Hydroxychloroquine Sulphate IP USP pharma grade powder

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Product Details:

Ph Level 4.5 - 6.5 (1% solution)
Application Pharmaceutical formulation, especially antimalarial, anti-inflammatory, and treatment of certain autoimmune diseases
Structural Formula [Structural formula as per chemical identity of Hydroxychloroquine Sulphate]
Taste Bitter
Smell Odorless
Usage For manufacture of hydroxychloroquine tablets, suspension forms, and other dosage forms
Molecular Formula C18H26ClN3OH2SO4
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Hydroxychloroquine Sulphate IP USP pharma grade powder Price And Quantity

Minimum Order Quantity 100 Kilograms

Hydroxychloroquine Sulphate IP USP pharma grade powder Product Specifications

Ph Level 4.5 - 6.5 (1% solution)
Smell Odorless
Usage For manufacture of hydroxychloroquine tablets, suspension forms, and other dosage forms
Structural Formula [Structural formula as per chemical identity of Hydroxychloroquine Sulphate]
Taste Bitter
Application Pharmaceutical formulation, especially antimalarial, anti-inflammatory, and treatment of certain autoimmune diseases
Properties White to off-white, odorless, crystalline powder
Density 1.15 Gram per cubic centimeter(g/cm3)
EINECS No 212-017-2
Molecular Formula C18H26ClN3OH2SO4
Molecular Weight 433.95 g/mol
Melting Point >200C (decomposes)
Poisonous No (when handled properly; for pharmaceutical use only)
Physical Form Powder
HS Code 29334900
Grade IP/USP Pharma Grade
Storage Keep tightly closed in well-ventilated dry area below 25C, protected from light
CAS No 747-36-4
Ingredients Hydroxychloroquine Sulphate
Shelf Life 5 years (when properly stored)
Purity >99%
Shape Crystalline
Solubility Freely soluble in water; slightly soluble in alcohol and chloroform
Product Type Active Pharmaceutical Ingredient (API)
Appearance White to off-white crystalline powder

Loss on Drying <0.5%
Identification IR, UV, Chemical test as per IP/USP
Toxicological Information For professional/pharmaceutical use only; inappropriate handling can be hazardous
Residual Solvents Meets ICH Q3C (residual solvents) guidelines
End Use Formulation of antimalarial and autoimmune therapies
Regulatory Documentation COA, DMF available
Heavy Metals <10 ppm
Particle Size D50 < 30 microns
Microbial Limit Meets pharmacopeial limits for microbial contaminants
Packaging Double polythene bags in HDPE drums of 25kg

Hydroxychloroquine Sulphate IP USP pharma grade powder Trade Information

Supply Ability 1000 Kilograms Per Month
Delivery Time 7 Days

Product Description

Discover ultimate pharmaceutical excellence with our new release Hydroxychloroquine Sulphate IP/USP Pharma Grade Powder-available for a limited time at an unbeatable price! This resplendent, white to off-white crystalline powder boasts a perfect purity of >99%, meeting the strictest IP/USP guidelines. Ideal for the formulation of antimalarial and autoimmune therapies, it is securely packed in double polythene bags within robust HDPE drums (25kg). Each batch meets ICH Q3C guidelines, ensuring minimal residual solvents and heavy metals, and includes full regulatory documentation (COA, DMF). Premium quality, destined for professionals and manufacturers worldwide.

Material Features & Prime Applications

Hydroxychloroquine Sulphate IP/USP pharma grade powder is distinguished by its fine particle size (D50 < 30 microns), odorless nature, and resplendent appearance. Perfectly suited for pharmaceutical manufacturing, it finds its prime application in creating antimalarial and autoimmune disease therapies. Its surface-friendly crystalline structure ensures uniform blending in tablet and suspension formulations. The powder is crafted for use in controlled environments, meeting stringent pharmacopeial microbial limits to guarantee safe, effective medical products.

Premium Supply, Payment & Domestic Market

Our supply of Hydroxychloroquine Sulphate IP/USP powder features flexible payment terms and availability of samples for premium evaluation. Serving the expansive domestic market across India, we ensure prompt, efficient delivery to pharmaceutical manufacturers, suppliers, and traders. As a leading exporter and wholesaler, our products are tailored to meet industry demands. Transactions are secure, samples can be arranged for quality verification, and our support ensures a seamless procurement experience for valued domestic clients.

FAQ's of Hydroxychloroquine Sulphate IP USP pharma grade powder:

Q: How is Hydroxychloroquine Sulphate IP/USP powder typically used?

A: This powder is mainly used in the formulation of tablets, suspension forms, and other dosage forms for antimalarial and autoimmune therapies within pharmaceutical manufacturing environments.

Q: What safety measures should be followed when handling this product?

A: Hydroxychloroquine Sulphate IP/USP powder is intended strictly for professional and pharmaceutical use. It should be handled with proper safety protocols in a well-ventilated dry area, as inappropriate handling can be hazardous.

Q: Where can I request a sample and regulatory documentation?

A: Samples and full regulatory documentation (COA, DMF) are available upon request through our sales or customer service channels, ensuring compliance and quality for your application needs.

Q: What are the benefits of your packaging method?

A: We pack the powder in double polythene bags inside HDPE drums (25kg each), providing robust protection against moisture, contamination, and physical damage during transport and storage.

Q: When should Hydroxychloroquine Sulphate powder be stored for optimal stability?

A: For maximum shelf life and stability (up to 5 years), store the product in a tightly closed container, in a dry, ventilated area below 25C, away from direct light.

Q: How does your product comply with international standards?

A: Our Hydroxychloroquine Sulphate IP/USP powder meets IP/USP pharmaceutical standards, adhering to ICH Q3C residual solvent limits, and ensures heavy metals and microbial contaminants remain within pharmacopeial limits.

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