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Literatura científica selecionada sobre o tema "Azo compounds Toxicology"

Autor: Grafiati

Publicado: 4 de junho de 2021

Última modificação: 19 de fevereiro de 2022

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Artigos de revistas sobre o assunto "Azo compounds Toxicology"

1

Sarah Mohammed Abed e Hasan Thamer Ghanem. "Synthesis and characterization Some of heterocyclic compounds from Nitrogen derivative". International Journal of Research in Pharmaceutical Sciences 10, n.º 4 (16 de outubro de 2019): 3186–96. http://dx.doi.org/10.26452/ijrps.v10i4.1621.

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This paper involves the synthesis of new oxazepine derivatives by multi-reaction steps. The first step synthesis azo derivative from 2-naphthol with 3-aminoacetophenone. The second step was the condensation reaction between ketone group of the azo compound and different primary aromatic amines (4-amino phenol, 3-nitro aniline and 4-methyl aniline) to yiled new azo Schiff base compounds (S1-S3) respectively. In the final step, Oxazepine compounds (L1-L3)and (L4-L6)were prepared from reaction imine compounds (S1-S3) with maleic and phthalic anhydride in toluene as solvent. All these derivatives were characterized by melting point, FTIR, HNMR and 13CNMR.

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Gadaleta, Domenico, Nicola Porta, Eleni Vrontaki, Serena Manganelli, Alberto Manganaro, Guido Sello, Masamitsu Honma e Emilio Benfenati. "Integrating computational methods to predict mutagenicity of aromatic azo compounds". Journal of Environmental Science and Health, Part C 35, n.º 4 (2 de outubro de 2017): 239–57. http://dx.doi.org/10.1080/10590501.2017.1391521.

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Tsuda, Shuji, Naonori Matsusaka, Hiroo Madarame, Shunji Ueno, Nobuyuki Susa, Kumiko Ishida, Noriko Kawamura, Kaoru Sekihashi e Yu F. Sasaki. "The comet assay in eight mouse organs: results with 24 azo compounds". Mutation Research/Genetic Toxicology and Environmental Mutagenesis 465, n.º 1-2 (fevereiro de 2000): 11–26. http://dx.doi.org/10.1016/s1383-5718(99)00199-0.

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4

Weber, Eric J., e N. Lee Wolfe. "Kinetic studies of the reduction of aromatic AZO compounds in anaerobic sediment/water systems". Environmental Toxicology and Chemistry 6, n.º 12 (dezembro de 1987): 911–19. http://dx.doi.org/10.1002/etc.5620061202.

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ELENA, PERDUM, MEDVEDOVICI ANDREI VALENTIN, TACHE FLORENTIN, VISILEANU EMILIA, DUMITRESCU IULIANA, MITRAN CORNELIA-ELENA, IORDACHE OVIDIU-GEORGE e RADULESCU ION RAZVAN. "Some validation aspects on the analytical method for assaying carcinogenic amines from textile dyes". Industria Textila 69, n.º 03 (1 de julho de 2018): 249–56. http://dx.doi.org/10.35530/it.069.03.1521.

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Chemicals safety control and ecological properties have become a priority for the textile industry in order to avoid the negative effects on humans and environment. The increasing interest for toxicology of textiles is determined by the presence of dangerous compounds in clothes generated from dyeing and finishing processes. In order to protect human health, European Regulations as Oeko Tex Standard 100 and REACH Regulation limit the presence of dangerous chemicals, such as aromatic amines, generated by reductive cleavage of azo dyes, by no more than 30 mg/kg of textile material. The main goal of this research work was to develop and validate a HPLC/MWD method for precise and reliable identification and quantification of carcinogenic aromatic amines derived from banned azo dye specific to the textile industry. The simultaneous determination of 24 regulated aromatic amines has been conducted by two chromatographic methods according to SR EN ISO 14362-1:2017 in order to avoid matrix interferences and compounds misidentification due to the presence of structural isomers. Preliminary analyses to establish the maximum absorption wavelength of each standard solution of aromatic amine were performed simultaneously at four wavelengths, 240, 280, 305 and 380 nm. With the scope of demonstrating the consistency, reliability and accuracy of the analysed data, both liquid and gas chromatographic method were validated. Parameters as selectivity, precision, limit of detection and limit of quantification of the analytical methods were evaluated. The certainty of the determinations was also proved by the results of proficiency testing conducted by IIS Netherlands on azo dyes in textiles.

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Shao, Jie, Nicholas E. Geacintov e Vladimir Shafirovich. "Oxidation of 8-Oxo-7,8-dihydro-2′-deoxyguanosine by Oxyl Radicals Produced by Photolysis of Azo Compounds". Chemical Research in Toxicology 23, n.º 5 (17 de maio de 2010): 933–38. http://dx.doi.org/10.1021/tx100022x.

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Rafii, F., e C. E. Cerniglia. "Reduction of azo dyes and nitroaromatic compounds by bacterial enzymes from the human intestinal tract." Environmental Health Perspectives 103, suppl 5 (junho de 1995): 17–19. http://dx.doi.org/10.1289/ehp.95103s417.

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Cox, Julie A., e Paul A. White. "The mutagenic activity of select azo compounds in MutaMouse target tissues in vivo and primary hepatocytes in vitro". Mutation Research/Genetic Toxicology and Environmental Mutagenesis 844 (agosto de 2019): 25–34. http://dx.doi.org/10.1016/j.mrgentox.2019.06.003.

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Li, Xue, e Yong-min Zhang. "Study on the reactions of azo compounds with acyl halides mediated by Sm/TiCl4". Journal of Zhejiang University SCIENCE B 7, n.º 3 (março de 2006): 198–201. http://dx.doi.org/10.1631/jzus.2006.b0198.

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Telke, Amar A., Dayanand C. Kalyani, Vishal V. Dawkar e Sanjay P. Govindwar. "Influence of organic and inorganic compounds on oxidoreductive decolorization of sulfonated azo dye C.I. Reactive Orange 16". Journal of Hazardous Materials 172, n.º 1 (dezembro de 2009): 298–309. http://dx.doi.org/10.1016/j.jhazmat.2009.07.008.

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Mais fontes

Livros sobre o assunto "Azo compounds Toxicology"

1

R, Cary, Dobson S, Ball Ellen M, World Health Organization, International Program on Chemical Safety. e Inter-Organization Programme for the Sound Management of Chemicals., eds. Azodicarbonamide. Geneva: World Health Organization, 1999.

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Capítulos de livros sobre o assunto "Azo compounds Toxicology"

1

de Almeida, Érica Janaina Rodrigues, Guilherme Dilarri e Carlos Renato Corso. "Evaluation of the Toxicity of Azo Dyes by Allium cepa and Study to Remove These Compounds in Aqueous Solution by Saccharomyces cerevisiae". In Methods in Pharmacology and Toxicology, 297–309. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7425-2_15.

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