InChI key
XCOBLONWWXQEBS-UHFFFAOYSA-N
InChI
1S/C8H18F3NOSi2/c1-14(2,3)12-7(8(9,10)11)13-15(4,5)6/h1-6H3
grade
derivatization grade (GC derivatization)
reaction suitability
reagent type: derivatization reagent
reaction type: Acylations, reagent type: derivatization reagent
reaction type: Silylations
packaging
pkg of 20 × 1 mL
technique(s)
GC/MS: suitable
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Application
Suitable for the derivatization of acetaminophen, acetanilide, n-acetylneuraminic acid, U-aminobutyric acid, sulfur amino acids, arginine, dipeptides, dopamine O-sulfate (3- and 4-isomers), amino sugar methyl glycosides, glycosphingolipi, glysine, n-hydroxylamines, lysine, nitrilotriacetate, phenacetin, phenols, phenols (sterically hindered), phospholipids, phosphoserine and phosphothreonine, prostaglandins F2α, prostaglandin H2 methyl ester, psiocin, psiocybin, dopamine O-sulfate (3- and 4-isomers), terephthalate prepolymer mixture, thiohydantoins of amino acids, and thromboxane B2.
Other Notes
Reagent for N-acetyl, O-trimethylesilyl, trimethylsilyl, trimethylsilyl ether, trimethylsilyl thiohydantoins, sulfonyl trimethylsilyl esters and trimethylsilyl diglyceride.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2
存储类别
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
法规信息
危险化学品
此项目有
C.W. Gehrke and K. Leimer
Journal of Chromatography A, 59, 219-219 (1971)
D B Repke et al.
Journal of pharmaceutical sciences, 66(5), 743-744 (1977-05-01)
With the combined technique of GLC-mass spectrometry, psilocin and psilocybin, two hallucinogenic indoles, were analyzed as their trimethylsilyl derivatives. The method was applied to these two components in an extract of Psilocybe cubensis (Earle) Sing.
E.R.Atkinson and S.I. Calouche
Analytical Chemistry, 43, 460-460 (1971)
R L Bronaugh et al.
The Journal of pharmacology and experimental therapeutics, 195(3), 441-452 (1975-12-01)
A method is described for the isolation and measurement of dopamine 3-O-sulfate and dopamine 4-O-sulfate. The sulfate isomers of dopamine were synthesized chemically by the reaction of dopamine with sulfuric acid. The isomers were isolated by anion-exchange column chromatography and
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)
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