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2-(4-Chlorophenoxy)-2-methylpropionic acid

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2-(4-Chlorophenoxy)-2-methylpropionic acid manufacturers

  • Clofibric acid
  • Clofibric acid pictures
  • $43.00
  • 2026-08-11
  • CAS:882-09-7
  • Purity: 99.97%
  • Supply Ability: 10g
2-(4-Chlorophenoxy)-2-methylpropionic acid Basic information
Product Name:2-(4-Chlorophenoxy)-2-methylpropionic acid
Synonyms:4-Chorophenoxy-d-methylpropionicacid;4-CPIB;Chlorobenzene oxygenisobutyrate;Acetic acid, (p-chlorop;Prestwick_39;2-(4-Chlorophe;Acetic acid, (p-chlorophenoxy)dimethyl-;Acide (p-chlorophenoxy)-2 methyl-2 propionique
CAS:882-09-7
MF:C10H11ClO3
MW:214.65
EINECS:212-925-9
Product Categories:Organic acids;Aromatics Compounds;Intracellular receptor;Acids and Derivatives;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals;CLOFIBRIN;882-09-7
Mol File:882-09-7.mol
2-(4-Chlorophenoxy)-2-methylpropionic acid Structure
2-(4-Chlorophenoxy)-2-methylpropionic acid Chemical Properties
Melting point 120-122 °C(lit.)
Boiling point 308.11°C (rough estimate)
density 1.2413 (rough estimate)
refractive index 1.5220 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility Chloroform, Methanol
form Crystals or Crystalline Powder
pka3.18±0.10(Predicted)
color Pale yellow to brownish
Merck 14,2378
BRN 1874067
InChI1S/C10H11ClO3/c1-10(2,9(12)13)14-8-5-3-7(11)4-6-8/h3-6H,1-2H3,(H,12,13)
InChIKeyTXCGAZHTZHNUAI-UHFFFAOYSA-N
SMILESCC(C)(Oc1ccc(Cl)cc1)C(O)=O
CAS DataBase Reference882-09-7(CAS DataBase Reference)
NIST Chemistry ReferenceClofibric acid(882-09-7)
EPA Substance Registry SystemPropanoic acid, 2-(4-chlorophenoxy)-2-methyl- (882-09-7)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-20/21/22
Safety Statements 36-24/25
WGK Germany 3
RTECS UE9455000
HazardClass IRRITANT
HS Code 29189900
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
2-(4-Chlorophenoxy)-2-methylpropionic acid Usage And Synthesis
DescriptionClofibric acid is a peroxisome proliferator-activated receptor α (PPARα) agonist (EC50 = 50 μM in a transactivation assay) and the active metabolite of clofibrate . It is formed from clofibrate by tissue and serum esterases. Dietary administration of clofibric acid (0.067-0.22%) reduces serum cholesterol, phospholipid, and triglyceride levels in rats. It decreases glutamate oxaloacetate transaminase (GOT) levels and increases glutamate pyruvate transaminase (GPT) and lactate dehydrogenase (LDH) levels, markers of xenobiotic stress, in the plasma of carp (C. carpio) when administered in tank water at a concentration of 10 μg/L. Clofibric acid has been found in wastewater effluent.
Chemical PropertiesPale Yellow Solid
UsesAntilipemic.
Usesherbicide, antihyperlipoproteinemic, antineoplastic
UsesA hypolipidemic compound
DefinitionChEBI: A monocarboxylic acid that is isobutyric acid substituted at position 2 by a p-chlorophenoxy group. It is a metabolite of the drug clofibrate.
Biological ActivityPPAR agonist. Antihyperlipoproteinemic.
Mechanism of actionAuxin-transport inhibitor
Synthesis
Clofibrate

637-07-0

2-(4-Chlorophenoxy)-2-methylpropionic acid

882-09-7

Step 2: Synthesis of 2-(4-chlorophenoxy)-2-methylpropionic acid To a solution of ethyl 2-(4-chlorophenoxy)-2-methylpropionate (2.0 g, 8.24 mmol) in tetrahydrofuran (16 mL) was added sequentially water (4 mL) and lithium hydroxide monohydrate (0.69 g, 16.4 mmol) at room temperature. The reaction mixture was stirred at room temperature for 16 hours. After completion of the reaction, the mixture was diluted with water and washed with dichloromethane (DCM). The aqueous phase was separated and acidified with 1 M aqueous hydrochloric acid to pH about 2, followed by extraction with dichloromethane (DCM, 2 times). The organic extracts were combined, washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give 2-(4-chlorophenoxy)-2-methylpropionic acid (p-chlorophenoxyisobutyric acid) as a white solid (1.45 g, 82% yield). 1H NMR (400 MHz, chloroform-d): δ 1.62 (6H, s), 6.89 (2H, d, J = 9.0 Hz), 7.24 (2H, d, J = 9.0 Hz).

References[1] Journal of Medicinal Chemistry, 2017, vol. 60, # 2, p. 681 - 694
[2] Patent: WO2009/105509, 2009, A1. Location in patent: Page/Page column 36-37
[3] Journal of Pharmaceutical Sciences, 1980, vol. 69, # 1, p. 92 - 93
[4] Patent: WO2008/104994, 2008, A2. Location in patent: Page/Page column 32-33
[5] Patent: US2009/197959, 2009, A1. Location in patent: Page/Page column 18
Pesticide TypePlant Growth Regulator; Herbicide
Tag:2-(4-Chlorophenoxy)-2-methylpropionic acid(882-09-7) Related Product Information
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