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Tizanidine CAS NO 51322-75-9
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CAS No.:51322-75-9
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Tizanidine CAS NO 51322-75-9 is a centrally acting skeletal muscle relaxant belonging to the imidazoline chemical class. This high-purity active pharmaceutical ingredient (API) is critical for the formulation of medications that effectively manage spasticity associated with conditions like multiple sclerosis and spinal cord injuries. It is primarily required by pharmaceutical manufacturers and research institutions engaged in the development and production of generic and branded neurological therapeutics.
Application
- Pharmaceutical API: Primary use as the active ingredient in prescription muscle relaxant tablets and capsules.
- Neurological Disorder Treatment: Formulation of drugs for managing spasticity in patients with multiple sclerosis, spinal cord injury, and other neurological disorders.
- Generic Drug Manufacturing: Sourcing for the production of bioequivalent generic versions of branded tizanidine medications.
- Clinical Research: Utilization in preclinical and clinical studies for new therapeutic applications or dosage forms.
- Reference Standard: Serves as a high-purity chemical standard for analytical testing and quality control in laboratories.
- Contract Manufacturing: Supply to CDMOs (Contract Development and Manufacturing Organizations) for finished dosage form production.
Basic Information
| Product Name | Tizanidine |
| CAS No. | 51322-75-9 |
| Molecular Formula | C9H8ClN5S |
| Molecular Weight | 253.71 g/mol |
| Synonyms | 5-Chloro-N-(4,5-dihydro-1H-imidazol-2-yl)-2,1,3-benzothiadiazol-4-amine; Zanaflex; Sirdalud; DS-103-282; 4-(2-Benzothiazolyl)-2-imidazolidinone derivative; Tizanidine Hydrochloride (salt form); Tizanidin; Tizanidina |
| EINECS | Contact for details |
Quality Control
Our Tizanidine is manufactured under strict quality systems to meet the rigorous standards required for pharmaceutical intermediates and APIs. We ensure compliance with relevant pharmacopeial guidelines, and every batch is supported by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. Our quality assurance protocols are designed to guarantee batch-to-batch consistency and supply reliability for our global B2B partners.
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 away from incompatible materials and moisture.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to reference standard |
| Identification (HPLC) | Retention time matches reference |
| Assay (HPLC) | 98.0% - 102.0% (on anhydrous basis) |
| Related Substances (HPLC) | Individual impurity ≤ 0.5%; Total impurities ≤ 1.5% |
| 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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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
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