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4-Chlorochalcone

    • Product Name 4-Chlorochalcone
    • Alias 1-(4-Chlorophenyl)-3-phenylprop-2-en-1-one
    • Einecs 210-548-4
    • 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

    431008

    Chemicalname 4-Chlorochalcone
    Molecularformula C15H11ClO
    Molecularweight 242.70 g/mol
    Casnumber 4219-80-5
    Appearance Yellow crystalline powder
    Meltingpoint 108-110°C
    Boilingpoint 394.1°C at 760 mmHg
    Density 1.17 g/cm³
    Solubility Slightly soluble in water, soluble in organic solvents
    Iupacname 1-(4-chlorophenyl)-3-phenylprop-2-en-1-one

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

    Packing & Storage
    Packing 4-Chlorochalcone is packaged in a 25g amber glass bottle with a tamper-evident cap, labeled with safety and chemical details.
    Shipping 4-Chlorochalcone is shipped in tightly sealed containers to prevent moisture and contamination. The packaging complies with hazardous material regulations, ensuring safe transport. It is handled with appropriate labeling and documentation, including safety data sheets. During transit, the chemical is stored in cool, dry conditions, away from incompatible substances and direct sunlight.
    Storage 4-Chlorochalcone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep it away from incompatible substances such as strong oxidizing agents. Store at room temperature and avoid moisture exposure. Proper labeling and secure storage are essential to prevent accidental contamination or hazardous reactions.
    Application of 4-Chlorochalcone

    Applications of 4-Chlorochalcone in Industrial Manufacturing

    4-Chlorochalcone serves as a valuable core building block for downstream chemical synthesis in multiple industrial sectors. Our manufacturing expertise ensures consistent quality and purity, enabling reliable performance wherever precision intermediates are required in formulation and processing. Below, we highlight practical industrial application scenarios where this compound plays a vital role, detailing compliance standards, precise ingredient ratios, process steps, and final product types relevant to each field.

    1. Pharmaceutical Intermediates for API Synthesis

    In pharmaceutical manufacturing, 4-Chlorochalcone functions as an advanced intermediate in the synthesis of selective anti-infective and anti-inflammatory active pharmaceutical ingredients (APIs). During multi-step organic synthesis, this aromatic ketone structure provides a high-reactivity site for coupling or modification, supporting downstream drug development pipelines targeting diseases that demand halogen-substituted scaffolds. Regulatory frameworks mandate strict traceability and compositional control to ensure patient safety and batch consistency throughout the API lifecycle.

    Industry compliance standards

    • Current Good Manufacturing Practices (cGMP) – ICH Q7
    • United States Pharmacopeia (USP) standards for intermediates
    • European Pharmacopoeia (Ph. Eur.) reference monographs for pharmaceutical synthesis
    • Drug Master File (DMF) supporting documentation for regulated markets

    Typical usage ratio

    • Reaction starting ratios typically range from 1 molar equivalent per target synthetic step, adjustable from 0.8 to 1.2 equivalents depending on route optimization, impurity profile, and target API yield requirements.

    Downstream process integration

    • Inserted during stepwise batch or flow synthesis, specifically within Claisen-Schmidt condensation, cyclization, or functionalization stages en route to final API structure.

    Final product types

    • Active pharmaceutical ingredients (APIs) such as substituted flavones, chalcone-derived antibiotics, and anti-inflammatory compounds

    2. Fine Chemical Synthesis for Agrochemical Actives

    Chemical manufacturers use 4-Chlorochalcone as an essential synthetic intermediate in the development of agrochemical agents, specifically for designing new herbicide and fungicide actives with chlorinated aryl features. Its selective reactivity supports carbon-carbon coupling and ring-closure reactions required to achieve tailored molecular profiles in crop-protection product portfolios, adhering to agricultural regulatory standards for both process safety and environmental controls.

    Industry compliance standards

    • Food and Agriculture Organization (FAO) pesticide specification standards
    • OECD Guidelines for the Testing of Chemicals
    • REACH (EU Regulation 1907/2006) registration and assessment
    • ISO 9001:2015 Certified QMS for agrochemical intermediate production

    Typical usage ratio

    • Standard addition levels range from 0.7 to 1.1 molar equivalents relative to downstream reactants, modulated by chemoselectivity and the efficiency of subsequent transformations depending on targeted agrochemicals.

    Downstream process integration

    • Incorporated during staged synthesis to yield chlorinated diaryl or heterocyclic scaffolds, typically as a core reactant or coupling partner in batch or continuous flow reactors.

    Final product types

    • Herbicide actives based on chalcone derivatives
    • Fungicidal intermediates and end-use agents with halogenated structures

    3. Dye Intermediates for Specialty Pigment Manufacturing

    Producers of high-value dyes and pigments employ 4-Chlorochalcone to construct azo, anthraquinone, or flavonoid-based chromophores with controlled aromatic substitution. Its well-defined structure and purity allow colorant manufacturers to synthesize pigments with unique shade and fastness characteristics required in textile, plastics, and coatings sectors. Process compliance with occupational health and effluent management standards remains vital to quality assurance and environmental responsibility.

    Industry compliance standards

    • OEKO-TEX® Standard 100 textile chemical evaluation
    • Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) for dye intermediates
    • ISO 14001:2015 Environmental Management System
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) guidelines

    Typical usage ratio

    • Charged at 5–15% by mass of the targeted pigment reactant batch, with concentration adjusted for desired color depth and chromaticity, specific to pigment type and application substrate.

    Downstream process integration

    • Introduced during primary pigment synthesis, typically via condensation or cyclization with complementary coupling agents, prior to purification and blending for pigment dispersion.

    Final product types

    • Azo and anthraquinone pigments for textiles and plastics
    • Flavone-based specialty dyes for coatings and printing inks

    4. Specialty Polymer Monomer Synthesis

    In the advanced materials sector, researchers and polymer producers leverage 4-Chlorochalcone as a monomer precursor for engineering specialty polymers. Its conjugated structure permits controlled copolymerization or functionalization, imparting desired UV-absorbing, electrical, or mechanical attributes to end-use polymers. Downstream processors must comply with industry guidelines for monomer purity, polymer handling, and product safety, especially in regulated technical applications.

    Industry compliance standards

    • ISO 9001:2015 quality management for polymer synthesis
    • ASTM D4762-10 (Standard Guide for Identification and Classification of Polymers)
    • Directive 2011/65/EU (RoHS) for electronic and electrical polymers
    • REACH substance registration for monomer use

    Typical usage ratio

    • Employed as 1–10 mol% in copolymerization reactions, tunable depending on the target physical property profile and final application requirements in plastics or coatings engineering.

    Downstream process integration

    • Fed into bulk or solution polymerization units as a functional comonomer or as a chain-modifying precursor during the synthesis of phenylenevinylene, chalcone-based, or photoactive copolymer systems.

    Final product types

    • UV-absorbing optical polymers
    • Electroactive and photoconductive polymeric materials

    5. Research and Development: Reference Compound for Bioactive Molecule Screening

    Academic laboratories and pharmaceutical R&D units employ 4-Chlorochalcone as a benchmark compound for high-throughput screening in medicinal chemistry, where structural analogs are synthesized to evaluate structure-activity relationships against various molecular targets. Strict documentation and chemical registry protocols support research traceability and reproducibility in these discovery settings, shaping the development of new therapeutic candidates.

    Industry compliance standards

    • Good Laboratory Practices (GLP, OECD Principles)
    • Standard Operating Procedures for compound management
    • Material Transfer Agreements (MTA) for inter-institutional studies
    • Local chemical safety and biological hazard regulations

    Typical usage ratio

    • Stock solution concentrations range from 0.01 M to 10 mM, calculated according to micromolar screening requirements; dosing adapted for assay format and detection limits.

    Downstream process integration

    • Utilized during initial molecule library construction, SAR testing, and as a starting point for targeted functionalization in bench-scale or pilot-scale chemical synthesis protocols.

    Final product types

    • Bioactive screening libraries
    • Prototype preclinical lead compounds
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