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4,4'-Cyclohexylidenebis[N,N-Bis(4-Methylphenyl)Aniline]

    • Product Name 4,4'-Cyclohexylidenebis[N,N-Bis(4-Methylphenyl)Aniline]
    • Alias CHI-1
    • Einecs 401-720-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    567465

    Chemical Name 4,4'-Cyclohexylidenebis[N,N-Bis(4-Methylphenyl)Aniline]
    Molecular Formula C49H48N2
    Molecular Weight 664.92 g/mol
    Cas Number 1174026-86-2
    Appearance Off-white to pale yellow powder
    Melting Point 185-190°C
    Solubility Insoluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Application Intermediate for OLED materials, organic electronics
    Storage Conditions Store in a cool, dry place, away from light
    Boiling Point Decomposes before boiling
    Synonyms TAPC-CHC, Bis(4-(N,N-dip-tolylamino)phenyl)cyclohexane
    Density 1.18 g/cm³ (approximate)

    As an accredited 4,4'-Cyclohexylidenebis[N,N-Bis(4-Methylphenyl)Aniline] factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250 grams of 4,4'-Cyclohexylidenebis[N,N-Bis(4-Methylphenyl)Aniline] is packaged in a sealed amber glass bottle with tamper-evident cap.
    Shipping This chemical, **4,4'-Cyclohexylidenebis[N,N-Bis(4-Methylphenyl)Aniline]**, is shipped in tightly sealed containers to prevent contamination and moisture exposure. Standard shipping involves sturdy, cushioned packaging that complies with relevant chemical transport regulations. It is typically transported at ambient temperature and is labeled according to hazard, handling, and safety guidelines.
    Storage 4,4'-Cyclohexylidenebis[N,N-bis(4-methylphenyl)aniline] should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible materials such as strong oxidizing agents. Keep the storage area free from moisture and sources of ignition. Ensure appropriate chemical labeling and secure storage to prevent unauthorized access or accidental release.
    Application of 4,4'-Cyclohexylidenebis[N,N-Bis(4-Methylphenyl)Aniline]

    Applications of 4,4'-Cyclohexylidenebis[N,N-Bis(4-Methylphenyl)Aniline] in Industrial Manufacturing

    4,4'-Cyclohexylidenebis[N,N-Bis(4-Methylphenyl)Aniline] serves as a specialty intermediate and functional ingredient across several advanced materials sectors. The following application pathways reflect its established industrial deployment, based on regulatory compliance, formulation expertise, and production integration seen among global manufacturing clients.

    1. High-Performance Polyimide Resin Synthesis

    This raw material functions as a high-temperature, high-clarity diamine in polyimide resin formulations. Its use supports demanding requirements for electronic substrates and insulating films due to excellent mechanical strength and hydrolytic stability besides improved thermal properties in final polyimide matrices. Manufacturers incorporate it into dianhydride-diamine condensation processes under inert atmospheric conditions, targeting fine-tuned dielectric and physical profiles for electronic component applications.

    Industry compliance standards

    • UL 94 V-0 Flammability Standard for Plastics
    • RoHS Directive (2011/65/EU)
    • REACH Regulation (EC) No 1907/2006
    • IEC 61249-2-21 for PCB Base Materials

    Typical usage ratio

    • Diamine component: 15–30 wt% of total monomers, with actual percentage adjusted based on the target molecular weight and final thermal properties required by the polyimide resin type.

    Downstream process integration

    • Added directly to the diamine solution during the polyamic acid synthesis stage prior to imidization by thermal or chemical methods.

    Final product types

    • Flexible copper-clad laminates (FCCL) for high-frequency printed circuit boards
    • Adhesiveless base films for electronics
    • Insulating films for aerospace electrical systems
    • Optical display substrates

    2. Advanced Epoxy Curing Agents for Electronic Encapsulation

    This molecule acts as a specialty curing agent or co-curing agent in highly cross-linked epoxy systems used for semiconductor encapsulation and potting resins. Its symmetrical structure and cyclohexyl bridge enhance the thermal stability, glass transition temperature, and dielectric performance, supporting package integrity under high thermal cycling and moisture exposure. Manufacturers choose it to meet electrical and mechanical reliability standards in epoxy molding compounds for integrated circuit applications.

    Industry compliance standards

    • JEDEC JESD22-A101 Moisture Resistance Test
    • IPC/JEDEC J-STD-020 for Soldering Heat Resistance
    • RoHS Directive (2011/65/EU)
    • UL 94 V-0 Flammability for Encapsulants

    Typical usage ratio

    • 1–10 phr (parts per hundred resin), with concentration adjusted according to the desired cure time, heat distortion temperature, and mechanical requirements per resin formulation.

    Downstream process integration

    • Blended into the epoxy resin base prior to molding or transfer encapsulation, followed by thermal curing at 150–180°C in bulk or mold cavity.

    Final product types

    • Integrated circuit and semiconductor packages
    • LED encapsulants
    • Electronic potting compounds
    • SMD device coatings

    3. High-End Polyurethane Formulations for Optical Lenses

    4,4'-Cyclohexylidenebis[N,N-Bis(4-Methylphenyl)Aniline] finds established use as a chain extender and aromatic building block in polyurethane (PU) optical lens materials and high-strength coatings. Its controlled reactivity and steric configuration support PU networks with excellent transparency, low birefringence, and dimensional stability critical for precision optical components. The material is incorporated during the isocyanate-prepolymer stage, enabling customized optical and mechanical profiles for downstream lens casting and curing operations.

    Industry compliance standards

    • ISO 8980-1 Ophthalmic Optics – Uncut Finished Spectacle Lenses
    • EN 166:2001 For Personal Eye Protection
    • FDA 21 CFR Part 801 (US labeling requirements for medical devices)
    • REACH Regulation (EC) No 1907/2006

    Typical usage ratio

    • Chain extender content: 2–6 mole %, with variation depending on final PU hardness and optical transmission targets.

    Downstream process integration

    • Charged during the chain extension step immediately following isocyanate prepolymer formation; process conditions are tightly controlled to prevent excess crosslinking that may compromise transparency.

    Final product types

    • Ophthalmic lenses
    • Protective visors
    • Photochromic lens substrates
    • High-clarity optical coatings

    4. Engineering Thermoplastic Modifiers for High-Temperature Nylon Compounds

    This aromatic diamine can act as a chain modifier or comonomer for specialty high-temperature-resistant nylon (polyamide) resins. Its introduction during polymerization alters the crystalline structure and enhances thermal softening points as well as electrical insulation. Drives adoption in electrical and automotive component manufacture where thermoplastics must retain mechanical integrity in demanding service conditions.

    Industry compliance standards

    • UL 746B Polymeric Materials Standard
    • ISO 11469 for Plastics Identification
    • IEC 60695-11-10 Glow-Wire Test
    • RoHS Directive (2011/65/EU)

    Typical usage ratio

    • Comonomer content: 3–12 wt% based on polymer backbone type, with dosage tuned to optimize melt viscosity and glass transition for the specific engineering plastic grade.

    Downstream process integration

    • Dosed into the melt-phase polycondensation reactor with caprolactam or other lactam monomers; forms block or random copolymers during chain growth.

    Final product types

    • Automotive electrical connectors
    • High-temperature fuse holders
    • Insulated switch housings
    • Precision instrument components

    5. Organic Semiconductor Synthesis for OLED Display Materials

    This intermediate serves as a central core for the synthesis of hole-transporting molecules in organic light-emitting diode (OLED) displays. Its rigid structure provides high glass transition and morphological stability, supporting consistent charge mobility and efficiency in multilayer OLED stacks. The material enters custom organic semiconductor synthesis routes where downstream users build on the aromatic core to attach functional groups, yielding tailored charge transport layers for advanced display units.

    Industry compliance standards

    • IEC 62341-5-1 OLED Testing Methods
    • RoHS Directive (2011/65/EU)
    • Regulations for Persistent Organic Pollutants (if applicable to national legislation)
    • UL 8750 for LED Component Safety

    Typical usage ratio

    • Integrated as a molecular core at 100% of the semiconductor precursor in the synthesis step; blends at 10–40 wt% into device ink or solution for spin or slot-die coating based on desired thickness and layer uniformity.

    Downstream process integration

    • Enters organic synthesis as initial aromatic diamine precursor; final transporting agent solution processed by vacuum evaporation or solution coating onto display substrates in device fabrication lines.

    Final product types

    • OLED display panel charge transport layers
    • Mobile phone and television screens
    • Wearable display modules
    • Flexible display films

    6. Synthesis of Specialty Polybenzoxazine Resins for Aerospace

    4,4'-Cyclohexylidenebis[N,N-Bis(4-Methylphenyl)Aniline] is used as a diamine source for benzoxazine resin synthesis, imparting superior flame resistance, low viscosity, and dimensional stability valued in aerospace composites. The cyclohexyl and methyl-substituted aromatic structure helps achieve low moisture uptake and stable physical properties in prepreg and laminate structures after high-temperature curing.

    Industry compliance standards

    • ASTM D3410 Standard Test for Composite Materials
    • FAR 25.853 Aircraft Flammability Requirements
    • SAE AMS 2759 for Aerospace Material Processing
    • NADCAP Accreditation for Composites Processing (where required)

    Typical usage ratio

    • Diamine content: 20–35 wt% of total resin monomers, proportion tailored according to crosslinking density and final composite layer thickness.

    Downstream process integration

    • Reacted with phenolic and formaldehyde sources in the initial benzoxazine ring-forming step; resin impregnates carbon or glass fiber in next composite layup stage.

    Final product types

    • Aerospace prepreg tapes
    • Structural composite panels
    • Aircraft interior panels with flammability certification
    • High-performance adhesive films
    Free Quote

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