Description

Potassium Acetate, Crystalline Powder, USP

Potassium Acetate, crystalline powder, USP is a high-purity, water-soluble salt used in pharmaceutical, nutraceutical, and clinical applications as an electrolyte, buffering agent, and stabilizer. As the USP-grade crystalline form of potassium acetate, it provides reliable and precise dosing of potassium for oral, parenteral, and compounding applications.

• USP-compliant crystalline Potassium salt
• Used as an electrolyte in oral, intravenous, and parenteral solutions
• Functions as a pH buffer, stabilizer, and source of potassium ions
• Suitable for pharmaceutical preparations, laboratory reagents, and clinical nutrition
• Manufactured under Good Manufacturing Practice (GMP) conditions
• Supplied with complete regulatory documentation including Certificate of Analysis (CoA) and technical data

Potassium Acetate, crystalline powder, USP is a white, hygroscopic powder that dissolves readily in water to yield potassium and acetate ions. Its stability, purity, and solubility make it ideal for use in solutions requiring precise electrolyte balance and pH control.

In pharmaceutical and clinical applications, Potassium Acetate, crystalline powder, USP is used in:

• Oral rehydration solutions and electrolyte supplements
• Intravenous and parenteral nutrition formulations for potassium supplementation
• Buffering systems in tablets, capsules, and liquid dosage forms
• Laboratory reagents and research-grade solutions requiring stable potassium sources
• Clinical formulations for metabolic, renal, or acid-base management

Potassium acetate provides both potassium supplementation and buffering capacity, helping maintain physiological electrolyte balance and prevent acid-base disturbances during medical treatments.

CarboMer supplies Potassium Acetate, crystalline powder, USP with strict control over assay, moisture content, heavy metals, and microbial purity. Material meets USP monograph specifications and is suitable for human use in regulated pharmaceutical and nutritional products.

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 (Potassium content), 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, Potassium Acetate, crystalline powder, USP is supported by formulation guidance, regulatory assistance, and reliable global supply to help develop safe, effective, and compliant dosage forms.