CHEBI:34247 - 2,6-di-tert-butyl-4-methylphenol

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ChEBI Name 2,6-di-tert-butyl-4-methylphenol
ChEBI ID CHEBI:34247
ChEBI ASCII Name 2,6-di-tert-butyl-4-methylphenol
Definition A member of the class of phenols that is 4-methylphenol substituted by tert-butyl groups at positions 2 and 6.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C15H24O
Net Charge 0
Average Mass 220.35046
Monoisotopic Mass 220.18272
InChI InChI=1S/C15H24O/c1-10-8-11(14(2,3)4)13(16)12(9-10)15(5,6)7/h8-9,16H,1-7H3
InChIKey NLZUEZXRPGMBCV-UHFFFAOYSA-N
SMILES Cc1cc(c(O)c(c1)C(C)(C)C)C(C)(C)C
Metabolite of Species Details
Homo sapiens (NCBI:txid9606) Found in saliva (UBERON:0001836). See: PubMed
Roles Classification
Chemical Role(s): antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Biological Role(s): food additive
Any substance which is added to food to preserve or enhance its flavour and/or appearance.
ferroptosis inhibitor
Any substance that inhibits the process of ferroptosis (a type of programmed cell death dependent on iron and characterized by the accumulation of lipid peroxides) in organisms.
Application(s): food additive
Any substance which is added to food to preserve or enhance its flavour and/or appearance.
geroprotector
Any compound that supports healthy aging, slows the biological aging process, or extends lifespan.
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ChEBI Ontology
Outgoing 2,6-di-tert-butyl-4-methylphenol (CHEBI:34247) has functional parent phenol (CHEBI:15882)
2,6-di-tert-butyl-4-methylphenol (CHEBI:34247) has role antioxidant (CHEBI:22586)
2,6-di-tert-butyl-4-methylphenol (CHEBI:34247) has role ferroptosis inhibitor (CHEBI:173084)
2,6-di-tert-butyl-4-methylphenol (CHEBI:34247) has role food additive (CHEBI:64047)
2,6-di-tert-butyl-4-methylphenol (CHEBI:34247) has role geroprotector (CHEBI:176497)
2,6-di-tert-butyl-4-methylphenol (CHEBI:34247) is a phenols (CHEBI:33853)
IUPAC Name
2,6-di-tert-butyl-4-methylphenol
Synonyms Sources
1-hydroxy-4-methyl-2,6-di-tert-butylbenzene ChemIDplus
2,6-bis(1,1-dimethylethyl)-4-methylphenol KEGG COMPOUND
2,6-di-t-butyl-4-methylphenol KEGG COMPOUND
2,6-di-t-butyl-p-cresol ChemIDplus
2,6-di-tert-butyl-1-hydroxy-4-methylbenzene ChemIDplus
2,6-di-tert-butyl-4-cresol ChemIDplus
2,6-di-tert-butyl-4-hydroxytoluene ChemIDplus
2,6-di-tert-butyl-4-methylhydroxybenzene ChemIDplus
2,6-di-tert-butyl-p-cresol KEGG COMPOUND
BHT KEGG COMPOUND
butylated hydroxytoluene KEGG COMPOUND
butylhydroxytoluene KEGG COMPOUND
FEMA 2184 HMDB
o-di-tert-butyl-p-methylphenol ChemIDplus
Manual Xrefs Databases
13835296 ChemSpider
Butylated_hydroxytoluene Wikipedia
C14693 KEGG COMPOUND
D02413 KEGG DRUG
FDB011992 FooDB
HMDB0033826 HMDB
LSM-19020 LINCS
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Registry Numbers Types Sources
128-37-0 CAS Registry Number NIST Chemistry WebBook
128-37-0 CAS Registry Number ChemIDplus
1911640 Beilstein Registry Number Beilstein
1911640 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
11837686 PubMed citation Europe PMC
24612426 PubMed citation Europe PMC
24617543 PubMed citation Europe PMC
29864697 PubMed citation Europe PMC
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33519739 PubMed citation Europe PMC
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448040 PubMed citation Europe PMC
Last Modified
22 September 2021