- Tributylchlorosilane
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- $2.00 / 1KG
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2019-07-06
- CAS:995-45-9
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: customsie
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| | Tributylchlorosilane Basic information |
| Product Name: | Tributylchlorosilane | | Synonyms: | TRIBUTYLSILYL CHLORIDE;TRIBUTYLCHLOROSILANE;TRI-N-BUTYLCHLOROSILANE;Tri-n-butylchlorosilane(Chlorotri-n-butylsilane);Silane, tributylchloro-;tributylchloro-silan;tri-n-butylsilyl chloride;CHLOROTRIBUTYLSILANE | | CAS: | 995-45-9 | | MF: | C12H27ClSi | | MW: | 234.88 | | EINECS: | 213-627-1 | | Product Categories: | | | Mol File: | 995-45-9.mol |  |
| | Tributylchlorosilane Chemical Properties |
| Boiling point | 250-252 °C (lit.) | | density | 0.879 g/mL at 25 °C (lit.) | | refractive index | n20/D 1.446(lit.) | | Fp | 220 °F | | storage temp. | Store at room temperature, keep dry and cool | | form | clear liquid | | color | Colorless to Light yellow | | Specific Gravity | 0.879 | | Water Solubility | Reacts with water. | | Sensitive | Moisture Sensitive | | Hydrolytic Sensitivity | 8: reacts rapidly with moisture, water, protic solvents | | BRN | 1742537 | | InChI | InChI=1S/C12H27ClSi/c1-4-7-10-14(13,11-8-5-2)12-9-6-3/h4-12H2,1-3H3 | | InChIKey | JSQJUDVTRRCSRU-UHFFFAOYSA-N | | SMILES | [Si](CCCC)(CCCC)(CCCC)Cl | | CAS DataBase Reference | 995-45-9(CAS DataBase Reference) | | NIST Chemistry Reference | Silane, tributylchloro-(995-45-9) | | EPA Substance Registry System | Silane, tributylchloro- (995-45-9) |
| Hazard Codes | C | | Risk Statements | 34-37 | | Safety Statements | 26-36/37/39-45 | | RIDADR | UN 2987 8/PG 2 | | WGK Germany | 1 | | F | 10-21 | | TSCA | TSCA listed | | HazardClass | 8 | | PackingGroup | II | | HS Code | 29349990 | | Storage Class | 8A - Combustible corrosive hazardous materials | | Hazard Classifications | Eye Dam. 1
Skin Corr. 1B |
| | Tributylchlorosilane Usage And Synthesis |
| Description | Tributylchlorosilane is a silanising agent widely used as a surface modification reagent and coupling agent in various chemical processes. It enhances hydrophobicity and improves adhesion properties by reacting with hydroxyl groups on surfaces to form stable siloxane bonds. Therefore, it is valuable in applications such as coating materials, silicone polymer manufacturing, and reagents for chromatographic analysis. The mechanism is that the chlorosilane group reacts with the surface hydroxyl group, replacing the surface chlorine atom by a covalent bond, while the butyl group provides hydrophobic properties. | | Uses | Chlorotri-n-butylsilane is as silylating agent. It can react with bromo-trifluoro-methane, to product tributyl-trifluoromethyl-silane. | | Application | Tributylchlorosilane can be used as one of the chlorosilane compounds for the preparation of lithium sulfide. Lithium sulfide is the most important basic raw material in a new type of high-energy and high-safety solid-state lithium-ion battery. | | General Description | Visit our Sensor Applications portal to learn more. | | Purification Methods | Fractionally distil it and store it in small aliquots in sealed ampoules. [Gilman et al. J Am Chem Soc 74 1361 1952, Osthoff & Clark J Org Chem 24 219 1959, Beilstein 4 IV 4072.] |
| | Tributylchlorosilane Preparation Products And Raw materials |
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