Merck
CN

06735

Supelco

丁基二甲基氯硅烷

for GC derivatization, LiChropur, ≥99.0% (GC)

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别名:
TBDMSCl, 叔丁基(氯)二甲基硅烷, 叔丁基二甲基氯硅烷
线性分子式:
(CH3)3CSi(CH3)2Cl
CAS号:
分子量:
150.72
Beilstein:
505999
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

等级

for GC derivatization

质量水平

检测方案

≥99.0% (GC)

质量

LiChropur

反应适用性

reagent type: derivatization reagent
reaction type: Silylations

技术

gas chromatography (GC): suitable

bp

125 °C (lit.)

mp

86-89 °C (lit.)

SMILES字符串

CC(C)(C)[Si](C)(C)Cl

InChI

1S/C6H15ClSi/c1-6(2,3)8(4,5)7/h1-5H3

InChI key

BCNZYOJHNLTNEZ-UHFFFAOYSA-N

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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

Aquatic Chronic 2 - Eye Dam. 1 - Flam. Sol. 1 - Skin Corr. 1A

储存分类代码

4.1B - Flammable solid hazardous materials

WGK

WGK 2

闪点(°F)

71.6 °F

闪点(°C)

22 °C

法规信息

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Hiroaki Wakimoto et al.
Clinical cancer research : an official journal of the American Association for Cancer Research, 20(11), 2898-2909 (2014-04-10)
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Some observations on the t-butyldimethylchlorosilane derivatization reaction.
K Bricknell et al.
Biochemical medicine, 23(1), 119-121 (1980-02-01)
P Huttenloch et al.
Environmental science & technology, 35(21), 4260-4264 (2001-11-23)
The efficacy of the surface modification of natural diatomite and zeolite material by chlorosilanes is demonstrated. Chlorosilanes used were trimethylchlorosilane (TMSCI), tert-butyldimethylchlorosilane (TBDMSCI), dimethyloctadecylchlorosilane (DMODSCI), and diphenyldichlorosilane (DPDSCI) possessing different headgroups and chemical properties. Silanol groups of the diatomite and
Rie Harboe Nielsen et al.
Journal of applied physiology (Bethesda, Md. : 1985), 117(7), 694-698 (2014-08-12)
The classic form of Ehlers-Danlos syndrome (cEDS) is an inherited connective tissue disorder, where mutations in type V collagen-encoding genes result in abnormal collagen fibrils. Thus the cEDS patients have pathological connective tissue morphology and low stiffness, but the rate
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Journal of biochemistry, 119(4), 823-827 (1996-04-01)
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Results of a study involving the ability few Fluka silylating reagents to form GC-MS-compatible trimethylsilylmethyl derivatives of NSAIDs

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