Description

Artemifone CAS NO 255730-18-8 is a high-purity synthetic chemical compound of significant interest in advanced pharmaceutical research and development. This compound serves as a critical intermediate or active pharmaceutical ingredient (API) in the synthesis of novel therapeutic agents. It is primarily utilized by research institutions and pharmaceutical companies engaged in the development of new drug candidates, particularly within specialized therapeutic areas. Our supply ensures consistent quality and reliable availability for critical R&D and scale-up processes.

Application

• Pharmaceutical Intermediate: A key building block in the multi-step synthesis of potential drug candidates.
• Active Pharmaceutical Ingredient (API) Development: Serves as the core active moiety in preclinical and clinical-stage pharmaceutical formulations.
• Biochemical Research: Used as a reference standard or probe compound in pharmacological and mechanism-of-action studies.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for cGMP production of clinical trial materials.
• Academic Research: Utilized in university and institutional labs for medicinal chemistry and synthetic methodology projects.
• Process Chemistry Optimization: Employed in route scouting and process development for efficient and scalable API manufacturing.

Basic Information

Product Name	Artemifone
CAS No.	255730-18-8
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Artemifone; 255730-18-8; UNII-8V71L1X0Y6; 8V71L1X0Y6; SCHEMBL2334221; DTXSID701318920; AKOS040750212; ZINC000003918756; (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
EINECS	Contact for details

Quality Control

Every batch of Artemifone is manufactured and tested under a strict quality management system. We provide material that meets high-purity standards suitable for pharmaceutical research and development. Comprehensive analytical testing, including identity confirmation, purity assay, and impurity profiling, is performed. A Certificate of Analysis (COA) detailing all test results and methods is provided with each shipment to ensure full traceability and compliance with your quality requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (typically 15-25°C). Keep the container tightly sealed to protect from moisture. For long-term storage, consider inert atmosphere conditions to maintain optimal stability.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 1.0%
Heavy Metals	≤ 20 ppm

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