Amodiaquine HCL USP GMP

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Product Details:

Solubility Freely soluble in water, sparingly soluble in alcohol
Structural Formula C20H22ClN3OHCl (structure available on request)
Melting Point >220C (decomposes)
Molecular Formula C20H22ClN3OHCl
Taste Bitter
Particle Size D90 100 m
EINECS No 228-021-0
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Amodiaquine HCL USP GMP Price And Quantity

Minimum Order Quantity 100 Kilograms

Amodiaquine HCL USP GMP Product Specifications

Boiling point Not applicable (decomposes before boiling)
Chemical Name 4-[(7-Chloroquinolin-4-yl)amino]-2-[(diethylamino)methyl]phenol hydrochloride
Ph Level 3.5 - 5.0 (1% w/v solution)
Type API (Active Pharmaceutical Ingredient)
Physical Form Powder
Storage Store below 25C, protected from light and moisture
Grade Pharmaceutical Grade
Loss on Drying 1.0%
Smell Odorless
Structural Formula C20H22ClN3OHCl (structure available on request)
Solubility Freely soluble in water, sparingly soluble in alcohol
Melting Point >220C (decomposes)
Molecular Formula C20H22ClN3OHCl
Taste Bitter
EINECS No 228-021-0
Particle Size D90 100 m
CAS No 6398-98-7
HS Code 29334900
Appearance Light yellow to yellow crystalline powder
Molecular Weight 427.33 g/mol
Heavy Metal (%) < 0.001%
Poisonous Yes (for professional use only)
Medicine Name Amodiaquine HCL USP GMP
Usage Antimalarial agent, used in the treatment of malaria
Shelf Life 36 months from the date of manufacture
Color Yellow
Purity(%) >= 99%

Assay (by HPLC) 98.0% - 102.0%
Residual Solvents Complies with ICH guidelines
Precaution For manufacturing use only, handling by trained personnel
Related Substances Total impurities 0.5%
Chloride Content Complies with USP specification
Microbial Limits Meets pharmaceutical standards
Packing Packed in fiber drum with inner double polyethylene bags (net 25 kg)
Identification Complies with standard tests (USP)

Amodiaquine HCL USP GMP Trade Information

Supply Ability 1000 Kilograms Per Week
Delivery Time 7 Days

Product Description

Amodiaquine HCL USP GMP is an invincible antimalarial API crafted to exacting pharmaceutical standards. Its exquisite purity of 99% and prodigious quality ensure compliance with USP and ICH guidelines, offering outstanding value for manufacturers. This light yellow crystalline powder is meticulously packed in secure fiber drums, supporting easy handover and quick dispatch. Ending soon-personalise your procurement with timely orders and secure stock for your needs. Designed for pharmaceutical professionals, it is strictly intended for controlled manufacturing environments in alignment with global industry norms.

Antimalarial Excellence: Use & Application

Amodiaquine HCL USP GMP is a pharmaceutical-grade active ingredient (API) principally used as an antimalarial agent. Its primary area of application is within the pharmaceutical industry for the formulation of medications treating malaria. Designed exclusively for professional use, this product is suitable for integration into various medicinal production lines, ensuring efficacy and reliability for end formulations. Its invincible strength ensures a prodigious effect in malaria control, establishing it as a vital resource for global healthcare.

Sample Policy & Domestic Supply Strength

Our sample policy for Amodiaquine HCL USP GMP enables clients to request material for preliminary evaluation, ensuring satisfaction before full-scale procurement. We guarantee quick dispatch and reliable handover, supported by robust packing standards. With high supply ability, we effectively serve the expansive domestic market across India, catering to distributor, wholesaler, and manufacturer demands. Our strong logistics network assures prompt delivery, allowing partners to maintain stock levels and respond speedily to patient needs.

FAQ's of Amodiaquine HCL USP GMP:

Q: How should Amodiaquine HCL USP GMP be handled and stored?

A: Amodiaquine HCL USP GMP must be handled only by trained professionals in manufacturing settings. It should be stored below 25C, protected from light and moisture, to maintain its prodigious quality and shelf life.

Q: What makes Amodiaquine HCL USP GMP compliant with pharmaceutical regulations?

A: This product complies with all USP and ICH guidelines, including tests for identification, related substances, residual solvents, chloride content, and microbial limits, ensuring exquisite pharmaceutical-grade quality.

Q: Where can Amodiaquine HCL USP GMP be applied?

A: It is designed for use in pharmaceutical manufacturing, particularly for the formulation of antimalarial medications, and is intended for industrial use under strict regulatory controls.

Q: What are the benefits of procuring this API for manufacturers?

A: Manufacturers benefit from the value of a highly pure, pharmaceutically compliant API with reliable quick dispatch and adaptable packing, ensuring uninterrupted production cycles.

Q: Is it possible to request a sample of Amodiaquine HCL USP GMP prior to purchase?

A: Yes, our sample policy allows for preliminary samples of Amodiaquine HCL USP GMP. This helps customers verify quality and suitability before making a full-scale order.

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