V900578
Phenyl salicylate
Vetec™, reagent grade, 98%
Synonym(s):
Salol
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About This Item
Linear Formula:
2-(HO)C6H4CO2C6H5
CAS Number:
Molecular Weight:
214.22
EC Number:
204-259-2
UNSPSC Code:
12352103
PubChem Substance ID:
Beilstein/REAXYS Number:
393969
MDL number:
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
grade
reagent grade
product line
Vetec™
assay
98%
form
liquid crystal
bp
172-173 °C/12 mmHg (lit.)
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Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
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
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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
Contact dermatitis from phenyl salicylate in a galenic cream.
M Fimiani et al.
Contact dermatitis, 22(4), 239-239 (1990-04-01)
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
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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