grade
derivatization grade (GC derivatization)
description
Silylation reagent
reaction suitability
reagent type: derivatization reagent
reaction type: Acylations, reagent type: derivatization reagent
reaction type: Silylations
packaging
pkg of 144 × 0.1 mL
technique(s)
GC/MS: suitable
InChI
1S/C8H18F3NOSi2/c1-14(2,3)12-7(8(9,10)11)13-15(4,5)6/h1-6H3
InChI key
XCOBLONWWXQEBS-UHFFFAOYSA-N
Application
Suitable for the derivatization of acetaminophen, acetanilide, n-acetylneuraminic acid, U-aminobutyric acid, arginine, dipeptides, dopamine O-sulfate (3- and 4-isomers), glycine, amino sugar methyl glycosides, glycosphingolipi, n-hydroxylamines, lysine, nitrilotriacetate, phenacetin, phenols, phospholipids, phosphoserine and phosphothreonine, prostaglandin H2 methyl ester, sulfur amino acids and terephthalate prepolymer mixture, and thromboxane B2.
Other Notes
Reagent for N-acetyl, O-trimethylesilyl, trimethylsilyl, trimethylsilyl diglyceride, sulfonyl trimethylsilyl esters, thiohydantoins of amino acids., and trimethylsilyl thiohydantoins.
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
93.2 °F
flash_point_c
34 °C
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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C.W. Gehrke and K. Leimer
Journal of Chromatography A, 57, 219-219 (1971)
Rapid determination of twenty amino acids by gas chromatography.
J P Hardy et al.
Analytical chemistry, 44(8), 1497-1499 (1972-07-01)
A new silylation reagent for amino acids bis(trimethylsilyl)trifluoroacetamide (BSTFA).
D L Stalling et al.
Biochemical and biophysical research communications, 31(4), 616-622 (1968-05-23)

