P1001
Phenoxyacetic acid
~99%
Synonym(s):
Glycolic acid phenyl ether
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About This Item
Linear Formula:
C6H5OCH2CO2H
CAS Number:
Molecular Weight:
152.15
Beilstein/REAXYS Number:
907949
EC Number:
MDL number:
UNSPSC Code:
12352103
Recommended Products
assay
~99%
mp
98-100 °C (lit.)
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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Description
Pricing
signalword
Warning
hcodes
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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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.
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
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.
Giuseppe Fracchiolla et al.
ChemMedChem, 2(5), 641-654 (2007-03-16)
Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors that govern lipid and glucose homeostasis, and play a central role in cardiovascular disease, obesity, and diabetes. Thus, there is significant interest in developing new and specific agonists for these receptors. Herein
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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