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Merck
CN

33155-U

BSTFA + TMCS,99:1

别名:

Trimethylchlorosilane, 三甲基氯硅烷, 三甲基硅基氯

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UNSPSC Code:
12352200
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description

(SYLON BFT)

reaction suitability

reagent type: derivatization reagent
reaction type: Silylations

packaging

pkg of 1 × 25 mL

concentration

(BSTFA+TMCS, 99:1)

Quality Level

General description

BSTFA is a stronger silylating reagent compared to BSA. In most cases, BSTFA is used in place of BSA as the reaction products are more volatile avoiding interference with early peaks in a chromatogram. BSTFA along with TMCS is considered suitable reagent for quantitative reactions.

Application

It was used in the derivatization of water during determination of trace levels of bisphenol A from plastic water containers using solid-phase microextraction (SPME) coupled with GC-MS.

Other Notes

Reagent for isothiocyanate (amino compounds), oxime, trimethylsilyl (TMS), trimethylsilyl deacylated polyphosphoinositides and trimethylsilyl glycerophosphate esters.

pictograms

FlameExclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

75.2 °F - closed cup

flash_point_c

24 °C - closed cup

ppe

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

法规信息

危险化学品
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分析证书(COA)

Lot/Batch Number

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Ryan R Lappe et al.
Proceedings of the National Academy of Sciences of the United States of America, 115(1), E24-E33 (2017-12-20)
Maize
Dale R Gardner et al.
Phytochemistry, 178, 112465-112465 (2020-09-06)
Broom snakeweed (Gutierrezia sarothrae) and threadleaf snakeweed (G. microcephala) are suffrutescent plants found in many parts of western US rangelands and are possibly toxic to grazing livestock. The toxic components are not known, but it has been suggested that the
D.R. Knapp
Handbook of Analytical Derivatization Reactions, 214-214 (1979)
N.Narasimhachari et al.
Journal of Chromatographic Science, 9, 502-502 (1971)
Combined gas chromatography-mass spectrometry of brain polyphosphoinositides.
T J Cicero et al.
Biochemical and biophysical research communications, 42(3), 428-433 (1971-02-05)

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