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Chemical Compound Review

Musk xylene     1,3-dimethyl-2,4,6-trinitro- 5-tert-butyl...

Synonyms: Xylene musk, CHEMBL228513, CCRIS 2391, Musk xylol, HSDB 7692, ...
 
 
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Disease relevance of Musk xylene

 

High impact information on Musk xylene

 

Biological context of Musk xylene

 

Associations of Musk xylene with other chemical compounds

 

Analytical, diagnostic and therapeutic context of Musk xylene

  • Musk xylene (MX) (1,3,5-trinitro-2-t-butylxylene) is a nitromusk perfume ingredient that although uniformly negative in a battery of genotoxicity tests, produces a high incidence of liver tumors in mice [9].
  • 1. Musk xylene (1-tert-butyl-3,5-dimethyl-2,4,6-trinitrobenzene) is used as a fragrance component in toiletries, detergents and skin care products [10].
  • Musk xylene (MX; 1,3,5-trinitro-2-t-butylxylene), another nitromusk, is not genotoxic but has been reported to produce mouse liver tumors in a chronic bioassay [11].

References

  1. Musk xylene induces and inhibits mouse hepatic cytochrome P-450 2B enzymes. Lehman-McKeeman, L.D., Caudill, D., Young, J.A., Dierckman, T.A. Biochem. Biophys. Res. Commun. (1995) [Pubmed]
  2. Long-term toxicity/carcinogenicity of musk xylol in B6C3F1 mice. Maekawa, A., Matsushima, Y., Onodera, H., Shibutani, M., Ogasawara, H., Kodama, Y., Kurokawa, Y., Hayashi, Y. Food Chem. Toxicol. (1990) [Pubmed]
  3. An evaluation of musk xylene in a battery of genotoxicity tests. Api, A.M., Ford, R.A., San, R.H. Food Chem. Toxicol. (1995) [Pubmed]
  4. Musk xylene: analysis, occurrence, kinetics, and toxicology. Käfferlein, H.U., Göen, T., Angerer, J. Crit. Rev. Toxicol. (1998) [Pubmed]
  5. Nitro musks are cogenotoxicants by inducing toxifying enzymes in the rat. Mersch-Sundermann, V., Emig, M., Reinhardt, A. Mutat. Res. (1996) [Pubmed]
  6. Musk xylene is a novel specific inducer of cytochrome P-450IA2. Iwata, N., Minegishi, K., Suzuki, K., Ohno, Y., Kawanishi, T., Takahashi, A. Biochem. Biophys. Res. Commun. (1992) [Pubmed]
  7. Determination of musk ambrette, musk xylol, and musk ketone in fragrance products by capillary gas chromatography with electron capture detection. Wisneski, H.H. Journal of AOAC International. (2001) [Pubmed]
  8. In vitro percutaneous absorption of the fragrance ingredient musk xylol. Hood, H.L., Wickett, R.R., Bronaugh, R.L. Food Chem. Toxicol. (1996) [Pubmed]
  9. Induction and inhibition of mouse cytochrome P-450 2B enzymes by musk xylene. Lehman-McKeeman, L.D., Johnson, D.R., Caudill, D. Toxicol. Appl. Pharmacol. (1997) [Pubmed]
  10. Haemoglobin binding of a musk xylene metabolite in man. Riedel, J., Birner, G., van Dorp, C., Neumann, H.G., Dekant, W. Xenobiotica (1999) [Pubmed]
  11. Characterization of the effects of musk ketone on mouse hepatic cytochrome P450 enzymes. Stuard, S.B., Caudill, D., Lehman-McKeeman, L.D. Fundamental and applied toxicology : official journal of the Society of Toxicology. (1997) [Pubmed]
 
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