B1507
tert-Butyl(chloro)dimethylsilane
Synonym(s):
tert-Butyldimethylchlorosilane, tert-Butyldimethylsilyl chloride, TBDMSCl
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About This Item
Empirical Formula (Hill Notation):
C6H15ClSi
CAS Number:
Molecular Weight:
150.72
EC Number:
242-042-4
UNSPSC Code:
12352103
PubChem Substance ID:
Beilstein/REAXYS Number:
505999
MDL number:
InChI key
BCNZYOJHNLTNEZ-UHFFFAOYSA-N
InChI
1S/C6H15ClSi/c1-6(2,3)8(4,5)7/h1-5H3
SMILES string
CC(C)(C)[Si](C)(C)Cl
storage temp.
2-8°C
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signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Dam. 1 - Flam. Sol. 1 - Skin Corr. 1A
Storage Class
4.1B - Flammable solid hazardous materials
wgk
WGK 2
flash_point_f
71.6 °F - closed cup
flash_point_c
22 °C - closed cup
Regulatory Information
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Akshanth R Polepally et al.
Journal of clinical pharmacology, 55(10), 1101-1108 (2015-04-24)
A classic 2-period crossover bioavailability study was conducted to evaluate the relative and absolute bioavailability of immediate-release (IR) and extended-release (XR) lamotrigine formulations under steady-state conditions in elderly patients with epilepsy. On treatment days, each subject's morning dose (IR or
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)
Grethe M Olsen et al.
Neurochemistry international, 88, 47-52 (2014-12-03)
Pyruvate carboxylation, the anaplerotic reaction in the brain, has been demonstrated in astrocytes but not neurons. Since anaplerosis cannot proceed without cataplerosis in a closed system such as the brain, there have to be mechanisms to degrade molecules such as
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
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