Pharmaceutical Intermediate Sodium Acetate Anhydrous
CAS NO.: 127-09-3
Molecular Formula: CH3COONa
Molecular Weight: 82.03
Character: white crystal powder; specific gravity is 1.528 and melting point is 324℃.
Usage: It is a kind of chemical raw material and is widely used in dye, pharmaceutical, chemical reagent fields, sewagement and etc.
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 Sodium Acetate Anhydrous
SHANXI ZHAOYI CHEMICAL CO., LTD offers premium Pharmaceutical Intermediate Sodium Acetate Anhydrous (CAS: 127-09-3) fabricated beneath strict GMP benchmarks with over thirty a long time of industry encounter. This high-purity, water-free acetic acid derivation salt conveys ≥99.0% substance with uncommon debasement control for pharmaceutical amalgamation applications. Our enterprise-grade arrangement highlights 24/7 specialized bolster, 5-7 working days generation lead time, and keeps up significant security stock for prompt fulfillment. With yearly generation capacity of 150,000 tons and ISO, KOSHER, HALAL certifications, we guarantee consistent batch stability and 2-hour response times for technical inquiries.
Key Features & Advantages
Superior Purity Standards
Our anhydrous sodium acetic acid derivation surpasses pharmaceutical middle of the road necessities with ≥99.0% substance and ultra-low pollution levels. Overwhelming metals stay underneath 0.002%, whereas press substance remains beneath 0.0005%, guaranteeing ideal response performance.
Moisture-Free Formulation
Unlike trihydrate variations, this water-free definition anticipates dampness obstructions in touchy natural amalgamation. You get higher acetic acid derivation particle thickness per kilogram and exact stoichiometric calculations for water-sensitive reactions.
Enhanced Stability
The crystalline white powder keeps up great stream properties and chemical soundness. Our specialized bundling with desiccants jam item keenness amid capacity and transportation.
Regulatory Compliance
Full compliance with USP, EP, and JP pharmacopeial benchmarks. Total documentation bolster counting MSDS, COA, and multilingual similarity articulations for worldwide administrative requirements.
Technical Specifications
| Parameter | Specification |
|---|---|
| Content (CH3COONa) | ≥99.0% |
| pH Value | 7.5-9.2 |
| Clarity Test | Qualified |
| Water Insoluble | ≤0.01% |
| Chloride (Cl) | ≤0.002% |
| Sulfate (SO4) | ≤0.01% |
| Phosphate (PO4) | ≤0.001% |
| Magnesium (Mg) | ≤0.002% |
| Calcium (Ca) | ≤0.05% |
| Iron (Fe) | ≤0.0005% |
| Heavy Metals (as Pb) | ≤0.002% |
Physical Properties:
- Molecular Formula: CH3COONa
- Molecular Weight: 82.03 g/mol
- Appearance: White crystalline powder
- Specific Gravity: 1.528
- Melting Point: 324℃
Our Factory
30-YEAR ACETATE SPECIALIST | Non-caking, High Purity, Global Supply Chain
Applications
Hemodialysis Solutions
Critical component in dialysate concentrates where Pharmaceutical Intermediate Sodium Acetate Anhydrous prevents calcium and magnesium precipitation while maintaining pH stability during sterilization processes.
Biopharmaceutical Manufacturing
Essential carbon source for aging forms creating recombinant proteins and immunizations. Tall virtue anticipates overwhelming metal defilement in delicate cell cultures.
API Synthesis
Serves as gentle base and acetylating operator in beta-lactam anti-microbial union. The anhydrous nature anticipates hydrolysis of middle of the road compounds in non-aqueous solvents.
Buffer Systems
Provides exact pH control in pharmaceutical details requiring feebly antacid buffering capacity between 7.5-9.0 range.
Production & Quality Control
Our state-of-the-art office actualizes thorough quality administration frameworks with ISO 9001, 14001, and 45001 certifications. Each group experiences comprehensive testing utilizing progressed explanatory methods.
Quality Assurance Process:
- Raw fabric confirmation and testing
- In-process checking at basic control points
- Final item examination against pharmacopeial standards
- Batch discharge certification and traceability
Environmental Compliance:
Complete natural security offices guarantee all generation forms meet Chinese and universal controls, supporting your ESG compliance requirements.
Packaging & Storage
Standard Packaging Options:
- 25kg plastic woven sacks with PE liner
- 1000kg enormous packs for bulk orders
- Custom bundling accessible per your specifications
Storage Requirements:
Store in dry, ventilated stockrooms absent from warm and dampness. Keep up relative stickiness underneath 50% to anticipate caking. Keep partitioned from incongruent substances and guarantee legitimate dealing with to dodge bundle damage.
Packing
Logistics Excellence:
Our vital organizations with universal shipping companies give competitive rates and ensured space assignment. Comprehensive trade documentation bolster guarantees smooth traditions clearance worldwide.
Shipment
Why Choose Us
Proven Experience
Over thirty a long time of chemical fabricating mastery with profound understanding of pharmaceutical middle of the road necessities and worldwide showcase needs.
Supply Chain Reliability
Stable upstream organizations and chance administration frameworks guarantee reliable accessibility. Crisis reaction plans and reinforcement frameworks ensure against supply disruptions.
Flexible Service
Multiple exchange terms (Coxcomb, CIF, DAP) and installment alternatives. Long-term system understandings accessible for key partnerships.
Technical Excellence
24/7 specialized bolster group gives application direction, test testing, and optimization proposals. Joint advancement programs for specialized requirements.
Whether you require standard grades or ultra-high virtue variations, our Pharmaceutical Intermediate Sodium Acetate Anhydrous delivers the reliability and performance your pharmaceutical operations demand.
FAQ
Q: What's the difference between anhydrous and trihydrate forms?
A: The anhydrous form contains no water molecules, offering higher acetate concentration and preventing moisture interference in water-sensitive synthesis reactions.
Q: How do you prevent caking during storage?
A: Our double-lined packaging with desiccants maintains product flow properties. Store in sealed containers under 50% relative humidity.
Q: Is this suitable for injectable products?
A: Yes, we offer low-endotoxin grades meeting USP/EP injection standards with detailed COAs for parenteral applications.
Q: What's the typical shelf life?
A: Two years when stored properly in original sealed packaging under recommended conditions.
Q: Can you provide custom specifications?
A: Absolutely. Our JDR program supports customized formulations, concentrations, and performance requirements.
Contact Us
Ready to use the Pharmaceutical Intermediate Sodium Acetate Anhydrous to enhance your pharmaceutical processes? Contact our expert team at sxzy@sxzhaoyi.com for technical consultation, samples, and competitive quotations today.
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