Benzylpenicillin Potassium (Penicillin G Potassium)
1. Product OverviewBenzylpenicillin Potassium, also known as Penicillin G Potassium, is a classic first-generation β-lactam antibiotic API. It is produced via microbial deep fermentation followed by crystallization and purification processes, presenting as white crystalline powder with strong broad-spectrum bactericidal activity against gram-positive bacteria and partial gram-negative pathogens. Our product complies with major international pharmacopoeia standards (USP, EP, BP, CP), manufactured in GMP-certified workshops, and serves as the core raw material for sterile injectable penicillin powder for global pharmaceutical manufacturers.
2. Core Technical Specifications- Active Ingredient: Benzylpenicillin Potassium (Penicillin G Potassium)
- CAS Number: 113-98-4
- Chemical Formula: C₁₆H₁₇KN₂O₄S
- Molecular Weight: 372.48
- Assay: 98.0% ~ 102.0% (anhydrous basis)
Place of Origin: China
3. Pharmacological MechanismBenzylpenicillin Potassium exerts bactericidal effects by inhibiting the synthesis of bacterial cell walls. It blocks the cross-linking reaction of peptidoglycan, the key structural component of bacterial cell membranes, leading to incomplete cell wall formation, osmotic lysis and death of sensitive bacteria.It shows potent activity against Streptococcus, Staphylococcus, Pneumococcus, Neisseria gonorrhoeae, Clostridium tetani and other gram-positive pathogenic bacteria.
4. Main Application Fields- Human Pharmaceutical APIRaw material for sterile injectable Benzylpenicillin Potassium powder, clinically used for the treatment of respiratory tract infections, skin and soft tissue infections, septicemia, syphilis, tetanus and other bacterial infectious diseases.
- Veterinary Antibiotic Raw MaterialFor prevention and treatment of livestock and poultry bacterial infections in animal health preparations.
Biochemical Research ReagentUsed as antibacterial additive for microbial culture medium in laboratory research.
5. Core Product Advantages- Stable Crystalline Form & Low ImpuritiesUniform crystal particles, low polymer and protein residue, effectively reducing the risk of allergic reactions in finished injections.
- Consistent Potency Batch to BatchStrict fermentation and purification control ensures stable antibacterial titer, meets strict injection-grade raw material requirements.
- Complete Compliance DocumentationEach batch is supplied with full COA, HPLC purity test, heavy metal, microbial limit and residual solvent inspection reports; GMP production certification available for import registration.
- Factory Direct Bulk SupplyAdequate spot inventory, flexible MOQ, customized packaging and stable long-term delivery for global pharmaceutical importers and preparation factories.
Strict Quality Traceability SystemWhole production chain tracking from fermentation raw materials to finished crystals, fully traceable for global regulatory audits.
6. Target Global BuyersPharmaceutical API importers, sterile powder for injection manufacturers, veterinary drug factories, pharmaceutical wholesale distributors, biomedical research laboratories, hospital pharmaceutical procurement groups.
