sativene
ylangocamphene
Identification
| Name | sativene |
| IUPAC | (1R,2S,3S,6S,8S)-6-methyl-7-methylidene-3-propan-2-yltricyclo[4.4.0.02,8]decane |
| CAS Number | 3650-28-0 |
| FDA UNII | Search |
| Molecular Formula | C15 H24 |
| Molecular Weight | 204.35628000 |
| MDL Number | MFCD00084731 |
| Nikkaji Number | J20.776D |
| Beilstein | 6566323 |
Regulatory
Physical Properties
| Appearance | colorless clear liquid (est) |
| Assay | 97.00 to 100.00 sum of isomers |
| Food Chemicals Codex Listed | No |
| Boiling Point | 255.00 to 257.00 °C. @ 760.00 mm Hg |
| Vapor Pressure | 0.025000 mmHg @ 25.00 °C. (est) |
| Flash Point | 221.00 °F. TCC ( 105.00 °C. ) |
| logP (o/w) | 6.166 (est) |
| Shelf Life | 12.00 month(s) or longer if stored properly. |
| Storage | refrigerate in tightly sealed containers. |
| Soluble in | alcohol |
| Insoluble in | water |
No sensory data available
Safety Information
| Preferred SDS | View |
| 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 sativene usage levels up to | not for fragrance use. |
| Recommendation for sativene flavor usage levels up to | not for flavor use. |
No supplier data available
Potential Uses
Natural Occurrence
Synonyms
(1R,2S,3S,6S,8S)-6-
methyl-7-methylidene-3-propan-2-yltricyclo[4.4.0.02,8]decane
(+)-
sativene
7(12)-
sativene
ylangocamphene
PubMed:
Identification of volatiles produced by Cladosporium cladosporioides CL-1, a fungal biocontrol agent that promotes plant growth.
PubMed:
Theoretical calculations on carbocations involved in the biosynthesis of bergamotenes and related terpenes--the same and not the same.
PubMed:
Computational studies on biosynthetic carbocation rearrangements leading to sativene, cyclosativene, alpha-ylangene, and beta-ylangene.
PubMed:
Rare sesquiterpenes from the algicolous fungus Drechslera dematioidea.
PubMed:
A formal total synthesis of racemic sesquiterpenoid sativene.
PubMed:
Synthesis of campherenone, epicampherenone, beta-santalene, epi-beta-santalene, alpha-santalene, ylangocamphor, copacamphor, and sativene.
PubMed:
SATIVENE, PARENT OF THE TOXIN FROM HELMINTHOSPORIUM SATIVUM.