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Merck
CN

15222

Supelco

N,O-双(三甲基硅基)三氟乙酰胺

for GC derivatization, LiChropur, ≥99.0%

别名:

BSTFA

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About This Item

线性分子式:
CF3C[=NSi(CH3)3]OSi(CH3)3
CAS号:
分子量:
257.40
Beilstein:
2050024
EC 号:
MDL编号:
UNSPSC代码:
41116105
PubChem化学物质编号:
NACRES:
NA.22

等级

for GC derivatization

质量水平

方案

≥99.0% (GC)
≥99.0%

表单

liquid

质量

LiChropur

反应适用性

reagent type: derivatization reagent
reaction type: Silylations

技术

gas chromatography (GC): suitable

折射率

n20/D 1.384 (lit.)
n20/D 1.384

沸点

45-50 °C/14 mmHg (lit.)

密度

0.969 g/mL at 25 °C (lit.)

SMILES字符串

C[Si](C)(C)O\C(=N\[Si](C)(C)C)C(F)(F)F

InChI

1S/C8H18F3NOSi2/c1-14(2,3)12-7(8(9,10)11)13-15(4,5)6/h1-6H3/b12-7+

InChI key

XCOBLONWWXQEBS-KPKJPENVSA-N

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一般描述

N,O-双(三甲基硅烷基)三氟乙酰胺(BSTFA)是一种优良的硅基化试剂。对于一些空间位阻的一级或二级硝基化合物,N,O-双(三甲基硅基)乙酰胺和BSTFA比常规硅基化条件结果更佳。BSTFA已在胺衍生化中得到应用。其适于羧酸、酚类、脲类、酰胺类、醇类的水化反应。

应用

更多信息请参见产品信息
BSTFA + 1% TMCS(三甲基硅基)溶于乙酸乙酯、乙腈和二氯甲烷溶剂中的情况下,可用于通过气相色谱-质谱联用技术(GC-MS)进行的甾体激素17a-乙炔雌醇(EE2)硅基化反应。此外,其还可用于内源性2-单甘油酯(存在于与大麻素受体结合的犬肠道中)的硅基化。

法律信息

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

象形图

FlameExclamation mark

警示用语:

Warning

危险声明

危险分类

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

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

93.2 °F

闪点(°C)

34 °C

个人防护装备

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

法规信息

危险化学品

从最新的版本中选择一种:

分析证书(COA)

Lot/Batch Number

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访问文档库

Houben-Weyl Methods of Molecular Transformations.
Aggarwal VK
Science of Synthesis Knowledge Updates, 27, 593-594 (2014)
Greene's Protective Groups in Organic Synthesis.
Science (2014)
Bo Wang et al.
Foods (Basel, Switzerland), 9(5) (2020-05-24)
A method based on accelerated solvent extraction (ASE) coupled with gas chromatography tandem mass spectrometry (GC-MS/MS) was developed for the quantitative analysis of spectinomycin and lincomycin in poultry egg (whole egg, albumen and yolk) samples. In this work, the samples
R Mechoulam et al.
Biochemical pharmacology, 50(1), 83-90 (1995-06-29)
In this study, we report the isolation from canine intestines of 2-arachidonyl glycerol (2-Ara-Gl). Its structure was determined by mass spectrometry and by direct comparison with a synthetic sample. 2-Ara-Gl bound to membranes from cells transiently transfected with expression plasmids
Modern Methods of Pharmaceutical Analysis.
Schirmer RE.
Science, 2, 215-216 (1990)

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