Pharmaceutical Intermediate 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
Pharmaceutical Intermediate Solid Potassium Acetate
SHANXI ZHAOYI CHEMICAL's Pharmaceutical Intermediate Solid Potassium Acetate conveys uncommon immaculateness and consistency for basic pharmaceutical fabricating forms. Our white crystalline item keeps up ≥99.0% substance with ultra-low overwhelming metal defilement (≤0.0005% Pb) and negligible press pollutions (≤0.0005% Fe). With over thirty a long time of industry encounter and yearly generation capacity of 150,000 tons, we guarantee solid supply chains supported by comprehensive quality certifications counting ISO 9001, KOSHER, and HALAL approvals. Your generation groups advantage from our 24/7 specialized back and 2-hour reaction times for pressing inquiries.
Key Features & Advantages
Our strong potassium acetic acid derivation stands out through predominant chemical steadiness and pharmaceutical-grade immaculateness. The crystalline structure avoids caking issues common in hygroscopic materials, guaranteeing reliable flowability amid capacity and handling.
You get exact pH buffering capabilities with 5% watery arrangements keeping up ideal ranges for touchy API amalgamation. The tall water solvency (253 g/100 mL at 20°C) and fabulous natural dissolvable compatibility make it perfect for differing pharmaceutical applications.
Quality points of interest incorporate rigid overwhelming metal controls, decreased chloride defilement (≤0.01%), and sulfate confinements (≤0.02%). These determinations anticipate downstream filtration issues and ensure catalyst productivity in your fabricating processes.
Our item meets worldwide pharmacopoeia benchmarks counting BP, EP, and USP monographs, guaranteeing worldwide administrative compliance for your pharmaceutical operations.
Technical Specifications
| Parameter | Specification | Unit |
|---|---|---|
| Content (CH3COOK) | ≥99.0 | % |
| Water insoluble | Qualified | % |
| Basicity (as K2CO3) | ≤0.12 | % |
| Acidity (as HA) | ≤0.05 | % |
| Chloride (Cl) | ≤0.01 | % |
| Sulfate (SO4) | ≤0.02 | % |
| Ferrum (Fe) | ≤0.0005 | % |
| Heavy metal (as Pb) | ≤0.0005 | % |
| Potassium permanganate-reducing | Qualified | - |
| Molecular Formula | CH3COOK | - |
| Molecular Weight | 98.14 | g/mol |
| CAS Number | 127-08-2 | - |
Our Factory
30-YEAR ACETATE SPECIALIST | Non-caking, High Purity, Global Supply Chain



Applications
Pharmaceutical Intermediate Solid Potassium Acetate serves as a basic component in beta-lactam anti-microbial union, especially for Penicillin G Potassium generation. Your API fabricating benefits from its exact pH control, avoiding hydrolytic corruption amid touchy response stages.
Hemodialysis arrangement definition speaks to another key application. The acetic acid derivation buffer changes over to bicarbonate in patients, anticipating metabolic acidosis whereas keeping up strict aluminum substance limits for persistent safety.
Protein decontamination forms utilize this halfway for affront extraction and biopharmaceutical fabricating. Its tall dissolvability empowers quick harmony in cold-process situations, stabilizing protein structures amid crystallization phases.
Buffer arrangement for pharmaceutical investigate and quality control testing depends on reliable pH execution. Your research facility operations accomplish reproducible comes about through our product's solid chemical composition.
Chemical union applications incorporate catalyst bolster and response medium arrangement where potassium particle nearness is particularly required over sodium alternatives.






Production & Quality Control
Our fabricating office executes comprehensive quality administration frameworks surpassing universal guidelines. Each clump experiences thorough testing utilizing Gas Chromatography (GC) for unstable natural debasements and ICP-MS examination for overwhelming metal verification.
Raw fabric sourcing takes after strict seller capability conventions with approaching assessment strategies. Generation lines keep up controlled situations avoiding cross-contamination and guaranteeing batch-to-batch consistency.
Quality control laboratories operate under Good Manufacturing Practice (GMP) rules with approved expository strategies. Certificate of Analysis (COA) documentation goes with each shipment, giving total traceability for your administrative requirements.
Environmental checking frameworks track generation parameters ceaselessly. Crisis reaction conventions guarantee quick remedial activities when deviations happen, ensuring item quality and conveyance schedules.
Third-party testing confirmation approves our inner comes about, giving extra affirmation for basic pharmaceutical applications requiring most extreme reliability.






Packaging & Storage
Standard bundling incorporates 25kg plastic woven packs with moisture-resistant internal liners. Large-volume necessities utilize 1000kg ton-bags planned for mechanical dealing with hardware and bulk capacity systems.
Custom bundling arrangements oblige particular client prerequisites counting OEM labeling and specialized holder groups. Our bundling group plans arrangements adjusting security, dealing with productivity, and fetched optimization.
Packing

Storage proposals indicate dry, ventilated stockroom conditions with temperature control underneath 25°C. Relative mugginess ought to stay beneath 60% to anticipate dampness assimilation and potential caking issues.
Transportation conventions guarantee item astuteness amid shipping. We arrange with worldwide cargo accomplices experienced in chemical coordinations, giving competitive rates and dependable travel times.
Shelf life amplifies 24 months beneath legitimate capacity conditions. Standard quality observing tracks steadiness parameters guaranteeing reliable execution all through the capacity period.
Shipment



Why Choose Us
SHANXI ZHAOYI CHEMICAL combines three decades of specialized encounter with advanced generation capabilities. Our 150,000-ton yearly capacity guarantees steady supply for your biggest volume prerequisites whereas keeping up reliable quality standards.
Safety stock programs keep commonly utilized items promptly accessible for quick shipment. Standard orders transport inside 5-7 working days, with crisis necessities satisfied inside 24 hours when stock permits.
Technical skill gives important application back past essential supply. Our groups offer free meeting on item optimization, investigating, and prepare enhancement suggestions based on broad pharmaceutical industry knowledge.
Global send out encounter ranges major markets counting Europe, America, Southeast Asia, and the Middle East. We understand regional regulatory requirements and assist with documentation, customs clearance, and compliance verification.
Flexible cooperation models accommodate various business needs through FOB, CIF, and DAP terms. Long-term system assentions give estimating soundness and ensured assignment for vital partnerships.
FAQ
Q: How does your solid potassium acetate prevent caking during humid conditions?
A: Our crystalline structure and moisture-controlled packaging with desiccant inter-layers minimize atmospheric moisture absorption. Storage below 60% relative humidity maintains optimal flowability.
Q: Can this product replace sodium acetate in pharmaceutical formulations?
A: Not directly. Potassium acetate provides specific potassium ion functionality and higher organic solvent solubility compared to sodium acetate. Application requirements determine the appropriate choice.
Q: What aluminum content limits apply for hemodialysis applications?
A: Strict aluminum limits typically remain below 0.2 ppm for renal applications. Standard pharmaceutical grades may allow slightly higher levels unless specifically designated for dialysis use.
Q: How do you ensure compliance with ICH Q3C residual solvent guidelines?
A: Gas Chromatography testing verifies absence of Class 1 solvents. Our manufacturing process avoids problematic solvents, ensuring compliance with international pharmaceutical solvent residue standards.
Q: What quality documentation accompanies each shipment?
A: Complete Certificate of Analysis (COA), Material Safety Data Sheet (MSDS), and relevant certifications including ISO, KOSHER, and HALAL documentation for pharmaceutical traceability requirements.
Contact Us
Ready to use the Pharmaceutical Intermediate Solid Potassium Acetate to secure your pharmaceutical intermediate supply? Contact our technical team at sxzy@sxzhaoyi.com for pricing, samples, and custom solutions.
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