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Merck
CN

75986

Chlorotriethylsilane

Wacker Chemie AG, ≥99.0%

Synonym(s):

Silane E3, TESCl, Triethylchlorosilane

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About This Item

Linear Formula:
(C2H5)3SiCl
CAS Number:
994-30-9
Molecular Weight:
150.72
UNSPSC Code:
12352103
NACRES:
NA.22
PubChem Substance ID:
57652599
EC Number:
213-615-6
Beilstein/REAXYS Number:
1732860
MDL number:
MFCD00000507
Assay:
≥99.0%
Form:
liquid

Key Documents

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InChI key

DCFKHNIGBAHNSS-UHFFFAOYSA-N

InChI

1S/C6H15ClSi/c1-4-8(7,5-2)6-3/h4-6H2,1-3H3

SMILES string

CC[Si](Cl)(CC)CC

assay

≥99.0%

form

liquid

manufacturer/tradename

Wacker Chemie AG

refractive index

n20/D 1.43 (lit.)

bp

142-144 °C (lit.)

density

0.898 g/mL at 25 °C (lit.)

Quality Level

200

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Application

Chlorotriethylsilane may be used to catalyze transesterification of triglycerides of natural refined sunflower oil with alcohols to synthesize fatty acid esters It may also be used as a silylating agent to synthesize triethylsilylated cellulose acetate.

Other Notes

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signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A

supp_hazards

EUH014,EUH071

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

86.0 °F

flash_point_c

30 °C

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN6374
BCCN1283
BCCN1026
BCCM0491
BCCK6919

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Synthesis, characterization, and gas permeation properties of the silyl derivatives of cellulose acetate.
Morita R, et al.
Journal of Membrane Science, 305(1-2), 136-145 (2007)
Sustainable formation of fatty acid alkyl esters by transesterification of triglycerides with chlorotrimethylsilane.
Salvini A
Royal Society of Chemistry Advances, 2(11), 4864-4868 (2012)

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