share

Diphemanil Methylsulfate CAS NO 62-97-5


Unit Price:

CAS No.:62-97-5

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Diphemanil Methylsulfate is a quaternary ammonium anticholinergic agent with specific pharmacological activity. This compound is valued for its role as a key intermediate and active pharmaceutical ingredient (API) in the synthesis of specialized therapeutic agents. It is primarily required by pharmaceutical manufacturers and research institutions engaged in developing treatments for gastrointestinal disorders and other conditions involving smooth muscle spasm.

Application

  • Pharmaceutical Intermediate: Serves as a critical building block in the synthesis of anticholinergic and antispasmodic drug formulations.
  • Active Pharmaceutical Ingredient (API): Used as the primary active component in the manufacture of prescription medications targeting hypermotility of the gastrointestinal tract.
  • Research & Development: Employed in preclinical and clinical research studies investigating muscarinic receptor antagonists.
  • Chemical Synthesis: Utilized in organic synthesis for introducing quaternary ammonium functionalities into complex molecules.
  • Reference Standard: Sourced for use as an analytical standard in quality control laboratories for method development and validation.

Basic Information

Item Detail
Product Name Diphemanil Methylsulfate
CAS No. 62-97-5
Molecular Formula C20H27NO5S
Molecular Weight 393.50 g/mol
Synonyms Diphemanil Metilsulfate; 4-(Diphenylmethylene)-1,1-dimethylpiperidinium Methyl Sulfate; Prantal; Diphemanil Metilsulphate; 4-(Benzhydrylidene)-1,1-dimethylpiperidinium Methylsulfate; 1,1-Dimethyl-4-(diphenylmethylene)piperidinium Methyl Sulfate; Prantal Methylsulfate; Diphemanyl Methylsulfate
EINECS 200-549-8

Quality Control

Our Diphemanil Methylsulfate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency, meeting the stringent requirements for pharmaceutical intermediates. A Certificate of Analysis (COA) detailing specific results for assay, related substances, and residual solvents is provided with every 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 to minimize exposure to atmospheric moisture.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to structure
Assay (HPLC) 98.0% - 102.0% (on anhydrous basis)
Water Content (KF) ≤ 5.0%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Residual Solvents (GC) Complies with ICH Q3C guidelines

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

Complete Your RFQ

0/ 2000

Why choose US

Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.