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Key Documents

34366

Supelco

Phenoxyacetic acid

PESTANAL®, analytical standard

Synonym(s):

Glycolic acid phenyl ether

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About This Item

Linear Formula:
C6H5OCH2CO2H
CAS Number:
Molecular Weight:
152.15
Beilstein:
907949
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

98-100 °C (lit.)

application(s)

agriculture
cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

format

neat

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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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Legal Information

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

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Guan-Sheng Jiao et al.
Bioorganic & medicinal chemistry letters, 22(6), 2242-2246 (2012-02-22)
Four core structures capable of providing sub-nanomolar inhibitors of anthrax lethal factor (LF) were evaluated by comparing the potential for toxicity, physicochemical properties, in vitro ADME profiles, and relative efficacy in a rat lethal toxin (LT) model of LF intoxication.
Katarzyna Ignatowicz
Journal of hazardous materials, 169(1-3), 953-957 (2009-05-19)
This paper presents research on phenoxyacid pesticides removal using sorption methods on activated carbons. It was noted, that physico-chemical properties of adsorbent and adsorbate as well as parameters of the process have influence on adsorption of pesticides, derivatives of phenoxyacetic
Maria G Margariti et al.
Therapeutic drug monitoring, 29(2), 150-163 (2007-04-10)
Extensive use of synthetic pesticides for agricultural and nonagricultural purposes began in the past 50 years. As a result of their wide and extensive application, exposure to hazardous pesticides is a concern to the general population and occupationally exposed persons.
Ming-Kung Yeh et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 27(1), 49-54 (2011-01-15)
Dynamic liquid-liquid-liquid microextraction coupled with ion-pair liquid chromatography (IP-LC) and photodiode array detection was developed and used for the extraction and analysis of chlorinated phenoxyacetic acids (CPAs) and chlorophenols (CPs) from water samples. An organic extraction solvent mixture was chosen
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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