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HS Code |
802270 |
| Cas Number | 13355-96-9 |
| Molecular Formula | C10H4Cl3NO2 |
| Molecular Weight | 276.5 g/mol |
| Appearance | Yellow to yellow-green crystalline powder |
| Melting Point | 232-235°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in organic solvents; insoluble in water |
| Storage Temperature | Store at 2-8°C |
| Boiling Point | Decomposes before boiling |
| Density | 1.61 g/cm³ |
| Synonyms | 2,4,6-Trichloro-N-phenylmaleimide |
| Ec Number | 236-400-6 |
As an accredited N-(2,4,6-Trichlorophenyl)Maleimide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle with a tight-sealed lid, affixed with a white label displaying the chemical name, hazard symbols, and supplier. |
| Shipping | N-(2,4,6-Trichlorophenyl)maleimide should be shipped in tightly sealed containers, protected from moisture and light. It must be labeled as a hazardous chemical and packed according to applicable regulations. Use secondary containment, such as cushioned boxes or absorbent liners, and ensure compliance with local and international transport guidelines for chemicals. |
| Storage | Store **N-(2,4,6-Trichlorophenyl)maleimide** in a tightly sealed container in a cool, dry, well-ventilated area away from direct sunlight, heat, and moisture. Keep away from incompatible substances such as strong oxidizing agents and bases. Use with proper personal protective equipment and avoid prolonged exposure. Always label containers clearly and follow all relevant safety guidelines and local regulations. |
Applications of N-(2,4,6-Trichlorophenyl)Maleimide in Industrial ManufacturingN-(2,4,6-Trichlorophenyl)maleimide serves as a specialty imide additive in multiple high-value chemical manufacturing sectors. Our factory supplies this material for downstream integrators who require precision intermediates for advanced polymer synthesis, electronic component fabrication, and specialty coatings. Below is a breakdown of its proven applications by industry track, including regulatory standards, mixing protocols, process entry points, and intended end-use products. 1. High-Performance Polyimide Resin SynthesisOur material functions as a key monomeric component in the production of polyimide-based resins. Polyimides require maleimide derivatives with high purity and defined reactivity to impart thermal stability and mechanical strength. End users in this sector utilize N-(2,4,6-Trichlorophenyl)maleimide in melt or solution-polymerization steps to form imide linkages. The final polymers withstand harsh environments, aligning with aerospace and electronics manufacturing needs. Industry compliance standards
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2. Semiconductor Photoresist Crosslinking AgentN-(2,4,6-Trichlorophenyl)maleimide acts as an effective crosslinking imide in the manufacture of negative-tone photoresists for semiconductor wafer processing. Its specific halogenation pattern improves UV-initiated crosslink density and etch resistance, making it suitable for lithography layers in advanced node fabrication environments. Strict control of additive concentration and residue mandates the use of this material only by qualified cleanroom processors. Industry compliance standards
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3. Speciality Reactive Dyes and Pigment IntermediateDownstream colorant and pigment producers source this maleimide derivative as a building block in the synthesis of halogenated dyes and specialty pigments. Its electron-withdrawing groups enhance chromophore reactivity, enabling fine-tuning of color performance and stability against chemical oxidants and acids. Typically, the material is used in multi-step organic transformations, with strict traceability on intermediate handling and environmental compliance for effluent treatment. Industry compliance standards
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4. Heat-Resistant Adhesives for Electronics AssemblyThis intermediate is utilized by formulators of specialty adhesives where temperature and flame resistance are critical. For electronics, compounders select N-(2,4,6-Trichlorophenyl)maleimide for its ability to form thermoset networks with high aromatic content, resulting in adhesives that maintain bonding integrity during solder reflow or under operational device stress. Quality control mandates accurate dosing and full cure verification to meet device reliability standards. Industry compliance standards
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5. Advanced Composite Materials for Aerospace StructuresAerospace composite fabricators depend on this chlorinated maleimide for matrix modification in fiber-reinforced thermoset prepregs. The compound increases cross-link density and improves matrix-to-fiber adhesion for composites exposed to continuous high-temperature and aggressive chemical environments. Production teams control the precise addition to resin baths to match pre-preg tow specifications and final lamination schedules. Industry compliance standards
Typical usage ratio
Downstream process integration
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