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Merck
CN

33350-U

HMDS, Derivatization Grade

Synonym(s):

Hexamethyldisilazane

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About This Item

CAS Number:
UNSPSC Code:
12352200
EC Number:
213-668-5
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form

liquid

InChI key

FFUAGWLWBBFQJT-UHFFFAOYSA-N

InChI

1S/C6H19NSi2/c1-8(2,3)7-9(4,5)6/h7H,1-6H3

grade

derivatization grade ((GC derivatization))

reaction suitability

reagent type: derivatization reagent
reaction type: Silylations

packaging

pkg of 1 × 30 mL

Other Notes

Reagent for schiff base, trimethylsilyl and trimethylsilyl ether.

pictograms

FlameSkull and crossbones

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

52.5 °F - closed cup

flash_point_c

11.4 °C - closed cup

ppe

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

Regulatory Information

危险化学品
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Activity of crude and fractionated extracts by lactic acid bacteria (LAB) isolated from local dairy, meat, and fermented products against Staphylococcus aureus.
Yong, Cheng-Chung, et al.
Annals of Microbiology, 65, 1037-1047 (2014)
E.F. Vansant, P. Van Der Voort, K.C. Vrancken
Characterization and Chemical Modification of the Silica Surface, 83-83 (1995)
D.R. Knapp
Handbook of Analytical Derivatization Reactions, 213-213 (1979)
SEPARATION AND IDENTIFICATION OF TRYPTAMINE-RELATED INDOLE BASES BY GAS CHROMATOGRAPHIC METHODS.
B HOLMSTEDT et al.
Analytical biochemistry, 8, 151-157 (1964-06-01)
Simultaneous GLC estimation of salicylic acid and aspirin in plasma.
L J Walter et al.
Journal of pharmaceutical sciences, 63(11), 1754-1758 (1974-11-01)

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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