Antibiotic Solid Potassium Acetate
CAS NO.: 127-08-2
Molecular Formula: CH3COOK
Molecular Weight: 98.14
Character: white crystal and it is easily soluble in water, acid and alcohol.
Usage: It is used as buffer agent, diuretic of Benzylpenicillin potassium, chemical reagent, industrial catalyst, auxiliaries, and also used in snow & ice melting agent, fertilizer and oilfield drilling.
Package: 25kg plastic woven bag or 1000kg Ton-bag
Storage: It should be stored in a dry and ventilative warehouse, kept away from heat and moisture during transportation, unloaded with care so as to avoid damage. Furthermore, it must be stored separately from poisonous substances.
- Product Description
Antibiotic Solid Potassium Acetate – Pharmaceutical Grade Buffer & Precipitating Agent
SHANXI ZHAOYI CHEMICAL CO., LTD delivers pharmaceutical-grade Antibiotic Solid Potassium Acetate with ≥99.0% purity, specifically engineered for antibiotic synthesis and injectable drug formulations. Our product ensures consistent batch quality with chloride content ≤0.01% and heavy metals ≤0.0005%, meeting strict pharmacopeia standards.
Backed by 35+ years of manufacturing expertise since 1988, our 150,000-ton annual production capacity across a 27,000 m² facility guarantees stable supply for your API production needs. The white crystalline powder demonstrates superior solubility in water and maintains pH stability (7.5-9.0 in 5% solution), critical for preventing acid-induced degradation in antibiotic manufacturing. Our ISO, KOSHER, and HALAL certifications confirm commitment to pharmaceutical-grade quality control.
Key Features & Benefits
Ultra-High Immaculateness for Basic Applications
You get ≥99.0% substance with negligible debasements – chloride ≤0.01%, press ≤0.0005%, and overwhelming metals ≤0.0005%. This remarkable immaculateness avoids catalyst deactivation and guarantees fast crystallization in penicillin G potassium synthesis.
Stable pH Buffering Performance
Our item keeps up reliable pH levels (7.5-9.0) all through anti-microbial union forms. This soundness secures beta-lactam rings from acid-induced corruption, specifically progressing your last item surrender and potency.
Batch-to-Batch Consistency
Every shipment conveys indistinguishable execution characteristics. You dispose of quality vacillations that cause conflicting blend comes about, lessening squander and generation delays in your fabricating line.
Superior Compatibility
The detailing coordinating consistently with natural solvents like butyl acetic acid derivation. You dodge undesirable by-products that complicate downstream filtration processes.
Fast Disintegration Rate
The white crystalline structure breaks down quickly in watery and alcoholic media. This quickens your response times and diminishes handling cycles.

Technical Specifications
Parameter | Specification | Test Method |
Content (CH₃COOK) | ≥99.0% | Titration |
Water Insoluble Matter | Qualified | Visual inspection |
Basicity (as K₂CO₃) | ≤0.12% | Titration |
Acidity (as HA) | ≤0.05% | Titration |
Chloride (Cl) | ≤0.01% | Ion chromatography |
Sulfate (SO₄) | ≤0.02% | Gravimetric |
Iron (Fe) | ≤0.0005% | Spectrophotometry |
Heavy Metal (as Pb) | ≤0.0005% | Atomic absorption |
Potassium Permanganate Reducing | Qualified | Color comparison |
pH (5% Solution) | 7.5-9.0 | pH meter |
Molecular Weight | 98.14 g/mol | - |
CAS Number | 127-08-2 | - |
Appearance | White crystal | Visual |
How It Works?
In Penicillin G Potassium Production
When you introduce Antibiotic Solid Potassium Acetate into your solvent system containing penicillin, the potassium ions immediately attach to the antibiotic molecule. The high purity accelerates crystal nucleation, giving you uniform particle size and maximum API recovery.
As a pH Buffer in Injectable Formulations
The acetate component neutralizes acids generated during antibiotic reconstitution. This buffering action keeps your solution within the narrow pH window required for drug stability, extending shelf life post-mixing.
In Dialysate Manufacturing
Your patients' livers convert acetate ions to bicarbonate for acid-base balance. The precise potassium content ensures electrolyte levels remain within therapeutic ranges during hemodialysis treatments.
The mechanism relies on the compound's dual functionality – providing both ionic exchange capacity and buffering reserve. You achieve stable reaction environments that protect sensitive antibiotic structures.
Our Factory
30-YEAR ACETATE SPECIALIST | Non-caking, High Purity, Global Supply Chain



Applications
Penicillin G Potassium Synthesis
You utilize it as the accelerating specialist in butyl acetic acid derivation dissolvable frameworks. The item conveys 95%+ crystallization yields with negligible pollution carryover into your last API.
Injectable Anti-microbial Formulations
Formulators depend on this buffer for ceftriaxone, ampicillin, and other parenteral anti-microbials. It avoids pH float amid capacity and keeps up medicate power through termination dates.
Hemodialysis Concentrates
Dialysate producers consolidate it as the acetic acid derivation and potassium source. The pyrogen-free review meets USP measures for persistent security in renal substitution therapy.
Veterinary Anti-microbial Production
Animal wellbeing companies utilize it in procaine penicillin and oxytetracycline fabricating. The food-grade compliance bolsters veterinary pharmaceutical regulations.
Research & Advancement Labs
Pharmaceutical R&D groups utilize it for anti-microbial amalgamation pathway investigation. The steady quality dispenses with factors in strategy improvement considers.
Antibiotic Solid Potassium Acetate vs Other Products
Feature | Our Pharma Grade | Standard Industrial Grade | Competitor Pharma Grade |
Purity (CH₃COOK) | ≥99.0% | 95-98% | 98.5-99.0% |
Heavy Metals (Pb) | ≤0.0005% | ≤0.003% | ≤0.001% |
Chloride Content | ≤0.01% | ≤0.05% | ≤0.02% |
Batch Consistency | ±0.1% variation | ±0.5% variation | ±0.2% variation |
pH Stability | 7.5-9.0 | 7.0-10.0 | 7.5-9.5 |
Dissolution Time | <3 minutes | <10 minutes | <5 minutes |
Certifications | ISO/KOSHER/HALAL | ISO only | ISO/HALAL |
Technical Support | Dedicated team | Limited | Basic |
Supply Capacity | 150,000 tons/year | Varies | 50,000 tons/year |
Lead Time | 7-14 days | 21-30 days | 14-21 days |
Certifications & Compliance
Our manufacturing facility holds ISO quality management certification, ensuring every production batch meets international pharmaceutical standards. The product complies with KOSHER and HALAL requirements, expanding your market access to regions with specific religious dietary laws.
We maintain strict adherence to Good Manufacturing Practices (GMP) for pharmaceutical-grade chemicals. Documentation packages include Certificate of Analysis (CoA), Material Safety Data Sheet (MSDS), and batch traceability records.
Third-party testing through accredited laboratories like SGS validates our specifications. You receive complete regulatory documentation supporting your own quality audits and regulatory submissions.

Manufacturing Process
Crude Fabric Selection
We source pharmaceutical-grade acidic corrosive and potassium hydroxide from certified providers. Approaching materials experience thorough testing some time recently entering production.
Neutralization Reaction
Controlled expansion of potassium hydroxide to acidic corrosive happens in glass-lined reactors. Temperature and pH checking guarantees total change with negligible by-products.
Crystallization & Filtration
The arrangement experiences moderate cooling to frame uniform precious stones. Multi-stage filtration evacuates water-insoluble pollutions to accomplish target immaculateness levels.
Drying & Milling
Low-temperature vacuum drying jam item soundness. Exactness processing produces reliable molecule sizes for ideal disintegration characteristics.
Quality Control & Packaging
Each bunch completes a 12-point quality assessment some time recently discharge. Computerized bundling lines keep up contamination-free exchange from generation to fixed holders.

Packaging Options
25kg Plastic Woven Bags
Our standard bundling suits little to medium clump operations. The moisture-resistant internal liner secures against mugginess amid capacity and transportation.
1000kg Ton-Bags (Enormous Bags)
High-volume producers advantage from bulk bundling that decreases dealing with recurrence. The food-grade PP development avoids defilement whereas optimizing distribution center space.
Custom Bundling Solutions
We oblige your particular necessities counting littler lab-size holders or specialized moisture-barrier bundling for touchy climate zones.
All bundling incorporates clear labeling with clump numbers, generation dates, close dates, and risk images. The tear-resistant development minimizes item misfortune amid shipment.
Packing

Why Choose Us?
35+ A long time of Fabricating Excellence
Since 1988, we've culminated acetic acid derivation generation forms. Your orders advantage from decades of investigating information and prepare optimization that more current producers lack.
Unmatched Generation Capacity
Our 150,000-ton yearly capacity implies you never confront supply deficiencies. We keep up buffer stock for pharmaceutical-grade items, guaranteeing prompt accessibility amid your critical requirements.
Technical Interview Team
Our chemists get it anti-microbial blend challenges. You get free specialized bolster for handle optimization, solvency questions, and administrative documentation assistance.
Global Conveyance Network
With set up trade channels to Europe, America, and Asia, we handle universal shipping coordinations. You get items with legitimate hazmat documentation and traditions compliance.
Competitive Estimating Without Compromise
Large-scale generation proficiency deciphers to taken a toll investment funds. You get pharmaceutical-grade quality at costs competitive with industrial-grade options from littler suppliers.
Customer-Centric Benefit Philosophy
We prioritize long-term associations over single exchanges. Your input straightforwardly impacts our quality changes and item advancement activities.
FAQ
Q: What makes your product suitable for penicillin production?
A: The ≥99.0% purity and ≤0.0005% heavy metal content prevent impurity-related yield losses. The rapid dissolution accelerates crystal formation, giving you higher API recovery rates.
Q: Can I use this for both research and commercial manufacturing?
A: Absolutely. The same batch quality serves lab-scale synthesis and full production runs. You eliminate variables when scaling up from development to commercial operations.
Q: How do you ensure batch-to-batch consistency?
A: Our automated production line maintains identical reaction conditions. Statistical process control monitors 12 quality parameters in real-time, with ±0.1% maximum variation between batches.
Q: What is the shelf life under proper storage?
A: When stored in dry, ventilated warehouses away from moisture, the product maintains specifications for 24 months. We provide storage guidelines with every shipment.
Q: Do you provide samples for testing?
A: Yes, we offer 500g to 2kg samples with full CoA documentation. This allows your quality team to validate compatibility before placing bulk orders.
Q: What documentation supports regulatory submissions?
A: You receive CoA, MSDS, test reports, manufacturing flow diagrams, and compliance certificates. Our team assists with additional documentation your regulatory affairs department may require.
Q: How quickly can you fulfill urgent orders?
A: Standard lead time is 7-14 days. For urgent requirements with existing stock, we arrange expedited shipping within 3-5 days to your facility.
Q: Is the product compatible with organic solvents?
A: Yes, it dissolves readily in water, alcohols, and mixed solvent systems like butyl acetate. The high purity prevents phase separation or precipitation issues.



Request a Quote
Ready to improve your antibiotic production efficiency with Antibiotic Solid Potassium Acetate? Contact our team for customized pricing, technical specifications, and sample requests.
Email: sxzy@sxzhaoyi.com
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