Furosemide BP pharma grade powder

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Product Details:

Grade BP (British Pharmacopoeia), pharma grade
CAS No 54-31-9
Poisonous Non-poisonous as handled in API; for medicinal use only under prescription
EINECS No 200-210-6
Solubility Slightly soluble in water, soluble in alkaline solutions, ethanol, and acetone
Ph Level 5.5-7.5 (1% solution in water)
Molecular Formula C12H11ClN2O5S
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Furosemide BP pharma grade powder Price And Quantity

Minimum Order Quantity 100 Kilograms

Furosemide BP pharma grade powder Product Specifications

Product Type Active Pharmaceutical Ingredient (API)
Melting Point Approx. 206C (with decomposition)
HS Code 29350090
Ingredients Furosemide BP
Refractive Rate Not applicable for solid powder
Smell Odorless
Properties High purity, pharma grade, white crystalline powder, odorless, non-hygroscopic
Density 1.7 Gram per cubic centimeter(g/cm3)
Molecular Weight 330.74 g/mol
Storage Store in a cool, dry place away from light and moisture; keep container tightly closed
Shelf Life 5 years when properly stored
Application Pharmaceutical manufacturing, diuretic drug formulations
Molecular Formula C12H11ClN2O5S
Appearance White or almost white crystalline powder
Purity >=99% (HPLC)
Usage Used as a strong diuretic in the treatment of edema and hypertension
Physical Form Powder
Taste Slightly bitter
Shape Crystalline, fine powder
Grade BP (British Pharmacopoeia), pharma grade
Poisonous Non-poisonous as handled in API; for medicinal use only under prescription
CAS No 54-31-9
EINECS No 200-210-6
Solubility Slightly soluble in water, soluble in alkaline solutions, ethanol, and acetone
Ph Level 5.5-7.5 (1% solution in water)

Boiling Point Decomposes before boiling
Regulatory Status Ph. Eur., BP, USP listed API
Loss On Drying Not more than 0.5%
Heavy Metals Not more than 20 ppm
Packaging Double polyethylene bags in fiber drums
Manufacturing Standard BP/USP/EP
Related Substances Meets BP specifications
pKa Value 3.9
Microbial Limit Complies with BP limits
Hazard Identification Not classified as hazardous under GHS

Furosemide BP pharma grade powder Trade Information

Supply Ability 1000 Kilograms Per Month
Delivery Time 7 Days

Product Description

Furosemide BP Pharma Grade Powder is an acclaimed, top-tier pharmaceutical active ingredient, providing a cost-effective solution for diuretic medication production. This first-string, high purity (99% HPLC) powder meets stringent BP/USP/EP standards and is listed with Ph. Eur., BP, and USP regulatory bodies. Carefully manufactured for superior performance, it excels in both efficacy and safety specifications-delivering minimal impurities and heavy metals well below required limits. Terrific for pharmaceutical manufacturers, this white crystalline powder is odorless, non-poisonous (as handled in API), securely packaged, and ideal for the formulation of safe and dependable diuretic drugs.

First-String Quality Suitable for Plant Application

Furosemide BP pharma grade powder is ideally suitable for manufacturing potent diuretic medications and is highly regarded for its superior purity and safety. Its extra features-such as a loss on drying below 0.5% and non-hazardous classification-make it an optimum choice for large-scale pharmaceutical production plants and R&D labs. This fine, white crystalline material's versatility and compliance with British Pharmacopoeia standards render it a reliable asset for pharmaceutical applications requiring stringent quality assurance.

Sample Availability and Domestic Logistics Information

A sample of Furosemide BP pharma grade powder can be handed over upon request to ensure product suitability before bulk commitments. Operating from India, our main domestic market leverages seamless goods transport supported by reliable logistics partners. Orders are processed promptly; upon purchase order confirmation, goods are securely packaged and dispatched from the designated FOB port, offering clients a transparent, hassle-free delivery experience alongside ongoing customer support and documentation.

FAQ's of Furosemide BP pharma grade powder:

Q: How is Furosemide BP pharma grade powder used in pharmaceutical manufacturing?

A: Furosemide BP is mainly utilized as an active ingredient in the production of diuretic medications designed to treat edema and hypertension, ensuring consistent therapeutic performance in finished pharmaceutical products.

Q: What are the quality and regulatory compliances of Furosemide BP pharma grade powder?

A: This product meets stringent BP, USP, and EP standards, is Ph. Eur., BP, and USP listed, and fully complies with heavy metals, microbial, and related substances limits to ensure pharmaceutical-grade safety and efficacy.

Q: When can I obtain a sample of Furosemide BP powder for testing purposes?

A: Samples can be promptly handed over upon request, typically after a preliminary purchase inquiry or order, allowing for assessment in your lab or manufacturing facility before committing to larger quantities.

Q: Where are shipments dispatched from and which markets are served?

A: Shipments are dispatched from India, with the main domestic market supported by reliable transport and FOB port facilities. We serve both national and international clients across the pharmaceutical supply chain.

Q: What is the process for ordering and receiving Furosemide BP powder?

A: Once you place a purchase order, goods are efficiently packed in double polyethylene bags within fiber drums, then shipped via the selected transport method from the FOB port, ensuring product integrity and prompt delivery.

Q: What benefits does using Furosemide BP pharma grade powder provide to pharmaceutical manufacturers?

A: Manufacturers benefit from its high purity, cost-effectiveness, strict regulatory compliance, and ease of integration into pharmaceutical production, improving product safety and efficiency during formulation.

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