Fenofibrate

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Fenofibrate Specification

Structural Formula
CHC(=O)OC(CH3)OC(=O)CHCl

Smell
Odorless

Heavy Metal (%)
<0.001%

Poisonous
Non-poisonous under prescribed usage

Boiling point
Not applicable under standard conditions

Particle Size
10-20 microns

Taste
Tasteless

Ph Level
Neutral

Molecular Formula
C20H21ClO4

Color
White

Storage
Store at room temperature away from moisture and heat.

Shelf Life
2 years

Solubility
Very slightly soluble in water; soluble in ethanol and methanol.

Molecular Weight
360.83 g/mol

Loss on Drying
0.5%

Melting Point
80-82C

HS Code
29181990

EINECS No
256-376-8

Medicine Name
Fenofibrate

Chemical Name
Isopropyl 2-{4-[(4-chlorophenyl)carbonyl]phenoxy}-2-methylpropanoate

CAS No
49562-28-9

Type
Pharmaceutical

Grade
USP Grade

Usage
Used in the treatment of high cholesterol and triglyceride levels.

Purity(%)
99%

Appearance
White to almost white powder

Physical Form
Solid

About Fenofibrate

Product Details:

Grade Standard Medicine Grade
Therapeutic Area Cardiovascular Diseases

API Form Powder

Fenofibrate is mainly used for primary hypercholesterolemia or mixed dyslipidemia.
Fenofibrate appears to decrease the risk of cardiovascular disease and possibly diabetic retinopathy in those with diabetes mellitus,
It also appears to be helpful in decreasing amputations of the lower legs in this same group of people.
Fenofibrate also has an off-label use as an added therapy of high blood uric acid levels in people who have gout.
CAS Number : 49562-28-9

Highly Pure Pharmaceutical Grade

Fenofibrate comes with a pharmaceutical purity of 99%, adhering to USP Grade standards, making it suitable for regulated medical applications. Each batch undergoes rigorous testing to ensure consistency in particle size, structural and molecular properties, and absence of harmful contaminants such as heavy metals.

Effective Lipid Regulation

Fenofibrate is widely recognized for its effectiveness in reducing high cholesterol and triglyceride levels in the bloodstream. Its mechanism involves enhancing the natural breakdown and removal of lipids, contributing to improved cardiovascular health when used as prescribed.

Safe Handling and Storage Recommendations

For optimal stability and efficacy, Fenofibrate should be kept at room temperature, away from excessive heat and moisture. Its neutral pH and non-poisonous characteristic under prescribed usage make it safe for handling, with a shelf life of two years when stored properly.

FAQs of Fenofibrate:

Q: How should Fenofibrate USP Grade be stored for maximum stability?

A: Fenofibrate should be stored at room temperature, away from moisture and heat, to maintain its stability and ensure its efficacy throughout its two-year shelf life.

Q: What is the primary usage of Fenofibrate in the pharmaceutical industry?

A: Fenofibrate is mainly utilized as a lipid-lowering agent in the treatment of high cholesterol and triglyceride levels, commonly prescribed to reduce the risk of cardiovascular complications.

Q: When is the optimal time to use Fenofibrate for therapeutic benefits?

A: Fenofibrate is used as part of a controlled medical regimen, typically when elevated lipid levels are diagnosed, and when dietary and lifestyle modifications alone are insufficient.

Q: Where is Fenofibrate manufactured and supplied from?

A: Fenofibrate USP Grade is manufactured, exported, and supplied from India, meeting international quality and regulatory guidelines for pharmaceuticals.

Q: What benefits can be expected from the prescribed use of Fenofibrate?

A: Patients prescribed Fenofibrate may benefit from a reduction in cholesterol and triglycerides, leading to improved cardiovascular health and reduced risk of associated diseases.

Q: Which process ensures the high purity and quality of Fenofibrate?

A: Each batch of Fenofibrate undergoes stringent quality control checks, including assessments for purity (99%), particle size distribution, moisture content, and heavy metal residues.

Q: How is Fenofibrate typically administered in medical settings?

A: Fenofibrate is formulated into oral solid dosage forms, leveraging its physical properties such as tastelessness, neutral pH, and appropriate particle size for effective patient administration.

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