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6,7-Dimethoxy-4-Methylcoumarin

    • Product Name 6,7-Dimethoxy-4-Methylcoumarin
    • Alias PMA
    • Einecs 244-682-6
    • 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
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    Specifications

    HS Code

    115444

    Chemical Name 6,7-Dimethoxy-4-Methylcoumarin
    Cas Number 4845-20-7
    Molecular Formula C12H12O4
    Molecular Weight 220.22 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 150-153°C
    Solubility Slightly soluble in water, soluble in organic solvents like ethanol and DMSO
    Purity Typically ≥98%
    Iupac Name 6,7-dimethoxy-4-methyl-2H-chromen-2-one
    Smiles COC1=CC2=C(C(=O)OC=C2C(=C1)OC)C
    Storage Conditions Store at 2-8°C, protect from light and moisture
    Synonyms 4-Methyl-6,7-dimethoxycoumarin

    As an accredited 6,7-Dimethoxy-4-Methylcoumarin 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 25 grams of 6,7-Dimethoxy-4-Methylcoumarin, sealed with a screw cap and labeled with safety information.
    Shipping 6,7-Dimethoxy-4-Methylcoumarin is shipped in tightly sealed containers, protected from light, moisture, and extreme temperatures. Transport complies with local and international regulations for chemical handling. Packaging ensures product stability and prevents contamination or leakage during transit. Shipping documents include safety data and handling instructions for safe and compliant delivery.
    Storage Store 6,7-Dimethoxy-4-Methylcoumarin in a tightly sealed container, in a cool, dry, and well-ventilated area. Protect from light, moisture, and incompatible substances such as strong oxidizers and acids. Keep away from sources of ignition and heat. Proper labeling and secondary containment are recommended to prevent accidental exposure or spills. Use appropriate personal protective equipment when handling.
    Application of 6,7-Dimethoxy-4-Methylcoumarin

    Applications of 6,7-Dimethoxy-4-Methylcoumarin in Industrial Manufacturing

    As a chemical manufacturer specializing in the production of 6,7-Dimethoxy-4-Methylcoumarin, we serve key sectors where this high-purity intermediate fulfills specific technical roles. Our expertise supports industries with stringent compliance requirements and proven process integration. Below we present focused industrial application scenarios, each supported by operational details reflecting real-world usage downstream.

    1. Photoinitiators for UV-Curable Coatings

    Industrial coating formulators use 6,7-Dimethoxy-4-Methylcoumarin as a specialty coumarin photoinitiator in UV-curable resin systems, where reliable radical formation is required for rapid surface curing. The compound integrates during photoinitiator blending steps, contributing efficient absorption at targeted UV wavelengths and minimizing residual odor in cured films. Coating producers deploy this material for high-gloss overprint varnishes and wood finishes that must comply with industrial emission and performance standards while maintaining optimal process speed and finish durability.

    Industry compliance standards

    • EN 71-3:2019 (Safety of toys – migration of certain elements for coatings used on children's furniture and toys)
    • EU Regulation (EC) No 1935/2004 (Framework for materials and articles intended for food contact – relevant for packaging coatings)
    • ISO 12944 (Corrosion protection of steel structures by protective paint systems)
    • REACH Annex XVII (Restrictions on manufacture, placing on market, and use of certain dangerous substances)

    Typical usage ratio

    • 0.4–1.5% by weight of total resin formulation; formulators adjust based on UV intensity, pigment content, and desired cure speed

    Downstream process integration

    • Added during the photoinitiator masterbatch compounding stage prior to dispersion into the main resin mix; compatibility with acrylate, epoxy, or polyester binder systems required for uniform film formation

    Final product types

    • UV-cured overprint varnishes for paperboard packaging
    • High-durability wood flooring coatings
    • Protective coatings for industrial electronics housings
    • Surface finishes for PVC profiles

    2. Laser Dye Intermediate for Fluorescent Markers

    Manufacturers of specialty laser dyes and fluorescent marker inks rely on this coumarin derivative for its high quantum yield and sharp emission profile in the blue-green region. The compound enters the dye synthesis process as a key intermediate, forming the chromophore backbone in spectral grade dyes. Strict photophysical property control during production ensures consistent marker intensity and resistance to photobleaching, which is crucial for applications in security printing and analytical instrumentation.

    Industry compliance standards

    • DIN EN ISO 11664-1 (Colorimetry – Specification of CIE standard illuminants and measurement)
    • RoHS Directive (2011/65/EU) on restriction of hazardous substances in electrical and electronic equipment
    • ISO 14184-1:2011 (Determination of formaldehyde in textile products – relevant for ink safety on apparel)
    • German Blue Wool Scale (for assessing lightfastness in printing inks)

    Typical usage ratio

    • 80–95% of the chromophore precursor batch; actual mass depending on targeted molar extinction coefficient and solvent system for dye processing

    Downstream process integration

    • Undergoes condensation reactions during fine chemical synthesis to form the functional dye; downstream purification via recrystallization or chromatography before blending into ink vehicles or marker gels

    Final product types

    • Laser dyes for scientific and medical lasers
    • Security inks for anti-counterfeiting packaging
    • Highlighters and marking pen inks
    • Fluorescent labeling reagents for laboratory assays

    3. Specialty Fragrance Ingredients for Fine Perfumery

    The compound finds targeted use as a precursor in the synthesis of musk and floral fragrance aldehydes for high-value fine perfumery bases. Its structural motif enables downstream chemists to construct fragrance molecules with persistent, diffusive qualities required in both luxury perfumes and high-end personal care products. Production runs align with IFRA and cosmetic ingredient quality frameworks, placing responsibility on the manufacturer to ensure low impurity profiles and traceability of all raw materials entering the olfactory synthesis sequence.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association – Compliance for consumer safety)
    • ISO 9235:2013 (Aromatic natural raw materials – Terminology for ingredient traceability)
    • EU Regulation (EC) No 1223/2009 (Cosmetics Regulation – requirements for ingredient safety and purity)
    • Good Manufacturing Practices (cosmetic ingredients): ISO 22716

    Typical usage ratio

    • 10–25% by weight in fragrance ingredient synthesis steps; actual ratio determined by yield pathway and downstream aldehyde conversion efficiency

    Downstream process integration

    • Engaged as an initial feedstock in multi-step organic transformations, including O-demethylation and side-chain alkylation, ahead of distillation and fine purification for perfumery application

    Final product types

    • Fine fragrance ingredients for Eau de Parfum and cologne bases
    • Perfumed lotions and creams
    • Luxury bar soaps
    • Home fragrance diffuser bases

    4. Organic Synthesis Intermediate in Pharmaceutical R&D

    API and chemical research laboratories employ 6,7-Dimethoxy-4-Methylcoumarin as a scaffold for building advanced molecular structures during the development of kinase inhibitors and enzyme interaction studies. It provides a highly-functionalized backbone for diversification in medicinal chemistry, improving lead compound selectivity. Integration occurs under GMP conditions with strict analytical validation, maintaining compliance with pharmacopoeial standards to support progression from discovery to preclinical studies.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients)
    • Ph. Eur (European Pharmacopoeia) reference standards
    • USP General Chapters (pharmaceutical use)
    • 21 CFR Part 211 (FDA – cGMP for finished pharmaceuticals)

    Typical usage ratio

    • 0.5–5.0 mmol scale per medicinal chemistry batch; the precise amount tailored by synthetic yield optimization and screening library design

    Downstream process integration

    • Engaged as a diversification handle during the lead optimization stage, where chemists introduce substitution groups for SAR (structure-activity relationship) exploration; added into multi-step batch reactors or parallel synthesis blocks in early-phase R&D

    Final product types

    • Lead compound libraries for kinase and protease inhibition studies
    • Chemical probes for academic research
    • Preclinical development candidates
    • Segments of reference standards for analytical validation

    5. Optical Brightener Precursor for Specialty Paper Manufacturing

    Specialty paper mills utilize this compound as an intermediate in the synthesis of coumarin-type optical brightening agents (OBAs), where it imparts strong fluorescence under UV illumination. The process involves reacting the coumarin building block during OBA synthesis, followed by downstream sulfonation and purification steps. Brightener producers must guarantee consistency in fluorescence intensity and compatibility with both acidic and neutral paper pulping operations, ensuring compliance with environmental and food packaging paper safety standards.

    Industry compliance standards

    • FDA 21 CFR 176.170 (Components of paper and paperboard in contact with aqueous and fatty foods)
    • ISO 2470-2:2016 (Paper, board and pulps – Measurement of diffuse blue reflectance factor)
    • Nordic Swan Ecolabel (paper products)
    • EN 646 (Paper and board intended to come into contact with foodstuffs – Determination of color transfer)

    Typical usage ratio

    • 5–12% by weight in OBA synthesis batches, later diluted to achieve 0.01–0.2% in final wet-end paper addition based on brightness requirement and stock flow rate

    Downstream process integration

    • Enters at the OBA synthesis phase, with subsequent integration into paper mill wet-end chests for dispersion prior to sheet formation on the paper machine

    Final product types

    • High-brightness copy paper and inkjet photo papers
    • Food-grade packaging liners
    • Banknote paper substrates
    • Security watermarked papers
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