Description

17,18-Didehydrovincamine is a high-purity alkaloid derivative of significant interest in pharmaceutical research and development. This compound serves as a crucial intermediate and reference standard for the synthesis and analysis of advanced therapeutic agents targeting neurological and cardiovascular systems. It is primarily utilized by research institutions, pharmaceutical manufacturers, and fine chemical suppliers engaged in the development of nootropic and vasodilatory drugs. Our product is supplied with guaranteed purity and stability to meet the stringent demands of modern pharmaceutical applications.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of advanced Vinca alkaloid derivatives and related active pharmaceutical ingredients (APIs).
• Reference Standard: Used for analytical method development, validation, and quality control (QC) testing in pharmaceutical laboratories.
• Neurological Research: Investigated in preclinical studies for its potential effects on cerebral metabolism and cognitive function.
• Vasodilatory Agent Research: Studied for its potential role in improving cerebral and peripheral blood flow.
• Fine Chemical Synthesis: Employed in the production of specialized, high-value compounds for medicinal chemistry.
• Biochemical Research: Used as a tool compound to study biological pathways and mechanisms of action related to alkaloids.

Basic Information

Product Name	17,18-Didehydrovincamine
CAS No.	32790-09-3
Molecular Formula	C21H24N2O3
Molecular Weight	352.43 g/mol
Synonyms	17,18-Dehydrovincamine; Didehydrovincamine; Vincaminor; (3α,16α)-Eburnamenine-14-carboxylic acid methyl ester; 14,15-Didehydrovincamine; Eburnamenine-14-carboxylic acid, methyl ester, (3α,16α)-; Methyl (3α,16α)-14,15-didehydroeburnamenine-14-carboxylate
EINECS	Contact for details

Quality Control

Our 17,18-Didehydrovincamine is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. Each lot is subjected to comprehensive analytical testing, including identity confirmation, purity assay, and impurity profiling. A Certificate of Analysis (COA) detailing all test results is provided with every shipment. We support compliance with cGMP and ICH guidelines for pharmaceutical ingredients, and specifications can be aligned with client-specific pharmacopeial requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a 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 powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0% Any single impurity ≤0.5%
Loss on Drying	≤0.5%
Residue on Ignition	≤0.1%
Heavy Metals	≤20 ppm

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