Description

Cinepazet CAS NO 23887-41-4 is a synthetic organic compound belonging to the class of cinepazic acid derivatives, recognized for its specific pharmacological activity. This high-purity chemical intermediate is critical for research and development in the pharmaceutical sector, where precise molecular structure and consistent quality are paramount. It is primarily utilized by pharmaceutical manufacturers and advanced research institutions focused on developing novel therapeutic agents.

Application

• Pharmaceutical Intermediate: Serves as a key building block in the synthesis of active pharmaceutical ingredients (APIs) for cardiovascular research.
• Biochemical Research: Used as a reference standard or reagent in studies investigating vasodilatory and anti-anginal mechanisms.
• Preclinical Development: Employed in the formulation and testing stages of new drug candidates during non-clinical studies.
• Process Chemistry: Acts as a starting material or intermediate in scale-up and optimization of synthetic routes within GMP environments.

Basic Information

Product Name	Cinepazet
CAS No.	23887-41-4
Molecular Formula	C20H28N2O5
Molecular Weight	376.45 g/mol
Synonyms	Cinepazic acid ethyl ester; Ethyl cinepazate; Cinepazet maleate (salt form); DL-Cinepazet; Ethyl 3,4,5-trimethoxycinnamoyl(piperazin-1-yl)acetate; (±)-Cinepazet; Vascoril (associated trade name)
EINECS	Contact for details

Quality Control

Our Cinepazet is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. The product undergoes comprehensive analytical testing, including HPLC for assay and related substances, residual solvent analysis, and identity confirmation. A 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, and well-ventilated area at a controlled room temperature (15-25°C). The product is hygroscopic (moisture-sensitive) and should be handled under dry conditions to maintain stability.

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	≤ 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.