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Merck
CN

33068-U

Supelco

TMSI,衍生化级

pkg of 25 mL

别名:

Trimethylsilylimidazole

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EC 号:
UNSPSC代码:
12352200
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等级

derivatization grade

描述

Silylation reagent

反应适用性

reagent type: derivatization reagent
reaction type: Silylations

包装

pkg of 25 mL

技术

GC/MS: suitable (SIM)
gas chromatography (GC): suitable

一般描述

N-trimethylsilyl-imidazole (TMSI) is a silylating agent. It is effective to improve hydrophobicity and catalytic activity of Ti-MCM-41. It is also considered suitable for silanization of silica based amino phases as it reacts selectively with silanol groups.

应用

TMSI was used in derivatization procedure during sample extraction, for GC/MS analysis done for determination of sugar anhydride levoglucosan.

其他说明

Reagent for oxime, trimethylsilyl (TMS) and O-trimethylsilyl.

象形图

FlameExclamation mark

警示用语:

Danger

危险分类

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

42.8 °F - closed cup

闪点(°C)

6 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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A new method for the separation of the catecholamines by gas-liquid chromatography.
M G Horning et al.
Biochimica et biophysica acta, 148(2), 597-600 (1967-11-28)
H. Brandenberger and D. Schnyder, Z.
Analytical Chemistry, 261, 297-297 (1972)
Christopher D Simpson et al.
Journal of the Air & Waste Management Association (1995), 54(6), 689-694 (2004-07-10)
A microanalytical method suitable for the quantitative determination of the sugar anhydride levoglucosan in low-volume samples of atmospheric fine particulate matter (PM) has been developed and validated. The method incorporates two sugar anhydrides as quality control standards. The recovery standard
Silylation of Ti-MCM-41 by trimethylsilyl-imidazole and its effect on the olefin epoxidation with aqueous H2O2.
Bu, Jie, and Hyun-Ku Rhee
Catalysis Letters, 66, 245-249 (2000)
New gas chromatographic method for the analysis of 5-hydroxytryptamine and 5-hydroxyindoleacetic acid in the brain.
Y Maruyama et al.
Biochemical pharmacology, 20(8), 1833-1841 (1971-08-01)

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