ylangocamphene

CAS: 3650-28-0 C15 H24 MW: 204.35628000

Identification

Namesativene
IUPAC(1R,2S,3S,6S,8S)-6-methyl-7-methylidene-3-propan-2-yltricyclo[4.4.0.02,8]decane
CAS Number3650-28-0
FDA UNIISearch
Molecular FormulaC15 H24
Molecular Weight204.35628000
MDL NumberMFCD00084731
Nikkaji NumberJ20.776D
Beilstein6566323

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 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 sativene usage levels up tonot for fragrance use.
Recommendation for sativene flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

cedarwood oil lebanon @ 0.10% Data mikania cordata (burm. f.) b.l. robinson var. cordata leaf oil france @ 1.40% Data

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.