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158518

Sigma-Aldrich

Phenoxyacetic acid

98%

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Synonym(s):
Glycolic acid phenyl ether
Linear Formula:
C6H5OCH2CO2H
CAS Number:
Molecular Weight:
152.15
Beilstein/REAXYS Number:
907949
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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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1 of 4

This Item
24238134366240834
Phenoxyacetic acid 98%

158518

Phenoxyacetic acid

Benzoic acid ACS reagent, ≥99.5%

242381

Benzoic acid

Phenoxyacetic acid PESTANAL®, analytical standard

34366

Phenoxyacetic acid

Diphenyl ether ReagentPlus®, ≥99%

240834

Diphenyl ether

solubility

ethanol: soluble 10%, clear, colorless

solubility

water: soluble (2.9 g/l at 25 °C)

solubility

-

solubility

alcohol: soluble(lit.), benzene: soluble(lit.), diethyl ether: soluble(lit.), glacial acetic acid: soluble(lit.), water: insoluble(lit.)

form

solid

form

crystalline

form

-

form

crystalline

mp

98-100 °C (lit.)

mp

121-125 °C (lit.)

mp

98-100 °C (lit.)

mp

25-27 °C (lit.)

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

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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Selective separation of penicillin V from phenoxyacetic acid using liquid membranes.
Cascaval D, et al.
Biochemical Engineering Journal, 55(1), 45-50 (2000)
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)
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
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
Huiting Zhang et al.
Bioorganic & medicinal chemistry, 15(18), 6089-6095 (2007-07-07)
Molecular imprinted polymers (MIPs) binding with phenoxyacetic acid (PA) as a dummy template molecule were synthesized via thermal initiation in aqueous medium. The retention behaviors of benzoic acid (BA), PA, 2-methyl-4-chlorophenoxyacetic acid (MCPA), 4-chlorophenoxyacetic acid (4-CPA), and 2,4-dichlorophenoxyacetic acid (2,4-D)

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