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3',5'-Dichloro-2'-Hydroxyacetophenone

    • Product Name 3',5'-Dichloro-2'-Hydroxyacetophenone
    • Einecs 405-040-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    611515

    Chemical Name 3',5'-Dichloro-2'-Hydroxyacetophenone
    Cas Number 17969-19-2
    Molecular Formula C8H6Cl2O2
    Molecular Weight 205.04 g/mol
    Appearance White to off-white solid
    Melting Point 87-89°C
    Boiling Point No data available
    Solubility Slightly soluble in water, soluble in organic solvents
    Density No data available
    Purity Typically ≥98%
    Smiles CC(=O)C1=CC(=C(C(=C1)Cl)O)Cl
    Storage Conditions Store in a cool, dry place; keep tightly closed
    Synonyms 2-Hydroxy-3,5-dichloroacetophenone
    Refractive Index No data available
    Hazard Statements May cause skin and eye irritation

    As an accredited 3',5'-Dichloro-2'-Hydroxyacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 10-gram bottle of 3',5'-Dichloro-2'-Hydroxyacetophenone is packed in a sealed amber glass vial with clear hazard labeling.
    Shipping 3',5'-Dichloro-2'-Hydroxyacetophenone is shipped in tightly sealed containers to prevent contamination and moisture absorption. It is packaged in compliance with chemical safety regulations, accompanied by appropriate labeling and documentation. The chemical is handled and transported as per MSDS guidelines, ensuring the safety of handlers and environmental protection during transit.
    Storage 3',5'-Dichloro-2'-hydroxyacetophenone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Keep away from direct sunlight, heat sources, and incompatible substances like strong oxidizers or acids. Store at room temperature, avoiding excessive moisture and humidity, and ensure proper chemical labeling. Restrict access to authorized personnel and follow all relevant safety protocols.
    Application of 3',5'-Dichloro-2'-Hydroxyacetophenone

    Applications of 3',5'-Dichloro-2'-Hydroxyacetophenone in Industrial Manufacturing

    3',5'-Dichloro-2'-Hydroxyacetophenone serves as a key intermediate in specialized chemical synthesis, demanded primarily for its unique reactivity profile in regulated and quality-driven downstream industries. As a manufacturer, we supply this compound in support of critical applications across agrochemicals, pharmaceuticals, dye intermediates, and specialty polymers production, where strict compliance, batch formulation, and product traceability are vital.

    1. Agrochemical Synthesis – Herbicide and Fungicide Active Ingredient Intermediates

    This compound functions as a core building block in synthesizing selective herbicide and fungicide active ingredients within crop protection manufacturing. Its dichloro and hydroxy substitutions enable downstream producers to construct tailored chlorinated acetophenone scaffolds, influencing target spectrum and degradation profiles for field applications. Industrial users in the agrochemical sector must ensure traceable sourcing and batch consistency to pass stringent multi-jurisdictional requirements, balancing the addition level based on bioactivity screen and compatibility with coupling reagents.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • REACH Registration (EU Regulation No 1907/2006)
    • US EPA Pesticide Registration (40 CFR Part 158 and 180)

    Typical usage ratio

    • 0.9–3.5% w/w as intermediate feedstock, optimized according to targeted active ingredient synthesis pathway and batch reactor volume. Formulators may adjust upward for specific coupling reactions or in process scale-up.

    Downstream process integration

    • Introduced during early-stage condensation or Friedel-Crafts acylation steps as the aromatic precursor. Reaction temperature and solvent choice influence yield and impurity profile before the downstream halogenation or sulfonation stage.

    Final product types

    • Commercial herbicide actives (e.g., chlorinated acetophenone analogues)
    • Fungicide active ingredient concentrates
    • Emulsifiable concentrate (EC) crop protection products
    • Technical grade agrochemical formulations

    2. Pharmaceutical Intermediate Manufacturing

    Pharmaceutical companies value this material as a strategic intermediate for constructing molecular frameworks in select active pharmaceutical ingredient (API) and advanced intermediate syntheses. Its substitution pattern allows medicinal chemists to introduce specific steric and electronic effects, influencing subsequent functionalization processes. Transparent source control and conformity to pharmacopeia impurity benchmarks remain central during procurement and quality assessment for GMP-compliant API manufacturing lines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs — relevant for related intermediates
    • 21 CFR Part 211 (US FDA current GMP for finished pharmaceuticals)
    • Drug Master File (DMF) submission for regulated market access

    Typical usage ratio

    • 0.25–1.2% molar equivalent relative to target API batch size; precise loadings are determined in route scouting and scale-up protocols according to reaction conversion and side product formation rates.

    Downstream process integration

    • Added at the heterocycle formation or side-chain introduction steps during stage-wise organic synthesis. Handled under segregated GMP zones with in-process analytical control and stringent solvent residue monitoring until the intermediate stage is cleared for downstream isolation or derivatization.

    Final product types

    • Specialty API intermediates (e.g., for anti-inflammatory, antifungal, or CNS agents)
    • Advanced intermediates for contract synthesis supply chains
    • Custom pharmaceutical research compounds
    • Regulatory submission batches for generic drug manufacturers

    3. Dye and Pigment Intermediate Production

    This compound acts as a crucial ingredient in the synthesis of specific high-performance azo and anthraquinone dye intermediates. The pattern of halogenation and hydroxylation enables downstream colorant producers to achieve shade strength, dispersion stability, and resistance properties required for textile, plastic, and ink applications. Users in this segment establish quality plans both for finished color yield and for reducing banned amine impurities, adhering to established global standards in dye manufacturing.

    Industry compliance standards

    • OEKO-TEX STANDARD 100 (chemical safety requirements for textiles)
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 9001:2015 and ISO 14001:2015 Environmental Management System
    • EU REACH Annex XVII (restriction of hazardous substances)

    Typical usage ratio

    • 1.8–4.0% w/w of total dye batch, subject to tuning for chromophore strength and target application substrate; higher additions may be specified when achieving deeper shades for technical textiles.

    Downstream process integration

    • Employed in coupling reactions and as a nucleophile in directed ortho-metalation or diazotization processes, typically entering the batch after diazo component generation and prior to final pigment coupling and salt purification.

    Final product types

    • Synthesized azo dyes for cellulose and synthetic fibers
    • Organic pigments for plastics and paint masterbatches
    • Specialty inks for digital textile printing
    • Colorant dispersions for technical coatings applications

    4. Specialty Polymer Initiator and Crosslinker Component

    High-value specialty polymers integrate this chemical as part of their crosslinking or initiator systems to impart modified mechanical, thermal, or barrier performance. Its specific aromatic core and halogen substitution deliver controlled reaction rates and enable easier tuning of final polymer structure. Industrial customers benefit from the stability and morphology adjustments obtainable through precise feed timing of this intermediate at the polymerization or curing stage, with close attention to final monomer conversion efficiency and end-use compliance.

    Industry compliance standards

    • ISO 9001:2015
    • RoHS Directive (2011/65/EU) for electric and electronic applications
    • FDA 21 CFR 177.2600 for elastomeric materials (if targeting food contact use)
    • GMP for polymer additive manufacturing (per customer audit)

    Typical usage ratio

    • 0.2–0.7% by weight of total polymer formulation; determined by polymer backbone chemistry and desired crosslink density or molecular weight profile for application-specific properties.

    Downstream process integration

    • Dispensed at the controlled addition stage, either as a pre-dissolved solution or melt, prior to final polycondensation or radical initiation. May be used in co-initiator systems for block copolymer or specialized elastomer manufacture.

    Final product types

    • High-performance thermoset resins
    • Specialty block copolymer elastomers
    • Functionalized thermoplastic masterbatches
    • Barrier coatings for packaging and electronics
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