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Mosapride CAS NO 112885-41-3
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CAS No.:112885-41-3
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Mosapride is a selective 5-HT4 receptor agonist belonging to the benzamide class of compounds. This pharmaceutical active ingredient is valued for its prokinetic properties, which enhance gastrointestinal motility. It is primarily utilized in the development and manufacturing of prescription medications targeting functional dyspepsia and gastroesophageal reflux disease (GERD). Our supply of Mosapride CAS NO 112885-41-3 meets the stringent purity requirements of the global pharmaceutical industry.
Application
- Active Pharmaceutical Ingredient (API): Core component in the formulation of prescription drugs for gastrointestinal disorders.
- Gastroprokinetic Agent: Used in medications to treat symptoms of functional dyspepsia, such as postprandial fullness and early satiety.
- GERD Management: Incorporated into therapeutic regimens for gastroesophageal reflux disease to improve esophageal clearance.
- Pharmaceutical Research & Development: Serves as a reference standard and key intermediate in preclinical and clinical studies for new GI therapeutics.
- Generic Drug Manufacturing: Essential for producing generic versions of established prokinetic medications for global markets.
- Veterinary Pharmaceuticals: Potential application in veterinary medicine for treating gastrointestinal motility issues in animals.
Basic Information
| Product Name | Mosapride |
| CAS No. | 112885-41-3 |
| Molecular Formula | C21H25ClFN3O3 |
| Molecular Weight | 421.89 g/mol |
| Synonyms | 4-Amino-5-chloro-2-ethoxy-N-[[4-[(4-fluorophenyl)methyl]-2-morpholinyl]methyl]benzamide; Mosapride Citrate (common salt form); AS-4370; Gasmotin (brand name); 5-HT4 receptor agonist; Benzamide derivative |
| EINECS | Contact for details |
Quality Control
Our Mosapride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency, meeting or exceeding relevant pharmacopeial standards. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting key parameters such as assay, related substances, and residual solvents. We support compliance with GMP, ICH Q7, and other global regulatory guidelines for active pharmaceutical ingredients.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (typically 15-25°C). Keep the container tightly sealed to protect from moisture.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to reference spectrum |
| Identification (HPLC) | Retention time corresponds to reference standard |
| Assay (HPLC) | 98.0% - 102.0% (on anhydrous basis) |
| Related Substances (HPLC) | Individual impurity: ≤ 0.5% Total impurities: ≤ 1.5% |
| Loss on Drying | ≤ 0.5% |
| Residue on Ignition | ≤ 0.1% |
| Heavy Metals | ≤ 20 ppm |
| 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.
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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.






