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Merck
CN

92718

1-(Trimethylsilyl)imidazole - Pyridine mixture

derivatization grade (GC derivatization), LiChropur

Synonym(s):

Silylating mixture VII, TMSI+Pyridine

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About This Item

CAS Number:
UNSPSC Code:
23151816
eCl@ss:
39151701
PubChem Substance ID:
NACRES:
NA.22
MDL number:
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Product Name

1-(Trimethylsilyl)imidazole - Pyridine mixture, derivatization grade (GC derivatization), LiChropur

SMILES string

c1ccncc1.C[Si](C)(C)n2ccnc2

InChI

1S/C6H12N2Si.C5H5N/c1-9(2,3)8-5-4-7-6-8;1-2-4-6-5-3-1/h4-6H,1-3H3;1-5H

InChI key

PFVKFOIOKNIZKY-UHFFFAOYSA-N

grade

derivatization grade (GC derivatization)

description

1:4 (v/v)

form

liquid

quality

LiChropur

reaction suitability

reagent type: derivatization reagent
reaction type: Silylations

technique(s)

gas chromatography (GC): suitable

density

0.98 g/mL at 20 °C

storage temp.

2-8°C

Quality Level

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Application

Learn more in the Product Information

General description

1-(Trimethylsilyl)imidazole-Pyridine mixture is useful for derivatizing wet sugar samples, hindered hydroxyl groups in steroids and, in conjunction with fluorinated acylation reagents, amino acids. For moderately hindered or slowly reacting compounds, pyridine is an especially useful solvent for TMSI because of its ability to act as an HCl acceptor in silylation reactions involving organochlorosilanes.

Other Notes

Silylating mixture for the mild silylation of alcohols. It is often called Tri-Sil Z

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

62.6 °F - closed cup

flash_point_c

17 °C - closed cup

ppe

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

Regulatory Information

危险化学品
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G. Van Ling
Journal of Chromatography A, 44, 175-175 (1969)
M A Andrews
Carbohydrate research, 194, 1-19 (1989-12-01)
Two new procedures for the gas-chromatographic analysis of monosaccharides are reported. One involves derivatization of the sugars by reaction with O-benzylhydroxylamine followed by trifluoroacetylation with N-methylbis(trifluoroacetamide) and chromatography on a DB-1701 capillary column. This technique probably provides the best resolution

Articles

Results of a study involving the ability few Fluka silylating reagents to form GC-MS-compatible trimethylsilylmethyl derivatives of NSAIDs

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