추천 제품
Grade
for GC derivatization
Quality Level
분석
≥94.0%
품질
LiChropur™
반응 적합성
reagent type: derivatization reagent
reaction type: Silylations
기술
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
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일반 설명
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
애플리케이션
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
기타 정보
Reagent for trimethylsilyl and trimethylsilyl ether.
법적 정보
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany
신호어
Danger
유해 및 위험 성명서
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
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
Silylation of Ti-MCM-41 by trimethylsilyl-imidazole and its effect on the olefin epoxidation with aqueous H2O2.
Catalysis Letters, 66 (4), 245-249 (2000)
Synthesis and crystal structure of an O-silylated hexahomotriazacalix [3] arene.
Tetrahedron Letters, 39 (31), 5473-5476 (1998)
Analysis of nanogram quantities of norethisterone in plasma using a GC-MS-COM selective ion detection procedure.
Steroids and lipids research, 5(2), 79-90 (1974-01-01)
Letter: Analysis of bile acids by mass fragmentography -application of 1:1 mixture technique by use of stable isotope labeled compounds.
Chemical & pharmaceutical bulletin, 22(8), 1949-1950 (1974-08-01)
CRC Handbook of Basic Tables for Chemical Analysis, 111-111 (2010)
문서
Results of a study involving the ability few Fluka silylating reagents to form GC-MS-compatible trimethylsilylmethyl derivatives of NSAIDs
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