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Coumalic Acid

    • Product Name Coumalic Acid
    • Alias 2-Oxo-2H-1-benzopyran-3-carboxylic acid
    • Einecs 207-572-8
    • 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

    841474

    Name Coumalic Acid
    Iupac Name 2-oxo-2H-pyran-5-carboxylic acid
    Cas Number 603-91-2
    Molecular Formula C6H4O4
    Molar Mass 140.09 g/mol
    Appearance White to pale yellow powder
    Melting Point 210-215 °C (decomposes)
    Solubility In Water Slightly soluble
    Density 1.564 g/cm³
    Boiling Point Decomposes before boiling
    Pka 3.1 (carboxylic acid group)
    Synonyms 2-Oxocoumalic acid; 5-Carboxy-2H-pyran-2-one

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

    Packing & Storage
    Packing Coumalic Acid is packaged in a 25g amber glass bottle, sealed with a screw cap, and labeled with safety and identification details.
    Shipping Coumalic Acid should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It must be clearly labeled and handled according to all relevant regulations for chemical substances. Store and transport it at room temperature, ensuring it remains upright, away from direct sunlight, and in compliance with hazardous materials shipping protocols.
    Storage Coumalic acid should be stored in a tightly sealed container, away from moisture and incompatible substances, such as strong bases and oxidizing agents. Keep it in a cool, dry, and well-ventilated area, protected from direct sunlight and sources of ignition. Proper labelling and segregation from food and drink are essential to prevent accidental ingestion or contamination.
    Application of Coumalic Acid

    Applications of Coumalic Acid in Industrial Manufacturing

    Coumalic acid, a heterocyclic carboxylic acid, is widely valued in specialized industrial fields for its unique aromatic and reactive properties. As an original manufacturer, we supply coumalic acid to multiple segments where it serves distinct functions in well-established downstream production lines. Below, we detail how our material integrates into real formulations and regulatory frameworks in key industries.

    1. Fine Chemical Intermediates for Dye and Pigment Synthesis

    In the colorant sector, companies use coumalic acid as a crucial intermediate for synthesizing specialty dyes and complex pigment molecules. Its furanone core structure provides reactive sites essential for condensation and coupling reactions, enabling generation of azo and anthraquinone-based chromophores. The value of coumalic acid lies in its contribution to high-purity, high-stability dye lots demanded by precision textile, ink, and polymer coloration markets.

    Industry compliance standards

    • REACH Annex XVII, Regulation (EC) No 1907/2006
    • EN 71-3 (Safety of Toys - Migration of certain elements)
    • Oeko-Tex Standard 100—Approved colorant content
    • Chinese National Standard GB/T 22899 for dye intermediates

    Typical usage ratio

    • Ranges from 1.5%–5% by weight of total reactants, determined by the molar ratios required for specific dye coupling and degree of color depth; levels are adjusted based on desired hue and target purity.

    Downstream process integration

    • Added during the initial condensation or coupling stage when building core chromophores; may be introduced as a pure acid or in pre-neutralized salt form, depending on the solvent system and pH requirements of the given synthesis.

    Final product types

    • Azo dyes for textile fiber dyeing
    • Organic pigments for printing inks
    • Water-soluble colorants for marker ink manufacturing
    • Complex intermediates for plastics color concentrates

    2. Agrochemical Synthesis: Herbicidal Active Ingredient Manufacturing

    Chemical corporations incorporate coumalic acid as a structurally unique building block in the assembly of innovative herbicidal molecules. Its reactivity is exploited in stepwise acylation and esterification reactions to construct substituted phthalide or coumarin frameworks, which perform as active herbicidal moieties or core scaffolds in patented active ingredients. This application is characterized by strictly controlled batch manufacturing to meet the high standards demanded by agrochemical registrants.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market
    • US EPA Title 40—Pesticide Registration Standards
    • Good Manufacturing Practice (GMP) for Agrochemicals

    Typical usage ratio

    • Employed at 2%–7% by mass in precursor synthesis, with dosing adjusted in proportion to the intended yield of the intermediate herbicidal structure; precise addition is calculated stoichiometrically based on target molecule synthesis routes.

    Downstream process integration

    • Charged during multi-step chemical synthesis, primarily in the cyclization or acylation stages; process engineers add it either as a solid or slurried input under tightly monitored temperature and solvent conditions.

    Final product types

    • Selective and non-selective herbicide technical concentrates
    • Formulated aqueous solutions for direct crop application
    • Wettable powders for arable land treatment
    • Granular pre-emergent herbicidal actives

    3. Pharmaceutical Research and Active Pharmaceutical Ingredient (API) Synthesis

    R&D-driven pharma firms leverage coumalic acid as a chemical precursor in route scouting of several heterocyclic drug candidates, prioritizing its furanone motif for the construction of pharmacologically relevant frameworks. Most uses center around pilot-scale route development, impurity profile characterization, and scale-up studies for preclinical actives where traceability and documentation are addressed by stringent international regulations.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP)
    • European Pharmacopoeia (Ph. Eur.)
    • China Pharmacopoeia (ChP) for bulk pharmaceutical intermediates

    Typical usage ratio

    • Used at 0.5%–2.5% of total reactant load, meticulously scaled in API route development labs; ratio depends on target scaffold complexity, with engineers adjusting to minimize waste and residual byproducts.

    Downstream process integration

    • Fed into pilot reactors during nucleophilic addition or condensation stages; handled as a solid with dedicated containment procedures to prevent cross-contamination in API GMP suites.

    Final product types

    • Generic and proprietary API intermediates
    • Advanced pharmaceutical intermediates for scale-up supply
    • Analytical reference standards for regulatory submissions
    • Non-commercial R&D drug substance samples

    4. Functional Additives for Specialty Polymer Modification

    Polymer producers rely on coumalic acid to introduce tailored functionality or reactivity into engineering resins and specialty copolymers. Its structural features enable the formation of cross-links or pendant groups that improve heat resistance, UV stability, or adhesion properties in performance polymers. Manufacturers commonly apply it in the formulation of plastics used in electrical insulation, automotive coatings, and protective films, aiming for consistent material upgrades compliant with international quality protocols.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • RoHS Directive (EU 2015/863) for plastics additives
    • UL 746C (Polymeric Materials—Use in Electrical Equipment)
    • ASTM D638 (Standard Test Method for Tensile Properties of Plastics)

    Typical usage ratio

    • Between 0.3%–2% by weight of polymer composition, exact amount tailored to desired performance features and compatibility with other reactive additives or fillers.

    Downstream process integration

    • Blended directly during compounding in melt-kneader or twin-screw extrusion lines; introduced with other functional additives before final pelletization or molding, with strict in-process QC for dispersion and reactivity retention.

    Final product types

    • Cross-linked engineering thermoplastics
    • Enhanced UV-resistant films for electronics
    • Automotive exterior paint systems
    • Protective coatings for industrial metal substrates

    5. Analytical Chemistry Reagent Manufacturing

    Chemical analysis product manufacturers utilize coumalic acid to prepare specialty reagents, reference materials, and derivatization agents for analytical laboratories. Due to its specific reactivity with certain classes of analytes, it is a choice reagent in qualitative and quantitative methods used in wet chemistry and instrumental assays.

    Industry compliance standards

    • ISO/IEC 17025 (General requirements for the competence of testing and calibration laboratories)
    • Analytical reagent specifications—ACS and ISO Reagent Grade
    • USP-NF for lab reagent purity
    • Good Laboratory Practice (GLP) standards

    Typical usage ratio

    • Formulated at concentrations of 0.05%–0.5% in final reagent solutions; ratio determined by sensitivity requirements of the analytical procedure and expected detection levels.

    Downstream process integration

    • Dissolved or suspended during reagent synthesis prior to bottling; producers carefully standardize concentration and perform batch validation to meet defined analytical performance criteria.

    Final product types

    • Colorimetric assay kits for laboratory use
    • Derivatization agents for chromatography sample prep
    • Spectrophotometric analysis reagents
    • Certified reference materials for QA/QC labs
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