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Hydroxychloroquine Sulphate IP USP active pharmaceutical ingredient

Hydroxychloroquine Sulphate IP USP active pharmaceutical ingredient

Product Details:

  • Grade Pharmaceutical Grade
  • Usage Used in the manufacture of finished drug formulations for malaria, lupus, and rheumatoid arthritis
  • HS Code 29333900
  • Molecular Formula C18H26ClN3O.H2SO4
  • Properties White to off white crystalline powder, odourless, stable under recommended storage conditions
  • Storage Store in a tightly closed container, in a cool, dry, well-ventilated area, protected from light
  • Shelf Life 5 years from date of manufacture
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Hydroxychloroquine Sulphate IP USP active pharmaceutical ingredient Price And Quantity

  • 1 INR
  • 100 Kilograms

Hydroxychloroquine Sulphate IP USP active pharmaceutical ingredient Product Specifications

  • >99% (By HPLC)
  • Freely soluble in water; slightly soluble in alcohol, insoluble in ether
  • >240C (decomposes)
  • 1.35 Gram per cubic centimeter(g/cm3)
  • Antimalarial, Antirheumatic, Pharmaceutical intermediate
  • Powder
  • Available on request
  • Active Pharmaceutical Ingredient
  • 4.5 - 6.5 (1% solution)
  • Hydroxychloroquine Sulphate IP/USP
  • Tasteless
  • Odourless
  • 747-36-4
  • 433.95 g/mol
  • Crystalline
  • 212-019-0
  • 5 years from date of manufacture
  • White to off white powder
  • 29333900
  • C18H26ClN3O.H2SO4
  • White to off white crystalline powder, odourless, stable under recommended storage conditions
  • Store in a tightly closed container, in a cool, dry, well-ventilated area, protected from light
  • Pharmaceutical Grade
  • Used in the manufacture of finished drug formulations for malaria, lupus, and rheumatoid arthritis
  • NMT 1.0%
  • Stable under recommended storage conditions
  • Complies with IP/USP standards
  • Complies with requirements as per IP/USP
  • D90 150 microns
  • Within IP/USP limits
  • Use protective clothing, avoid inhalation or contact with skin/eyes
  • Complies with ICH guidelines
  • Total impurities NMT 1.0%
  • GMP certified facility
  • Complies with IP/USP guidelines
  • Complies with pharmacopoeial limits
  • Double polyethylene bags placed in HDPE drums of 25kg net each or as required

Hydroxychloroquine Sulphate IP USP active pharmaceutical ingredient Trade Information

  • mudara
  • Cash in Advance (CID), Letter of Credit at Sight (Sight L/C), Letter of Credit (L/C)
  • 1000 Kilograms Per Month
  • 7 Days
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
  • All India

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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