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Details

Stereochemistry MIXED
Molecular Formula C16H22O3
Molecular Weight 262.3441
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HOMOSALATE

SMILES

CC1CC(CC(C)(C)C1)OC(=O)C2=C(O)C=CC=C2

InChI

InChIKey=WSSJONWNBBTCMG-UHFFFAOYSA-N
InChI=1S/C16H22O3/c1-11-8-12(10-16(2,3)9-11)19-15(18)13-6-4-5-7-14(13)17/h4-7,11-12,17H,8-10H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C16H22O3
Molecular Weight 262.3441
Charge 0
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: http://www.fda.gov/downloads/ForConsumers/ConsumerUpdates/UCM258718.pdf

Homosalate is used as a broad-band UV filter in concentrations of up to 10% in the EU or 15% depending upon where the product is used (e.g. in the USA) in sunscreen products alone or in combination with other UV absorbers to protect the skin against harmful effects of the UV radiation.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Preventing
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Korean women: breast cancer knowledge, attitudes and behaviors.
2001
Determination of the UV filters worldwide authorised in sunscreens by high-performance liquid chromatography. Use of cyclodextrins as mobile phase modifier.
2001 Jul 6
In vitro and in vivo estrogenicity of UV screens.
2001 Mar
Determination of sixteen UV filters in suncare formulations by high-performance liquid chromatography.
2004 Sep 17
Influence of anatomical site and topical formulation on skin penetration of sunscreens.
2005 Sep
3,3,5-Trimethylcyclohexanols and derived esters: green synthetic procedures, odour evaluation and in vitro skin cytotoxicity assays.
2006 Dec
Design of a photostabilizer having built-in antioxidant functionality and its utility in obtaining broad-spectrum sunscreen formulations.
2006 May-Jun
Quercetin and rutin as potential sunscreen agents: determination of efficacy by an in vitro method.
2008 Jun
Non-porous membrane-assisted liquid-liquid extraction of UV filter compounds from water samples.
2009 Jun 12
On-line renewable solid-phase extraction hyphenated to liquid chromatography for the determination of UV filters using bead injection and multisyringe-lab-on-valve approach.
2010 May 28
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 Oct 1
FDA-approved drugs and other compounds tested as inhibitors of human glutathione transferase P1-1.
2013 Sep 5
Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: 30 min after application the remaining product was removed from the skin with two dry cotton swabs and the skin was tape-stripped 16 times with D-Squames. The total amount of UV filters penetrating into the stratum corneum (strips 2–16) from the emulsion gel formulation was 25.7+/-6.4 ug/cm2 (23.2 % applied dose). The total amount of UV filters penetrating from the petroleum formulation was 8.3+/-3.6 ug/cm2 (9.0 % applied dose).
2 mg/cm2 Homosalate was applied to area (2x2 cm) on the volar side of the forearm.
Route of Administration: Other
In Vitro Use Guide
Human full-thickness skin was mounted in a conventional static Franz diffusion cells with a receptor volume of 12.4 ml. The UV filters were readily soluble in the receptor fluid. Epidermis and dermis separated by the hot plate method (60°C for 2 min) and punch biopsies (8 mm) from the tissue samples were taken. Homosalate did not permeate through the skin after 6 h application.
Substance Class Chemical
Created
by admin
on Sun Dec 18 18:28:28 UTC 2022
Edited
by admin
on Sun Dec 18 18:28:28 UTC 2022
Record UNII
V06SV4M95S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HOMOSALATE
INCI   INN   MART.   MI   USAN   USP   USP-RS   VANDF   WHO-DD  
USAN   INN   INCI  
Official Name English
HOMOSALATE [USP MONOGRAPH]
Common Name English
HOMOMENTHYL SALICYLATE
Common Name English
HOMOSALATE [INCI]
Common Name English
3,3,5-Trimethylcyclohexyl salicylate
Systematic Name English
HOMOSALATE [MART.]
Common Name English
Homosalate [WHO-DD]
Common Name English
HOMOSALATE [MI]
Common Name English
2-HYDROXYBENZOIC ACID 3,3,5-TRIMETHYLCYCLOHEXYL ESTER
Systematic Name English
NSC-164918
Code English
EUSOLEX
Brand Name English
homosalate [INN]
Common Name English
HOMOSALATE [USP-RS]
Common Name English
HOMOSALATE [USAN]
Common Name English
BENZOIC ACID, 2-HYDROXY-, 3,3,5-TRIMETHYLCYCLOHEXYL ESTER
Common Name English
HOMOSALATE [USP IMPURITY]
Common Name English
SALICYLIC ACID 3,3,5-TRIMETHYLCYCLOHEXYL ESTER
Systematic Name English
Classification Tree Code System Code
CFR 21 CFR 352.10
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
CFR 21 CFR 352.20
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
EPA PESTICIDE CODE 76603
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
NCI_THESAURUS C851
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
Code System Code Type Description
INN
3183
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
PRIMARY
MESH
C060446
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
PRIMARY
NCI_THESAURUS
C83760
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
PRIMARY
ECHA (EC/EINECS)
204-260-8
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
PRIMARY
EPA CompTox
DTXSID1026241
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
PRIMARY
ChEMBL
CHEMBL1377575
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
PRIMARY
RXCUI
91326
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
PRIMARY RxNorm
RS_ITEM_NUM
1311408
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
PRIMARY
DAILYMED
V06SV4M95S
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
PRIMARY
NSC
164918
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
PRIMARY
DRUG BANK
DB11064
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
PRIMARY
WIKIPEDIA
HOMOSALATE
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
PRIMARY
USAN
KK-99
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
PRIMARY
EVMPD
SUB08053MIG
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
PRIMARY
PUBCHEM
8362
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
PRIMARY
CAS
118-56-9
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
PRIMARY
MERCK INDEX
M6047
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
PRIMARY Merck Index
DRUG CENTRAL
3279
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
PRIMARY
FDA UNII
V06SV4M95S
Created by admin on Sun Dec 18 18:28:28 UTC 2022 , Edited by admin on Sun Dec 18 18:28:28 UTC 2022
PRIMARY
Related Record Type Details
ACTIVE MOIETY