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BENZO(C)PHENANTHRENE

BENZO(C)PHENANTHRENE Structure
BENZO(C)PHENANTHRENE
  • CAS No.195-19-7
  • Chemical Name:BENZO(C)PHENANTHRENE
  • CBNumber:CB6484398
  • Molecular Formula:C18H12
  • Formula Weight:228.29
  • MOL File:195-19-7.mol
BENZO(C)PHENANTHRENE Property
  • Melting point 158-160℃
  • Boiling point 305.1°C (rough estimate)
  • Density 1.1209 (estimate)
  • refractive index 1.5500 (estimate)
  • storage temp. Sealed in dry,2-8°C
  • solubility Acetonitrile (Slightly), Chloroform (Slightly)
  • color Needles from EtOH or pet ether
  • BRN 1909296
  • Stability Light Sensitive
  • InChIKey TUAHORSUHVUKBD-UHFFFAOYSA-N
  • EWG's Food Scores 2
  • FDA UNII H22XVR3V8A
  • IARC 2B (Vol. 92, Sup 7) 2010
  • EPA Substance Registry System Benzo[c]phenanthrene (195-19-7)
Safety
  • Hazard Codes  :Xn
  • Risk Statements  :20/21/22-36/37/38
  • Safety Statements  :26-37/39
  • RIDADR  :2811
  • WGK Germany  :3
  • RTECS  :DI8225000
  • HazardClass  :6.1(b)
  • PackingGroup  :III
  • Toxicity :mma-sat 25 nmol/plate CNREA8 40,2876,80
Hazard and Precautionary Statements (GHS)
  • Symbol(GHS)
  • Signal wordWarning
  • Hazard statements H302-H312-H315-H319-H332-H335
  • Precautionary statements P261-P280-P305+P351+P338

BENZO(C)PHENANTHRENE Chemical Properties,Usage,Production

  • Chemical Properties Yellow Solid
  • Uses A PAH metabolite having a toxic effect on fish bone metabolite. Also, it is used as a marker of the carcinogenic potency of the polycyclic aromatic hydrocarbons (PAH) mixture. A genotoxic agent.
  • Definition ChEBI: An ortho-fused polycyclic arene resulting from the symmetrical fusion of the C1-C2 bonds of two naphthalene units.
  • Safety Profile Questionable carcinogen withexperimental tumorigenic data. Mutation data reported.When heated to decomposition it emits acrid and irritatingfumes.
  • Carcinogenicity Dermal administration (initiation– promotion protocols) to mice showed benzo[c]phenanthrene was a tumor-initiating agent. Repeated dermal administration in mice or subcutaneous injection into mice or rats gave results considered to be inadequate for evaluation (3). Intraperitoneal injection of benzo[c]phenanthrene into infant mice resulted in a substantial induction of lung tumors. Seven suspected activated metabolites were also active, as well as in two-stage mouse carcinogenesis assays.
  • Purification Methods Crystallise benzo[c]phenanthrene from EtOH, pet ether, or EtOH/Me2CO. [Beilstein 5 III 2378, 5 IV 2552.]
BENZO(C)PHENANTHRENE Preparation Products And Raw materials
Raw materials
Preparation Products
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  • 195-19-7
  • Benzo(c)phenanthrene in Acetonitrile
  • Benzo(c)phenanthrene in Cyclohexane
  • L20631500CY Benzo[c]phenanthrenE10μg/mLin Cy
  • C20631500 Benzo[c]phenanthrene
  • Zavegepant Impurity 6
  • Benzo(c)phenanthrene@50 μg/mL in Toluene
  • Tetrahelicene
  • Benzo-3,4-phenanthrene
  • 3,4-Benzphenanthrene
  • 3,4-Benzophenanthrene
  • AR-G 3 BENZO(C)PHENANTHRENE
  • 3,4-Benzo[c]phenthrene
  • 3,4-Benzo[c]phenanthrene
  • 60624, Benzo[c]phenanthrene (purity)
  • Benzo[c]phenanthrene (purity)
  • BENZO(C)PHENANTHRENE

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