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308617

Sigma-Aldrich

tert-Butyltrichlorosilane

96%

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About This Item

Linear Formula:
(CH3)3CSiCl3
CAS Number:
18171-74-9
Molecular Weight:
191.56
Beilstein/REAXYS Number:
1736174
EC Number:
242-059-7
MDL number:
MFCD00000480
UNSPSC Code:
12352103
PubChem Substance ID:
24858681
NACRES:
NA.23

assay

96%

form

solid

bp

132-134 °C (lit.)

mp

97-100 °C (lit.)

SMILES string

CC(C)(C)[Si](Cl)(Cl)Cl

InChI

1S/C4H9Cl3Si/c1-4(2,3)8(5,6)7/h1-3H3

InChI key

MOOUPSHQAMJMSL-UHFFFAOYSA-N

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General description

tert-Butyltrichlorosilane is a tert-alkyltrichlorosilane that can be prepared by reacting trimethyl chloride and silicon tetrachloride. It can be used in the synthesis of tert-butyl silsequioxanes by hydrolytic condensation in DMSO.

Application

Hydrolytic condensation of tert-butyltrichlorosilane (tBuSiCl3)in DMSO and water was investigated. The process results in the formation of tBu2Si2O(OH)4, the Ti complex of the intermediate produce active heterogeneous epoxidation catalysts.

pictograms

FlameCorrosion
GHS02,GHS05

signalword

Danger

hcodes

H228,H314

Hazard Classifications

Flam. Sol. 1 - Skin Corr. 1B

supp_hazards

EUH014

Storage Class

4.1B - Flammable solid hazardous materials

wgk_germany

WGK 3

flash_point_f

104.0 °F - closed cup

flash_point_c

40 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Silsesquioxane-Based Homogeneous and Heterogeneous Epoxidation Catalysts Developed by Using High-Speed Experimentation,
Pescarmona PP, et al.
Chemistry (Weinheim An Der Bergstrasse, Germany), 116 (38), 20433-20437 (2012)
Silsesquioxane-Based Homogeneous and Heterogeneous Epoxidation Catalysts Developed by Using High-Speed Experimentation
Pescarmona PP, et al.
Chemistry?A European Journal , 10(7), 1657-1665 (2004)
Organomagnesium synthesis of sec-butyl-and tert-alkylchlorogermanes and their reaction with ethynylmagnesium bromide
Yarosh OG, et al.
Russ. J. Gen. Chem., 75(5), 714-718 (2005)

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