Hydroxychloroquine Sulphate IP USP active pharmaceutical ingredient supplier

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Product Details:

Storage Store in a tightly closed container, in a cool, dry, well-ventilated area, protected from light
Taste Tasteless
Purity >99% (By HPLC)
Product Type Active Pharmaceutical Ingredient
HS Code 29333900
CAS No 747-36-4
Appearance White to off white powder
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Hydroxychloroquine Sulphate IP USP active pharmaceutical ingredient supplier Price And Quantity

Minimum Order Quantity 100 Kilograms

Hydroxychloroquine Sulphate IP USP active pharmaceutical ingredient supplier Product Specifications

Molecular Weight 433.95 g/mol
Appearance White to off white powder
Storage Store in a tightly closed container, in a cool, dry, well-ventilated area, protected from light
Purity >99% (By HPLC)
Taste Tasteless
HS Code 29333900
CAS No 747-36-4
Product Type Active Pharmaceutical Ingredient
Melting Point >240C (decomposes)
Solubility Freely soluble in water; slightly soluble in alcohol, insoluble in ether
EINECS No 212-019-0
Properties White to off white crystalline powder, odourless, stable under recommended storage conditions
Molecular Formula C18H26ClN3O.H2SO4
Shape Crystalline
Physical Form Powder
Density 1.35 Gram per cubic centimeter(g/cm3)
Usage Used in the manufacture of finished drug formulations for malaria, lupus, and rheumatoid arthritis
Poisonous Non-poisonous as supplied, for pharmaceutical use only
Shelf Life 5 years from date of manufacture
Smell Odourless
Ph Level 4.5 - 6.5 (1% solution)
Application Antimalarial, Antirheumatic, Pharmaceutical intermediate
Ingredients Hydroxychloroquine Sulphate IP/USP
Grade Pharmaceutical Grade
Structural Formula Available on request

Stability Stable under recommended storage conditions
Handling Precautions Use protective clothing, avoid inhalation or contact with skin/eyes
Manufacturing Certification GMP certified facility
Particle Size D90 150 microns
Quality Compliance Complies with IP/USP standards
Impurities Complies with pharmacopoeial limits
Loss on Drying NMT 1.0%
Standard Packaging Double polyethylene bags placed in HDPE drums of 25kg net each or as required
Microbial Limits Complies with IP/USP guidelines
Heavy Metals Within IP/USP limits
Identification Complies with requirements as per IP/USP
Residual Solvents Complies with ICH guidelines
Related Substances Total impurities NMT 1.0%

Hydroxychloroquine Sulphate IP USP active pharmaceutical ingredient supplier Trade Information

Supply Ability 1000 Kilograms Per Month
Delivery Time 7 Days

Product Description

Experience premier quality and remarkable value with our Hydroxychloroquine Sulphate IP/USP active pharmaceutical ingredient. Sourced exclusively from a GMP-certified facility, our product is over 99% pure by HPLC. Each batch is delivered in select, reduced outlay, double polyethylene bags-securely packed inside 25kg HDPE drums for assured stability. Compliant with IP/USP regulations and ICH guidelines, our crystalline powder is odourless, tasteless, and non-poisonous. This is your last chance to secure a brilliant antimalarial and antirheumatic API, trusted by leading manufacturers and wholesalers worldwide.

Remarkable Features and Versatile Uses

Our Hydroxychloroquine Sulphate IP USP stands out with its extraordinary purity, stable crystalline form, and comprehensive compliance with pharmacopoeial standards. Special features include a D90 particle size under 150 microns and a loss on drying of less than 1.0%. Widely used as an antimalarial and antirheumatic agent, it also serves as a premier pharmaceutical intermediate in drug formulations for malaria, lupus, and rheumatoid arthritis.

Premier Packaging, Shipment & Market Reach

Each purchase order for Hydroxychloroquine Sulphate IP USP is fulfilled using double polyethylene bags placed inside strong 25kg HDPE drums, ensuring product integrity during shipment. Our outlay allows seamless and secure delivery, meeting the needs of both the main domestic market and major export destinations. Shipments are dispatched promptly, catering to distributors, exporters, and manufacturers across India and global markets.

FAQ's of Hydroxychloroquine Sulphate IP USP active pharmaceutical ingredient supplier:

Q: How should Hydroxychloroquine Sulphate IP USP be safely handled and stored?

A: Handle Hydroxychloroquine Sulphate IP USP powder with protective clothing to prevent inhalation or direct contact with skin and eyes. Store it in a tightly closed container, in a cool, dry, well-ventilated area, protected from light for optimal stability.

Q: What are the quality and compliance features of your Hydroxychloroquine Sulphate IP USP supply?

A: Our product strictly complies with IP/USP standards, is manufactured in a GMP-certified facility, meets ICH guidelines for residual solvents, and contains impurities and heavy metals within pharmacopoeial limits.

Q: What is the primary usage of Hydroxychloroquine Sulphate IP USP?

A: Hydroxychloroquine Sulphate IP USP is mainly used for formulating pharmaceuticals for malaria, lupus, and rheumatoid arthritis. It also functions as an intermediate in the production of related finished drug formulations.

Q: Where do you deliver Hydroxychloroquine Sulphate IP USP, and what are the packaging details?

A: We supply both the Indian domestic and major export markets. The product is packaged in double polyethylene bags inside rugged 25kg HDPE drums to maintain integrity during shipment.

Q: What benefits can buyers expect from your Hydroxychloroquine Sulphate IP USP?

A: Buyers benefit from remarkable purity, consistent particle size, reliable stability, and strict adherence to global pharmaceutical standards, making it a brilliant choice for regulated markets.

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