Weight | 178.234 g/mol |
---|---|
Formula | C14H10 |
Hydrogen Acceptors | 0 |
Hydrogen Donors | 0 |
Aromatic Rings | 3 |
Rotatable Bonds | 0 |
Phenanthrene
85-01-8, 65996-93-2, 50-32-8
Score:
#52 in Environmental science
,
#313 in Biology
,
#329 in Chemistry
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- Polarization of the Luminescence of Phenanthrene (Journal of Chemical Physics, 1962)
- The ratios of dibenzothiophene to phenanthrene and pristane to phytane as indicators of depositional environment and lithology of petroleum source rocks (Geochimica et Cosmochimica Acta, 1995)
- Synthetic oestrogenic agents without the phenanthrene nucleus (Nature, 1936)
- Plant uptake, accumulation and translocation of phenanthrene and pyrene in soils (Chemosphere, 2004)
- Degradation of phenanthrene, fluorene, fluoranthene, and pyrene by a Mycobacterium sp (Applied and Environmental Microbiology, 1993)
- Carboxylation as an Initial Reaction in the Anaerobic Metabolism of Naphthalene and Phenanthrene by Sulfidogenic Consortia (Applied and Environmental Microbiology, 1997)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H400: Very toxic to aquatic life
Warning Hazardous to the aquatic environment, acute hazard - Category 1 -
SMILESC1=CC=C2C(=C1)C=CC3=CC=CC=C32
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- Pubchem - Phenanthrene
- Wikipedia - phenanthrene
Phenanthrene is a polycyclic aromatic hydrocarbon composed of three fused benzene rings. The name 'phenanthrene' is a composite of phenyl and anthracene. In its pure form, it is found in cigarette smoke and is a known irritant, photosensitizing skin to light.
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Alternate Names
Estimated Properties
Boiling Point | 332.23 C | EPA T.E.S.T. |
---|---|---|
Density | 1.12 g/cm3 | EPA T.E.S.T. |
Flash Point | 147.41 C | EPA T.E.S.T. |
Water Solubility | 0.57 mg/L | EPA T.E.S.T. |
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