149187
Phenyl salicylate
ReagentPlus®, 99%
Synonym(s):
Salol
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About This Item
Linear Formula:
2-(HO)C6H4CO2C6H5
CAS Number:
Molecular Weight:
214.22
Beilstein:
393969
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23
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Quality Level
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
Signal Word
Warning
Hazard Statements
Precautionary Statements
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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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)
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)
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)
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
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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