ChemicalBook Product Catalog Analytical Chemistry Standard Volatile organic compounds (VOCs) BENZO(C)PHENANTHRENE

BENZO(C)PHENANTHRENE

BENZO(C)PHENANTHRENE Basic information
Product Name:BENZO(C)PHENANTHRENE
Synonyms:BENZO(C)PHENANTHRENE;Benzo[c]phenanthrene (purity);60624, Benzo[c]phenanthrene (purity);3,4-Benzo[c]phenanthrene;3,4-Benzo[c]phenthrene;AR-G 3 BENZO(C)PHENANTHRENE;3,4-Benzophenanthrene;3,4-Benzphenanthrene
CAS:195-19-7
MF:C18H12
MW:228.29
EINECS:205-896-9
Product Categories:Aromatics;Intermediates & Fine Chemicals;Alphabetic;B;Mutagenesis Research Chemicals;Pharmaceuticals;BA - BH
Mol File:195-19-7.mol
BENZO(C)PHENANTHRENE Structure
BENZO(C)PHENANTHRENE Chemical Properties
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)
form neat
color Needles from EtOH or pet ether
BRN 1909296
Stability:Light Sensitive
InChIKeyTUAHORSUHVUKBD-UHFFFAOYSA-N
IARC2B (Vol. 92, Sup 7) 2010
EPA Substance Registry SystemBenzo[c]phenanthrene (195-19-7)
Safety Information
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
Toxicitymma-sat 25 nmol/plate CNREA8 40,2876,80
MSDS Information
BENZO(C)PHENANTHRENE Usage And Synthesis
Chemical PropertiesYellow Solid
UsesA 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.
DefinitionChEBI: An ortho-fused polycyclic arene resulting from the symmetrical fusion of the C1-C2 bonds of two naphthalene units.
Safety ProfileQuestionable carcinogen withexperimental tumorigenic data. Mutation data reported.When heated to decomposition it emits acrid and irritatingfumes.
CarcinogenicityDermal 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 MethodsCrystallise 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 materialsBENZO(B)CHRYSENE-->BENZO(G,H,I)FLUORANTHENE-->1-METHYLANTHRACENE
Preparation ProductsCYCLOPENTA(C,D)PYRENE-->Phenanthrene
BENZO(G,H,I)PERYLENE D12 Fullerene C60 Hypericin 1,12-BENZOPERYLENE (13C12) OVALENE 1,12-BENZOPERYLENE CORONENE (D12) PYRANTHRENE BENZO(C)PHENANTHRENE protohypericin 1.12,2.3,4.5,6.7,8.9,10.11-HEXABENZOCORONENE NAPHTHO[1,2,3,4-GHI]PERYLENE (5)HELICENE BENZO[G]CHRYSENE 3-METHYLPHENANTHRO[3,4-C]PHENANTHRENE (6)HELICENE BENZO[A]CORONENE DIBENZO[A,G]CORONENE
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