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Hydrofhobic
Hydrofhobic
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In Japan: For commercial and research quantities contact: AZmax Co. Ltd. Tokyo Office Matsuda Yaesudori Bld F8 1-10-7 Hatchoubori, Chuo-Ku Tokyo 104-0032 Tel: 81-3-5543-1630 Fax: 81-3-5543-0312 e-mail: [email protected] on-line catalog: www.azmax.co.jp
In South-East Asia: For commercial and research quantities contact: Altus Technologies Pte Ltd 196 Pandan Loop #06-09 Pantech Industrial Complex Singapore 128384 Tel: (65) 6779 7666 Fax: (65) 6779-7555 www.altus.com.sg
Front Cover Photos: Water rolls off a ducks back. Lotus leaves exhibit superhydrophobicity. Biological systems are dependent on water, but at the same time must control the interaction. In a sense, all living organisms exhibit behaviors that can be described as both hydrophobic and hydrophilic.
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Hydrophobicity, Hydrophilicity
and Silane Surface Modification
TABLE OF CONTENTS
Silanes and Surface Modification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 Water, Hydrophobicity and Hydrophilicity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 Wettability and Contact Angle . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 Critical Surface Tension and Adhesion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 How does a Silane Modify a Surface? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 Selecting a Silane for Surface Modification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 Hydrophobic Surface Treatments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 Hydrophilic Surface Treatments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 Range of Water Interaction with Surfaces . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11 Reacting with the Substrate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Special Topics:
Dipodal Silanes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13 Linker Length. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14 Partition, Orientation and Self-Assembly in Bonded Phases . . . . . . . . . . . . . . . . . . . 15 Modification of Metal Substrates . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16 Difficult Substrates . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17 Applying a Silane Surface Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18 Hydrophobic Silane Selection Guide. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Silane Properties:
Hydrophobic Silanes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30 Hydrophobic Silanes - Dipodal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56 Hydrophobic Silanes - Polymeric . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59 Hydrophilic Silanes - Polar . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60 Hydrophilic Silanes - Hydrogen Bonding . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 62 Hydrophilic Silanes - Hydroxylic . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66 Hydrophilic Silanes - Ionic / Charge Inducible. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 67 Hydrophilic Silanes - Polymeric . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 70 Hydrophilic Silanes - Epoxy / Masked . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 71 Silyl Hydrides . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 72
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Property modifications include: Hydrophobicity Release Dielectric Absorption Orientation Hydrophilicity Charge Conduction
Applications include: Architectural Coatings Water-Repellents Anti-stiction Coatings for MEMs Mineral Surface Treatments Fillers for Composites Pigment Dispersants Dielectric Coatings Anti-fog Coatings Release Coatings Optical (LCD) Coatings Bonded Phases Self-Assembled Monolayers (SAMs) Crosslinkers for Silicones Nanoparticle Synthesis
In contrast with silanes utilized as coupling agents in adhesive applications, silanes used to modify the surface energy or wettability of substrates under normal conditions do not impart chemical reactivity to the substrate. They are often referred to as non-functional silanes. The main classes of silanes utilized to effect surface energy modification without imparting reactivity are: Hydrophobic Silanes Methyl Linear Alkyl Branched Alkyl Fluorinated Alkyl Aryl Dipodal Hydrophilic Silanes Polar Hydroxylic Ionic Charge inducible /charge switchable Embedded Hydrophilicity Masked
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Hydrogen Oxygen
This brief description of water is provided in order to give the insight that whenever a solid surface interacts with bulk water it is interacting with a soft matter structure, not simply a collection of individual molecules. Surface interactions with water must compete with a variety of internal interactions of liquid phase water: van der Waals forces, dipole interactions, hydrogen bonding and proton exchange.
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115 108-112 108 110 102-109 104 104 95-105 100 90-100 88-103 94 90 75-90 87 86 86-88 50-55 80-81 70-75 70 66 50-60 49 42-46 40 28-30 17 <15 <10
Hydrophobicpoor wetting
Hydrophilicgood wetting
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heptadecafluorodecyltrichlorosilane poly(tetrafluoroethylene) octadecyltrichlorosilane methyltrimethoxysilane nonafluorohexyltrimethoxysilane vinyltriethoxysilane paraffin wax ethyltrimethoxysilane propyltrimethoxysilane glass, soda-lime (wet) poly(chlorotrifluoroethylene) poly(propylene) poly(propylene oxide) polyethylene trifluoropropyltrimethoxysilane 3-(2-aminoethyl)-aminopropyltrimethoxysilane poly(styrene) p-tolyltrimethoxysilane cyanoethyltrimethoxysilane aminopropyltriethoxysilane polymethylmethacrylate polyvinylchloride phenyltrimethoxysilane chloropropyltrimethoxysilane mercaptopropyltrimethoxysilane glycidoxypropyltrimethoxysilane poly(ethyleneterephthalate) poly(ethylene oxide) copper (dry) aluminum (dry) iron (dry) nylon 6/6 glass, soda-lime (dry) silica, fused titanium dioxide (anatase) ferric oxide tin oxide
12.0 18.5 20-24 22.5 23.0 25 25.5 27.0 28.5 30.0 31.0 31.0 32 33.0 33.5 33.5 34 34 34 35 39 39 40.0 40.5 41 42.5 43 43-45 44 45 46 45-6 47 78 91 107 111
Note: Critical surface tensions for silanes refer to smooth treated surfaces.
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Hydrolysis Considerations
Water for hydrolysis may come from several sources. It may be added, it may be present on the substrate surface, or it may come from the atmosphere. The degree of polymerization of the silanes is determined by the amount of water available and the organic substituent. If the silane is added to water and has low solubility, a high degree of polymerization is favored. Multiple organic substitution, particularly if phenyl or tertiary butyl groups are involved, favors formation of stable monomeric silanols. The thickness of a polysiloxane layer is also determined by the concentration of the siloxane solution. Although a monolayer is generally desired, multilayer adsorption results from solutions customarily used. It has been calculated that deposition from a 0.25% silane solution onto glass could result in three to eight molecular layers. These multilayers could be either interconnected through a loose network structure, or intermixed, or both, and are, in fact, formed by most deposition techniques. The orientation of functional groups is generally horizontal, but not necessarily planar, on the surface of the substrate. The formation of covalent bonds to the surface proceeds with a certain amount of reversibility. As water is removed, generally by heating to 120C for 30 to 90 minutes or evacuation for 2 to 6 hours, bonds may form, break, and reform to relieve internal stress.
- CH3OH
H3C Si CH3 O
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OH
H O
H O H HO OH
H O
Factors influencing silane surface modification selection include: Concentration of surface hydroxyl groups Type of surface hydroxyl groups Hydrolytic Stability of the bond formed Physical dimensions of the substrate or substrate features Surface modification is maximized when silanes react with the substrate surface and present the maximum number of accessible sites with appropriate surface energies. An additional consideration is the physical and chemical properties of the interphase region. The interphase can promote or detract from total system properties depending on its physical properties such as modulus or chemical properties such as water/hydroxyl content. Hydroxyl-containing substrates vary widely in concentration and type of hydroxyl groups present. Freshly fused substrates stored under neutral conditions have a minimum number of hydroxyls. Hydrolytically derived oxides aged in moist air have significant amounts of physically adsorbed water which can interfere with coupling. Hydrogen bonded vicinal silanols react more readily with silane coupling agents, while isolated or free hydroxyls react reluctantly. Silanes with three alkoxy groups are the usual starting point for substrate modification. These materials tend to deposit as polymeric films, effecting total coverage and maximizing the introduction of organic functionality. They are the primary materials utilized in composites, adhesives, sealants, and coatings. Limitations intrinsic in the utilization of a polylayer deposition are significant for nano-particles or nano-composites where the interphase dimensions generated by polylayer deposition may approach those of the substrate. Residual (non-condensed) hydroxyl groups from alkoxysilanes can also interfere in activity. Monoalkoxy-silanes provide a frequently used alternative for nano-featured substrates since deposition is limited to a monolayer. If the hydrolytic stability of the oxane bond between the silane and the substrate is poor or the application is in an aggressive aqueous environment, dipodal silanes often exhibit substantial performance improvements. These materials form tighter networks and may offer up to 105x greater hydrolysis resistance making them particularly appropriate for primer applications.
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Water droplets on a (heptadecafluoro-1,1,2,2-tetrahydrodecyl)trimethoxysilane-treated silicon wafer exhibit high contact angles, indicative of the low surface energy. Surfaces are both hydrophobic and resist wetting by hydrocarbon oils. (water droplets contain dye for photographic purposes).
Amount of Silane
(minimum of monolayer coverage) 1.5% 1.0% 0.75% 0.1% or less
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Hydrophobicity is frequently associated with oleophilicity, the affinity of a substance for oils, since nonpolar organic substitution is often hydrocarbon in nature and shares structural similarities with many oils. The hydrophobic and oleophilic effect can be differentiated and controlled. At critical surface tensions of 20-30, surfaces are wetted by hydrocarbon oils and are water repellent. At critical surface tensions below 20, hydrocarbon oils no longer spread and the surfaces are both hydrophobic and oleophobic. The most oleophobic silane surface treatments have fluorinated long-chain alkyl silanes and methylated medium chain alkyl silanes. Superhydrophobic surfaces are those surfaces that present apparent contact angles that exceed the theoretical limit for smooth surfaces, i.e. >120. The most common examples of super-hydrophobicity are associated with surfaces that are rough on a sub-micron scale and contact angle measurements are composites of solid surface asperities and air denoted the Cassie state. Perfectly hydrophobic surfaces (contact angles of 180) have been prepared by hydrolytic deposition of methylchlorosilanes as microfibrillar structures.
Hydrophobicity vs W a t e r P e r m e a b i l i t y Although silane and silicone derived coatings are in general the most hydrophobic, they maintain a high degree of permeability to water vapor. This allows coatings to breathe and reduce deterioration at the coating interface associated with entrapped water. Since ions are not transported through non-polar silane and silicone coatings, they offer protection to composite structures ranging from pigmented coatings to rebar reinforced concrete.
Superhydrophobic Surface:
Cassie State
Automotive side windows are treated with fluoroalkylsilanes to provide self-cleaning properties. Water beads remove soil as they are blown over the glass substrate during acceleration.
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The selection of the class of hydrophilic subsitution is dependent on the application. If it is sufficient for water to spread evenly over a surface to form a thin film that washes away and dries off quickly without leaving 'drying spots', then a polar aprotic silane is preferred. If a coating is desired that reduces non-specific binding of proteins or other biofoulants, then a polar hydrogenbonding material such as a polyether functional silane is preferred. A very different application for a polar non-hydroxylic materials is thin film proton conduction electrolytes. Lubricious coatings are usually hydroxylic since they require a restrained adsorbed phase of water. Antistatic coatings are usually charged or charge-inducible as are ion-conductive coatings used in the construction of thin-film batteries. A combination of hydrophilicity and hydrophobicity may be a requirement in coatings which are used as primers or in selective adsorption applications such as chromatography. Formulation limitations may require that hydrophilicity is latent and becomes unmasked after application. Factors affecting the intrinsic hydrolytic stability of silane treated surfaces are magnified when the water is drawn directly into the interface. Even pure silicon dioxide is ultimately soluble in water (at a level of 2-6ppm), but the kinetics, low concentration for saturation and phase separation, make this a negligible consideration in most applications. The equilibrium constant for the rupture of a Si-O-Si bond by water to two Si-OH bonds is estimated at 10 -3. Since at minimum 3 Si-O-Si bonds must be simultaneously broken under equilibrium conditions to dissociate an organosilane from a surface, in hydrophobic environments the long-term stability is a minor consideration. Depending on the conditions of exposure to water of a hydrophilic coating, the long-term stability can be an important consideration. Selection of a dipodal, polypodal or other network forming silane as the basis for inducing hydrophilicity or as a component in the hydrophilic surface treatment is often obligatory.
description
superhydrophobic oleophobic lipophobic oleophilic lipophilic hydrophobic polar hydrophilic hygroscopic hydrogel film
surface example
fluorocarbon
measurement parameter
contact angle
water-sliding angle critical surface tension heat of immersion water activity equilibrium water absorption swell
moderate
strong
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Advantage
reactive, volatile byproduct reactive, volatile byproduct volatile moderate reactivity, neutral byproduct low toxicity
Disadvantage
toxic
hydrogen chloride
corrosive
ethoxy
lower reactivity
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Special Topics
Dipodal Silanes
Functional dipodal silanes and combinations of nonfunctional dipodal silanes with functional silanes have significant impact on substrate bonding, hydrolytic stability and mechanical strength of many composites systems. They possess enabling activity in many coatings, particularly primer systems and aqueous immersion applications. The effect is thought to be a result of both the increased crosslink density of the interphase and a consequence of the fact that the resistance to hydrolysis of dipodal materials (with the ability to form six bonds to a substrate) is estimated at close to 100,000 times greater than conventional coupling agents (with the ability to form only three bonds to a substrate). Both because dipodal silanes may not have functional groups identical to conventional coupling agents or because of economic considerations, conventional coupling agents are frequently used in combination with a non-functional dipodal silanes. In a typical application a dipodal material such as bis(triethoxysilyl)ethane (SIB1817.0) is combined at a 1:5 to 1:10 ratio with a traditional coupling agent. It is then processed in the same way as the traditional silane coupling agent.
Effect of dipodal -SiCH2CH2Si- on the bond strength of a crosslinkable ethylene-vinyl acetate primer formulation Wet adhesion to metals (N/cm) Primer on metal 10% in i-PrOH No silane Methacryloxypropylsilane Methacryloxypropylsilane + 10% dipodal Titanium Nil 0.25 10.75 Cold-rolled steel Nil 7.0 28.0 (cohesive failure)
H N CH2 CH2 CH2 CH2 CH2 CH2 (CH3O)3Si Si(OCH 3)3 SIB1833.0
Multilayer printed circuit boards use dipodal silanes to maintain the integrity of the bond between metal and resins by reducing interfacial water adsorption.
Si(OC2H5)3
SIB1831.0
N CH2CH2 N
(C2H5O)3Si
H C C CH2
CH2
CH2 CH2
CH2 CH2
Hydrophobic coatings applied to antennas inhibit the formation of adsorbed water layers which become dielectric layers that absorb signals and cause high losses. If the water is in beads, the energy will be slightly diffracted because the water droplets have dimensions much less than a wavelength at these frequencies.
Si(OC H )
(C2H5O)3Si
SB1820..0 SIB1142.0
SIB1824.6 SIB1824.82
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Linker Length
An important factor in controlling the effectiveness and properties of a coupled system is the linker between the organic functionality and the silicon atom. The linker length imposes a number of physical property and reactivity limitations. The desirability of maintaining the reactive centers close to the substrate are most important in sensor applications, in heterogeneous catalysis, fluorescent materials and composite systems in which the interfacing components are closely matched in modulus and coefficient of thermal expansion. On the other hand, inorganic surfaces can impose enormous steric constraints on the accessibility of organic functional groups in close proximity. If the linker length is long the functional group has greater mobility and can extend further from the inorganic substrate. This has important consequences if the functional group is expected to react with a single component in a multi-component organic or aqueous phases found in homogeneous and phase transfer catalysis, biological diagnostics or liquid chromatography. Extended linker length is also important in oriented applications such as self-assembled monolayers (SAMs). The typical linker length is three carbon atoms, a consequence of the fact that the propyl group is synthetically accessible and has good thermal stability. Silanes with short linker length
CH3 CH3 Cl
H3C Si O Si Cl Cl
OCH 2CH3 N C CH2CH2 Si OCH 2CH3 OCH 2CH3
SIT8572.6
SIH5925.0
Cl N C CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2
OCH 3
Si Cl Cl
SIC2445.0 SIC2456.3
Cl
SIH6175.0
CH2CH2CH2CH2 Si Cl Cl
SIP6724.9
Cl
SIA0055.0
CH3OCH 2CH2O
CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2CH2
Si Cl Cl
SIM6491.5
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A Self-Assembled Monolayer (SAM) is a one molecule thick layer of material that bonds to a surface in an ordered way as a result of physical or chemical forces during a deposition process. Silanes can form SAMs by solution or vapor phase deposition processes. Most commonly, chlorosilanes or alkoxysilanes are used and once deposition occurs a chemical (oxane) bond forms with the surface rendering a permanent modification of the substrate. Applications for SAMs include micro-contact printing, N-METHYLAMINOPROPYLTRIMETHOXYSILANE (SIM6500.0) soft lithography, dip-pen nanolithography, anti-stiction coatings and orientation layers involved in nanofabrication of MEMs, fluidic microassemblies, semiconductor sensors and memory devices. Common long chain alkyl silanes used in the formation of SAMs are simple hydrocarbon, fluoroalkyl and end-group substituted silanes. Silanes with one hydrolyzeable group maintain interphase structure after deposition by forming a single oxane bond with the subF. Kahn., Appl. Phys. Lett. 22, 386, 1973 strate. Silanes with three hydrolyzeable groups form Micro-Contact Printing Using SAMs siloxane (silsesquioxane) polymers after deposition, bonding both with each other as spin casting of sol-gel precursor well as the substrate. For non-oxide metal and soft bake PDMS substrates, silyl hydrides may be used, reactinked with solution ing with the substrate by a dehydrogenative amorphous oxide of C18-Silane in hexane Substrate Substrate coupling. The perpendicular orientation of silanes microcontact printing of C18-Silane polishing and crystallization with C10 or greater length can be utilized in micro-contact printing and other soft lithogSAMs of C18-Silane crystallization oxide Substrate (2-3nm) raphy methods. Here the silane may effect a Substrate simple differential adsorption, or if functionalized have a direct sensor effect.
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figure courtesy of
M. Banaszak-Holl
Metals that form stable hydrides, e.g. titanium, zirconium, nickel. In a significant departure from traditional silane coupling agent chemistry, the ability of certain metals to form so-called amorphous alloys with hydrogen is exploited in an analogous chemistry in which hydride functional silanes adsorb and then coordinate with the surface of the metal. Most silanes of this class possess only simple hydrocarbon substitution such as octylsilane. However they do offer organic compatibility and serve to markedly change wet-out of the substrate. Both hydride functional silanes and treated metal substrates will liberate hydrogen in the presence of base or with certain precious metals such as platinum and associated precautions must be taken.
(see p72.)
Coupling Agents for Metals* Metal Copper Gold Class Amine Sulfur Phosphorus Amine Sulfur Amine Screening Candidates SSP-060 SIT7908.0 SID4558.0 SIB1834.0 SIB1824.6 SIB1835.5 SIG5840.0 SIU9048.0 SSP-060 SIT8402.0 SIE6668.0 SIT8398.0 SIP6926.2 SIB1091.0 WSA-7011 SIM6476.0
Iron
Tin
OCH 3
OCH 3
SIT8398.0 SIT8192.6
*These coupling agents are almost always used in conjunction with a second silane with organic reactivity or a dipodal silane.
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Difficult Substrates
Silane coupling agents are generally recommended for applications in which an inorganic surface has hydroxyl groups and the hydroxyl groups can be converted to stable oxane bonds by reaction with the silane. Substrates such as calcium carbonate, copper and ferrous alloys, and high phosphate and sodium glasses are not recommended substrates for silane coupling agents. In cases where a more appropriate technology is not available a number of strategies have been devised which exploit the organic functionality, film-forming and crosslinking properties of silane coupling agents as the primary mechanism for substrate bonding in place of bonding through the silicon atom. These approaches frequently involve two or more coupling agents. Calcium carbonate fillers and marble substrates do not form stable bonds with silane coupling agents. Applications of mixed silane systems containing a dipodal silane or tetraethoxysilane in combination with an organofunctional silane frequently increases adhesion. The adhesive mechanism is thought to be due to the low molecular weight and low surface energy of the silanes which allows them initially to spread to thin films and penetrate porous structures followed by the crosslinking which results in the formation of a silica-rich encapsulating network. The silica-rich encapsulating network is then susceptible to coupling chemistry comparable to siliceous substrates. Marble and calciferous substrates can also benefit from the inclusion of anhydride-functional silanes which, under reaction conditions, form dicarboxylates that can form salts with calcium ions. Metals and many metal oxides can strongly adsorb silanes if a chelating functionality such as diamine or dicarboxylate is present. A second organofunctional silane with reactivity appropriate to the organic component must be present. Precious metals such as gold and rhodium form weak coordination bonds with phosphine and mercaptan functional silanes. High phosphate and sodium content glasses are frequently the most frustrating substrates. The primary inorganic constituent is silica and would be expected to react readily with silane coupling agents. However alkali metals and phosphates not only do not form hydrolytically stable bonds with silicon, but, even worse, catalyze the rupture and redistribution of silicon-oxygen bonds. The first step in coupling with these substrates is the removal of ions from the surface by extraction with deionized water. Hydrophobic dipodal or multipodal silanes are usually used in combination with organofunctional silanes. In some cases polymeric silanes with multiple sites for interaction with the substrate are used. Some of these, such as the polyethylenimine functional silanes can couple to high sodium glasses in an aqueous environment.
OH O
+
O Ca
- +
Na
Substrates with low concentrations of non-hydrogen bonded hydroxyl groups, high concentrations of calcium, alkali metals or phosphates pose challenges for silane coupling agents.
Removing Surface Impurities Eliminating non-bonding metal ions such as sodium, potassium and calcium from the surface of substrates can be critical for stable bonds. Substrate selection can be essential. Colloidal silicas derived from tetraethoxysilane or ammonia sols perform far better than those derived from sodium sols. Bulk glass tends to concentrate impurities on the surface during fabrication. Although sodium concentrations derived from bulk analysis may seem acceptable, the surface concentration is frequently orders of magnitude higher. Surface impurities may be reduced by immersion in 5% hydrochloric acid for 4 hours, followed by a deionized water rinse, and then immersion in deionized water overnight followed by drying. Oxides with high isoelectric points can adsorb carbon dioxide, forming carbonates. These can usually be removed by a high temperature vacuum bake.
Increasing Hydroxyl Concentration Hydroxyl functionalization of bulk silica and glass may be increased by immersion in a 1:1 mixture of 50% aqueous sulfuric acid : 30% hydrogen peroxide for 30 minutes followed by rinses in D.I. water and methanol and then air drying. Alternately, if sodium ion contamination is not critical, boiling with 5% aqueous sodium peroxodisulfate followed by acetone rinse is recommended1.
1. K. Shirai et al, J. Biomed. Mater. Res. 53, 204, 2000.
Catalyzing Reactions in Water-Free Environments Hydroxyl groups without hydrogen bonding react slowly with methoxy silanes at room temperature. Ethoxy silanes are essentially non-reactive. The methods for enhancing reactivity include transesterification catalysts and agents which increase the acidity of hydroxyl groups on the substrate by hydrogen bonding. Transesterification catalysts include tin compounds such as dibutyldiacetoxytin and titanates such as titanium isopropoxide. Incorporation of transesterification catalysts at 2-3 weight % of the silane effectively promotes reaction and deposition in many instances. Alternatively, amines can be premixed with solvents at 0.01-0.5 weight % based on substrate prior or concurrent to silane addition. Volatile primary amines such as butylamine can be used, but are not as effective as tertiary amines such as benzyldimethylamine or diamines such as ethylenediamine. The more effective amines, however, are more difficult to remove after reaction1.
1. S. Kanan et al, Langmuir, 18, 6623, 2002.
Hydroxylation by Water Plasma & Steam Oxidation Various metals and metal oxides including silicon and silicon dioxide can achieve high surface concentrations of hydroxyl groups after exposure to H2O/O2 in high energy environments including steam at 1050 and water plasma1.
1. N. Alcanter et al, in Fundamental & Applied Aspects of Chemically Modified Surfaces ed. J. Blitz et al, 1999, Roy. Soc. Chem., p212.
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Gelest, Inc.
Applying Silanes
Deposition from aqueous alcohol solutions is the most facile method for Fig. 1 Reactor for slurry preparing silylated surfaces. A 95% ethanol-5% water solution is adjusted to treatment of powders. Separate filtration and pH 4.5-5.5 with acetic acid. Silane is added with stirring to yield a 2% final concentration. Five minutes should be allowed for hydrolysis and silanol for- drying steps are required. mation. Large objects, e.g. glass plates, are dipped into the solution, agitated gently, and removed after 1-2 minutes. They are rinsed free of excess materials by dipping briefly in ethanol. Particles, e.g. fillers and supports, are silylated by stirring them in solution for 2-3 minutes and then decanting the solution. The particles are usually rinsed twice briefly with ethanol. Cure of the silane layer is for 5-10 mins at 110C or 24 hours at room temperature (<60% relative humidity). Deposition from aqueous solution is employed for most commercial fiberglass systems. The alkoxysilane is dissolved at 0.5-2.0% concentration in water. For less soluble silanes, 0.1% of a nonionic surfactant is added prior to the silane and an emulsion rather than a solution is prepared. The solution is adjusted to pH 5.5 with acetic acid. The solution is either sprayed onto the substrate or employed as a dip bath. Cure is at 110-120C for 20-30 minutes. Stability of aqueous silane solutions varies from 2-12 hours for the simple alkyl silanes. Poor solubility parameters limit the use of long chain alkyl and aromatic silanes by this method. Distilled water is not necessary, but water containing fluoride ions must be avoided. Bulk deposition onto powders, e.g. filler treatment, is usually accomplished by a spray-on method. It assumes that the total Fig. 2 Vacuum tumble amount of silane necessary is known and that sufficient adsorbed dryers can be used for moisture is present on the filler to cause hydrolysis of the silane. slurry treatment of The silane is prepared as a 25% solution in alcohol. The powder is powders. placed in a high intensity solid mixer, e.g. twin cone mixer with intensifier. The methods are most effective. If the filler is dried in trays, care must be taken to avoid wicking or skinning of the top layer of treated material by adjusting heat and air flow. Integral blend methods are used in composite formulations. In this method the silane is used as a simple additive. Composites can be prepared by the addition of alkoxysilanes to dry-blends of polymer and filler prior to compounding. Generally 0.2 to 1.0 weight percent of silane (of the total mix) is dispersed by spraying the silane in an alcohol carrier onto a preblend. The addition of the silane to non-dispersed filler is not desirable in this technique since it can lead to agglomeration. The mix is dry-blended briefly and then melt compounded. Vacuum devolatization of byproducts of silane reaction during melt compounding is necessary to achieve optimum properties. Properties are sometimes enhanced by adding 0.5-1.0% of tetrabutyl titanate or benzyldimethylamine to the silane prior to dispersal. Anhydrous liquid phase deposition of chlorosilanes, methoxysilanes, aminosilanes and cyclic azasilanes is preferred for small particles and nano-featured substrates. Toluene, tetrahydrofuran or hydrocarbon solutions are prepared containing 5% silane. The mixture is refluxed for 12-24 hours with the substrate to be treated. It is washed with the solvent. The solvent is then removed by air or explosion-proof oven drying. No further cure is necessary. This reaction involves a direct nucleophilic displacement of the silane chlorines by the surface silanol. If monolayer deposition is desired, substrates should be predried at 150C for 4 hours. Bulk deposition results if adsorbed water is present on the substrate. This method is cumbersome for large scale preparations and rigorous controls must be established to ensure reproducible results. More reproducible coverage is obtained with monochlorosilanes. Chlorosilanes can also be deposited from alcohol solution. Anhydrous alcohols, particularly ethanol or isopropanol are preferred. The chlorosilane is added to the alcohol to yield a 2-5% solution. The chlorosilane reacts with the alcohol producing an alkoxysilane and HCl. Progress of the reaction is observed by halt of HCl evolution. Mild warming of the solution (30-40C) promotes completion of the reaction. Part of the HCl reacts with the alcohol to produce small quantities of alkyl halide and water. The water causes formation of silanols from alkoxysilanes. The silanols condense on the substrate. Treated substrates are cured for 5-10 mins. at 110C or allowed to stand 24 hours at room temperature. PLEASE INQUIRE ABOUT BULK QUANTITIES
18
Fig. 3 Twin-cone blenders with intensive mixing bars are used for bulk deposition of silanes onto powders.
Gelest, Inc.
Applying Silanes
Vapor Phase Deposition Silanes can be applied to substrates under dry aprotic conditions by chemical vapor deposition methods. These methods favor monolayer deposition. Although under proper conditions almost all silanes can be applied to substrates in the vapor phase, those with vapor pressures >5 torr at 100C have achieved the greatest number of commercial applications. In closed chamber designs, substrates are supported above or adjacent to a silane reservoir and the reservoir is heated to sufficient temperature to achieve 5mm vapor pressure. Alternatively, vacuum can be applied until silane evaporation is observed. In still another variation the silane can be prepared as a solution in toluene, and the toluene brought to reflux allowing sufficient silane to enter the vapor phase through partial pressure contribution. In general, substrate temperature should be maintained above 50 and below 120 to promote reaction. Cyclic azasilanes deposit the quickestusually less than 5 minutes. Amine functional silanes usually deposit rapidly (within 30 minutes) without a catalyst. The reaction of other silanes requires extended reaction times, usually 4-24 hours. The reaction can be promoted by addition of catalytic amounts of amines. Spin-On Spin-On applications can be made under hydrolytic conditions which favor maximum functionalization and polylayer deposition or dry conditions which favor monolayer deposition. For hydrolytic deposition 2-5% solutions are prepared (see deposition from aqueous alcohol). Spin speed is low, typically 500 rpm. Following spin-deposition a hold period of 3-15 minutes is required before rinse solvent. Dry deposition employs solvent solutions such as methoxypropanol or ethyleneglycol monoacetate (EGMA). Aprotic systems utilize toluene or THF. Silane solutions are applied at low speed under a nitrogen purge. If strict monolayer deposition is preferred, the substrate should be heated to 50. In some protocols, limited polylayer formation is induced by spinning under an atmospheric ambient with 55% relative humidity. Spray application Formulations for spray applications vary widely depending on end-use. They involve alcohol solutions and continuously hydrolyzed aqueous solutions employed in architectural and masonry applications. The continuous hydrolysis is effected by feeding mixtures of silane containing an acid catalyst such as acetic acid into a water stream by means of a venturi (aspirator). Stable aqueous solutions (see water-borne silanes), mixtures of silanes with limited stability (4-8 hours) and emulsions are utilized in textile and fiberglass applications. Complex mixtures with polyvinyl acetates or polyesters enter into the latter applications as sizing formulations.
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Gelest, Inc.
Methyl-Silanes very hydrophobic, hydrolysates stable to 425C, acceptable performance to 600C reported, volatile
3 Hydrolyzeable Groups
Hydrolyzeable Groups chloro methoxy ethoxy propoxy methoxyalkoxy acetoxy dimethylamine other amine silazane (NH) oxime Product Code SIM6520.0 SIM6560.0 SIM6555.0 SIM6579.0 SIM6585.0 SIM6519.0 SIT8712.0 SIT8710.0 SIM6590.0 Product Name methyltrichlorosilane methyltrimethoxysilane methyltriethoxysilane methyltri-n-propoxysilane methyltris(methoxyethoxy)silane methyltriacetoxysilane tris(dimethylamino)methylsilane tris(cyclohexylamino)methylsilane methyltris(methylethylketoximino)silane
Methyl-SiloxanylSilanes
3 Hydrolyzeable Groups
Hydrolyzeable Groups Product Code SIT8572.6 Product Name trimethylsiloxytrichlorosilane
2 silicon atom compounds chloro ethoxy acetoxy 3 silicon atom compounds chloro methoxy ethoxy chloro oligomeric polysiloxanes chloro methoxy ethoxy amine/silazane silanol selected specialties
SID4236.0
dimethyltetramethoxydisiloxane
Gelest, Inc.
2 Hydrolyzeable Groups
Product Code SID4120.0 SID4123.0 SID4121.0 SID4076.0 SIB1072.0 SIB1068.0 SIH6102.0 Product Name dimethyldichlorosilane dimethyldimethoxysilane dimethyldiethoxysilane dimethyldiacetoxysilane bis(dimethylamino)dimethylsilane bis(diethylamino)dimethylsilane hexamethylcyclotrisilazane
1 Hydrolyzeable Group
Product Code SIT8510.0 SIT8566.0 SIT8515.0 SIT8568.0 SIM6492.8 SIA0110.0 SID3605.0 SID3398.0 SIH6110.0 Product Name trimethylchlorosilane trimethylmethoxysilane trimethylethoxysilane trimethyl-n-propoxysilane methoxypropoxytrimethylsilane acetoxytrimethylsilane dimethylaminotrimethylsilane diethylaminotrimethylsilane hexamethyldisilazane
2 Hydrolyzeable Groups
Product Code SID3372.0 SIT7534.0 Product Name dichlorotetramethyldisiloxane tetramethyldiethoxydisiloxane
1 Hydrolyzeable Group
Product Code Product Name
SIP6717.0
pentamethylacetoxydisiloxane
dichlorohexamethyltrisiloxane SIB1843.0 1,5-diethoxyhexamethyltrisiloxane bis(trimethylsiloxy)dichlorosilane chlorine terminated polydimethylsiloxane methoxy terminated polydimethylsiloxane ethoxy terminated polydimethylsiloxane dimethylamine terminated polydimethylsiloxane silanol terminated polydimethylsiloxane SID4125.0 SIT8719.5
Space Shuttle tiles are treated with dimethylethoxysilane to reduce water absorption.
bis(trimethylsiloxy)methylmethoxysilane
dimethylethoxysilane [tris(trimethylsiloxy)silylethyl]dimethylchlorosilane
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21
Gelest, Inc.
3 Hydrolyzeable Groups
Hydrolyzeable Groups
C2
Product Code
Product Name
C3
C4
C5
C6
C7 C8
C10
C11 C12
C14 C16
C18
hydrophobic, treatment for microporous mineral powders used as fillers for plastics chloro SIE4901.0 ethyltrichlorosilane methoxy SIE4901.4 ethyltrimethoxysilane ethoxy SIE4901.2 ethyltriethoxysilane acetoxy SIE4899.0 ethyltriacetoxysilane hydrophobic, treatment for microporous mineral powders used as fillers for plastics chloro SIP6915.0 propyltrichlorosilane methoxy SIP6918.0 propyltrimethoxysilane ethoxy SIP6917.0 propyltriethoxysilane amine/silazane moderate hydrophobicity, penetrates microporous structures, minimal organic compatibility chloro SIB1982.0 n-butyltrichlorosilane methoxy SIB1988.0 n-butyltrimethoxysilane amine/silazane moderate hydrophobicity with minimal organic compatibility chloro SIP6720.0 pentyltrichlorosilane ethoxy SIP6720.2 pentyltriethoxysilane moderate hydrophobicity with moderate organic compatibility chloro SIH6167.0 hexyltrichlorosilane methoxy SIH6168.5 hexyltrimethoxysilane ethoxy SIH6167.5 hexyltriethoxysilane moderate hydrophobicity with moderate organic compatibility chloro SIH5846.0 heptyltrichlorosilane hydrophobic with moderate organic compatibility - generally most economical chloro SIO6713.0 octyltrichlorosilane methoxy SIO6715.5 octyltrimethoxysilane ethoxy SIO6715.0 octyltriethoxysilane amine silazane (NH) hydrophobic, concentrates on surface of microporous structures chloro SID2663.0 decyltrichlorosilane ethoxy SID2665.0 decyltriethoxysilane hydrophobic, concentrates on surface of microporous structures, forms SAMs chloro SIU9050.0 undecyltrichlorosilane hydrophobic, concentrates on surface of microporous structures, forms SAMs chloro SID4630.0 dodecyltrichlorosilane ethoxy SID4632.0 dodecyltriethoxysilane hydrophobic, concentrates on surface of microporous structures, forms SAMs chloro SIT7093.0 tetradecyltrichlorosilane forms hydrophobic and oleophilic coatings, liquid a room temperature, forms SAMs chloro SIH5920.0 hexadecyltrichlorosilane methoxy SIH5925.0 hexadecyltrimethoxysilane ethoxy SIH5922.0 hexadecyltriethoxysilane forms hydrophobic and oleophilic coatings allowing full miscibility with parafinic materials, forms SAMs chloro SIO6640.0 octadecyltrichlorosilane methoxy SIO6645.0 octadecyltrimethoxysilane ethoxy SIO6642.0 octadecyltriethoxysilane amine proprietary SIS6952.0/PPI-GC18 Siliclad/Glassclad 18 forms hydrophobic and oleophilic coatings, solid at room temperature chloro SIE4661.0 eicosyltrichlorosilane forms hydrophobic and oleophilic coatings, solid at room temperature chloro SID4621.0 docosyltrichlorosilane blend forms hydrophobic and oleophilic coatings, solid at room temperature chloro SIT8048.0 triacontyltrichlorosilane blend
22
Gelest, Inc.
2 Hydrolyzeable Groups
Product Code
SIE4896.0
1 Hydrolyzeable Group
Product Code
SIE4892.0
Product Name
ethylmethyldichlorosilane
Product Name
ethyldimethylchlorosilane
SIP6912.0 SIP6914.0
propylmethyldichlorosilane propylmethyldimethoxysilane
Long chain alkylsilanes are processing additives for crosslinked polyethylene (XLPE) used in wire and cable.
SIH6165.6
hexylmethyldichlorosilane
heptylmethyldichlorosilane octylmethyldichlorosilane octylmethyldiethoxysilane SIO6711.3 SID4404.0 octyldimethyl(dimethylamino)silane dioctyltetramethyldisilazane decyldimethylchlorosilane SIO6711.0 SIO6711.1 octyldimethylchlorosilane octyldimethylmethoxysilane
SID2662.0
decylmethyldichlorosilane
SID2660.0
SID4628.0 SID4629.0
dodecylmethyldichlorosilane dodecylmethyldiethoxysilane
SID4627.0
dodecyldimethylchlorosilane
Surface conductivity of glass substrates is reduced by application of hydrophobic coatings. Surface arc-tracking is eliminated on fluorescent light bulbs.
Control d 18 Glasscla
SID4620.0
23
Gelest, Inc.
3 Hydrolyzeable Groups
Hydrolyzeable Groups Product Code Product Name
C3
chloro
C4
chloro methoxy ethoxy chloro SII6453.0 SII6453.7 SII6453.5 SIB1985.0 SIC2555.0 SIC2557.0 SID4069.0 SIT7906.6 SIC2480.0 SIC2482.0 SIB0997.0 SIC2470.0 SII6457.0 SII6458.0 SIC2490.0 isobutyltrichlorosilane isobutyltrimethoxysilane isobutyltriethoxysilane t-butyltrichlorosilane cyclopentyltrichlorosilane cyclopentyltrimethoxysilane (3,3-dimethylbutyl)trichlorosilane thexyltrichlorosilane cyclohexyltrichlorosilane cyclohexyltrimethoxysilane bicycloheptyltrichlorosilane (cyclohexylmethyl)trichlorosilane isooctyltrichlorosilane isooctyltrimethoxysilane cyclooctyltrichlorosilane
C5
chloro methoxy
C6
chloro chloro chloro methoxy
C7 C8
C10 C12
SIA0325.0 adamantylethyltrichlorosilane 7-(trichlorosilylmethyl)pentadecane (di-n-octylmethylsilyl)ethyltrichlorosilane
C16
SIT8162.4
C18 C24
SID4401.5
C28
chloro SIT8162.0 13-(trichlorosilylmethyl)heptacosane
24
Gelest, Inc.
2 Hydrolyzeable Groups
Product Code
SII6463.0
1 Hydrolyzeable Group
Product Code
SII6462.0 SII6452.5
Product Name
isopropylmethyldichlorosilane
Product Name
isopropyldimethylchlorosilane isobutyldimethylchlorosilane
SII6452.8 SIB1972.2
SIC2468.0 SIC2469.0
cyclohexylmethyldichlorosilane cyclohexylmethyldimethoxysilane
SIB0994.0
bicycloheptyldimethylchlorosilane
SII6456.6
isooctyldimethylchlorosilane
SID4074.0
(dimethylchlorosilyl)methylpinane
25
Gelest, Inc.
3 Hydrolyzeable Groups
Hydrolyzeable Groups
spacer atoms = 0 chloro methoxy ethoxy acetoxy oxime/amine spacer atoms = 1 chloro ethoxy chloro spacer atoms = 2 chloro methoxy amine/silazane spacer atoms = 3 chloro spacer atoms = 4 chloro chloro spacer atoms > 4 chloro chloro SIP6736.4 SIP6723.4 phenoxyundecyltrichlorosilane phenylhexyltrichlorosilane SIP6724.9 SIP6723.3 4-phenylbutyltrichlorosilane phenoxypropyltrichlorosilane SIP6722.0 SIP6722.6 phenethyltrichlorosilane phenethyltrimethoxysilane SIB0970.0 SIB0971.0 SIP6813.0 benzyltrichlorosilane benzyltriethoxysilane 1-phenyl-1-trichlorosilylbutane SIP6810.0 SIP6822.0 SIP6821.0 SIP6790.0 SIP6826.5 phenyltrichlorosilane phenyltrimethoxysilane phenyltriethoxysilane phenyltriacetoxysilane phenyltris(methylethylketoximino)silane
Product Code
Product Name
Napthyl-Silanes
methoxy chloro SIN6597.0 SIN6596.0 1-napthyltrimethoxysilane (1-napthylmethyl)trichlorosilane
Gelest, Inc.
2 Hydrolyzeable Groups
Product Code
SIP6738.0 SIP6740.0 SIP6739.0 SIP6736.8
1 Hydrolyzeable Group
Product Code
SIP6728.0 SIP6728.4
Product Name
phenylmethyldichlorosilane phenylmethyldimethoxysilane phenylmethyldiethoxysilane phenylmethylbis(dimethylamino)silane
Product Name
phenyldimethylchlorosilane phenyldimethylethoxysilane
SIB0962.0 SIP6738.5 SIP6721.5 1-phenyl-1-methyldichlorosilylbutane phenethylmethyldichlorosilane SP6721.0 SIP6721.2 SIP6744.0 SIP6724.8 SIP6723.25 (3-phenylpropyl)methyldichlorosilane 4-phenylbutylmethyldichlorosilane phenoxypropylmethyldichlorosilane SIP6743.0 SIP6724.7 SIP6723.2
benzyldimethylchlorosilane
SIT8035.0
p-tolylmethydichlorosilane
SIT8030.0
p-tolyldimethylchlorosilane
SIM6511.0
SIM6492.4
3-(p-methoxyphenyl)propylmethyldichlorosilane
SIP6723.0 SIN6598.0
m-phenoxyphenyldimethylchlorosilane p-nonylphenoxypropyldimethylchlorosilane
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27
Gelest, Inc.
3 Hydrolyzeable Groups
Hydrolyzeable Groups Product Code
SIT8371.0 SIT8372.0
Product Name
(3,3,3-trifluoropropyl)trichlorosilane (3,3,3-trifluoropropyl)trimethoxysilane
C3
chloro methoxy amine/silazane
C6
chloro methoxy ethoxy amino SIN6597.6 SIN6597.7 SIN6597.65 SIN6597.4 SIT8174.0 SIT8176.0 SIT8175.0 SIH5841.0 SIH5841.5 SIH5841.2 nonafluorohexyltrichlorosilane nonafluorohexyltrimethoxysilane nonafluorohexyltriethoxysilane nonafluorohexyltris(dimethylamino)silane (tridecafluoro-1,1,2,2-tetrahydrooctyl)trichlorosilane (tridecafluoro-1,1,2,2-tetrahydrooctyl)trimethoxysilane (tridecafluoro-1,1,2,2-tetrahydrooctyl)triethoxysilane (heptadecafluoro-1,1,2,2-tetrahydrodecyl)trichlorosilane (heptadecafluoro-1,1,2,2-tetrahydrodecyl)trimethoxysilane (heptadecafluoro-1,1,2,2-tetrahydrodecyl)triethoxysilane
C8
chloro methoxy ethoxy
C10
chloro methoxy ethoxy
DiAlkyl Silanes
2 Hydrolyzeable Groups
Highest Carbon # Next Carbon # Hydrolyzeable Groups
chloro ethoxy
Product Code
SID3402.0 SID3404.0 SID3537.0 SID3538,0 SID3203.0 SID3214.0 SID3530.0 SID3528.0 SII6452.6 SID3390.0 SID3391.0 SID3510.0 SID3382.0 SID4400.0
Product Name
diethyldichlorosilane diethyldiethoxysilane diisopropyldichlorosilane diisopropyldimethoxysilane di-n-butyldichlorosilane di-n-butyldimethoxysilane diisobutyldimethoxysilane diisobutyldiethoxysilane isobutylisopropyldimethoxysilane dicyclopentyldichlorosilane dicyclopentyldimethoxysilane di-n-hexyldichlorosilane dicyclohexyldichlorosilane di-n-octyldichlorosilane
C2 C3 C4
C2 C3
chloro methoxy
C4
chloro methoxy methoxy ethoxy
C4 C5
C3
methoxy
C5
chloro methoxy
C6
C6
chloro chloro
C8
C8
chloro
28
Gelest, Inc.
2 Hydrolyzeable Groups
Product Code Product Name
SIT8369.0 SIT8370.0 (3,3,3-trifluoropropyl)methyldichlorosilane (3,3,3-trifluoropropyl)methyldimethoxysilane
1 Hydrolyzeable Group
Product Code
SIT8364.0 SIB1828.4
Product Name
(3,3,3-trifluoropropyl)dimethylchlorosilane bis(trifluoropropyl)tetramethyldisilazane nonafluorohexyldimethylchlorosilane
SIN6597.5
nonafluorohexylmethyldichlorosilane
SIN6597.3
SIT8172.0
(tridecafluoro-1,1,2,2-tetrahydrooctyl)methyldichlorosilane
SIT8170.0
(tridecafluoro-1,1,2,2-tetrahydrooctyl)dimethylchlorosilane
SH5840.6
(heptadecafluoro-1,1,2,2-tetrahydrodecyl)methyldichlorosilane
SIH5840.4
(heptadecafluoro-1,1,2,2-tetrahydrodecyl)dimethylchlorosilane
Pigments treated with hydrophobic silanes resist agglomeration in highly polar vehicle and film-forming compositions such as those used in nail polish.
29
Gelest, Inc.
bp/mm (mp)
D420
0.891
nD20
1.3890
HYDROLYTIC SENSITIVITY: 4 no reaction under neutral conditions TSCA HMIS: 3-4-1-X 25g/$11.00
135/3 (36-7)mp flashpoint: 155C (310F) forms silica bonded phases for reverse phase chromatography1. 1. Yang et al, Anal. Chem., 59, 2750, 1988
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-1-1-X 5.0g/$73.00
297.73
[37843-11-1]
CH 3 CH 2Si Cl CH 3
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 10g/$43.00
50g/$172.00
Cl CH2Si Cl Cl
OC 2H 5 CH 2Si OC 2H 5 OC 2H 5
225.58 140-2/10 1.288 1.527 TOXICITY- oral rat, LD50: 2830mg/kg flashpoint: 87C (189F) 100g/$152.00 0.986 1.462825
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 25g/$47.00
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-1-0-X 10g/$39.00
Si(CH 3)2Cl
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 25g/$68.00
SiCl 3
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 10g/$31.00
(C2H5)2N Si (C2H5)2N
CH3 CH3
SIB1068.0 BIS(DIETHYLAMINO)DIMETHYLSILANE 202.42 192-5 flashpoint: 35C (95F) C10H26N2Si silylates diamines to cyclic diaminosilanes1. 1. E. Schwartz et al, J. Org. Chem., 50, 5469, 1985. [4669-59-4]
HYDROLYTIC SENSITIVITY: 8 Si-NR reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-3-1-X 50g/$127.00
(CH3)2N Si (CH3)2N
CH3 CH3
146.31
0.810
1.416922
HYDROLYTIC SENSITIVITY: 8 Si-NR reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-4-1-X 25g/$23.00
50g/$148.00
30
Gelest, Inc.
name
SIB1837.0 BIS(TRIMETHYLSILOXY)DICHLOROSILANE
CH3
MW
bp/mm (mp)
D420
nD20
Cl Si Cl
CH3
CH3 O Si CH3
277.37
3,3-DICHLOROHEXAMETHYLTRISILOXANE
C6H18CI2O2Si3 [2750-44-9] HMIS: 3-2-1-X SIB1843.0 BIS(TRIMETHYLSILOXY)METHYMETHOXY SILANE METHOXYHEPTAMETHYLTRISILOXANE C8H24O3Si3 [7671-19-4] HMIS: 3-2-1-X SIB1846.0 N,O-BIS(TRIMETHYLSILYL)ACETAMIDE C8H21NOSi2 BSA versatile blocking agent. [10416-59-8]
173 1.0017 1.3983 (-53)mp vapor pressure, 57: 12mm 25g/$96.00 82/47 25g/$68.00 0.862 1.3883225
HYDROPHOBIC
252.53
203.43
71-3/35 0.832 1.418 (-24)mp flashpoint: 42C (108F) TOXICITY - oral rat, LD50: 1580mg/kg 100g/$52.00 2kg/$560.00 0.969 1.3840
COMMERCIAL
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-3-1-X 25g/$16.00
SIB1876.0 BIS(TRIMETHYLSILYL)TRIFLUOROACETAMIDE 257.40 45-50/15 BSTFA (-10)mp flashpoint: 24C (75F) C8H18F3NOSi2 silylation reagent for preparing derivatives of amino acids1. 1. D. Stalling et al, Biochem. Biophys., Res. Comm., 31, 616, 1968. [25561-30-2]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-3-1-X 25g/$49.00 100g/$152.00
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3 -3-1-X 25g/$43.00
100g/$140.00
SIB1935.0 t-BUTYLDIMETHYLCHLOROSILANE 150.72 124-6 0.83 (87-90)mp C6H15ClSi vapor pressure, 100: 476mm flashpoint: 22C (73F) silylation reagent - derivatives resistant to Grignards, alkyl lithium compounds etc. blocking agent widely used in prostaglandin synthesis [18162-48-6]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-4-1-X 25g/$36.00 100g/$117.00
COMMERCIAL
SIB1937.0 n-BUTYLDIMETHYL(DIMETHYLAMINO)SILANE 159.35 47-9/12 flashpoint: 26C (79F) N(CH 3)2 C8H21NSi highly reactive reagent for bonded phases without acidic byproduct [181231-67-4]
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture TSCA-L HMIS: 3-3-1-X 10g/$38.00
190.36
1.0424 1.4312
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents TSCA HMIS: 3-3-1-X
171.14
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents HMIS: 3-3-1-X
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31
Gelest, Inc.
name
CH3 H3C C CH3 CH3 CH2 CH2 SiCl CH3
MW
254.87
bp/mm (mp)
122-3/2
D420
0.95
nD20
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents HMIS: 3-2-1-X
25g/$78.00
SIB1973.0 p-(t-BUTYL)PHENETHYLTRICHLOROSILANE CH2 CH2 SiCl3 C12H17Cl3Si mixed isomers for HPLC bonded phase
1.16
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents HMIS: 3-2-1-X
CH3CH2CH2CH2SiCl3
191.56 142-3 1.1608 1.4364 flashpoint: 45C (114F) vapor pressure, 31: 10mm 100g/$121.00
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents TSCA HMIS: 3-3-1-X 25g/$37.00
191.56
1.1608 1.436
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents TSCA HMIS: 3-3-1-X 10g/$41.00
50g/$164.00 0.9312 1.3979 100g/$136.00 140-1 10g/$143.00 200-210/0.01 0.84825 1.454230 0.903 1.3941
CH3CH2CH2CH2Si(OCH 3)3
CH3 OCH 3 H3C C Si OCH 3 CH3 OCH 3
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-2-1-X 25g/$42.00
178.30
487.37
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents 10g/$117.00 [194243-00-0] TSCA-L HMIS: 3-1-1-X
H3C
Si CH3 Cl
SIC2266.5 11-(CHLORODIMETHYLSILYLMETHYL)TRICOSANE C26H55ClSi forms self-assembled oleophilic monolayers employed as bonded phase in HPLC
HMIS: 3-1-1-X
431.27
170/0.075
1.457522
H3C
Si CH3 Cl
CH3 Si H3C Cl
SIC2465.0 CYCLOHEXYLDIMETHYLCHLOROSILANE 176.76 52-3/2 flashpoint: 63C (145F) C8H17ClSi silane blocking agent with good resistance to Grignard reagents. [71864-47-6]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS:: 3-2-1-X 25g/$36.00
COMMERCIAL
Cl Si H3C Cl
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 25g/$25.00
2 kg/$402.00
Gelest, Inc.
name
SIC2469.0 CYCLOHEXYLMETHYLDIMETHOXYSILANE C9H20O2Si vapor pressure, 20: 12mm donor for polyolefin polymerization [17865-32-6]
MW
bp/mm (mp)
D420
nD20
COMMERCIAL
188.34 196 0.9472 1.4354 TOXICITY- oral rat, LD50: 3000mg/kg flashpoint: 66C (151F) 100g/$37.00 94-8/11 2kg/$496.00
HYDROPHOBIC
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-3-1-X 25g/$11.00
231.62
[18388-16-4]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 10g/$93.00
Cl Si Cl Cl
SIC2480.0 CYCLOHEXYLTRICHLOROSILANE 217.60 90-1/10 flashpoint: 91C (195F) C6H11Cl3Si intermediate for melt-processable silsesquioxane-siloxanes1. employed in solid-phase extraction columns2. 1. J. Lichtenhan et al, Macromolecules, 26, 2141, 1993. 2. B. Tippins, Nature, 334, 273, 1988. [98-12-4]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 25g/$34.00
1.222
1.4774
100g/$110.00
204.34
207-9 50g/$124.00 85-9/1.25 1.19 50g/$148.00 1.2255 1.4713 100g/$146.00 0.99025 1.424025 50g/$136.00 0.866 1.441
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture HMIS: 2-3-1-X 10g/$31.00
SiCl3
245.65
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 10g/$37.00
SiCl3
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 25g/$45.00
Si(OCH 3)3
CH3 CH3(CH2)9 Si CH3 Cl
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture HMIS: 3-3-1-X 10g/$34.00
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-1-1-X 25g/$36.00
Cl CH3(CH2)9 Si Cl Cl CH3(CH2)9 Si Cl
OC2H5 CH3(CH2)9 Si OC2H5 OC2H5
CH3
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-1-1-X 25g/$30.00
Cl
275.72 133-7/5 1.0540 1.4528 flashpoint: >110C (>230F) 100g/$65.00 0.8790 1.4220
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-1-1-X 25g/$20.00
SID2665.0 n-DECYLTRIETHOXYSILANE C16H36O3Si see also SIB1829.0 for dipodal version [2943-73-9]
304.54
150/8
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture HMIS: 2-1-0-X 25g/$54.00
100g/$175.00
(215) 547-1015
www.gelest.com
33
Gelest, Inc.
name MW bp/mm (mp) D420
0.991
nD20
1.4448
Cl Cl OCH 3 OCH 3
CH3 Si nC4H9 CH3
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 10g/$52.00
50g/$208.00 0.861
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA-L HMIS: 3-2-1-X
0.80
1.4353
100g/$240.00 1.4071
CH3 Cl CH3
CH3 CH3
CH3 O Si CH3 Cl
Si O Si
184 1.018 (-53)mp flashpoint: 76C (169F) vapor pressure:, 50: 1mm
277.37
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents [3582-71-6] TSCA HMIS: 3-2-1-X 25g/$37.00
Cl Cl
Cl Si Cl Cl
SID3367.6 DICHLOROPHENYLTRICHLOROSILANE, 95% C6H3Cl5Si-isomeric mixture vapor pressure, 102: 7mm [27137-85-5]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-1-1-X 25g/$45.00
CH3 Cl CH3
CH3 Cl CH3
Si O Si
SID3372.0 1,3-DICHLOROTETRAMETHYLDISILOXANE C4H12Cl2OSi2 vapor pressure, 25: 8mm blocking agent [2401-73-2]
203.22
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-4-1-X 25g/$36.00
100g/$117.00 1.103
Si
Cl Cl
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-1-1-X 25g/$60.00
Cl
Si Cl
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 10g/$29.00
H3CO Si OCH 3
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-1-1-X 10g/$24.00
SID3394.0 1,5-DIETHOXYHEXAMETHYLTRISILOXANE 296.59 51-2/0.8 C2H5O Si O Si O Si OC2H5 C10H28O4Si3 [17928-13-1] HMIS: 2-2-1-X 25g/$118.00 CH3 CH3 CH3 SID3398.0 (DIETHYLAMINO)TRIMETHYLSILANE 145.32 126-7 TMSDEA (-10)mp flashpoint: 10C (50F) C7H19NSi CH3CH2 Hform: -87.7kcal/mole NSi(CH 3)3 silylation reagent: F&F: 3, 317; 4, 544; 6, 634; 18, 382 CH CH
CH3 CH3 CH3
3 2
0.7627 1.4109
[996-50-9]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-4-1-X 25g/$28.00
100g/$90.00
Gelest, Inc.
name
SID3402.0 DIETHYLDICHLOROSILANE C4H10Cl2Si Hvap: 10.0 kcal/mole dipole moment: 2.4 surface tension: 30.3 dynes/cm vapor pressure, 21: 10mm [1719-53-5]
MW
157.11
bp/mm (mp)
D420
nD20
CH3CH2 Si CH3CH2
Cl Cl
130 1.0504 1.4309 (-96.5)mp TOXICITY- oral rat, LD20: 1000mg/kg flashpoint: 27C (81F) thermal conductivity: 0.134 W/mC 100g/$75.00 0.8622 1.4022
HYDROPHOBIC
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-3-1-X 25g/$23.00
CH3CH2 Si CH3CH2
OC2H5 OC2H5
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-3-1-X 10g/$36.00
CH3(CH2)5 Si CH3(CH2)5
H3C
Cl Cl
CH3 CH CH2 Si Cl
SID3510.0 DI-n-HEXYLDICHLOROSILANE C12H26Cl2Si [18204-93-8] SID3526.0 DIISOBUTYLCHLOROSILANE C8H19ClSi [18279-73-7] SID3528.0 DIISOBUTYLDIETHOXYSILANE C12H28O2Si [18297-14-8] HMIS: 2-2-1-X
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 10g/$41.00
H3C
CH3 CH
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-3-1-X 25g/$127.00
232.44
221 10g/$86.00
0.8450 1.4179
CH3O
SID3530.0 DIISOBUTYLDIMETHOXYSILANE 204.39 120/6 flashpoint: 102C (216F) C10H24O2Si intermediate for diisobutylsilanediol, a liquid crystal. employed in polyolefin polymerization [17980-32-4]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-1-1-X 10g/$20.00
0.87
1.4167
H3C
CH3 CH CH CH3
CH3 CH Si OCH 3 CH CH3
Cl Si Cl H3C
H3C CH3O H3C
SID3537.0 DIISOPROPYLDICHLOROSILANE 185.17 64-5/25 flashpoint: 43C (109F) C6H14Cl2Si forms bis(blocked) or tethered alcohols1,2. 1. J. Hutchinson et al, Tet. Lett., 32, 573, 1991. 2. C. Bradford et al, Tet. Lett., 36, 4189, 1995. [7751-38-4]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-3-1-X 10g/$21.00
SID3538.0 DIISOPROPYLDIMETHOXYSILANE C8H20O2Si cocatalyst for -olefin polymerization1. 1. S. Lee et al, US Pat. 5,223,466, 1993 [18230-61-0]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-3-1-X 10g/$39.00
Si(OC2H5)3
300.43
CH3O
OCH 3
CH3 CH3
SID3605.0 (N,N-DIMETHYLAMINO)TRIMETHYLSILANE 117.27 85-6 0.741 TMSDMA PENTAMETHYLSILANAMINE flashpoint: -19C (-3F) C5H15NSi Hvap: 7.6 kcal/mole stronger silylation reagent than HMDS; silylates amino acids1. selectively silylates equatorial hydroxyl groups in prostaglandin synthesis2. 1. K. Rhlman, Chem. Ber., 94, 1876, 1961. 2. E. Yankee et al, J. Am. Chem. Soc., 94, 3651, 1972. [2083-91-2]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-4-1-X 25g/$38.00
COMMERCIAL
100g/$123.00
2kg/$920.00
(215) 547-1015
www.gelest.com
35
Gelest, Inc.
name
CH3CHCH 2CH3 H3C Si H3C NH CH3CHCH 2CH3 NH
MW
202.42
bp/mm (mp)
D420
nD20
82/15 0.810 1.4271 (<-50)mp TOXICITY- oral rat, LD50: 907mg/kg flashpoint: 40C (104F) 100g/$133.00 0.849 1.4240
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-3-1-X 25g/$41.00
CH3CCH2CH2Si
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-3-1-X 25g/$34.00
CH3CCH2CH2Si
SID4069.0 (3,3-DIMETHYLBUTYL)TRICHLOROSILANE NEOHEXYLTRICHLOROSILANE C6H13Cl3Si [105732-02-3] HMIS: 3-2-1-X SID4074.0 (DIMETHYLCHLOROSILYL)METHYLPINANE C12H23ClSi
219.61
183-4 25g/$48.00
Cl
230.85 93-4/2 0.957 1.4780 flashpoint: 92C (198F) 1*S,2*S,5*S []D: -5.15; >95% optical purity acetylenic derivative forms chiral polymer membrane that resolves amino acids1. 1. T. Aoki et al, Makromol. Chem. Rapid Commun, 13, 565, 1992
[2182-66-3]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 10g/$37.00
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture 100g/$20.00 TSCA HMIS: 2-4-1-X
CH3 O CH3
CH3CO Si OCCH 3
SID4076.0 DIMETHYLDIACETOXYSILANE 176.24 164-6 flashpoint: 37C (98F) C6H12O4Si reagent for the preparation of cis-diols and corticosteroids1. 1. R. Kelley, J. Chromatog., 43, 229, 1969; F&F 3, 113 [2182-66-3]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-3-1-X 100g/$30.00
500g/$120.00
CH3 Cl Si Cl CH3
COMMERCIAL
70-1 1.0637 1.4055 (-76)mp TOXICITY- ihl rat: LC50: 930ppm/4H viscosity: 0.47 cSt flashpoint: -10C (14F) Hvap: 8.0 kcal/mole Hcomb: -491 kcal/mole vapor pressure, 17: 100mm specific heat: 0.22 cal/g/ surface tension: 20.1 dynes/cm coefficient of thermal expansion: 1.3 x 10-3 critical temperature: 247.2 critical pressure: 34.4 atm autoignition temperature: 410 flammability limits: 3.4-10.4% fundamental monomer for silicones; hydrophobic surface treatment
129.06
[75-78-5]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-4-2-X 500g/$25.00 2kg/$58.00 18kg/$477.00*+container *zDR-S-019 or zCYL-S-019 required
CH3 Cl Si Cl CH3
129.06
1.0637 1.4055
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-4-2-X 25g/$11.00 500g/$68.00 18kg/$1224.00*+container *zDR-S-019 or zCYL-S-019 required
Gelest, Inc.
name
MW
bp/mm (mp)
D420
nD20
SID4121.0 DIMETHYLDIETHOXYSILANE 148.28 114-5 0.8395 1.3805 (-97)mp C6H16O2Si viscosity; 0.53cSt TOXICITY- oral rat, LDLo: 1000mg/kg vapor pressure, 25: 15mm flashpoint: 11C (51F) Hvap: 9.8 kcal/mole Hcomb: -1119 kcal/mole Hform: 200 kcal/mole dipole moment: 1.39 coefficient of thermal expansion: 1.3 x 10-3 hydrophobic surface treatment and release agent [78-62-6]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-4-1-X 100g/$12.00
HYDROPHOBIC
COMMERCIAL
2kg/$144.00
SID4123.0 DIMETHYLDIMETHOXYSILANE C4H12O2Si Hcomb: 832 kcal/mole Hform: 171 kcal/mole vapor pressure, 36: 100mm coefficient of thermal expansion: 1.3 x 10-3 [1112-39-6]
120.22
82 (-80)mp flashpoint: -8C (18F) dipole moment 1.33 viscosity, 20C: 0.44cSt 2kg/$110.00 82 (-80)mp 500g/$89.00
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-4-1-X 25g/$10.00
120.22
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-4-1-X
SID4125.0 DIMETHYLETHOXYSILANE 104.22 54-5 0.757 1.3683 TOXICITY- oral rat, LD50: 5000mg/kg C4H12OSi vapor pressure, 25: 281mm flashpoint: 15C (59F) CH3 undergoes hydrosilylation reactions waterproofing agent for space shuttle thermal tiles1. Si OC2H5 1. W. Hill et al, Poly. Mat. Sci. Eng., 62, 668, 1990
CH3
CH 3 CH 3O Si Cl CH 3
OCH 3 OCH 3 H3C Si O Si CH3 OCH 3 OCH 3
[14857-34-2]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-4-1-X 25g/$30.00
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-4-1-X 25g/$48.00
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture HMIS: 3-3-1-X 10g/$30.00
CH3(CH2)7 Si CH3(CH2)7
Cl Cl
325.44
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 25g/$38.00
SID4401.0 (DI-n-OCTYLMETHYLSILYL)ETHYLDIMETHYL- 391.23 CHLOROSILANE C21H47ClSi2 forms bonded phases for reverse phase chromatography [472513-03-7]
165-6/0.1
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 25g/$117.00
(215) 547-1015
www.gelest.com
37
Gelest, Inc.
name
MW
bp/mm (mp)
166-8/0.1
D420
0.966
nD20
Cl H3C SiCH2CH2Si Cl Cl
SID4401.5 (DI-n-OCTYLMETHYLSILYL)ETHYLTRI432.06 CHLOROSILANE C19H41Cl3Si2 forms bonded phases for reverse phase HPLC
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 25g/$117.00
CH3 CH3(CH2)7 Si
CH3
flashpoint: >110C (>230F) N Si (CH2)7CH3 HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture CH3 H CH3 [69519-51-3] HMIS: 2-1-0-X 10g/$49.00 SID4510.0 DIPHENYLDICHLOROSILANE, 95% 253.20 304-5 1.2216 1.5819 (-22)mp C12H10Cl2Si vapor pressure, 125: 2mm TOXICITY- ipr mus, LD50: 383mg/kg Hvap: 15.0 kcal/mole flashpoint: 157C (314F) dipole moment: 2.6 debye coefficient of thermal expansion: 0.7 x 10-3 specific heat: 0.30 viscosity, 25: 4.1 cSt silicone monomer; forms diol on contact with water [80-10-4]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-1-1-X 100g/$19.00 2kg/$90.00
357.77
160-5/1
0.826
1.4500
Cl Si Cl
COMMERCIAL
20kg/$720.00
Cl Si Cl
253.20
304-5 1.2216 1.5819 (-22)mp TOXICITY- ipr mus, LD50: 383mg/kg flashpoint: 157C (314F) 2kg/$390.00 1.0329 1.5269
[80-10-4]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-1-1-X 25g/$11.00 100g/$36.00
OC2H5 Si OC2H5
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-1-0-X 25g/$19.00
Si OCH 3
COMMERCIAL
OCH 3
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-1-1-X 100g/$16.00
2kg/$190.00 1.5742
CH3 Si Cl
SID4552.0 DIPHENYLMETHYLCHLOROSILANE 232.78 295 1.128 C13H13ClSi (-22C)mp vapor pressure, 125: 3mm flashpoint: 141C (286F) Hvap: 149 kcal/mole viscosity, 25: 5.3 cSt surface tension: 40.0 dynes/cm thermal conductivity: 0.112 W/mC silylates esters, lactones; precursors to silyl enolates1. 1. G. Larson et al, J. Am. Chem. Soc., 103, 2418, 1981. [144-79-6]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS 3-1-1-X 25g/$19.00 100g/$62.00
241.41
98-9/0.25
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA-L HMIS: 3-3-1-X 25g/$34.00
Gelest, Inc.
name
SID4553.0 DIPHENYLMETHYLETHOXYSILANE C15H18OSi Hvap: 14.8 kcal/mole vapor pressure: 125: 3mm [1825-59-8]
CH3 Si NH CH3 2
MW
242.39
bp/mm (mp)
D420
1.018
nD20
1.544025
CH3 Si OC2H5
HYDROPHOBIC
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-0-0-X 10g/$23.00
50g/$92.00
0.985
1.5384
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture TSCA-L HMIS: 3-1-1-X 5.0g/$30.00
25g/$120.00
0.800
1.4290
SID4598.0 DI(p-TOLYL)DICHLOROSILANE, 95% C14H14Cl2Si forms polymers w/ liquid crystal behavior1. 1. M. Lee et al, Polymer, 34, 4882, 1993. [18414-38-5]
1.568
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 10g/$37.00
50g/$148.00
272.42
140/0.5 25g/$155.00
1.023
1.535525
CH3(CH2)20CH2 Cl Si Cl H3C
423.62
0.93
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-1-1-X 50g/$130.00
CH3(CH2)20CH2 Cl Si Cl Cl
CH3(CH2)10CH2 CH3 Si H3C Cl CH3(CH2)10CH2 Cl Si H3C Cl
CH3(CH2)10CH2 OCH 2CH3 Si OCH 2CH3 H3C
444.04
0.94
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-1-1-X 25g/$85.00
262.94
291-3
0.865
1.445
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 25g/$58.00
0.955
1.4581
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS:3-1-1-X 25g/$48.00
0.84525
(215) 547-1015
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39
Gelest, Inc.
name
SID4630.0 DODECYLTRICHLOROSILANE C12H25Cl3Si [4484-72-4]
MW
303.77
bp/mm (mp)
D420
nD20
CH3(CH2)10CH2SiCl3
1.0242 1.4581
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-1-1-X 25g/$16.00
250g/$112.00
CH3(CH2)10CH2Si(OC2H5)3
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture TSCA HMIS: 2-1-0-X 25g/$27.00
CH3(CH2)18CH2SiCl3
CH3 CH3CH2 Si Cl CH3
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-0-1-X 25g/$160.00
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-4-1-X 10g/$24.00
CH3 Si CH3CH2
Cl Cl
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-4-1-X 25g/$31.00
65/75
CH3CH2
CH2CH2Si(OMe) 3
O OCCH 3 O CH3CH2 Si O O CCH3 OCCH 3
SIE4897.5 m,p-ETHYLPHENETHYLTRIMETHOXYSILANE, 95% C13H22O3Si component in optical hard coating resins [259818-29-6]
254.40
243.28
COMMERCIAL
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture [17689-77-9] TSCA HMIS: 3-1-1-X 25g/$10.00
2.0kg/$148.00
Cl CH3CH2 Si Cl Cl
SIE4901.0 ETHYLTRICHLOROSILANE C2H5Cl3Si vapor pressure, 20: 26mm, 30.4; 66mm Hvap: 9.0 kcal/mole coefficient of expansion: 1.5x10-3 viscosity: 0.48 cSt [115-21-9]
100-1 1.237 1.426 (-106)mp TOXICITY- oral rat, LD50: 1330mg/kg flashpoint: 27C (80F) dipole moment: 2.1 critical temperature: 287 4kg/$176.00
163.51
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-3-1-X 25g/$10.00 500g/$29.00
SIE4901.2 ETHYLTRIETHOXYSILANE C8H20O3Si viscosity: 0.70 cSt vapor pressure, 50: 10mm coefficient of thermal expansion: 1.5 x 10-3 Hvap: 7.8 kcal/mole
192.33
[78-07-9]
158-9 0.8963 1.3955 (-78)mp TOXICITY- oral rat, LD50: 13,720 mg/kg flashpoint: 40C (104F) autoignition temperature: 235C (455F) specific heat: 0.43/g/ c of treated surface: 26.3 dynes/cm critical temperature: 314 100g/$37.00 500g/$148.00
Gelest, Inc.
name MW bp/mm (mp) D420 nD20
0.9488 1.3838
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture TSCA HMIS: 3-3-1-X 25g/$10.00
HYDROPHOBIC
17kg/$816.00 0.88
COMMERCIAL
trol Con
c of treated glass surface: 31 dynes/cm coefficient of friction of treated glass surface: 0.2-0.3 surface resistivity of treated surface: 1.2 x 1013 ohms reduces blood protein adsorption1. 1. B. Arkles et al in Silanes Surfaces & Interfaces D. Leyden ed, Gordon & Breach, 1986, p91 TSCA HMIS: 2-3-1-X 100g/$19.00 1.5kg/$148.00 15kg/$399.00 197-8 1.51 1.3410
CF3(CF2)7CH2CH2
SIH5840.4 (HEPTADECAFLUORO-1,1,2,2-TETRA540.72 CH3 HYDRODECYL)DIMETHYLCHLOROSILANE PERFLUORODECYL-1H,1H,2H,2H-DIMETHYLCHLOROSILANE Si Cl C H ClF Si 12 10 17 derivatizing agent for fluorous phase synthesis. CH3 [74612-30-9] SIH5840.6 (HEPTADECAFLUORO-1,1,2,2-TETRAHYDRODECYL)METHYLDICHLOROSILANE C11H7Cl2F17Si [3102-79-2]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents HMIS: 3-2-1-X 5.0g/$41.00
CH3 CF3(CF2)7CH2CH2 Si Cl Cl
561.14
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents HMIS: 3-2-1-X 5.0g/$48.00
25g/$192.00
Cl CF3(CF2)7CH2CH2 Si Cl Cl
SIH5841.0 (HEPTADECAFLUORO-1,1,2,2-TETRA581.56 216-8 1.703 1.3490 HYDRODECYL)TRICHLOROSILANE TOXICITY- oral rat, LD50: >5000 mg/kg PERFLUORODECYL-1H,1H,2H,2H-TRICHLOROSILANE C10H4Cl3F17Si c of treated surfaces: 12 dynes/cm1. 1. J. Brzoska et al, Langmuir, 10, 4367, 1994 [78560-44-8]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents TSCA HMIS: 3-2-1-X 5.0g/$36.00
25g/$144.00
SIH5841.2 (HEPTADECAFLUORO-1,1,2,2-TETRA610.38 103-6/3 1.40725 1.3419 HYDRODECYL)TRIETHOXYSILANE C16H19F17O3Si hydrolysis in combination with polydimethoxysiloxane gives hard hydrophobic coatings1. 1. T. Oota et al, Jpn. Kokai JP 06,293,782, 1993; CA 122: 136317d, 1995 [101947-16-4]
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture HMIS: 3-2-1-X 5g/$42.00
568.30
F3C F F3C C O
361.55
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents HMIS: 3-3-1-X
Cl CH3(CH2)6 Si CH3 Cl
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents TSCA HMIS: 3-2-1-X
(215) 547-1015
www.gelest.com
41
Gelest, Inc.
name
SIH5846.0 n-HEPTYLTRICHLOROSILANE C7H15Cl3Si [871-41-0]
MW
bp/mm (mp)
D420
1.087
nD20
1.443925
CH3(CH2)6SiCl3
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents HMIS: 3-2-1-X
H2C
CHCF 2(CF2)6CF2CH2CH2SiCl3
SIH5918.0 HEXADECAFLUORODODEC-11-ENE-1-YL589.61 94-6/0.6 TRICHLOROSILANE C12H7Cl3F16Si forms self-assembled monolayers/ reagent for immobilization of DNA
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture HMIS: 3-1-1-X
1.626
1.3713
CH3(CH2)14CH2SiCl3
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents TSCA HMIS: 3-1-1-X 25g/$13.00
388.71
346.63
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture TSCA HMIS: 2-2-1-X 25g/$18.00
16kg/$1536.00 1.4448
COMMERCIAL
CH3
H N
186-8 0.922 (-10)mp flashpoint: 61C (142F) Hform: 132 kcal/mole dipole moment: 0.92 viscosity, 20: 1.7 cSt dielectric constant, 1000Hz: 2.57 modifies positive resists for O2 plasma resistance1. polymerizes to polydimethylsilazane oligomer in presence of Ru/H22. silylation reagent for diols3. 1. E. Babich et al, Microelectron. Eng., 11, 503, 1990. 2. Y. Blum et al, US Pat., 4,216,383, 1986; US Pat. 4,788,309, 1988. 3. L. Birkofer et al, J. Orgmet. Chem., 187, 21, 1980. see also SID4074.4
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture TSCA HMIS: 2-2-1-X 25g/$29.00
219.51
[1009-93-4]
100g/$94.00
2kg/$636.00
SIH6110.0 HEXAMETHYLDISILAZANE 161.39 126-7 0.7742 1.4080 TOXICITY- oral rat, LD50: 850mg/kg C6H19NSi2 HMDS, HMDZ viscosity: 0.90 cSt TOXICITY- ipr mus, LDLo: 650mg/kg vapor pressure, 50: 50mm flashpoint: 14C (57F) pKa: 7.55 Hvap: 8.3 kcal mole surface tension: 18.2 dynes/cm dielectric constant, 1000 Hz: 2.27 specific wetting surface: 485 m2/g Ea, reaction w/SiO2 surface: 17.6 kcal/mole versatile silylation reagent; creates hydrophobic surfaces [999-97-3]
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture TSCA HMIS: 2-4-1-X 25g/$10.00
1.5kg/$60.00
14kg/$305.00
SIH6110.1 HEXAMETHYLDISILAZANE, 99% C6H19NSi2 HMDS, HMDZ <5ppm chloride photoresist adhesion promoter [999-97-3]
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture TSCA HMIS: 2-4-1-X 25g/$13.00
CH3(CH2)4CH2 Cl Si Cl CH3
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 25g/$31.00
Gelest, Inc.
name MW bp/mm (mp) D420
1.107
nD20
1.3473
CH3(CH2)4CH2 Cl Si Cl Cl
CH3(CH2)4CH2Si(OC2H5)3
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 25g/$15.00
100g/$49.00
HYDROPHOBIC
0.860
1.40825
100g/$100.00
COMMERCIAL
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture TSCA HMIS: 3-2-1-X 50g/$31.00
CH3 CHCH 2Si CH3 CH3 CHCH 2Si OCH 3 OCH 3 Cl CHCH 2Si Cl Cl Cl
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS:3-4-1-X 10g/$28.00
0.851
1.3962
H3C H3C
1.162
1.4335
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-3-1-X 25g/$11.00
100g/$36.00
H3C H3C
220.38 190-1 0.9104 1.3908 TOXICITY- oral rat, LD50: >5000mg/kg flashpoint: 63C (145F)
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-2-1-X 25g/$10.00
COMMERCIAL
2kg/$92.00
16kg/$528.00
H3C H3C
SII6453.7 ISOBUTYLTRIMETHOXYSILANE 178.30 154 0.933 1.3960 TRIMETHOXYSILYL-2-METHYLPROPANE flashpoint: 42C (107F) TOXICITY- oral rat,LD50: >2000mg/kg C7H18O3Si viscosity: 0.8 cSt branched structure provides hydrophobic surface treatments for architectural coatings [18395-30-7]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-2-1-X 50g/$11.00
2kg/$110.00
17kg/$493.00
CH3CCH2CHCH 2SiCl
SII6456.6 ISOOCTYLDIMETHYLCHLOROSILANE C10H23ClSi [79957-95-2] HMIS: 3-3-1 SII6457.0 ISOOCTYLTRICHLOROSILANE 1-TRICHLOROSILYL-2,4,4-TRIMETHYLPENTANE C8H17Cl3Si [18379-25-4]
206.83
83-5/10 25g/$72.00
0.852
1.0684 1.4510
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 25g/$22.00
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-2-1-X 25g/$12.00
2kg/$190.00
(215) 547-1015
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43
Gelest, Inc.
name MW bp/mm (mp) D420
0.873
nD20
1.4138
H3C H3C
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-4-1-X 25g/$48.00
100g/$156.00
CH3O
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents 25g/$68.00 HMIS: 3-1-1-X store <5
CH3O
[163155-57-5]
CH3O H2C CH3 CH O H3C Si CH3 CH3
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-1-1-X 25g/$68.00
162.30
0.83
1.3965
[55816-62-1]
H3C
SIM6511.0 (p-METHYLPHENETHYL)METHYLDICHLORO- 233.21 103-5/2 flashpoint: 95C (203F) CH2CH2 Cl SILANE, 95% (p-TOLYLETHYL)METHYLDICHLOROSILANE Si C10H14Cl2Si : 40:60 H3C Cl HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture [63126-87-4] TSCA-L HMIS: 3-1-1-X 50g/$88.00
1.1
1.510025
Si
Cl Cl
233.21
104-5/9
1.1165 1.5152
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture TSCA HMIS: 3-1-1-X 25g/$45.00
SIM6519.0 METHYLTRIACETOXYSILANE, 95% 220.25 87-8/3 (40)mp C7H12O6Si vapor pressure, 94: 9mm flashpoint: 85C (185F) most common crosslinker for condensation cure silicone RTVs [4253-34-3]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-2-1-X 50g/$19.00
2kg/$280.00
18kg/$576.00
COMMERCIAL
H3C Si Cl
Cl Cl
SIM6520.0 METHYLTRICHLOROSILANE CH3Cl3Si vapor pressure, 13.5: 100mm Hvap: 7.4 kcal/mole viscosity: 0.46 cSt critical pressure: 39 atm specific heat: 0.22 cal/g/ coefficient of thermal expansion: 1.3 x 10-3 [75-79-6]
66.4 1.275 1.4110 (-78)mp TOXICITY- ihl rat,LDLo: 450ppm/4H flashpoint: -15C (5F) autoignition temperature: 395 critical temperature: 243C ionization potential: 11.36 eV surface tension: 20.3 dynes/cm 500g/$26.00 20kg/$480.00*+container
*zDR-S-019 or zCYL-S-019 required
149.48
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture TSCA HMIS: 3-4-2-X 25g/$11.00
H3C Si Cl
Cl Cl
SIM6520.1 METHYLTRICHLOROSILANE, 99% CH3Cl3Si in combination w/H2 forms SiC by CVD1. 1. A. Josiek et al, Chem. Vap. Dep., 2, 17, 1996 [75-79-6]
149.48
66.4 (-78)mp
1.275
1.4110
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture TSCA HMIS: 3-4-2-X 25g/$36.00
500g/$252.00
Gelest, Inc.
name MW bp/mm (mp) D420 nD20
SIM6555.0 METHYLTRIETHOXYSILANE C7H18O3Si vapor pressure, 25: 6mm dipole moment: 1.72 debye viscosity: 0.6 cSt [2031-67-6]
H3C Si C2H5O
OC2H5 OC2H5
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 1-3-1-X 25g/$11.00
178.30 142 0.8948 1.3832 TOXICITY- oral rat, LD50: 12,500mg/kg flashpoint: 30C (86F) autoignition temperature: 225C (437F) Hcomb: 1831 kcal/mole 2.0kg/$100.00 15kg/$360.00
HYDROPHOBIC
COMMERCIAL
H3C Si CH3O
OCH 3 OCH 3
SIM6560.0 METHYLTRIMETHOXYSILANE C4H12O3Si viscosity: 0.50 cSt dipole moment: 1.60 debye intermediate for coating resins [1185-55-3]
136.22
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-4-1-X 25g/$11.00
102-3 0.955 1.3696 (-78)mp TOXICITY- oral rat, LD50: 12,500mg/kg flashpoint: 8C (46F) autoignition temperature: 255 Hcomb: 1142 kcal/mole 2.0kg/$68.00 17kg/$323.00
H3C Si CH3O
OCH 3 OCH 3
SIM6560.1 METHYLTRIMETHOXYSILANE, 99+% C4H12O3Si viscosity: 0.50 cSt dipole moment: 1.60 debye intermediate for coating resins [1185-55-3] TSCA HMIS: 3-4-1-X SIM6579.0 METHYLTRI-n-PROPOXYSILANE C10H24O3Si [5581-66-8]
136.22
102-3 0.955 1.3696 (-78)mp TOXICITY- oral rat, LD50: 12,500mg/kg flashpoint: 8C(46F) autoignition temperature: 255 Hcomb: 1142 kcal/mole 100g/$91.00 220.38 83-4/13 flashpoint: 60C (130F) 25g/$51.00 145/15 25g/$34.00 1.045 1.4178 0.878 1.4085
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-2-1-X
268.38
SIM6590.0 METHYLTRIS(METHYLETHYLKETOXIME)301.46 110-1/2 0.982 1.454825 SILANE, 95% METHYLTRIS(2-BUTANONEOXIME)SILANE (-22)mp TOXICITY- oral rat, LD50: 2000-3000mg/kg C13H27N3O3Si flashpoint: 90C (194F) neutral crosslinker for condensation cure silicones [22984-54-9]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-2-1-X 100g/$16.00
COMMERCIAL
2kg/$170.00
CH2SiCl3
275.64
150-1/7
1.3112 1.5974
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 10g/$123.00
Si(OCH 3)3
SIN6597.0 1-NAPTHYLTRIMETHOXYSILANE 248.35 C13H16O3Si employed in high refractive index surface modification [18052-76-1]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture HMIS: 3-2-1-X
1.5562
340.69
Cl
381.53 10g/$27.00
70-2/15
1.542 50g/$108.00
(215) 547-1015
www.gelest.com
45
Gelest, Inc.
name
OCH 2CH3 CF3CF2CF2CF2CH2CH2Si OCH 2CH3
MW
410.35
bp/mm (mp)
D420
nD20
SIN6597.65 C12H19F9O3Si [102390-98-7] 25g/$74.00 368.27 10g/$32.00 355.04 181/0.75 68-9/15 1.335 1.3376
SIN6597.7 NONAFLUOROHEXYLTRIMETHOXYSILANE C9H13F9O3Si c of treated surface: 23 dynes/cm [85877-79-8] TSCA HMIS: 3-2-1-X SIN6598.0 p-NONYLPHENOXYPROPYLDIMETHYLCHLOROSILANE, 90% C20H35CIOSi
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-1-1-X 10g/$95.00
COMMERCIAL
SIO6615.0 n-OCTADECYLDIMETHYLCHLOROSILANE 347.10 159/0.1 0.85629 1.499829 DIMETHYL-n-OCTADECYLCHLOROSILANE (28-30)mp flashpoint: 201C (394F) C20H43ClSi contains 5-10% C18 isomers employed in bonded HPLC reverse phases1. 1. S. Wise et al in Silanes Surfaces & Interfaces D. Leyden ed., Gordon & Breach, 1986, p349. [18643-08-8]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-1-1-X 25g/$25.00
SIO6615.1 n-OCTADECYLDIMETHYLCHLOROSILANE, 97% DIMETHYL-n-OCTADECYLCHLOROSILANE C20H43ClSi contains 3-6% C18 isomers [18643-08-8]
347.10
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-1-1-X 25g/$51.00
100g/$165.00 0.854
COMMERCIAL
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-3-1-X 25g/$21.00
2kg/$350.00
355.72
160/0.1
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-3-1-X 10g/$42.00
SIO6618.0 n-OCTADECYLDIMETHYLMETHOXYSILANE 342.68 contains 5-10% C18 isomers C21H46OSi employed in SAM resist 1. 1. T. Oh et al, Mol. Cryst. Liq. Cryst. Sci. A, 337, 7, 1999. [71808-65-6]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-1-0-X 25g/$52.00
100g/$169.00 1.452
Cl CH3(CH2)16CH2 Si OCH 3 Cl
SIO6624.0 n-OCTADECYLMETHOXYDICHLORO383.51 144-7/1.5 0.9425 SILANE, 95% C19H40Cl2OSi maintains reactivity of octadecyltrichlorosilane, but with reduced HCl byproduct
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-1-1-X 25g/$39.00
100g/$127.00 0.930
Cl CH3(CH2)16CH2 Si CH3 Cl
OC2H5 CH3(CH2)16CH2 Si CH3 OC2H5
46
367.52
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-1-1-X 25g/$20.00
500g/$262.00 1.4407
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-1-0-X
Gelest, Inc.
name
MW
358.68
bp/mm (mp)
D420
nD20
1.4427
HYDROPHOBIC
[70851-50-2]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-1-0-X 25g/$52.00
100g/$169.00
387.93
Cl CH3(CH2)16CH2 Si Cl Cl
0.95022 1.4602
COMMERCIAL
provides lipidophilic surface coatings employed in patterning and printing of electroactive molecular films1,2. see also SIO6624.0 1. Z. Huan et al, Synth. Met., 85, 1375, 1997. 2. N. Jeon et al, Langmuir, 13, 3382, 1997. [112-04-9]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-1-1-X 25g/$11.00 1kg/$119.00
Cl CH3(CH2)16CH2 Si Cl Cl
OC2H5 CH3(CH2)16CH2 Si OC2H5
SIO6640.1 n-OCTADECYLTRICHLOROSILANE 387.93 C18H37Cl3Si contains <3% C18 isomers highest concentration of terminal silane substitution [112-04-9]
160-2/3 (22)mp
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-1-1-X 25g/$20.00
100g/$65.00 1.4386
SIO6642.0 n-OCTADECYLTRIETHOXYSILANE, 95% OC2H5 C24H52O3Si contains 5-10% C18 isomers forms hydrophobic, oleophilic coatings [7399-00-0]
416.76
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture HMIS: 2-1-0-X 25g/$30.00
100g/$96.00
CH3(CH2)16CH2
SIO6645.0 n-OCTADECYLTRIMETHOXYSILANE, 95% 374.68 170/1 0.885 1.439 OCH 3 (13-17)mp C21H46O3Si contains 5-10% C18 isomers see also SIH5925.0 TOXICITY- oral rat, LD50: >5000mg/kg Si OCH 3 forms clear, ordered, films w/ tetramethoxysilane1. flashpoint: 140C (284F) 1. A. Shimjima et al, J. Am. Chem. Soc., 120, 4258, 1998. OCH
3
COMMERCIAL
[3069-42-9]
H 3C H N CH 3 Si CH 3 N H CH 3 Si N CH 3 H Si CH 3 N CH 3 CH 3
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-1-1-X 25g/$15.00
Si
SIO6698.0 OCTAMETHYLCYCLOTETRASILAZANE 292.68 225 C8H28N4Si4 (97)mp Hform: 188 kcal/mole flashpoint: 66C (150F) forms -Si3N4 by ammonia thermal synthesis1. 1. S. Schaible et al, Applied Organomet. Chem., 7, 53, 1993 [1020-84-4]
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture TSCA HMIS: 2-2-1-X 25g/$27.00
100g/$88.00 1.4550
H3C
CH3 CH CH CH3
CH3 CH CH CH3
CH3(CH2)6CH2 Si Cl H3C
H3C
SIO6710.5 n-OCTYLDIISOPROPYLCHLOROSILANE 262.94 95-9/0.5 0.875 C14H31ClSi flashpoint: >110C (>230F) reagent for preparation of HPLC stationary phases w/high stability and efficiency1. 1. J. Kirkland et al, J. Chrom. Sci., 32, 473, 1994. [117559-37-2]
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture HMIS: 3-1-1-X
271.57
25g/$250.00
(215) 547-1015
www.gelest.com
47
Gelest, Inc.
name MW bp/mm (mp) D420
0.794
nD20
1432825
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-1-1-X 25g/$28.00
CH3 CH3(CH2)6CH2
202.42 221-223 flashpoint: 82C(181F) 25g/$84.00 215.45 94-6/10 flashpoint: 69C (156F) 25g/$52.00 227.25 94/6 flashpoint: 98C (209F)
CH3 CH3
0.8025
[2530-86-1]
Cl Cl
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 25g/$20.00
OC2H5 n-OCTYLMETHYLDIETHOXYSILANE
C13H30O2Si [2652-38-2]
246.47 80-2/2 0.8478 1.4190 flashpoint: >110C (>230F) 100g/$68.00 0.858 1.4190
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture HMIS: 2-2-0-X 25g/$21.00
SIO6712.4 n-OCTYLMETHYLDIMETHOXYSILANE C11H26O2Si [85712-15-8] HMIS: 3-2-1-X SIO6713.0 n-OCTYLTRICHLOROSILANE C8H17Cl3Si vapor pressure, 140: 2mm [5283-66-9]
218.42 87-9/5 flashpoint: 94C(201F) 25g/$30.00 224-6 (<-50)mp flashpoint: 96C (204F) 247.67
Cl CH3(CH2)6CH2 Si Cl Cl
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-1-1-X 25g/$11.00
COMMERCIAL
SIO6715.0 n-OCTYLTRIETHOXYSILANE 276.48 98-9/2 (<-40)mp C14H32O3Si viscosity: 1.9 cSt flashpoint: 100C (212F) vapor pressure, 75: 1mm may be formulated to stable water emulsions1. 1. R. Depasquale et al, US Pat. 4,648,904, 1987. [2943-75-1]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-1-0-X 50g/$10.00
2.0kg/$140.00
SIO6715.5 n-OCTYLTRIMETHOXYSILANE 234.41 191-2 flashpoint: 68C (154F) C11H26O3Si vapor pressure, 75: 0.1mm see also- SII6458.0 ISOOCTYLTRIMETHOXYSILANE [3069-40-7]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-2-1-X 25g/$10.00
O Si O Si
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-2-1-X 10g/$36.00
Cl C5H11Si Cl Cl
SIP6720.0 PENTYLTRICHLOROSILANE AMYLTRICHLOROSILANE mixed isomers C5H11Cl3Si specific heat: 0.35 cal/g/ [107-72-2]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-3-1-X 25g/$45.00
Gelest, Inc.
name MW bp/mm (mp) D420
0.895
nD20
1.4059
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-2-1-X
HYDROPHOBIC
SIP6720.5 PERFLUORODODECYL-1H,1H,2H,2H-TRIETHOXY- 710-810 157-198/1.5 SILANE -PERFLUOROTETRADECYL-1H,1H,2H,2H(70-85)mp TRIETHOXYSILANE MIXTURE, 80% (contains ~ 5% SIH5841.2, balance higher homologs) for the preparation of low surface energy substrates
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture HMIS: 2-1-1-X
5.0g/$127.00
C8F17
SiCl3
SIP6720.7 PERFLUOROOCTYLPHENYLTRICHLOROSILANE 629.60 67-9/3 thermally stable to >300 C14H4Cl3F17Si contact angle treated glass surface, water: 115.1 1.Y. Kondo, J. Oleoscience, 53, 143, 2004 [753025-21-7] HMIS: 3-1-1-X 1.0g/$232.00 SIP6720.8 PHENETHYLDIISOPROPYLCHLOROSILANE, C8H22ClSi contains ,-isomers [151613-24-4] TSCA HMIS: 3-2-1-X SIP6721.0 PHENETHYLDIMETHYLCHLOROSILANE contains ,-isomers C10H15ClSi see also SIP6724.7 [17146-08-6] 254.87 105-9/0.3 5.0g/$120.00 198.77 56/0.2 flashpoint: 70C (158F) 0.999 1.5185 0.97
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 50g/$170.00
207.39
109/2
0.890
Cl
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 25g/$38.00
100g/$124.00
Cl CH2 CH2 Si Cl Cl
239.60 93-6/3 1.240 1.5185 TOXICITY- oral rat, LD50: 2830mg/kg flashpoint: 91C (196F) 100g/$82.00
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-1-1-X 25g/$25.00
COMMERCIAL
OCH 3
1.037
1.4753
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-1-1-X 25g/$28.00
CH3 O Si Cl CH3
SIP6723.0 m-PHENOXYPHENYLDIMETHYLCHLORO262.81 SILANE, 95% contains other isomers C14H15ClOSi end-capper for low-temperature lubricating fluids1. 1. M. Gardos, ASLE Transactions, 18, 31, 1972. SIP6723.2 3-PHENOXYPROPYLDIMETHYLCHLOROSILANE C11H17ClOSi [69733-73-9]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 5.0g/$94.00
228.78
90-2/0.25 100g/$138.00
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 25g/$42.00
49
Gelest, Inc.
name
Cl O CH2CH2CH2Si Cl
Cl O CH2CH2CH2Si Cl Cl
MW
bp/mm (mp)
110/1 25g/$84.00
D420
nD20
CH3
SIP6723.25 3-PHENOXYPROPYLMETHYLDICHLOROSILANE 249.21 C10H14OCl2Si [28229-56-3] HMIS: 3-2-1-X SIP6723.3 3-PHENOXYPROPYLTRICHLOROSILANE C9H11Cl3OSi [60333-76-8]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 25g/$36.00
Cl O (CH2)10CH2Si Cl Cl
SIP6723.4 11-PHENOXYUNDECYLTRICHLOROSILANE C17H27Cl3OSi forms SAMs that orient pentacene [526204-46-6] HMIS: 3-1-1-X SIP6724.7 4-PHENYLBUTYLDIMETHYLCHLOROSILANE C12H19ClSi
381.85 5.0g/$210.00
1.497925
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 25g/$110.00
Cl (CH2)4Si Cl
Cl Cl
CH3
1.0925
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 25g/$110.00
CH2CH2CH2CH2
1.5121
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 25g/$110.00
CH3 CH3
Si O CCH3
1.006
1.4907
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-2-1-X
CH3 Si Cl CH3
COMMERCIAL
SIP6728.0 PHENYLDIMETHYLCHLOROSILANE C8H11ClSi vapor pressure, 25: 1 mm viscosity: 1.4 cSt [768-33-2] TSCA HMIS: 3-2-1-X SIP6728.4 PHENYLDIMETHYLETHOXYSILANE C10H16OSi viscosity: 1.3 cSt dipole moment: 1.34 [1825-58-7]
170.71 192-3 flashpoint: 61C (141F) Hvap: 11.4 kcal/mole 25g/$26.00 100g/$84.00
1.032
1.5082
2kg/$700.00
180.32 93/25 0.926 1. 4799 TOXICITY- oral rat, LD50: 2460mg/kg flashpoint: 61C (141F) 50g/$80.00 1.5321
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-2-0-X 10g/$20.00
Cl Si C2H5 Cl
Cl CH2CH2CH2CH2CH2CH2Si Cl Cl
205.16 225-6 1.184 flashpoint: 92C (198F) vapor pressure, 100: 13mm
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 25g/$110.00
295.71
95/0.1 5.0g/$96.00
1.505225
Gelest, Inc.
name
N(CH 3)2 Si CH3 N(CH 3)2
MW
bp/mm (mp)
D420
nD20
1.4982
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 10g/$38.00
HYDROPHOBIC
Cl Si CH3 Cl
SIP6738.0 PHENYLMETHYLDICHLOROSILANE C7H8Cl2Si vapor pressure:, 82.5: 13mm Hvap: 11.5 kcal/mole [149-74-6]
205-6 1.187 1.5180 (-53)mp TOXICITY- ipr mus, LD50: 300mg/kg flashpoint: 82C (180F) 500g/$64.00 1.10 1.5120
191.13
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 25g/$12.00
CH2CH2CH3 CH Cl Si Cl CH3
247.24 87-9/1 flashpoint: >110C(>230F) 25g/$120.00 210.35 117-8/31 flashpoint: 89C (192F)
0.963
1.4690
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-2-1-X 25g/$23.00
100g/$78.00
182.29 199-200 0.9934 1.4694 TOXICITY- oral rat, LD50: 892 mg/kg flashpoint: 76C (168F) 250g/$105.00 0.963 50g/$119.00 1.08625 1.509025
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-2-1-X 25g/$15.00
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-1-1-X 5.0g/$17.00
CH3
233.21
96-8/4
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 25g/$87.00
1.194
1.4708
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-2-1-X 25g/$64.00
100g/$208.00
Cl Si Cl Cl
SIP6810.0 PHENYLTRICHLOROSILANE C6H5Cl3Si Hvap: 11.4 kcal/mole vapor pressure, 75: 10mm surface tension: 27.9 dynes/cm specific heat: 0.24 cal/g/ coefficient of thermal expansion: 1.2 x 10-3 [98-13-5]
201 1.324 1.5247 (-33)mp TOXICITY- oral rat, LD50: 2340mg/kg flashpoint: 91C (195F) viscosity: 1.08 cSt dipole moment: 2.41 critical temperature: 438 18kg/$576.00 1.201 1.5180
211.55
COMMERCIAL
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 25g/$11.00 2kg/$76.00
CH2CH2CH3 CH Cl Si Cl Cl
(215) 547-1015
www.gelest.com
51
Gelest, Inc.
name MW bp/mm (mp) D420 nD20
OC2H5 Si
COMMERCIAL
C2H5O
OC2H5
SIP6821.0 PHENYLTRIETHOXYSILANE 240.37 112-3/10 0.996 1.4718 TOXICITY- oral rat, LD50: 2830mg/kg C12H20O3Si vapor pressure, 75: 1mm flashpoint: 96C (205F) surface tension 28 dynes/cm coefficient of thermal expansion: 0.9 x 10-3 dipole moment: 1.85 debye dielectric constant: 4.12 viscosity, 25: 1.7 cSt improves photoresist adhesion to silicon nitride effective treatment for organic-grafted clays1. 1. K. Canrado et al, Chem. Mater. 13, 3766, 2001. [780-69-8]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-1-1-X 100g/$11.00
2kg/$112.00
17kg/$510.00
SIP6822.0 PHENYLTRIMETHOXYSILANE C9H14O3Si viscosity, 25: 2.1 cSt vapor pressure, 108: 20mm dipole moment: 1.77 intermediate for silicone resin coatings [2996-92-1]
211 1.064 1.4734 (-25)mp TOXICITY- ivn mus, LD50: 180mg/kg flashpoint: 86C (187 F) dielectric constant: 4.44 2kg/$98.00 18kg/$562.00 0.995
198.29
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-2-1-X 100g/$11.00
H3C CH3CH2 C N O Si 3
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-2-1-X 50g/$17.00
HYDROLYTIC SENSITIVITY: 8 Si-Cl reacts rapidly with water/moisture TSCA HMIS: 3-4-1-X 25g/$49.00
132.28
Cl CH3CH2CH2 Si CH3 Cl
OCH 3 CH3CH2CH2 Si CH3 OCH 3
1.027
1.425
HYDROLYTIC SENSITIVITY: 8 Si-Cl reacts rapidly with water/moisture TSCA HMIS: 3-3-1-X 25g/$38.00
SIP6914.0 PROPYLMETHYLDIMETHOXYSILANE C6H16O2Si [18173-73-4] HMIS: 3-3-1-X SIP6915.0 n-PROPYLTRICHLOROSILANE C3H7Cl3Si vapor pressure, 16: 10mm [141-57-1]
148.28
Cl CH3CH2CH2 Si Cl Cl
COMMERCIAL
1.185
1.4290
HYDROLYTIC SENSITIVITY: 8 Si-Cl reacts rapidly with water/moisture TSCA HMIS: 3-3-1-X 25g/$13.00
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-3-1-X 25g/$12.00
SIP6918.0 n-PROPYLTRIMETHOXYSILANE C6H16O3Si c of treated surface: 28.5 dynes/cm utilized in architectural hydrophobic coatings [1067-25-0]
164.27 142 0.93225 1.3880 TOXICITY- oral rat, LD50: 7420mg/kg flashpoint: 34C (93F) 2kg/$102.00 16kg/$368.00
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-3-1-X 25g/$11.00
Gelest, Inc.
name MW bp/mm (mp) D420 nD20
SIS6952.0 0.88 SILICLAD OCTADECYL FUNCTIONAL SILANE flashpoint: 25C (77F) 20% in t-AMYL ALCOHOL and DIACETONE ALCOHOL amber liquid c of treated glass surface: 31 dynes/cm coefficient of friction of treated glass surface: 0.2-0.3 surface resistivity of treated surface: 1.2 x 1013 ohms reduces blood protein adsorption1. hydrophobic, anti-stiction coating for silicon substrates2. 1. B. Arkles et al, in Silanes Surfaces & Interfaces D. Leyden ed, Gordon & Breach, 1986, p 91. 2. A. Almanza-Workman et al, J. Electro Chem. Soc. 149, H6, 2002 for application information see Performance Products Brochure [39443-39-5]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-3-1-X 100g/$20.00
O (CH3(CH2)17Si O O
HYDROPHOBIC
COMMERCIAL
OH H3C Si O Na OH
+
116.12 pH: 13.0 viscosity: 10 cSt. 500g/$17.00 2.0kg/$50.00 331.83 155-6/3 25g/$80.00 282.48 205 flashpoint: 58C (136F) 25g/$57.00
CH3(CH2)13SiCl3
OC2H5 OC2H5 H3C Si O Si CH3 OC2H5 OC2H5
SIT7093.0 TETRADECYLTRICHLOROSILANE C14H29Cl3Si [18402-22-7] TSCA HMIS: 3-1-1-X SIT7095.0 1,1,3,3-TETRAETHOXY-1,3-DIMETHYLDISILOXANE, 95% C10H26O5Si2 [18001-60-0]
0.953
1.3912
CH3 CH3
CH3 CH3
C2H5O Si O Si OC2H5
222.43
0.879
1.3880
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-2-0-X 25g/$28.00
100g/$90.00
H H3C Si N Si CH3
218-220/1.5 (91)mp flashpoint: >110C (>230F) deactivates glass capillary columns by persilylation1. 1. K. Grob et al, High Resol. Chrom. & Col Chrom., 3, 197, 1980. 25g/$102.00 0.911 1.4490
409.68
[7453-26-1]
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture TSCA-L HMIS: 2-1-0-X 5.0g/$25.00
H3C H3C
SIT7906.0 THEXYLDIMETHYLCHLOROSILANE
t-HEXYLDIMETHYLCHLOROSILANE
178.78
C8H19ClSi [67373-56-2]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents, protic solvents HMIS: 3-2-1-X 5.0g/$16.00
25g/$64.00
H3C H3C
219.61
70-2/15
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents, protic solvents HMIS: 3-3-1-X 10g/$101.00
H3C
Si Cl CH3
1.00725 1.5055
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents, protic solvents TSCA HMIS: 3-2-1-X 5.0g/$37.00
Cl H3C Si CH3 Cl
1.1609 1.5330
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents, protic solvents TSCA HMIS: 3-2-1-X 25g/$114.00
53
Gelest, Inc.
name
Cl H3C Si Cl Cl
SIT8040.0 p-TOLYLTRICHLOROSILANE C7H7Cl3Si c of treated surface: 34 dynes/cm [701-35-9]
MW
bp/mm (mp)
D420
1.28
nD20
1.522425
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents, protic solvents TSCA HMIS: 3-2-1-X 25g/$31.00
H3C
SIT8042.0 p-TOLYLTRIMETHOXYSILANE 212.32 75-8/8 C10H16O3Si flashpoint: 94C (201C) OCH 3 c of treated surface: 34 dynes/cm Si OCH 3 charge control surface treatment for electrostatic copier particles1. 1. H. Yamazaki, Jpn. Kokai, JP 06027719 A2, 1994.
OCH 3
[17873-01-7]
50g/$152.00
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents, protic solvents TSCA HMIS: 3-1-0-X 25g/$52.00
Cl CH3(CH2)28CH2 Si Cl Cl
SIT8048.0 TRIACONTYLTRICHLOROSILANE, blend 556.26 (60-82)mp 80% C30 and higher, 20% C22-C28 C30H61Cl3Si employed in bonded phases for HPLC of carotenes [70851-48-8]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents, protic solvents TSCA HMIS: 3-1-1-X 25g/$52.00
100g/$169.00 0.946
Cl Si Cl Cl
528.21
215/0.01 (20-35)mp
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA-L HMIS: 3-1-1-X 10g/$127.00
Cl
Si Cl Cl
359.88
146-9/0.2 10g/$174.00
0.985
SIT8170.0 (TRIDECAFLUORO-1,1,2,2-TETRAHYDRO440.70 189-91 1.473 OCTYL)DIMETHYLCHLOROSILANE flashpoint: 52C (127F) PERFLUOROOCTYL-1H,1H,2H,2H-DIMETHYLCHLOROSILANE C10H10ClF13Si employed in column chromatography where low protein retention is required1. CH3 employed in solid phase extraction of fluorous phases2. modification of layered silicate yields material w/ film forming properties3. CF3CF2CF2CF2CF2CF2CH2CH2Si Cl 1. G. Xindu et al, J. Chromatog, 269, 96, 1983. CH3 2. D. Curran, J. Org. Chem. 62,6714, 1997. 3. M. Ogawa et al, Chem. Mater., 10, 3787, 1998. [102488-47-1]
Cl CF3CF2CF2CF2CF2CF2CH2CH2Si CH3 Cl
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-3-1-X 10g/$31.00
1.3453
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-3-1-X 10g/$41.00
SIT8174.0 (TRIDECAFLUORO-1,1,2,2-TETRAHYDRO481.55 84-5/17 OCTYL)TRICHLOROSILANE flashpoint: 54C (129F) Cl C8H4Cl3F13Si CF3CF2CF2CF2CF2CF2CH2CH2Si Cl lowers the coefficient of friction of silicon substrates1. 1. V. DePalma et al, Langmuir, 5, 868, 1989. Cl [78560-45-9]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA-L HMIS: 3-3-1-X 10g/$28.00
COMMERCIAL
510.36
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture TSCA HMIS: 2-2-1-X 10g/$26.00
50g/$104.00
54
Gelest, Inc.
name
SIT8176.0 (TRIDECAFLUORO-1,1,2,2-TETRAHYDROCF3CF2CF2CF2CF2CF2CH2CH2Si OCH 3 OCTYL)TRIMETHOXYSILANE C11H13F13O3Si
OCH 3 OCH 3
MW
468.29
bp/mm (mp)
60-2/0.5
D420
1.44
nD20
1.3322
[85857-16-5]
50g/$148.00
HYDROPHOBIC
Cl CF3CH2CH2 Si Cl Cl CF3CH2CH2 Si Cl
OCH 3 CF3CH2CH2 Si OCH 3
CH3
211.08 121-2 1.2611 1.3850 TOXICITY- ipr mus: 254mg/kg flashpoint: 15C (59F) 50g/$128.00 1.395 1.385
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-4-1-X 10g/$32.00
Cl
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-4-1-X 10g/$32.00
50g/$128.00
OCH 3
SIT8372.0 (3,3,3-TRIFLUOROPROPYL)TRIMETHOXYSILANE 218.25 144 1.137 1.3546 flashpoint: 38C (100F) C6H13F3O3Si HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture c of treated surface: 33.5 dynes/cm [429-60-7] TSCA HMIS: 3-3-1-X 5.0g/$34.00 25g/$136.00 SIT8510.0 TRIMETHYLCHLOROSILANE TMCS C3H9ClSi 57.6 0.8580 1.3885 (-57.7)mp TOXICITY- ihl mus, LDLo: 500mg/m3/10M vapor pressure, 20: 190mm; 50: 591 mm flashpoint: -27C (-17F) Hvap: 6.6 kcal/mole autoignition temperature: 395 most economical and broadly used silylation reagent [75-77-4] TSCA HMIS: 3-4-2-X 25g/$11.00 750g/$48.00 3kg/$160.00 118.25 75-6 0.7573 1.3742 (-83)mp flashpoint: -27C (-17F) vapor pressure, 25: 111mm Hvap: 33.5 kcal/mole 1.5kg/$138.00 14kg/$672.00 0.7560 1.3678 108.64
COMMERCIAL
SIT8515.0 TRIMETHYLETHOXYSILANE ETHOXYTRIMETHYLSILANE C5H14OSi dipole moment: 1.2 Hcomb: 970.4 kcal/mole critical temperature: 233 [1825-62-3]
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture TSCA HMIS: 2-4-1-X 25g/$10.00
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture TSCA HMIS: 3-4-1-X 25g/$19.00
100g/$62.00 1.126
Cl Cl
CH3 CH3 CH3 CH3
CH 3 Si O Si CH 3 Si(CH 3)3
H3C Si O Si Cl
SIT8572.6 TRIMETHYLSILOXYTRICHLOROSILANE C3H9Cl3OSi2 [2750-45-0] HMIS: 3-4-1-X SIT8712.0 TRIS(DIMETHYLAMINO)METHYLSILANE C7H21N3Si [3768-57-8]
223.63 128 flashpoint: 16C (61F) 25g/$72.00 55-6/17 (-11)mp flashpoint: 30C (86F) 175.35
0.85022 1.43222
Si N N
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture TSCA HMIS: 3-3-1-X 10g/$29.00
(CH 2)2 H 3C Si Cl CH 3
417.32
HYDROLYTIC SENSITIVITY: 8 Si-CI reacts rapidly with water/moisture, protic solvents HMIS: 3-2-1-X 10g/$84.00
CH3(CH2)9CH2SiCl3
1.02
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-1-1-X 25g/$104.00
55
Gelest, Inc.
MW
bp/mm (mp)
D420
1.02
nD20
ClMe 2SiCH2CH2
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-1-1-X 50g/$204.00
Cl(CH3)2SiCH2CH2Si(CH3)2Cl
SIB1042.0 1,2-BIS(CHLORODIMETHYLSILYL)ETHANE 215.27 198-9 TETRAMETHYLDICHLORODISILETHYLENE (36-9)mp flashpoint: 40C (104F) C6H16Cl2Si2 reagent for protection of primary amines, including amino acids1. 1. S. Djuric et al, Tet. Lett., 22, 1787, 1981 [13528-93-3]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 25g/$21.00
100g/$68.00
Cl(CH3)2Si(CH2)6Si(CH3)2Cl
0.961
1.4538
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-1-1-X 25g/$52.00
100g/$169.00
Cl(CH3)2Si(CH2)8Si(CH3)2Cl
1.4540
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-1-1-X 25g/$41.00
100g/$134.00
SIB1048.2 1,3-BIS(CHLORODIMETHYLSILYL)PROPANE 229.30 94/19 1.0244 1.4647 C7H18Cl2Si2 forms cyclic derivatives of polyalkyleneoxides suitable for anionic copolymerization1. 1. T. Zundel et al, Macromol, 31, 2724, 1998 [2295-06-9]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 5.0g/$102.00
Cl
Cl Cl
C2H5O
Cl Cl
OC2H5 OC2H5
CH3SiCH2CH2SiCH3
SIB1614.0 BIS(METHYLDICHLOROSILYL)ETHANE 256.11 208-210 1,4-DIMETHYL-1,1,4,4-TETRACHLORO-1,4-DISILABUTANE (31-3)mp flashpoint: 94C (201F) C4H10Cl4Si2 dipodal coupling agent [3353-69-3]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 25g/$31.00
1.2628 1.4760
CH3SiCH2CH2SiCH3 C2H5O
294.54
80/1.5 25g/$62.00
F F
F F
190.29
114
1.118
CH3SiCH2CH2SiCH3
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-3-1-X 10g/$69.00
409.16
114/1 25g/$85.00
1.2496 1.4754
Gelest, Inc.
name
CF2CF2CF2CF2CF2CF2CF2CF2 CH2 CH2 CH2 SiCl3 CH2 SiCl3
MW
725.06
bp/mm (mp)
142-4/0.6 (69-70)mp 5.0g/$170.00
D420
nD20
DIPODAL HYDROPHOBIC
Cl Cl Cl
Cl Cl Cl
Si(CH2)6Si
1.4759
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 10g/$41.00
Cl Cl Cl
Cl Cl Cl
Cl Cl Cl
Cl Cl
Cl Cl Cl
Cl Cl
SiCH2Si Cl
SIB1813.0 BIS(TRICHLOROSILYL)METHANE CH2Cl6Si2 nucleus for star polymers and dendrimers [4142-85-2]
282.9
183
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 5.0g/$80.00
Si(CH2)8Si
1.22
1.4757
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-1-1-X 25g/$36.00
SiCH2CH2CH2Si
310.97
115-7/4 (29-30)mp
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 10g/$85.00
Cl3Si
(CH2)11O(CH 2)11
SIB1816.6 1,4-BIS(TRIETHOXYSILYL)BENZENE 402.64 C18H34O6Si2 Si OC2H5 forms thermally stable hybrid silica fibers1. 1. Y. Yang et al, Chem. Mater., 18, 1324, 2006 OC2H5
OC2H5
[52217-60-4]
5.0g/$60.00
C2H5O
SIB1817.0 BIS(TRIETHOXYSILYL)ETHANE 354.59 96/0.3 0.957 1.4052 HEXAETHOXYDISILETHYLENE flashpoint: 107C (225F) vapor pressure, 150: 10mm C14H34O6Si2 Hvap: 101.5 kj/mole TOXICITY - oral rat, LD50: 161mg/kg additive to silane coupling agent formulations that enhances hydrolytic stability OC2H5 OC2H5 employed in corrosion-resistant coatings/primers for steel and aluminum1,2. sol-gels of ,-bis(trimethoxysilyl)alkanes reported 3. SiCH2CH2Si OC2H5 forms mesoporous, derivatizeable molecular sieves4. OC2H5 OC2H5 1. W. Van Ooij et al, J. Adhes. Sci. Tech. 11, 29, 1997. 2. W. Van Ooij et al, Chemtech., 28, 26, 1998. 3. D. A. Loy et al, J. Am. Chem. Soc., 121, 5413, 1999. 4. B. Molde et al, Chem. Mat., 11, 3302, 1999. [16068-37-4]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA-S HMIS: 3-1-1-X 25g/$15.00
COMMERCIAL
100g/$49.00
OEt OEt
SiCH2Si OEt
SIB1821.0 BIS(TRIETHOXYSILYL)METHANE 340.56 114-5/3.5 4,4,6,6-TETRAETHOXY-3,7-DIOXA-4,6-DISILANONANE C13H32O6Si2 intermediate for sol-gel coatings, hybrid inorganic-organic polymers [18418-72-9]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture HMIS: 2-3-0-X 5.0g/$24.00
25g/$96.00
(215) 547-1015
www.gelest.com
57
Gelest, Inc.
name
MW
bp/mm (mp)
172-5/0.75
D420
0.926
nD20
1.4240
SIB1824.0 BIS(TRIETHOXYSILYL)OCTANE 438.76 C20 H46 O6Si2 employed in sol-gel synthesis of mesoporous structures (C2H5O)3Si(CH2)8Si(OC2H5)3 sol-gels of , -bis(trimethoxysilyl)alkanes reported1. 1. D. A. Loy et al, J. Am. Chem. Soc., 121, 5413, 1999. [52217-60-4]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA-L HMIS: 2-1-1-X 25g/$30.00
SIB1829.0 1,2-BIS(TRIMETHOXYSILYL)DECANE 382.65 C16H38O6Si2 pendant dipodal silane; employed in high pH HPLC
Si(OCH 3)3 Si(OCH 3)3
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture HMIS: 3-2-1-X 25g/$51.00
100g/$165.00 1.4091
OCH 3 OCH 3
OCH 3 OCH 3
SIB1830.0 BIS(TRIMETHOXYSILYL)ETHANE 270.43 103-4/5 1.068 flashpoint: 65 (149F) C8H22O6Si2 CAUTION: INHALATION HAZARD vapor pressure, 20: 0.08mm employed in fabrication of multilayer printed circuit boards 1. J. Palladino, U.S. Pat. 5,073,456, 1991. see also SIB1817.0 [18406-41-2]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 4-2-1-X 25g/$64.00
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-1-0-X 10g/$33.00
OCH 3 OCH 3
OCH 3 OCH 3
SIB1832.0 1,6-BIS(TRIMETHOXYSILYL)HEXANE 326.54 161/2 flashpoint: 95C (203F) C12H30O6Si2 sol-gels of , -bis(trimethoxysilyl)alkanes reported1. 1. D. A. Loy et al, J. Am. Chem. Soc., 121, 5413, 1999. [87135-01-1] SIB1832.2
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture HMIS: 3-2-1-X 10g/$38.00
OCH 3 p-BIS(TRIMETHOXYSILYLMETHYL)BENZENE 346.53 CH2 Si OCH 3 C14H26O6Si2 OCH 3 HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture
[193358-40-6]
HMIS: 3-1-1-X
(CH3O)3SiCH2CH2CH2
CH2CH2CH2Si(OCH 3)3
402.64 5.0g/$145.00
CH3 Cl Si CH3
SIC2265.5 (CHLORODIMETHYLSILYL)-6-[2-(CHLORODI309.43 1.03 1.4863 CH3 METHYLSILYL)ETHYL]BICYCLOHEPTANE mixture of 1 and 2 regio isomers, exo and endo CH2CH2Si Cl C13H26Cl2Si2 forms polymers CH3
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture HMIS: 3-2-1-X
SiCH2CH2Si
COMMERCIAL
SIT8185.8 1-(TRIETHOXYSILYL)-2-(DIETHOXYMETHYL324.56 100/0.5 SILYL)ETHANE flashpoint:102C (215F) C13H32O5Si dipodal silane; forms abrasion-resistant sol-gel coatings [18418-54-7]
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture TSCA HMIS: 3-2-1-X 25g/$40.00
100g/$130.00
2kg/$840.00
Gelest, Inc.
POLYMERIC HYDROPHOBIC
name
MW
bp/mm (mp)
D420
nD20
Polybutadiene
CH2 CH CH2 CH CH2CH2Si(OC2H5)3
SSP-055 TRIETHOXYSILYL MODIFIED POLY-1,2-BUTADIENE, 50% in toluene viscosity: 100-200 cSt. coupling agent for EPDM resins [72905-90-9] TSCA HMIS: 2-4-1-X store <5 SSP-056 TRIETHOXYSILYL MODIFIED POLY-1,2-BUTADIENE, 50% in volatile silicone viscosity: 100-200 cSt. primer coating for silicone rubbers [72905-90-9] TSCA HMIS: 2-3-1-X store <5
3500-4500
0.90
100g/$60.00 3500-4500
2.0kg/$780.00 0.93
CH2 CH
CH2 CH CH2CH2Si(OC2H5)3
100g/$68.00 0.90
SSP-058 DIETHOXYMETHYLSILYL MODIFIED POLY-1,2-BUTA- 3500-4500 DIENE, 50% in toluene viscosity: 75-150 cSt. water tree resistance additive for crosslinkable HDPE cable cladding HMIS: 2-4-1-X store <5 100g/$86.00 SSP-255 (30-35%TRIETHOXYSILYLETHYL)ETHYLENE4500-5500 (35-40% 1,4-BUTADIENE) - (25-30% STYRENE) terpolymer, 50% in toluene HMIS: 2-3-1-X viscosity: 20-30 cSt. 100g/$86.00
(CH2CH)m (CH2CH)n(CH2CH
CHCH 2)p
CH2CH2Si(OC2H5)3
59
Gelest, Inc.
bp/mm (mp)
180-2/1
D420
0.985
nD20
OCH 3 OCH 3
5.0g/$112.00 1.45225
CH3O CH3O
CH3
OCH 3 OCH 3
COMMERCIAL
SIB1660.0 BIS[(3-METHYLDIMETHOXYSILYL)PROPYL]600-800 1.00 POLYPROPYLENE OXIDE flashpoint: >110C (>230F) viscosity: 6000-10,000 cSt. w/tin catalyst forms moisture-crosslinkable resins hydrophilic dipodal silane [75009-88-0]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-1-1-X 100g/$24.00
2.0kg/$288.00
SIB1824.9 1,3-[BIS(3-TRIETHOXYSILYLPROPYL)POLY1113.5 (CH2)3 ETHYLENOXY]-2-METHYLENEPROPANE Si(OCH 2CH3)3 C 50H104O20Si2 (average) vinyl functional hydrophilic dipodal coupling agent for protein immobilization HMIS: 2-2-1-X 1.0g/$292.00 SIC2436.0 (3-CYANOBUTYL)DIMETHYLCHLOROSILANE C7H14ClNSi
HMIS: 3-2-1-X
CH 3 N C CHCH 2CH 2 CH 3 Si Cl H 3C
175.73 25g/$40.00
80-4/1
CH 3 N C CHCH 2CH2 Cl Si Cl H 3C
SIC2437.0 (3-CYANOBUTYL)METHYLDICHLOROSILANE 196.17 63/0.3 4-(DICHLOROMETHYLSILYL)-2-METHYLBUTYRONITRILE C6H11Cl2NSi [71550-62-4] TSCA HMIS: 3-2-1-X 25g/$40.00 SIC2437.5 (3-CYANOBUTYL)METHYLDIMETHOXYSILANE C8H17NO2Si [793681-94-4] TSCA HMIS: 3-2-1-X SIC2438.0 (3-CYANOBUTYL)TRICHLOROSILANE C5H8Cl3NSi [163155-56-4] HMIS: 3-2-1-X SIC2439.0 3-CYANOBUTYLTRIETHOXYSILANE C11H23NO3Si
HMIS: 2-2-1-X
187.32 77/1.5 flashpoint: 93C (199F) 25g/$88.00 216.57 25g/$39.00 245.39 25g/$62.00 61-3/0.2
1.220
1.469025
100g/$127.00
N C CH2CH2 Cl Si H3C Cl
SIC2440.0 2-CYANOETHYLMETHYLDICHLOROSILANE 168.10 60-2/4 C4H7Cl2NSi flashpoint: 60C (140F) monomer for polar silicones used in GC phases [1070-18-4]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents TSCA HMIS: 3-2-1-0
1.2015 1.455025
25g/$123.00
CH 2CH 2SiCl3
SIC2442.0 2-CYANOETHYLTRICHLOROSILANE C3H4Cl3NSi Hvap: 11.2 kcal/mole vapor pressure, 85: 12mm [10731-22-3]
188.52
84-6/10 1.356 1.4615 (32-3)mp TOXICITY- oral rat, LD50: 2000mg/kg 50g/$108.00
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents TSCA HMIS: 3-2-1-0-X 10g/$27.00
Gelest, Inc.
name
OCH 2CH3 N C CH2CH2 Si OCH 2CH3 OCH 2CH3
SIC2445.0 2-CYANOETHYLTRIETHOXYSILANE C9H19NO3Si [919-31-3]
MW
bp/mm (mp)
D420
nD20
COMMERCIAL
217.34 224-5 0.9792 1.4140 TOXICITY- oral rat, LD50: 5630mg/kg flashpoint: 86C (186F) 100/$49.00 2kg/$360.00 1.079 1.4126
POLAR HYDROPHILIC
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-2-0-X 25g/$15.00
N C CH2CH2Si(OCH 3)3
SIC2446.0 2-CYANOETHYLTRIMETHOXYSILANE C6H13NO3Si c of treated surface: 34 dynes/cm crosslinker for moisture-cure silicone RTVs [2526-62-7]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-2-1-X 25g/$42.00
100g/$138.00
SIC2451.0 3-CYANOPROPYLDIISOPROPYLDIMETHYL226.44 96-8/0.2 0.89 AMINOSILANE 4-[DIMETHYLAMINOBIS(1-METHYLETHYL)SILYL]BUTANENITRILE C12H26N2Si stable cyanofunctional bonded phase [163794-91-0]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-2-1-X
SIC2452.0 3-CYANOPROPYLDIMETHYLCHLOROSILANE 161.71 108-9/15 4-(CHLORODIMETHYLSILYL)BUTYRONITRILE flashpoint: 85C (185F) C6H12ClNSi coupling agent for antibodies1. 1. S. Falipou et al, Bioconjugate Chem., Am. Chem. Soc., 1989 [18156-15-5]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents TSCA HMIS: 3-2-1-X 25g/$36.00
100g/$117.00
Cl N C CH2CH2CH2Si Cl
182.12 79-82/1 1.14525 1.455125 TOXICITY- oral, rat, LD50: 2830mg/kg flashpoint: 92C (198F) 100g/$127.00 0.9970 1.4235 25g/$114.00 1.302 1.465
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents TSCA HMIS: 3-2-1-X 25g/$39.00
82-3/3
Cl N C CH2CH2CH2Si Cl
OC2H5 N C CH2CH2CH2Si OC2H5
Cl
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents TSCA HMIS: 3-2-1-X 25g/$24.00
100g/$78.00
231.37 79-80/0.6 0.961 1.4174 TOXICITY- oral rat, LD50: 2460mg/kg flashpoint: 74C (165F) 100g/$104.00 90-2/7 1.02625 1.4167 50g/$140.00 162-4/1 1.075
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-2-1-X 25g/$32.00
189.29
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA-L HMIS: 3-2-1-X 10g/$30.00
314.76
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 5.0g/$155.00
(215) 547-1015
www.gelest.com
61
Gelest, Inc.
MW
221.33
bp/mm (mp)
162-5/2-3 10g/$120.00
D420
nD20
1.4410
CH3 Cl CH3
CH3COCH 2CH2Si
1.03125 1.430125
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-2-1-X 25g/$61.00
Cl CH3 Cl
CH3COCH 2CH2Si
1.17725 1.439025
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 25g/$55.00
Cl Cl Cl
CH3COCH 2CH2Si
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 25g/$51.00
CH3COCH 2CH2Si
SIA0025.0 ACETOXYETHYLTRIETHOXYSILANE 250.35 60/0.2 C10H22O5Si >280 rearranges to acetoxytriethoxysilane w/ extrusion of ethylene1. [22538-45-0]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture HMIS: 2-2-1-X
0.983
1.410
1. K. Ezbiansky et al, in Chemical Process. of Dielectrics, Insulators & Electronic Ceramics MRS Proc. 2000.
25g/$49.00
CH3COCH 2CH2Si
208.29
108-9/27 25g/$48.00
1.061
CH3 O CH3
1.0420 1.4388
OC2H5 OC2H5
SIA0050.0 ACETOXYMETHYLTRIETHOXYSILANE 236.34 106/15 C9H20O5Si hydrolyzes to form stable silanol solutions in neutral water [5630-83-1]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture HMIS: 2-2-1-X 25g/$58.00
1.04225 1.4092
100g/$190.00
OCH 3 OCH 3
1.085 50g/$180.00
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture 10g/$45.00 TSCA-L HMIS: 3-3-1-X
OCH 3 OCH 3
500-700 25g/$78.00
1.04
Gelest, Inc.
name
O Cl CH3 Cl
SIA0090.0 ACETOXYPROPYLMETHYLDICHLOROSILANE C6H12Cl2O2Si [5290-24-4]
MW
bp/mm (mp)
D420
nD20
1.15125 1.443425
CH3COCH 2CH2CH2Si
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 25g/$58.00
CH3COCH 2CH2CH2Si
1.062
1.4146
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture HMIS: 3-1-1-X 25g/$19.00
100g/$62.00
O CH3COCH 2(CH2)10SiCl3
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-1-1-X 10g/$85.00
293.37
CH3
CH3
SIA0599.4 N-3-[(AMINO(POLYPROPYLENOXY)]AMINO337-435 PROPYLTRIMETHOXYSILANE 60-65% 3-4 propyleneoxy units contains 30-35% amine terminated polypropylene oxide coupling agent with film-forming capability HMIS: 2-2-1-X 25g/$76.00 SIB0959.0 BENZOYLOXYPROPYLTRIMETHOXYSILANE C13H20O5Si [76241-02-6] 284.38 145/0.2 25g/$68.00
1.104
1.4806
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA-L HMIS: 3-2-1-X
583.40
190-200/0.4
1.158
10g/$124.00
O O CH 2 CH 2 CH 2 CH 2 Si Cl Cl Cl C CH 2 O CH 2 CH 2 CH 2 Si Cl Cl Cl
CH 2 CH 3
SIB1815.3 3,3-BIS(TRICHLOROSILYLPROPOXYMETHYL)- 597.42 220-2/0.9 1.13 5-OXA-TRIDECANE C20H40O3Cl6Si2 dipodal hydrophobic surface treatment with buried hydrophilicity for chromatography
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents HMIS: 3-1-1-X 10g/$84.00
SIB1824.82 BIS[N,N'-(TRIETHOXYSILYLPROPYL)AMINO1000-1200 CARBONYL]POLYETHYLENE OXIDE (10-15 EO) dipodal hydrophilic silane [178884-91-8] TSCA HMIS: 1-1-1-X 25g/$60.00 SIB1824.84 BIS(TRIETHOXYSILYLPROPYL)POLYETHYLENE OXIDE (25-30 EO)
HMIS: 2-1-1-X
1.085
1400-1600 25g/$104.00
(215) 547-1015
www.gelest.com
63
Gelest, Inc.
name
S H N N H CH2 CH2 CH2 CH2 (C2H5O)3Si CH2 CH2 Si(OC2H5)3 C
MW
bp/mm (mp)
D420
nD20
SIB1827.0 BIS[3-(TRIETHOXYSILYL)PROPYL]THIO484.40 UREA tech -90 C19H44N2O6SSi2 forms films on electrodes for determination of mercury1. 1. Y. Guo et al, J. Pharm. Biol. Anal., 19, 175, 1999 [69952-89-2] HMIS: 2-1-1-X SIB1828.0 BIS[3-(TRIETHOXYSILYL)PROPYL]UREA, 60% in ethanol C O C H N O Si 19 44 2 7 2 [69465-84-5]
25g/$134.00
H ((C2H5O)3SiCH2CH2CH2 N)2
0.923
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture HMIS: 2-1-1-X 25g/$34.00
100g/$110.00
384.58 1.102 flashpoint: >110C (>230F) viscosity: 100-250 cSt. 25g/$20.00 100g/$65.00
CH3 Cl CH3
CH3OC(CH 2)10Si
0.950
1.448325
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents [53749-38-5] HMIS: 3-1-1-X 10g/$42.00
CH3OC(CH 2)10Si
288.50
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture HMIS: 2-1-1-X 10g/$51.00
Cl Cl
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents [18163-42-3] TSCA HMIS: 3-2-1-X
Cl Cl
CH3OCCH 2CH2Si Cl
SIC2070.0 2-(CARBOMETHOXY)ETHYLTRICHLORO221.54 90-2/25 1.325 SILANE, 95% contains ~ 20% 1-(carbomethoxy)ethyltrichlorosilane isomer METHYL(3-TRICHLOROSILYLPROPIONATE) flashpoint: > 43C (>110F) C4H7Cl3O2Si
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents [18147-81-4] TSCA HMIS: 3-3-1-X 25g/$36.00
1.448
100g/$117.00
CH3OCCH 2CH2Si
SIC2072.0 2-(CARBOMETHOXY)ETHYLTRIMETHOXY208.29 SILANE, 95% contains ~ 20% 1-(carbomethoxy)ethyltrimethoxysilane isomer METHYL(3-TRIMETHOXYSILYLPROPIONATE) flashpoint: > 43C (>110F) C7H16O5Si [76301-00-3] HMIS: 3-3-1-X 10g/$88.00 SID4465.0 N,N-DIOCTYL-N-TRIETHOXYSILYLPROPYLUREA 488.83 C26H56N2O4Si forms hydrophobic phases with embedded hydrophilicity [259727-10-1]
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture HMIS: 2-2-1-X
1.069
1.410
0.92425 1.452125
CH3CH2CH2CH2CH2CH2CH2CH2 CH3CH2CH2CH2CH2CH2CH2CH2
O N C N(CH 2)3Si(OC2H5)3 H
25g/$82.00
Gelest, Inc.
name
MW
bp/mm (mp)
145-9/1.25
D420
1.07
nD20
SIM6491.5 METHOXYETHOXYUNDECYLTRICHLOROSILANE 363.83 C14H29Cl3O2Si forms self-assembled monolayers with hydrophilic tips
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents 5.0g/$76.00 HMIS: 3-2-1-X
SIM6492.66 2-[METHOXY(POLYETHYLENEOXY)PROPYL]- 472-604 TRICHLOROSILANE, 90% CH3O(C2H4O)6-9C3H6Cl3Si forms hydrophilic surfaces provides protein antifouling surface1. 1. F. Cecchet et al., Langmuir, 22, 1173, 2006 [36493-41-1]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture HMIS: 3-2-1-X
1.13
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-2-1-X 25g/$76.00
100g/$247.00
2-[METHOXY(POLYETHYLENEOXY)PROPYL]TRIMETHOXYSILANE, 90% CH3(OC2H4)9-12(CH2)3Si(OCH3)3 [65994-07-2] TSCA HMIS: 2-2-1-X SIM6493.0 3-METHOXYPROPYLTRIMETHOXYSILANE C7H18O4Si [33580-59-5]
1.09 100g/$247.00
0.995 100g/$110.00
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture HMIS: 3-2-1-X 25g/$34.00
339.71
1.163
SIM6493.4
CH3O (CH2CH2O)3 (CH2)3Si(OCH 3)3 METHOXYTRIETHYLENOXYPROPYLTRI-
326.46 METHOXYSILANE C13H30O7Si forms polymeric proton-conducting electrolytes1. 1. J. Ritchie et al, Chem. Mater., 18, 504, 2006 [132388-45-5] HMIS: 3-2-1-X SIT8186.0 (2-TRIETHOXYSILYLPROPOXY)ETHOXYSULFOLANE, 95% C15H32O7SSi forms hydrophilic surfaces [502925-40-8] 384.56
1.034
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-1-1-X 25g/$12.00
2.0kg/$380.00
(215) 547-1015
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65
Gelest, Inc.
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-4-0-X 25g/$30.00
100g/$98.00 0.985
SIB1142.0 N,N-BIS(HYDROXYETHYL)-N,N-BIS472.73 (TRIMETHOXYSILYLPROPYL)ETHYLENEDIAMINE 66-68% in methanol C18H44N2O8Si2 flashpoint: 11C(52F) [214362-07-9] HMIS: 3-4-1-X 25g/$66.00 SIB1824.2 BIS-[3-(TRIETHOXYSILYLPROPOXY)700-800 2-HYDROXYPROPOXY]POLYETHYLENE OXIDE 65% in methanol HMIS: 2-4-1-X 25g/$74.00 SIB1824.4 2,2-BIS(3-TRIETHOXYSILYLPROPOXY542.86 METHYL)BUTANOL, 50% in ethanol C24H54O9Si2 for solid state synthesis of oligonucleotides for solid state synthesis of oligonucleotides
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture HMIS: 2-4-1-X
CH2CHCH 2O OCH 2CHCH 2 O (CH2CH2O) 5-10 CH2 CH2 CH2 CH2 (C2H5O)3Si CH2 CH2 Si(OC2H5)3
0.899
500-550
OC2H5 OC2H5
SIH6172.0 N-(HYDROXYETHYL)-N-METHYLAMINO237.37 PROPYLTRIMETHOXYSILANE, 75% in methanol flashpoint: 16C (61F) C9H23NO4Si HMIS: 3-4-1-X 25g/$55.00 SIH6175.0 HYDROXYMETHYLTRIETHOXYSILANE, 50% 194.31 in ethanol TRIETHOXYSILYLMETHANOL C7H18O4Si contains equilibrium condensation oligomers hydrolysis yields analogs of silica- hydroxymethylsilanetriol polymers1. 1. B. Arkles, US Pat. 5,371,262, 1994. [162781-73-9] HMIS: 2-4-0-X 25g/$96.00 SIT8189.0 N-(3-TRIETHOXYSILYLPROPYL)GLUCONAMIDE 399.51 50% in ethanol flashpoint: 8C (46F) C15H33NO9Si water soluble, hydrophilic silane [104275-58-3] HMIS: 2-4-1-X 25g/$28.00 SIT8189.5 N-(3-TRIETHOXYSILYLPROPYL)-4-HYDROXY307.47 BUTYRAMIDE C13H29NO5Si anchoring reagent for light-directed synthesis of DNA on glass1. 1. G. McGall et al, J. Am. Chem. Soc., 119, 5081, 1997. [186543-03-3] HMIS: 2-2-1-X 10g/$31.00 SIT8192.0 N-(TRIETHOXYSILYLPROPYL)-O-POLY400-500 ETHYLENE OXIDE URETHANE, 95% viscosity: 75-125 cSt C10H22NO4SiO(CH2CH2O)4-6H contains some bis(urethane) analog hydrophilic surface modifier stabilizes Si3N4 aqueous colloids1. 1. J. Yanez et al, J. Eur. Ceram. Soc., 18, 1993, 1998 [74695-91-3]
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture HMIS: 2-1-1-X 25g/$16.00
100g/$179.00 0.866
0.951
COMMERCIAL
100g/$52.00
2kg/$728.00
66
Gelest, Inc.
MW
bp/mm (mp)
D420
0.942
nD20
1.4104
SIB0957.0 (2-N-BENZYLAMINOETHYL)-3-AMINOPROPYL- 348.25 TRIMETHOXYSILANE, hydrochloride 50% in methanol C15H28N2O3Si.HCl amber liquid flashpoint: 9C (48F) [623938-90-9] TSCA HMIS: 3-3-1-X 25g/$16.00 SIB1835.0 BIS(3-TRIMETHOXYSILYLPROPYL)N-METHYLAMINE C13H33NO6Si2 [31024-70-1]
100g/$52.00
1.023
1.4300
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture HMIS: 2-1-0-X 25g/$68.00
100g/$221.00 1.1725
O Na
+-
OH O Na
+
OCCH 2CH2Si OH
196.14 pH:12-12.5
100g/$146.00 1.37
ClSO2
CH2CH2SiCl3
338.11
Solid Phase Extraction (SPE) columns with benzenesulfonic acid functionalized silica are utilized to analyze urine samples for amino acids and drugs of abuse.
contains 30% free sulfonic acid analog and small amounts of silylsulfonic acid condensation products employed in preparation of solid phase extraction columns
[79793-00-3]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents TSCA HMIS: 4-2-2-X 25g/$48.00
100g/$156.00
338.11
1.08
contains 30% free sulfonic acid analog and small amounts of silylsulfonic acid condensation products
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with water/moisture, protic solvents TSCA HMIS: 4-4-2-X 25g/$52.00
100g/$169.00
ClSO2
CH2CH2Si(OCH 3)3
SIC2417.0 2-(4-CHLOROSULFONYLPHENYL)ETHYLTRI324.85 1.3025 METHOXYSILANE, 50% in methylene chloride C11H17ClO5SSi contains free sulfonic acid; amber color treated silica acts as etherification catalyst1. treatment of surface oxidized PMDSO supports electroosmotic flow 2. 1. B. Sow et al, Microporous & Mesoporous Materials, 79, 129, 2005 2. B. Wang et al, Micro Total Analysis Systems 2004 Vol 2., Roy Soc. Chem., 297, p109 [126519-89-9] HMIS: 3-2-1-X 25g/$72.00 100g/$234.00 SID3392.0 N,N-DIDECYL-N-METHYL-N-(3-TRIMETHOXYSILYL- 510.32 PROPYL)AMMONIUM CHLORIDE, 42% in methanol flashpoint: 13C (55F) contains 3-5% Cl(CH2)3Si(OMe)3 C27H60ClNO3Si [68959-20-6]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-4-0-X
CH3(CH2)9 CH3(CH2)9
0.863
1.4085
CH3CH2 CH3CH2
SID3395.4 DIETHYLAMINOMETHYLTRIETHOXYSILANE C11H27NO3Si catalyst for neutral cure 1-part RTVs [15180-47-9]
249.43
25g/$49.00
(215) 547-1015
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67
Gelest, Inc.
name
SID3396.0 (N,N-DIETHYL-3-AMINOPROPYL)TRIMETHOXYSILANE C10H25NO3Si [41051-80-3]
MW
bp/mm (mp)
D420
0.934
nD20
1.423
CH3CH2 CH3CH2
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 2-2-1-X 25g/$62.00
100g/$202.00
SIO6620.0 OCTADECYLDIMETHYL(3-TRIMETHOXYSILYL496.29 0.89 PROPYL)AMMONIUM CHLORIDE, 60% in methanol C26H58ClNO3Si contains 3-5% Cl(CH2)3Si(OMe)3 flashpoint: 15C (59F) employed as lubricant/anti-static surface treatment orients liquid crystals dispersion/coupling agent for high density magnetic recording media1. application as immobilizeable antimicrobial reported2. 1. H. Vincent in Chemically Modified Oxide Surfaces, ed. D. Leyden, Gordon & Breach,1990, p. 305. 2. W. White et al in Silanes, Surfaces & Interfaces ed. D. Leyden, Gordon & Breach, 1986, p. 107. [27668-52-6]
HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture TSCA HMIS: 3-4-0-X 25g/$18.00
COMMERCIAL
301.48
SIP6926.4 2-(4-PYRIDYLETHYL)THIOPROPYLTRI301.48 160-2/0.2 METHOXYSILANE pKa: 4.8 C13H23NO3SSi immobilizeable ligand for immunoglobulin IgG separation using hydrophobic charge induction chromatography (HCIC) [198567-47-4] HMIS: 3-2-1-X 10g/$124.00 SIP6928.0 2-(4-PYRIDYLETHYL)TRIETHOXYSILANE C13H23NO3Si see also SIT8396.0 [98299-74-2] 269.43 105/0.9 amber liquid 10g/$119.00
1.00
1.462424
240.59
CH2CH2SiCl3
[17082-69-8]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-2-1-X 25g/$45.00
CH2CH2SiCl3
SIT8158.0 4-[2-(TRICHLOROSILYL)ETHYL240.59 0.93 PYRIDINE, 15-20% in toluene flashpoint: 4C (39F) hazy liquid; extremely moisture sensitive C7H8Cl3NSi see also SIT8396.0 2-(TRIMETHOXYSILYLETHYL)PYRIDINE employed in polypyridine self-assembled monolayers1. 1. S. Paulson et al, J. Chem. Soc. Chem. Comm., 21, 1615, 1992. [17082-70-1]
HYDROLYTIC SENSITIVITY: 8 reacts rapidly with moisture, water, protic solvents TSCA HMIS: 3-4-1-X 25g/$29.00
100g/$96.00
Gelest, Inc.
name MW bp/mm (mp) D420 nD20
1.452
SIT8187.5 N-(3-TRIETHOXYSILYLPROPYL)274.43 134/2 1.005 4,5-DIHYDROIMIDAZOLE flashpoint: >110C (>230F) 3-(2-IMIDAZOLIN-1-YL)PROPYLTRIETHOXYSILANE C12H26N2O3Si viscosity: 5 cSt. OC2H5 utilized in HPLC of metal chelates1. N CH2CH2CH2Si OC2H5 forms proton vacancy conducting polymers w/sulfonamides by sol-gel2. ligand for molecurlarly imprinting silica w/ chymotrypsin transition state analog3. OC2H5 1. T. Suzuki et al, Chem. Lett, 881, 1994. 2. V. De Zea Bermudez et al, Sol-Gel Optics II, SPIE Proc. 1728, 180, 1992. 3. M. Markowitz et al, Langmuir, 1989. [58068-97-6]
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture TSCA HMIS: 2-1-1-X 25g/$18.00
COMMERCIAL
100g/$62.00 (-62)
2.0kg/$680.00 1.12
O HOSCH 2CH2CH2Si(OH) 3 O
HYDROLYTIC SENSITIVITY: 0 forms stable aqueous solutions TSCA HMIS: 3-0-0-X 25g/$51.00
O CH3PO(CH 2)3Si(OH) 3 O Na
+
SIT8378.5 3-TRIHYDROXYSILYLPROPYLMETHYL238.18 PHOSPHONATE, SODIUM SALT, 42% in water flashpoint: 79C (174F) C4H12NaO6PSi contains 4-5% methanol, sodium methylphosphonate [84962-98-1]
HYDROLYTIC SENSITIVITY: 0 forms stable aqueous solutions TSCA HMIS: 1-2-0-X 100g/$16.00
500g/$64.00 0.966
CH2CH2Si(OCH 3)3
SIT8395.0 N-(TRIMETHOXYSILYLETHYL)BENZYL-N,N,N333.93 TRIMETHYLAMMONIUM CHLORIDE, 60% in methanol flashpoint: 25C (77F) C15H28ClNO3Si candidate for exchange resins and extraction phases
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture HMIS: 3-3-1-X
25g/$80.00 1.4755
CH2CH2Si(OCH 3)3
50g/$164.00
COMMERCIAL
265.43 114-8/2 1.030 1.4590 flashpoint: 137C (279F) c of treated surface: 37.5 dynes/cm 2.0kg/$248.00 1.26
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture TSCA HMIS: 3-1-1-X 100g/$20.00
Na OOCCH 2 Na OOCCH 2
+-
CH2COO Na CH2
SIT8402.0 N-(TRIMETHOXYSILYLPROPYL)ETHYLENE462.42 DIAMINE TRIACETIC ACID, TRISODIUM SALT, 45% in water essentially silanetriol, contains NaCl C14H25N2Na3O9Si chelates metal ions [128850-89-5]
HYDROLYTIC SENSITIVITY: 0 forms stable aqueous solutions TSCA HMIS: 2-0-0-X 25g/$42.00
H2N H2N
SIT8405.0 N-(TRIMETHOXYSILYLPROPYL)ISOTHIOURONIUM CHLORIDE, 50% in water C7H19ClN2O3SSi antimicrobial activity reported [84682-36-0]
274.84 pH: 6
25g/$45.00 0.92
C4H9
+
C4H9
N C4H9
Br CH2CH2CH2Si(OCH 3)3
SIT8412.0 N-TRIMETHOXYSILYLPROPYL-N,N,N-TRI428.52 n-BUTYLAMMONIUM BROMIDE, 50% in methanol flashpoint: 11C (52F) C18H42BrNO3Si immobilizable phase transfer catalyst
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture HMIS: 3-4-1-X
25g/$89.00
(215) 547-1015
www.gelest.com
69
Gelest, Inc.
name
C4H9
+ -
MW
bp/mm (mp)
D420
0.88
nD20
C4H9
N C4H9
Cl CH2CH2CH2Si(OCH 3)3
SIT8414.0 N-TRIMETHOXYSILYLPROPYL-N,N,N-TRI384.08 n-BUTYLAMMONIUM CHLORIDE, 50% in methanol flashpoint: 11C (52F) C18H42ClNO3Si contains 3-5% chloropropyltrimethoxysilane and Bu3NH+ClHYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture HMIS: 3-4-1-X
CH3 - Cl
+
H3C
N CH3
CH2CH2CH2Si(OCH 3)3
SIT8415.0 N-TRIMETHOXYSILYLPROPYL-N,N,N-TRI257.83 METHYLAMMONIUM CHLORIDE, 50% in methanol N,N,N-TRIMETHYL-3-(TRIMETHOXYSILYL)-1-PROPANAMINIUM CHLORIDE C9H24ClNO3Si flashpoint: 16C (61F) employed for bonded chromatographic phases anti-static agent used to treat glass substrates employed in electroblotting see also SIT8395.0 [35141-36-7]
HYDROLYTIC SENSITIVITY: 7 reacts slowly with water/moisture TSCA HMIS: 2-4-1-X 25g/$18.00
COMMERCIAL
2.0kg/$390.00
H N
+ Cl
Si(OCH 3)3
H N
+ Cl
COMMERCIAL
n N
4n
TSCA
H2
C Si
H2 CH 2 CH
2
N H2 H NH
2 +
CH C 2
CH Si O Si m
O OH
OH n
H O O Si H O C 2 H2 C H 2 C H
OH
Functional Molecular Weight % Specific Code Group Mole % Weight in solution Gravity Viscosity pH Price/100g 3kg Aminopropyl 65-75 250-500 25-28 1.10 5-15 10-10.5 $29.00 $435.00 WSA-7011 Aminopropyl WSA-9911* 100 270-550 22-25 1.06 5-15 10-10.5 $24.00 $360.00 Aminoethylaminopropyl 65-75 370-650 25-28 1.10 5-10 10-11 $29.00 $435.00 WSA-7021 WSAV-6511** Aminopropyl, vinyl 60-65 250-500 25-28 1.11 3-10 10-11 $35.00 $480.00
*CAS [29159-37-3] **[207308-27-8]
Gelest, Inc.
Aqueous exposure of treated surfaces converts Epoxy-Silanes to Hydrophilic-Diols
1.015
1.4455
2.0kg/$320.00
CH2CH2Si(OCH 3)3
SIE4670.0 2-(3,4-EPOXYCYCLOHEXYL)ETHYL246.38 95-7/0.25 1.065 1.449 TRIMETHOXYSILANE TOXICITY- oral rat, LD50: 12,300mg/kg flashpoint: 146C (295F) C11H22O4Si viscosity: 5.2 cSt c of treated surface: 39.5 dynes/cm specific wetting surface: 317 m2/g coefficient of thermal expansion: 0.8 x 10-3 vapor pressure, 152: 10mm ring epoxide more reactive than glycidoxypropyl systems. UV initiated polymerization of epoxy group with weak acid donors. forms UV-cureable coating resins by controlled hydrolysis1. 1. J. Crivello et al, Chem. Mater. 9, 1554, 1997. [3388-04-3] TSCA HMIS: 3-1-1-X 100g/$24.00 2.0kg/$270.00 18kg/$1044.00 120/2 1.070 1.4290 (<-70)mp C9H20O5Si TOXICITY- oral rat, LD50: 8,400 mg/kg coupling agent for epoxy composites employed in electronic chip encapsulation. [2530-83-8] TSCA HMIS: 3-1-1-X 100g/$16.00 2.0kg/$138.00 18kg/$693.00
3-(2,3-EPOXYPROPOXY)PROPYLTRIMETHOXYSILANE
COMMERCIAL
SIG5840.0 (3-GLYCIDOXYPROPYL)TRIMETHOXYSILANE
236.34
CH3CH2O
1.00
1.425
2.0kg/$580.00
C9H20O5Si [2530-83-8]
120/2 1.070 1.4290 (<-70)mp TOXICITY- oral rat, LD50: 8,400 mg/kg 25g/$180.00 in fluoropolymer bottle 0.96025 1.425425
DEVELOPMENTAL
248.39 122-6/5 0.97825 1.431 TOXICITY- oral rat, LD50: >2000mg/kg flashpoint: 122C (252F) viscosity: 3.0 cSt employed in scratch-resistant coatings for eyeglasses. [2897-60-1] TSCA HMIS: 2-1-1-X 25g/$38.00 100g/$124.00 2.0kg/$580.00 SIG5836.0 (3-GLYCIDOXYPROPYL)METHYLDIMETHOXYSILANE C9H20O4Si relative hydrolysis rate vs. SIG5840.0: 7.5:1 [65799-47-5] TSCA-L HMIS: 3-1-1-X 220.34 100/4 flashpoint: 105C (221F) 1.02 1.43125
COMMERCIAL
DEVELOPMENTAL
25g/$50.00
100g/$162.00
50g/$160.00
(215) 547-1015
www.gelest.com
71
Gelest, Inc.
Silyl Hydrides
Silyl Hydrides are a distinct class of silanes that behave and react very differently than conventional silane coupling agents. Their application is limited to deposition on metals (see discussion on p. 17). They liberate hydrogen on reaction and should be handled a with appropriate caution.
name
H CH3(CH2)10CH2Si H H SID4629.6 DODECYLSILANE C12H28Si forms SAMS on gold surfaces 872-19-5 HMIS: 2-2-1-X
MW
200.44
bp/mm (mp)
80/7
D420
0.7753
nD20
1.438025
10g/$78.00
H CH3(CH2)16CH2 Si H H
SIO6635.0 n-OCTADECYLSILANE 284.60 195/15 C18H40Si contains 4-6% C18 isomers (29)mp forms self-assembled monolayers on titanium1. flashpoint: >110C (>230F) 1. A. Fadeau et al, J. Am. Chem. Soc., 121, 12184, 1999 [18623-11-5] TSCA HMIS: 2-1-1-X 25g/$46.00 SIT8173.0 (TRIDECAFLUORO-1,1,2,2-TETRA378.22 75/251.446 HYDROOCTYL)SILANE C8H7F13Si provides vapor-phase hydrophobic surfaces on titanium, gold, silicon [469904-32-3] HMIS: 3-3-1-X 10g/$190.00 SIU9048.0 10-UNDECENYLSILANE C11H24Si
HMIS: 2-3-1-X
0.794
100g/$150.00
H CF3CF2CF2CF2CF2CF2CH2CH2Si H H
1.3184
184.40 2.5g/$180.00
0.78
MethylHydrosiloxane homopolymers are used as water-proofing agents, reducing agents and as components in some foamed silicone systems.
Tg: -119 V.T.C: 0.50 polyMethylHydrosiloxanes, Trimethylsiloxy terminated Molecular Mole % Equivalent Specific Refractive Code Viscosity Weight (MeHSiO) Weight Gravity Index HMS-991 15-25 1400-1800 100 67 0.98 1.395 HMS-992 25-35 1800-2100 100 65 0.99 1.396 HMS-993 35-45 2100-2400 100 64 0.99 1.396
COMMERCIAL
Gelest, Inc.
Surface Modification with Silanes: Whats not covered in Hydrophobicity, Hydrophilicity and Silane Surface Modification? Silanes which are expected to form covalent bonds after deposition onto surfaces are discussed in the Gelest brochure entitled Silane Coupling Agents: Connecting Across Boundaries Aminosilanes which are important in some hydrophilic surface treatments are covered in detail.
Further Reading
Silane Coupling Agents - General References and Proceedings 1. B. Arkles, Tailoring Surfaces with Silanes, CHEMTECH, 7, 766-778, 1977. 2. E. Plueddemann, Silane Coupling Agents, Plenum, 1982. 3. K. Mittal, Silanes and Other Coupling Agents, VSP, 1992. 4. D. Leyden and W. Collins, Silylated Surfaces, Gordon & Breach, 1980. 5. D. E. Leyden, Silanes, Surfaces and Interfaces, Gordon & Breach 1985. 6. J. Steinmetz and H. Mottola, Chemically Modified Surfaces, Elsevier, 1992. 7. J. Blitz and C. Little, Fundamental & Applied Aspects of Chemically Modified Surfaces, Royal Society of Chemistry, 1999. Substrate Chemistry - General References and Proceedings 8. R. Iler, The Chemistry of Silica, Wiley, 1979. 9. S. Pantelides, G. Lucovsky, SiO2 and Its Interfaces, MRS Proc. 105, 1988. Hydrophobicity & Hydrophilicity 10. C. Tanford, The Hydrophobic Effect Wiley, 1973. 11. H. Butt, K. Graf, M. Kappl, Physics and Chemistry of Interfaces, Wiley, 2003. 12. A. Adamson, Physical Chemistry of Surfaces. Wiley, 1976. 13. F. Fowkes, Contact Angle, Wettability and Adhesion, American Chemical Society, 1964. 14. D. Quere Non-sticking Drops Rep. Prog. Phys. 68, 2495, 2005. 15. McCarthy, T. A Perfectly Hydrophobic Surface, J. Am. Chem. Soc., 2006, 128, 9052.
Product Information
Product Code Product Name
Molecular Weight Boiling Point/mm (Melting Point) Refractive Index Specific Gravity
H2NCH 2CH2NHCH 2
SIA0588.0 (AMINOETHYLAMINOMETHYL)PHENETHYL-298.46 126-30/0.2 1.02 1.5083 TRIMETHOXYSILANE, 90% mixed m,p isomers flashpoint: > 110C (>230F) Other Physical Properties C14H26N2O3Si coupling agent for polyimides photochemically sensitive (194nm)1 self-assembled monolayers2. 1. W. Dressick et al, Thin Solid Films, 284, 568, 1996. References 2. C Harnett et al, Appl. Phys. Lett., 76, 2466, 2000. HYDROLYTIC SENSITIVITY: 7 Si-OR reacts slowly with water/moisture 25g/$82.00 100g/$266.00 [74113-77-2] TSCA HMIS: 3-1-1-X
CAS# Hazardous Rating Information (Health-Flammability-Reactivity)
Indicates Product listed in TSCA Inventory (L = Low Volume Exemption; S = Significant New Use Restriction)
73
The Stenocara beetle, an African desert species, harvests water that adsorbs on superhydrophilic bumps on its back, then transfers droplets into superhydrophophic channels that lead to its mouth.
Gelest Inc. 11 East Steel Road Morrisville, PA 19067 Phone (215) 547-1015 Fax: (215) 547-2484 www.gelest.com