Molecular structure of 4,4′-Diaminoazobenzene, CAS Number: 538-41-0
4,4′-Diaminoazobenzene (CAS 538-41-0)
Alternate Names:
4,4′-Azodianiline
CAS Number:
538-41-0
Purity:
95%
Molecular Weight:
212.26
Molecular Formula:
C12H12N4
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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4,4′-Diaminoazobenzene is an artificial organic substance classified within the azo dye group. It serves multiple purposes, including as a reagent in organic synthesis, a dye for biological uses, and a catalyst in various reactions. The azo group has the ability to undergo nucleophilic attacks.
4,4′-Diaminoazobenzene (CAS 538-41-0) References
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- Synthesis of novel amphiphilic azobenzenes and X-ray scattering studies of their Langmuir monolayers. | Sørensen, TJ., et al. 2008. Langmuir. 24: 3223-7. PMID: 18302427
- Label-free electrochemical detection of short sequences related to the hepatitis B virus using 4,4'-diaminoazobenzene based on multiwalled carbon nanotube-modified GCE. | Li, XM., et al. 2008. Oligonucleotides. 18: 321-7. PMID: 18928329
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- A plasmon-driven selective surface catalytic reaction revealed by surface-enhanced Raman scattering in an electrochemical environment. | Cui, L., et al. 2015. Sci Rep. 5: 11920. PMID: 26145715
- Evaluation of the mutagenicity of azo dyes in Salmonella typhimurium: a study of structure-activity relationships. | Shahin, MM. 1989. Mutagenesis. 4: 115-25. PMID: 2659922
- Selective plasmon-driven catalysis for para-nitroaniline in aqueous environments. | Cui, L., et al. 2016. Sci Rep. 6: 20458. PMID: 26857259
- Toward Spatiotemporally Controlled Synthesis of Photoresponsive Polymers: Computational Design of Azobenzene-Containing Monomers for Light-Mediated ROMP. | Zhou, Q., et al. 2016. J Phys Chem A. 120: 7101-11. PMID: 27552379
- Observation of Olefin/Paraffin Selectivity in Azo Compound and Its Application into a Metal-Organic Framework. | Kim, SY., et al. 2018. ACS Appl Mater Interfaces. 10: 27521-27530. PMID: 30040880
- Electronic band structures of pristine and chemically modified cellulose allomorphs. | Srivastava, D., et al. 2020. Carbohydr Polym. 243: 116440. PMID: 32532390
- Studies on carcinogenic bifunctional aminoazo dyes. I. Syntheses and physico-chemical properties of [N', N',-dimethyl-4'-amino]-N-monomethyl-4-aminoazobenzene and 4,4'-diaminoazobenzene. | Lin, JK., et al. 1971. Taiwan Yi Xue Hui Za Zhi. 70: 147-58. PMID: 5281517
- Lack of carcinogenicity in mice of 4,4-'diaminobenzanilide and 4,4'-diaminoazobenzene, two intermediates used in the manufacture of azo dyes. | Della Porta, G. and Dragani, TA. 1981. Cancer Lett. 14: 329-36. PMID: 7332908
- Host–guest complexes of cucurbituril with 4-amino-4′-nitroazobenzene and 4, 4′-diaminoazobenzene in acidic aqueous solutions | Neugebauer, R., & Knoche, W. 1998. Journal of the Chemical Society, Perkin Transactions 2. (3): 529-534.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
4,4′-Diaminoazobenzene, 250 mg | sc-277686 | 250 mg | $108.00 |