lactarorufin A

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azuleno(5,6-c)furan-1(3H)-one, 4,4a,5,6,7,7a,8,9-octahydro-4,8-dihydroxy-6,6,8-trimethyl-, (4S-(4alpha,4aalpha,7aalpha,8alpha))-

CAS: 35008-20-9 C15 H22 O4 MW: 266.33714000
All Ingredients Aromatic Ingredients CAS Numbers Found in Nature

Identification

Namelactarorufin A
IUPAC(5R,5aS,8aR,9S)-5,9-dihydroxy-5,7,7-trimethyl-4,5a,6,8,8a,9-hexahydro-1H-azuleno[5,6-c]furan-3-one
CAS Number35008-20-9
FDA UNIISearch
Molecular FormulaC15 H22 O4
Molecular Weight266.33714000

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 472.61 °C. @ 760.00 mm Hg (est)
Flash Point 352.00 °F. TCC ( 177.50 °C. ) (est)
logP (o/w) 1.270 (est)
Soluble in water, 1084 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 lactarorufin A usage levels up tonot for fragrance use.
Recommendation for lactarorufin A flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

mushrooms PMC

Synonyms

azuleno(5,6-c)furan-1(3H)-one, 4,4a,5,6,7,7a,8,9-octahydro-4,8-dihydroxy-6,6,8-trimethyl-, (4S-(4alpha,4aalpha,7aalpha,8alpha))- (5R,5aS,8aR,9S)-5,9- dihydroxy-5,7,7-trimethyl-4,5a,6,8,8a,9-hexahydro-1H-azuleno[5,6-c]furan-3-one (4S-(4alpha,4aalpha,7aalpha,8alpha))-4,4a,5,6,7,7a,8,9- octahydro-4,8-dihydroxy-6,6,8-trimethyl azuleno(5,6-c)furan-1(3H)-one PubMed: Clavicorolides A and B, sesquiterpenoids from the fermentation products of edible fungus Clavicorona pyxidata. PubMed: [Chemical constituents study on the fruiting bodies of Lactarius rufus]. PubMed: 1,2-Dehydrolactarolide A, a new plant growth regulatory lactarane sesquiterpene from Lactarius vellereus. PubMed: [Influence of newly synthesized sesquiterpenes--analogs of taxol on multiplication of herpes simplex virus (HSV-1MC) and retrovirus (Mo-MSV)].