CHEBI:48945 - 2-methylbutan-1-ol

Main ChEBI Ontology Automatic Xrefs
ChEBI Name 2-methylbutan-1-ol
ChEBI ID CHEBI:48945
Definition A primary alcohol that is isopentane substituted by a hydroxy group at position 1.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Save molfile Download Molfile
Formula C5H12O
Net Charge 0
Average Mass 88.14818
InChI InChI=1S/C5H12O/c1-3-5(2)4-6/h5-6H,3-4H2,1-2H3
InChIKey QPRQEDXDYOZYLA-UHFFFAOYSA-N
SMILES CCC(C)CO
Roles Classification
Biological Role(s): Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2-methylbutan-1-ol (CHEBI:48945) has parent hydride isopentane (CHEBI:30362)
2-methylbutan-1-ol (CHEBI:48945) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
2-methylbutan-1-ol (CHEBI:48945) is a alkyl alcohol (CHEBI:50584)
2-methylbutan-1-ol (CHEBI:48945) is a primary alcohol (CHEBI:15734)
Incoming 2-methylbutyl acetate (CHEBI:50585) has functional parent 2-methylbutan-1-ol (CHEBI:48945)
2-methylbutyl decanoate (CHEBI:87330) has functional parent 2-methylbutan-1-ol (CHEBI:48945)
(R)-2-methylbutan-1-ol (CHEBI:50624) is a 2-methylbutan-1-ol (CHEBI:48945)
(S)-2-methylbutan-1-ol (CHEBI:50625) is a 2-methylbutan-1-ol (CHEBI:48945)
IUPAC Name
2-methylbutan-1-ol
Synonyms Sources
2-methyl butanol-1 ChemIDplus
2-methyl-1-butanol ChemIDplus
2-methyl-n-butanol ChemIDplus
2-methylbutanol NIST Chemistry WebBook
2-methylbutyl alcohol ChemIDplus
active amyl alcohol NIST Chemistry WebBook
active primary amyl alcohol ChemIDplus
CH3CH2CH(CH3)CH2OH NIST Chemistry WebBook
methyl-2-butan-1-ol NIST Chemistry WebBook
primary active amyl alcohol ChemIDplus
sec-butylcarbinol ChemIDplus
Database Links Databases
CPD-7033 MetaCyc
HMDB31527 HMDB
View more database links
Registry Numbers Types Sources
137-32-6 CAS Registry Number NIST Chemistry WebBook
137-32-6 CAS Registry Number ChemIDplus
1718810 Reaxys Registry Number Reaxys
1718810 Beilstein Registry Number ChemIDplus
600874 Gmelin Registry Number Gmelin
Citations Waiting for Citations Types Sources
20812374 PubMed citation CiteXplore
22821412 PubMed citation CiteXplore
Last Modified
05 August 2015