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Merck
CN

W396001

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
Flavis number:
9.689
PubChem Substance ID:
24901954
UNSPSC Code:
12164502
FEMA Number:
3960
NACRES:
NA.21
EC Number:
204-259-2
MDL number:
MFCD00002213
Beilstein/REAXYS Number:
393969
Organoleptic:
fruity; sweet
Grade:
FG
Biological source:
synthetic
Agency:
meets purity specifications of JECFA
Food allergen:
no known allergens

Key Documents

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biological source

synthetic

Quality Level

300, 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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Related Categories

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

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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Certificates of Analysis (COA)

Lot/Batch Number
SHBT0394
SHBS7083
SHBR2052
SHBQ8590
SHBQ2354

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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
Contact dermatitis from phenyl salicylate in a galenic cream.
M Fimiani et al.
Contact dermatitis, 22(4), 239-239 (1990-04-01)
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
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
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Global Trade Item Number

SKUGTIN
W396001-5KG04061835516537
W396001-1KG04061837608292
W396001-SAMPLE04061837608308

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