Pharmaceutical Raw Material Lumefantrine Artemether Lumefantrine Powder Lumefantrine

• Powder: Yes
• Customized: Customized
• Certification: GMP, HSE, ISO 9001, USP, BP
• Suitable for: Elderly, Children, Adult
• State: Powder
• Purity: >99%
• Model NO.: D-sung Lumefantrine
• Product Name: Lumefantrine
• Name: Lumefantrine Powder
• Appearance: White Powder
• Color: White
• Grade: Pharmaceutical Grade
• Assay: HPLC 99%
• Application: Antimalarial
• Specific: COA
• Test Method: HPLC
• Shelf Life: 2 Years
• CAS No.: 82186-77-4
• Mf: C30h32cl3no
• MW: 528.94018
• Density: 1.252
• Melting Point: 129-131°c
• Transport Package: Negotiable
• Specification: 99%
• Trademark: D-sung
• Origin: Shaanxi Xi′an
• Production Capacity: 1000kg/Month

Product Description

Pharmaceutical Raw Material Lumefantrine Artemether Lumefantrine Powder Lumefantrine

Product Description

Product Details

Product name	Lumefantrine
Cas number	82186-77-4
Apperance	Yellow Crystal Powder
MF	C30H32Cl3NO
MW	528.94018
Density	1.252
Melting point	129-131°C

Lumefantrine (or benflumetol) is an antimalarial pharm. It is only used in combination with artemether.The term "co-artemether" is sometimes used to describe this combination. Lumefantrine has a much longer half-life compared to artemether, and is therefore thought to clear any residual parasites that remain after combination treatment.

Application&Function

Lumefantrine (benflumetol) is created for our class of drug mefloquine on Plasmodium vivax sexual and asexual body a clear killing effect on P. vivax has a good effect to prevent.

Lumefantrine (Benflumetol) is a new kinds of mefloquine drug. Obvious Effect of killing vivax malaria, as well as in preventing.

It also can kill the Falciparum malaria phorozoon, but slow effect.
It can reduce the gametophyte rate in blood, suppression the development of the gametophyte in mosquitoes.The cure rate of chloroquine-resistant and multidrug-resistant falciparum malaria is more than 95%.Animal experiments show that the toxicity of this product is very low, and no adverse reaction on the clinical.

Specification