Description

Deserpidine CAS NO 131-01-1 is a high-purity alkaloid derived from *Rauwolfia canescens*. This compound is a critical intermediate and active pharmaceutical ingredient (API) valued for its specific pharmacological profile. It is primarily utilized by pharmaceutical manufacturers and research institutions engaged in the development of cardiovascular and neurological therapeutics.

Application

• Pharmaceutical API: Serves as a key active ingredient in the formulation of antihypertensive and antipsychotic medications.
• Biochemical Research: Used as a reference standard and tool compound in neurological and cardiovascular research studies.
• Precision Medicine: Employed in the development of targeted therapies due to its specific receptor activity.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for the production of finished dosage forms.
• Analytical Standard: Provides a high-purity benchmark for quality control and method validation in analytical laboratories.

Basic Information

Product Name	Deserpidine
CAS No.	131-01-1
Molecular Formula	C32H38N2O8
Molecular Weight	578.66 g/mol
Synonyms	11-Desmethoxyreserpine; Canescine; Harmonyl; Raunormine; Recanescine; Deserpidin; Deserpidinum; (3β,16β,17α,18β,20α)-11,17-Dimethoxy-18-[(3,4,5-trimethoxybenzoyl)oxy]yohimban-16-carboxylic acid methyl ester
EINECS	205-019-7

Quality Control

Our Deserpidine is manufactured under strict quality management systems. Each batch is subjected to comprehensive analytical testing, including HPLC for purity and identity confirmation, to ensure it meets stringent pharmaceutical-grade specifications. A detailed Certificate of Analysis (COA) is provided with every shipment to guarantee traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store under an inert atmosphere (e.g., nitrogen or argon) at a controlled room temperature of 15-25°C to prevent oxidation and degradation. The container should be kept in a cool, dry, and well-ventilated area.

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)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.5% 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.