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Details

Stereochemistry ACHIRAL
Molecular Formula C13H10O3
Molecular Weight 214.2167
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHENYL SALICYLATE

SMILES

OC1=CC=CC=C1C(=O)OC2=CC=CC=C2

InChI

InChIKey=ZQBAKBUEJOMQEX-UHFFFAOYSA-N
InChI=1S/C13H10O3/c14-12-9-5-4-8-11(12)13(15)16-10-6-2-1-3-7-10/h1-9,14H

HIDE SMILES / InChI
Molecular Formula C13H10O3
Molecular Weight 214.2167
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 based on several sources, including http://www.ncbi.nlm.nih.gov/pubmed/23387858

Phenyl salicylate belongs to the family of hydroxybenzoic acid derivatives. Phenyl salicylate is used as a food additive. Antimycobacterial activity of phenyl salicylates (salols) was studied in connection with antituberculotic activity of salicylic derivatives. Phenyl salicylates are esters. Phenyl salicylates (salols) represent a new group of antimycobacterial compounds. Phenyl salicylate is included in the number of medications, indicated for the treatment of symptoms of irritative voiding, used to relieve the discomfort, pain, frequent urge to urinate, and cramps/spasms of the urinary tract caused by an infection or a medical procedure. Phenyl salicylate works as a pain reliever in these combinations.

Originator

Approval Year

1921
1468
Targets

Targets

Primary TargetPharmacologyConditionPotency
Agonist
2752
 49.78 µM [EC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Approved
8583
PROSED EC

Approved Use

PROSED EC is indicated for the relief of discomfort of the lower urinary tract caused by hypermotility resulting from inflammation or diagnostic procedures and in the treatment of cystitis, urethritis and trigonitis when caused by organisms which maintain or produce an acid urine and are susceptible to formaldehyde.
PubMed

PubMed

TitleDatePubMed
Simultaneous determination of the UV-filters benzyl salicylate, phenyl salicylate, octyl salicylate, homosalate, 3-(4-methylbenzylidene) camphor and 3-benzylidene camphor in human placental tissue by LC-MS/MS. Assessment of their in vitro endocrine activity.
2013-10-01
The estrogenic potential of salicylate esters and their possible risks in foods and cosmetics.
2012-03-07
Phenyl 3,5-di-tert-butyl-2-hy-droxy-benzoate.
2010-11-24
A new semi-empirical kinetic method for the determination of ion exchange constants for the counterions of cationic micelles.
2010-09-15
Determination of an ion exchange constant by the use of a kinetic probe: a new semiempirical kinetic approach involving the effects of 3-F- and 4-F-substituted benzoates on the rate of piperidinolysis of anionic phenyl salicylate in aqueous cationic micelles.
2010-07-06
The role of nucleation in vitrification of supercooled liquids.
2010-04-21
Infrared spectroscopy study of structural changes in glass-forming salol.
2010-03
Kinetic evidence for the occurrence of independent ion-exchange processes in the cationic micellar-mediated reaction of piperidine with anionic phenyl salicylate.
2009-06-11
The temperature dependence of free volume in phenyl salicylate and its relation to structural dynamics: a positron annihilation lifetime and pressure-volume-temperature study.
2009-04-14
A direct test of the correlation between elastic parameters and fragility of ten glass formers and their relationship to elastic models of the glass transition.
2009-02-14
Mass spectrometric identification of covalent adducts of the skin allergen 2,4-dinitro-1-chlorobenzene and model skin proteins.
2008-08
Degradation kinetics of hydrolytically susceptible drugs in O/W emulsions--effects of interfacial area and lecithin.
2007-09-05
Investigating protein haptenation mechanisms of skin sensitisers using human serum albumin as a model protein.
2007-06
Fragrance material review on phenyl salicylate.
2007
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Depolarized light scattering versus optical Kerr effect spectroscopy of supercooled liquids: comparative analysis.
2006-09-21
Pharmaceutical quality control of acid and neutral drugs based on competitive self-assembly in amphiphilic systems.
2006-01
Interfacial effects on vitrification of confined glass-forming liquids.
2005-11-15
Oxidation of anthracyclines by peroxidase metabolites of salicylic Acid.
2005-10
Viscosity at the dynamic crossover in o-terphenyl and salol under high pressure.
2004-06-18
Lobatamide C: total synthesis, stereochemical assignment, preparation of simplified analogues, and V-ATPase inhibition studies.
2003-07-02
Effect of ultraviolet light absorbers on photostabilization of azadirachtin-A in solution (part: II).
2003-01
Effect of some ultraviolet light absorbers on photo-stabilization of azadirachtin-A.
2002-10
Synthesis and V-ATPase inhibition of simplified lobatamide analogues.
2002-09-05
Estrogenic activity of phenolic additives determined by an in vitro yeast bioassay.
2001-02
Patents

Patents

JP2000044925A
2
JP2000159880A
1
JP2000159963A
1
JPH0328248A
2
JPH06166602A
1
JPH07177826A
1
JPS56118424A
1
JPS59206452A
2
JPS5951232A
1
JPS61115950A
1

Sample Use Guides

In Vivo Use Guide
One tablet of PROSED EC orally 4 times per day followed by liberal fluid intake. Each tablet of PROSED EC contains: Phenyl Salicylate 36.2 mg
Route of Administration: Oral
In Vitro Use Guide
Phenyl Salicylate at 10 uM increased the number of MCF-7 cells by approximately 1.8 fold
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:35:41 GMT 2025
Edited
by admin
on Mon Mar 31 18:35:41 GMT 2025
Record UNII
28A37T47QO
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PHENYL SALICYLATE
FHFI   INCI   MI   VANDF   WHO-DD  
INCI  
Official Name English
SALOL
HPUS   MART.   VANDF  
Preferred Name English
PHENYL SALICYLATE [VANDF]
Common Name English
PHENYL SALICYLATE [USP-RS]
Common Name English
Phenyl salicylate [WHO-DD]
Common Name English
FEMA NO. 3960
Code English
PHENYL SALICYLATE MELTING POINT STANDARD
USP-RS  
Common Name English
SALOL [HPUS]
Common Name English
PHENYL SALICYLATE [FHFI]
Common Name English
PHENYL SALICYLATE [MI]
Common Name English
NSC-33406
Code English
SALOL [MART.]
Common Name English
SALOL [VANDF]
Common Name English
Classification Tree Code System Code
JECFA EVALUATION PHENYL SALICYLATE
Created by admin on Mon Mar 31 18:35:41 GMT 2025 , Edited by admin on Mon Mar 31 18:35:41 GMT 2025
WHO-VATC QG04BX12
Created by admin on Mon Mar 31 18:35:41 GMT 2025 , Edited by admin on Mon Mar 31 18:35:41 GMT 2025
WHO-ATC G04BX12
Created by admin on Mon Mar 31 18:35:41 GMT 2025 , Edited by admin on Mon Mar 31 18:35:41 GMT 2025
NCI_THESAURUS C2356
Created by admin on Mon Mar 31 18:35:41 GMT 2025 , Edited by admin on Mon Mar 31 18:35:41 GMT 2025
Code System Code Type Description
NCI_THESAURUS
C75079
Created by admin on Mon Mar 31 18:35:41 GMT 2025 , Edited by admin on Mon Mar 31 18:35:41 GMT 2025
PRIMARY
EPA CompTox
DTXSID6021957
Created by admin on Mon Mar 31 18:35:41 GMT 2025 , Edited by admin on Mon Mar 31 18:35:41 GMT 2025
PRIMARY
MERCK INDEX
m8690
Created by admin on Mon Mar 31 18:35:41 GMT 2025 , Edited by admin on Mon Mar 31 18:35:41 GMT 2025
PRIMARY Merck Index
JECFA MONOGRAPH
607
Created by admin on Mon Mar 31 18:35:41 GMT 2025 , Edited by admin on Mon Mar 31 18:35:41 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-259-2
Created by admin on Mon Mar 31 18:35:41 GMT 2025 , Edited by admin on Mon Mar 31 18:35:41 GMT 2025
PRIMARY
WIKIPEDIA
PHENYL SALICYLATE
Created by admin on Mon Mar 31 18:35:41 GMT 2025 , Edited by admin on Mon Mar 31 18:35:41 GMT 2025
PRIMARY
RS_ITEM_NUM
1534209
Created by admin on Mon Mar 31 18:35:41 GMT 2025 , Edited by admin on Mon Mar 31 18:35:41 GMT 2025
PRIMARY
DAILYMED
28A37T47QO
Created by admin on Mon Mar 31 18:35:41 GMT 2025 , Edited by admin on Mon Mar 31 18:35:41 GMT 2025
PRIMARY
ChEMBL
CHEMBL1339216
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PRIMARY
RXCUI
895808
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ALTERNATIVE
MESH
C026041
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PRIMARY
CHEBI
34918
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PRIMARY
DRUG CENTRAL
3462
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PRIMARY
EVMPD
SUB14839MIG
Created by admin on Mon Mar 31 18:35:41 GMT 2025 , Edited by admin on Mon Mar 31 18:35:41 GMT 2025
PRIMARY
FDA UNII
28A37T47QO
Created by admin on Mon Mar 31 18:35:41 GMT 2025 , Edited by admin on Mon Mar 31 18:35:41 GMT 2025
PRIMARY
RXCUI
36122
Created by admin on Mon Mar 31 18:35:41 GMT 2025 , Edited by admin on Mon Mar 31 18:35:41 GMT 2025
PRIMARY
DRUG BANK
DB11071
Created by admin on Mon Mar 31 18:35:41 GMT 2025 , Edited by admin on Mon Mar 31 18:35:41 GMT 2025
PRIMARY
PUBCHEM
8361
Created by admin on Mon Mar 31 18:35:41 GMT 2025 , Edited by admin on Mon Mar 31 18:35:41 GMT 2025
PRIMARY
CAS
118-55-8
Created by admin on Mon Mar 31 18:35:41 GMT 2025 , Edited by admin on Mon Mar 31 18:35:41 GMT 2025
PRIMARY
SMS_ID
100000079433
Created by admin on Mon Mar 31 18:35:41 GMT 2025 , Edited by admin on Mon Mar 31 18:35:41 GMT 2025
PRIMARY
NSC
33406
Created by admin on Mon Mar 31 18:35:41 GMT 2025 , Edited by admin on Mon Mar 31 18:35:41 GMT 2025
PRIMARY
Related Record Type Details
Structure of PHENYL SALICYLATE
ACTIVE MOIETY
NIH
NCATS
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