Description

Sodium Acetate, Anhydrous USP

Sodium Acetate, Anhydrous USP is a high-purity, crystalline salt used in pharmaceutical, nutraceutical, and laboratory applications as a buffering agent, pH stabilizer, and source of sodium ions. Compliant with United States Pharmacopeia (USP) standards, it provides consistent solubility, stability, and precise dosing for oral, parenteral, and compounding applications. Sodium Acetate, Anhydrous USP
• Is a USP-compliant sodium salt for pharmaceutical and laboratory use
• Is used as a buffer, pH regulator, and electrolyte source
• Is suitable for oral solutions, tablets, capsules, and parenteral formulations
• Supports formulation stability, controlled pH, and shelf-life extension
• Is manufactured under Good Manufacturing Practice (GMP) certified conditions
• Is supplied with complete regulatory documentation including Certificate of Analysis (CoA) and technical data
Sodium Acetate, Anhydrous USP is chemically designated as CH3COONa. It appears as a white, free-flowing crystalline powder that is highly soluble in water, forming clear solutions suitable for a wide range of formulations.
In pharmaceutical and laboratory applications, Sodium Acetate, Anhydrous USP is used in:
• Oral rehydration solutions, syrups, and electrolyte supplements
• Parenteral nutrition and intravenous formulations for sodium supplementation
• Buffering systems in tablets, capsules, and liquid dosage forms
• Stabilization of pH-sensitive actives and compounds
• Laboratory and research-grade reagents requiring controlled ionic strength
Sodium Acetate, Anhydrous USP provides consistent ion delivery and pH control, ensuring stability and efficacy of sensitive pharmaceutical and nutritional formulations.
CarboMer supplies Sodium Acetate, Anhydrous USP with control over assay, moisture content, particle size, and microbial purity. The material meets USP monograph specifications and is suitable for regulated pharmaceutical and laboratory applications.
The material is packaged in sealed, moisture-resistant, tamper-evident containers. Available in laboratory, pilot, and commercial-scale volumes. Minimum order quantities (MOQ), lead times, and documentation including CoA and SDS are provided upon request.
Each batch is tested for identity (IR, titration), assay, loss on drying, pH, heavy metals, and microbial limits. Certificates of Analysis (CoA), Safety Data Sheets (SDS), and full traceability documentation accompany every shipment.
As with all CarboMer pharmaceutical salts and excipients, Sodium Acetate, Anhydrous USP is supported by formulation guidance, regulatory expertise, and reliable global supply to ensure safe, effective, and compliant product development.