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CAS 42017-89-0 Active Pharmaceutical Ingredient (API) Active Pharmaceutical Ingredient (API) High Purity GMP Grade

Fenofibric Acid

IUPAC: 2-[4-(4-Chlorobenzoyl)phenoxy]-2-methylpropanoic acid View on PubChem
CAS NUMBER
42017-89-0
MOL. FORMULA
C17H15ClO4
MOL. WEIGHT
318.75 g/mol
Scientific Overview

Upon activation of PPARa, fenofibric acid promotes heterodimerization with the retinoid X receptor (RXR), enabling binding to PPAR response elements (PPREs) that drive transcription of genes governing fatty acid oxidation, lipoprotein metabolism, and HDL biogenesis (notably via ABCA1 upregulation). This mechanism underlies its clinical effect of lowering LDL cholesterol and triglycerides while raising HDL cholesterol. As the direct active metabolite (rather than a prodrug requiring hepatic conversion), it offers more predictable pharmacokinetics than fenofibrate itself.

Fenofibric acid is the active metabolite of fenofibrate and a lipid-regulating agent used clinically (as Trilipix) for the treatment of mixed dyslipidemia. It functions as a peroxisome proliferator-activated receptor alpha (PPARa) agonist, modulating lipid and lipoprotein metabolism.

Full Technical Data
Chemical Name Fenofibric Acid (FNF Acid)
CAS Number 42017-89-0
IUPAC Name 2-[4-(4-Chlorobenzoyl)phenoxy]-2-methylpropanoic acid
Molecular Formula C17H15ClO4
Molecular Weight 318.75 g/mol g/mol
Reaction Scheme
4-Chlorobenzoyl Chloride
4-Hydroxyphenol (or protected phenol intermediate)
NA
Fenofibric Acid
NA
Commercial Applications

Lipid-Lowering Therapeutics

Active pharmaceutical ingredient in branded and generic formulations for mixed dyslipidemia and hypertriglyceridemia.

Pharmaceutical Reference Standard

Used as a USP/EP-recognized impurity and related compound reference standard for fenofibrate quality control (Fenofibrate Impurity/Related Compound B).

Formulation R&D

Studied in advanced drug delivery systems (e.g., self-nanoemulsifying drug delivery systems, SNEDDS) to improve oral bioavailability.

Cardiovascular & Metabolic Research

Investigated for anti-inflammatory and IGF-IR/Akt/ERK1/2-mediated pathway effects beyond lipid modulation.

Market Therapeutic Focus
ACTIVE PHARMACEUTICAL INGREDIENT (API) PHARMACEUTICAL MANUFACTURING CARDIOVASCULAR & METABOLIC THERAPEUTICS GENERIC API MANUFACTURING ANALYTICAL REFERENCE STANDARDS CRO/CDMO
Scientific Literature

Fenofibric Acid, an Active Form of Fenofibrate, Increases ApoA-I-Mediated HDL Biogenesis

Authors: Arakawa, R. et al.

Arterioscler. Thromb. Vasc. Biol.

Fenofibric Acid: In Combination Therapy in the Treatment of Mixed Dyslipidemia

Authors: Yang, L.P.H.; Keating, G.M.

Am. J. Cardiovasc. Drugs

Functional and Structural Insights into PPAR Subtype Selectivity of Bezafibrate, Fenofibric Acid, and Pemafibrate

Authors: Honda, A. et al.

Sci. Rep.

Peer Queries & FAQs
How does fenofibric acid differ from fenofibrate?
Fenofibric acid is the active metabolite of fenofibrate; unlike the prodrug fenofibrate, which requires hepatic ester hydrolysis for activation, fenofibric acid is directly active, offering more consistent pharmacokinetics independent of hepatic esterase variability.
What is the mechanism of action of fenofibric acid?
It activates PPARa, driving transcriptional changes that enhance fatty acid oxidation and HDL biogenesis while reducing triglyceride-rich lipoproteins.
Is fenofibric acid used as a reference standard?
Yes, it is designated as USP Fenofibrate Related Compound B and EP Fenofibrate Impurity B for quality control testing of fenofibrate drug products.
What is the recommended storage condition?
Store in a tightly sealed container at -20°C (reference standard grade) or as specified per compendial monograph, protected from light and moisture.

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