mansonone H
naphtho[1,8-bc]pyran-7,8-dione, 2,3-dihydro-4-hydroxy-3,6,9-trimethyl-
Identification
| Name | mansonone H |
| CAS Number | 13383-59-0 |
| FDA UNII | Search |
| Molecular Formula | C15 H14 O4 |
| Molecular Weight | 258.27338000 |
| Nikkaji Number | J14.080E |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 437.00 °C. @ 760.00 mm Hg (est) |
| Flash Point | 332.00 °F. TCC ( 166.60 °C. ) (est) |
| logP (o/w) | 2.750 (est) |
| Soluble in | water, 563.5 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 H usage levels up to | not for fragrance use. |
| Recommendation for mansonone H flavor usage levels up to | not for flavor use. |
No supplier data available
Potential Uses
Natural Occurrence
Synonyms
4-
hydroxy-3,6,9-trimethyl-2,3-dihydrobenzo[de]chromene-7,8-dione
naphtho[1,8-bc]pyran-7,8-dione, 2,3-dihydro-4-hydroxy-3,6,9-trimethyl-
PubMed:
[Chemical constituents from wood of the Chinese Hainan mangrove-associated plant, Thespesia populnea].
PubMed:
Acetyl- and butyryl-cholinesterase inhibitory activities of mansorins and mansonones.
PubMed:
Constituents from the stems of Hibiscus taiwanensis.
PubMed:
Cytotoxicity and superoxide anion generation by some naturally occurring quinones.
PubMed:
Inhibition of the cytotoxicity of protein toxins by a novel plant metabolite, mansonone-D.