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Merck
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725986

Sigma-Aldrich

Trimethylsilanol

≥97.5% (GC)

Sinónimos:

TMS, TMSiOH, Hydroxytrimethylsilane

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About This Item

Fórmula lineal:
(CH3)3SiOH
Número de CAS:
1066-40-6
Peso molecular:
90.20
Beilstein/REAXYS Number:
1361356
EC Number:
213-914-1
MDL number:
MFCD02751657
UNSPSC Code:
12352103
PubChem Substance ID:
329764205
NACRES:
NA.22

assay

≥97.5% (GC)

form

liquid

SMILES string

C[Si](C)(C)O

InChI

1S/C3H10OSi/c1-5(2,3)4/h4H,1-3H3

InChI key

AAPLIUHOKVUFCC-UHFFFAOYSA-N

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Application

Trimethylsilanol (TMS) can be used to prepare tris(trimethylsiloxy) aluminum (I) by reacting with triethylaluminum.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

44.6 °F - closed cup

flash_point_c

7 °C - closed cup

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Saegusa T, et al.
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Drug development and industrial pharmacy, 45(1), 159-167 (2018-09-21)
Establish an effective experimental strategy to determine the compatibility of rubber closures for drugs. Various types of rubber closures with different compositions are available for drug packaging. Many additives of rubber closures can be released from rubber closures and may
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In most reported cases of lung trauma with water proofing products, volatile organic compounds (VOC) have a prominent role. Here we report on a case involving ten workers exposed to a sprayed product containing nanoparticles in a water solution with
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Organic & biomolecular chemistry, 1(7), 1106-1111 (2003-08-21)
A convenient and efficient method for the cleavage of 1,3-oxazolidin-5-ones and 1,3-oxazolidin-2-ones utilising potassium trimethylsilanolate in tetrahydrofuran is described. The benzyloxycarbonyl-protecting group is readily removed under the reaction conditions, whereas the N-benzoyl group is stable. A synthesis of (R)-salmeterol exploiting
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