suberenol

2H-1-benzopyran-2-one, 6-(3-hydroxy-3-methyl-1-butenyl)-7-methoxy-, (E)-

CAS: 18529-47-0 C15 H16 O4 MW: 260.28932000

Identification

Namesuberenol
IUPAC6-[(E)-3-hydroxy-3-methylbut-1-enyl]-7-methoxychromen-2-one
CAS Number18529-47-0
FDA UNIISearch
Molecular FormulaC15 H16 O4
Molecular Weight260.28932000
Nikkaji NumberJ103.428F

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 466.89 °C. @ 760.00 mm Hg (est)
Flash Point 350.00 °F. TCC ( 176.70 °C. ) (est)
logP (o/w) 2.042 (est)
Soluble in water, 707.9 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 suberenol usage levels up tonot for fragrance use.
Recommendation for suberenol flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

citrus nobilis orange root bark wood-apple

Synonyms

2H-1- benzopyran-2-one, 6-(3-hydroxy-3-methyl-1-butenyl)-7-methoxy-, (E)- coumarin, 6-(3-hydroxy-3-methyl-1-butenyl)-7-methoxy-, (E)- (E)-6-(3- hydroxy-3-methyl-1-butenyl)-7-methoxy-2H-1-benzopyran-2-one 6-[(E)-3- hydroxy-3-methylbut-1-enyl]-7-methoxychromen-2-one (E)- suberenol trans- suberenol PubMed: Anticoagulant activity of isolated coumarins (suberosin and suberenol) and toxicity evaluation of Ferulago carduchorum in rats. PubMed: [Chemical studies on roots of Ficus hirta]. PubMed: Alkaloids and Coumarins from the Leaves of Amyris diatripa.