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208329

Sodium amide

Name: Sodium amide
Brand: ALDRICH

98%

Synonym(s):

Sodamide

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About This Item

Linear Formula:

NaNH₂

CAS Number:

7782-92-5

Molecular Weight:

39.01

NACRES:

NA.22

PubChem Substance ID:

57647875

UNSPSC Code:

12352301

EC Number:

231-971-0

MDL number:

MFCD00011117

Assay:

98%

Form:

powder

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Properties

Quality Level

200

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

Enabling,

SMILES string

N[Na]

InChI

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

InChI key

ODZPKZBBUMBTMG-UHFFFAOYSA-N

Description

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

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pictograms

GHS02,GHS05

signalword

Danger

Storage Class

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

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

Hazard Classifications

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

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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)

Stannylated allyl carbonates as versatile building blocks for the diversity oriented synthesis of allylic amines and amides.

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

M. Bakavoli, et al.,

Journal of Heterocyclic Chemistry, 48, 149-152 (2010)

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Global Trade Item Number

SKU	GTIN
208329-250G	04061838769671
208329-1KG	04061826680209
208329-50G	04061838769688