| Weight | 202.256 g/mol |
|---|---|
| Formula | C16H10 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 4 |
| Rotatable Bonds | 0 |
PYRENE (129-00-0)
Score:
#139 in Physics
,
#385 in Biology
,
#403 in Chemistry
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- Environmental effects on vibronic band intensities in pyrene monomer fluorescence and their application in studies of micellar systems (Journal of the American Chemical Society, 1977)
- Preferential Formation of Benzo[a]pyrene Adducts at Lung Cancer Mutational Hotspots in P53 (Science, 1996)
- Benzo[alpha]pyrene metabolism, activation and carcinogenesis: role and regulation of mixed-function oxidases and related enzymes. (Physiological Reviews, 1980)
- Metabolic activation of benzo(a)pyrene proceeds by a diol-epoxide. (Nature, 1974)
- Bioremediation of high molecular weight polycyclic aromatic hydrocarbons: a review of the microbial degradation of benzo[a]pyrene (International Biodeterioration & Biodegradation, 2000)
- Pyrene-Based Materials for Organic Electronics (Chemical Reviews, 2011)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C3C(=C1)C=CC4=CC=CC(=C43)C=C2
-
InChIKeyBBEAQIROQSPTKN-UHFFFAOYSA-N
- Pubchem - PYRENE
- Wikipedia - pyrene
Pyrene is a polycyclic aromatic hydrocarbon (PAH) consisting of four fused benzene rings, resulting in a flat aromatic system. The chemical formula is C 16H 10. This colorless solid is the smallest peri-fused PAH (one where the rings are fused through more than one face).
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Estimated Properties
| Boiling Point | 408.64 C | EPA T.E.S.T. |
|---|---|---|
| Density | 1.24 g/cm3 | EPA T.E.S.T. |
| Flash Point | 180.35 C | EPA T.E.S.T. |
| Water Solubility | 0.0306 mg/L | EPA T.E.S.T. |
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PYRENE
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