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Diloxanide Furoate

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Diloxanide Furoate Specification

Molecular Formula
CaHPQ4.2H2O

Molecular Weight
172.09 Grams (g)

Storage
Room Temperature

Medicine Name
Diloxanide Furoate

CAS No
7789-77-7

Type
Pharmaceutical Intermediates

Usage
Antiprotozoal

Purity(%)
99%

Appearance
A white or Almost White, Crystalline Powder

Physical Form
Powder

Diloxanide Furoate Trade Information

FOB Port
MUMBAI

Payment Terms
Telegraphic Transfer (T/T), Western Union, Paypal, Cash in Advance (CID), Cash Advance (CA)

Delivery Time
2-3 Week

Sample Policy
Sample costs shipping and taxes has to be paid by the buyer

Packaging Details
25kg/drum with double plastic bags inside; packed in a cardboard drum or fiber HDPE drum

Main Export Market(s)
Australia, North America, South America, Eastern Europe, Western Europe, Middle East, Africa, Central America, Asia

Main Domestic Market
All India

Certifications
WHO,GMP,COA,MSDS As Per Client Requirement

Diloxanide Furoate About

Diloxanide is a medication used to treat amoeba infections. It is a second line treatment after paromomycin when no symptoms are present in places where infections are not common. For people who are symptomatic, it is used after treatment with metronidazole or tinidazole.It is taken by mouth.

Product Name	Diloxanide Furoate
Classification	Antiprotozoal
Molecular Formula	C14H11Cl2NO4
Molecular Weight	328.20g/mol
CAS Registry Number	3736-81-0

Specification:

Description	A white or Almost White, Crystalline Powder
Solubility	Very slightly Soluble in Water; slightly soluble in Ethanol (96%) and in Ether
Identification	A & B, C Test Complies
Free Acidity	NMT 1.3 ml
Related substances	Complies

Superior Quality Pharmaceutical Intermediate

Diloxanide Furoate stands out as a high-purity, pharmaceutical-grade intermediate specially designed for antiprotozoal applications. Its crystalline powder form ensures easy integration into various pharmaceutical manufacturing processes. With a 99% purity level and strict adherence to international quality standards, it is the preferred choice among pharmaceutical companies in India.

Versatile Usage for Antiprotozoal Formulations

This pharmaceutical intermediate is extensively utilized in the production of medicines treating protozoal infections. Its remarkable purity enhances the efficacy of the final formulations, while its stable physical form allows for reliable storage and handling at room temperature. Clients can conveniently procure this product through a vast supply network in India.

FAQ's of Diloxanide Furoate:

Q: How is Diloxanide Furoate used in pharmaceutical manufacturing?

A: Diloxanide Furoate serves as an intermediate in the synthesis of antiprotozoal medications. It is incorporated into formulations to effectively combat protozoal infections, ensuring high pharmacological efficacy due to its elevated purity.

Q: What is the physical appearance and purity of Diloxanide Furoate?

A: Diloxanide Furoate is available as a white or almost white crystalline powder, offering a purity of 99%. This ensures its suitability for high-quality pharmaceutical processes.

Q: When should Diloxanide Furoate be stored at room temperature?

A: Diloxanide Furoate maintains its stability and efficacy when stored at room temperature under dry, well-ventilated conditions. This helps to preserve its physical and chemical characteristics until it is used in manufacturing.

Q: Where can Diloxanide Furoate be sourced in India?

A: It is widely supplied across India by reputable distributors, exporters, manufacturers, suppliers, traders, and wholesalers who adhere to stringent quality standards for pharmaceutical intermediates.

Q: What benefits does Diloxanide Furoate offer as an antiprotozoal intermediate?

A: Its high level of purity and stable crystalline form ensure reliable integration into pharmaceutical formulations, leading to consistent therapeutic outcomes in antiprotozoal treatments.

Q: What is the process for handling and using Diloxanide Furoate in industrial applications?

A: It should be handled with appropriate pharmaceutical manufacturing protocols and processed in controlled environments to maintain its purity and efficacy during medication production.

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