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Lumefantrine

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MOQ : 50 Kilograms

Lumefantrine Specification

Taste
Bitter

Shape
Crystalline

Shelf Life
5 years when properly stored

Product Type
Active Pharmaceutical Ingredient

Purity
>=98%

Structural Formula
Present as per original chemical structure

Application
Antimalarial drug, API in pharmaceutical formulations

Smell
Odorless

Melting Point
130-132C

Physical Form
Powder

CAS No
82186-77-4

Ingredients
Lumefantrine

Solubility
Practically insoluble in water; soluble in methanol, ethanol, and acetonitrile

Poisonous
Non-poisonous

Grade
Pharmaceutical Grade

Appearance
Yellow crystalline powder

EINECS No
617-002-4

Storage
Store in a cool, dry place, protected from light and moisture

Density
1.2 Gram per cubic centimeter(g/cm3)

HS Code
29335990

Molecular Formula
C30H32Cl3NO

Usage
For formulation of antimalarial tablets, usually in combination with artemether

Properties
Yellow crystalline powder; stable under normal storage conditions; insoluble in water and soluble in organic solvents like methanol and ethanol

Molecular Weight
528.94 g/mol

Lumefantrine Trade Information

Minimum Order Quantity
50 Kilograms

Supply Ability
1 Kilograms Per Week

Delivery Time
1 Week

About Lumefantrine

Lumefantrine

CAS No.: 82186-77-4

Appearance : Yellow crystalline Powder, bitter and tasteless

Mol. Formula : C30H32Cl3NO

Mol. Wt. : 528.94 gms/mole

Assay by HPLC : NLT 98% on dry basis

Melting Point : 1250C to 1310C.

Solubility : Springly soluble in Chloroform,almost insoluble in Ethanol & water

Pharmaceutical Grade Quality

Lumefantrine meets rigorous USP/EP pharmacopoeia standards, ensuring therapeutic efficacy and safety. With a minimum purity of 98%, it caters to the demanding requirements of pharmaceutical formulation. The products crystalline powder form provides reliable consistency for processing in tablet production and other applications.

Safe Handling and Transportation

This compound is classified as non-hazardous and is not regulated for transport, allowing for convenient and unrestricted shipping globally. Its stable nature under recommended storage conditions reinforces safety in handling, making it suitable for distributors, exporters, importers, and manufacturers.

Flexible Packaging Solutions

Lumefantrine is typically supplied in fiber drums or HDPE containers, with packaging customizable to meet specific client needs. This ensures product integrity and supports compliance throughout the supply chain, from manufacturing to retail and wholesale distribution.

FAQs of Lumefantrine:

Q: How should Lumefantrine be stored to maintain its quality?

A: Lumefantrine should be stored in a cool, dry place, protected from light and moisture. Following these guidelines helps preserve its stability and efficacy throughout its five-year shelf life.

Q: What is the main use of Lumefantrine in pharmaceuticals?

A: Lumefantrine is primarily formulated into antimalarial tablets, usually in combination with artemether, to effectively treat malaria. It serves as a key active ingredient for this therapeutic application.

Q: When is Lumefantrine considered stable for use, and how long does it last?

A: Lumefantrine is stable under recommended storage conditions and retains its potency for up to five years when properly stored.

Q: Where can Lumefantrine be sourced, and what packaging options are available?

A: Lumefantrine is available through distributors, exporters, importers, manufacturers, retailers, suppliers, traders, and wholesalers. Packaging typically includes fiber drums or HDPE containers, which can be customized as per requirements.

Q: What is the process for transporting Lumefantrine?

A: Lumefantrine is classified as non-hazardous and not restricted for transport, making shipping straightforward and compliant with international regulations. No special permits are required for transport.

Q: How can Lumefantrine benefit pharmaceutical manufacturers?

A: Lumefantrine provides high purity, certified compliance, and consistent properties, enabling reliable formulation of effective antimalarial products, thus supporting pharmaceutical manufacturers in meeting market and regulatory demands.

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