A96606
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:
Molecular Weight:
116.08
Beilstein:
1704003
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
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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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Resp. Sens. 1
Supplementary Hazards
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
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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)
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)
Azodicarboxamides as template binding motifs for the building of hydrogen-bonded molecular shuttles.
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
Catalytic oxidation of hydrazodicarboxamide to azodicarboxamide by oxygen.
Kaszonyi A, et al.
J. Mol. Catal., 80(3), L13-L17 (1993)
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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