Description

Rociverine CAS NO 53716-44-2 is a synthetic organic compound belonging to the class of antispasmodic agents. It is valued for its pharmacological activity in targeting smooth muscle spasms, making it a critical intermediate in the development of therapeutic formulations. This compound is primarily required by pharmaceutical manufacturers and research institutions engaged in the synthesis of anticholinergic and spasmolytic medications.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of prescription antispasmodic drugs.
• Research & Development: Used in preclinical and clinical studies for investigating smooth muscle relaxants.
• Active Pharmaceutical Ingredient (API) Manufacturing: Serves as a precursor in the production of finished dosage forms.
• Chemical Synthesis: Intermediate for creating novel derivatives with potential therapeutic applications.
• Reference Standard: Serves as an analytical standard for quality control and regulatory testing in pharmaceutical labs.

Basic Information

Item	Detail
Product Name	Rociverine
CAS No.	53716-44-2
Molecular Formula	C₂₀H₂₅NO₃
Molecular Weight	327.42 g/mol
Synonyms	Rociverine; 53716-44-2; 2-(Diethylamino)ethyl 1-phenylcyclopentanecarboxylate; 1-Phenylcyclopentanecarboxylic acid 2-(diethylamino)ethyl ester; Rociverinum; UNII-7D3Q5K5A04
EINECS	Contact for details

Quality Control

Our Rociverine is produced 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 impurity profiling, to meet the stringent requirements of pharmaceutical applications. A Certificate of Analysis (COA) detailing identity, purity, and related substances is provided with each shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed after opening to minimize exposure to atmospheric moisture.

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 ≤ 1.0% 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.