Disinfection Preparation 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
Disinfection Preparation Solid Potassium Acetate
Shanxi Zhaoyi Chemical Co., Ltd. proudly manufactures pharmaceutical-grade Disinfection Preparation Solid Potassium Acetate (CAS 127-08-2) at our 27,000 m² production facility established in 1988. Our product achieves ≥99.0% purity with strict heavy metal limits (Pb ≤0.0005%, Fe ≤0.0005%) and meets USP, EP, and BP pharmacopeial standards.
With an annual production capacity of 150,000 tons across acetate series products, we deliver pharmaceutical-grade material featuring high solubility (253g/100ml at 20°C) and precise pH buffering (7.5-8.5 in 5% solution). Our product serves as a critical component in hemodialysis concentrates, pharmaceutical CIP systems, and sterile injectable manufacturing, ensuring microbial stability and chemical homogeneity for your medical and industrial applications.
Key Features & Benefits
Superior Pharmaceutical Purity
Our product delivers ≥99.0% assay purity on a dried basis, ensuring consistent performance in critical healthcare applications. You benefit from extremely low bacterial endotoxins (<2.5 EU/g) and strict heavy metal controls.
Exceptional Buffering Stability
The pH range of 7.5-8.5 in 5% solution provides optimal conditions for biocide efficacy and prevents microbial proliferation. Your formulations maintain stable pH environments essential for disinfection preparation integrity.
High Solubility Performance
With approximately 253g/100ml solubility at 20°C, you achieve rapid dissolution without residue. This characteristic streamlines your production processes and ensures uniform distribution in liquid preparations.
Comprehensive Safety Standards
Our product meets USP, EP, and BP specifications with rigorous testing for aluminum (<0.2ppm for dialysis safety). You gain confidence in regulatory compliance and patient safety.

Technical Specifications
Parameter | Specification |
Content (CH3COOK) | ≥99.0% |
Molecular Formula | CH3COOK |
Molecular Weight | 98.14 g/mol |
CAS Number | 127-08-2 |
Appearance | White crystalline powder |
Water Insoluble Matter | Qualified |
Basicity (as K2CO3) | ≤0.12% |
Acidity (as HA) | ≤0.05% |
Chloride (Cl) | ≤0.01% |
Sulfate (SO4) | ≤0.02% |
Iron (Fe) | ≤0.0005% |
Heavy Metals (as Pb) | ≤0.0005% |
pH (5% solution) | 7.5-8.5 |
Solubility at 20°C | ~253g/100ml |
Loss on Drying | <1.0% |
How It Works?
The item capacities through numerous synergistic instruments in pharmaceutical and therapeutic applications. As a vigorous alkalizing operator, it neutralizes acidic situations whereas keeping up exact pH control basic for dynamic biocide stability.
The acetic acid derivation particle gives bacteriostatic buffering activity that makes unfavorable conditions for microbial development. When broken down, it dissociates to discharge potassium and acetic acid derivation particles that control electrolyte adjust in dialysis liquids and therapeutic preparations.
Its tall solvency empowers fast integration into fluid frameworks without particulate arrangement. You accomplish homogeneous dispersion that guarantees steady antimicrobial assurance all through your cleansing arrangements. The buffering capacity anticipates pH float amid capacity and utilize, keeping up the adequacy of temperature-sensitive dynamic fixings.
Our Factory
30-YEAR ACETATE SPECIALIST | Non-caking, High Purity, Global Supply Chain



Applications
Hemodialysis Concentrate Fabricating
You'll discover our item broadly utilized in defining corrosive concentrate parcels of dialysis liquids. It gives basic potassium electrolyte sourcing whereas acting as a bacteriostatic buffer that avoids microbial development in liquid lines some time recently sterilization.
Pharmaceutical Clean-In-Place Frameworks
Our fabric serves as a neutralizing operator and buffer in CIP cleaning arrangements for biopharmaceutical tanks. It upgrades antacid cleanser adequacy against natural buildups in high-purity channeling environments.
Sterile Injectable Generation
In affront and antibody fabricating, it acts as a exact pH controller amid extraction and refinement stages. The sanitization arrangement perspective keeps up conditions unfavorable for contaminant expansion amid amalgamation of sterile injectables.
Medical Gadget Sanitization
Your cleansing liquid details advantage from steady pH support that optimizes biocide execution. It guarantees steady antimicrobial action over changed temperature and capacity conditions.
Airport Runway
This product provides solid ice and snow evacuation for runways



Disinfection Preparation Solid Potassium Acetate vs Other Products
Feature | Our Disinfection Preparation Grade | Technical Grade Potassium Acetate | Sodium Acetate Alternative |
Purity (CH3COOK) | ≥99.0% | ≥98.0% | ≥99.0% |
Heavy Metals (Pb) | ≤0.0005% | ≤0.001% | ≤0.002% |
Bacterial Endotoxins | <2.5 EU/g | Not controlled | Not controlled |
Aluminum Content | <0.2 ppm | Not specified | Not specified |
Pharmacopeial Compliance | USP/EP/BP | Industrial standards | Food/Industrial grade |
Dialysis Safety | Yes | No | No |
Loss on Drying | <1.0% | <2.0% | <1.5% |
Application Suitability | Medical/Pharma | De-icing/Industrial | Food/Industrial |
GMP Production | Yes | No | Varies |
Certifications & Compliance
Our manufacturing facility holds ISO 9001 certification, ensuring rigorous quality management systems. We've achieved KOSHER and HALAL certifications, expanding your market reach across diverse regions and customer requirements.
Our Disinfection Preparation Solid Potassium Acetate strictly adheres to USP (United States Pharmacopeia), EP (European Pharmacopoeia), and BP (British Pharmacopoeia) specifications. Production occurs in GMP-certified facilities with validated cleanroom environments.
We maintain comprehensive documentation including Certificate of Analysis, Material Safety Data Sheets, and Drug Master Files. Our quality control laboratory performs batch testing for bacterial endotoxins via LAL method, heavy metals via ICP-MS, and microbial limits (TAMC/TYMC) according to pharmacopeial requirements.

Manufacturing Process
Our generation starts with high-purity acidic corrosive and potassium hydroxide sourced from certified providers. Controlled neutralization responses happen in stainless steel reactors beneath strict temperature and pH monitoring.
Crystallization takes put in temperature-controlled situations to accomplish ideal gem estimate and immaculateness. Numerous washing stages evacuate leftover debasements counting chlorides, sulfates, and overwhelming metals.
Centrifugation and vacuum drying diminish dampness substance to <1.0% while preventing thermal degradation. Our quality control team samples each batch for comprehensive testing including microbial limits, endotoxins, and elemental analysis.
Final packaging occurs in climate-controlled cleanrooms meeting pharmaceutical production standards. We implement continuous process validation and maintain full traceability from raw materials through finished product.

Packaging Options
25kg Plastic Woven Packs
Perfect for medium-volume operations, these packs highlight double-lined PE development that ensures against dampness entrance. You get helpful dealing with for group generation processes.
1000kg Ton-Bags
Idealize for high-volume pharmaceutical producers, our gigantic sacks diminish taking care of recurrence and capacity space prerequisites. They keep up item astuteness through fortified development and dampness barriers.
Custom Bundling
We oblige your particular necessities counting littler research facility amounts or specialized holder setups. All bundling incorporates desiccant assurance and dampness indicators.
Each bundle incorporates batch-specific documentation
Certificate of Investigation, generation date, termination date, and capacity enlightening. We guarantee tamper-evident seals and clear labeling for administrative compliance.
Packing

Why Choose Us?
37 A long time of Fabricating Brilliance
Since 1988, we've refined our acetic acid derivation generation ability. You accomplice with a provider illustrating demonstrated soundness and persistent advancement in chemical manufacturing.
Massive Generation Capacity
Our 150,000-ton yearly capacity over acetic acid derivation items guarantees steady supply accessibility. You maintain a strategic distance from stock-out dangers that seem disturb your basic therapeutic generation schedules.
Global Quality Benchmarks
We're one of few Chinese producers accomplishing USP/EP/BP compliance with ISO, Legitimate, and HALAL certifications. Your administrative endorsement forms ended up smoother with our comprehensive documentation.
Technical Back Group
Our 60-person staff incorporates experienced chemists who get it pharmaceutical applications. You get responsive specialized help for definition optimization and troubleshooting.
Competitive Estimating Structure
Coordinate producer estimating disposes of mediator costs. You accomplish superior edges whereas keeping up the pharmaceutical-grade quality your applications demand.
Flexible Arrange Amounts
From research facility tests to bulk shipments, we suit your volume necessities. You scale generation without changing providers as your trade develops.
FAQ
Q: How should we prevent caking during storage?
A: Due to high hygroscopicity, store in double-lined PE bags within sealed drums at <60% relative humidity. Open packages require immediate use or resealing in inert atmosphere to prevent moisture absorption.
Q: What distinguishes Disinfection Preparation Grade from Technical Grade?
A: Our pharmaceutical grade follows strict USP/EP standards with controlled endotoxins, nitrates, and aluminum content. Technical grades permit higher impurities suitable only for industrial de-icing applications.
Q: Can this product function directly as a disinfectant?
A: No. It serves as a preparation agent—a buffer and electrolyte source used to manufacture disinfection fluids, dialysis solutions, or pharmaceutical products. It supports final product stability and efficacy.
Q: Does dissolution generate significant heat?
A: The dissolution is slightly exothermic/neutral with high solubility. However, control rapid addition to acidic solutions to manage pH buffering reactions effectively during your formulation process.
Q: What shelf life can we expect?
A: Sealed containers maintain quality for 2-3 years. Once opened, immediate moisture absorption occurs (deliquescence), requiring complete use or proper resealing to preserve product integrity.
Q: Do you provide batch-specific analytical certificates?
A: Yes. Every shipment includes comprehensive CoA with test results for all pharmacopeial parameters, including endotoxins, heavy metals, and microbial limits specific to your batch.



Request a Quote
Ready to secure your pharmaceutical-grade supply with Disinfection Preparation Solid Potassium Acetate? Contact us today at sxzy@sxzhaoyi.com for competitive pricing, technical specifications, and sample requests.
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