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235083

Sigma-Aldrich

Sodium bis(trimethylsilyl)amide

95%

Synonym(s):

Hexamethyldisilazane sodium salt

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About This Item

Linear Formula:
[(CH3)3Si]2NNa
CAS Number:
1070-89-9
Molecular Weight:
183.37
Beilstein:
3629917
EC Number:
213-983-8
MDL number:
MFCD00009835
UNSPSC Code:
12352111
PubChem Substance ID:
24854078
NACRES:
NA.22

Assay

95%

mp

171-175 °C (lit.)

SMILES string

C[Si](C)(C)N([Na])[Si](C)(C)C

InChI

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

InChI key

WRIKHQLVHPKCJU-UHFFFAOYSA-N

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Application

Useful for the generation of carbenes, the amination of sulfenamides, and the preparation of lanthanide complexes.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Supplementary Hazards

EUH014

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Journal of the Chemical Society. Perkin Transactions 1, 1923-1923 (1992)
Angewandte Chemie (International Edition in English), 32, 1208-1208 (1993)
Journal of the American Chemical Society, 116, 7637-7637 (1994)
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
Adrienne C Greene et al.
Biomaterials, 32(34), 8860-8869 (2011-09-03)
Chemical and topographical cues can be used to guide dissociated neurons into user-defined network geometries on artificial substrates, yet control of neuron polarity (differentiation into axons and dendrites) remains an elusive goal. We developed a dual guidance cue strategy for
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