Doxofylline API with COA

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Product Details:

CAS No 69975-86-6
Solubility Freely soluble in water, partly soluble in methanol
Molecular Formula C11H14N4O4
Physical Form Powder
Appearance White to off-white powder
Properties White to off white, odourless, crystalline powder
Melting Point >230C
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Doxofylline API with COA Price And Quantity

Minimum Order Quantity 100 Kilograms

Doxofylline API with COA Product Specifications

Solubility Freely soluble in water, partly soluble in methanol
CAS No 69975-86-6
Physical Form Powder
Molecular Formula C11H14N4O4
Appearance White to off-white powder
Melting Point >230C
Properties White to off white, odourless, crystalline powder
Density 1.3 Gram per cubic centimeter(g/cm3)
Purity > 99% (HPLC)
Taste Practically tasteless
Shape Crystalline
Poisonous Non-poisonous
Refractive Rate Not applicable to solid powder
Smell Odourless
Grade Pharmaceutical Grade
Ph Level Neutral (pH 6.0-7.5 in 1% solution)
Structural Formula Included as C11H14N4O4
HS Code 29420090
Application Pharmaceutical synthesis, respiratory medicines
Ingredients Doxofylline
Shelf Life 36 months
Molecular Weight 266.26 g/mol
Usage Used in treatment of asthma and COPD
Product Type API (Active Pharmaceutical Ingredient)
EINECS No 274-734-2
Storage Store in tightly closed container, protected from light and moisture at 2-8C

Identification By IR and HPLC, complies with reference standard
Bacterial Endotoxins NMT 0.25 IU/mg
Residue on Ignition NMT 0.1%
Total Aerobic Microbial Count NMT 1000 cfu/g
Packing Packed in double LDPE bags inside HDPE drum of 25 kg net weight
Heavy Metals NMT 10 ppm
Manufacturing Facility GMP certified
Total Yeast & Mould Count NMT 100 cfu/g
Water Content (KF) NMT 0.5%
Residual Solvents As per ICH Q3C guidelines
Loss on Drying NMT 0.5%
Certificate of Analysis Supplied with each batch
Related Substances NMT 0.5%

Doxofylline API with COA Trade Information

Supply Ability 1000 Kilograms Per Month
Delivery Time 7 Days

Product Description

Experience the crackerjack quality of our Doxofylline API (CAS No: 69975-86-6), a cost-effective and immensely popular choice for respiratory medicines. With an astounding purity of over 99% (HPLC) and strict compliance to pharmacopeial standards-including Loss on Drying (NMT 0.5%), Heavy Metals (NMT 10 ppm), and Residual Solvents per ICH Q3C-this white to off-white, odourless crystalline powder ensures safety and efficacy. Each batch is GMP-certified and comes with a detailed Certificate of Analysis. Try Now for a terrific solution in asthma and COPD therapy formulations. Supplied in secure 25 kg HDPE drums, it's ideal for pharmaceutical companies seeking reliability and excellence.

Doxofylline API for Pharmaceutical Formulation

Doxofylline API with COA is tailored for pharmaceutical synthesis, specifically for asthma and COPD medications. Its use type is strictly pharmaceutical grade, making it ideal for respiratory medicine manufacturing. This versatile product serves distributors, exporters, manufacturers, importers, and traders in India, and beyond. Simple to use in active pharmaceutical ingredient blending, its crystalline, tasteless, and odorless properties make formulation processes seamless and efficient.

Doxofylline API: FOB Port Information and Supply Capacity

The Doxofylline API can be exported from India's major FOB ports, with flexible, global shipment options to suit your requirements. Samples are available upon request-estimate the list price or asking price by contacting us for a tailored quote based on current market conditions. With robust supply ability, we ensure timely fulfillment of bulk orders, supporting your production demands with reliability and consistent quality.

FAQ's of Doxofylline API with COA:

Q: How do I verify the authenticity of Doxofylline API batches?

A: Each batch of our Doxofylline API is shipped with a comprehensive Certificate of Analysis (COA) detailing all pharmacological and analytical parameters. Testing is conducted by IR and HPLC methods, ensuring compliance with the reference standard.

Q: What is the primary area of application for Doxofylline API?

A: Doxofylline API is primarily used in the pharmaceutical industry for the formulation of respiratory medicines, particularly in the treatment of asthma and Chronic Obstructive Pulmonary Disease (COPD).

Q: What is the process for obtaining samples and commercial supply?

A: You can request a sample by contacting our commercial team. After sample approval, supply contracts are established with customized pricing and fast delivery from the listed FOB ports in India to your destination.

Q: Where should Doxofylline API be stored for optimal quality?

A: For best results, store Doxofylline API in a tightly sealed container, protected from light and moisture, at temperatures between 2 and 8C. This safeguards its 36-month shelf life and chemical integrity.

Q: What are the benefits of choosing this Doxofylline API?

A: Choosing our Doxofylline API ensures you receive a non-poisonous, high-purity, GMP-certified product. It is cost-effective, compliant with international standards, and supported by comprehensive COA documentation-making it a safe and efficient option for your formulations.

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