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Isoperisone CAS NO 64840-92-2
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CAS No.:64840-92-2
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Isoperisone is a pharmaceutical intermediate and active ingredient with the CAS registry number 64840-92-2. This compound is valued for its role as a skeletal muscle relaxant, primarily used to alleviate muscle stiffness and pain associated with various conditions. It is a critical component for manufacturers in the pharmaceutical industry developing formulations for neurological and musculoskeletal disorders. Our supply ensures high purity and consistent quality for reliable integration into your production processes.
Application
- Pharmaceutical Active Ingredient (API): Primary use as a centrally-acting muscle relaxant in prescription medications.
- Neurological Disorder Treatments: Formulation component for drugs targeting spasticity, cervical spondylosis, and related conditions.
- Musculoskeletal Pain Management: Used in products designed to relieve pain from muscle strains, lower back pain, and shoulder stiffness.
- Generic Drug Manufacturing: Key intermediate for the production of generic muscle relaxant formulations.
- Research & Development: Reference standard and building block in pharmacological research for new neuro-muscular therapies.
- Veterinary Pharmaceuticals: Potential application in veterinary medicine for animal muscle relaxation.
Basic Information
| Product Name | Isoperisone |
| CAS No. | 64840-92-2 |
| Molecular Formula | C₁₆H₂₅NO₂ |
| Molecular Weight | 263.38 g/mol |
| Synonyms | 4-(1-Methylethyl)-2-methyl-3-(1-pyrrolidinyl)-1-(2,4,6-trimethoxyphenyl)-1-butanone; 3-Pyrrolidinyl-1-(2,4,6-trimethoxyphenyl)-1-butanone; Isoprenaline related compound; Eperisone impurity; Myonal (brand name reference); Muscle relaxant intermediate |
| EINECS | Contact for details |
Quality Control
Our Isoperisone is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for assay and purity, residual solvent analysis, and identification by IR and NMR, to ensure it meets high-grade pharmaceutical standards. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming compliance with agreed specifications. We support compliance with GMP, ICH Q7 guidelines, and relevant pharmacopoeial requirements.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric 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) | Total impurities ≤ 2.0% Any single unknown impurity ≤ 0.5% |
| Water Content (KF) | ≤ 1.0% |
| 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.
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