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1-(4-Chlorophenyl)-1,2-Propandione

    • Product Name 1-(4-Chlorophenyl)-1,2-Propandione
    • Alias 4-Chlorophenylchloromethylketone
    • Einecs 241-850-7
    • 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

    873115

    Productname 1-(4-Chlorophenyl)-1,2-Propandione
    Casnumber 1885-14-9
    Molecularformula C9H7ClO2
    Molecularweight 182.61
    Appearance Yellow crystalline solid
    Meltingpoint 66-68 °C
    Boilingpoint 320.7 °C at 760 mmHg
    Density 1.267 g/cm3
    Solubility Soluble in organic solvents like ethanol and ether
    Smiles CC(=O)C(=O)C1=CC=C(C=C1)Cl
    Inchi InChI=1S/C9H7ClO2/c1-6(11)9(12)7-2-4-8(10)5-3-7/h2-5H,1H3
    Pubchemcid 16733

    As an accredited 1-(4-Chlorophenyl)-1,2-Propandione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 100 grams of 1-(4-Chlorophenyl)-1,2-Propandione; sealed cap; safety label with hazard symbols.
    Shipping 1-(4-Chlorophenyl)-1,2-Propandione should be shipped in tightly sealed containers, protected from light and moisture. It must be packaged according to relevant chemical transport regulations, including DOT and IATA guidelines. Use appropriate hazard labeling, and include safety documentation. Ensure shipment is handled by trained personnel and kept at a controlled ambient temperature.
    Storage Store **1-(4-Chlorophenyl)-1,2-propanedione** in a tightly closed container, kept in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers and acids. Ensure the storage area is secure, clearly labeled, and equipped with appropriate spill control and fire safety measures. Avoid exposure to moisture and protect from physical damage.
    Application of 1-(4-Chlorophenyl)-1,2-Propandione

    Applications of 1-(4-Chlorophenyl)-1,2-Propandione in Industrial Manufacturing

    As a direct manufacturer, we supply 1-(4-Chlorophenyl)-1,2-propandione to certified industrial clients operating in specialized downstream sectors. Below, we detail verified industrial applications, each reflecting precise formulation practices, compliance with essential standards, and concrete end-use product contexts within their respective value chains.

    1. Pharmaceutical Intermediate for Pyrazole-based API Synthesis

    This diketone serves as a critical intermediate in the manufacture of pyrazole derivative active pharmaceutical ingredients via condensation and cyclization reactions. Its introduction occurs during key condensation steps, securing high chemical yields and structural consistency in downstream drug candidates. API manufacturers integrate this compound after strict raw material qualification, under cGMP conditions for innovative and generic pharma pipelines, notably for anti-inflammatory and anticancer small molecules.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP, EP, JP pharmacopoeia specifications depending on end-market
    • 21 CFR Part 211 (US FDA cGMPs)
    • ISO 9001:2015 Quality Management System certification

    Typical usage ratio

    • Varies from 0.08 to 0.25 molar equivalents per API batch, adjusted according to target moiety and overall route optimization

    Downstream process integration

    • Dosed during cyclization and pyrazole ring-forming condensation after base pre-treatment; monitored for purity pre-isolation

    Final product types

    • Anti-inflammatory drug substances (e.g., selective inhibitors)
    • Oncology candidate APIs containing arylpyrazole motifs
    • Pharmaceutical intermediates exported for further downstream synthesis

    2. Agrochemical Intermediate for Fungicide Precursors

    Major agrochemical producers rely on this compound to synthesize arylpyrazole precursors, further transformed into active fungicidal ingredients. Its insertion as a core building block in solution-based or semi-batch processes enables selective functionalization at defined process points, supporting reproducibility in crop-protection molecule manufacturing under stringent environmental and pesticide compliance frameworks.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • OECD GLP (Good Laboratory Practice) for agrochemical production
    • Regulation (EC) No 1107/2009 for EU plant protection products
    • China GB/T 31270.1-2014 for pesticide industry quality

    Typical usage ratio

    • Used at 5–12% weight in pre-coupling formulations, exact proportion determined by target compound and process scale

    Downstream process integration

    • Introduced post-activation of halide intermediates; undergoes condensation and subsequent chlorination or nitration as required by final molecule design

    Final product types

    • Triazole- and pyrazole-based agrochemical actives
    • Arylpyrazole fungicide intermediates for further derivatization
    • Active ingredients supplied to plant protection product formulators

    3. Fine Chemical Synthesis: Flavor and Fragrance Intermediates

    Specialty aroma chemical producers utilize this diketone as a precursor for synthesizing aromatic aldehydes through subsequent reduction and selective oxidation steps. Its defined substitution pattern allows for the generation of unique aromatic profiles essential for flavor house libraries and fragrance ingredient manufacturing. All processes operate within REACH and sector-specific regulatory limits, prioritizing batch traceability and analytical monitoring to ensure downstream olfactory consistency.

    Industry compliance standards

    • EU REACH Regulation (EC) No 1907/2006
    • IFRA (International Fragrance Association) Standards
    • ISO 9001:2015 for fine chemical manufacturing
    • FCC (Food Chemicals Codex) and FEMA GRAS for food-grade intermediates

    Typical usage ratio

    • Formulated at 2.5–7.0% weight in intermediate synthesis solutions; adjusted based on aldehyde output yield targets and downstream reduction route

    Downstream process integration

    • Added after base-catalyzed aldol formation stage; further processed via hydrogenation and oxidation in continuously monitored reactors

    Final product types

    • Chlorinated aromatic aldehydes used as fragrance top notes
    • Flavor intermediates for compounding houses
    • Custom aroma building blocks for personal care formulation

    4. Polymerization Modifier in Specialty Resin Manufacturing

    Producers of high-performance specialty resins, particularly those focused on halogenated thermosets and engineering polymers, employ this diketone as a polymerization modifier to control molecular weight and introduce specific functional handles into the polymer backbone. Applied in resin batch reactors, its use ensures consistency in batch-to-batch polymer network architecture and meets precise spectral signature requirements for advanced composite and coating applications.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management for Polymer Manufacturers)
    • RoHS 2011/65/EU (Restriction of Hazardous Substances in Electronics where relevant)
    • UL 94 Standard for Safety of Flammability of Resin Materials
    • ASTM D638 for physical property consistency

    Typical usage ratio

    • Added at 0.5–3.2% weight to monomer or pre-polymer charge, tailored to desired crosslinking density and target final mechanical properties

    Downstream process integration

    • Injected into polymerization vessel post-monomer mixing but prior to initiation; participates in condensation and branching reactions monitored by in-line spectroscopy

    Final product types

    • Halogenated epoxy resins for corrosion-resistant coatings
    • Specialty thermosetting polymers for composite prepregs
    • Molded electronic encapsulation components

    5. Research Reagent for Heterocyclic Compound Development

    Analytical and contract research organizations integrate this compound as a core diketone scaffold for synthesizing custom heterocyclic compounds. Used extensively in route development, screening libraries, and SAR optimization, it provides access to new chemical entities for lead optimization in medicinal and material chemistry R&D workflows. Research teams document all usage in compliance with laboratory best practices and safety requirements.

    Industry compliance standards

    • OECD GLP (Good Laboratory Practice) for chemical research
    • ISO/IEC 17025:2017 for analytical laboratory competence
    • National/institutional chemical safety and hazardous substance handling protocols
    • Material transfer documentation and full batch traceability

    Typical usage ratio

    • Applied in screening reactions at 1–10 mmol scale; amount tailored for target library size and final molecule creativity during high-throughput synthesis

    Downstream process integration

    • Employed during early-stage substrate assembly; typically involved in condensation or cycloaddition reactions under controlled atmosphere conditions

    Final product types

    • Custom heterocyclic scaffolds for early-stage drug discovery
    • Lead molecule synthons for patent portfolio expansion
    • Material science testing samples for advanced polymer or sensor research
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