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| | 7,8,9,10-TETRAHYDRO-BENZO[A]PYREN-7-OL Basic information |
| Product Name: | 7,8,9,10-TETRAHYDRO-BENZO[A]PYREN-7-OL | | Synonyms: | 7,8,9,10-TETRAHYDRO-BENZO[DEF]CHRYSEN-7-OL;7,8,9,10-tetrahydro-benzo(a)pyren-7-o;7-Hydroxy-7,8,9,10-tetrahydrobenzo[a]pyrene;7,8,9,10-TETRAHYDROBENZO(A)PYREN-7-OL, 9 9%;Benzo[a]pyren-7-ol, 7,8,9,10-tetrahydro-;7,8,9,10-Tetrahydrobenzo[pqr]tetraphen-7-ol | | CAS: | 6272-55-5 | | MF: | C20H16O | | MW: | 272.34 | | EINECS: | | | Product Categories: | Alcohols;C9 to C30;Oxygen Compounds;Building Blocks;C11 to C30+;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds | | Mol File: | 6272-55-5.mol | ![7,8,9,10-TETRAHYDRO-BENZO[A]PYREN-7-OL Structure](CAS/GIF/6272-55-5.gif) |
| | 7,8,9,10-TETRAHYDRO-BENZO[A]PYREN-7-OL Chemical Properties |
| Melting point | 142-144 °C(lit.) | | Boiling point | 508.5±19.0 °C(Predicted) | | density | 1.323±0.06 g/cm3(Predicted) | | storage temp. | 2-8°C | | solubility | DMF: 30 mg/ml; DMSO: 30 mg/ml; Ethanol: 0.2 mg/ml | | form | A crystalline solid | | pka | 14.36±0.20(Predicted) |
| WGK Germany | 3 | | RTECS | DJ8304000 |
| | 7,8,9,10-TETRAHYDRO-BENZO[A]PYREN-7-OL Usage And Synthesis |
| Description | 7,8,9,10-Tetrahydrobenzo[a]pyren-7-ol is a benzopyrene derivative that is activated by hepatic cytosol into electrophilic sulfuric acid esters, which are capable of forming covalent DNA adducts and inducing mutations. | | Chemical Properties | Yellow Solid | | Uses | 7,8,9,10-Tetrahydrobenzo[a]pyren-7-ol is a benzopyrene derivative that is activated by hepatic cytosol into electrophilic sulfuric acid esters, which are capable of forming covalent DNA adducts and inducing mutations.[Cayman Chemical] | | Uses | 7,8,9,10-Tetrahydro-benzo[a]pyren-7-ol is a Benzopyrene (B205800) derivative, activated by hepatic cytosol. | | General Description | 7,8,9,10-Tetrahydrobenzo[a]pyren-7-ol (7-hydroxy-7,8,9,10-tetrahydrobenzo[a]pyrene), a polycyclic aromatic hydrocarbon (PAH), is a substituted benzopyrene. Its bromination reaction with N-bromosaccharin (NBSac) has been investigated. The sulfotransferase-assisted activation of 7-hydroxy-7,8,9,10-tetrahydrobenzo[a]pyrene to form electrophilic, mutagenic, or tumorigenic sulfuric acid ester metabolite, which binds covalently to DNA and leads to mutation, has been reported. |
| | 7,8,9,10-TETRAHYDRO-BENZO[A]PYREN-7-OL Preparation Products And Raw materials |
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