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Chromone

    • Product Name Chromone
    • Alias 4H-1-benzopyran-4-one
    • Einecs 202-207-7
    • 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

    386427

    Chemical Name Chromone
    Molecular Formula C9H6O2
    Molar Mass 146.15 g/mol
    Cas Number 491-38-3
    Appearance Yellow crystalline solid
    Melting Point 73-76°C
    Boiling Point 273°C
    Solubility In Water Slightly soluble
    Density 1.28 g/cm³
    Synonyms 1,4-Benzopyrone
    Smiles O=C1C=CC2=CC=CC=C2O1
    Pubchem Cid 10258
    Refractive Index 1.656

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

    Packing & Storage
    Packing Chromone is packaged in a 100-gram amber glass bottle with a secure screw cap, labeled with hazard warnings and product details.
    Shipping Chromone should be shipped in tightly sealed containers, away from incompatible substances, in accordance with local, national, and international regulations. Store and transport in a cool, dry, well-ventilated area. Ensure proper labeling and documentation, including hazard classifications. Handle with appropriate protective equipment and avoid release to the environment during shipping.
    Storage Chromone should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight. Keep it separated from strong oxidizing agents and sources of ignition. Store at room temperature and avoid excessive heat or moist conditions to prevent decomposition or degradation. Properly label the container and ensure access to appropriate safety data sheets.
    Application of Chromone

    Applications of Chromone in Industrial Manufacturing

    Chromone, as a highly pure chemical intermediate produced at scale using controlled synthetic methods, supports a range of precision applications across the pharmaceutical, agrochemical, and specialty polymer sectors. The following detailed scenarios reflect established downstream applications, with specific focus on manufacturing process flows, regulatory frameworks, additive ranges, and the nature of finished products that rely on this critical raw material.

    1. Synthesis of Respiratory Pharmaceutical Actives

    Pharmaceutical manufacturers source chromatographically pure chromone derivatives as building blocks for ion channel modulators and anti-inflammatory drugs targeting respiratory pathways. Consistent batch quality and trace metal control are essential due to strict compliance mandates for API precursors. Chromone commonly enters the process through catalytic acylation or hydroxylation steps, forming the core scaffold of finished molecules. Finished products include prescription bronchodilators and non-steroidal anti-asthmatic agents, requiring rigorous documentation of additive percentages and validation against pharmacopeia guidelines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for chromone derivatives
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • Chinese Pharmacopoeia (ChP) raw material chapters

    Typical usage ratio

    • Between 0.5%–10% w/w in the precursor stage, adjusted based on the synthetic route and yield optimization during API synthesis

    Downstream process integration

    • Introduced in reactor charging for direct acylation, prior to condensation or cyclization steps
    • Forms part of the key intermediate mixture before final purification and crystallization

    Final product types

    • Pharmaceutical-grade anti-asthmatic tablets
    • Inhalable dry powder formulations for respiratory conditions
    • Sterile injectable preparations of chromone derivatives

    2. Fungicide and Pesticide Intermediates in Crop Protection

    Agrochemical companies integrate chromone as a core intermediate during the multistep synthesis of systemic fungicides and selective herbicides. Functionality as a heterocyclic precursor supports oxime ether and carboxamide fungicide scaffolds, with direct implications for spectrum activity and persistence in field applications. Regulatory conditions demand clear material identification, impurity profiles, and environmental risk disclosures, especially for global registration and export. Usage levels vary with targeted molecule and extraction efficiency, monitored through in-line analytics across the reaction batch.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC) No 1907/2006 for agrochemical raw materials
    • China GB 2763 Maximum Residue Limits for Pesticides
    • OECD Test Guidelines for environmental safety assessment

    Typical usage ratio

    • Range of 1%–8% weight fraction in intermediates, subject to conversion rate and final fungicide structure

    Downstream process integration

    • Fed into main synthesis reactor at the heterocyclic formation stage
    • Participates in cross-coupling or halogenation before formulation of active pesticide ingredient

    Final product types

    • Systemic grain fungicides for disease prevention
    • Lawn and turf weed control herbicide blends
    • Seed treatment agents for row crops

    3. UV-Absorber Precursors in Engineering Polymers

    Specialty chemical producers rely on chromone moieties for developing polymer stabilizers and ultraviolet-light absorbers designed for high-performance plastics and coatings. The material’s functionality enables enhanced weathering resistance in automotive parts and construction polymers, entering the value chain through melt-blend compounding or inline reactive extrusion with engineering resins. Regulatory systems require full characterization of the intermediate and residue levels, frequently aligned with toxicity and migration standards for consumer exposure.

    Industry compliance standards

    • EU Regulation (EU) No 10/2011 on plastic materials and articles intended for food contact
    • US FDA 21 CFR §177.1520 for olefin polymers
    • ISO 4892 for artificial weathering testing of plastics
    • Automotive OEM specification for interior part weathering

    Typical usage ratio

    • Incorporated at 0.2%–3% by polymer mass, modulated by required light stabilization effect and matrix compatibility

    Downstream process integration

    • Compounded during resin pelletization or introduced in liquid masterbatch solution
    • Dispersed prior to polymer extrusion, blown film formation, or injection molding

    Final product types

    • UV-stabilized automotive trim and dashboards
    • Clear construction panel sheets
    • Outdoor-use polycarbonate and polypropylene housings

    4. Colorant Intermediate for Textile and Leather Dye Production

    Dye manufacturers employ chromone as a reactive precursor for the synthesis of specialty azo and anthraquinone dyes, valued for their unique colorfast properties on synthetic and natural fibers. It enters sulfonation and diazotization stages, affecting the tone and fastness of resultant pigments. The integration into dye production requires strict compliance with international textile chemical standards, careful management of residual byproducts, and documentation of batch traceability for downstream finishing houses and export regulatory checks.

    Industry compliance standards

    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • Oeko-Tex Standard 100 for textile chemical safety
    • EU REACH SVHC (Substances of Very High Concern) requirements
    • ISO 105-B02 lightfastness test for dyed textiles

    Typical usage ratio

    • Typically added at 1%–5% mass fraction in dye intermediate synthesis, adjusted by target chromophore concentration and dye class

    Downstream process integration

    • Reacted in primary dye coupling reaction before purification and standardization
    • Formulates substrate for finishing and coloration processes in textile and leather manufacturing

    Final product types

    • High-fastness direct dyes for cotton and polyester
    • Specialty leather finish colorants
    • Industrial pigment dispersions for thread and fiber spinning

    5. Fragrance and Flavor Synthesis Intermediate

    Fine chemical firms apply chromone in controlled syntheses of aroma compounds and complex fragrance bases, leveraging its aromatic structure to introduce lactone or aldehyde groups critical for nuanced scent formation. The substance typically enters aldehyde condensation or ring functionalization steps, producing ingredients compliant with international food and fragrance codes. Batch tracking and contaminant thresholds must be tightly monitored to fulfill food safety and labeling responsibilities across export markets.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • US FDA 21 CFR §172 for approved flavoring substances
    • EU Regulation (EC) No 1334/2008 on flavorings and food ingredients
    • FEMA GRAS (Generally Recognized As Safe) guidelines

    Typical usage ratio

    • Applied at 0.05%–1.5% in intermediate blends, adjusted according to target flavor intensity and downstream combinatorial reactions

    Downstream process integration

    • Condensed with aliphatic aldehydes or esters before fractional distillation and purification
    • Subjected to hydrogenation or enzymatic transformation for final aroma molecule production

    Final product types

    • Ready-to-use fragrance bases for personal care products
    • Encapsulated flavor additives for confectionery and beverages
    • Solvent-free aroma concentrates for ESS (Encapsulated Scent Systems)
    Free Quote

    Competitive Chromone prices that fit your budget—flexible terms and customized quotes for every order.

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