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HS Code |
433510 |
| Cas Number | 24589-78-4 |
| Molecular Formula | C5H2Cl3N |
| Molecular Weight | 198.44 g/mol |
| Iupac Name | 3,4,5-Trichloropyridine |
| Appearance | White to off-white crystalline solid |
| Melting Point | 60-64°C |
| Boiling Point | 256°C |
| Density | 1.58 g/cm³ |
| Solubility In Water | Slightly soluble |
| Flash Point | 110°C |
| Refractive Index | 1.628 |
| Ec Number | 246-330-7 |
As an accredited 3,4,5-Trichloropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100 grams, sealed with a screw cap; hazard and chemical labels indicating "3,4,5-Trichloropyridine", CAS number displayed. |
| Shipping | 3,4,5-Trichloropyridine is shipped in tightly sealed containers, protected from moisture and incompatible substances. It should be transported according to local, national, and international regulations for hazardous chemicals, typically under the classification of toxic and environmentally hazardous substances. Proper labeling, documentation, and safety precautions must be strictly followed during transit. |
| Storage | Store 3,4,5-Trichloropyridine in a cool, dry, well-ventilated area away from heat, open flames, and direct sunlight. Keep container tightly closed and properly labeled. Isolate from incompatible substances such as strong oxidizers and acids. Use appropriate chemical-resistant containers and avoid moisture contact. Implement spill containment measures and ensure access to safety equipment like eyewash stations and emergency showers. |
Applications of 3,4,5-Trichloropyridine in Industrial Manufacturing3,4,5-Trichloropyridine serves as a high-value intermediate in several industrial verticals. Our manufacturing expertise supports downstream integration for agrochemical actives, pharmaceutical synthesis, dye development, and specialty polymer additives. Each application demands strict adherence to compliance, precision in formulation, and detailed process control for consistent end-use performance. 1. Synthesis of Agrochemical Active IngredientsDownstream producers utilize 3,4,5-trichloropyridine as a building block for selective herbicide and pesticide intermediates. The compound undergoes nucleophilic substitution or coupling reactions, often forming pyridine-based frameworks within crop protection molecules. Its halogenation profile allows for precise control of reactivity, streamlining the scale-up from laboratory to industrial formulation. Formulators adjust batch sizes and stoichiometry according to crop-specific requirements and regional regulations. Stringent impurity monitoring ensures suitability for subsequent use in regulated agricultural applications. Industry compliance standards
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2. Pharmaceutical Intermediate for Antiviral APIsIn pharmaceutical manufacturing, companies employ 3,4,5-trichloropyridine in the synthesis of heterocyclic scaffolds relevant to antiviral and anti-inflammatory drugs. Strict batch documentation and impurity tracking are mandatory under cGMP conditions. Process chemists incorporate the chlorinated pyridine nucleus via regioselective reactions to construct core fragments for further diversification, such as amidation and cross-coupling. Validation batches determine the precise load, with variations allowed only within pharmacopeia-defined limits. Industry compliance standards
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3. Precursor in High-Performance Dye SynthesisDye manufacturers select 3,4,5-trichloropyridine for chromophore extension and stability in industrial colorants. The compound enables fine-tuned halogenation, supporting synthesis of pyridine-based dyes for use in textile, paper, and printing sectors. Color fastness and solubility adjustments often depend on the position and density of chlorine substituents. Manufacturing lines establish fixed ratios, but process engineers regularly recalibrate input based on the chromatic properties demanded by end-users and environmental regulation regarding aromatic amines and organohalogens. Industry compliance standards
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4. Functional Monomer in Specialty PolymersProducers of engineering polymers adopt 3,4,5-trichloropyridine as a reactive monomer or crosslinker to enhance chemical resistance and thermal stability in specialty plastics. Its electronic configuration and chlorine substituents facilitate graft polymerization and copolymerization, especially for high-end paints, coatings, and adhesive segments. Process control teams maintain consistent feed qualities for predictable molecular weight distribution and performance parameters, closely monitoring the integration of halogen functionalities versus other nucleophilic monomers or comonomers. Industry compliance standards
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