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A96606

Sigma-Aldrich

Azodicarboxamide

97%

Synonym(s):

1,1′-Azobis[formamide], 1,1′-Azobiscarbamide, 1,1′-Azodiformamide, Diazenedicarboxamide (9CI)

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About This Item

Linear Formula:
NH2CON=NCONH2
CAS Number:
123-77-3
Molecular Weight:
116.08
Beilstein:
1704003
EC Number:
204-650-8
MDL number:
MFCD00007958
UNSPSC Code:
12352100
PubChem Substance ID:
24891486
NACRES:
NA.22

Quality Level

100

Assay

97%

form

powder

mp

220-225 °C (dec.) (lit.)

solubility

water: soluble 0.033 g/L at 20 °C

SMILES string

NC(=O)\N=N\C(N)=O

InChI

1S/C2H4N4O2/c3-1(7)5-6-2(4)8/h(H2,3,7)(H2,4,8)/b6-5+

InChI key

XOZUGNYVDXMRKW-AATRIKPKSA-N

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Related Categories

Pictograms

FlameHealth hazard
GHS02,GHS08

Signal Word

Danger

Hazard Statements

H228 - H334

Hazard Classifications

Flam. Sol. 1 - Resp. Sens. 1

Supplementary Hazards

EUH044

Storage Class Code

4.1A - Other explosive hazardous materials

WGK

WGK 1

Flash Point(F)

392.0 °F

Flash Point(C)

> 200 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

EU REACH SVHC Candidate List

CAS No.

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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Catalytic oxidation of hydrazodicarboxamide to azodicarboxamide by oxygen.
Kaszonyi A, et al.
J. Mol. Catal., 80(3), L13-L17 (1993)
José Berná et al.
Journal of the American Chemical Society, 132(31), 10741-10747 (2010-08-05)
Azodicarboxamides (R(2)NCON=NCONR(2)) are shown to act as new templates for the assembly of unprecedented azo-functionalized hydrogen-bond-assembled [2]rotaxanes. Moreover, these binding sites can be reversibly and efficiently interconverted with their hydrazo forms through a hydrogenation-dehydrogenation strategy of the nitrogen-nitrogen bond. This
The catalytic oxidation of biurea by hydrogen peroxide for preparing azodicarboxamide.
Bingjun S, et al.
Journal of Fuzhou University (Natural Sciences Edtion), 4, 014-014 (1984)
Effect of additives on flexible PVC foam formation.
Demir H, et al.
Journal of Materials Processing Technology, 195(1), 144-153 (2008)
Fourier transform infrared spectrometry (FTIR) for qualitative and quantitative analysis of azodicarboxamide and its potential impurities.
Otte X, et al.
Analytica Chimica Acta, 355(1), 7-13 (1997)
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