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Merck

208329

Sigma-Aldrich

Sodium amide

greener alternative

98%

Sinónimos:

Sodamide

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About This Item

Fórmula lineal:
NaNH2
Número de CAS:
Peso molecular:
39.01
EC Number:
MDL number:
UNSPSC Code:
12352301
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

98%

form

powder

greener alternative product characteristics

Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

bp

400 °C (lit.)

mp

210 °C (lit.)

greener alternative category

SMILES string

N[Na]

InChI

1S/H2N.Na/h1H2;/q-1;+1

InChI key

ODZPKZBBUMBTMG-UHFFFAOYSA-N

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General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency. Find details here.

Application

Reagent for:
Synthesis of allylic amines and amides
Synthesis of antibacterials
Aggregative activation and heterocyclic chemistry
Phenylation with diphenyliodonium chloride
Sodium amide (NH2Na) (98%) can be used for a variety of applications such as:
  • production of a hydrogen storage system
  • adsorption of CO2
  • fabrication of fuel cells

pictograms

FlameCorrosion

signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B - Water-react 2

Storage Class

4.3 - Hazardous materials which set free flammable gases upon contact with water

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Visite la Librería de documentos

M. Bakavoli, et al.,
Journal of Heterocyclic Chemistry, 48, 149-152 (2010)
Thermal decomposition kinetics of light-weight composite NaNH2-NaBH4 hydrogen storage materials for fuel cells
Bai Y, et al.
International Journal of Hydrogen Energy, 37(17), 12973-12979 (2012)
Christian Bukovec et al.
Organic & biomolecular chemistry, 9(8), 2743-2750 (2011-03-08)
Stannylated allylic carbonates are suitable substrates for Pd-catalyzed allylic aminations. In DMF and with [allylPdCl](2) as catalyst the stannylated allyl amines formed can be directly coupled with electrophiles according to the Stille protocol, giving rise to highly functionalized building blocks
Highly efficient CO2 adsorption by nitrogen-doped porous carbons synthesized with low-temperature sodium amide activation
Wang L, et al.
Carbon, 130(16), 31-40 (2018)
C. Caubere, et al.,
Tetrahedron, 50, 11903-11920 (1994)

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