N,N-Bis(4-Ethoxycarbonylphenyl)-N-Benzylformamidine Bulk Price
Procurement teams and R&D chemists frequently face volatility in securing high-purity N,N-Bis(4-ethoxycarbonylphenyl)-N-benzylformamidine. Inconsistent supply chains and variable analytical data often delay formulation timelines for critical industrial grade applications.
Technical Specifications and Analytical Methods
To ensure a reliable drop-in replacement for existing formulations, precise adherence to physical and chemical parameters is essential. The following table outlines the critical specifications for this Formamidine UV absorber, validated against international standards.
| Parameter | Specification |
|---|---|
| CAS Number | 586400-06-8 |
| Molecular Formula | C26H26N2O4 |
| Molecular Weight | 430.5 g/mol |
| Purity (HPLC) | ≥ 99.0% |
| Refractive Index | 1.564 |
| Density | 1.11 g/cm³ |
| Boiling Point | 581.8±60.0 °C |
For detailed performance benchmarking data regarding thermal stability in polyurethane foam, please review our technical page on UV Absorber NP3.
Troubleshooting Common Impurities and Yield Issues
Manufacturing UV NP3 equivalents requires strict control over reaction conditions to avoid downstream performance failures.
Residual Benzylamine Content
Elevated levels of unreacted benzylamine can compromise the thermal stability of the final polymer matrix. Our synthesis protocol utilizes optimized stoichiometry to minimize this residual impurity below detectable limits.
Hydrolysis During Storage
Improper packaging can lead to ester hydrolysis, affecting the bulk price value by reducing effective potency. We recommend moisture-barrier packaging and storage in cool, dry environments to maintain the integrity of Ethyl 4-[(E)-({benzyl[4-(ethoxycarbonyl)phenyl]amino}methylene)amino]benzoate.
Color Stability Variance
Yellowing issues often stem from trace metal catalysts remaining from the formamidine synthesis. Advanced purification steps ensure the equivalent product maintains clarity required for high-end coatings.
Strict Quality Assurance (QA) Workflow and COA Verification
At NINGBO INNO PHARMCHEM CO.,LTD., every batch undergoes rigorous testing before release. Our quality assurance workflow includes multi-point HPLC analysis and GC-MS verification to confirm identity and purity. Each shipment is accompanied by a comprehensive COA that allows your QC team to verify specifications immediately upon receipt. For a deeper analysis of market supply dynamics, consult our report on Uv Absorber Np3 Bulk Price Global Manufacturer trends.
Securing a stable supply of high-performance additives is critical for maintaining production schedules and product quality.
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