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About This Item
Empirical Formula (Hill Notation):
C6H12N2Si
CAS Number:
Molecular Weight:
140.26
UNSPSC Code:
41115716
NACRES:
NA.22
PubChem Substance ID:
EC Number:
242-040-3
Beilstein/REAXYS Number:
606148
MDL number:
Assay:
≥94.0%
grade
derivatization grade (GC derivatization)
Quality Level
assay
≥94.0%
quality
LiChropur™
reaction suitability
reagent type: derivatization reagent
reaction type: Silylations
technique(s)
gas chromatography (GC): suitable
refractive index
n20/D 1.475 (lit.)
bp
93-94 °C/14 mmHg (lit.)
density
0.956 g/mL at 25 °C (lit.)
SMILES string
C[Si](C)(C)n1ccnc1
InChI
1S/C6H12N2Si/c1-9(2,3)8-5-4-7-6-8/h4-6H,1-3H3
InChI key
YKFRUJSEPGHZFJ-UHFFFAOYSA-N
General description
1-(Trimethylsilyl)imidazole (TMSIM) has high silyl donor ability. It does not react with amino groups and also does not help in formation of enol-ether on unprotected ketone groups. It is useful as a silylating agent for ecdysones, norepinephrine, dopamine, steroids, sugars, sugar phosphates and ketose isomers.
Powerful silylating agent, particularly for alcohols; Synthesis of acyl imidazolides
Application
1-(Trimethylsilyl) imidazole may be used for the synthesis an O-silylated derivative of a hexahomotriazacalix[3]arene. It may also be used for the silylation of Ti-MCM-41 catalyst, to study its effect on the olefin epoxidation with aqueous H2O2, 1-(Trimethylsilyl) imidazole was found to improve the hydrophobicity and the catalytic performance of Ti-MCM-41.
Learn more in the Product Information
Other Notes
Reagent for 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 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
42.8 °F - closed cup
flash_point_c
6 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Related Content
Letter: Analysis of bile acids by mass fragmentography -application of 1:1 mixture technique by use of stable isotope labeled compounds.
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Chemical & pharmaceutical bulletin, 22(8), 1949-1950 (1974-08-01)
Thomas J. Bruno, Paris D.N. Svoronos,
CRC Handbook of Basic Tables for Chemical Analysis, 111-111 (2010)
Silylation of Ti-MCM-41 by trimethylsilyl-imidazole and its effect on the olefin epoxidation with aqueous H2O2.
Jie Bu and Rhee HK.
Catalysis Letters, 66 (4), 245-249 (2000)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 394874-1ML | 04061837683039 |
| 394874-5ML | 04061837683749 |
| 394874-25ML | 04061831982558 |
| 394874-10X1ML | 04061831982534 |

