
CAS 158776-07-9
:Formule :C24H14
InChI :InChI=1S/C24H14/c1-3-7-19-15(5-1)13-17-9-10-18-14-16-6-2-4-8-20(16)22-12-11-21(19)23(17)24(18)22/h1-14H/i1D,2D,3D,4D,5D,6D,7D,8D,9D,10D,11D,12D,13D,14D
Code InChI :TUGYIJVAYAHHHM-WZAAGXFHSA-N
SMILES :[2H]C1=C(C(=C2C3=C4C(=C(C2=C1[2H])[2H])C(=C(C5=C(C6=C(C(=C(C(=C6C(=C54)C(=C3[2H])[2H])[2H])[2H])[2H])[2H])[2H])[2H])[2H])[2H])[2H]
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3 produits trouvés.
Dibenzo[a,i]pyrene-d14
CAS :Degré de pureté :98 atom % DCouleur et forme :Yellow SolidMasse moléculaire :316.46Deuterated PAH Mixture 918 200 µg/mL in Dichloromethane
CAS :Produit contrôléFormule :C12H10Couleur et forme :MixtureMasse moléculaire :164.27Dibenzo[a,i]pyrene-d14
CAS :Produit contrôléApplications Labelled analogue of Dibenzo[a,i]pyrene, a polycyclic aromatic hydrocarbon (PAH) with potent carcinogenic activity. Dibenzo[a,i]pyrene was shown to induce DNA adduction, tumorigenicity as well as Ki-ras oncogene mutations in strain A/J mouse lung. Dibenzo[a,i]pyrene has been shown to be present in cigarette smoke condensate and in automobile exhaust gas in small quantities.
References Prahalad, A.K. et al.: Carcinogenesis, 18, 1955 (1997); Wynder, E.L. et al.: Nature, 192, 1092 (1961); Homburger, F. et al.: J. Nat. Cancer Inst., 44, 357 (1970);Formule :C24D14Couleur et forme :NeatMasse moléculaire :316.45



