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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 | 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. |
Applications of N-(4,6-Dimethylpyrimidin-2-Yl)Benzene-1,4-Diamine in Industrial ManufacturingAs 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 FormulationGlobal 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
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2. Specialty Polymer Additive in Antistatic Fiber ProductionTechnical 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
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3. Intermediary Precursor in High-Performance Organic Pigment SynthesisProducers 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
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4. Analytical Reagent Manufacturing for Diagnostic KitsLife 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
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