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Antazoline Methanesulfonate CAS NO 3131-32-6
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CAS No.:3131-32-6
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Antazoline Methanesulfonate is a high-purity pharmaceutical salt form of the antihistamine compound antazoline. This material is a critical active pharmaceutical ingredient (API) and intermediate valued for its precise chemical structure and consistent performance in formulation. It is primarily required by pharmaceutical manufacturers and research institutions engaged in the development and production of ophthalmic solutions, nasal sprays, and other therapeutic agents targeting allergic responses. Our supply ensures the reliability and stringent quality control necessary for advanced medical applications.
Application
- Primary Active Pharmaceutical Ingredient (API) in ophthalmic solutions for allergic conjunctivitis.
- Key intermediate in the synthesis of advanced antihistamine formulations.
- Research and development of novel nasal decongestant and anti-allergy medications.
- Reference standard for analytical method development and quality control laboratories.
- Manufacturing of veterinary pharmaceutical products for allergic conditions.
- Component in stability studies and formulation optimization for drug delivery systems.
Basic Information
| Product Name | Antazoline Methanesulfonate |
| CAS No. | 3131-32-6 |
| Molecular Formula | C₁₇H₁₉N₃·CH₄O₃S |
| Molecular Weight | 377.46 g/mol |
| Synonyms | Antazoline Mesylate; 2-[(N-Benzylanilino)methyl]-2-imidazoline methanesulfonate; Antazoline methanesulphonate; Antistin methanesulfonate; Phenazoline Methanesulfonate; Antazoline Metilsulfate; N-(Benzylphenyl)-N',N'-dimethyl-2-imidazolin-2-ylamine methanesulfonate |
| EINECS | 221-525-8 |
Quality Control
Our Antazoline Methanesulfonate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical applications. We provide Certificates of Analysis (COA) detailing purity, identity, and impurity profiles, with testing performed in accordance with validated methods. Specifications can be aligned with pharmacopeial standards (such as USP/EP) upon request to support global regulatory submissions.
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 (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) |
| Water Content (KF) | ≤ 1.0% |
| Residue on Ignition | ≤ 0.1% |
| Heavy Metals | ≤ 20 ppm |
| Related Substances (HPLC) | Total impurities ≤ 2.0% Any single impurity ≤ 0.5% |
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.
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Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.






