A96606
Azodicarboxamide
97%
Synonym(s):
1,1′-Azobis[formamide], 1,1′-Azobiscarbamide, 1,1′-Azodiformamide, Diazenedicarboxamide (9CI)
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All Photos(3)
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)
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)
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)
P P J Mulder et al.
Analytica chimica acta, 586(1-2), 366-373 (2007-03-28)
Recently doubts have arisen on the usefulness of semicarbazide as marker residue for the illegal use of the antibiotic nitrofurazone (NFZ) in aquaculture and poultry production. Most notably azodicarbonamide (ADC) has been implicated as an alternative source of semicarbazide. ADC
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