CHEBI:41308 - benzophenone

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ChEBI Name benzophenone
ChEBI ID CHEBI:41308
Definition The simplest member of the class of benzophenones, being formaldehyde in which both hydrogens are replaced by phenyl groups.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:41306, CHEBI:3034
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Formula C13H10O
Net Charge 0
Average Mass 182.21790
Monoisotopic Mass 182.073
InChI InChI=1S/C13H10O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H
InChIKey RWCCWEUUXYIKHB-UHFFFAOYSA-N
SMILES O=C(c1ccccc1)c1ccccc1
Roles Classification
Biological Role(s): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
Application(s): photosensitizing agent
A chemical compound that can be excited by light of a specific wavelength and subsequently transfer energy to a chosen reactant. This is commonly molecular oxygen within a cancer tissue, which is converted to (highly rective) singlet state oxygen. This rapidly reacts with any nearby biomolecules, ultimately killing the cancer cells.
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ChEBI Ontology
Outgoing benzophenone (CHEBI:41308) has role photosensitizing agent (CHEBI:47868)
benzophenone (CHEBI:41308) has role plant metabolite (CHEBI:76924)
benzophenone (CHEBI:41308) is a benzophenones (CHEBI:22726)
Incoming demethylsulochrin (CHEBI:48948) has functional parent benzophenone (CHEBI:41308)
fenofibrate (CHEBI:5001) has functional parent benzophenone (CHEBI:41308)
mesotrione (CHEBI:38321) has functional parent benzophenone (CHEBI:41308)
Ro 48-8071 (CHEBI:101064) has functional parent benzophenone (CHEBI:41308)
IUPAC Names
benzophenone
diphenylmethanone
Synonyms Sources
α-oxodiphenylmethane NIST Chemistry WebBook
α-oxoditane NIST Chemistry WebBook
Benzophenone KEGG COMPOUND
benzoylbenzene NIST Chemistry WebBook
Diphenyl ketone KEGG COMPOUND
DIPHENYLMETHANONE PDBeChem
Ph2CO ChEBI
Database Links Databases
Benzophenone Wikipedia
BZQ PDBeChem
C06354 KEGG COMPOUND
DB01878 DrugBank
HMDB0032049 HMDB
View more database links
Registry Numbers Types Sources
119-61-9 CAS Registry Number ChemIDplus
119-61-9 CAS Registry Number NIST Chemistry WebBook
1238185 Beilstein Registry Number Beilstein
1238185 Reaxys Registry Number Reaxys
4256 Gmelin Registry Number Gmelin
Citations Waiting for Citations Types Sources
17439666 PubMed citation Europe PMC
19939518 PubMed citation Europe PMC
20534002 PubMed citation Europe PMC
21238557 PubMed citation Europe PMC
21277784 PubMed citation Europe PMC
21919502 PubMed citation Europe PMC
Last Modified
31 March 2016
General Comment
2011-03-24 Benzophenone is widely used as a building block in organic synthesis, and as a photosensitizer and photo-initiator in UV-curing applications such as inks, imaging, and clear coatings in the printing industry. It also prevents UV light from damaging scents and colors in products such as perfumes and soaps, and can be added to plastic packaging as a UV blocker, so allowing manufacturers to package UV-sensitive products in clear glass or plastic. Substituted benzophenones such as oxybenzone and dioxybenzone are used in some sunscreens.