Description

Deoxydihydroartemisinin Acetate is a key pharmaceutical intermediate and derivative of artemisinin, a natural product renowned for its antimalarial properties. This compound is valued for its role in the research and synthesis of novel therapeutic agents, particularly in the development of next-generation antimalarial drugs and other bioactive molecules. It is essential for pharmaceutical R&D laboratories, fine chemical manufacturers, and academic institutions engaged in medicinal chemistry and drug discovery programs.

Application

• Pharmaceutical Intermediate: A critical building block in the synthetic pathway for advanced antimalarial compounds and other artemisinin-based derivatives.
• Medicinal Chemistry Research: Used in structure-activity relationship (SAR) studies to develop new drug candidates with improved efficacy and reduced resistance.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method development in pharmaceutical analysis.
• Active Pharmaceutical Ingredient (API) Synthesis: Employed in the production of potent antimalarial APIs and combination therapies.
• Biochemical Research: Utilized in studies investigating the mechanism of action of artemisinin and its analogs against *Plasmodium* parasites.
• Fine Chemical Production: A specialized reagent for the custom synthesis of complex, high-value organic molecules for clinical and preclinical testing.

Basic Information

Product Name	Deoxydihydroartemisinin Acetate
CAS No.	90935-12-9
Molecular Formula	C17H26O5
Molecular Weight	310.39 g/mol
Synonyms	Deoxy Dihydroartemisinin Acetate; Dihydroartemisinin Acetate, Deoxy-; Arteannuin B Acetate Derivative; (3R,5aS,6R,8aS,9R,10S,12R,12aR)-Decahydro-3,6,9-trimethyl-3,12-epoxy-12H-pyrano[4,3-j]-1,2-benzodioxepin-10-ol, acetate ester (derivative); Artemisinin derivative acetate; Deoxy-DHA Acetate
EINECS	Contact for details

Quality Control

Our Deoxydihydroartemisinin Acetate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via spectroscopic methods, to ensure it meets the high standards required for pharmaceutical research and development. Certificates of Analysis (COA) with detailed specifications are provided for every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). The product is light-sensitive and should be handled under appropriate conditions to maintain stability.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Conforms to reference
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.