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ChEBI
> Main
CHEBI:49000 - 2-phenylethanol
Main
ChEBI Ontology
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ChEBI Name
2-phenylethanol
ChEBI ID
CHEBI:49000
Definition
A primary alcohol that is ethanol substituted by a phenyl group at position 2.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:8096, CHEBI:44780
Supplier Information
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Formula
C8H10O
Net Charge
0
Average Mass
122.16440
Monoisotopic Mass
122.07316
InChI
InChI=1S/C8H10O/c9-7-6-8-4-2-1-3-5-8/h1-5,9H,6-7H2
InChIKey
WRMNZCZEMHIOCP-UHFFFAOYSA-N
SMILES
OCCc1ccccc1
Metabolite of Species
Details
Saccharomyces cerevisiae
(NCBI:txid4932)
Source: yeast.sf.net See:
PubMed
Aspergillus niger
(NCBI:txid5061)
of strain var. Tieghem. See: Phytochemistry, 1988, 27(10), 3169-3173
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.
Aspergillus metabolite
Any fungal metabolite produced during a metabolic reaction in the mould,
Aspergillus
.
plant growth retardant
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (
Saccharomyces cerevisiae
).
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
2-phenylethanol (
CHEBI:49000
)
has role
Aspergillus
metabolite (
CHEBI:76956
)
2-phenylethanol (
CHEBI:49000
)
has role
Saccharomyces cerevisiae
metabolite (
CHEBI:75772
)
2-phenylethanol (
CHEBI:49000
)
has role
fragrance (
CHEBI:48318
)
2-phenylethanol (
CHEBI:49000
)
has role
plant growth retardant (
CHEBI:35219
)
2-phenylethanol (
CHEBI:49000
)
has role
plant metabolite (
CHEBI:76924
)
2-phenylethanol (
CHEBI:49000
)
is a
benzenes (
CHEBI:22712
)
2-phenylethanol (
CHEBI:49000
)
is a
primary alcohol (
CHEBI:15734
)
Incoming
2-(2-hydroxyphenyl)ethanol (
CHEBI:64803
)
has functional parent
2-phenylethanol (
CHEBI:49000
)
2-(4-hydroxyphenyl)ethanol (
CHEBI:1879
)
has functional parent
2-phenylethanol (
CHEBI:49000
)
2-phenylethyl β-primeveroside (
CHEBI:136550
)
has functional parent
2-phenylethanol (
CHEBI:49000
)
2-phenylethyl 1
H
-indol-3-ylacetate (
CHEBI:141317
)
has functional parent
2-phenylethanol (
CHEBI:49000
)
2-phenylethyl formate (
CHEBI:87417
)
has functional parent
2-phenylethanol (
CHEBI:49000
)
2-phenylethyl pentanoate (
CHEBI:87323
)
has functional parent
2-phenylethanol (
CHEBI:49000
)
2-phenylethyl pivalate (
CHEBI:87336
)
has functional parent
2-phenylethanol (
CHEBI:49000
)
ethyl 2-phenylethyl dimethylmalonate (
CHEBI:87278
)
has functional parent
2-phenylethanol (
CHEBI:49000
)
phenethyl acetate (
CHEBI:31988
)
has functional parent
2-phenylethanol (
CHEBI:49000
)
phenethyl benzoate (
CHEBI:156233
)
has functional parent
2-phenylethanol (
CHEBI:49000
)
phenethyl butyrate (
CHEBI:87413
)
has functional parent
2-phenylethanol (
CHEBI:49000
)
phenethyl isobutyrate (
CHEBI:87409
)
has functional parent
2-phenylethanol (
CHEBI:49000
)
IUPAC Name
2-phenylethanol
Synonyms
Sources
2-Hydroxyethylbenzene
ChemIDplus
2-PEA
ChEBI
2-PHENYL-ETHANOL
PDBeChem
2-phenylethanol
UniProt
2-Phenylethanol
KEGG COMPOUND
Benzeneethanol
ChemIDplus
Benzylmethanol
ChemIDplus
β-PEA
NIST Chemistry WebBook
β-Phenethyl alcohol
NIST Chemistry WebBook
β-Phenylethanol
NIST Chemistry WebBook
β-Phenylethyl alcohol
NIST Chemistry WebBook
Phenethyl alcohol
KEGG COMPOUND
Phenylethyl alcohol
KEGG COMPOUND
Manual Xrefs
Databases
C00002663
KNApSAcK
C05853
KEGG COMPOUND
CPD-7035
MetaCyc
D00192
KEGG DRUG
DB02192
DrugBank
HMDB0033944
HMDB
PEL
PDBeChem
Phenethyl_alcohol
Wikipedia
View more database links
Registry Numbers
Types
Sources
1905732
Beilstein Registry Number
Beilstein
1905732
Reaxys Registry Number
Reaxys
240469
Gmelin Registry Number
Gmelin
60-12-8
CAS Registry Number
KEGG COMPOUND
60-12-8
CAS Registry Number
NIST Chemistry WebBook
60-12-8
CAS Registry Number
ChemIDplus
Citations
Types
Sources
19517523
PubMed citation
Europe PMC
22690913
PubMed citation
Europe PMC
23385159
PubMed citation
Europe PMC
23836015
PubMed citation
Europe PMC
24423498
PubMed citation
Europe PMC
Last Modified
24 July 2020