| Weight | 234.342 g/mol |
|---|---|
| Formula | C18H18 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 1 |
RETENE (483-65-8)
7-isopropyl-1-methylphenanthrene
Score:
#19 in Environmental health
,
#194 in Environmental science
,
#4201 in Biology
,
#5298 in Chemistry
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- Retenea molecular marker of wood combustion in ambient air (Nature, 1983)
- Toxicity of retene to early life stages of two freshwater fish species (Environmental Toxicology and Chemistry, 1999)
- CYP1A INDUCTION AND BLUE SAC DISEASE IN EARLY DEVELOPMENTAL STAGES OF RAINBOW TROUT (ONCORHYNCHUS MYKISS) EXPOSED TO RETENE (Journal of Toxicology and Environmental Health, 2003)
- Chronic retene exposure causes sustained induction of CYP1A activity and protein in rainbow trout (Oncorhynchus mykiss) (Environmental Toxicology and Chemistry, 1998)
- AhR2-mediated, CYP1A-independent cardiovascular toxicity in zebrafish (Danio rerio) embryos exposed to retene. (Aquatic Toxicology, 2011)
- Occurrence of retene and resin acids in sediments and fish bile from a lake receiving pulp and paper mill effluents (Environmental Toxicology and Chemistry, 1999)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 7-isopropyl-1-methylphenanthrene
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SMILESCC1=CC=CC2=C1C=CC3=C2C=CC(=C3)C(C)C
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InChIKeyNXLOLUFNDSBYTP-UHFFFAOYSA-N
- Pubchem - RETENE
- Wikipedia - retene
Retene, methyl isopropyl phenanthrene or 1-methyl-7-isopropyl phenanthrene, C18H18, is a polycyclic aromatic hydrocarbon present in the coal tar fraction, boiling above 360 C. It occurs naturally in the tars obtained by the distillation of resinous woods. It crystallizes in large plates, which melt at 98.5 C and boil at 390 C.
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