CHEBI:48945 - 2-methylbutan-1-ol

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ChEBI Name 2-methylbutan-1-ol
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
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Formula C5H12O
Net Charge 0
Average Mass 88.14818
Monoisotopic Mass 88.08882
InChI InChI=1S/C5H12O/c1-3-5(2)4-6/h5-6H,3-4H2,1-2H3
Metabolite of Species Details
Saccharomyces cerevisiae (NCBI:txid4932) Source: See: PubMed
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 butanoate (CHEBI:156490) has functional parent 2-methylbutan-1-ol (CHEBI:48945)
2-methylbutyl decanoate (CHEBI:87330) has functional parent 2-methylbutan-1-ol (CHEBI:48945)
2-methylbutyl hexanoate (CHEBI:156542) 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)
Synonyms Sources
2-methyl butanol-1 ChemIDplus
2-methyl-1-butanol ChemIDplus
2-methyl-n-butanol ChemIDplus
2-methylbutan-1-ol UniProt
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
Manual Xrefs Databases
CPD-7033 MetaCyc
HMDB0031527 HMDB
View more database links
Registry Numbers Types Sources
137-32-6 CAS Registry Number ChemIDplus
137-32-6 CAS Registry Number NIST Chemistry WebBook
1718810 Reaxys Registry Number Reaxys
1718810 Beilstein Registry Number ChemIDplus
600874 Gmelin Registry Number Gmelin
Citations Waiting for Citations Types Sources
20812374 PubMed citation Europe PMC
22821412 PubMed citation Europe PMC
Last Modified
10 September 2020