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Shaanxi Kaishi Biotechnology Co., Ltd
Product Description
Sulfaquinoxaline Sodium Powder is a sulfonamide pharmaceutical ingredient widely used in veterinary medicine and animal health product development. Supplied as a high-quality active pharmaceutical ingredient, sulfaquinoxaline sodium features controlled purity, analytical verification, and documentation support for professional veterinary formulation and manufacturing applications.
Sulfaquinoxaline Sodium is the sodium salt form of sulfaquinoxaline, a sulfonamide compound developed for veterinary pharmaceutical applications. It is commonly used as an active ingredient in animal health formulations due to its defined chemical structure and established pharmaceutical properties.
Commercial sulfaquinoxaline sodium is produced through controlled chemical synthesis and purification processes. Product quality depends on raw material control, synthesis consistency, purity level, impurity profile, and analytical verification methods.
For veterinary pharmaceutical procurement, buyers should evaluate active ingredient identity, assay level, impurity control, manufacturing documentation, analytical methods, and suitability for the intended dosage form.
| Item | Specification |
|---|---|
| Product Name | Sulfaquinoxaline Sodium Powder |
| Product Category | Veterinary Pharmaceutical API / Sulfonamide Ingredient |
| Active Compound | Sulfaquinoxaline Sodium |
| CAS Number | 967-80-6 |
| Molecular Formula | C14H11N4NaO2S |
| Molecular Weight | 306.32 g/mol |
| Appearance | White to slightly yellow crystalline powder |
| Assay | Common veterinary pharmaceutical grades are supplied according to API specification requirements |
| Identification | Conforms to sulfaquinoxaline sodium reference standard identification requirements |
| Standard Test Method | HPLC and pharmaceutical analytical methods |
| Production Method | Chemical synthesis and purification process |
| Solubility | Soluble in water depending on formulation conditions |
| Particle Size | Fine powder; customized according to formulation requirements |
| Residual Solvents | Controlled according to pharmaceutical quality standards |
| Heavy Metals | Controlled according to applicable pharmaceutical requirements |
| Microbial Quality | Controlled according to veterinary pharmaceutical standards |
| Shelf Life | Typically 24 months under recommended storage conditions |
| Storage | Store tightly sealed in a cool, dry place protected from moisture, heat, and direct light |
| Packaging | Aluminum foil bags or pharmaceutical-grade containers; bulk packaging customized according to requirements |
The main sourcing consideration for sulfaquinoxaline sodium is maintaining pharmaceutical-grade quality and consistency. Veterinary API buyers should focus on chemical identity, purity profile, impurity control, and documentation quality to ensure compatibility with animal health product manufacturing.
| Evaluation Factor | Why It Matters | Buyer Consideration |
|---|---|---|
| API Purity | Determines active ingredient quality and formulation reliability | Review assay results and impurity profile data |
| Chemical Identity | Confirms the correct sodium salt structure | Verify analytical identification methods |
| Solubility Characteristics | Affects dosage form design and processing | Consider formulation requirements and application type |
| Documentation Package | Supports veterinary pharmaceutical qualification | Review COA, TDS, SDS, and technical records |
Veterinary Pharmaceutical Ingredients require consistent impurity management because raw material quality directly affects formulation control. Analytical testing helps verify active compound content, chemical identity, and batch-to-batch consistency.
Sulfaquinoxaline Sodium quality control focuses on API identity, assay verification, impurity management, and pharmaceutical quality systems.
COA, TDS, SDS, and technical documentation can be provided for veterinary pharmaceutical ingredient evaluation and procurement.
Sulfaquinoxaline Sodium Powder is supplied in sealed pharmaceutical-grade packaging designed to protect product quality during storage and transportation.
The product should be stored in a cool and dry environment, protected from moisture, heat, and direct light. Proper storage helps maintain API stability and quality.
Sulfaquinoxaline Sodium can support veterinary pharmaceutical projects requiring API sourcing, technical documentation, specification review, and customized packaging solutions according to project requirements.
Sulfaquinoxaline Sodium is the sodium salt form of sulfaquinoxaline, a sulfonamide pharmaceutical ingredient used in veterinary medicine and animal health product development.
HPLC testing helps verify assay, chemical identity, and impurity profile. It supports reliable quality evaluation of veterinary pharmaceutical active ingredients.
Buyers should evaluate API purity, analytical methods, impurity control, manufacturing documentation, and suitability for the intended veterinary formulation.
Sulfaquinoxaline sodium powder should be stored in tightly sealed packaging under cool and dry conditions, protected from moisture, heat, and direct light.
Sulfaquinoxaline Sodium Powder is a veterinary pharmaceutical active ingredient requiring accurate identification, purity control, and reliable analytical documentation. With controlled API specifications and professional supply support, it provides a dependable raw material solution for animal health formulation projects. Contact us today to request samples, a COA, technical documents, and a wholesale quotation for Sulfaquinoxaline Sodium Powder.
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