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197777

Sigma-Aldrich

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:
882-09-7
Molecular Weight:
214.65
EC Number:
212-925-9
MDL number:
MFCD00004192
UNSPSC Code:
12352100
PubChem Substance ID:
24851846
NACRES:
NA.22

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

human ... PPARA(5465) , PPARG(5468)
mouse ... Ppara(19013) , Pparg(19016)

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Hazard Classifications

Acute Tox. 4 Oral

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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Certificates of Analysis (COA)

Lot/Batch Number
STBC3913V
05019CJ
01220BT
S26379
0316BL

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Sigma-Aldrich

L1376

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Sigma-Aldrich

O1008

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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
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
Chao-meng Dai et al.
Environmental science and pollution research international, 20(8), 5492-5501 (2013-02-26)
A novel double templates-molecularly imprinted polymer (MIP) was prepared by precipitation polymerization using carbamazepine (CBZ) and clofibric acid (CA) as the double templates molecular and 2-vinylpyridine as functional monomer. The equilibrium data of MIP was well described by the Freundlich
Julia Martín et al.
Journal of environmental management, 102, 18-25 (2012-03-20)
In this work, the distribution and the ecotoxicological risk of sixteen pharmaceutically active compounds belonging to seven different therapeutic groups (five anti-inflammatory drugs, two antibiotics, an anti-epileptic drug, a β-blocker, a nervous stimulant, four estrogens and two lipid regulators) have
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
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