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2,3,6-Trichlorobenzaldehyde

    • Product Name 2,3,6-Trichlorobenzaldehyde
    • Alias 2,3,6-Trichlorobenzal
    • Einecs 211-012-6
    • 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

    625453

    Cas Number 87-72-9
    Molecular Formula C7H3Cl3O
    Molecular Weight 209.46 g/mol
    Appearance White to off-white crystalline solid
    Melting Point 57-61°C
    Boiling Point 266°C
    Density 1.56 g/cm³
    Solubility In Water Insoluble
    Flash Point 165°C
    Purity Typically ≥98%
    Synonyms 2,3,6-Trichloro-1-benzaldehyde
    Refractive Index 1.603
    Storage Temperature Store at room temperature
    Smiles Clc1cccc(Cl)c1C=O
    Ec Number 201-760-7

    As an accredited 2,3,6-Trichlorobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle containing 100 grams of 2,3,6-Trichlorobenzaldehyde, tightly sealed with a red screw cap and hazard labeling.
    Shipping 2,3,6-Trichlorobenzaldehyde should be shipped in tightly sealed, clearly labeled containers, stored in a cool, dry, and well-ventilated area. Follow all regulatory guidelines for hazardous materials; protect from moisture and physical damage. Ensure appropriate documentation, hazard labels, and use secondary containment to prevent leaks during transport. Handle with proper PPE.
    Storage 2,3,6-Trichlorobenzaldehyde should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Ensure appropriate labeling and secure storage to prevent spillage or accidental contact. Use chemical safety cabinets if possible and avoid sources of ignition, as the compound may be combustible.
    Application of 2,3,6-Trichlorobenzaldehyde

    Applications of 2,3,6-Trichlorobenzaldehyde in Industrial Manufacturing

    2,3,6-Trichlorobenzaldehyde serves as a strategic intermediate in multiple value chains, supporting the synthesis and modification of specialty chemicals for regulated manufacturing environments. Our production expertise ensures material consistency and compliance required in each downstream industry. Below, we detail application scenarios with industry-specific formulation, compliance, process, and finished goods insights.

    1. Synthesis of Crop Protection Active Ingredients

    Agrochemical manufacturers incorporate our material in key steps when developing selective herbicide molecules, notably for chloroaromatic scaffolds. Stringent monitoring tracks batch identity and purity as the aldehyde forms core structures of target actives. Scaling protocols require closed-system handling, with integration in controlled condensation and chlorination stages. End users focus on regulated pesticides adaptable for both pre-emergence and post-emergence formulations.

    Industry compliance standards

    • Food and Agriculture Organization (FAO) pesticide specification procedure
    • European REACH Regulation EC 1907/2006 for agricultural chemicals
    • US EPA FIFRA registration for technical grade active ingredients
    • ISO 9001:2015 Quality Management for chemical intermediates

    Typical usage ratio

    • 10–45% by molecular composition, varying by target herbicidal structure and downstream synthetic route optimization

    Downstream process integration

    • Input as starting aromatic aldehyde for condensation with amines or phenols under controlled temperature and pH in slurry reactors
    • Feeds into chlorination or alkylation post-processing to yield final technical active ingredient
    • Compatible with catalytic continuous-flow processes for large-scale production

    Final product types

    • Selective herbicides (e.g., pretilachlor, fluchloralin)
    • Crop-specific weed control technical concentrates
    • Suspension concentrates and emulsifiable concentrates for field application

    2. Fine Chemical Intermediates for Pharmaceutical Synthesis

    Pharma API and intermediate manufacturers use 2,3,6-Trichlorobenzaldehyde for synthesizing halogenated aromatic building blocks, relevant to certain cardiovascular and antimicrobial compounds. Strict process validation and impurity profiling align with multi-stage manufacturing, where the aldehyde serves as a base for Grignard or Wittig reactions. Documentation ensures traceability across each step, from reaction monitoring to final intermediate assay before API conversion.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for intermediates
    • FDA 21 CFR Part 211 – Current Good Manufacturing Practice for Finished Pharmaceuticals
    • USP General Chapters for residual solvents and impurities

    Typical usage ratio

    • 15–40% of the reaction substrate, adjusted according to reaction stoichiometry and yield requirements in multiple step synthesis

    Downstream process integration

    • Initial condensation or reductive amination baseline step in aromatic ring modification
    • Intermediary for coupling with heterocyclic precursors and subsequent reduction or oxidation
    • Monitored addition under nitrogen atmosphere to minimize side reactions and byproduct formation

    Final product types

    • Pharmaceutical intermediates for benzyl halide derivatives
    • Key starting materials (KSMs) for specialty APIs
    • Advanced intermediates for late-stage functionalization

    3. Polymer Additive Manufacturing

    Specialty polymer and resin producers employ this chlorinated aldehyde as a monomer or crosslinking agent precursor in the synthesis of functional resins, including thermoset and thermoplastic blends. Quality assurance involves close analysis for residual monomers and organochlorine content. The aldehyde acts in the aromatic backbone build, influencing glass transition temperature and crosslink density. Processing occurs under controlled mixing and curing cycles in batch or continuous equipment.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronic components
    • ASTM D3648 for resin composition purity
    • ISO 14001 Environmental Management for additive usage
    • DIN EN ISO 1043-1 nomenclature for polymer modification

    Typical usage ratio

    • 0.5–5% as a functional monomer or crosslinker, modulated by target thermal and chemical property demands

    Downstream process integration

    • Entry in prepolymer or oligomer formation during resin synthesis
    • Combined with epoxy, acrylic, or phenolic systems during batch mixing
    • Heat-initiated or catalyzed cure for final polymer structure stabilization

    Final product types

    • High-performance polymer resins for industrial coatings
    • Specialty thermosets with halogenated aromatic content
    • Adhesives and encapsulants for electronics or automotive applications

    4. Dye and Pigment Intermediate Production

    Dyestuff and pigment manufacturers integrate this compound as a key starting material for synthesizing complex chlorinated aromatic chromophores. The feedstock undergoes condensation and oxidative coupling steps in multi-stage syntheses. Material traceability supports final batch uniformity, while routine QC verifies isomeric purity and absence of unwanted byproducts. Application aligns with the demand for high-purity intermediates in specialty dye manufacture for plastics, textiles, and printing inks.

    Industry compliance standards

    • OEKO-TEX Standard 100 for restricted aromatic amines
    • Chemical Control Act (TSCA) for imported/exported dye intermediates
    • REACH Annex XVII for colorant ingredients
    • ISO 9001:2015 for pigment and dye process control

    Typical usage ratio

    • 3–20% of total batch mass, with adjustments based on target pigment density and chromophore functionalization efficiency

    Downstream process integration

    • Initial aromatic core in condensation with amines or hydrazine for azo or anthraquinone dye synthesis
    • Sulfonation or halogenation carried out post-integration for enhanced color fastness
    • Controlled multi-stage batch reaction monitored for color yield and contaminant residuals

    Final product types

    • High-fastness plastic and fiber dyes
    • Colorants for industrial printing inks
    • Chlorinated pigment intermediates for specialty polymers
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