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Merck

W396001

Phenyl salicylate

≥99%, FG

Synonym(s):

Salol

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About This Item

Linear Formula:
2-(HO)C6H4CO2C6H5
CAS Number:
Molecular Weight:
214.22
Flavis number:
9.689
PubChem Substance ID:
UNSPSC Code:
12164502
FEMA Number:
3960
NACRES:
NA.21
EC Number:
204-259-2
MDL number:
Beilstein/REAXYS Number:
393969
Organoleptic:
fruity; sweet
Grade:
FG
Biological source:
synthetic
Agency:
meets purity specifications of JECFA
Food allergen:
no known allergens
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InChI key

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

SMILES string

Oc1ccccc1C(=O)Oc2ccccc2

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.)

Quality Level

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

fruity; sweet

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Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


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P T Deota et al.
Natural product research, 17(1), 21-26 (2003-04-04)
The effect of photostabilization of azadirachtin-A (Aza-A) was examined in solutions when exposed to UV radiation, in the presence of four structurally different UV absorbers namely, p-aminobenzoic acid, 2,4-dihydroxybenzophenone, 4,4'-dihydroxybenzophenone and phenyl salicylate. The percentages of Aza-A recovered from the
C D Calnan et al.
Contact dermatitis, 7(4), 208-211 (1981-07-01)
Six cases of contact dermatitis from a lip salve are described. Five were allergic to phenyl salicylate and one to geraniol in the fragrance. The dermatitis spread in a ring around the mouth. Phenyl salicylate has been removed from the
Cross-sensitivity between resorcinol, resorcinol monobenzoate and phenyl salicylate.
M Nakagawa et al.
Contact dermatitis, 27(3), 199-200 (1992-09-01)
D P Krickau et al.
International journal of pharmaceutics, 342(1-2), 62-71 (2007-06-29)
To investigate the influence of the interfacial area and the emulsifier lecithin on the degradation rate of drugs prone to hydrolysis in parenteral lipid O/W emulsions we measured the degradation kinetics of phenyl salicylate in systems consisting of Miglyol as
J Baran et al.
Physical review. E, Statistical, nonlinear, and soft matter physics, 81(3 Pt 1), 031503-031503 (2010-04-07)
We report the investigation of glass-forming salol upon different courses of the temperature changes from liquid to glass state and back using FT-IR spectroscopy measurements in the wide spectral and temperature ranges. The formation of the ordered clusters in supercooled

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