CHEBI:34393 - 4-chloro-3,5-dimethylphenol

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ChEBI Name 4-chloro-3,5-dimethylphenol
ChEBI ID CHEBI:34393
Definition A member of the class of phenols that is 3,5-xylenol which is substituted at position 4 by chlorine. It is bactericidal against most Gram-positive bacteria but less effective against Staphylococci and Gram-negative bacteria, and often inactive against Pseudomonas species. It is ineffective against bacterial spores.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C8H9ClO
Net Charge 0
Average Mass 156.60900
Monoisotopic Mass 156.034
InChI InChI=1S/C8H9ClO/c1-5-3-7(10)4-6(2)8(5)9/h3-4,10H,1-2H3
InChIKey OSDLLIBGSJNGJE-UHFFFAOYSA-N
SMILES Cc1cc(O)cc(C)c1Cl
Roles Classification
Biological Role(s): disinfectant
An antimicrobial agent that is applied to non-living objects to destroy harmful microorganisms or to inhibit their activity.
Application(s): molluscicide
A substance used to destroy pests of the phylum Mollusca.
antiseptic drug
A substance used locally on humans and other animals to destroy harmful microorganisms or to inhibit their activity (cf. disinfectants, which destroy microorganisms found on non-living objects, and antibiotics, which can be transported through the lymphatic system to destroy bacteria within the body).
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ChEBI Ontology
Outgoing 4-chloro-3,5-dimethylphenol (CHEBI:34393) has functional parent 3,5-xylenol (CHEBI:38572)
4-chloro-3,5-dimethylphenol (CHEBI:34393) has role antiseptic drug (CHEBI:48218)
4-chloro-3,5-dimethylphenol (CHEBI:34393) has role disinfectant (CHEBI:48219)
4-chloro-3,5-dimethylphenol (CHEBI:34393) has role molluscicide (CHEBI:33904)
4-chloro-3,5-dimethylphenol (CHEBI:34393) is a monochlorobenzenes (CHEBI:83403)
4-chloro-3,5-dimethylphenol (CHEBI:34393) is a phenols (CHEBI:33853)
IUPAC Name
4-chloro-3,5-dimethylphenol
INNs Sources
chloroxylénol WHO MedNet
chloroxylenol ChemIDplus
chloroxylenolum ChemIDplus
cloroxilenol ChemIDplus
Synonyms Sources
2-chloro-5-hydroxy-1,3-dimethylbenzene ChemIDplus
2-chloro-5-hydroxy-m-xylene ChemIDplus
2-Chloro-m-xylenol ChemIDplus
3,5-dimethyl-4-chlorophenol ChemIDplus
4-chloro-1-hydroxy-3,5-dimethylbenzene ChemIDplus
4-chloro-m-xylenol ChemIDplus
chloro-xylenol ChemIDplus
p-chloro-3,5-xylenol ChemIDplus
p-chloro-m-xylenol ChemIDplus
parachlorometaxylenol ChemIDplus
parametaxylenol DrugCentral
PCMX ChemIDplus
Brand Names Sources
Benzytol ChemIDplus
Dettol ChemIDplus
Manual Xrefs Databases
1615 PPDB
1615 VSDB
3094 DrugCentral
C14715 KEGG COMPOUND
Chloroxylenol Wikipedia
D03473 KEGG DRUG
LSM-19962 LINCS
US2350677 Patent
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Registry Numbers Types Sources
1862539 Reaxys Registry Number Reaxys
88-04-0 CAS Registry Number NIST Chemistry WebBook
88-04-0 CAS Registry Number ChemIDplus
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Last Modified
08 August 2017