Tetraethyl Ammonium Iodide High-Purity Reagent for Synthesis & Electrolytes
- Introduction to Tetraethyl Ammononium Iodide
- Technical Advantages and Performance Metrics
- Market Comparison: Leading Suppliers Analyzed
- Customized Solutions for Industry-Specific Needs
- Application Case Studies Across Key Sectors
- Quality Assurance and Compliance Standards
- Future Trends in Ammonium Iodide Derivatives
(tetraethyl ammonium iodide)
Understanding Tetraethyl Ammonium Iodide in Modern Chemistry
Tetraethyl ammonium iodide (CAS 68-05-3) serves as a critical quaternary ammonium salt with broad applications in organic synthesis, electrochemistry, and pharmaceutical research. This crystalline compound, often abbreviated as TEAI, exhibits a molecular weight of 257.12 g/mol and decomposes at 150°C. Recent market analysis shows a 12.7% CAGR growth in demand since 2020, driven by its role as a phase-transfer catalyst and conductivity enhancer.
Technical Superiority in Ionic Compound Manufacturing
Our tetraethyl ammonium iodide
surpasses competitors through three core innovations:
- 99.5% minimum purity via multi-stage crystallization
- Halogen content controlled below 50 ppm
- Custom particle size distribution (10-200 μm)
Comparative conductivity tests demonstrate 18% higher ionic mobility than standard ammonium iodide compounds under identical conditions (25°C, 0.1M solution).
Competitive Landscape: Supplier Benchmarking
| Parameter | Our Product | Vendor A | Vendor B |
|---|---|---|---|
| Purity (%) | 99.5 | 98.2 | 97.8 |
| Moisture (ppm) | ≤200 | 500 | 800 |
| Lead Time (days) | 7-10 | 14-21 | 28+ |
Tailored Formulations for Specialized Applications
We provide modified tetra ethyl ammonium iodide variants for specific industrial requirements:
- Pharma-grade: <500 CFU/g microbial limits
- Battery-grade: <5 ppb heavy metal content
- Research-grade: Custom isotopic labeling (¹³C, ²H)
Documented Success in Electrochemical Systems
A 2023 case study with a lithium battery manufacturer achieved:
- 23% increase in electrolyte conductivity
- 15°C extension in thermal stability range
- 0.02% batch-to-batch variability
Certifications and Manufacturing Excellence
Our ammonium iodide production facilities maintain:
- ISO 9001:2015 certified quality systems
- REACH/OSHA compliance documentation
- 21 CFR Part 11 compliant data tracking
Innovation Pathways for Tetraethyl Ammonium Derivatives
Ongoing R&D focuses on developing non-hygroscopic tetraethyl ammonium iodide formulations with 40% improved shelf life. Collaborative studies with electrochemical research consortiums aim to enhance ionic liquid applications through structural modifications, targeting 30% reduction in charge transfer resistance by 2025.
(tetraethyl ammonium iodide)
FAQS on tetraethyl ammonium iodide
Q: What is tetraethyl ammonium iodide used for?
A: Tetraethyl ammonium iodide is commonly used as a phase-transfer catalyst in organic synthesis. It also serves as an electrolyte in electrochemical studies. Additionally, it aids in ion channel research in biological sciences.
Q: Is tetraethyl ammonium iodide the same as tetra ethyl ammonium iodide?
A: Yes, "tetraethyl ammonium iodide" and "tetra ethyl ammonium iodide" refer to the same compound. The spacing in the name does not alter its chemical structure. Both terms denote (C₂H₅)₄N⁺I⁻.
Q: How should tetraethyl ammonium iodide be stored safely?
A: Store tetraethyl ammonium iodide in a cool, dry place away from light and moisture. Keep it sealed in an airtight container to prevent decomposition. Avoid contact with strong oxidizing agents.
Q: Can ammonium iodide be substituted for tetraethyl ammonium iodide in reactions?
A: No, ammonium iodide (NH₄I) lacks the organic tetraethyl group, making it unsuitable for applications requiring quaternary ammonium salts. Their reactivity and solubility profiles differ significantly. Use depends on the specific reaction mechanism.
Q: How is tetraethyl ammonium iodide synthesized?
A: Tetraethyl ammonium iodide is typically synthesized by reacting triethylamine with ethyl iodide. The reaction forms a quaternary ammonium salt through alkylation. Purification is achieved via crystallization from organic solvents.
Post time: May . 07, 2025 18:22
