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N-(4,6-Dimethylpyrimidin-2-Yl)Benzene-1,4-Diamine

    • Product Name N-(4,6-Dimethylpyrimidin-2-Yl)Benzene-1,4-Diamine
    • Alias Trimethoprim
    • Einecs 629-43-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    459764

    Iupac Name N-(4,6-dimethylpyrimidin-2-yl)benzene-1,4-diamine
    Molecular Formula C12H14N4
    Molecular Weight 214.27 g/mol
    Cas Number 569-61-9
    Appearance Light brown to brown solid
    Melting Point 181-183 °C
    Solubility In Water Slightly soluble
    Smiles CC1=NC(=NC(=N1)N2C=CC=C2N)C
    Inchi InChI=1S/C12H14N4/c1-8-9(2)15-12(14-8)16-11-6-4-10(13)5-7-11/h4-7H,13H2,1-2H3
    Pubchem Cid 69241

    As an accredited N-(4,6-Dimethylpyrimidin-2-Yl)Benzene-1,4-Diamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle with a tightly sealed cap, labeled with chemical name, CAS number, hazard symbols, and handling instructions.
    Shipping For shipping, **N-(4,6-Dimethylpyrimidin-2-Yl)Benzene-1,4-Diamine** should be packed in tightly sealed containers, protected from light, moisture, and extreme temperatures. Label all containers per relevant regulations (such as GHS/OSHA). Ship as a chemical reagent with appropriate documentation, using a reliable carrier experienced in transporting laboratory chemicals. Avoid physical damage or contamination during transit.
    Storage Store **N-(4,6-Dimethylpyrimidin-2-yl)benzene-1,4-diamine** in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Keep away from sources of ignition and moisture. Ensure appropriate labeling and access to safety equipment, such as gloves and goggles, to prevent skin and eye contact.
    Application of N-(4,6-Dimethylpyrimidin-2-Yl)Benzene-1,4-Diamine

    Applications of N-(4,6-Dimethylpyrimidin-2-Yl)Benzene-1,4-Diamine in Industrial Manufacturing

    As a direct manufacturer specializing in advanced chemical intermediates, we supply N-(4,6-Dimethylpyrimidin-2-Yl)Benzene-1,4-Diamine to a select number of focused downstream industries where its specific reactivity and physicochemical stability play a critical role in demanding production environments. Each application below reflects verified industrial usage and incorporates requirements and insights from customer implementation, compliance protocols, and formulation methods.

    1. Hair Dye Formulation

    Global hair colorant manufacturers incorporate this compound as a primary oxidative dye intermediate due to its strong color-developing capabilities and resistance to fading under consumer-use conditions. Integration into professional and retail permanent color systems requires strict monitoring of ingredient purity, reaction kinetics during processing, and color fastness in end-use applications, with attention to regulatory concentration limits driven by regional safety assessments and consumer product standards.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No 1223/2009, Annex III and IV
    • US FDA 21 CFR 73.2396 (Hair Dye Exemptions)
    • Japan Ministry of Health, Labour and Welfare - Standards for Cosmetics
    • Good Manufacturing Practices (GMP) for Cosmetics ISO 22716

    Typical usage ratio

    • Generally formulated at 0.2%–1.0% by weight in the final mix, subject to local regulatory maximums; precise dosage is balanced based on desired shade intensity, compatibility with other dye intermediates, and base formulation (cream, gel, or liquid systems).

    Downstream process integration

    • Added during the blending phase alongside developers and modifiers; undergoes oxidative coupling with hydrogen peroxide under pH-controlled conditions, forming chromophore molecules essential for permanent color development.

    Final product types

    • Permanent hair color creams
    • Professional hair dye developer kits
    • Boxed retail hair coloring solutions
    • Salon-use colorant systems targeting durable and high-intensity results

    2. Specialty Polymer Additive in Antistatic Fiber Production

    Technical textile manufacturers operating melt-spinning and solution polymerization lines utilize this diamine derivative as a charge-control or functional comonomer to impart antistatic properties and UV-stabilization in PET, polyamide, and selected acrylic fibers. Its integration delivers long-term charge dissipation and pigment binding characteristics without compromising fiber tensile strength or process throughput in filament drawing lines and high-speed texturizing.

    Industry compliance standards

    • OEKO-TEX Standard 100
    • REACH Regulation (EC) No 1907/2006 for additives
    • ISO 9001:2015 Quality Management System for Textiles
    • ISO 11484:2019 (Textile fibers – identification)

    Typical usage ratio

    • Employed at 0.05%–0.25% by polymer weight, adjusted for target conductivity, polymer matrix compatibility, and permissible additive levels in technical fiber specification.

    Downstream process integration

    • Directly dosed into the polymer melt during compounding or introduced as a masterbatch prior to spinning, ensuring molecular-level dispersion before extrusion, spinning, and post-processing.

    Final product types

    • Antistatic polyester industrial yarns
    • Technical workwear linings
    • High-performance filter fibers for clean rooms
    • Conductive carpet and upholstery fibers

    3. Intermediary Precursor in High-Performance Organic Pigment Synthesis

    Producers of advanced organic pigments employ this intermediate in multiple-step syntheses where its unique substitution pattern facilitates precision control over final dye crystal habit, purity, and photostability. It serves as a nucleophilic aromatic amine source during key coupling reactions or as a building block for heteroaromatic pigment frameworks, enabling repeatable color rendition in demanding coatings and plastics coloration applications.

    Industry compliance standards

    • DIN EN 71 Part 3 (Safety of Toys – Migration of Certain Elements)
    • AP(89)1 - Council of Europe Resolution on food contact materials (if applicable)
    • Chemical Control Law (Japan)
    • Toy Safety Directive 2009/48/EC (when used in toy colorants)

    Typical usage ratio

    • Functions as a core building block; precise feedstock ratio set at 1.0–1.5 molar equivalents against coupling partners, controlled to minimize byproducts and optimize color strength.

    Downstream process integration

    • Introduced at the azo-coupling or condensation phase under controlled temperature and solvent systems; followed by purification, milling, and pigment finishing processes.

    Final product types

    • High-purity organic pigments for plastics and laminates
    • Architectural and automotive coating colorants
    • Ink jet and offset print base pigments
    • Thermoplastic masterbatches for extruded goods

    4. Analytical Reagent Manufacturing for Diagnostic Kits

    Life science reagent companies depend on this compound for synthesis of colorimetric and fluorometric probes used in in-vitro diagnostics. Its ability to undergo controlled aromatic substitutions and metal-complex formation under mild conditions is leveraged to develop assay reagents with sharp absorbance spectra, chemical stability, and batch-to-batch reproducibility, serving as key components in immunoassay platforms and enzymatic detection kits.

    Industry compliance standards

    • ISO 13485:2016 Medical Devices – Quality management for IVDs
    • CLSI Document M29-A4 – Protection of Laboratory Workers from Occupationally Acquired Infections
    • 21 CFR Part 820 – FDA QSR (for US-bound diagnostics)
    • EC Directive 98/79/EC on In Vitro Diagnostic Medical Devices

    Typical usage ratio

    • Formulated at 0.01–0.10% by assay buffer volume or per test kit, adjusted based on required sensitivity, signal response, and background noise thresholds.

    Downstream process integration

    • Reacted into probe molecules during organic synthesis or metal-complexation step, followed by purification, lyophilization, and precise dosing into single-use kit packaging lines.

    Final product types

    • Colorimetric immunoassay diagnostic kits
    • Point-of-care analytical reagents
    • Enzyme substrate buffer packs
    • Quantitative test strips for medical laboratories
    Free Quote

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