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50 ML
€132.00
250 ML
€459.00
About This Item
Empirical Formula (Hill Notation):
C6H12N2Si
CAS Number:
Molecular Weight:
140.26
Beilstein:
606148
EC Number:
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22
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grade
synthesis grade
Quality Level
Assay
≥98.0% (T)
≥98.0%
form
liquid
refractive index
n20/D 1.475 (lit.)
bp
93-94 °C/14 mmHg (lit.)
density
0.957 g/mL at 20 °C
0.956 g/mL at 25 °C (lit.)
storage temp.
2-8°C
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
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Application
1-(Trimethylsilyl)imidazole may be used as an effective alternative to N,O-bis(trimethylsilyl)trifluoroacetamide (BSTFA) and N-methyl-N-(trimethylsilyl)trifluoroacetamide (MSTFA) for the efficient silylation of Ti-MCM-41, a titanium substituted mesoporous molecular sieve. This process enhances the hydrophobicity and catalytic activity of Ti-MCM-41 catalyst for cyclohexene epoxidation with aqueous hydrogen peroxide.[1]
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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
42.8 °F - closed cup
Flash Point(C)
6 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Silylation of Ti?MCM?41 by trimethylsilyl?imidazole and its effect on the olefin epoxidation with aqueous H 2 O 2.
Bu J & Rhee HK
Catalysis Letters, 66(4), 245-249 (2000)
Lukas Schmidt et al.
Archives of toxicology, 91(2), 677-687 (2015-12-19)
We studied the human in vivo metabolism and the elimination kinetics of α-pinene (αPN), a natural monoterpene which commonly occurs in the environment. Four volunteers were exposed to a single oral dose of 10 mg αPN. Each subject provided one pre-exposure
G.S. Bates et al.
Tetrahedron Letters, 4423-4423 (1976)
J.D. Nicholson
Analyst, 103, 193-193 (1978)
K. Blau et al.
Handbook of Derivatives for Chromatography (1993)
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