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
SHANXI ZHAOYI CHEMICAL's Antibiotic Solid Potassium Acetate is a high-purity, pharmaceutical-grade chemical planned particularly for anti-microbial union and pharmaceutical applications. Our premium item accomplishes ≥99.0% immaculateness with entirely controlled pollutions counting chloride ≤0.01% and overwhelming metals ≤0.0005%, assembly USP, BP, and EP pharmacopoeial guidelines. With over thirty a long time of industry involvement, we keep up security stock for prompt conveyance inside 24 hours and offer 5-7 working days generation lead time for custom orders. Our 24/7 specialized bolster group gives reactions inside 2 hours, guaranteeing consistent integration into your pharmaceutical fabricating processes.
Key Features & Advantages
Superior Purity Standards
Our pharmaceutical-grade potassium acetic acid derivation surpasses industry prerequisites with negligible overwhelming metal defilement. This anticipates catalytic debasement of touchy anti-microbial atoms and guarantees reliable bunch quality.
Optimized Physical Properties
The white crystalline powder highlights controlled molecule estimate dispersion for fast disintegration in natural solvents. Moo dampness substance (<1.0% LOD) prevents hydrolysis risks during storage and processing.
Regulatory Compliance
Certified with ISO 9001, ISO 14001, and ISO 45001 management systems. KOSHER and HALAL certifications available for food-grade applications. All products meet strict pharmaceutical industry standards with comprehensive documentation support.
Enhanced Stability
Low iron content (<10ppm) prevents discoloration and oxidation of active pharmaceutical ingredients. Engineered for low bacterial endotoxins, complying with injection-grade safety requirements.
Technical Specifications
| Parameter | Specification | Test Method |
|---|---|---|
| Content (CH₃COOK) | ≥99.0% | Titration |
| Water Insoluble | Qualified | Filtration |
| 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 | Redox Titration |
| pH (5% solution) | 7.5-8.5 | pH meter |
| Loss on Drying | ≤1.0% | Gravimetric |
Our Factory
30-YEAR ACETATE SPECIALIST | Non-caking, High Purity, Global Supply Chain
Applications
Penicillin G Potassium Synthesis
Acts as the basic accelerating specialist in API fabricating, presenting potassium particles to penicillin particles in dissolvable media. Tall virtue guarantees fast crystallization and greatest abdicate without metallic impurities.
Injectable Pharmaceutical Buffering
Functions as a pH controller and electrolyte replenisher in parenteral medicate conveyance frameworks. Keeps up anti-microbial arrangement soundness post-reconstitution, anticipating acid-induced beta-lactam ring degradation.
Hemodialysis Solutions
Serves as Antibiotic Solid Potassium Acetate particle source in dialysate concentrates, acting as a bicarbonate forerunner in the liver. Basic for exact potassium level control in understanding electrolyte adjust applications.
Chemical Synthesis
Utilized as a buffering specialist and catalyst in different pharmaceutical amalgamation responses requiring exact pH control and negligible contamination.
Production & Quality Control
Our state-of-the-art office works with an yearly generation capacity of 150,000 tons, including profoundly adaptable generation lines. We execute inner control benchmarks stricter than universal necessities with full-process quality observing and traceability.
Quality Assurance Process:
- Raw fabric confirmation and testing
- In-process quality control at each generation stage
- Final item testing against pharmaceutical standards
- Batch-to-batch consistency validation
- Comprehensive documentation and certification
Our quality administration framework guarantees each bunch of item meets your correct determinations with total traceability and steadiness data.
Packaging & Storage
Packaging Options:
- 25kg plastic woven sacks with polyethylene liners
- 1000kg ton sacks for bulk orders
- Custom bundling accessible upon request
Packing
Storage Requirements:
Store in dry, ventilated stockrooms absent from warm and dampness. Keep up relative mugginess underneath 60% to avoid caking. Keep partitioned from inconsistent substances and handle with care to dodge bundle damage.
Shelf Life: 2-3 a long time when appropriately put away in unique fixed packaging.
Shipment
Why Choose Us
Supply Chain Reliability
With steady upstream crude fabric channels and strong hazard administration, we ensure steady long-term supply. Our crisis reaction plans incorporate reinforcement frameworks and elective coordinations to handle startling disruptions.
Competitive Advantages
Large-scale generation capabilities, optimized forms, and proficient coordinations control empower competitive estimating whereas keeping up predominant quality standards.
Global Export Expertise
Extensive encounter with universal shipping methods and documentation necessities for major worldwide ports. Key associations with famous shipping companies guarantee steady transportation solutions.
Flexible Service Options
Support for different exchange terms (Dandy, CIF, DAP) with adaptable installment strategies. Custom definition capabilities and OEM administrations accessible to meet particular requirements.
FAQ
Q: How does humidity affect storage of this product?
A: Due to hygroscopicity, maintain storage below 60% relative humidity in climate-controlled environments. Use multi-layer packaging with moisture barriers.
Q: What differentiates antibiotic grade from technical grade?
A: Our antibiotic grade undergoes additional recrystallization to remove impurities like formates and excess iron, meeting strict USP/EP pharmaceutical limits.
Q: Is this suitable for both oral and injectable formulations?
A: Yes, our product meets endotoxin limits for injectable applications while maintaining the chemical purity required for oral formulations.
Q: How does particle size impact antibiotic synthesis?
A: Our controlled fine crystalline powder ensures rapid dissolution in organic solvents, reducing reaction time and improving energy efficiency in synthesis processes.
Q: What quality documentation do you provide?
A: Complete batch certificates, MSDS, COA, and conformity statements in multiple languages. Custom documentation available for specific regulatory requirements.
Contact Us
Ready to use the Antibiotic Solid Potassium Acetate to enhance your pharmaceutical manufacturing? Contact our expert team today for technical consultation and competitive quotes at sxzy@sxzhaoyi.com.
USER EVALUATE
Here is the customer's evaluation of us
YOU MAY LIKE
VIEW MOREIndustrial Solid Potassium Acetate
VIEW MOREPharmaceutical Solid Potassium Acetate
VIEW MOREDisinfection Preparation Solid Potassium Acetate
VIEW MORECatalytic Solid Potassium Acetate
VIEW MOREOilfield Solid Potassium Acetate
VIEW MOREDrilling Solid Potassium Acetate
VIEW MORESnow Melting Solid Potassium Acetate
VIEW MOREAirport Runway Solid Potassium Acetate