4253-34-3CC(=O)O[Si](C)(OC(C)=O)OC(C)=OTVJPBVNWVPUZBM-UHFFFAOYSA-N4253-34-3DTXSID0027565CHEMBL3184776Liquid; Other Solid; Liquid
Solid; [Alfa Aesar MSDS]
Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.
This chemical does not meet GHS hazard criteria for 0.9% (5 of 561) of reports.
Danger
H302 (73.6%): Harmful if swallowed [Warning Acute toxicity, oral]
P260, P261, P264, P264+P265, P270, P271, P280, P301+P317, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P351+P338, P305+P354+P338, P316, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P363, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 561 reports by companies from 22 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Danger
Chemical: Silanetriol, methyl-, triacetate
Silanetriol, 1-methyl-, 1,1,1-triacetate is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Silanetriol, 1-methyl-, 1,1,1-triacetate are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)
Status: Active Update: 04-08-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/14400
Silanetriol, methyl-, triacetate, >5% in a non hazardous diluent: Does not have an individual approval but may be used under an appropriate group standard
Causes severe irritation and burns to skin and eyes in rabbits; Rapidly hydrolyzed by moisture/water forming acetic acid and the corresponding trisilanols (observed toxicity attributed to acetic acid); [OECD SIDS: Methyltriacetoxysilane - 2005] An irritant; Harmful by ingestion; [Alfa Aesar MSDS] See Acetic acid. See Ethyltriacetoxysilane.
Acute Tox. 4 (73.6%)
Acute toxicity (Oral) - Category 4
6.2 [mg/m3]
68 [mg/m3]
410 [mg/m3]
Used as a cross-linker for silicone sealants and adhesives (completely reacts during curing); [OECD SIDS: Methyltriacetoxysilane - 2005]
Working with Glues and Adhesives [Category: Other]
Adhesive Manufacturing
Silanetriol, 1-methyl-, 1,1,1-triacetate: ACTIVE
UsesMethyltriacetoxysilane is used as a silane coupling agent.
PreparationCurrently, in industry, methyltrichlorosilane and acetic anhydride are commonly used as raw materials for acylation reactions to synthesize methyltriacetoxysilane products. The content can reach over 95%, and the total chlorine content is ≤100ppm. The reaction formula is as follows: CH3SiCl3 + 3C4H6O3 → (CH3CO2)3SiCH3 + 3C2H3ClO. The production process is as follows: Using methyltrichlorosilane and acetic anhydride as raw materials, the materials are added to the synthesis reactor in a certain proportion for the acylation reaction. The temperature is first raised to 80℃ for atmospheric pressure reflux reaction, and acetyl chloride is collected while refluxing at 80~95℃ until the flow is stopped. The semi-finished methyltriacetoxysilane in the synthesis reactor is transferred to a crude synthesis tank. The semi-finished product is then pumped to an acetyl chloride vacuum thin-film evaporator, where the feeding temperature is controlled at 100℃ to distill off acetic anhydride and acetyl chloride. The material is then pumped to an acetic anhydride vacuum thin-film evaporator, where the feeding temperature is controlled at 105-115℃ to obtain the finished methyltriacetoxysilane. Material containing a large amount of acetic anhydride is extracted from both vacuum thin-film evaporators and returned to the synthesis reactor. The finished methyltriacetoxysilane is then decolorized in a decolorization reactor using activated carbon at 70℃. After decolorization, the material is filtered through a candle filter into a modification reactor to obtain pure methyltriacetoxysilane.
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