Skip to Content
Merck
CN
All Photos(2)

Documents

Safety Information

226890

Sigma-Aldrich

2-(Trimethylsilyl)ethanol

96%

Sign Into View Organizational & Contract Pricing

Synonym(s):
(2-Hydroxyethyl)trimethylsilane
Linear Formula:
(CH3)3SiCH2CH2OH
CAS Number:
Molecular Weight:
118.25
Beilstein:
1732034
EC Number:
MDL number:
UNSPSC Code:
12352000
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

96%

form

liquid

refractive index

n20/D 1.423 (lit.)

bp

71-73 °C/35 mmHg (lit.)

density

0.825 g/mL at 25 °C (lit.)

SMILES string

C[Si](C)(C)CCO

InChI

1S/C5H14OSi/c1-7(2,3)5-4-6/h6H,4-5H2,1-3H3

InChI key

ZNGINKJHQQQORD-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Protecting reagent for carboxyl and phosphate groups.
Used to synthesize Teoc-protected amines via alcoholysis of the corresponding isocyanates.

Pictograms

Flame

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Flam. Liq. 3

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Tetrahedron Letters, 33, 7685-7685 (1992)
A Aberman et al.
Biochimica et biophysica acta, 791(2), 278-280 (1984-12-07)
Several trimethylsilyl derivatives were found to be ligands of acetylcholinesterase (acetylcholine acetylhydrolase, EC 3.1.1.7): trimethylsilylethyl acetate (III) and trimethylsilylmethyl acetate (V) are substrates of the enzyme, whereas trimethylsilylethanol (VIII) is a competitive inhibitor. The silicon compounds have kinetic parameters similar
Seth L Crawley et al.
Organic letters, 8(18), 3995-3998 (2006-08-25)
A new protocol for generating aza-ortho-xylylenes via acid-catalyzed or fluoride-promoted ring opening of 2-(2-acylaminophenyl)aziridines is described. This methodology has been exploited in the rapid construction of a hexacyclic substructure of communesin B.
Journal of the Chemical Society. Perkin Transactions 1, 2639-2639 (1993)
Tetrahedron Letters, 35, 757-757 (1994)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service