bilobol

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21:1-.omega.7-cardol

CAS: 22910-86-7 C21 H34 O2 MW: 318.50038000
All Ingredients Aromatic Ingredients CAS Numbers Found in Nature

Identification

Namebilobol
CAS Number22910-86-7
FDA UNIISearch
Molecular FormulaC21 H34 O2
Molecular Weight318.50038000
MDL NumberMFCD27968631
Nikkaji NumberJ167.340H

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Soluble in water, 0.003336 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Preferred SDSView
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 bilobol usage levels up tonot for fragrance use.
Recommendation for bilobol flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

ginkgo biloba fruit

Synonyms

1,3- benzenediol, 5-(8-pentadecenyl)-, (Z)- 21:1-.omega.7- cardol 5-[(Z)- pentadec-8-enyl]benzene-1,3-diol 5-(8- pentadecenyl)-1,3-benzenediol PubMed: Bilobol inhibits the lipopolysaccharide-induced expression and distribution of RhoA in HepG2 human hepatocellular carcinoma cells. PubMed: [Chronotropic properties of adaptogenic drugs]. PubMed: [The optimizing influence of melatonin on the behavioral activity of cognitive enhancers]. PubMed: Synthesis and biological evaluation of bilobol and adipostatin A. PubMed: Evidence for toxic effects of alkylphenols from Ginkgo biloba in the hen's egg test (HET). PubMed: Alkylresorcinols in fruit pulp and leaves of Ginkgo biloba L. PubMed: Higher cardol homologs (5-alkylresorcinols) in rye seedlings. PubMed: Phospholipase Cgamma1 inhibitory principles from the sarcotestas of Ginkgo biloba. PubMed: Comparison of the effects of bilobol and 12-O-tetradecanoylphorbol-13-acetate on skin, and test of tumor promoting potential of bilobol in CD-1 mice. PubMed: Analogues of poison ivy urushiol. Synthesis and biological activity of disubstituted n-alkylbenzenes.