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Merck
CN

90383

Supelco

三乙基氯硅烷

for GC derivatization, LiChropur, ≥97.0% (GC)

别名:

TESCl, Triethylchlorosilane

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About This Item

线性分子式:
(C2H5)3SiCl
CAS号:
分子量:
150.72
Beilstein:
1732860
EC 号:
MDL编号:
UNSPSC代码:
12000000
PubChem化学物质编号:
NACRES:
NA.22

等级

for GC derivatization

质量水平

方案

≥97.0% (GC)

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 1.43 (lit.)

沸点

142-144 °C (lit.)

密度

0.898 g/mL at 25 °C (lit.)

SMILES字符串

CC[Si](Cl)(CC)CC

InChI

1S/C6H15ClSi/c1-4-8(7,5-2)6-3/h4-6H2,1-3H3

InChI key

DCFKHNIGBAHNSS-UHFFFAOYSA-N

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一般描述

Chlorotriethylsilane may be used as a silylating reagent for the preparation of trisilyl ethers from alcohols in the presence of a base such as imidazole, pyridine or 4-(dimethylamino)pyridine. It is found to be more reactive when used with pyridine as a solvent.

应用

Chlorotriethylsilane may be used as a derivatizing reagent for the determination of fluoride, in toothpaste samples using headspace solid-phase microextraction and gas chromatography–flame ionization detection.

其他说明

本品是一种硅烷化试剂,在某些合成或者分析应用方面优于三甲基硅烷化试剂

法律信息

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

警示用语:

Danger

危险声明

危险分类

Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A

补充剂危害

储存分类代码

3 - Flammable liquids

WGK

WGK 1

闪点(°F)

86.0 °F

闪点(°C)

30 °C

个人防护装备

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

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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在文件库中查找您最近购买产品的文档。

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J. Heberle et al.
Silylating Agents, 2nd ed. (1995)
W.C. Still et al.
Journal of the American Chemical Society, 99, 948-948 (1977)
Determination of fluoride in toothpaste using headspace solid-phase microextraction and gas chromatography?flame ionization detection
Wejnerowska G, et al.
Journal of Chromatography A, 1150(1-2), 173-177 (2007)
Science of Synthesis: Houben-Weyl Methods of Molecular Transformations, 4 (2014)
C.F. Poole et al.
Journal of Chromatographic Science, 17, 115-115 (1979)

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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