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W396001

Sigma-Aldrich

Phenyl salicylate

≥99%, FG

Synonym(s):

Salol

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About This Item

Linear Formula:
2-(HO)C6H4CO2C6H5
CAS Number:
118-55-8
Molecular Weight:
214.22
FEMA Number:
3960
Beilstein:
393969
EC Number:
204-259-2
MDL number:
MFCD00002213
UNSPSC Code:
12164502
PubChem Substance ID:
24901954
Flavis number:
9.689
NACRES:
NA.21

biological source

synthetic

grade

FG

Agency

meets purity specifications of JECFA

reg. compliance

EU Regulation 1334/2008 & 872/2012
FDA 21 CFR 110

Assay

≥99%

bp

172-173 °C/12 mmHg (lit.)

mp

41-43 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

Organoleptic

fruity; sweet

SMILES string

Oc1ccccc1C(=O)Oc2ccccc2

InChI

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

InChI key

ZQBAKBUEJOMQEX-UHFFFAOYSA-N

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Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H315,H317,H319,H411

Hazard Classifications

Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Contact dermatitis from phenyl salicylate in a galenic cream.
M Fimiani et al.
Contact dermatitis, 22(4), 239-239 (1990-04-01)
M Niyaz Khan
Advances in colloid and interface science, 159(2), 160-179 (2010-08-03)
A new method, based upon semi-empirical kinetic approach, for the determination of ion exchange constant for ion exchange processes occurring between counterions at the cationic micellar surface is described in this review article. Basically, the method involves a reaction kinetic
K Inoue et al.
Toxicology letters, 7(3), 211-215 (1981-01-01)
The in vitro carcinogenic activities of 3-(N-salicyloyl)amino-1,2,4-triazole (SAT) and its two components, 3-amino-1,2,4-triazole and phenyl salicylate were examined in a transformation assay with cryopreserved hamster embryo cells. SAT induced morphological transformation at certain doses between 10 microgram/ml and 100 microgram/ml
M Paulí et al.
Acta odontologica latinoamericana : AOL, 10(1), 1-9 (1997-01-01)
The mutans group of streptococci is considered to play a key role in the etiology of dental caries. We have evaluated the ability of different substances to prevent dental plaque formation without affecting Streptococcus sobrinus viability. Viable organisms were detected
H Lygre et al.
Acta odontologica Scandinavica, 53(6), 397-401 (1995-12-01)
The aromatic compounds phenyl benzoate (PB), phenyl salicylate (PS), and biphenyl (BP), which have previously been found to leach from poly(methyl methacrylate) denture base materials, were tested for cytotoxicity and biologic effects by L929 cells in culture. The octanol-water partition
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