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.
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Flam. Liq. 2
存储类别
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
法规信息
危险化学品
此项目有
E.F. Vansant, P. Van Der Voort, K.C. Vrancken
Characterization and Chemical Modification of the Silica Surface, 83-83 (1995)
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)
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)
商品
Results of a study involving the ability few Fluka silylating reagents to form GC-MS-compatible trimethylsilylmethyl derivatives of NSAIDs
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