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Product Attributes
Model No.: 5749-67-7
Product Description
Carbasalate Calcium Powder is a pharmaceutical active ingredient derived from acetylsalicylic acid and calcium urea, commonly used in pharmaceutical formulation development. Supplied as a controlled-quality powder with defined chemical specifications, carbasalate calcium is evaluated through analytical testing, purity verification, and documentation support for professional pharmaceutical sourcing.
Carbasalate Calcium, also known as calcium acetylsalicylate, is a calcium salt complex of acetylsalicylic acid and urea. It is a white crystalline powder used as an active pharmaceutical ingredient (API) in specific pharmaceutical formulations.
Commercial carbasalate calcium is produced through controlled chemical synthesis and purification processes. The final quality profile depends on synthesis conditions, purity control, particle characteristics, residual solvent management, and analytical verification.
For pharmaceutical procurement, buyers should evaluate API identity, assay level, impurity profile, compliance documentation, analytical methods, and suitability for the intended dosage form.
| Item | Specification |
|---|---|
| Product Name | Carbasalate Calcium Powder |
| Alternative Name | Calcium Acetylsalicylate; Carbasalate Calcium |
| Product Category | Pharmaceutical Active Ingredient (API) |
| Active Compound | Carbasalate Calcium |
| CAS Number | 5749-67-7 |
| Molecular Formula | C19H18CaN2O9 |
| Molecular Weight | 458.43 g/mol |
| Appearance | White crystalline powder |
| Assay | Common pharmaceutical grades are supplied according to API specification requirements |
| Identification | Conforms to carbasalate calcium reference standard identification requirements |
| Standard Test Method | HPLC and pharmaceutical analytical methods |
| Production Method | Chemical synthesis and purification process |
| Particle Size | Fine powder; customized according to formulation requirements |
| Residual Solvents | Controlled according to pharmaceutical quality requirements |
| Heavy Metals | Controlled according to pharmaceutical standards |
| Microbial Quality | Controlled according to applicable pharmaceutical requirements |
| Shelf Life | Typically 24 months under recommended storage conditions |
| Storage | Store in a tightly sealed container in a cool, dry place protected from moisture and direct light |
| Packaging | Aluminum foil bags or pharmaceutical-grade containers; bulk packaging customized according to requirements |
The primary sourcing consideration for carbasalate calcium is pharmaceutical-grade quality control. Unlike general Nutritional Ingredients, API materials require strict evaluation of chemical identity, impurity profile, analytical validation, and regulatory documentation to support pharmaceutical 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 correct active pharmaceutical ingredient structure | Verify analytical identification methods |
| Manufacturing Process | Affects consistency and impurity control | Review production process and quality documentation |
| Documentation Package | Supports pharmaceutical qualification | Evaluate COA, TDS, SDS, and technical records |
Pharmaceutical active ingredients require consistent impurity control because even small variations can affect formulation quality. Analytical testing helps confirm purity, chemical identity, and batch consistency during pharmaceutical manufacturing.
Carbasalate Calcium quality control focuses on API identity, assay verification, impurity control, and pharmaceutical quality management.
COA, TDS, SDS, and technical documentation can be provided for pharmaceutical ingredient evaluation and procurement processes.
Carbasalate Calcium 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.

Carbasalate Calcium can support pharmaceutical projects requiring API sourcing, technical documentation, specification review, and customized packaging solutions according to project requirements.
Carbasalate calcium is a calcium salt complex related to acetylsalicylic acid and urea. It is supplied as a pharmaceutical active ingredient for specific formulation applications.
HPLC testing helps verify assay, chemical identity, and impurity profile. It supports reliable quality evaluation of pharmaceutical active ingredients.
Buyers should evaluate API purity, analytical methods, impurity control, manufacturing documentation, and suitability for the intended pharmaceutical formulation.
Carbasalate calcium powder should be stored in tightly sealed packaging under cool and dry conditions, protected from moisture, heat, and direct light.
Carbasalate Calcium Powder is a 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 pharmaceutical formulation projects. Contact us today to request samples, a COA, technical documents, and a wholesale quotation for Carbasalate Calcium Powder.

Packaging & Delivery
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