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384429

Sigma-Aldrich

tert-Butyldimethylsilyl chloride solution

1.0 M in methylene chloride

Sinónimos:

tert-Butylchlorodimethylsilane solution, tert-Butyldimethylchlorosilane, tert-Butyldimethylsilyl chloride, TBDMSCl solution

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About This Item

Fórmula lineal:
(CH3)3CSi(CH3)2Cl
Número de CAS:
18162-48-6
Peso molecular:
150.72
Beilstein/REAXYS Number:
505999
MDL number:
MFCD00000501
UNSPSC Code:
12352103
PubChem Substance ID:
24863996
NACRES:
NA.22

form

liquid

concentration

1.0 M in methylene chloride

density

0.87 g/mL at 20 °C (lit.)
1.225 g/mL at 25 °C

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

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Descripción
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tert-Butyldimethylsilyl chloride, reagent grade, 97%

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N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide with 1% tert-Butyldimethylchlorosilane, ≥95%

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tert-Butylchlorodimethylsilane solution, 50 wt. % in toluene

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tert-Butyldimethylsilyl chloride solution, 1.0 M in THF

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tert-Butyldimethylsilyl trifluoromethanesulfonate, reagent grade, 98%

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1-(tert-Butyldimethylsilyl)imidazole, ≥95%

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t-Butyldimethylsilylimidazole solution, TBDMSIM in DMF, pkg of 10 × 1 mL

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tert-Butyldimethylsilyl chloride, for GC derivatization, LiChropur™, ≥99.0% (GC)

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tert-Butyldimethylsilyl trifluoromethanesulfonate, for GC derivatization, LiChropur™, ≥98.0% (T)

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N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide, for GC derivatization, LiChropur™, ≥98.0% (GC)

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N-tert-Butyldimethylsilyl-N-methyltrifluoroacetamide with 1% tert-Butyldimethylchlorosilane, for GC derivatization, LiChropur™, ≥95.0% (GC)

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N,O-Bis(tert-butyldimethylsilyl)acetamide, for GC derivatization, LiChropur™, ≥98.0% (GC)

signalword

Danger

Hazard Classifications

Aquatic Chronic 2 - Carc. 2 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A - STOT SE 3

target_organs

Central nervous system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

136.4 °F - closed cup

flash_point_c

58 °C - closed cup

ppe

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

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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
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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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Some observations on the t-butyldimethylchlorosilane derivatization reaction.
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