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6-Chloro-4-Hydroxycoumarin

    • Product Name 6-Chloro-4-Hydroxycoumarin
    • Alias 4-Hydroxy-6-chlorocoumarin
    • Einecs 217-948-7
    • 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

    323370

    Chemicalname 6-Chloro-4-Hydroxycoumarin
    Casnumber 2107-69-9
    Molecularformula C9H5ClO3
    Molecularweight 196.59
    Appearance Pale yellow to beige powder
    Meltingpoint 238-241°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles C1=CC2=C(C=C1Cl)C(=O)C=CC2=O
    Inchi InChI=1S/C9H5ClO3/c10-5-1-2-7-6(3-5)8(11)4-9(12)13-7/h1-4,11H
    Storageconditions Store in a cool, dry place, protected from light

    As an accredited 6-Chloro-4-Hydroxycoumarin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g package of 6-Chloro-4-Hydroxycoumarin comes in a sealed amber glass bottle with a white, tamper-evident cap and hazard labeling.
    Shipping 6-Chloro-4-Hydroxycoumarin is shipped in tightly sealed containers to prevent contamination and moisture ingress. It should be packaged in accordance with relevant regulations, including labeling for hazardous chemicals if applicable. The container must be handled with care, stored in a cool, dry place, and protected from light during transit.
    Storage 6-Chloro-4-Hydroxycoumarin should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. The storage area should be clearly labeled and access restricted to trained personnel. Minimize exposure to moisture, and handle under inert atmosphere if necessary to prevent degradation.
    Application of 6-Chloro-4-Hydroxycoumarin

    Applications of 6-Chloro-4-Hydroxycoumarin in Industrial Manufacturing

    Our facility manufactures 6-Chloro-4-Hydroxycoumarin for established industrial sectors. This material enters downstream processes serving highly regulated and technically demanding verticals, where traceability, process control, and purity are required for successful formulation and product release.

    1. Intermediate for Pharmaceutical Anticoagulants

    6-Chloro-4-Hydroxycoumarin functions as a key intermediate in synthesizing several coumarin-derived anticoagulant APIs. Downstream pharmaceutical companies incorporate this raw material during critical coupling reactions, where batch traceability, impurity profile, and moisture control are mandatory for regulatory drug registration and batch release. Final APIs often serve regulated therapeutics and require exhaustive validation at every processing stage, including raw material qualification, in-process analytical testing, and contamination risk minimization.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • EDQM/CEP (Europe) and USP monograph specifications
    • 21 CFR Part 211 (US FDA drug GMPs)
    • China Pharmacopoeia (ChP) requirements for intermediates

    Typical usage ratio

    • 0.95:1 to 1.05:1 molar ratio with condensation partners
    • Adjusted per downstream process yield and residual solvent targets
    • Material assay above 99% to ensure yield consistency
    • Moisture content controlled below 0.1% w/w in critical syntheses

    Downstream process integration

    • Charged at catalyst-coupling stage during API synthesis
    • Subjected to in-process purity and identity checks
    • Residue management monitored at each reaction stage
    • Final purification status matches release specifications

    Final product types

    • Warfarin sodium bulk active ingredient
    • Acenocoumarol and phenprocoumon APIs
    • Finished oral anticoagulant tablets (hospital supply)
    • Parenteral anticoagulant injectables (clinical use)

    2. Intermediate for Coumarin-Based Optical Brighteners

    This raw material serves as a functional intermediate in the production of selected optical brighteners used in industrial textile dyeing, high-performance papers, and polymer film coatings. Its structure enables downstream synthesis of specialty coumarin derivatives requiring precise control of substituents for color-fastness and ultraviolet absorption properties. Downstream processors monitor this intermediate for batch-to-batch consistency, residual halide content, and polymerization compatibility before introducing into thermal or solution-phase reactions.

    Industry compliance standards

    • OEKO-TEX Standard 100 limits on residual chemicals for textiles
    • GB/T 22864 for paper-processing chemicals (China)
    • REACH Annex XVII and SVHC screening for non-pharma use in EU
    • ISO 9001-driven QC for specialty chemical intermediates

    Typical usage ratio

    • 3% to 5% w/w relative to total brightener mass
    • Optimized based on target polymer and end-product absorbance
    • Adjusted for retention rate and solution viscosity in coatings
    • Maintained below 0.05% residual halide to prevent yellowing

    Downstream process integration

    • Fed into esterification or alkylation reaction vessels
    • Entering polymer chain extension phase for optical effect
    • Dosed in closed reactors with monitored temperature and solvent recovery
    • Post-reaction purification for color clarity and shelf stability

    Final product types

    • Textile optical brightener agents
    • Fluorescent whitening agents for specialty papers
    • Film additives for UV protection in plastics
    • High-efficiency printing inks with coumarin structure

    3. Raw Material for Agrochemical Synthesis (Rodenticides)

    The compound is an established intermediate for manufacturing certain second-generation coumarin-based rodenticides. Agrochemical producers require defined purity, limited trace impurities, and halogen specification to ensure end-product regulatory compliance. The synthesis pathway relies on robust analytical oversight, minimizing contaminants that may impact field efficacy or introduce toxic secondary byproducts monitored by national pesticide regulations.

    Industry compliance standards

    • FAO/WHO "Specification of plant protection products" for rodenticides
    • US EPA 40 CFR Part 180 residue limitations
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • GB 38502 (China) for pesticide intermediate safety and control

    Typical usage ratio

    • 1:1 molar ratio to aldehyde/carbonyl partners for condensation
    • Batch optimization based on target rodenticide compound
    • Impurity profile targets <0.5% for downstream regulatory approval
    • Moisture and solvent content below 0.2% w/w in final blend

    Downstream process integration

    • Initial stage in condensation synthesis of active rodenticide ingredient
    • Purpose-specific monitoring for halide and byproduct residues
    • Subjected to batch QC and API standard analytical release
    • Passed to formulation or granulation for finished product manufacturing

    Final product types

    • Brodifacoum and difenacoum technical concentrates
    • Commercial rodenticide pellets and blocks for pest control
    • Ready-to-use agricultural bait formulations
    • Export-grade pest management actives

    4. Synthesis of Specialty Dyes

    Downstream dye manufacturers process this material to generate coumarin-based colorants for high-value specialty inks and dyes. The compound enters coupling and cyclization steps requiring tightly managed reaction conditions to produce pure, high-intensity chromophores. Final dyes must comply with end-use restrictions for application in textiles, packaging, and regulated marking, often requiring full traceability and robust documentation of raw material origin, impurity status, and batch release analytics.

    Industry compliance standards

    • REACH registration dossier for colorants in the EU
    • ISO 1833-24:2010 for dye and pigment evaluation
    • EN 71-3 safety for allowable migration in consumer goods
    • ZDHC MRSL for restricted substances in manufacturing

    Typical usage ratio

    • 1.0 to 2.5 equivalents per total dye intermediate charged
    • Adjusted for absorption intensity and end-product solubility
    • Chemical purity greater than 98.5% for high-resolution color targets
    • Total batch impurity below 1% to meet global dye standards

    Downstream process integration

    • Added at the cyclization and coloration synthesis step
    • Incorporated under controlled reflux or pressure conditions
    • In-line HPLC or GC confirmation of structure before move to finishing
    • Post-reaction purification enables registration for branded colorant systems

    Final product types

    • Coumarin-based fluorescent textile dyes
    • High-performance inkjet and offset printing inks
    • Food packaging colorants requiring migration safety testing
    • Specialty marking inks for industrial traceability applications
    Free Quote

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