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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
Organoleptic:
fruity; sweet
grade:
FG
biological source:
synthetic
Agency:
meets purity specifications of JECFA
food allergen:
no known allergens

biological source

synthetic

Quality Level

400

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

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Certificates of Analysis (COA)

Lot/Batch Number
SHBR2052
SHBQ8590
SHBQ2354
SHBN2207
SHBM3413

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Karel Waisser et al.
Ceska a Slovenska farmacie : casopis Ceske farmaceuticke spolecnosti a Slovenske farmaceuticke spolecnosti, 61(6), 282-284 (2013-02-08)
Antimycobacterial activity of phenyl salicylates (salols) was studied in connection with antituberculotic activity of salicylic derivatives. Phenyl salicylates are esters. Our attention was previously oriented on amides. Phenyl salicylates (salols) represent a new group of antimycobacterial compounds. They are less
N Miyatake et al.
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 116(1), 65-70 (1996-01-01)
The stability and degradation pathways of phenyl salicylate (PS) in 50 v/v% aqueous ethanol were investigated over the pH range of 3.2-8.4. The experiments were performed at three different temperatures (5, 23 and 50 degrees C) for four months by
Olga Trofymluk et al.
The Journal of chemical physics, 123(19), 194509-194509 (2005-12-03)
Mesoporous silica phases, with uniform pores of dimensions in the 2-30 nm range, offer a uniquely well-defined environment for the study of the effects of two-dimensional spatial confinement on the properties of glass-forming liquids. We report observations by differential scanning
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
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