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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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Pictograms

Health hazard
GHS08

Signal Word

Danger

Hazard Statements

H334

Precautionary Statements

P261 - P284 - P501

Hazard Classifications

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

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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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)
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)
J Tassignon et al.
Clinical immunology (Orlando, Fla.), 100(1), 24-30 (2001-06-21)
We recently demonstrated that azodicarbonamide is an immunosuppressive compound that inhibits calcium mobilization in T lymphocytes. In this study, we show that azodicarbonamide prevents the progression of human CD4+ T lymphocytes into the G1 phase of the cell cycle, inhibits
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