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About This Item
Linear Formula:
CH3C[=NSi(CH3)3]OSi(CH3)3
CAS Number:
Molecular Weight:
203.43
UNSPSC Code:
41116105
NACRES:
NA.22
PubChem Substance ID:
EC Number:
233-892-7
Beilstein/REAXYS Number:
1306669
MDL number:
Assay:
≥98.5% (GC)
Form:
liquid
grade
derivatization grade (GC derivatization)
Quality Level
assay
≥98.5% (GC)
form
liquid
quality
LiChropur™
reaction suitability
reagent type: derivatization reagent
reaction type: Silylations
technique(s)
gas chromatography (GC): suitable
refractive index
n20/D 1.417
bp
71-73 °C/35 mmHg (lit.)
density
0.832 g/mL at 20 °C (lit.)
SMILES string
C\C(O[Si](C)(C)C)=N/[Si](C)(C)C
InChI
1S/C8H21NOSi2/c1-8(9-11(2,3)4)10-12(5,6)7/h1-7H3/b9-8+
InChI key
SIOVKLKJSOKLIF-CMDGGOBGSA-N
General description
N,O-Bis(trimethylsilyl)acetamide is an excellent silylation reagent. For some sterically hindered primary or secondary nitro compounds, N,O-bis(trimethylsilyl)acetamide and BSTFA achieve better results than normal silylation conditions.
Application
Learn more in the Product Information
Suitable for the derivatization of 2-amino-2-dexoxyhexoses, ecdysones, hexosamines in glycosaminoglycans, 18-hydroxycorticosteroids, 15-Oxo-prostaglandin F2α, prostaglandins A,B and E and F, F2α, prostaglandins and metabolites, prostaglandins Emetabolites, sugar phosphates, steroids and testosterone.
Other Notes
Powerful silylating agent
Reagent for o-trimethylsilyl-aldono-1,4-lactones, trimethylsilyl and trimethylsilyl ether.
Legal Information
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 3 - Skin Corr. 1B
supp_hazards
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
111.2 °F - closed cup
flash_point_c
44 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Related Content
K. Blau et al.
Handbook of Derivatives for Chromatography (1993)
J. Heberle et al.
Silylating Agents, 2nd ed. (1995)
Houben-Weyl Methods of Molecular Transformations. Heteroatom Analogues of Aldehydes and Ketones.
Aggarwal VK
Science of Synthesis Knowledge Updates, 27, 593-594 (2014)


