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158518

Sigma-Aldrich

Phenoxyacetic acid

98%

Synonym(s):

Glycolic acid phenyl ether

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About This Item

Linear Formula:
C6H5OCH2CO2H
CAS Number:
122-59-8
Molecular Weight:
152.15
Beilstein/REAXYS Number:
907949
EC Number:
204-556-7
MDL number:
MFCD00004296
UNSPSC Code:
12352100
PubChem Substance ID:
24849763
NACRES:
NA.22

Quality Level

100

assay

98%

form

solid

mp

98-100 °C (lit.)

solubility

ethanol: soluble 10%, clear, colorless

SMILES string

OC(=O)COc1ccccc1

InChI

1S/C8H8O3/c9-8(10)6-11-7-4-2-1-3-5-7/h1-5H,6H2,(H,9,10)

InChI key

LCPDWSOZIOUXRV-UHFFFAOYSA-N

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General description

Phenoxyacetic acid is a herbicide and its photodegradation using TiO2 as photocatalyst has been studied. Selective separation of penicillin V from phenoxyacetic acid using liquid membranes consisting of 1,2-dichloroethane and Amberlite LA-2 as carrier has been studied.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Rudina Bleta et al.
Langmuir : the ACS journal of surfaces and colloids, 30(39), 11812-11822 (2014-09-16)
A series of mesoporous titania photocatalysts with tailorable structural and textural characteristics was prepared in aqueous phase via a colloidal self-assembly approach using various cyclodextrins (CDs) as structure-directing agents. The photocatalysts and the structure-directing agents were characterized at different stages
Photocatalyzed Degradation of Phenol, 2, 4-Dichlorophenol, Phenoxyacetic Acid and 2, 4-Dichlorophenoxyacetic Acid over SupportedTiO2 in a Flow System.
Trillas M, et al.
Journal of Chemical Technology and Biotechnology, 67(3), 237-242 (1996)
Selective separation of penicillin V from phenoxyacetic acid using liquid membranes.
Cascaval D, et al.
Biochemical Engineering Journal, 55(1), 45-50 (2000)
Charles Timchalk
Toxicology, 200(1), 1-19 (2004-05-26)
Phenoxyacetic acids including 2,4-dichlorophenoxyacetic acid (2,4-D) and 4-chloro-2-methylphenoxyacetic acid (MCPA) are widely utilized organic acid herbicides that have undergone extensive toxicity and pharmacokinetic analyses. The dog is particularly susceptible to the toxicity of phenoxyacetic acids and related organic acids relative
M Shahar Yar et al.
Journal of enzyme inhibition and medicinal chemistry, 24(3), 876-882 (2008-10-28)
Several substituted phenoxy acetic acid derived pyrazolines were synthesized by the reaction between 2-{4-[3-(2,4-dihydroxyphenyl)-3-oxo-1-propenyl]-2-methoxyphenoxy} acetic acid and substituted acid hydrazides and were tested for their in vitro cytotoxicity and antiviral activity. None of the compounds showed any specific antiviral activity
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