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06735

tert-Butyldimethylsilyl chloride

LiChropur™, ≥99.0% (GC)

Synonyme(s) :

tert-Butyl(chloro)dimethylsilane, tert-Butyldimethylchlorosilane, TBDMSCl

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A propos de cet article

Formule linéaire :
(CH3)3CSi(CH3)2Cl
Numéro CAS:
18162-48-6
Poids moléculaire :
150.72
UNSPSC Code:
41116105
NACRES:
NA.22
PubChem Substance ID:
329748269
EC Number:
242-042-4
Beilstein/REAXYS Number:
505999
MDL number:
MFCD00000501
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grade

derivatization grade ((GC derivatization))

Quality Level

100

assay

≥99.0% (GC)

quality

LiChropur™

reaction suitability

reagent type: derivatization reagent
reaction type: Silylations

technique(s)

gas chromatography (GC): suitable

bp

125 °C (lit.)

mp

86-89 °C (lit.)

SMILES string

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

Other Notes

Discover LiChropur™ reagents ideal for HPLC or LC-MS analysis

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

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Danger

Hazard Classifications

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

Classe de stockage

4.1B - Flammable solid hazardous materials

wgk

WGK 2

flash_point_f

71.6 °F - closed cup

flash_point_c

22 °C - closed cup

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Certificats d'analyse (COA)

Lot/Batch Number

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Articles

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Results of a study involving the ability few Fluka silylating reagents to form GC-MS-compatible trimethylsilylmethyl derivatives of NSAIDs

Hiroaki Wakimoto et al.
Clinical cancer research : an official journal of the American Association for Cancer Research, 20(11), 2898-2909 (2014-04-10)
Isocitrate dehydrogenase (IDH) gene mutations occur in low-grade and high-grade gliomas. We sought to identify the genetic basis of malignant phenotype heterogeneity in IDH-mutant gliomas. We prospectively implanted tumor specimens from 20 consecutive IDH1-mutant glioma resections into mouse brains and
Some observations on the t-butyldimethylchlorosilane derivatization reaction.
K Bricknell et al.
Biochemical medicine, 23(1), 119-121 (1980-02-01)
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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Numéro d'article de commerce international

RéférenceGTIN
06735-10G04061833379011
06735-10X1G04061833379028