U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C13H10O
Molecular Weight 182.2179
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BENZOPHENONE

SMILES

O=C(C1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=RWCCWEUUXYIKHB-UHFFFAOYSA-N
InChI=1S/C13H10O/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H

HIDE SMILES / InChI

Molecular Formula C13H10O
Molecular Weight 182.2179
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: Description was created using several sources including: http://apps.who.int/iris/bitstream/10665/42578/1/WHO_TRS_909.pdf; http://www.fda.gov/food/ingredientspackaginglabeling/foodadditivesingredients/ucm091048.htm; http://www.fda.gov/downloads/drugs/developmentapprovalprocess/developmentresources/over-the-counterotcdrugs/statusofotcrulemakings/ucm090435.pdf; https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5a68508b-f1fa-4f03-b28a-554e24cf58d6; https://clinicaltrials.gov/ct2/show/NCT01695356?term=BENZOPHENONE&rank=1; https://clinicaltrials.gov/ct2/show/NCT01695356?term=BENZOPHENONE&rank=1; https://www.ncbi.nlm.nih.gov/pubmed/26753716

Benzophenone is the organic compound. It is a flavouring agent evaluated as safe at current levels of intake by joint FAO/WHO Expert Committee on Food Additives (JECFA) and approved by FDA as a food additive and as UV protector. Substituted benzophenones such as oxybenzone (benzophenone-3) and dioxybenzone are used in sunscreens in cosmetics and as a sunscreen ingredients in some topical drugs in combination with skin lighteners for gradual fading of dark (brownish) areas in the skin such as freckles, age and liver spots or treatment of melanosis. Benzophenone derivatives can be used as a photo initiators. Benzophenone used in practical synthesis of some drugs.

Originator

Curator's Comment: C. S. Marvel and W. M. Sperry described the synthesis of benzothenone in 1928

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
METASOL

Approved Use

For the gradual fading of dark (brownish) areas in the skin such as freckles, age and liver spots
PubMed

PubMed

TitleDatePubMed
Biochemical and structural studies with prenyl diphosphate analogues provide insights into isoprenoid recognition by protein farnesyl transferase.
2003-04-08
Catalytic asymmetric Mannich reactions of glycine derivatives with imines. A new approach to optically active alpha,beta-diamino acid derivatives.
2003-04-04
Diazotrifluoropropionamido-containing prenylcysteines: syntheses and applications for studying isoprenoid-protein interactions.
2003-03-06
Cryptophycin affinity labels: synthesis and biological activity of a benzophenone analogue of cryptophycin-24.
2003-02-24
Determination of benzophenones in a cosmetic matrix by supercritical fluid extraction and capillary electrophoresis.
2003-02-14
Structure-activity relationships of novel anti-malarial agents: part 5. N-(4-acylamino-3-benzoylphenyl)-[5-(4-nitrophenyl)-2-furyl]acrylic acid amides.
2003-02-10
Three-fold interpenetrating three-dimensional networks based on C-methylcalix[4]resorcinarene incorporating benzophenone guest molecules.
2003-02-07
Unexpected differences in the alpha-halogenation and related reactivity of sulfones with perhaloalkanes in KOH-t-BuOH.
2003-01-24
High-intensity ultrasound-promoted reformatsky reactions.
2003-01-24
Tuning copper-dioxygen reactivity and exogenous substrate oxidations via alterations in ligand electronics.
2003-01-22
New series of N-substituted phenyl ketone oxime ethers: synthesis and bovine beta3-adrenergic agonistic activities.
2003-01
Methionine proximity assay, a novel method for exploring peptide ligand-receptor interaction.
2002-12-31
Migration of surrogate contaminants in paper and paperboard into water through polyethylene coating layer.
2002-12
Benzophenone-induced estrogenic potency in ovariectomized rats.
2002-12
p-Nitrobenzenesulfenate esters as precursors for laser flash photolysis studies of alkyl radicals.
2002-11-29
Molecular structure of the solvated proton in isolated salts. Short, strong, low barrier (SSLB) H-bonds.
2002-11-20
Photoinduced electron transfer cleavage of oxetane adducts of uracil and cytosine.
2002-09
Biotransformation of cyclizine in greyhounds. 2: N(1)-dealkylation and identification of some neutral and phenolic metabolites in canine urine by gas chromatography-mass spectrometry.
2002-09
Modulation of GABA(A) receptor-mediated currents by benzophenone derivatives in isolated rat Purkinje neurones.
2002-09
Identification of the extracellular loop 2 as the point of interaction between the N terminus of the chemokine MIP-1alpha and its CCR1 receptor.
2002-09
Genotoxic activation of benzophenone and its two metabolites by human cytochrome P450s in SOS/umu assay.
2002-08-26
Triplet energy distribution in photoinitiators containing two dissociable groups.
2002-08-23
The development of an improved carrier system for sunscreen formulations based on crystalline lipid nanoparticles.
2002-08-21
4,4'-Benzophenone-O,O'-disulfamate: a potent inhibitor of steroid sulfatase.
2002-08-19
Oligonucleotides containing 7-vinyl-7-deazaguanine as a facile strategy for expanding the functional diversity of DNA.
2002-08-05
[Determination of alkylphenols, bisphenol A, benzophenone and phthalates in containers of baby food, and migration into food simulants].
2002-08
New photoactivators for multiphoton excited three-dimensional submicron cross-linking of proteins: bovine serum albumin and type 1 collagen.
2002-08
Hydrogenation without a transition-metal catalyst: on the mechanism of the base-catalyzed hydrogenation of ketones.
2002-07-24
Identification of two tamoxifen target proteins by photolabeling with 4-(2-morpholinoethoxy)benzophenone.
2002-07-18
[Results of a French nationwide survey of cutaneous side effects of ketoprofen gel reported between September 1996 and August 2000].
2002-07-02
Identification of the principal binding site for RGD-containing ligands in the alpha(V)beta(3) integrin: a photoaffinity cross-linking study.
2002-07-02
Relationship between estrogen receptor-binding and estrogenic activities of environmental estrogens and suppression by flavonoids.
2002-07
New cytotoxic coumarins and prenylated benzophenone derivatives from the bark of Ochrocarpos punctatus from the Madagascar rainforest.
2002-07
Stability indicating methods for the determination of loratadine in the presence of its degradation product.
2002-06-15
Synthesis and protein kinase inhibitory activity of balanol analogues with modified benzophenone subunits.
2002-06-06
Synthesis and structure-activity relationship of 2-aminobenzophenone derivatives as antimitotic agents.
2002-06-06
Polarographic determination of phenytoin and benzophenone (as impurity) in pharmaceutical preparations.
2002-05-15
[Cross-reaction potentials of ketoprofen].
2002-05-12
Oxidation of sulfides and disulfides under electron transfer or singlet oxygen photosensitization using soluble or grafted sensitizers.
2002-05
Oxygen transfer from sulfoxides: oxidation of alkylarenes catalyzed by a polyoxomolybdate, [PMo12O40]3-.
2002-04-24
Experimental study on phototoxicity and the photosensitization potential of ketoprofen, suprofen, tiaprofenic acid and benzophenone and the photocross-reactivity in guinea pigs.
2002-04
Complete LC/MS analysis of a Tinnevelli senna pod extract and subsequent isolation and identification of two new benzophenone glucosides.
2002-04
Fate of excited probes in micellar systems.
2002-03-29
Stereoselective intramolecular hydrogen abstraction by a chiral benzophenone derivative.
2002-02-07
Structure-reactivity relationships in the photoreduction of n,pi*-excited ketones and azoalkanes: the effect of reaction thermodynamics, excited-state electrophilicity, and antibonding character in the transition state.
2002-02
Photoimmobilization of biomolecules within a 3-dimensional hydrogel matrix.
2002
Structure based design of benzophenone-based non-thiol farnesyltransferase inhibitors.
2002
The use of a photoactivatable kaempferol analogue to probe the role of flavonol 3-O-galactosyltransferase in pollen germination.
2002
Evaluating the potential for recycling all PET bottles into new food packaging.
2002
Hydrogen abstraction from ionic liquids by benzophenone triplet excited states.
2001-11-21
Patents

Sample Use Guides

Apply a small amount of gel as a thin layer on the affected area twice daily, or use as directed by a doctor (50 g of gel contains 1 g of hydroquinone and 0.05 g benzophenone)
Route of Administration: Topical
The patterned co-culture of different types of living cells in a microfluidic device is crucial for the analysis of cellular interactions and cell-cell communication. Cell patterning was achieved by photocrosslinking 0.2 M benzophenone-4-isocyocyanate in a microfluidic channel. Patterning and co-culture of non-adherent K562 cells and adherent RF-6A cells was achieved by successive rounds of patterning. The present approach is expected to be useful for the development of in vitro methods for studying cell signaling.
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:33:01 GMT 2025
Edited
by admin
on Mon Mar 31 17:33:01 GMT 2025
Record UNII
701M4TTV9O
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIMENHYDRINATE IMPURITY J
EP  
Preferred Name English
BENZOPHENONE
FCC   FHFI   HSDB   INCI   MI   USP-RS   WHO-DD  
INCI  
Official Name English
Benzophenone [WHO-DD]
Common Name English
BENZOPHENONE [HSDB]
Common Name English
DIPHENYLMETHANONE
Systematic Name English
PHENYTOIN SODIUM IMPURITY A [EP IMPURITY]
Common Name English
PHENYTOIN IMPURITY BENZOPHENONE [USP IMPURITY]
Common Name English
HYDROCODONE HYDROGEN TARTRATE 2.5-HYDRATE IMPURITY H [EP IMPURITY]
Common Name English
BENZOPHENONE [USP IMPURITY]
Common Name English
KAYACURE BP
Common Name English
DIMENHYDRINATE IMPURITY J [EP IMPURITY]
Common Name English
FEMA NO. 2134
Code English
BENZOPHENONE [FHFI]
Common Name English
BENZOYLBENZENE
Systematic Name English
ADJUTAN 6016
Common Name English
PHENYL KETONE
Systematic Name English
PHENYTOIN SODIUM IMPURITY BENZOPHENONE [USP IMPURITY]
Common Name English
DIPHENHYDRAMINE HYDROCHLORIDE IMPURITY E [EP IMPURITY]
Common Name English
DIPHENYL KETONE
Systematic Name English
NSC-8077
Code English
.ALPHA.-OXODIPHENYLMETHANE
Common Name English
BENZOPHENONE [FCC]
Common Name English
DAROCUR BP
Common Name English
DIPHENHYDRAMINE IMPURITY E
Common Name English
.ALPHA.-OXODITANE
Common Name English
BENZOPHENONE [MI]
Common Name English
BENZOPHENONE [IARC]
Common Name English
SPEEDCURE BP
Common Name English
BENZOPHENONE [USP-RS]
Common Name English
PHENYTOIN IMPURITY A [EP IMPURITY]
Common Name English
Classification Tree Code System Code
JECFA EVALUATION BENZOPHENONE
Created by admin on Mon Mar 31 17:33:01 GMT 2025 , Edited by admin on Mon Mar 31 17:33:01 GMT 2025
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 17:33:01 GMT 2025 , Edited by admin on Mon Mar 31 17:33:01 GMT 2025
EPA PESTICIDE CODE 315
Created by admin on Mon Mar 31 17:33:01 GMT 2025 , Edited by admin on Mon Mar 31 17:33:01 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID0021961
Created by admin on Mon Mar 31 17:33:01 GMT 2025 , Edited by admin on Mon Mar 31 17:33:01 GMT 2025
PRIMARY
HSDB
6809
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PRIMARY
RS_ITEM_NUM
1056130
Created by admin on Mon Mar 31 17:33:01 GMT 2025 , Edited by admin on Mon Mar 31 17:33:01 GMT 2025
PRIMARY
CAS
119-61-9
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PRIMARY
EVMPD
SUB13019MIG
Created by admin on Mon Mar 31 17:33:01 GMT 2025 , Edited by admin on Mon Mar 31 17:33:01 GMT 2025
PRIMARY
WIKIPEDIA
BENZOPHENONE
Created by admin on Mon Mar 31 17:33:01 GMT 2025 , Edited by admin on Mon Mar 31 17:33:01 GMT 2025
PRIMARY
NSC
8077
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PRIMARY
PUBCHEM
3102
Created by admin on Mon Mar 31 17:33:01 GMT 2025 , Edited by admin on Mon Mar 31 17:33:01 GMT 2025
PRIMARY
MERCK INDEX
m2370
Created by admin on Mon Mar 31 17:33:01 GMT 2025 , Edited by admin on Mon Mar 31 17:33:01 GMT 2025
PRIMARY Merck Index
SMS_ID
100000077159
Created by admin on Mon Mar 31 17:33:01 GMT 2025 , Edited by admin on Mon Mar 31 17:33:01 GMT 2025
PRIMARY
CHEBI
41308
Created by admin on Mon Mar 31 17:33:01 GMT 2025 , Edited by admin on Mon Mar 31 17:33:01 GMT 2025
PRIMARY
FDA UNII
701M4TTV9O
Created by admin on Mon Mar 31 17:33:01 GMT 2025 , Edited by admin on Mon Mar 31 17:33:01 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-337-6
Created by admin on Mon Mar 31 17:33:01 GMT 2025 , Edited by admin on Mon Mar 31 17:33:01 GMT 2025
PRIMARY
DRUG BANK
DB01878
Created by admin on Mon Mar 31 17:33:01 GMT 2025 , Edited by admin on Mon Mar 31 17:33:01 GMT 2025
PRIMARY
RXCUI
18997
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PRIMARY RxNorm
MESH
C047723
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PRIMARY
DAILYMED
701M4TTV9O
Created by admin on Mon Mar 31 17:33:01 GMT 2025 , Edited by admin on Mon Mar 31 17:33:01 GMT 2025
PRIMARY
JECFA MONOGRAPH
745
Created by admin on Mon Mar 31 17:33:01 GMT 2025 , Edited by admin on Mon Mar 31 17:33:01 GMT 2025
PRIMARY
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