Description

Rescinnamine is a crystalline alkaloid compound derived from various *Rauwolfia* species, recognized for its specific pharmacological profile. This high-purity active pharmaceutical ingredient (API) is critical for research and development in cardiovascular and neurological therapeutics. It is primarily utilized by pharmaceutical manufacturers, advanced research institutions, and fine chemical suppliers serving the global life sciences sector.

Application

• Pharmaceutical Active Ingredient (API): Serves as a key intermediate or direct component in the formulation of antihypertensive and psychotropic medications.
• Biochemical Research: Used as a reference standard and tool compound in pharmacological studies investigating adrenergic and serotonergic pathways.
• Analytical Chemistry: Employed as a certified reference material (CRM) for quality control and method validation in analytical laboratories.
• Fine Chemical Synthesis: Acts as a sophisticated building block for the semi-synthesis of novel derivatives and analogs in medicinal chemistry programs.

Basic Information

Product Name	Rescinnamine
CAS No.	24815-24-5
Molecular Formula	C35H42N2O9
Molecular Weight	634.72 g/mol
Synonyms	Rescinnamine; Apoterin; Anaprel; Cinnasil; Rescinnamin; Moderil; (3β,16β,17α,18β,20α)-11,17-Dimethoxy-18-[(3,4,5-trimethoxybenzoyl)oxy]yohimban-16-carboxylic acid methyl ester
EINECS	Contact for details

Quality Control

Our Rescinnamine is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. The product is tested against rigorous in-house specifications, which typically include identification, assay, and impurity profile analysis. A comprehensive Certificate of Analysis (COA) detailing all test results is provided with each shipment to support your quality assurance protocols.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container should be kept in a low-humidity environment and opened under dry conditions to minimize moisture uptake.

Specification

Item	Specification
Appearance	White to off-white crystalline 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 ≤ 0.5%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%

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