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Commercial Organofunctional Silanes for Coupling, Surface Modification and Thin-Film Deposition 03 OSiOOHN
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Gute Chemie. Foreword 1 Gute Chemie. Welcome to abcr. What do you think of when you hear the expression ‚Gute Chemie‘? Does it make you think of top-quality products or people that understand each other really well? Since we set up our company in 1987, we have consistently attempted to combine both. We offer Gute Chemie in the form of more than 400,000 specialty chemicals that we supply to major pharmaceuticals and chemical companies. And we also provide Gute Chemie in terms of our personal service coupled with an extensive network that links our clients, suppliers and partners all around the world. With this brochure, we would like to invite you to experience all the aspects of Gute Chemie. Dr. Jan Schuricht | Managing Director
Commercial Organofunctional Silanes Reagents for Coupling, Surface Modification and Thin-Film Deposition. Organofunctional silanes are widely used commer- cially due to their remarkable versatility. They are hy- brid molecules combining the functionality of a reac- tive organic group and inorganic functionality into a single molecule. This unique property is used as a molecular bridge to make inorganic materials organi- cally compatible. Typically, organofunctional silanes molecules have two reactive centers. One is characterized by at least one hydrolytically stable carbon-silicon bond, which allows the introduction of non-reactive or reactive organic functionality such as alkyl, aryl, arylalkyl, per- fluoropenylalkyl, amino, epoxy, aldehyde, ethylene and anhydride. Hydrolyzable groups, mainly chloro, alkoxy and amine, characterize the other reactive center of the silicon atom. The hydrolysable compo- nent of organofunctional silanes will hydrolyze readily with water to form silanols and allow silicon to cova- lently bond to inorganic surfaces via a condensation reaction to form a siloxane bond. In addition to forming covalent siloxane bonds with inorganic substrates, the hydrophobic nature of the silicon-carbon bond provides improved resistance to hydrolysis attack at the interphase between siloxane bond and substrate. This feature makes a matrix com- posite materials more hydrolytically stable; hence, increasing service life by providing protection against corrosion and enhancing its mechanical properties. The organofunctional silanes can be tri-functional, di-functional or mono-functional. Typical molecular structure for a tri-functional silane is: R X (CH 2 ) n Si R R R can an example be for chloro, dimethylamine or methoxy X can an example be for hydrogen, perfluorphenyl, phenyl, amino, oxy or cyano In order to initiate the hydrolysis reaction of organo- functional alkoxysilanes to subsequently form covalent siloxane bonds, a catalyst is generally required; typi- cally, a mild acid or base is sufficient. The most com- mon catalysts are acetic acid and ammonia. Chlorosi- lanes and aminosilanes are autocatalytic because the hydrolyzable groups will generate in situ hydrochloric acid or amine. The choice of hydrolyzable group de- pends on the desired rate of hydrolysis and application requirements. The tri-functional silanes, e.g. trimethoxysilanes, hy- drolyze first to form a silanol group and then condense with surface hydroxyl groups to form a hydrolytically stable covalent bond and crosslink to form a multilayer (silsequioxane) coating. This multilayer forms at the inorganic interphase and can diffuse into a porous matrix to create an interpenetrating network within the inorganic substrate; this, in turn, generates a more hydrolytically stable matrixcomposite material. The di-functional silanes, e.g. dimethothoxysilanes, also hydrolyze first to form a silanol group and then condense with surface hydroxyl groups to form hydro- lytically stable covalent bonds. The di-functional si- lanes can also form polymeric siloxane materials that
Gute Chemie. Commercial Organofunctional Silanes Reagents 2 | 3 can adhere to different types of surfaces. These types of organofunctional silanes are incorporated into for- mulations to tailor the mechanical properties of the matrix composite material. The mono-functional silanes, due to their single hydro- lyzable reactive group, form a self-assembled-monolay- er (SAM) on the inorganic substrate thus creating a uniform molecular layer on the inorganic substrate’s surface. This may offer advantages because the film thickness is easily controlled; whereas it is well known that for tri- and di-functional silanes, reproducibly con- trolling the film thickness can be quite challenging. vents are highly recommended. In order to facilitate analysis and process handling, these products are also offered as a solution in a non-polar solvent. In chromatography for example, mono-functional si- lanes are generally used to make bonded phases for analytical applications because results are more repro- ducible; whereas, due to the higher hydrolytic stability, the di- and tri-functional silanes are more commonly used to make bonded phases for sample-prep-scale chromatography, solid phase extraction (SPE) and pre- parative chromatography for the purification of active pharmaceutical ingredients (API). In addition, an important aspect of treating inorganic substrates is capping of unreacted hydroxyl groups left on the inorganic surfaces. These unreacted hydroxyl groups adversely affect performance and, therefore, are capped with a trimethysilyl group. Also, capping of hydroxyl groups eliminates hydrogen bonding and leads to free flowing particles. Hydroxyl and free water scavengers like trimethylchlorosilane and hexamethyl- disilazane are efficient; however, a customized solution of trimethylchlorosilane and hexamethyldisilazane has a higher reactivity and is more effective than either of the reagents alone. And, organofunctional silanes with a hydrolyzable dimethylamino group are versatile si- lylating reagents for capping hydroxyls. Due to it is ex- treme reactivity with hydroxyl groups, dimethylami- notrimethylsilane is a highly effective hydroxyl scavenger. The by-product formed, dimethylamine, can be easily removed by applying vacuum. It must be not- ed that dimethylamino silanes are extremely hydrolyti- cally sensitive, even more reactive than chlorosilanes. They will react almost instantaneously with moisture in the air; water contained in polar solvents, adsorbed on the surfaces of glass. When handling these types of products, the use of inert gases and anhydrous sol- Due to their versatility, organofunctional silanes in combination with metal alkoxide precursors are also used to make films and particles using sol-gel technol- ogy. Discovered and first used in the mid-1800s, a renewed interest in the sol-gel process emerged when it was found out that inorganic gels could be formed and turned into inorganic glasses without the use of a high temperature melting process. Today, the sol-gel process is extensively used for the synthesis of thin films, fibers, ceramic powders, and other organic-inor- ganic hybrid materials. Along with exceptionally low processing temperatures, this technique also creates a product with high chemical homogeneity and provides the ability to control precisely the size of its inter- spersed particles. Sol-gel technology makes possible the synthesis of materials that are otherwise difficult to obtain by regu- lar means due to problems of volatilization, high melt- ing temperatures, or crystallization. It creates hybrid materials with unique properties without the need for complex machinery or processes. Typically, reactions take place at room temperature with minimal sensitiv- ity towards atmospheric conditions and allow for fine
control of the product’s chemical composition and pu- rity; resulting in excellent homogeneity of the final gel. In particular, sol-gel technology is especially preferred for the toughness of its ceramic products, capable of withstanding much higher temperatures than conven- tional powders or coatings. The sol-gel process requires the use of appropriate chemical precursors and reagents in order to promote the growth of colloidal particles within the initial mix- ture solution. The “sol” referred to in the sol-gel pro- cess is a liquid containing a stable suspension of colloidal particles and/or monomers formed after hydrolysis and condensation of the metal alkoxide precursor solution. Through gelation, the monomers within the sol eventually link up and polymerize to form larger particles. The controlled growth of these particles causes the sol to thicken into a porous, three- dimensional gel network, which then can be dried in different ways to form the final “gel”. As listed below, the process (figure 1) can be broken down into the following major steps: hydrolysis and condensation of the metal alkoxide precursors with or without the use of a catalyst, gelation of the homogeneous sol mixture, and the removal of excess solvent and unre- acted precursors in order to dry and form the final oxide structure. Chemical precursors: These are the starting materials for the sol-gel process, the most common of which are metal alkoxides due to their high reactivity with water. They consist of a positively charged metal ion and a negatively charged alcohol part. Other organic or inor- ganic precursors include acetates, lactates, pentanedi- onates, nitrates, or chlorides. These are initially mixed with water during hydrolysis to form a solution that can then undergo a condensation reaction in order to en- courage polymerization. Precursors such as organo- functional silanes and metal alkoxides play a major role in the final gel’s effectiveness by directly affecting its porosity, refractive index, hardness, and other physical characteristics. Hydrolysis and condensation: When using a silicon- based precursor, the addition of water initiates a hy- drolysis reaction and causes the mixture solution to react and form silanol groups. Then they undergo a water condensation reaction that produces siloxane bonds in the sol that promote its polymerization. As the number of siloxane bonds begins to increase, more molecules aggregate together within the sol, turning it into a continuous gel network. The structure of the resulting gel can be anywhere from discreet colloidal particles within the mixture to a continuous polymer network. It is possible to control the structure and properties of the final gel product by carefully regulat- ing pH, temperature, and reagent concentrations throughout the reactions. Catalysts: Varying effects on gelation time, porosity, bulk, and apparent density of the final gel can be ob- tained through the use of a catalyst. Although catalysts for hydrolysis and condensation reactions are not typi- cally required, some metal alkoxides, such as alkoxysi- lanes, hydrolyze much more quickly with the addition of either an acidic or basic catalyst. If no catalyst is used during hydrolysis, the reaction may not finish complete- ly by the time condensation begins. Mineral acids, am- monia, alkali metal hydroxides, and fluoride anions are the most common types of catalysts used. It is the strength and concentration of either acid or base cata- lyst that determines the speed of the reaction. Drying: Once the gel product is obtained, it undergoes a drying process where the remaining solvent liquid is removed at room temperature and atmospheric pres- sure. This stage causes a significant amount of shrink- age and densification of the gel, creating a dried
Gute Chemie. Commercial Organofunctional Silanes Reagents 4 | 5 product referred to as a xerogel. When the gel is dried under supercritical conditions, a highly porous and lighter aerogel is produced. Specific uses for these gels are derived from the different material shapes obtained when processing the final gel product. These shapes include monoliths, films, fibers, and nanoparticles. Sol-gel derived materials have a diverse set of applica- tions. The most widespread commercial use of sol-gel products is in the fabrication of specialized material coatings. They can be either protective or decorative coatings applied to glass, metal or other types of sub- strates. These coatings provide a number of functions such as protection from corrosion and abrasion, en- hancing optoelectronic properties, and increasing con- ductivity. Sol-gel technology is used in the formation of ceramic fibers and thin glass films with practical appli- cations that include thermal insulation and fiber optic sensors, respectively. Increasing varieties of materials for dental and biomedical applications are being devel- oped using the sol-gel technology. Figure 1: Sol-gel process Sol-gel derived materials have a diverse set of appli- cations. The most widespread commercial use of sol-gel products is in the fabrication of specialized material coatings. They can be either protective or decorative coatings applied to glass, metal or other types of substrates. These coatings provide a number of functions such as protection from corrosion and abrasion, enhancing optoelectronic properties, and increasing conductivity. Sol-gel technology is used in the formation of ceramic fibers and thin glass films with practical applications that include thermal insula- tion and fiber optic sensors, respectively. Increasing varieties of materials for dental and biomedical applica- tions are being developed using the sol-gel technology. Condensation Gelation Precursor Solution Colloidal Solution (Sol) Gel Supercritical Drying Aerogel Normal Drying Xerogel
Gute Chemie. abcr and abcr labs. abcr GmbH Germany abcr Locations Worldwide
Gute Chemie. abcr and abcr labs 6 | 7 In 2010, abcr GmbH, located in Karlsruhe, Germany, established a new contract manufacturing facility for fine chemicals and specialty materials, abcr labs S.L. in Forcarei, Spain. The 6,000 m2 manufacturing site provides contract services for custom synthesis, product and process development, scale-up and com- mercialisation. abcr labs operates 24 hours a day, 5 days a week. The flexible manufacturing platform consists of a kilo lab, pilot plant and full-scale com- mercial production facilities. In addition, R&D and analytical laboratories provide technical support and testing for raw materials and in-process and finished products to support manufacturing operations. abcr labs’ bulk products are shipped to abcr’s logistics centre in Karlsruhe, Germany, for final packaging and global distribution. abcr GmbH has been delivering specialty chemicals to renowned pharmaceutical, chemical and material science-oriented companies worldwide since 1987. Via the 2,500 m2 logistic centre in Karlsruhe, Germany, abcr organises product shipping to more than 10,000 individual laboratories worldwide. Competent assis- tance from our chemists and engineers, worldwide sourcing activities, as well as reliable deliveries at fair prices and excellent quality have made abcr the “preferred supplier” of many customers. abcr keeps stock of most of their 50,000 items up to semi-bulk quantities, offering you immediate access to organo- silanes, silicones, fluorinated chemicals, organic and inorganic compounds, precious metal compounds, metal-organics, homogeneous and heterogeneous catalysts, nanomaterials, phosphines, rare earth com- pounds and many more. The products are available in regular catalogue units, as well as on a semi-bulk and bulk scale.
Custom synthesis. Gute Chemie paves the way for new products and processes. Lasting relationships abcr builds lasting relationships with customers by collaborating at all stages of product development, from laboratory scale to commercial production, from gram to ton quantities.
Gute Chemie. Custom synthesis 8 | 9 Chemical process equipment Applications abcr labs chemical process equipment makes use of batch, semi-batch, reactive distillations and continuous process technology. The portfolio of chemical processes consists of: For more than 30 years, abcr has been supplying specialty chemicals in laboratory-scale and semi-bulk quantities to companies worldwide. These products can be widely used as: › Condensation › Ammonolysis › Alkyllithium reaction › Grignard formation & reaction › Alkoxylation › Catalytic hydrogenation › Amination › Esterification › Transesterification › Halogenation › Hydrolysis › Hydrosilylation › LAH reduction › Lithiation reaction › Ring opening polymerisation › Silylation › Silylating and protecting groups › Adhesion promoters › Reducing agents › Derivatisation › Various reagents for organic synthesis › Reagents for bioactive reactions › Blocking agents › Surface modification › Thinfilm deposition › Optical and conductive coatings › Catalysis › Polymer synthesis › and many more
In-house production. Gute Chemie means trusting in the quality of the products you make. Kilo lab Pilot plant The kilo laboratory facilities manufacture products in the range of 5 to 15 kg; they are equipped with 6 walk-in fume hoods, one bench top fume hood for weighing and two distillation bench tops for fractional distillations. Pilot plant facilities are composed of six processing suites, two of which are equipped with two reactor pairs with working capacities of 160 and 400 litres. The automated reactors are Pfaudler-Pharmaglass® lined; they have azeotropic, flash and fractional distillation capabilities; they operate from full vacuum to 10 bars of pressure and temperature from -20 °C to 220 °C. A third suite is equipped with a continuous thin film eva- porator for purification of heat sensitive materials and low volatility products. The remaining suites are dedicated for special projects and future expansion.
Gute Chemie. In-house production 10 | 11 Commercial plant The full scale commercial plant facilities are equipped with automated reactors that are Pfaudler-Pharmaglass® lined; have azeotropic, flash and fractional distillation capabilities; operate from full vacuum to 10 bars of pressure and temperatures from -20 °C to 220 °C. Both reactors are supported by a 1,000 litre (1.2 m3) corrosion resistant alloy Neutsche Filter / dryer equipped with automatic cake discharge for rapid turnover and has an operating temperature range from -20 °C to 120 °C. The plant has the infrastructure in place for 4 reactors ranging from 2,500 to 8,000 litres.
Safety. Gute Chemie gives you a feeling of security – from procurement to delivery. Safety: As important as the air we breathe Quality with responsability As in the parent company abcr, at abcr labs highest standards of safety are also observed. This equally applies to environment, health and safety regulations. When it comes to quality assurance, abcr accepts no compromises. As is the case at abcr, the modern production facility is climatically supplied by an earth tube which cools the building by up to 7 °C in the summer and warms it accordingly in the winter. The plants on the roof serve as a natural buffer for tem- perature peaks. abcr has strict standards of quality and is committed to complying with all the environmental, health and safety regulations. Clients are welcome to audit the quality systems that are critical to our success.
Gute Chemie. Safety 12 | 13 Your professional partner for products and services › Custom synthesis for complex multi-step or air-sensitive reactions › Specialty chemicals outsourcing of small or medium-sized products › Tailor-made solutions according to customer needs › Transfer and up-scaling of new processes from laboratory to commercial scale › Silanes and specialty silicones › Metalorganic compounds › Organic intermediates › Organo-Silanes & Silicones
Flexible quantities. Gute Chemie is when you can order any different quantity from the same company.
Gute Chemie. Flexible quantities 14 | 15 Glass bottles Barrels Narrow neck bottle (brown) 5 - 2 500 ml Combination barrels Wide neck bottle (brown) 25 - 2 500 ml Steel barrels inside cover Septum bottle (brown) 50 - 1 000 ml Stainless steel barrels Lab glass bottle with scale (white) 100 - 2 500 ml Plastic barrels (incl. lid & clamping ring) Plastic bottles Aseptic Pharma Containers 6 - 216 l 6 - 220 l 30 - 220 l 30 - 220 l Narrow neck bottle (PFA) (off-white) Narrow neck bottle (PE) (off-white) 60 - 125 ml 60 - 125 ml Wide neck bottle (PE) (off-white) 250 - 2 500 ml Nalgene narrow neck bottle (HDPE) 15 - 1 000 ml Type series C (for aseptic application) 300 ml - 12 l Type series C M (with magnetic stirrer) 600 ml - 12 l Type series CD (M) (with double jacket and optional magnetic stirrer) 1,4 - 12 l Stainless steel bottles GL45 Stainless steel bottles with PE cap 250 - 3 000 ml Stainless steel bottles with Stainless steel cap 100 - 1 000 ml Cylinders Steel cylinders 25 - 2 400 ml Stainless steel cylinders 50 ml - 3.78 l (1 Gallone) Stainless steel bubblers Stainless steel bubblers with standard valve Stainless steel bubblers with cross-purge valve Plastic canisters Plastic canisters 1.5 l - 33 l 150 ml - 1 000 l 5 - 20 l
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Gute Chemie. Products 17 Coupling, Surface Modification, Thin-Film Deposition. Table of contents. Organofunctional Silanes Reagents for Coupling Acetoxy Organofunctional Silanes Acrylate Organofunctional Silanes Amino Organofunctional Silanes Bidentate Organofunctional Silanes Carboxylic Acid Organofunctional Silanes Cyanate Organofunctional Silanes Epoxy Organofunctional Silanes Halogen Organofunctional Silanes Olefin Organofunctional Silanes Phosphorous Organofunctional Silanes Sulfur Organofunctional Silanes Organofunctional Silanes Reagents for Surface Modification Alkyl Organofunctional Silanes Aryl Organofunctional Silanes Arylalkyl Organofunctional Silanes Polar Organofunctional Silanes Perfluorinated Organofunctional Silanes Organofunctional Silanes Reagents for Thin-Film Deposition Silicate Precursors Bidentate Alkyl Organofunctional Silanes Bidentate Aryl Organofunctional Silanes Siloxanes SiOx Precursors Silane Reagents for Microelectronics 19 20 22 26 27 28 30 32 35 39 39 40 52 54 57 59 62 63 65 66 66 68
Gute Chemie. Organofunctional Silanes Reagents for Coupling 19 Acetoxy Organofunctional Silanes AB110781 Acetoxyethyldimethylchlorosilane; 97% 18306-45-1 AB110782 Acetoxyethylmethyldichlorosilane; 97% 18163-34-3 AB110783 Acetoxyethyltrichlorosilane; 97% 18204-80-3 AB134426 Acetoxyethyltriethoxysilane 22538-45-0 AB153206 Acetoxyethyltrimethoxysilane; 95% 72878-29-6 AB110784 Acetoxymethyltriethoxysilane; 97% 5630-83-1 AB110785 Acetoxymethyltrimethoxysilane; 95% 65625-39-0 Cl Si O O Cl Cl Si Cl Cl Si Cl O O O O O O Si O O O O O O O Si O O O Si O O O O O Si O O O AB252438 2-(4-Acetoxyphenyl)ethyltrichlorosilane; 97% 627882-90-0 O O AB110787 3-Acetoxypropylmethyldichlorosilane; 97% 5290-24-4 AB110788 Acetoxypropyltrimethoxysilane; 97% 59004-18-1 Cl Si Cl Cl Cl Cl Si O O O O Si O O O AB153213 11-Acetoxyundecyltrichlorosilane; 95% 53605-77-9 Cl Cl Si Cl O O abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
20 Acrylate Organofunctional Silanes AB252441 (Acryloxymethyl)phenethyltrimethoxysilane; 95%, 141813-19-6 mixed m-, p-, alfa-, beta-isomers O O Si O O O AB252440 Acryloxymethyltrimethoxysilane; 95% 21134-38-3 AB108707 (3-Acryloxypropyl)dimethylmethoxysilane; 95% 111918-90-2 AB108959 (3-Acryloxypropyl)methyldichlorosilane; 95% 71550-63-5 AB108709 (3-Acryloxypropyl)methyldimethoxysilane; 95% 13732-00-8 AB108960 (3-Acryloxypropyl)trichlorosilane; 97% 38595-89-0 AB108961 (3-Acryloxypropyl)trimethoxysilane; 95% 4369-14-6 AB129149 O-(Methacryloxyethyl)-N-(triethoxysilylpropyl)urethane; 115396-93-5 90% AB108759 (Methacryloxymethyl)dimethylethoxysilane; 95% 5577-70-8 AB152157 (Methacryloxymethyl)methyldiethoxysilane; 97% 3978-58-3 AB152158 (Methacryloxymethyl)methyldimethoxysilane; 97% 121177-93-3 O O O Si O O O Si O O Cl Cl Si O O O O O O O O O Si O Cl Cl Si Cl O O Si O O O Si O H N O O O O O O Si O O O O O Si O O O Si O Gute Chemie
Gute Chemie. Organofunctional Silanes Reagents for Coupling 21 AB108761 Methacryloxymethyltriethoxysilane 5577-72-0 AB108998 (3-Methacryloxypropyl)dimethylchlorosilane; 92% 24636-31-5 AB108999 (3-Methacryloxypropyl)dimethylethoxysilane 13731-98-1 AB108766 Methacryloxypropyldimethylmethoxysilane; 92% 66753-64-8 AB109000 (3-Methacryloxypropyl)methyldichlorosilane; 95% 18301-56-9 AB109002 (3-Methacryloxypropyl)methyldiethoxysilane; 95% 65100-04-1 AB108767 3-Methacryloxypropylmethyldimethoxysilane; 92% 14513-34-9 AB253639 3-Methacryloxypropyltriacetoxysilane; 85% 51772-85-1 AB109004 (3-Methacryloxypropyl)trichlorosilane; 95% 7351-61-3 AB109005 (3-Methacryloxypropyl)triethoxysilane; 97% 21142-29-0 O O Si O O O Si Cl O O Si O O O O Si O O Cl Cl Si O O O O O O O Si O O Si O O O O O Si O O O Cl Cl Si Cl O O O O O Si O O O abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
22 Amino Organofunctional Silanes AB153224 N-(2-Aminoethyl)-3-aminoisobutyldimethylmethoxy- 31024-49-4 silane; 95% O Si NH2 N H AB110804 (Aminoethylaminomethyl)phenethyltrimethoxysilane; 74113-77-2 90% mixed m, p-isomers AB153226 N-(2-Aminoethyl)-3-aminopropyltriethoxysilane; 95% 5089-72-5 AB110806 N-(2-Aminoethyl)-3-aminopropyltrimethoxysilane; 1760-24-3 97% AB134430 N-(2-Aminoethyl)-11-aminoundecyltrimethoxysilane; 121772-92-7 95% AB182037 N-(6-Aminohexyl)aminomethyltriethoxysilane; 92% 15129-36-9 AB110807 N-(6-Aminohexyl)aminopropyltrimethoxysilane; 92% 51895-58-0 AB110808 3-(m-Aminophenoxy)propyltrimethoxysilane; 95% 71550-66-8 AB110809 3-Aminophenyltrimethoxysilane; 90% 70411-42-6 AB110810 p-Aminophenyltrimethoxysilane; 97% 33976-43-1 O O Si O O O Si O O O Si O O O Si O H N NH2 H N NH2 H N NH2 NH2 NH H2N O N H Si O O O O Si O H N NH2 O O Si O H2N O NH2 O O Si O NH2 O Si O O Gute Chemie
Gute Chemie. Organofunctional Silanes Reagents for Coupling 23 AB134431 N-3-[(Amino(polypropyleneoxy)]aminopropyl-triMeO- silane 60-65% in NH2-terminated Polypropylene oxide AB110812 3-Aminopropyldiisopropylethoxysilane; 95% 117559-36-1 AB146193 (3-Aminopropyl)dimethylethoxysilane; 95% 18306-79-1 AB110815 3-Aminopropyltriethoxysilane; 98% 919-30-2 AB153236 11-Aminoundecyltriethoxysilane; 95% 116821-45-5 AB153301 (9-Carbazolyl)ethyltriethoxysilane 1185252-84-9 AB152160 (N-Cyclohexylaminomethyl)methyldiethoxysilane; 27445-54-1 95% AB152159 (N-Cyclohexylaminomethyl)triethoxysilane; 95% 26495-91-0 AB153316 3-(N-Cyclohexylaminopropyl)trimethoxysilane 3068-78-8 AB111049 (N,N-Diethyl-3-aminopropyl)trimethoxysilane; 97% 41051-80-3 Si O NH2 O Si NH2 O O Si O NH2 O O Si O H2N O O Si O N H N H N O Si O O O Si O O O Si O O O Si O H N N abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
24 AB252529 (3-N,N-Dimethylaminopropyl)methyldimethoxysilane; 67353-42-8 97% AB336017 (3-N,N-Dimethylaminopropyl)triethoxysilane; 97% 43108-00-5 AB110559 (3-N,N-Dimethylaminopropyl)trimethoxysilane; 97% 2530-86-1 AB111094 3-(2,4-Dinitrophenylamino)propyltriethoxysilane; 71783-41-0 95% AB134451 (N-Ethylaminoisobutyl)trimethoxysilane; 95% 227085-51-0 AB129144 N-(Hydroxyethyl)-N-methylaminopropyltrimethoxy- 330457-46-0 silane; 75% in Methanol AB129192 N-Methylaminopropylmethyldimethoxysilane 31024-35-8 AB111230 N-Methylaminopropyltrimethoxysilane; 97% 3069-25-8 O Si O N O O Si O O O Si O N N NO2 O Si O O N H NO2 H N N OH O Si O H N O O Si O O O Si O H N O O Si O AB100555 Octadecyldimethyl[3-(trimethoxysilyl)-propyl]ammo- 27668-52-6 Cl- nium chloride; 40% in Methanol O O Si O N+ AB152161 (N-Phenylaminomethyl)trimethoxysilane; 95% 77855-73-3 AB111305 (N-Phenylaminopropyl)trimethoxysilane; 95% 3068-76-6 H O N O Si O O O Si O H N Gute Chemie
Gute Chemie. Organofunctional Silanes Reagents for Coupling 25 AB111326 (R)-N-1-Phenylethyl-N'-triethoxysilylpropylurea; 97% 131206-15-0 O O Si O NH N H O O O Si O S O O Si O N N AB182100 [2-(4-Pyridylethyl)thiopropyl]trimethoxysilane 198567-47-4 AB134601 2-(4-Pyridylethyl)triethoxysilane; 95% 98299-74-2 AB129310 Tetradecyldimethyl(3-trimethoxysilylpropyl)ammonium 41591-87-1 chloride; 50% in methanol O O Si O N Cl AB111452 N-(3-Triethoxysilylpropyl)-4,5-dihydroimidazole; 97% 58068-97-6 AB111451 N-(Triethoxysilylpropyl)dansylamide 70880-05-6 AB111458 N-(Triethoxysilylpropyl)-O-poly(ethylene oxide) 74695-91-3 urethane AB111457 3-(Triethoxysilylpropyl)-4-nitrobenzamide; 95% 60871-86-5 N N O Si O O O H N S O O O Si O H N O O OH O N O O Si O O Si O O O N H NO2 abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
26 AB129324 N-Triethoxysilylpropylquinineurethane; 95% 200946-85-6 AB111488 N-[3-Trimethoxysilyl)propyl]ethylenediamine triacetic 128850-89-5 acid trisodium salt, 45% in water AB111491 N-Trimethoxysilylpropyl-N,N,N-tri-n-butylammonium 147366-30-1 bromide, 50% in methanol AB111492 N-Trimethoxysilylpropyl-N,N,N-tri-n-butylammonium 143203-33-2 chloride; 50% in methanol AB111493 N-Trimethoxysilylpropyl-N,N,N-trimethylammonium 35141-36-7 chloride, 50% in methanol Bidentate Organofunctional Silanes AB129264 Bis(methyldiethoxysilylpropyl)amine; 90% 31020-47-0 AB153279 Bis(3-triethoxysilylpropyl)amine; 95% 13497-18-2 AB110557 Bis(3-trimethoxysilylpropyl)amine; 95% 82985-35-1 Gute Chemie O O Si O O N O H N H N O Na O O O Si O O Na O O N N O O Na O Si O O O Si O O N Br N Cl O O Si O N Cl O Si O O O Si O O O Si O N H H N H N O Si O O O Si O O O Si O
Gute Chemie. Organofunctional Silanes Reagents for Coupling 27 AB110558 Bis(3-trimethoxysilylpropyl)ethylenediamine; 62% in 68845-16-9 methanol AB131042 Bis(3-trimethoxysilylpropyl)ethylenediamine; 90% 68845-16-9 AB153286 Bis(3-trimethoxysilylpropyl)-N-methylamine; 95% 31024-70-1 Carboxylic Acid Organofunctional Silanes AB391080 5-Triethoxysilylpentanoic acid; tech. 1137665-94-1 AB391081 6-Triethoxysilylhexanoic acid; 95% 145045-54-1 AB391082 7-Triethoxysilylheptanoic acid; 95% 1858242-65-5 AB391083 8-Triethoxysilyloctanoic acid; 95% 1858255-00-1 AB391084 9-Triethoxysilylnonanoic acid; 95% 1858251-01-0 O O Si O O O Si O H N H N N H N H O Si O O O Si O O O O Si O N O Si O O O OH O O Si O O O Si O O OH O O Si O O O Si O O O Si O OH O O OH OH O abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
28 AB391085 10-Triethoxysilyldecanoic acid; 95% 1643983-72-5 AB391086 11-Triethoxysilylundecanoic acid; 95% 82784-73-4 Cyanate Organofunctional Silanes AB110845 Bis(3-cyanopropyl)dichlorosilane; 95% 1071-17-6 AB129109 (3-Cyanobutyl)methyldichlorosilane; 95% 71550-62-4 AB100242 (3-Cyanobutyl)trichlorosilane; 95% 163155-56-4 AB182062 (3-Cyanobutyl)triethoxysilane; 95% 1049679-56-2 AB110988 (2-Cyanoethyl)methyldichlorosilane; 97% 1071-21-2 AB131047 (2-Cyanoethyl)methyldimethoxysilane 2526-61-6 AB110989 (2-Cyanoethyl)trichlorosilane; 97% 1071-22-3 AB110992 3-Cyanopropyldiisopropylchlorosilane; 97% 113641-37-5 Gute Chemie O O Si O O O Si O O OH OH O N Si Cl Cl N Cl Cl Si N Cl Cl Si Cl N O O Si O Cl Cl Si O O Si Cl Cl Si Cl N N N N Si Cl N
Gute Chemie. Organofunctional Silanes Reagents for Coupling 29 AB110994 (3-Cyanopropyl)dimethylchlorosilane; 97% 18156-15-5 Cl Si N AB252516 (3-Cyanopropyl)dimethyl(dimethylamino)silane 111873-32-6 AB100249 3-Cyanopropyldimethylmethoxysilane; 95% 143203-47-8 AB110995 3-Cyanopropylmethyldichlorosilane; 97% 1190-16-5 AB109879 3-Cyanopropylmethyldimethoxysilane; 97% 153723-40-1 AB129111 (3-Cyanopropyl)phenyldichlorosilane; 97% 1078-96-2 AB153315 3-Cyanopropylphenyldimethoxysilane; 95% 204760-82-7 AB110996 (3-Cyanopropyl)trichlorosilane; 97% 1071-27-8 AB110997 3-Cyanopropyltriethoxysilane; 97% 1067-47-6 AB128523 (3-Cyanopropyl)trimethoxysilane; 97% 55453-24-2 N Si O Si Cl Cl Si O Si O Cl Si Cl O Si O Cl Cl Si Cl O O Si O O O Si O N N N N N N N N N AB111200 3-Isocyanatopropyldimethylchlorosilane; 95% 17070-70-1 Cl Si N C O abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
30 AB111201 3-Isocyanatopropyltriethoxysilane; 95% 24801-88-5 AB254789 3-Isothiocyanatopropyltriethoxysilane 58698-89-8 AB126796 (3-Triethoxysilylpropyl)-t-butylcarbamate; 95% 137376-38-6 AB111453 N-(3-Triethoxysilylpropyl)ethylcarbamate; 97% 17945-05-0 AB111456 (S)-N-Triethoxysilylpropyl-O-menthocarbamate 1438401-72-9 O O Si O O O Si O O O Si O O O Si O N C O N C S H N O O H N O O O O Si O H N O O Epoxy Organofunctional Silanes AB134442 Bis[2-(3,4-epoxycyclohexyl)ethyl]tetramethyldi- 18724-32-8 O siloxane AB153257 1,5-Bis(glycidoxypropyl)-3-phenyl-1,1,3,5,5-pentame- 865811-59-2 thyltrisiloxane Si Si O O O O O O Si O Si O Si Gute Chemie
Gute Chemie. Organofunctional Silanes Reagents for Coupling 31 AB110856 1,3-Bis(glycidoxypropyl)tetramethyldisiloxane; 97% 126-80-7 O O Si Si O O O AB129137 5,6-Epoxyhexyltriethoxysilane; 97% 86138-01-4 AB111147 (3-Glycidoxypropyl)bis(trimethylsiloxy)methylsilane; 7422-52-8 95% AB111148 (3-Glycidoxypropyl)dimethylethoxysilane; 97% 17963-04-1 AB111149 (3-Glycidoxypropyl)methyldiethoxysilane; 97% 2897-60-1 AB111150 (3-Glycidoxypropyl)methyldimethoxysilane; 97% 65799-47-5 AB111151 (3-Glycidoxypropyl)pentamethyldisiloxane; 95% 18044-44-5 AB252553 (3-Glycidoxypropyl)-1,1,3,3-tetramethyldisiloxane; 17980-29-9 95% AB111152 (3-Glycidoxypropyl)trimethoxysilane; 98% 2530-83-8 AB182131 Tris(glycidoxypropyldimethylsiloxy)phenylsilane; 95% 90393-83-2 O O O Si O Si O Si Si O O O Si O O O O Si O O O O O O O O O O Si O O Si Si O Si Si H O Si O O O O O O O Si Si Si O O Si O O O O abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
32 Halogen Organofunctional Silanes AB110841 Bis(chloromethyl)methylchlorosilane; 95% 18171-56-7 AB252493 (4-Bromobutyl)dimethylchlorosilane; 95% 52112-26-2 AB182051 7-Bromoheptyltrimethoxysilane; 95% 1193317-40-6 AB138167 Bromomethyldimethylchlorosilane; 95% 16532-02-8 AB100151 8-Bromooctyltrimethoxysilane 82985-34-0 AB110907 Bromophenyltrimethoxysilane, mixed isomers 17043-05-9 AB253779 (3-Bromopropyl)dimethylchlorosilane 74349-12-5 AB110908 3-Bromopropyltrichlorosilane; 97% 13883-39-1 AB110909 3-Bromopropyltrimethoxysilane; 97% 51826-90-5 Cl Si Cl Cl Cl Si Br Br O O Si O Cl Si Br O O Si O Br Br Br Br Br O O Si O Cl Si Cl Cl Si Cl O O Si O AB129273 11-Bromoundecyldimethylchlorosilane; 95% 330457-42-6 AB110910 11-Bromoundecyltrichlorosilane; 95% 79769-48-5 AB110911 11-Bromoundecyltrimethoxysilane; 95% 17947-99-8 Cl Si Cl Cl Si Cl O O Si O Br Br Br Gute Chemie
Gute Chemie. Organofunctional Silanes Reagents for Coupling 33 AB110938 4-Chlorobutyldimethylchlorosilane; 97% 18145-84-1 AB110943 2-Chloroethyltriethoxysilane; 95% 18279-67-9 AB153305 3-Chloroisobutyldimethylchlorosilane 18145-83-0 AB153306 3-Chloroisobutyldimethylmethoxysilane; 95% 18244-08-1 AB110945 2-(Chloromethyl)allyltrichlorosilane 18147-84-7 AB110946 2-(Chloromethyl)allyltrimethoxysilane; 95% 39197-94-9 AB110949 (Chloromethyl)dimethylchlorosilane; 97% 1719-57-9 AB139781 Chloromethyl(dichloro)methylsilane; 97% 1558-33-4 AB119076 (Chloromethyl)methylphenylchlorosilane 2632-83-9 AB110958 ((Chloromethyl)phenylethyl)methyldichlorosilane, 81870-64-6 mixed m,p isomers AB110960 [(Chloromethyl)phenylethyl]trichlorosilane, 58274-32-1 mixed m,p isomers AB110961 [(Chloromethyl)phenylethyl]trimethoxysilane, 68128-25-6 mixed m,p isomers Cl Si Cl O O Si O Cl Cl Si Cl Cl O Si Cl Cl Cl Cl Si Cl O O Si O Cl Si Cl Cl Cl Si Cl Cl Si Cl Cl Cl Si Cl Cl Cl Cl Cl Si Cl O O Si O abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
34 AB171802 4-(Chloromethyl)phenyltrichlorosilane; 97% 13688-90-9 AB110963 [4-(Chloromethyl)phenyl]trimethoxysilane; 95% 24413-04-5 AB110968 (Chloromethyl)triethoxysilane; 97% 15267-95-5 AB100224 (2-Chloro-2-phenylethyl)methyldichlorosilane; 95% 1858251-24-7 AB110977 (3-Chloropropyl)dimethylchlorosilane; 97% 10605-40-0 AB182060 3-Chloropropyldimethylethoxysilane; 95% 13508-63-9 AB110978 (3-Chloropropyl)dimethylmethoxysilane; 95% 18171-14-7 AB110980 3-Chloropropylmethyldichlorosilane; 97% 7787-93-1 AB119254 (3-Chloropropyl)trichlorosilane; 97% 2550-06-3 AB111195 3-Iodopropyltrimethoxysilane; 95% 14867-28-8 AB182119 3-(Trimethoxysilylpropyl)-2-bromo-2-methylpropionate; 314021-97-1 95% Gute Chemie Cl Cl Si Cl O O Si O Cl Cl O O Si O Cl Cl Cl Si Cl Cl Si Cl Cl O Si O Si Cl Cl Cl I Cl Cl Si Cl Cl Si Cl O O Si O O O Si O Br O O
Gute Chemie. Organofunctional Silanes Reagents for Coupling 35 Olefin Organofunctional Silanes AB108712 3-(N-Allylamino)propyltrimethoxysilane; 95% 31024-46-1 AB131214 Allylchlorodimethylsilane; 95% 4028-23-3 AB110793 Allyldichlorosilane 3937-28-8 AB110794 Allyldimethoxysilane 18147-35-8 AB177675 Allyldichloromethylsilane; 95% 1873-92-3 AB134428 11-Allyloxyundecyltrimethoxysilane; 95% 1196453-35-6 O O Si O H N Cl H Si Cl Cl Si O O Si H Cl Cl Si O O Si O O AB108965 Allyltrichlorosilane; 97% 107-37-9 AB177860 Allyltriethoxysilane; 97% 2550-04-1 AB108967 Allyltrimethoxysilane; 97% 2551-83-9 AB252453 [(Bicycloheptenyl)ethyl]methyldichlorosilane; 95%, 198570-38-6 mixed endo/exo isomers AB153239 [(Bicycloheptenyl)ethyl]trimethoxysilane; 95%, 68323-30-8 endo/exo isomers Cl Cl Si Cl O O Si O O O Si O Cl Si Cl H H O O Si O abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
36 AB108719 5-(Bicycloheptenyl)methyldichlorosilane; 95% 18245-94-8 AB108970 5-(Bicycloheptenyl)trichlorosilane; 97% 14319-64-3 AB108971 5-(Bicycloheptenyl)triethoxysilane; 97% 18401-43-9 AB110868 1,1-Bis(trichlorosilylmethyl)ethylene 78948-04-6 AB108727 1,2-Bis(triethoxysilyl)ethylene; 95% 87061-56-1 (80% trans-isomer) AB108735 3-Butenyltriethoxysilane; 95% 57813-67-9 AB126786 3-Cyclohexenyltrichlorosilane; 97% 10137-69-6 AB252521 Diallyldichlorosilane 3651-23-8 AB108987 1,4-Divinyl-tetramethyldisilylethane 84677-98-5 AB108992 5-Hexenyldimethylchlorosilane; 95% 30102-73-9 AB108993 5-Hexenyltrichlorosilane; 92% 18817-29-3 Gute Chemie Cl Si Cl Cl H Cl Si Cl H O SiO O Cl Cl Si Cl Cl Si Cl Cl O O Si O O O O Si O O O O Si O Cl Cl Si Cl Si Cl Cl Si Si Cl Si Cl Cl Si Cl
Gute Chemie. Organofunctional Silanes Reagents for Coupling 37 AB182071 5-Hexenyltriethoxysilane; 95% 52034-14-7 O O Si O AB111280 7-Octenyldimethylchlorosilane; 95% 17196-12-2 AB171364 7-Octenyldimethylmethoxysilane; 95% 204775-11-1 AB111281 7-Octenyltrichlorosilane; 95% 52217-52-4 (contains 10-30% isomers) AB111282 7-Octenyltrimethoxysilane; 95% 52217-57-9 Cl Si O Si Cl Cl Si Cl O O Si O AB110797 Allylphenyldichlorosilane; 95% 7719-03-1 Cl Si Cl AB129303 O-(Propargyloxy)-N-(triethoxysilylpropyl)urethane; 870987-68-1 90% AB111376 (Styrylethyl)trimethoxysilane; 97% 134000-44-5 AB108785 Trivinylethoxysilane; 95% 70693-56-0 AB129340 10-Undecenyldimethylchlorosilane; 95% 18406-97-8 AB134479 10-Undecenyltrichlorosilane; 95% 17963-29-0 O O Si O H N O O O O Si O Si O Cl Si Cl Cl Si Cl abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
38 AB153354 10-Undecenyltrimethoxysilane; 95% 872575-06-9 (sum of isomers, ca. 90% n-C11) O O Si O AB174304 Dimethylethoxyvinylsilane; 97% 5356-83-2 AB106075 Vinyldimethylmethoxysilane; 95% 16546-47-7 AB111581 Vinyldiphenylchlorosilane 18419-53-9 AB111582 Vinyldiphenylethoxysilane 17933-85-6 AB108800 Vinylmethyldimethoxysilane; 97% 16753-62-1 AB108802 Vinyloctyldichlorosilane 211985-85-2 AB111589 Vinylphenyldichlorosilane; 95% 7719-02-0 AB129343 Vinylphenyldiethoxysilane; 95% 4652-09-9 AB111590 Vinylphenylmethylchlorosilane; 95% 17306-05-7 AB129344 Vinylphenylmethylmethoxysilane 80252-60-4 AB111598 Vinyltrimethoxysilane; 99% 2768-02-7 Gute Chemie O Si O Si Cl Si Si O O O Si Si Cl Cl Cl Cl Si O Si O Cl Si O Si O Si O O
Gute Chemie. Organofunctional Silanes Reagents for Coupling 39 Phosphorous Organofunctional Silanes AB111061 (Diethylphosphatoethyl)triethoxysilane; 92% 757-44-8 AB129122 Diphenylphosphinoethyldimethylethoxysilane; 97% 359859-29-3 AB111108 2-(Diphenylphosphino)ethyltriethoxysilane; 97% 18586-39-5 Sulfur Organofunctional Silanes AB153280 Bis[3-(triethoxysilyl)propyl]disulfide; 90% 56706-10-6 AB111216 Mercaptomethylmethyldiethoxysilane; 95% 55161-63-2 AB111489 N-[3-(Trimethoxysilyl)propyl]isothiouronium chloride, 84682-36-0 50% in water O O Si O O O P O P Si O P O Si O O O O Si O S S O Si O O HS O Si O O O Si O Cl S NH2 NH2 abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
40 Alkyl Organofunctional Silanes AB110790 Adamantylethyltrichlorosilane; mixture of isomers, 37843-11-1 97% AB129069 2-(Bicycloheptyl)trichlorosilane; 97% 18245-29-9 AB129274 t-Butyldichlorosilane; 97% 85121-42-2 AB153294 t-Butyldimethylchlorosilane, 3M in tetrahydrofuran 18162-48-6 AB110913 n-Butyldimethylchlorosilane; 97% 1000-50-6 AB129275 n-Butyldimethyl(dimethylamino)silane; 95% 181231-67-4 AB252498 n-Butyldimethylmethoxysilane 64712-50-1 AB129279 t-Butyldiphenylmethoxysilane; 97% 76358-47-9 AB110923 n-Butylmethyldichlorosilane; 97% 18147-23-4 AB129277 t-Butylmethyldichlorosilane; 97% 18147-18-7 AB334058 n-Butylmethyldimethoxysilane; 97% 18294-08-1 AB110926 n-Butyltrichlorosilane; 97% 7521-80-4 Gute Chemie Cl Cl Si Cl H CH2 H2 C H CH2 H Cl H Cl Si Cl H Cl Si H Cl Si Cl Cl Si N Si O Si O Si Cl Cl Si Si Cl Cl O Si O Cl Si Cl Cl
Gute Chemie. Organofunctional Silanes Reagents for Surface Modification 41 AB110927 t-Butyltrichlorosilane 18171-74-9 AB252508 n-Butyltriethoxysilane; 95% 4781-99-1 AB110928 n-Butyltrimethoxysilane; 97% 1067-57-8 AB110998 Cyclohexyldimethylchlorosilane; 97% 71864-47-6 AB111000 Cyclohexylmethyldichlorosilane; 97% 5578-42-7 AB180151 Cyclohexyldimethoxymethylsilane; 98% 17865-32-6 AB111002 (Cyclohexylmethyl)trichlorosilane; 97% 18388-16-4 AB111003 Cyclohexyltrichlorosilane; 95% 98-12-4 AB111004 Cyclohexyltrimethoxysilane; 97% 17865-54-2 AB148726 1,1-Dichloro-1-silacycohexane; 95% 2406-34-0 AB111007 Cyclopentyltrichlorosilane; 95% 14579-03-4 AB173315 Cyclopentyltrimethoxysilane; 95% 143487-47-2 Cl Si Cl Cl O O Si O O Si O O Cl Si Cl Si Cl O Si O Cl Si Cl Cl Cl Cl Si Cl O O Si O Cl Cl Si Cl O O Si O Si Cl Cl abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
42 AB111014 n-Decyldimethylchlorosilane; 97% 38051-57-9 AB111015 n-Decylmethyldichlorosilane; 97% 18051-88-2 AB178102 n-Decyltrichlorosilane; 97% 13829-21-5 AB111017 n-Decyltriethoxysilane; 97% 2943-73-9 AB171953 n-Decyltrimethoxysilane; 95% 5575-48-4 AB111025 Di-t-butylchlorosilane; 95% 56310-18-0 AB111026 Di-n-butyldichlorosilane; 97% 3449-28-3 AB134449 Di-n-butyldimethoxysilane 18132-63-3 AB111028 Di-t-butylmethylchlorosilane; 97% 70892-81-8 AB111124 Dodecylmethyldichlorosilane 18407-07-3 Cl Cl Si AB110697 Dicyclohexyldichlorosilane; 97% 18035-74-0 AB111050 (N,N-Diethylamino)trimethylsilane; 97% 996-50-9 Gute Chemie Cl Si Cl Cl Si O O Si O Si Cl Cl Cl O Si O O Si ClH Si Cl Cl O Si O Si Cl Cl Cl Si Si N
Gute Chemie. Organofunctional Silanes Reagents for Coupling 43 AB129114 Diisobutylchlorosilane; 97% 18279-73-7 AB111066 Diisopropylchlorosilane; 97% 2227-29-4 AB111067 Diisopropyldichlorosilane; 97% 7751-38-4 AB111068 Diisopropyldimethoxysilane; 95% 18230-61-0 AB111074 (N,N-Dimethylamino)trimethylsilane; 97% 2083-91-2 AB129117 (3,3-Dimethylbutyl)dimethylchlorosilane; 95% 96220-76-7 AB252530 (3,3-Dimethylbutyl)trichlorosilane; 95% 105732-02-3 AB252531 (3,3-Dimethylbutyl)triethoxysilane 41966-94-3 AB290057 (3,3-Dimethylbutyl)trimethoxysilane; 98% 157223-36-4 AB111095 Di-n-octyldichlorosilane; 97% 18416-07-4 AB252533 Di-n-octyldimethoxysilane; 95% 947155-81-9 Si ClH H Si Cl Si Cl Cl O Si O Si N Si Cl Cl Si Cl Cl O O Si O O O Si O Si Cl Cl O Si O abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
44 AB111121 Docosylmethyldichlorosilane; 95%, 67892-56-2 contains C20 and C24 homologs Cl Cl Si AB129129 Dodecyldimethylchlorosilane; 95% 66604-31-7 AB111125 Dodecylmethyldiethoxysilane 60317-40-0 AB111126 Dodecyltrichlorosilane; 97% 4484-72-4 AB111127 Dodecyltriethoxysilane; 95% 18536-91-9 AB171666 n-Dodecyltrimethoxysilane; 95% 3069-21-4 AB180199 Ethoxytriethylsilane; 97% 597-67-1 AB111133 Ethyldimethylchlorosilane; 97% 6917-76-6 AB131056 Ethylphenethyltrimethoxysilane; 95%, 259818-29-6 mixture of m,p isomers AB121874 Ethyltrichlorosilane; 98% 115-21-9 AB111160 n-Heptylmethyldichlorosilane; 97% 18395-93-2 Cl Si O Si O Cl Cl Si Cl O O Si O O O Si O Si O Cl Si Cl Cl Si Cl O O Si O Cl Cl Si Gute Chemie
Gute Chemie. Organofunctional Silanes Reagents for Surface Modification 45 AB111161 n-Heptyltrichlorosilane; 95% 871-41-0 Cl Cl Si Cl AB111165 n-Hexadecyltrichlorosilane; 95% 5894-60-0 AB153343 Hexadecyltriethoxysilane, mixed isomers; 92% 16415-13-7 AB111166 Hexadecyltrimethoxysilane; 90% 16415-12-6 Cl Cl Si Cl O O Si O O O Si O AB111174 Hexamethyldisilazane; 98.5% 999-97-3 AB111184 Hexylmethyldichlorosilane; 95% 14799-94-1 AB111186 Hexyltrichlorosilane; 95% 928-65-4 AB174350 n-Hexyltriethoxysilane; 95% 18166-37-5 AB111188 n-Hexyltrimethoxysilane; 97% 3069-19-0 AB180168 Chlorodimethylisobutylsilane 27490-70-6 Si Si N H Cl Cl Si Cl Cl Si Cl O O Si O O O Si O Cl Si abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
46 AB174203 Dichloroisobutylmethylsilane; 97% 18028-96-1 AB111197 Isobutyltrichlorosilane; 98% 18169-57-8 AB111199 Isobutyltrimethoxysilane; 97% 18395-30-7 AB111202 Isooctyltrichlorosilane; 95% 18379-25-4 AB252563 Isooctyltriethoxysilane; 95% 35435-21-3 AB129146 Isooctyltrimethoxysilane; 95% 34396-03-7 AB111204 Isopropyldimethylchlorosilane; 90% 3634-56-8 AB111206 Isopropylmethyldichlorosilane; 97% 18236-89-0 AB252564 Isopropyltrichlorosilane; 95% 4170-46-1 AB105506 2-Butyldimethylchlorosilane 60090-96-2 AB111244 Methyltrimethoxysilane; 97% 1185-55-3 Gute Chemie Cl Cl Si Cl Cl Si Cl O O Si O Cl Si Cl Cl O Si O O O O Si O Cl Si Cl Cl Si Cl Cl Si Cl Cl Si O O Si O
Gute Chemie. Organofunctional Silanes Reagents for Surface Modification 47 AB252576 n-Octadecyldiisobutylchlorosilane; 97% 162578-86-1 AB252577 n-Octadecyldiisobutyl(dimethylamino)silane; 95% 151613-23-9 Si Cl Si N AB128282 n-Octadecyldimethylchlorosilane; 70% in toluene 18643-08-8 Cl Si AB111257 n-Octadecyldimethylchlorosilane; 97% 18643-08-8 (5-10% C18 isomers) Cl Si AB129205 n-Octadecyldimethyl(dimethylamino)silane; 76328-77-3 contains 5-10% C18 isomers N Si AB111258 Octadecyldimethylmethoxysilane; 95% 71808-65-6 O Si AB111263 n-Octadecylmethoxydichlorosilane; 90% 211934-50-8 O Si Cl Cl AB111265 Octadecylmethyldichlorosilane; 97% 5157-75-5 Cl Cl Si AB289989 Octadecylmethyldichlorosilane, 70% in toluene 5157-75-5 Cl Cl Si AB111267 n-Octadecylmethyldiethoxysilane 67859-75-0 O Si O abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
48 AB110682 Octadecylmethyldimethoxysilane (mixed isomers) 70851-50-2 AB111269 n-Octadecylsilane; 95% O Si O 18623-11-5 SiH3 AB334057 n-Octadecyltrichlorosilane; 70% in toluene 112-04-9 Cl Cl Si Cl AB108930 n-Octadecyltrichlorosilane; 95%, 112-04-9 cont. 5-10% branched isomers Cl Cl Si Cl AB111273 n-Octadecyltriethoxysilane; 95% 7399-00-0 (5-10% branched C18-isomers) O O Si O AB110648 n-Octadecyltrimethoxysilane; 95% 3069-42-9 (85% n-isomer) O O Si O AB111284 n-Octyldiisopropylchlorosilane; 90% 117559-37-2 AB129288 n-Octyldiisopropyl(dimethylamino)silane 151613-25-1 AB111285 n-Octyldimethylchlorosilane; 97% 18162-84-0 AB111286 n-Octyldimethyl(dimethylamino)silane; 95% 110348-62-4 Gute Chemie Si Cl N Si Cl Si N Si
Gute Chemie. Organofunctional Silanes Reagents for Surface Modification 49 AB131060 n-Octyldimethylmethoxysilane; 95% 93804-29-6 AB111287 n-Octylmethyldichlorosilane; 97% 14799-93-0 AB111288 n-Octylmethyldiethoxysilane 2652-38-2 AB134462 n-Octylmethyldimethoxysilane; 95% 85712-15-8 AB111290 n-Octyltrichlorosilane; 97% 5283-66-9 AB110649 n-Octyltriethoxysilane; 97% 2943-75-1 AB129289 n-Octyltrimethoxysilane; 97% 3069-40-7 AB182093 n-Pentylmethyldichlorosilane 13682-99-0 AB140272 Pentyltriethoxysilane; 95% 2761-24-2 AB142522 Dimethyl-n-propylchlorosilane (dimethyl-n-propylsi- 17477-29-1 lylating agent); 99% AB252616 n-Propyldimethylmethoxysilane; 95% 18182-14-4 O Si Cl Cl Si O Si O O Si O Cl Cl Si Cl O O Si O O Si O O Cl Si Cl O O Si O Cl Si O Si abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
Cl Cl Si O Si O Cl Cl Si Cl O O Si O O Si O O SiH SiH N H Cl Si 50 AB111355 n-Propylmethyldichlorosilane; 97% 4518-94-9 AB252617 n-Propylmethyldimethoxysilane; 95% 18173-73-4 AB141346 n-Propyltrichlorosilane; 99% 141-57-1 AB110555 n-Propyltriethoxysilane; 97% 2550-02-9 AB111357 n-Propyltrimethoxysilane; 97% 1067-25-0 AB178028 n-Tetradecyltrichlorosilane; 97% 18402-22-7 Cl Cl Si Cl AB111416 1,1,3,3-Tetramethyldisilazane; 97% 15933-59-2 AB111427 Thexyldimethylchlorosilane; 95% 67373-56-2 AB334055 TMS silylating solution 999-97-3 (hexamethyldisilazane/chlorotrimethylsilane) AB111433 n-Triacontyldimethylchlorosilane 70851-52-4 Cl Si AB111434 Triacontyltrichlorosilane; 70851-48-8 (80% C30 and higher, 20% C22-C28) Cl Cl Si Cl Gute Chemie
Gute Chemie. Organofunctional Silanes Reagents for Surface Modification 51 AB173994 Chlorotri-n-butylsilane; 97% 995-45-9 AB111461 Triethylbromosilane 1112-48-7 AB111462 Triethylchlorosilane; 98% 994-30-9 AB129325 Triisobutylchlorosilane; 99% 13154-25-1 AB111480 Triisopropylchlorosilane; 95% 13154-24-0 AB111495 Trimethylchlorosilane; 99% 75-77-4 AB111497 Trimethylethoxysilane; 95% 1825-62-3 AB210603 Methoxytrimethylsilane; 97% 1825-61-2 AB252562 Isooctyldimethylchlorosilane; 95% 79957-95-2 AB119949 N-(Trimethylsilyl)imidazole; 97% 18156-74-6 Si Cl Si Br Si Cl Si Cl Si Cl Cl Si Si O O Si Cl Si NSi N AB111577 Undecyltrichlorosilane; 97% 18052-07-8 Cl Cl Si Cl abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
52 Aryl Organofunctional Silanes AB304369 4-Biphenyldimethylchlorosilane; 95% 41081-31-6 Si Cl AB110922 t-Butyldiphenylchlorosilane; 98% 58479-61-1 AB173884 Chlorodiphenylsilane; 90% 1631-83-0 AB111101 Diphenyldichlorosilane; 98% 80-10-4 AB111104 Diphenyldimethoxysilane; 97% 6843-66-9 AB111105 Diphenylmethylchlorosilane; 97% 144-79-6 AB111106 Diphenylmethylethoxysilane; 95% 1825-59-8 AB111109 Diphenylsilane; 99% 775-12-2 AB129124 Di(p-tolyl)dichlorosilane; 95% 18414-38-5 AB153333 Di(p-tolyl)dimethoxysilane; 95% 92779-72-1 AB182087 1-Naphthyltriethoxysilane 17938-06-6 Gute Chemie Cl Si ClH Si Cl Cl Si O Si O Cl Si Si O HH Si Cl Cl Si O Si O O O Si O
Gute Chemie. Organofunctional Silanes Reagents for Surface Modification 53 AB134457 1-Naphthyltrimethoxysilane; 95% 18052-76-1 AB110768 Phenyldichlorosilane; 96% 1631-84-1 AB111320 Phenyldiethoxysilane 17872-93-4 AB111322 Phenyldimethylchlorosilane; 97% 768-33-2 AB111323 Phenyldimethylethoxysilane; 95% 1825-58-7 AB111330 Phenylmethylchlorosilane; 97% 1631-82-9 AB111332 Phenylmethyldiethoxysilane; 95% 775-56-4 AB111333 Phenylmethyldimethoxysilane; 97% 3027-21-2 AB111340 Phenyltriethoxysilane; 97% 780-69-8 AB111342 Phenyltrimethoxysilane; 97% 2996-92-1 AB111430 p-Tolyldimethylchlorosilane 35239-30-6 O O Si O Cl Si Cl Si H Cl H Si O O Si O Si H Cl O Si O O Si O O O Si O O O Si O Cl Si abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
54 AB111431 p-Tolylmethyldichlorosilane; 95% 25898-37-7 AB133000 p-Tolyltrichlorosilane; 95% 701-35-9 AB182110 p-Tolyltriethoxysilane 18412-57-2 AB129316 p-Tolyltrimethoxysilane; 95% 17873-01-7 AB121932 Triphenylchlorosilane; 95% 76-86-8 AB111546 Triphenylethoxysilane; 95% 1516-80-9 Arylalkyl Organofunctional Silanes AB110822 Benzyldimethylchlorosilane; 95% 1833-31-4 AB110825 Benzyltrichlorosilane; 97% 770-10-5 AB110826 Benzyltriethoxysilane; 96% 2549-99-7 Cl Si Cl Cl Cl Si Cl O O Si O O O Si O Cl Si Si O Si Cl Cl Si Cl Cl O Si O O AB110924 4-(t-Butyl)phenethyltrichlorosilane 211925-40-5 Cl Si Cl Cl Gute Chemie
Gute Chemie. Organofunctional Silanes Reagents for Surface Modification 55 AB129293 Phenethyldiisopropylchlorosilane 151613-24-0 AB111299 Phenethyldimethylchlorosilane; 97% 17146-08-6 AB129294 Phenethyldimethyl(dimethylamino)silane 181231-68-5 AB111300 Phenethylmethyldichlorosilane; 95% 772-65-6 AB111301 Phenethyltrichlorosilane, 940-41-0 contains some alpha-isomer; 97% AB111302 Phenethyltrimethoxysilane; 97% 49539-88-0 AB134465 4-Phenylbutyldimethylchlorosilane; 97% 32328-67-9 AB355878 (4-Phenylbutyl)(dimethyl)(diethylamino)silane 1858256-02-6 AB134466 (4-Phenylbutyl)methyldichlorosilane; 95% 17776-69-1 AB131061 4-Phenylbutyltrichlorosilane 17886-88-3 AB252611 6-Phenylhexyldimethylchlorosilane; 97% 97451-53-1 AB334056 6-Phenylhexyldimethyl(dimethylamino)silane; 95% 1223044-18-5 Si N Cl Si Cl Si Cl Si Cl Cl Cl Si Cl O O Si O Cl Si N Si Cl Si Cl Cl Cl Si Cl Si Cl Si N abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
56 Si O Cl Si Cl O Si O Cl Cl Si Cl O O Si O Si Cl O Si Cl Cl Si AB334062 6-Phenylhexyldimethylmethoxysilane; 97% 1858242-16-6 AB334060 6-Phenylhexylmethyldichlorosilane; 97% 97451-52-0 AB334061 6-Phenylhexylmethyldimethoxysilane; 97% 1858240-78-4 AB201456 6-Phenylhexyltrichlorosilane; 97% 18035-33-1 AB334063 6-Phenylhexyltrimethoxysilane; 97% 1640036-44-7 AB111335 (3-Phenylpropyl)dimethylchlorosilane; 97% 17146-09-7 AB331574 3-Phenylpropyldimethylmethoxysilane; 97% 52500-10-4 AB129299 (3-Phenylpropyl)methyldichlorosilane; 97% 17776-66-8 AB331582 (3-Phenylpropyl)methyldimethoxysilane; 97% 1233513-31-9 AB252612 (3-Phenylpropyl)trichlorosilane; 97% 13617-40-8 AB334059 (3-Phenylpropyl)trimethoxysilane; 97% 152958-90-2 O Si O Cl Si Cl Cl O Si O O Gute Chemie
Gute Chemie. Organofunctional Silanes Reagents for Surface Modification 57 Polar Organofunctional Silanes AB129259 3-Benzoyloxypropyltrimethoxysilane; 97% 76241-02-6 AB110931 10-(Carbomethoxy)decyldimethylchlorosilane; 97% 53749-38-5 AB153302 10-(Carbomethoxy)decyldimethylmethoxysilane; 1211488-83-3 95% AB110932 2-(Carbomethoxy)ethylmethyldichlorosilane; 92%, 18163-42-3 total of isomers AB110933 2-(Carbomethoxy)ethyltrichlorosilane; 95% 18147-81-4 AB110934 Carboxyethylsilanetriol, disodium salt; 25% in water 18191-40-7 AB110986 [2-(4-Chlorosulfonylphenyl)ethyl]trichlorosilane; 50% 79793-00-3 in methylene chloride AB129108 [2-(4-Chlorosulfonylphenyl)ethyl]trichlorosilane; 50% 79793-00-3 in toluene AB334066 N-[3-(Dimethoxymethylsilyl)propyl]hexadecanamide; 1858240-83-1 95% O Si O AB334065 N-[3-(Methoxydimethylsilyl)propyl]hexadecanamide; 1240493-11-1 95% O Si AB134454 [11-(2-Methoxyethoxy)undecyl]trichlorosilane 943349-49-3 O O N H N H O O O Si O O Cl Si O Si O O O O Cl Cl Si Cl Cl Si Cl O O O O OH HO Si HO Na O O O SO Cl O SO Cl Cl Si Cl Cl Cl Si Cl Cl Cl Cl Cl Si O O abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
58 AB111224 [3-(4-Methoxyphenyl)propyl]methyldichlorosilane 134438-26-9 AB128293 [3-(4-Methoxyphenyl)propyl]trichlorosilane; 95% 163155-57-5 AB153032 2-[Methoxy(polyethyleneoxy)propyl]trichlorosilane; 36493-41-1 90% AB212452 2-[Methoxy(polyethyleneoxy)propyl]trimethoxysilane; 65994-07-2 90%, 9-12 PE-units AB134143 (4-Nonylphenoxypropyl)dimethylchlorosilane 1274904-19-6 AB129295 3-Phenoxypropyldimethylchlorosilane; 95% 69733-73-9 AB129296 3-Phenoxypropyltrichlorosilane; 95% 60333-76-8 AB123804 Phenoxytrimethylsilane 1529-17-5 AB111438 Trichloromethyltrichlorosilane; 50% in toluene 17760-13-3 AB129323 N-(3-Triethoxysilylpropyl)-4-hydroxybutyramide; 95% 156214-80-1 AB128800 3-(Triethoxysilyl)propylsuccinic anhydride; 93642-68-3 tech. 60-70% Gute Chemie Cl Si Cl Cl Cl Si Cl O O Cl Cl Si Cl O O n Si Cl O Cl Si Cl Cl Si Cl O O Si O Cl Cl Cl Si Cl Cl Cl O O Si O H N O OH O Si O O O O O
Gute Chemie. Organofunctional Silanes Reagents for Surface Modification 59 AB152514 11-(Triethoxysilyl)undecanal; 90% 116047-42-8 O O Si O O AB130830 3-(Trihydroxysilyl)-1-propanesulfonic acid, 70942-24-4 30-35% in water HO Si HO OH HO O S O AB290843 N-[3-(Trimethoxysilyl)propyl]hexadecanamide; 95% 862822-32-0 O O Si O H N O Perfluorinated Organofunctional Silanes AB111157 (3-Heptafluoroisopropoxy)propyltrichlorosilane; 97% 15538-93-9 AB182089 (3,3,4,4,5,5,6,6,6-Nonafluorohexyl)dimethylchloro- 119386-82-2 silane; 97% CF3 F F3C O Cl Si Cl Cl Si Cl FF FF F F F F F AB252600 (3,3,3,4,4,5,5,6,6-Nonafluorohexyl)methyldichloro- 38436-16-7 F F F F silane; 97% AB129290 Pentafluorophenyldimethylchlorosilane; 95% 20082-71-7 AB129291 Pentafluorophenylpropyldimethylchlorosilane; 97% 157499-19-9 AB134463 Pentafluorophenylpropylmethyldichlorosilane; 97% 1220126-66-8 F F F F F F Cl Si Cl F FF F F Cl Si F F F F F F F F F Si Cl Cl Si Cl abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
60 AB334064 (Pentafluorophenylpropyl)methyldimethoxysilane; 1858256-21-9 97% AB126774 Pentafluorophenylpropyltrichlorosilane; 97% 78900-02-4 AB126792 Pentafluorophenylpropyltrimethoxysilane; 97% 303191-26-6 AB134664 Pentafluorophenyltriethoxysilane; 97% 20083-34-5 AB104055 1H,1H,2H,2H-Perfluorooctyltriethoxysilane; 97% 51851-37-7 F F F F F F F F F F F F F F F O Si O Cl Cl Si Cl O Si O O O O Si O F F F F F F F F F F O F F O Si O F F F F F F AB111154 (Heptadecafluoro-1,1,2,2-tetrahydrodecyl)dimethyl- 74612-30-9 F F F F F F F F chlorosilane; 95% AB129141 (Heptadecafluoro-1,1,2,2-tetrahydrodecyl)methyldi- 3102-79-2 chlorosilane; 97% AB111155 1H,1H,2H,2H-Perfluorodecyltrichlorosilane; 97% 78560-44-8 (stabilized with copper) F F F F F F F FF FF FF F F F F F F F F F FF FF FF F F F F F F F F F F F F F F F Si Cl Cl Si Cl Cl Cl Si Cl AB111156 (Heptadecafluoro-1,1,2,2-tetrahydrodecyl)triethoxy- 101947-16-4 silane; 97%, stabilized with copper F F F F F F F F AB153340 (Heptadecafluoro-1,1,2,2-tetrahydrodecyl)trimethoxy- 83048-65-1 silane; 95% (stab. with copper) F F F F F F F F F F F F F F F F F F F F FF FF FF O Si O O O Si O O Gute Chemie
Gute Chemie. Organofunctional Silanes Reagents for Surface Modification 61 AB200561 1H,1H,2H,2H-Perfluorododecyltrichlorosilane; 97% 102488-49-3 F F F F F F F F F F AB232454 1H,1H,2H,2H-Perfluorododecyltriethoxysilane; 97% 146090-84-8 AB182091 Nonafluorohexyltrichlorosilane; 95% 78560-47-1 AB252596 Nonafluorohexyltriethoxysilane; 95% 102390-98-7 AB182092 Nonafluorohexyltrimethoxysilane; 95% 85877-79-8 F F F F F F F F F F F Cl Cl Si Cl F F F F F F F F F F F F F F F F F F F F F O Si O O F F F F F F F FF Cl Si Cl Cl F F FF F F F F F O Si O O FF FF F FF FF O Si O O AB104048 1H,1H,2H,2H-Perfluorooctyldimethylchlorosilane; 102488-47-1 F F F F F 97% AB111443 (Tridecafluoro-1,1,2,2-tetrahydrooctyl)methyldichloro- 73609-36-6 silane; 97% AB108484 1H,1H,2H,2H-Perfluorooctylmethyldimethoxysilane; 85857-17-6 96% F F F F F F FF FF FF F F F F F FF FF FF F F F F F FF FF FF AB182112 (Tridecafluoro-1,1,2,2-tetrahydrooctyl)silane; 95% 469904-32-3 F F F F F F AB111444 (Tridecafluoro-1,1,2,2-tetrahydrooctyl)trichlorosilane; 78560-45-9 97% F F F F F F F F F F F F F F F F F F F F Cl Si Cl Si Cl O Si O SiH3 Cl Cl Si Cl abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
62 AB104055 1H,1H,2H,2H-Perfluorooctyltriethoxysilane; 97% 51851-37-7 O O Si O FF FF F F F F F F F F F AB108485 1H,1H,2H,2H-Perfluorooctyltrimethoxysilane; 97% 85857-16-5 F F F F F F F F F F F F F O O Si O AB231952 1H,1H,2H,2H-Perfluorotetradecyltriethoxysilane; 885275-56-9 97% O Si O O FF FF FF FF FF FF F F F F F F F F F F F F F AB111473 (3,3,3-Trifluoropropyl)trimethoxysilane; 97% 429-60-7 Silicate Precursors AB111024 Di-t-butoxydiacetoxysilane; tech grade 13170-23-5 AB111163 Hexachlorodisiloxane; 96% 14986-21-1 AB111381 Tetra-n-butoxysilane; 97% 4766-57-8 AB111383 Silicon(IV) chloride; 97% 10026-04-7 AB111385 Tetraethoxysilane; 99% 78-10-4 Gute Chemie O O Si O CF3 O O O Si O O O Cl Cl Si Si O Cl Cl Cl Cl O O Si O O Cl Cl Si Cl Cl O O Si O O
Gute Chemie. Organofunctional Silanes Reagents for Thin-Film Depositio 63 AB153256 Tetrakis(2-hydroxyethoxy)silane; 90% 17622-94-5 OH AB111410 Tetramethoxysilane; 98% 681-84-5 AB153260 Tetramethylammonium silicate, 16-20% in water 53116-81-7 AB111424 Tetra-n-propoxysilane; 97% 682-01-9 AB401821 Tri-t-butoxysilanol; (99.9+%-Si) 18166-43-3 AB153351 Tri-t-pentoxysilanol; 95% 17906-35-3 HO O O Si O HO O O O Si O O OH O O Si O O N 4 O O Si O O O Si O O OH O Si O O HO Bidentate Alkyl Organofunctional Silanes AB110835 1,2-Bis(chlorodimethylsilyl)ethane; 97% 13528-93-3 AB110836 1,6-Bis(chlorodimethylsilyl)hexane; 97% 14799-66-7 AB110837 1,8-Bis(chlorodimethylsilyl)octane; 90% 5089-28-1 AB100081 1,6-Bis(dichloromethylsilyl)hexane; 95% 18395-97-6 Cl Si Si Cl Cl Si Cl Si Si Cl Si Cl abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
64 AB110862 Bis(methyldichlorosilyl)ethane; 97% 3353-69-3 AB290842 1,8-Bis(methyldichlorosilyl)octane 5181-41-9 AB252462 1,2-Bis(methyldiethoxysilyl)ethane 18043-74-8 AB110865 1,2-Bis(trichlorosilyl)ethane; 95% 2504-64-5 AB110866 Bis(trichlorosilyl)hexane; 95% 13083-94-8 AB110867 Bis(trichlorosilyl)methane; 97% 4142-85-2 AB110869 Bis(trichlorosilyl)octane; 97% 52217-53-5 AB110871 Bis(triethoxysilyl)ethane; 97% 16068-37-4 AB110872 Bis(triethoxysilyl)methane; 97% 18418-72-9 AB128299 Bis(triethoxysilyl)octane; 97% 52217-60-4 Gute Chemie Cl Cl Si Cl Si Cl Cl Si Cl Cl Cl Si O Si O O Si O Cl Cl Si Cl Cl Si Cl Cl Cl Cl Si Cl Cl Si Cl Cl Cl Si Cl Cl Cl Si Cl Cl Cl Cl Si Cl Cl Si Cl Cl O O Si O O Si O O O O O O Si Si O O O O Si O O Si O O
Gute Chemie. Organofunctional Silanes Reagents for Thin-Film Depositio 65 AB110875 1,2-Bis(trimethoxysilyl)ethane; 97% 18406-41-2 AB110627 1,6-Bis(trimethoxysilyl)hexane; 97% 87135-01-1 AB252480 1,8-Bis(trimethoxysilyl)octane; 95% 105566-68-5 Bidentate Aryl Organofunctional Silanes AB129119 2,5-Disilahexane; 95% 4405-22-5 AB110855 1,4-Bis(dimethylsilyl)benzene; 97% 2488-01-9 AB110858 1,4-Bis(hydroxydimethylsilyl)benzene; 95% 2754-32-7 AB153274 1,4-Bis(triethoxysilyl)benzene; 95% 2615-18-1 AB110876 Bis(trimethoxysilylethyl)benzene 58298-01-4 AB153284 1,4-Bis(trimethoxysilylmethyl)benzene 193358-40-6 O O Si O O Si O O O O Si O O O Si O O O Si O O Si O O H2 Si Si H2 H Si Si H HO Si Si OH O O Si O O Si O O O Si O O O Si O O O O Si O O O Si O abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
66 Siloxanes AB291850 1,3-Bis-(3,3-dimethylbutyl)tetramethoxydisiloxane; 1858255-90-9 96% AB111033 1,3-Dichloro-1,3-diphenyl-1,3-dimethyldisiloxane; 3582-72-7 97% AB111034 1,5-Dichlorohexamethyltrisiloxane; 95% 3582-71-6 AB111039 1,7-Dichlorooctamethyltetrasiloxane; 90% 2474-02-4 AB111043 1,3-Dichlorotetramethyldisiloxane; 97% 2401-73-2 AB252525 1,5-Diethoxyhexamethyltrisiloxane; 95% 17928-13-1 AB108983 1,3-Divinyl-1,3-dimethyl-1,3-dichlorodisiloxane; 97% 15948-19-3 AB111393 1,1,3,3-Tetraisopropyl-1,3-dichlorodisiloxane; 96% 69304-37-6 SiOx Precursors AB111009 Cyclotetramethylenedichlorosilane; 97% 2406-33-9 AB111010 Cyclotetramethylenedimethylsilane; 95% 1072-54-4 AB111011 Cyclotrimethylenedichlorosilane; 97% 2351-33-9 Gute Chemie O O Si Si O O O Cl Cl Si Si O O O Si Si Si Cl Cl O O O Si Si Si Si Cl Cl Cl Cl Si Si O O O O O Si Si Si O Si Si Cl Cl O Si Si Cl Cl Si Cl Cl Si Cl Si Cl
Gute Chemie. Organofunctional Silanes Reagents for Thin-Film Depositio 67 AB109330 Cyclotrimethylenedimethylsilane; 97% 2295-12-7 AB129099 Cyclotrimethylenemethylchlorosilane; 97% 2351-34-0 AB111083 Dimethylethoxysilane; 97% 14857-34-2 AB111084 Dimethylmethoxychlorosilane; 90% 1825-68-9 AB111115 1,3-Disilabutane; 97% 6787-86-6 AB251646 Hexachlorodisilane; 98% 13465-77-5 AB252559 1,1,3,3,5,5-Hexaethoxy-1,3,5-trisilacyclohexane; 17955-67-8 95% AB111176 Hexamethyldisiloxane; 98% 107-46-0 AB111232 Methyldiethoxysilane; 95% 2031-62-1 AB111233 Methyldimethoxysilane; 97% 16881-77-9 AB111419 Tetramethylsilane; 99.9% (NMR grade) 75-76-3 AB254089 Trimethylsilane; 99.9% 993-07-7 Si Si Cl H Si O Cl Si O H3Si Si H2 Cl Cl Cl Si Si Cl Cl Cl O O O Si Si O Si O O Si Si O O O Si H O O H Si Si SiH abcr GmbH ▪ Phone +49 721 95061 - 0 ▪ Fax +49 721 95061 - 80 ▪ info@abcr.com ▪ www.abcr.com
68 Silane Reagents for Microelectronics AB111228 (3-Methoxypropyl)trimethoxysilane; 95% 33580-59-5 AB111418 1,1,3,3-Tetramethyldisiloxane; 99% 3277-26-7 AB111294 Pentamethyldisiloxane; 97% 1438-82-0 AB111159 1,1,1,3,3,5,5-Heptamethyltrisiloxane; 97% 2895-07-0 AB391536 9-Phenanthrenyltriethoxysilane; 95% 21591-53-7 AB357480 (N,N-Dimethylamino)trimethylsilane; 98% 2083-91-2 AB110883 Bis(trimethylsiloxy)methylsilane; 97% 1873-88-7 AB111051 Diethyldichlorosilane; 97% 1719-53-5 AB129115 Diiodosilane; 95% 13760-02-6 AB111030 Di-t-butylsilane; 97% 30736-07-3 O O O Si O SiH SiH O SiH Si O SiH Si Si O O O Si O O N Si Si SiH Si O O Cl Cl Si H2 Si I I Si H2 AB575692 1,1,5,5-Tetramethoxy-1,5-dimethyl-3,3-diphenyltri- 10175-48-1 siloxane O Si O O Si O O Si O Gute Chemie
Publishing details abcr GmbH Im Schlehert 10 76187 Karlsruhe Germany Phone +49 721 95061 - 0 Fax +49 721 95061 - 80 info@abcr.com ▪ www.abcr.com Registered office Karlsruhe Managing Director Dr. Jan Schuricht District court AG Mannheim HRB 104793 Tax number 35005/14749 VAT number DE 815518524 DUNS number 320054844 Publisher: abcr GmbH 369248.1113.6-23 © abcr - All rights reserved.
Gute Chemie. Greater diversity, choice and value. Make use of our e-papers to quickly and easily browse through our catalogues and flyers and search for products. All products listed in the e-papers are linked to the respective product detail page within our website where you will find further information. We can also send the catalogues and flyers by mail. Silicon Compounds Life Science Drug Design Fluorinated Compounds Organozinc Reagents Palladium Catalysts Aryne Precursors Freaky Amino Acids Catalysts Ligands Find 400,000 specialty chemicals in our webshop: www.abcr.com abcr GmbH Germany +49 721 95061-0 info@abcr.com abcr swiss AG +41 41 7201882 info@abcr-swiss.ch abcr france SAS +33 4 7291 3100 info@abcr-france.fr abcr IRL Ltd. +353 56 7738971 info@abcr-irl.ie abcr UK Ltd. +44 161 8187062 info@abcr-uk.com LLC ABCR CHEMI RUS +7 495 9664181 info@abcr-russia.ru (R,R)-Catalyst (35 mol-%)MnO2 (3 eq.), Li2CO3 (2 eq.)PhCF3, 115 °C, 24 hup to 86% yield) (2 eq.)NNOSO2RHHNNHSO2Rup to 94% yield(S,S)-ligand (8 mol-%)THF, diglyme-20°CRalkylNN)(S,S)-ligand (8 mol-%)R1CF3R1+F3C(S,S)-ligand (8 mol-%THF, diglym-20°alkylCoI2 (10 mol-%)(S,S)-ligand (12 mol-%)THF, -80°CArylMgBrROup to 96% yield)ROArylalkylCo(S,S)-ligand (12 mol-%THF, -80°CROBralkyl+ArylMgBrup to 96% yieldONNOCuTfOOTfNNO(R,R)-Catalyst (35 mol-%)MnO2 (3 eq.), Li2CO3 (2 eq.)PhCF3, 115 °C, 24 hup to 86% yield) (2 eq.)NNOSO2RHHNNHSO2RR2(DME)NiCl2 (5 mol-%)(S,S)-ligand (6 mol-%)TMEDA (1.6 eq.)THF, 0°Cup to 94% yieldR (5 mol-%) (6 mol-%)R1FFNOR2R2ZnClR1+BrFFNOR2R2(DME)NiCl(S,S)-ligandTMEDA (1.6 eq.)THF, 0°Cup to 94% yield(DME)NiCl2 (6 mol-%)(S,S)-ligand (8 mol-%)THF, diglyme-20°CRalkylONNO)(S,S)-ligand (8 mol-%)R1alkylCF3ZnClR1+F3C(DME)NiCl(S,S)-ligand (8 mol-%THF, diglym-20°XalkylCoI2 (10 mol-%)(S,S)-ligand (12 mol-%)THF, -80°CArylMgBrROup to 96% yield)ROArylalkylCo(S,S)-ligand (12 mol-%THF, -80°CROBralkyl+ArylMgBrup to 96% yieldNNO(S,S)-ligandONNOCuTfOOTfNNOCO2RArORArOCONR2OR1R2ArRNNNRONRNNR2R1NNRTsNR1R2R1CO2R2ONR1R2R3NR1R2R3OORetc.OTfTMSCsFCO2RArORArOCONR2OR1R2ArRNNNRONRNNR2R1NNRTsNR1R2R1CO2R2ONR1R2R3NR1R2R3OORetc.MeCNrtCommercial Organofunctional Silanes for Diagnostics and Separation01Commercial Organofunctional Silanes for Diagnostics and Separation01Life ScienceNew Chirals for Drug DesignNNNN01Life ScienceNew Chirals for Drug DesignNNNN0101Available in bulk quantities Fluoro Organic Intermediates01Available in bulk quantities Fluoro Organic IntermediatesNew Organozinc Reagents for Organic Synthesis01New Organozinc Reagents for Organic Synthesis01Palladium catalysts for C-C and C-N coupling reactions01Palladium catalysts for C-C and C-N coupling reactions01