auraptenol

8-(2-hydroxy-3-methyl-3-butenyl)-7-methoxycoumarin

CAS: 1221-43-8 C15 H16 O4 MW: 260.28932000

Identification

Nameauraptenol
IUPAC8-(2-hydroxy-3-methyl-3-buten-1-yl)-7-methoxy-2H-chromen-2-one
CAS Number1221-43-8
FDA UNIISearch
Molecular FormulaC15 H16 O4
Molecular Weight260.28932000
Nikkaji NumberJ14.363D

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 ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for auraptenol usage levels up tonot for fragrance use.
Recommendation for auraptenol flavor usage levels up tonot for flavor use.

BOC Sciences

Best of Chemicals Supplier

Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecul...

View All Website 1-631-485-4226 account@bocsci.com

Potential Uses

None Found

Natural Occurrence

citrus aurantium ssp. amara oil orange pericarp

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.