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Mebeverine CAS NO 3625-06-7
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CAS No.:3625-06-7
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Mebeverine CAS NO 3625-06-7 is a pharmaceutical active ingredient classified as an antispasmodic agent. It is primarily valued for its direct action on the smooth muscle of the gastrointestinal tract, providing relief from spasms without affecting normal gut motility. This compound is essential for manufacturers in the pharmaceutical industry producing medications for irritable bowel syndrome (IBS) and other functional gastrointestinal disorders.
Application
- Pharmaceutical Formulations: Primary active ingredient in antispasmodic medications for the treatment of irritable bowel syndrome (IBS).
- Gastrointestinal Spasm Relief: Used in drugs targeting abdominal pain, cramping, and bloating associated with functional bowel disorders.
- Tablet and Capsule Production: Incorporated into solid oral dosage forms for patient convenience and compliance.
- Clinical Research: Serves as a reference standard and active component in preclinical and clinical studies for new gastrointestinal therapies.
- Generic Drug Manufacturing: Key ingredient for companies producing bioequivalent versions of branded antispasmodic drugs.
- Compounding Pharmacy: Used in specialized pharmacy preparations for tailored patient treatment plans.
Basic Information
| Product Name | Mebeverine |
| CAS No. | 3625-06-7 |
| Molecular Formula | C25H35NO5 |
| Molecular Weight | 429.55 g/mol |
| Synonyms | Mebeverine Hydrochloride (common salt form); 4-[Ethyl[1-(4-methoxyphenyl)propan-2-yl]amino]butyl 3,4-dimethoxybenzoate; Duspatalin (brand name); Colofac (brand name); Mebeverinum; Mebeverini; 4'-(Ethyl[2-(4-methoxyphenyl)-1-methylethyl]amino)butyl veratrate |
| EINECS | 222-848-9 |
Quality Control
Our Mebeverine is manufactured under strict quality systems suitable for pharmaceutical use. It undergoes rigorous analytical testing to ensure compliance with relevant pharmacopoeial standards such as EP (European Pharmacopoeia) and USP (United States Pharmacopeia). Every batch is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles, available upon request to support your regulatory filings.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after each use to prevent degradation from atmospheric humidity.
Specification
| Item | Specification |
|---|---|
| Appearance | White or almost 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) |
| Water Content (KF) | ≤ 1.0% |
| Residue on Ignition | ≤ 0.1% |
| Related Substances (HPLC) | Individual impurity: ≤ 0.5%; Total impurities: ≤ 1.5% |
| Heavy Metals | ≤ 20 ppm |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
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