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2'-Hydroxy-4',5'-Dimethoxyacetophenone

    • Product Name 2'-Hydroxy-4',5'-Dimethoxyacetophenone
    • Alias Hesperetin 4’-methyl ether
    • Einecs 249-596-6
    • 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
    VTB
    Specifications

    HS Code

    886874

    Chemicalname 2'-Hydroxy-4',5'-Dimethoxyacetophenone
    Molecularformula C10H12O4
    Molecularweight 196.20 g/mol
    Casnumber 22131-39-5
    Appearance White to off-white solid
    Meltingpoint 83-85°C
    Solubility Soluble in organic solvents such as ethanol, methanol, and DMSO
    Pubchemcid 382105
    Smiles COC1=CC(=C(C=C1OC)O)CC(=O)C
    Inchi InChI=1S/C10H12O4/c1-6(11)5-7-8(12)3-4-9(13-2)10(7)14-3/h3-4,12H,5H2,1-2H3

    As an accredited 2'-Hydroxy-4',5'-Dimethoxyacetophenone 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 2'-Hydroxy-4',5'-Dimethoxyacetophenone, sealed with a screw cap and labeled for laboratory use.
    Shipping 2'-Hydroxy-4',5'-Dimethoxyacetophenone is shipped in secure, airtight containers to prevent contamination and moisture exposure. Packaging complies with chemical safety standards, featuring appropriate hazard labeling. The product is handled by trained personnel and transported under controlled conditions, ensuring safe and efficient delivery while meeting regulatory requirements for chemical shipments.
    Storage 2'-Hydroxy-4',5'-Dimethoxyacetophenone should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, well-ventilated area, ideally at room temperature. Avoid exposure to incompatible substances such as strong oxidizers. Properly label the container, and use appropriate personal protective equipment when handling this chemical to ensure safety.
    Application of 2'-Hydroxy-4',5'-Dimethoxyacetophenone

    Applications of 2'-Hydroxy-4',5'-Dimethoxyacetophenone in Industrial Manufacturing

    Our 2'-Hydroxy-4',5'-Dimethoxyacetophenone is utilized in demanding industrial segments where precise formulation, validated quality, and adherence to sector-specific regulations are key. As a specialized intermediate, it delivers established performance and consistency backed by over a decade of direct manufacturing experience. Below, we detail its main downstream applications, covering critical compliance, process integration, formulation range, and finished product use.

    1. UV Absorbers for High-Performance Polymer Stabilization

    This compound finds established use in synthesizing specialty benzophenone- and benzotriazole-type UV absorbers for engineering plastics. Polymer compounders dose these additives to prevent coloration or brittleness during sunlight exposure, particularly in automotive or electronics housings subjected to outdoor conditions. Material sourcing and batch supply involve close tracking to align with global regulatory and quality mandates.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • EU RoHS Directive 2011/65/EU
    • UL 94 Plastics Flammability Standard
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 2'-Hydroxy-4',5'-Dimethoxyacetophenone typically constitutes 0.8–3.0% of the UV absorber batch; compounders then dose the resulting UV absorber at 0.05–0.4% into the resin blend, adjusted depending on plastic resin and lightfastness requirement.

    Downstream process integration

    • The material is introduced during the fine chemical synthesis stage of UV stabilizer intermediates, followed by purification and integration in resin compounding lines (extrusion or masterbatch production).

    Final product types

    • Automotive exterior plastics (mirror housings, grilles)
    • Electronic device enclosures
    • Outdoor equipment casings
    • Clear packaging films with enhanced UV resistance

    2. Pharmaceutical Intermediate for Antipyretic and Analgesic API Synthesis

    Selective pharmaceutical manufacturers source our product as a high-purity building block for novel antipyretic and analgesic active pharmaceutical ingredients. We maintain stringent traceability and batch documentation to meet both local and international GMP process controls, with all handling geared to minimize impurities throughout multi-stage synthesis in regulated pharma plants.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.)
    • US FDA cGMP (21 CFR Parts 210 & 211)
    • ISO 14001 Environmental Management (where required for export markets)

    Typical usage ratio

    • Compound is metered at 5–18% w/w in key condensation or acylation steps, proportion based on molar equivalency specific to target API; excess or recycle fractions determined according to process efficiency and impurity profile requirements.

    Downstream process integration

    • Integration occurs during initial intermediate coupling or ring substitution stages before core API crystallization, often under controlled temperature and solvent recovery schemes mandated by pharma process validation teams.

    Final product types

    • Antipyretic bulk APIs (e.g., paracetamol derivatives)
    • Analgesic finished dosage forms
    • Combination fever-reducing agents for adult and pediatric formulations
    • Export-market generics in oral solid and liquid formats

    3. Fragrance Intermediate in Fine Aroma Chemicals Manufacturing

    Leading aroma chemical firms employ our material as a coupling agent to deliver stable ether or ester motifs used in perfumery and cosmetics. Batch consistency is critical for downstream distillation and quality control, especially for high-value fragrance bases destined for premium markets. All production fully traces raw material origin and purity to comply with IFRA and related regional standards.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association)
    • EU Cosmetics Regulation (EC) No 1223/2009
    • ISO 22716:2007 Cosmetics GMP
    • Product-specific allergen labeling requirements

    Typical usage ratio

    • Used at 3–12% of fragrance intermediate formulations, adjusted based on desired tonal profile and substrate volatility; higher ratios leveraged for fixing base notes in complex blends.

    Downstream process integration

    • Material enters during multi-stage etherification or esterification, with close pH and distillation monitoring to ensure aromatic purity pre-blending and packaging.

    Final product types

    • Fine fragrance compounds for perfumes
    • Creams, lotions, and cosmetic emulsions with tailored scents
    • Aroma additives in personal care and toiletries
    • Home care and air freshener bases

    4. Dye Intermediate in High-Purity Quinone and Phenolic Dyes

    Industrial dye manufacturers specify our product as a critical building block in advanced phenolic and quinone dye synthesis, required for demanding applications in textile and specialty printing sectors. Its well-characterized impurity profile ensures reliable color consistency in downstream grinding and blending operations. We support regular shipments with accompanying analytical COA to ease regulatory audits for compliance-focused dye converters.

    Industry compliance standards

    • OEKO-TEX® Standard 100
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • EU REACH Annex XVII (dye-specific restrictions)
    • ISO 9001:2015 production traceability

    Typical usage ratio

    • Compound represents 6–22% of dye synthesis batches, with final percentage tailored to chromophore loading and desired color strength.

    Downstream process integration

    • Introduced in the diazotization, coupling, or oxidation steps prior to crude dye precipitation, then carried through filtration and milling stages to produce fine, consistent dye powders and dispersions.

    Final product types

    • Reactive dyes for cotton and viscose fabrics
    • Specialty inkjet inks for textile printing
    • Technical paper dyes with anti-fading properties
    • Leather finishing colorants

    5. Photoinitiator Intermediate in Specialty Coatings

    Coating chemical formulators use our compound in synthesizing photoinitiators critical for UV-curable paints, inks, and adhesives. Due to stringent end-use requirements, we provide certificates of analysis for every lot, facilitating inclusion in regulated industrial and electronic assembly applications, where final product documentation and supply chain transparency are mandatory for global trade.

    Industry compliance standards

    • ISO 22196:2011 for antibacterial coatings (where required)
    • EU Packaging Ink Platform (PIP) compliance
    • ASTM D7767 for UV-cured coatings
    • REACH chemical safety dossiers

    Typical usage ratio

    • Typically dosed at 1.5–7.5% within the photoinitiator precursor stage; downstream formulators then incorporate the resulting photoinitiators at 0.1–3.0% into the resin matrix contingent on cure thickness and UV intensity.

    Downstream process integration

    • Incorporated at prepolymerization or during post-condensation steps of photoinitiator synthesis, followed by high-shear mixing into base resin systems and subsequent UV-curing formulation.

    Final product types

    • UV-curable industrial coatings for plastics and metal parts
    • High-speed printing inks for flexible packaging
    • Electronics assembly adhesives and encapsulants
    • Optically clear coating fluids
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