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4'-Aminobiphenyl-4-Carbonitrile

    • Product Name 4'-Aminobiphenyl-4-Carbonitrile
    • Alias 4'-Cyanobiphenyl-4-amine
    • Einecs 242-506-2
    • 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
    VTB
    Specifications

    HS Code

    806360

    Iupac Name 4'-Aminobiphenyl-4-carbonitrile
    Molecular Formula C13H10N2
    Molecular Weight 194.23 g/mol
    Cas Number 50648-46-7
    Appearance Light yellow to brown powder
    Melting Point 220-225°C
    Solubility In Water Insoluble
    Synonyms 4-Cyano-4'-aminobiphenyl
    Smiles C1=CC=C(C=C1)C2=CC=C(C#N)C=C2N
    Inchi InChI=1S/C13H10N2/c14-9-10-1-5-12(6-2-10)13-7-3-11(15)4-8-13/h1-8,15H

    As an accredited 4'-Aminobiphenyl-4-Carbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical, 4'-Aminobiphenyl-4-Carbonitrile (25g), is packaged in a sealed amber glass bottle with a secure screw cap.
    Shipping 4'-Aminobiphenyl-4-carbonitrile is typically shipped in tightly sealed containers to prevent moisture and contamination. It should be packaged in accordance with local, national, and international regulations, ensuring protection from physical damage. Store and ship at room temperature, away from strong oxidizing agents, and ensure appropriate labeling for safe transport and handling.
    Storage 4'-Aminobiphenyl-4-Carbonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition. Protect from moisture, light, and incompatible substances such as strong oxidizers and acids. Properly label the storage container, and ensure access is limited to trained personnel. Follow all applicable safety guidelines for hazardous chemical storage.
    Application of 4'-Aminobiphenyl-4-Carbonitrile

    Applications of 4'-Aminobiphenyl-4-Carbonitrile in Industrial Manufacturing

    As a direct manufacturer of high-purity 4'-Aminobiphenyl-4-Carbonitrile, we collaborate closely with downstream industrial partners operating in demanding synthesis environments. Below, we outline the core sectors and production contexts where our material plays a structurally essential role. Each use case references established industry norms, formulation ratios, process positioning, and downstream finished goods, reflecting the priorities of regulatory compliance and consistent formulation value for industrial clients.

    1. Organic Light-Emitting Diode (OLED) Intermediate Synthesis

    OLED display and lighting manufacturers rely on this intermediate as a building block for new generations of emitting and charge-transfer molecules. The aromatic structure and cyano functionality of the raw material are essential in constructing high-performance, thermally stable organic emitters. Our production supports high-purity specification requirements for electronic industry clients who apply vacuum deposition and solution-processable technologies.

    Industry compliance standards

    • IEC 62341 (Performance of OLED panels)
    • RoHS Directive (2011/65/EU) for hazardous substances
    • REACH Regulation (EC No 1907/2006) for chemical substances registration
    • ISO 9001:2015 certified quality management systems

    Typical usage ratio

    • 0.05–0.25 mole per mole of final emitter target; final amount depends on architecture and functionalization route within OLED molecule synthesis.

    Downstream process integration

    • Employed during the Buchwald-Hartwig amination or Suzuki coupling stage to introduce biphenyl core structures or terminal amino/cyano groups in OLED precursor molecules, followed by purification for thin-film deposition.

    Final product types

    • OLED emitter molecules
    • Hole-transport materials
    • Host materials for display and lighting panels
    • Functionalized intermediates for further optoelectronic device fabrication

    2. High-Performance Pigments and Dyes Manufacturing

    Producers of specialty dyes and pigments use this compound as a core intermediate for synthesizing colorants demanding high temperature resistance, particularly aza- and anthraquinone derivatives with strong chromatic performance. The benzene ring system and amino group provide structural integrity and tinctorial strength during pigment backbone assembly and halogenation or sulfonation transformations.

    Industry compliance standards

    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) risk assessment guidelines
    • OEKO-TEX® Standard 100 for textiles dyed with chemical intermediates
    • GB/T 5211.1 for pigment general test methods (China)
    • ISO 787 (General methods of test for pigments and extenders)

    Typical usage ratio

    • Varies by pigment batch, generally 0.8–1.1 equivalents relative to the main diazo or quinone core-forming agent; adjustments account for yield optimization or color tuning.

    Downstream process integration

    • Introduced at the condensation or coupling stage during fine chemical pigment synthesis, where precise control of reactant ratios ensures color purity and stability before milling and dispersion steps.

    Final product types

    • High-stability azo dyes
    • Anthraquinone-based pigments
    • Textile and plastic colorants used in demanding lightfastness and weatherability applications
    • Specialty printing inks

    3. Pharmaceutical Advanced Intermediate Production

    Pharmaceutical manufacturers use this raw material in small molecule R&D and scale-up synthesis, typically in the construction of biphenyl-framework intermediates. This compound’s unique substitution pattern allows for regioselective transformation and efficient downstream functionalization, especially when developing proprietary kinase inhibitors or anti-inflammatory lead compounds.

    Industry compliance standards

    • ICH Q7A (Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients)
    • US FDA 21 CFR Part 211 compliance for APIs
    • EU GMP (EudraLex Volume 4)
    • Ph. Eur., USP, JP raw material specifications as required for registered drug substances

    Typical usage ratio

    • Determined by target synthesis; typically 1 equivalent for each API backbone, occasionally used in slight excess (1.05 to 1.15 equiv.) for complete coupling or condensation reactions.

    Downstream process integration

    • Added at early or mid-stage in multi-step synthesis, especially during palladium-catalyzed C-N, C-C, or C-Ni coupling steps, ensuring high yield of biphenyl intermediates prior to final heterocycle closure or amide installation.

    Final product types

    • Custom pharmaceutical intermediates for clinical candidate APIs
    • Lead compounds for kinase and inflammatory disorders
    • Substituted biphenyl derivatives for agrochemical or veterinary drug R&D

    4. Agrochemical Active Ingredient Synthesis

    Agrochemical producers targeting advanced herbicide and fungicide formulations integrate this specialty aromatic as a core ring system builder, particularly within biphenyl and nitrile-containing active ingredient scaffolds. The compound’s precise structure supports site-specific substitution and subsequent formation of active ingredients with enhanced binding affinity and environmental stability.

    Industry compliance standards

    • FAO/WHO Specifications for pesticides (including purity and impurity limits)
    • ISO 9001:2015 for quality management in agrochemical synthesis
    • EU Regulation (EC) No 1107/2009 (Approval of plant protection products in the EU)
    • US EPA 40 CFR Part 180 for pesticide tolerances

    Typical usage ratio

    • Generally 0.9–1.2 equivalents per target molecule in the final coupling or condensation step; optimized by stoichiometry and desired functionalization pattern.

    Downstream process integration

    • Used in key condensation or cross-coupling reactions that define the agrochemical’s core, followed by purification, formulation with carriers, and granulation for field-ready products.

    Final product types

    • Herbicide active components
    • Broad-spectrum fungicides
    • Fine chemical intermediates for seed treatment products

    5. Specialty Polymer and High-Performance Resin Modifier

    Manufacturers of advanced engineering polymers incorporate this compound for functional group insertion—specifically amino or cyano terminals—when preparing resins designed for enhanced thermal characteristics and dielectric properties. It supports chain extension and end-capping in high Tg polyarylenes and copolymer materials destined for electronics and specialty composites.

    Industry compliance standards

    • UL 94 (Flammability standards for plastic materials)
    • IEC 60216 (Electrical insulating materials—thermal endurance)
    • RoHS and REACH environmental requirements for restricted substances
    • ISO 9001:2015 for polymer manufacturing

    Typical usage ratio

    • 0.5–2 wt% as a chain extender or terminating agent, with precise figures set by target molecular weight and polymer grade; higher concentrations suited for specialty end-use applications.

    Downstream process integration

    • Introduced during melt polycondensation or solution polymerization to achieve specific molar functionality, followed by extrusion, pelletization, and compounding with additives.

    Final product types

    • High-performance polyarylene resins
    • Functionalized specialty copolymers
    • Electronic encapsulants
    • Advanced thermoset matrix materials for high-reliability industrial components
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