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Merck

197777

2-(p-Chlorophenoxy)-2-methylpropionic acid

97%

Synonym(s):

α-(p-Chlorophenoxy)isobutyric acid, Clofibric acid

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About This Item

Linear Formula:
ClC6H4OC(CH3)2CO2H
CAS Number:
Molecular Weight:
214.65
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
212-925-9
MDL number:
Assay:
97%
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Quality Level

assay

97%

mp

120-122 °C (lit.)

functional group

carboxylic acid, chloro

SMILES string

CC(C)(Oc1ccc(Cl)cc1)C(O)=O

InChI

1S/C10H11ClO3/c1-10(2,9(12)13)14-8-5-3-7(11)4-6-8/h3-6H,1-2H3,(H,12,13)

InChI key

TXCGAZHTZHNUAI-UHFFFAOYSA-N

Gene Information



pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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R Salgado et al.
Journal of hazardous materials, 241-242, 182-189 (2012-10-16)
Clofibric acid (CLF) is the pharmaceutically active metabolite of lipid regulators clofibrate, etofibrate and etofyllinclofibrate, and it is considered both environmentally persistent and refractory. This work studied the biotransformation of CLF in aerobic sequencing batch reactors (SBRs) with mixed microbial
K Sumida et al.
Chemosphere, 33(11), 2201-2207 (1996-12-01)
Peroxisome proliferators are generally known as activators of fatty acid beta-oxidation which is one of degradation pathways. However, since it is unknown whether peroxisome proliferators have an effect on biosynthesis of fatty acid or not, we commenced to study if
Dong Qing Zhang et al.
Environmental pollution (Barking, Essex : 1987), 167, 124-131 (2012-05-09)
This study evaluated the effect of continuous and batch feeding on the removal of 8 pharmaceuticals (carbamazepine, naproxen, diclofenac, ibuprofen, caffeine, salicylic acid, ketoprofen and clofibric acid) from synthetic wastewater in mesocosm-scale constructed wetlands (CWs). Both loading modes were operated