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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/REAXYS Number:
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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pictograms

Health hazard
GHS08

signalword

Danger

hcodes

H334

Hazard Classifications

Resp. Sens. 1

supp_hazards

EUH044

Storage Class

4.1A - Other explosive hazardous materials

wgk_germany

WGK 1

flash_point_f

>392.0 °F

flash_point_c

> 200 °C

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCW8726
MKCS9169
MKCR3393
MKCS0670
MKCS6048

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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)
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
Effect of additives on flexible PVC foam formation.
Demir H, et al.
Journal of Materials Processing Technology, 195(1), 144-153 (2008)
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)
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