Polycyclic Aromatic Hydrocarbon (PAHs) Standards

Applications 1-Acenaphthenol is a product of the microbial metabolism and photolysis of acenaphthene, of acenaphthene, a polycyclic hydrocarbon that has potential to act as polyploidizing agents in plants. 1-Acenaphthenol is also a known substrate of dihydrodiol dehydrogenases.
References Reyes, C., et al.: J. Photochem. Photobiol. A, 112, 277 (1998); Šavlík, M., et al.: Res. Vet. Sci., 83, 20 (2007); Schocken, M. & Gibson, D.: Appl. Environ. Microb., 48, 10 (1984);

Applications 2,7-Dibromophenanthrene is a halogenated phenanthrene (P294800), a polycyclic aromatic hydrocarbons and environmental pollutant.
References Brown, W.G.,et al.: J. Am. Chem, Soc., 65, 1235 (1943); He, B.,et al.: J. Mat. Chem., 21, 14793 (2011);

Applications A mutagenic aromatic nitro compound.
References Kier, L., et al.: Pharmacol. Res., 7, 801 (1990), Benigni, R., et al.: J. Med. Chem., 38, 629 (1995), Benigni, R., et al.: Mutat. Res., 371, 29 (1996),

Applications 3,11-Dimethylchrysene is a derivative of Chrysene (C428000), both being part of a group of polycyclic aromatic compounds suspected to have tumour-initiating effects on humans.
References Schuetzle, D. & Daisey, J.: Genetic Toxicology of Complex Mixtures, No vol. given, 11 (1990); Shaw, G., et al.: Rev. Environ. Contam. T., No vol. given, 1 (1994)

Applications 3-Chloroacenaphthene is a chloro derivative of Acenaphthene (D448330); a polycyclic aromatic hydrocarbon serving as a carcinogenic agent.
References Hansen, B., et al.: Environ. Toxicol. Chem., 18, 772 (1999); Czub, G., et al.: Environ. Sci. Technol., 38, 2406 (2004)

Applications 3,​5,​6,​8-​Tetrabromo-​1,​2-​dihydro-acenaphthylene is a byproduct during the synthesis of 3,​5,​6-​Tribromo-​1,​2-​dihydroacenaphthylene (T771875), a derived from Acenaphthene (1,2-Dihydro Acenaphthylene) (D448330), which is a polycyclic aromatic hydrocarbons as carcinogenic agents.
References Hansen, B., et al.: Environ. Toxicol. Chem., 18, 772 (1999); Czub, G., et al.: Environ. Sci. Technol., 38, 2406 (2004)

Applications 1-Pyrenol Acetate is an intermediate in the synthesis of 8-Nitro-1-pyrenol-d8 (N519992), which is an urinary hydroxylated metabolites used as a biomarkers of exposure of polycyclic aromatic hydrocarbons. This is the labeled analog.
References Toriba, A., et al.: J. Health. Sci., 53; 631 (2007); Chae, Y.H., et al.: Cancer Res., 59, 1473 (1999); Sangaiah, R., et al.: Poly. Aro. Comp., 11, 283 (1996);

Stability Hygroscopic
Applications 9,10-Bis(bromomethyl)anthracene shows high antitumor activity against Ehrlich ascites tumor in mice.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Peck, R. M., et al.: J. Med. Chem., 15, 68 (1972)

Stability Light Sensitive
Applications Benz[l]aceanthrylene is a mutagenic agent.
References Bartczak, A., et al.: Mutagenesis, 2, 101 (1987); Nesnow, S., et al.: Cancer Res., 44, 4993 (1984)

Applications 3,5-Dichloroacenaphthene is a chlorinated derivative of Acenaphthene (D448330); a polycyclic hydrocarbon that has potential to act as polyploidizing agents in plants.
References Campbell, K., et al.: J. Org. Chem., 16, 1712 (1951); Reisen, F. & Arey J.: Env. Sci. Tech., 36, 4302 (2002)

Stability Store in Freezer
Applications This compound is an interesting intermediate in the synthesiis of the epoxy-diol derivtives of dibenz(a,h)acridine (Catalogue number D41690) which is the proximate or ultimate carcinogen.
References S. Kumar: JOC, 50, 3070-3073 (1985)

Applications Metabolite of 3,4-Benzopyrene. Carcinogenic.
References Peacock, P. R. et al.; Brit. J. Cancer 6, 407 (1952); Cook, J. W. et al.; Brit. J. Cancer 6, 400 (1952)