mansonone G
1,2-naphthalenedione, 6-hydroxy-3,8-dimethyl-5-(1-methylethyl)-
Identification
| Name | mansonone G |
| IUPAC | 6-hydroxy-3,8-dimethyl-5-propan-2-ylnaphthalene-1,2-dione |
| CAS Number | 7715-96-0 |
| FDA UNII | Search |
| Molecular Formula | C15 H16 O3 |
| Molecular Weight | 244.29012000 |
| Nikkaji Number | J14.091K |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 424.30 °C. @ 760.00 mm Hg (est) |
| Flash Point | 436.00 °F. TCC ( 224.50 °C. ) (est) |
| logP (o/w) | 3.530 (est) |
| Soluble in | water, 26.02 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 mansonone G usage levels up to | not for fragrance use. |
| Recommendation for mansonone G flavor usage levels up to | not for flavor use. |
No supplier data available
Potential Uses
Natural Occurrence
Synonyms
6-
hydroxy-3,8-dimethyl-5-propan-2-ylnaphthalene-1,2-dione
6-
hydroxy-5-isopropyl-3,8-dimethyl-1,2-naphthalenedione
1,2-
naphthalenedione, 6-hydroxy-3,8-dimethyl-5-(1-methylethyl)-
PubMed:
Anti-estrogenic activity of mansonone G and mansorin A derivatives.
PubMed:
Isolation and synthesis of two antiproliferative calamenene-type sesquiterpenoids from Sterculia tavia from the Madagascar rain forest.
PubMed:
Thespesenone and dehydrooxoperezinone-6-methyl ether, new sesquiterpene quinones from Thespesia populnea.