42017-89-0

  • Product Name:Fenofibric acid
  • Molecular Formula:C17H15ClO4
  • Purity:99%
  • Molecular Weight:318.757
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Product Details;

CasNo: 42017-89-0

Molecular Formula: C17H15ClO4

Appearance: white to off-white solid

Buy Reliable Quality Wholesale Fenofibric acid 42017-89-0 Cheapest Price

  • Molecular Formula:C17H15ClO4
  • Molecular Weight:318.757
  • Appearance/Colour:white to off-white solid 
  • Vapor Pressure:2.82E-10mmHg at 25°C 
  • Melting Point:177-179 °C 
  • Boiling Point:486.457 °C at 760 mmHg 
  • PKA:3.09±0.10(Predicted) 
  • Flash Point:248.001 °C 
  • PSA:63.60000 
  • Density:1.287 g/cm3 
  • LogP:3.81300 

Fenofibric acid(Cas 42017-89-0) Usage

Description

Fenofibric acid is a medication that effectively lowers triglyceride levels and increases good cholesterol levels in the blood. It is the active metabolite of fenofibrate. The compound works by enhancing the transcription of the ATP-binding cassette transporter A1 gene in a liver X receptor-dependent manner, thereby increasing Apolipoprotein A-I-mediated High-Density Lipoprotein (HDL) biogenesis.

Uses

This fibrate is prescribed to address severe hypertriglyceridemia, primary hypercholesterolemia, or mixed dyslipidemia. By reducing cholesterol and triglycerides, fenofibric acid plays a vital role in managing lipid levels and promoting cardiovascular health.

Definition

ChEBI: A monocarboxylic acid that is 2-methylpropanoic acid substituted by a 4-(4-chlorobenzoyl)phenoxy group at position 2. It is a metabolite of the drug fenofibrate.

Consumer Uses

ECHA has no public registered data indicating whether or in which chemical products the substance might be used. ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment.

InChI:InChI=1/C17H15ClO4/c1-17(2,16(20)21)22-14-9-5-12(6-10-14)15(19)11-3-7-13(18)8-4-11/h3-10H,1-2H3,(H,20,21)/p-1

42017-89-0 Relevant articles

Interesting morphological behavior of organic salt choline fenofibrate: Effect of supersaturation and polymeric impurity

Bordawekar, Shailendra,Kuvadia, Zubin,Dandekar, Preshit,Mukherjee, Samrat,Doherty, Michael

, p. 3800 - 3812 (2014)

Crystal habit of drug molecules can have...

Management of dyslipidemias with fibrates, alone and in combination with statins: role of delayed-release fenofibric acid

Elisavet Moutzouri,Anastazia Kei,Moses S Elisaf &Haralampos J Milionis

, Vascular Health and Risk Management Volume 6, 2010 - Issue

Fenofibrate is the most commonly used fibric acid derivative, exerts beneficial effects in several lipid and nonlipid parameters, and is considered the most suitable fibrate to combine with a statin. However, in clinical practice this combination raises concerns about safety. ABT-335 (fenofibric acid, Trilipix®) is the newest formulation designed to overcome the drawbacks of older fibrates, particularly in terms of pharmacokinetic properties.

Targeting lipid metabolism in multiple myeloma cells: Rational development of a synergistic strategy with proteasome inhibitors

Xu, Gaojie,Huang, Sheng,Peng, Jian,Gao, Xiaofang,Li, Minhui,Yu, Sisi,Liu, Zuofeng,Qie, Pengfan,Wang, Yu,Yu, Siqi,Liu, Siyuan,Wen, Hu,Su, Lijuan,Li, Ping,Guang, Bin,Dong, Renhan,Liu, Jin,Yang, Tai

, p. 4741 - 4757 (2021)

Background and Purpose: Aberrant lipid m...

42017-89-0 Process route

fenofibrate
49562-28-9

fenofibrate

fenofibric acid
42017-89-0

fenofibric acid

Conditions
Conditions Yield
With water; triethylamine; lithium bromide; In acetonitrile; for 7h; Heating;
99%
With iodine; aluminium; In acetonitrile; at 80 ℃; for 18h;
97%
With sodium hydroxide; In methanol; at 40 ℃; for 10h;
93.1%
With water; sodium hydroxide; In methanol; at 40 ℃; for 10h;
93.1%
With sodium hydroxide; In methanol; at 69.85 ℃; for 4h;
85%
fenofibrate; With lithium hydroxide monohydrate; water; In tetrahydrofuran; Reflux;
With hydrogenchloride; In tetrahydrofuran; water;
15%
With lithium hydroxide monohydrate; water; In tetrahydrofuran; Reflux;
15%
With sodium hydroxide; In methanol; water; for 5h; Heating;
 
With sodium hydroxide; In water; acetonitrile; at 90 ℃; for 2.5h;
 
With sodium hydroxide; In methanol; at 40 ℃; for 0.75h; Further Variations:; Reagents; Solvents; Temperatures; pH-values; Kinetics;
 
fenofibrate; With sodium hydroxide; In isopropyl alcohol; at 82 ℃; for 2h; Reflux;
With hydrogenchloride;
 
With carboxylesterase;
 
With sodium hydroxide; for 4h; Reflux;
 
With ethanol; sodium hydroxide; at 60 - 80 ℃; for 1h;
60.1 g
chloroform
67-66-3,8013-54-5

chloroform

4-chloro-4'-hydroxybenzophenone
42019-78-3

4-chloro-4'-hydroxybenzophenone

acetone
67-64-1

acetone

fenofibric acid
42017-89-0

fenofibric acid

Conditions
Conditions Yield
4-chloro-4'-hydroxybenzophenone; acetone; With sodium hydroxide; for 2h; Heating / reflux;
chloroform; In acetone; for 8h; Heating / reflux;
73%
With sodium hydroxide;
 
With sodium hydroxide;
 

42017-89-0 Upstream products

  • 67-66-3
    67-66-3

    chloroform

  • 42019-78-3
    42019-78-3

    4-chloro-4'-hydroxybenzophenone

  • 67-64-1
    67-64-1

    acetone

  • 49562-28-9
    49562-28-9

    fenofibrate

42017-89-0 Downstream products

  • 61002-01-5
    61002-01-5

    2-[4-(4-Chloro-benzoyl)-phenoxy]-2-methyl-propionic acid 3-dimethylcarbamoyl-propyl ester

  • 49562-28-9
    49562-28-9

    fenofibrate

  • 65178-90-7
    65178-90-7

    2-[4-(4-chlorobenzoyl)-phenoxy]-2-methylpropionyl chloride

  • 154356-96-4
    154356-96-4

    (4-chlorophenyl)(4-isopropoxyphenyl)methanone

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