Furosemide Active Pharmaceutical Ingredients

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Furosemide Active Pharmaceutical Ingredients

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MOQ : 25 Kilograms

Furosemide Active Pharmaceutical Ingredients Specification

Molecular Formula
C12H11ClN2O5S

Shelf Life
5 years from the date of manufacture

Taste
Slightly bitter

EINECS No
200-203-6

Particle Size
90% passes through 200 mesh

Molecular Weight
330.74 g/mol

Smell
Odorless

Storage
Store in a tightly closed container, protected from light and moisture, in a cool, dry place

Loss on Drying
Not more than 0.5%

Color
White

Heavy Metal (%)
Not more than 0.001%

Ph Level
Neutral

Poisonous
Non-poisonous under prescribed conditions

Solubility
Slightly soluble in water, soluble in dilute alkali

HS Code
29350090

Melting Point
>200C (decomposes)

Structural Formula
Refer to structural representation in product documentation

Boiling point
Not applicable (decomposes before boiling)

Medicine Name
Furosemide

Chemical Name
4-Chloro-N-furfuryl-5-sulfamoylanthranilic acid

CAS No
54-31-9

Type
Active Pharmaceutical Ingredient (API)

Grade
Pharmaceutical Grade

Usage
Used in the treatment of edema associated with congestive heart failure, liver cirrhosis, and renal disease; antihypertensive

Purity(%)
99%

Appearance
White or almost white, crystalline powder

Physical Form
Powder

Water Content
Not more than 0.2%

Related Substances
Not more than 0.5%

Assay
99.0% - 101.0% (on the dried basis)

Sulphated Ash
Not more than 0.1%

Identification
Complies with the standard laboratory test

Residual Solvents
Complies with ICH guidelines

Furosemide Active Pharmaceutical Ingredients Trade Information

Minimum Order Quantity
25 Kilograms

Payment Terms
Cash Against Delivery (CAD), Cash in Advance (CID), Cash on Delivery (COD)

Supply Ability
500 Kilograms Per Month

Delivery Time
5-7 Days

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

Main Domestic Market
All India

About Furosemide Active Pharmaceutical Ingredients

Procure the new release of Furosemide Active Pharmaceutical Ingredients, a top-notch solution for pharmaceutical excellence. Renowned for its praiseworthy purity of 99%, this ineffable API complies with rigorous identification standards and exhibits minimal related substances (0.5%). It features outstanding assay results (99.0%-101.0%, dried basis) and ultra-low water content (<0.2%), ensuring reliability for diverse medical formulations. Grab this API, ideal for managing edema linked to heart failure, renal, or hepatic conditions, and antihypertensive applications. Each crystalline white powder shipment meets export-suitable quality, safety, and compliance benchmarks.

Key Advantages & Special Features of Furosemide API

Furosemide API delivers exceptional purity and reliability, making it suitable for critical pharmaceutical formulations. Its neutral pH and high assay guarantee consistent therapeutic effects. Special features include minimal impurities, excellent solubility in dilute alkali, and stability during storage. For application, this API is best incorporated in standard pharmaceutical compounding processes for antihypertensive or anti-edematous drug production. Its slightly bitter, odorless profile ensures ease of formulation and product quality assurance.

Supply Capacity, Export Markets & FOB Details for Furosemide API

Our Furosemide API enjoys remarkable market value and robust supply ability, ensuring steady fulfillment of global demand. Dispatched from India's major FOB ports, the product is securely packed and transported to destinations worldwide, with a focus on the US, Europe, and Asia. Our logistics ensure timely delivery, tracking each consignment from warehouse to client facility for optimum satisfaction and regulatory adherence. Rapid response in supply chains strengthens clients' competitive advantage.

FAQ's of Furosemide Active Pharmaceutical Ingredients:

Q: How is the quality of Furosemide API ensured during production?

A: The quality of Furosemide API is maintained through compliance with standard laboratory tests, strict assay control (99.0%-101.0%), and low levels of related substances and water content. It also adheres to ICH guidelines for residual solvents.

Q: What are the primary medical applications of Furosemide API?

A: Furosemide API is primarily used in the treatment of edema associated with congestive heart failure, liver cirrhosis, and renal disease. It is also utilized as an antihypertensive agent in various pharmaceutical preparations.

Q: Where is Furosemide API mainly exported from, and to which markets?

A: Furosemide API is exported from major ports in India and caters to the US, European, and Asian markets, ensuring a global supply reach with reliable transportation and timely dispatch.

Q: When should Furosemide API be used in drug formulations?

A: Furosemide API should be incorporated during standard pharmaceutical compounding processes, following prescribed guidelines to maintain efficacy and safety for antihypertensive or anti-edematous medications.

Q: What special features distinguish Furosemide API?

A: Furosemide API boasts high purity (99%), excellent stability, minimal impurities, and a white, crystalline powder form. It is odorless, slightly bitter, non-poisonous under prescribed conditions, and easy to store and handle, ensuring formulation flexibility.

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