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Sigma-Aldrich

Sodium amide

greener alternative

98%

Synonym(s):

Sodamide

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About This Item

Linear Formula:
NaNH2
CAS Number:
7782-92-5
Molecular Weight:
39.01
EC Number:
231-971-0
MDL number:
MFCD00011117
UNSPSC Code:
12352301
PubChem Substance ID:
57647875
NACRES:
NA.22

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

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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
GHS02,GHS05

Signal Word

Danger

Hazard Statements

H261,H314,H412

Hazard Classifications

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

Supplementary Hazards

EUH014,EUH019,EUH029

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)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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K. G. Hampton, et al.,
Organic Syntheses, 51, 128-132 (1971)
C. Caubere, et al.,
Tetrahedron, 50, 11903-11920 (1994)
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
M. Bakavoli, et al.,
Journal of Heterocyclic Chemistry, 48, 149-152 (2010)
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