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BENZO(J)FLUORANTHENE

BENZO(J)FLUORANTHENE Basic information
Product Name:BENZO(J)FLUORANTHENE
Synonyms:Benzo[j]fluoranthene (purity);Benzo(J)fluoranthene [polycyclic aromatic compounds];Benzo(J)fluoranthene [polycyclic aromatic hydrocarbons];Benzo(j)fluoranthene 10mg [205-82-3];10,11-benzfluoranthene;10,11-benzofluoranthene;7,8-Benzofluoranthene;B(j)F
CAS:205-82-3
MF:C20H12
MW:252.31
EINECS:205-910-3
Product Categories:Benzo(a)pyrene and other PAH;A-BAlphabetic;Alpha Sort;B;BA - BHEnvironmental Standards;PAHs;Volatiles/ Semivolatiles
Mol File:205-82-3.mol
BENZO(J)FLUORANTHENE Structure
BENZO(J)FLUORANTHENE Chemical Properties
Melting point 166°C
Boiling point 330.49°C (rough estimate)
density 1.1549 (estimate)
refractive index 1.8390 (estimate)
storage temp. 2-8°C
solubility Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form Solid
color White
Water Solubility 2.5ug/L(temperature not stated)
Stability:Stable. Incompatible with strong oxidizing agents. Combustible.
IARC2B (Vol. 92) 2010
EPA Substance Registry SystemBenzo[j]fluoranthene (205-82-3)
Safety Information
Hazard Codes T,N
Risk Statements 45-50/53-63-43-36/37/38-23/24/25-67-52/53
Safety Statements 45-53-61-60-36/37-24/25-23-26
RIDADR 3077
WGK Germany 3
HazardClass 6.1(b)
PackingGroup III
Hazardous Substances Data205-82-3(Hazardous Substances Data)
MSDS Information
BENZO(J)FLUORANTHENE Usage And Synthesis
Chemical Propertiessolid
UsesBenzo[j]fluoranthene is a polycyclic aromatic hydrocarbon that has tumour initiating activity and can be found in soot, oil, water and soil extracts as a common pollutant.
DefinitionChEBI: Benzo[j]fluoranthene is a member of naphthalenes.
General DescriptionYellow crystals. Insoluble in water.
Air & Water ReactionsDust/air mixture may ignite and explode. Insoluble in water.
Reactivity ProfileVigorous reactions, sometimes amounting to explosions, can result from the contact between aromatic hydrocarbons, such as BENZO(J)FLUORANTHENE, and strong oxidizing agents. They can react exothermically with bases and with diazo compounds. Substitution at the benzene nucleus occurs by halogenation (acid catalyst), nitration, sulfonation, and the Friedel-Crafts reaction.
Health HazardBenzo[j]fluoranthene is a cancer suspectagent. Animal studies present sufficient evidence on its carcinogenicity. It may causetumor in lungs and skin.
CarcinogenicityBenzo[j]fluoranthene was tested for carcinogenicity by dermal application in mice in four studies, by intraperitoneal injection into newborn mice in two studies and by intrapulmonary implantation into rats in one study. With the exception of one study on newborn female mice, benzo[j] fluoranthene exhibited a significant carcinogenic activity in all of the assays.
BENZO(J)FLUORANTHENE Preparation Products And Raw materials
2.3,7.8-DI-(PERI-NAPHTHYLENE)-PYRENE BENZO(K)FLUORANTHENE SOLUTION IN METHANOL 100UG/ML IN METHANOL 5ML BENZO(J)FLUORANTHENE SOLUTION 100UG/ML IN METHANOL 5ML 4-fluorobenzo(j)fluoranthene 2-PHENYLBENZO[J]FLUORANTHENE BENZO(K)FLUORANTHENE (13C6) SOLUTION 100UG/ML IN N-NONANE 1.2ML 1.2,3.4,5.6,7.8-TETRA(PERI-NAPHTHYLENE)ANTHRACENE BENZO(K)FLUORANTHENE (D12) SOLUTION 200UG/ML IN ISOOCTANE 1.2ML BENZO(A)FLUORANTHENE,56549, Benzo[a]fluoranthene (purity) BENZO(K)FLUORANTHENE SOLUTION 100UG/ML IN METHANOL 1ML BENZO(B)FLUORANTHENE (D12) IN 0.01G [R] NAPHTHO[2,3-J]FLUORANTHENE BENZO(B)FLUORANTHENE (D12) SOLUTION 200UG/ML IN ISOOCTANE 1.2ML BENZO(J)FLUORANTHENE DIBENZO[J,L]FLUORANTHENE 10-fluorobenzo(j)fluoranthene 5-PHENYLBENZO[J]FLUORANTHENE BENZO(B)FLUORANTHENE (13C6)
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