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Merck
CN

702722

Potassium bis(trimethylsilyl)amide solution

1 M in THF

Synonym(s):

KHMDS, Hexamethyldisilazane potassium salt solution, Potassium hexamethyldisilazide solution

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About This Item

Linear Formula:
[(CH3)3Si]2NK
CAS Number:
Molecular Weight:
199.48
UNSPSC Code:
12352111
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4006754
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Product Name

Potassium bis(trimethylsilyl)amide solution, 1 M in THF

InChI key

IUBQJLUDMLPAGT-UHFFFAOYSA-N

SMILES string

C[Si](C)(C)N([K])[Si](C)(C)C

InChI

1S/C6H18NSi2.K/c1-8(2,3)7-9(4,5)6;/h1-6H3;/q-1;+1

vapor density

3.2 (vs air)

form

liquid

concentration

1 M in THF

density

0.915 g/mL at 25 °C

Quality Level

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Application

Potassium bis(trimethylsilyl)amide solution (1 M in THF) has been used as an anionic initiator in the polymerization of polyethylene oxide(PEO).

Packaging

The 25 mL Sure/Seal bottle is recommended as a single-use bottle. Repeated punctures will likely result in decreased performance of product.

Legal Information

Sure/Seal is a trademark of Sigma-Aldrich Co. LLC

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3

target_organs

Central nervous system, Respiratory system

supp_hazards

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

-2.0 °F

flash_point_c

-18.9 °C

ppe

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

Regulatory Information

危险化学品
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Journal of Colloid and Interface Science, 459, 175-182 (2015)
A Sebok et al.
Journal of chromatography. A, 1211(1-2), 104-112 (2008-10-14)
This paper presents a derivatization, mass fragmentation study relating to the most common six cholic acids, such as cholic, lithocholic, chenodeoxycholic, ursodeoxycholic, 3-hydroxy,7-ketocholanic and dehydrocholic acids, identified and quantified as pollutants in the aquatic environment at the first time. Derivatizations
Hexamethyldisilazane-mediated controlled polymerization of alpha-amino acid N-carboxyanhydrides.
Hua Lu et al.
Journal of the American Chemical Society, 129(46), 14114-14115 (2007-10-30)
Daniele Fabbri et al.
Environmental science & technology, 42(8), 2957-2963 (2008-05-24)
Using the pyrolysis-gas chromatography-mass spectrometry and off-line pyrolysis/silylation methods for lignites from three Miocene brown coal basins of Poland resulted in the characterization of many organic compounds, including dominant cellulose degradation products such as levoglucosan, 1,6-anhydro-beta-D-glucofuranose, and 1,4:3,6-dianhydroglucopyranose. Levoglucosan is
Marko Marinkovic et al.
Advanced materials (Deerfield Beach, Fla.), 24(29), 4005-4009 (2012-06-26)
A model is presented that describes the gate-voltage-dependent contact resistance and channel-length-dependent charge carrier mobility of small-molecule-based organic thin-film transistors in top and bottom drain/source contact configuration.

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