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149187

Sigma-Aldrich

Phenyl salicylate

ReagentPlus®, 99%

Synonym(s):

Salol

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About This Item

Linear Formula:
2-(HO)C6H4CO2C6H5
CAS Number:
118-55-8
Molecular Weight:
214.22
Beilstein:
393969
EC Number:
204-259-2
MDL number:
MFCD00002213
UNSPSC Code:
12352103
PubChem Substance ID:
24848935
NACRES:
NA.23

Quality Level

200

product line

ReagentPlus®

Assay

99%

form

liquid crystal

bp

172-173 °C/12 mmHg (lit.)

mp

41-43 °C (lit.)

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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Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

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
SDBB0358
STBJ4367
STBH2467
STBH9235
STBH7641

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Short-time dynamics of glass-forming liquids: Phenyl salicylate (salol) in bulk liquid, dilute solution, and confining geometries
Kalampounias, A. G., et al.
J. Chem. Phys. , 118(18), 8340-8349 (2003)
Different Polymorphic Modifications of Phenyl Salicylate
Davydova, N. A., Melnik, V. I., Nesprava, V. V., & Reznichenko, V. Y.
Ukrainian Journal of Physics, 57(2), 140-144 (2012)
Application of phenyl salicylate-sepiolite systems as ultraviolet radiation filters
Hoyo, C. D., Vicente, M. A., & Rives, V.
Clay Minerals, 33(3), 467-474 (1998)
Cross-sensitivity between resorcinol, resorcinol monobenzoate and phenyl salicylate.
M Nakagawa et al.
Contact dermatitis, 27(3), 199-200 (1992-09-01)
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
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