pogostol
2,3,3a,5,6,7,8,8a-octahydro-1,4-dimethyl-7-prop-1-en-2-yl-1H-azulen-4-ol
Identification
| Name | pogostol |
| IUPAC | 1,4-dimethyl-7-prop-1-en-2-yl-2,3,3a,5,6,7,8,8a-octahydro-1H-azulen-4-ol |
| CAS Number | 21698-41-9 |
| FDA UNII | Search |
| Molecular Formula | C15 H26 O |
| Molecular Weight | 222.37142000 |
| Nikkaji Number | J55.656D |
Regulatory
Physical Properties
| Assay | 90.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 303.00 to 304.00 °C. @ 760.00 mm Hg |
| Vapor Pressure | 0.000083 mmHg @ 25.00 °C. (est) |
| Flash Point | 263.00 °F. TCC ( 128.33 °C. ) |
| logP (o/w) | 4.965 (est) |
| Soluble in | alcohol |
| Insoluble in | water |
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 pogostol usage levels up to | not for fragrance use. |
| Recommendation for pogostol flavor usage levels up to | not for flavor use. |
No supplier data available
Potential Uses
Natural Occurrence
Synonyms
1,4-
dimethyl-7-prop-1-en-2-yl-2,3,3a,5,6,7,8,8a-octahydro-1H-azulen-4-ol
2,3,3a,5,6,7,8,8a-
octahydro-1,4-dimethyl-7-prop-1-en-2-yl-1H-azulen-4-ol
PubMed:
Pogostol biosynthesis by the endophytic fungus Geniculosporium.
PubMed:
Chemical composition and antimicrobial activity of three essential oils from Curcuma wenyujin.
PubMed:
Quantitative and physical evaluation of patchouli essential oils obtained from different sources of Pogostemon cablin.
PubMed:
Guaiane sesquiterpenes from Biscogniauxia nummularia featuring potent antigerminative activity.
PubMed:
Synthesis of the reported structure of pogostol and a total aynthesis of (+/-)-kessane without the use of protecting groups.
PubMed:
Anti-emetic principles of Pogostemon cablin (Blanco) Benth.