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1-TRIMETHYLSILYLMETHANOL

Basic information Safety Supplier Related

1-TRIMETHYLSILYLMETHANOL Basic information

Product Name:
1-TRIMETHYLSILYLMETHANOL
Synonyms:
  • (hydroxymethyl)trimethyl-silan
  • (trimethylsilyl)-methano
  • Methanol, (trimethylsilyl)-
  • Silane, (hydroxymethyl)trimethyl-
  • TRIMETHYLHYDROXYMETHYLSILANE
  • (TRIMETHYLSILYL)METHANOL
  • 1-TRIMETHYLSILYLMETHANOL
  • (HYDROXYMETHYL)TRIMETHYLSILANE
CAS:
3219-63-4
MF:
C4H12OSi
MW:
104.22
EINECS:
221-746-5
Product Categories:
  • Si (Classes of Silicon Compounds)
  • Si-(C)4 Compounds
  • Silicon Compounds (for Synthesis)
  • Synthetic Organic Chemistry
Mol File:
3219-63-4.mol
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1-TRIMETHYLSILYLMETHANOL Chemical Properties

Melting point:
<0°C
Boiling point:
120-122 °C754 mm Hg(lit.)
Density 
0.826 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.419(lit.)
Flash point:
88 °F
storage temp. 
2-8°C
form 
clear liquid
pka
15.92±0.10(Predicted)
Specific Gravity
0.827
color 
Colorless to Almost colorless
Water Solubility 
Fully miscible in water.
Hydrolytic Sensitivity
1: no significant reaction with aqueous systems
BRN 
1731486
CAS DataBase Reference
3219-63-4(CAS DataBase Reference)
EPA Substance Registry System
Methanol, (trimethylsilyl)- (3219-63-4)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
RIDADR 
UN 1987 3/PG 3
WGK Germany 
3
RTECS 
PC4100000
TSCA 
Yes
HS Code 
2931.90.9010
HazardClass 
3
PackingGroup 
III

MSDS

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1-TRIMETHYLSILYLMETHANOL Usage And Synthesis

Uses

1-Trimethylsilylmethanol is used as nucleophile to resolve the racemate obtained from enantioselective esterification of naproxen (2-(6-methoxy-2-naphthyl) propionic acid) by lipases. It was also used as a nucleophilic hydroxymethylation agent.

Purification Methods

If the NMR indicates impurities (should have only two signals), then dissolve it in Et2O, shake this with aqueous 5N NaOH, M H2SO4, saturated aqueous NaCl, dry (MgSO4) and distil it using an efficient column at atmospheric pressure. The 3,5-dinitrobenzoate has m 70-70.5o (from 95% EtOH). [Huang & Wang Acta Chem Sin 23 291 1957, cf. Chem Abstr 52 19911 1958, Speier et al. J Am Chem Soc 81 1844 1959 and Speier et al. J Am Chem Soc 70 1117 1948, Beilstein 4 III 1844, 4 IV 2876.]

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