• 1-Naphthol is used in each of the following chemical tests: Molisch's test gives a red- or purple-colored compound to indicate the presence of carbohydrate. (wikipedia.org)
  • Finding wide usage in textile, plastic, chemical and pharmaceutical industry, these when dyeing with naphthols offer economical usage. (sdinternational.com)
  • 1-Naphthol, or α-naphthol, is a fluorescent organic compound with the formula C10H7OH. (wikipedia.org)
  • Human udp-glucuronosyltransferases: isoform selectivity and kinetics of 4-methylumbelliferone and 1-naphthol glucuronidation, effects of organic solvents, and inhibition by diclofenac and probenecid. (chemchart.com)
  • It is an isomer of 2-naphthol differing by the location of the hydroxyl group on the naphthalene ring. (wikipedia.org)
  • The naphthols are naphthalene homologues of phenol, with the hydroxyl group being more reactive than in the phenols. (wikipedia.org)
  • In one method, naphthalene is nitrated to give 1-nitronaphthalene, which is hydrogenated to the amine followed by hydrolysis: C10H8 + HNO3 → C10H7NO2 + H2O C10H7NO2 + 3H2 → C10H7NH2 + 2H2O C10H7NH2 + H2O → C10H7OH + NH3 Alternatively, naphthalene is hydrogenated to tetralin, which is oxidized to 1-tetralone, which undergoes dehydrogenation. (wikipedia.org)
  • 1-Naphthol is a metabolite of the insecticide carbaryl and naphthalene. (wikipedia.org)
  • Sorption of naphthalene and 1-naphthol by biochars of orange peels with different pyrolytic temperatures. (chemchart.com)
  • 1-Naphthol biodegrades via formation of 1-naphthol-3,4-oxide, which converts to 1,4-naphthoquinone. (wikipedia.org)
  • Degradation of phenanthrene by different bacteria: evidence for novel transformation sequences involving the formation of 1-naphthol. (chemchart.com)