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4-Chlororesorcinol

    • Product Name 4-Chlororesorcinol
    • Alias 4-chlorobenzene-1,3-diol
    • Einecs 202-641-4
    • 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

    845942

    Cas Number 95-88-5
    Iupac Name 4-chlorobenzene-1,3-diol
    Molecular Formula C6H5ClO2
    Molar Mass 144.56 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 112-115°C
    Boiling Point 264°C
    Solubility In Water Slightly soluble
    Density 1.44 g/cm³
    Pka 8.62 (for the first hydroxyl group)
    Refractive Index 1.642
    Synonyms 4-chloro-1,3-benzenediol, p-chlororesorcinol
    Pubchem Cid 7418

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

    Packing & Storage
    Packing The 100g bottle of 4-Chlororesorcinol is supplied in an amber glass container with a secure screw cap and safety labeling.
    Shipping 4-Chlororesorcinol is typically shipped in tightly sealed containers to prevent moisture and contamination. It should be packed in accordance with local and international regulations for hazardous chemicals. Ensure labeling indicates its chemical identity and hazard information. Store and transport in a cool, dry place, away from incompatible materials and sources of ignition.
    Storage 4-Chlororesorcinol should be stored in a tightly closed container in a cool, dry, well-ventilated area away from sources of ignition, heat, and incompatible substances such as strong oxidizing agents. Protect it from light and moisture. Use non-sparking tools, and ensure good ventilation in the storage area. Keep out of reach of unauthorized personnel and label the storage container clearly.
    Application of 4-Chlororesorcinol

    Applications of 4-Chlororesorcinol in Industrial Manufacturing

    As a direct manufacturer of 4-Chlororesorcinol, we supply this specialty intermediate for several downstream industries. Each application utilizes unique compliance requirements, formulation ratios, manufacturing processes, and leads to distinct end-use products. Explore the main industrial sectors integrating our material.

    1. Hair Dye Formulation for Cosmetic Manufacturing

    4-Chlororesorcinol functions as a key primary intermediate in oxidative and semi-permanent hair dye formulations. Hair colorants require reliable tone stability, rapid oxidative coupling, and minimal impurities for consumer safety. Manufacturers control the input ratio to balance color intensity with toxicological limits. Quality control extends from incoming raw material through in-process color quality checks, using this ingredient in combination with others such as p-phenylenediamine and m-aminophenol to manufacture boxed hair coloring and salon tinting solutions.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No 1223/2009
    • US FDA 21 CFR 73 Subpart C
    • Japan Standards of Quasi-Drug Ingredients
    • ISO 22716 Good Manufacturing Practices for Cosmetics

    Typical usage ratio

    • Formulations use 0.1%–1.5% w/w, depending on target shade and cross-reactivity with other color precursors.
    • Exact loadings adjusted according to in-house toxicity assessment and performance tests.

    Downstream process integration

    • Added to blending tanks after initial aqueous base and before alkaline agents.
    • Incorporated together with other dye precursors during the batch mixing step.
    • Solution is filtered, standardized, and filled under nitrogen to minimize degradation.

    Final product types

    • Boxed consumer permanent and semi-permanent hair dyes
    • Salon hair coloring creams and lotions
    • Root touch-up applicator kits
    • Professional hair bleaching and coloring combos

    2. Pharmaceutical Intermediate for Antifungal API Synthesis

    Leading pharma producers utilize 4-Chlororesorcinol as a building block in synthesis routes for various phenolic antifungal active ingredients. The material is involved in multi-step reactions, typically after protection and chlorination operations. High purity and batch consistency matter, as downstream impurities can affect GMP compliance. This intermediate enables the creation of APIs for topical ointments and medical creams.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Ph. Eur. (European Pharmacopoeia) Monograph requirements
    • US Pharmacopeia (USP)
    • FDA Drug Master File (DMF) submissions

    Typical usage ratio

    • 5%–18% molar ratio in coupling reactions, based on batch stoichiometry for target API strength.
    • Adjusted to ensure full conversion and manageable purification yields.

    Downstream process integration

    • Introduced at the aromatic substitution or condensation stage in multi-step synthesis.
    • Solubilized or suspended in pre-dried solvents for purity control.
    • Follows by further protection or deprotection chemistry before API isolation.

    Final product types

    • Bulk phenolic antifungal active ingredients
    • Topical antifungal creams
    • Medicated ointments
    • Pharmaceutical intermediate stock solutions

    3. Intermediate for Specialty Polymer and Resin Manufacturing

    Producers of resins and high-performance polymers add 4-Chlororesorcinol to tailor-make monomer blends for coatings, adhesives, and engineered plastics. The product enables fine-tuning of cross-linking density and thermal stability in end polymers. Downstream engineers monitor input quality and precise batch ratios to maintain mechanical strength, optical clarity, and chemical resistance in the final material. Post-reaction purification and reactivity checks ensure downstream reliability.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for production plants
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EU 1907/2006)
    • ASTM D256, D638 for resin physical property testing
    • RoHS Directive for electronic and electrical equipment compatibility (where applicable)

    Typical usage ratio

    • Normally 0.5%–7% by weight in resin and monomer formulations.
    • Ratio depends on target functionality and downstream customer technical datasheet specifications.

    Downstream process integration

    • Blended with main polyol or epoxy stock prior to initiation stage.
    • May enter bulk or solution polymerization reactors, depending on desired polymer chain architecture.
    • Pre-dried and filtered before addition to avoid gel formation and impurities.

    Final product types

    • Resorcinol-formaldehyde resins for adhesives
    • Tailor-made engineering plastics for electronics
    • Cross-linked coatings for industrial applications
    • Composite matrix resin systems

    4. Synthesis of Agrochemical Intermediates

    Formulators use 4-Chlororesorcinol as a precursor in the synthesis of agrochemical molecules, such as selected fungicides and herbicidal agents. Its ability to introduce chlorinated phenol functional groups makes it crucial during early-stage organic synthesis. Precise ratio and monitoring are essential, as overuse leads to regulatory concerns, while underuse can limit final efficacy. Quality assurance laboratories track its purity and reaction conversion in process control samples throughout the entire production cycle.

    Industry compliance standards

    • FAO/WHO Specifications for pesticides
    • EPA FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act, USA)
    • ISO 17025 for lab validation of intermediates
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • Generally 2%–10% molar equivalent depending on the downstream molecule's synthetic pathway.
    • Ratio varies with batch scale, target conversion, and impurity profile.

    Downstream process integration

    • Charged at the chlorination or alkylation stage in plant batch reactors.
    • Heated and mixed to facilitate substitution on the aromatic ring.
    • Reaction monitored for conversion and isolated by extraction for subsequent reactions.

    Final product types

    • Pesticide and fungicide technical intermediates
    • Herbicidal pre-emergent formulations
    • Active ingredient stocks for crop protection
    • Bulk agrochemical active intermediates for blending
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