
Polycyclic Aromatic Hydrocarbons (PAHs)
Found 294 products of "Polycyclic Aromatic Hydrocarbons (PAHs)"
9,10-Bis(bromomethyl)anthracene
CAS:Controlled ProductStability 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)Formula:C16H12Br2Color and Shape:NeatMolecular weight:364.073-Methoxy Benzopyrene
CAS:Controlled ProductApplications 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)Formula:C21H14OColor and Shape:NeatMolecular weight:282.343,5-Dichloroacenaphthene
CAS:Controlled ProductApplications 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)Formula:C12H8Cl2Color and Shape:NeatMolecular weight:223.13,5,6-Tribromo-1,2-dihydroacenaphthylene
CAS:Controlled ProductApplications 3,5,6-Tribromo-1,2-dihydroacenaphthylene is 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)Formula:C12H7Br3Color and Shape:NeatMolecular weight:390.93,6-Dichloroacenaphthene
CAS:Controlled ProductApplications 3,6-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)Formula:C12H8Cl2Color and Shape:NeatMolecular weight:223.18,9,10,11-Tetrahydrodibenz(a,h)acridine
CAS:Controlled ProductStability 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)Formula:C21H17NColor and Shape:NeatMolecular weight:283.373-Vinylphenol
CAS:Controlled ProductStability Light Sensitive
Applications An oxidative metabolite of Styrene (S687790).
References Linhart, I. et al.: Chem. Res. Toxicol., 1, 251 (2010); Shen, S. et al.: Drug Metab. Disp., 38, 1934 (2010); Watabe, T. et al: Mutat. Res., 93, 45 (1982);Formula:C8H8OColor and Shape:NeatMolecular weight:120.151,2,3,4-Tetrahydronaphthalene
CAS:Controlled ProductFormula:C10H12Color and Shape:NeatMolecular weight:132.207H-Benzo[c]fluorene 10 µg/mL in Cyclohexane
CAS:Formula:C17H12Color and Shape:Single SolutionMolecular weight:216.28Isoviolanthrone
CAS:Formula:C34H16O2Color and Shape:Gray to Dark purple to Black powder to crystalMolecular weight:456.50



