CHEBI:89188 - 2,4-di-tert-butylphenol

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ChEBI Name 2,4-di-tert-butylphenol
ChEBI ID CHEBI:89188
ChEBI ASCII Name 2,4-di-tert-butylphenol
Definition A member of the class of phenols carrying two tert-butyl substituents at positions 2 and 4.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C14H22O
Net Charge 0
Average Mass 206.324
Monoisotopic Mass 206.16707
InChI InChI=1S/C14H22O/c1-13(2,3)10-7-8-12(15)11(9-10)14(4,5)6/h7-9,15H,1-6H3
InChIKey ICKWICRCANNIBI-UHFFFAOYSA-N
SMILES OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C
Metabolite of Species Details
Bacillus subtilis (NCBI:txid1423) See: PubMed
Ipomoea batatas (NCBI:txid4120) See: PubMed
Scolopendra subsp.nipes (NCBI:txid55038) See: PubMed
Streptomyces mutabilis (NCBI:txid67332) See: PubMed
Pseudomonas monteilii (NCBI:txid76759) of strain PsF84 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): bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
marine metabolite
Any metabolite produced during a metabolic reaction in marine macro- and microorganisms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2,4-di-tert-butylphenol (CHEBI:89188) has role antioxidant (CHEBI:22586)
2,4-di-tert-butylphenol (CHEBI:89188) has role bacterial metabolite (CHEBI:76969)
2,4-di-tert-butylphenol (CHEBI:89188) has role marine metabolite (CHEBI:76507)
2,4-di-tert-butylphenol (CHEBI:89188) is a alkylbenzene (CHEBI:38976)
2,4-di-tert-butylphenol (CHEBI:89188) is a phenols (CHEBI:33853)
Synonyms Sources
1-Hydroxy-2,4-di-tert-butylbenzene HMDB
2,4-Bis(1,1'-dimethylethyl)phenol HMDB
2,4-Bis(1,1-dimethylethyl)-Phenol HMDB
2,4-Bis(1,1-dimethylethyl)phenol NIST Chemistry WebBook
2,4-Bis(tert-butyl)phenol HMDB
2,4-Di-t-Butylphenol HMDB
2,4-Tert-butylphenol HMDB
Manual Xref Database
HMDB0013816 HMDB
View more database links
Registry Numbers Types Sources
1910383 Reaxys Registry Number Reaxys
1910383 Beilstein Registry Number ChemIDplus
96-76-4 CAS Registry Number ChemIDplus
96-76-4 CAS Registry Number NIST Chemistry WebBook
Citations Waiting for Citations Types Sources
16595909 PubMed citation Europe PMC
22020168 PubMed citation Europe PMC
23450232 PubMed citation Europe PMC
24074359 PubMed citation Europe PMC
24934765 PubMed citation Europe PMC
25641715 PubMed citation Europe PMC
27107984 PubMed citation Europe PMC
27524650 PubMed citation Europe PMC
Last Modified
11 November 2016