CHEBI:132899 - β-terpineol

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ChEBI Name β-terpineol
ChEBI ID CHEBI:132899
ChEBI ASCII Name beta-terpineol
Definition A member of the class of terpineols that is cyclohexanol carrying additional methyl and propenyl substituents at positions 1 and 4 respectively.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter qingping liu
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Formula C10H18O
Net Charge 0
Average Mass 154.250
Monoisotopic Mass 154.13577
InChI InChI=1S/C10H18O/c1-8(2)9-4-6-10(3,11)7-5-9/h9,11H,1,4-7H2,2-3H3
InChIKey RUJPNZNXGCHGID-UHFFFAOYSA-N
SMILES OC1(CCC(CC1)C(C)=C)C
Metabolite of Species Details
Amomum cannicarpum (NCBI:txid1540384) Found in rhizome (BTO:0001181). See: PubMed
Eucalyptus globulus (NCBI:txid34317) Found in whole plant (BTO:0001461). See: PubMed
Abies balsamea (NCBI:txid90345) Found in whole plant (BTO:0001461). Isolated from the essential oil See: Journal of essential oil research (1994), 6, 229-238
Roles Classification
Biological Role(s): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
volatile oil component
Any plant metabolite that is found naturally as a component of a volatile oil.
Application(s): fragrance
A substance, extract, or preparation for diffusing or imparting an agreeable or attractive smell.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing β-terpineol (CHEBI:132899) has role fragrance (CHEBI:48318)
β-terpineol (CHEBI:132899) has role plant metabolite (CHEBI:76924)
β-terpineol (CHEBI:132899) has role volatile oil component (CHEBI:27311)
β-terpineol (CHEBI:132899) is a terpineol (CHEBI:26876)
β-terpineol (CHEBI:132899) is a tertiary alcohol (CHEBI:26878)
IUPAC Name
1-methyl-4-(prop-1-en-2-yl)cyclohexan-1-ol
Synonyms Sources
1-Methyl-4-(1-methylethenyl)cyclohexanol ChemIDplus
1-methyl-4-(1-methylvinyl)cyclohexan-1-ol NIST Chemistry WebBook
1-Methyl-4-isopropenylcyclohexan-1-ol ChemIDplus
4-Isopropenyl-1-methyl-1-cyclohexanol HMDB
4-Isopropenyl-1-methyl-1-cyclohexanol ChemIDplus
beta-Terpineol KNApSAcK
p-Menth-8-en-1-ol ChemIDplus
Manual Xrefs Databases
C00048331 KNApSAcK
C17517 KEGG COMPOUND
HMDB0036996 HMDB
Terpineol Wikipedia
View more database links
Registry Numbers Types Sources
138-87-4 CAS Registry Number ChemIDplus
138-87-4 CAS Registry Number NIST Chemistry WebBook
2040100 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
16714091 PubMed citation Europe PMC
18640203 PubMed citation Europe PMC
23678820 PubMed citation Europe PMC
IND20412149 Agricola citation Europe PMC
Last Modified
31 January 2017