auraptenol
8-(2-hydroxy-3-methyl-3-butenyl)-7-methoxycoumarin
Identification
| Name | auraptenol |
| IUPAC | 8-(2-hydroxy-3-methyl-3-buten-1-yl)-7-methoxy-2H-chromen-2-one |
| CAS Number | 1221-43-8 |
| FDA UNII | Search |
| Molecular Formula | C15 H16 O4 |
| Molecular Weight | 260.28932000 |
| Nikkaji Number | J14.363D |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 446.73 °C. @ 760.00 mm Hg (est) |
| Flash Point | 334.00 °F. TCC ( 168.00 °C. ) (est) |
| logP (o/w) | 2.235 (est) |
| Soluble in | water, 504.3 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | natural substances and extractives |
| Recommendation for auraptenol usage levels up to | not for fragrance use. |
| Recommendation for auraptenol flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
8-(2-
hydroxy-3-methyl-3-butenyl)-7-methoxycoumarin
8-(2-
hydroxy-3-methyl-3-buten-1-yl)-7-methoxy-2H-chromen-2-one
PubMed:
Auraptenol attenuates vincristine-induced mechanical hyperalgesia through serotonin 5-HT1A receptors.
PubMed:
Antidepressant-like effects of auraptenol in mice.
PubMed:
Coumarins from the Herb Cnidium monnieri and chemically modified derivatives as antifoulants against Balanus albicostatus and Bugula neritina larvae.
PubMed:
[Coumarins from Leonurus japonicus and their anti-platelet aggregative activity].
PubMed:
Antifibrotic activity of coumarins from Cnidium monnieri fruits in HSC-T6 hepatic stellate cells.
PubMed:
Nonvolatiles of commercial lime and grapefruit oils separated by high-speed countercurrent chromatography.