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3,4-Dihydroxyacetophenone

    • Product Name 3,4-Dihydroxyacetophenone
    • Alias 3,4-DHAP
    • Einecs 207-750-3
    • 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

    691555

    Cas Number 99-50-3
    Iupac Name 1-(3,4-dihydroxyphenyl)ethan-1-one
    Molecular Formula C8H8O3
    Molecular Weight 152.15 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 109-113°C
    Boiling Point 329.1°C at 760 mmHg
    Solubility Soluble in ethanol, ether, and hot water
    Density 1.294 g/cm³
    Pubchem Cid 7434
    Smiles CC(=O)C1=CC(=C(C=C1)O)O

    As an accredited 3,4-Dihydroxyacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of 3,4-Dihydroxyacetophenone is supplied in a sealed amber glass bottle, labeled with hazard information and product details.
    Shipping 3,4-Dihydroxyacetophenone is securely packaged in sealed, chemical-resistant containers to prevent contamination or leakage. It is shipped following all regulations for chemical transport, including appropriate labeling and documentation. The package is protected from moisture, sunlight, and extreme temperatures, ensuring safe delivery to the destination. Handle with care upon receipt.
    Storage 3,4-Dihydroxyacetophenone should be stored in a cool, dry, and well-ventilated area, away from sources of heat, light, and incompatible substances such as strong oxidizers. The container must be tightly sealed to prevent moisture absorption and contamination. Proper chemical storage protocols, clearly labeling the container and keeping it away from food and drink, must be followed at all times.
    Application of 3,4-Dihydroxyacetophenone

    Applications of 3,4-Dihydroxyacetophenone in Industrial Manufacturing

    3,4-Dihydroxyacetophenone supports specialty production in life sciences, cosmetics, pharmaceutical intermediates, and analytical reagents. As an experienced manufacturer, we focus on processes where this compound’s properties align with high-value downstream use, detailed for each application pathway below.

    1. UV-Absorber in Cosmetic and Personal Care Formulations

    Major personal care brands leverage 3,4-Dihydroxyacetophenone for its photoprotective characteristics in sunscreen products and anti-aging formulations. Its aromatic, polyhydroxy structure provides efficient free-radical scavenging when integrated into cosmetic matrices. Research shows consistent performance as a UV filter stabilizer and mild skin-conditioning agent, particularly suited for premium sunscreen lotions, BB creams, and moisturizing creams targeting high-defense markets.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No. 1223/2009
    • US FDA 21 CFR Part 700: Cosmetics
    • China NMPA GB/T 29665 safety standards
    • ISO 16128 natural ingredient criteria (composition record)

    Typical usage ratio

    • 0.05% to 0.4% by weight, precisely modulated to formulation pH, photo-stability targets, and local regulatory limits. Dermatological products with higher SPF require the upper concentration range.

    Downstream process integration

    • In cosmetic manufacturing, technical staff introduce the additive during the oil or aqueous phase preparation under controlled temperatures. Dispersion and stabilization occur before emulsion formation or homogenization, ensuring full incorporation without crystallization or sediment.

    Final product types

    • Sunscreen lotions (SPF 15-50+)
    • Facial BB/CC creams
    • Day gel moisturizers
    • SPF lip balms

    2. Intermediate for Synthetic Pharmaceutical APIs

    Pharmaceutical synthesis units use 3,4-Dihydroxyacetophenone as a building block for drugs that require a catechol motif, supporting the preparation of advanced intermediates in antibacterials, anti-inflammatory agents, and neuroprotective compounds. The stability and reactivity allow controlled functionalization, endorsing its use in multi-stage chemical synthesis for the regulated pharmaceutical sector.

    Industry compliance standards

    • ICH Q7 GMP Guidelines for Active Pharmaceutical Ingredients
    • USP-NF / Ph.Eur monograph documentation for process validation
    • FDA 21 CFR Part 211 pharmaceutical cGMP
    • EMA: EDQM TSE/BSE statements for raw material sourcing

    Typical usage ratio

    • The input molar ratio ranges from 0.8 to 1.2 equivalents per stage depending on desired yield and downstream functionalization steps. R&D teams determine the loading in route optimization, with scale-up usually settling at stoichiometric or slight excess amounts for intermediate isolation consistency.

    Downstream process integration

    • Synthesizers introduce the compound during core ketone functionalization and ring-substitution. The material routinely feeds into Friedel–Crafts acylation or Mannich-type reactions. Chemists purify intermediates before coupling or cyclization to ensure compliance for further API processing.

    Final product types

    • Neuroprotective APIs (dopaminergic agents)
    • Topical wound-healing medication intermediates
    • Antioxidant pharmaceutical agents
    • Antibacterial precursor compounds

    3. Precursor for Food Contact Material Additives

    Food packaging manufacturers utilize 3,4-Dihydroxyacetophenone for the synthesis of antioxidant and UV-absorbing additives incorporated within polymer coatings. Specialty polymers bearing the catechol-type functionality improve packaging resistance to light-induced degradation and oxidation, ensuring shelf life extension for sensitive foods. Its role as a starting material for custom-tailored stabilizers delivers technical advantages in multilayer packaging films and resin-based food containers.

    Industry compliance standards

    • EU Regulation No. 10/2011 on plastic materials for food contact
    • US FDA 21 CFR 175.300-177.1520: adhesives, coatings, and plastics for food packaging
    • China GB 9685 food packaging additives regulation
    • ISO 22000 HACCP principles for indirect food additives

    Typical usage ratio

    • 0.01% to 0.12% by weight, tailored in masterbatch formulations according to substrate type, polymerization method, and barrier requirements. Regulatory migration limits often define the maximum permitted dosage in the final material.

    Downstream process integration

    • Resin plants add the compound during melt blending or in situ polymerization, preceding extrusion or film casting. Technicians confirm full dispersion through compounding prior to film conversion, printing, or lamination operations.

    Final product types

    • Thermoformed food trays
    • Laminated multi-barrier films
    • Flexible pouch liners
    • Beverage bottle coatings

    4. Reference Standard in Analytical Reagent Production

    Producers of analytical kits source high-purity 3,4-Dihydroxyacetophenone for calibration standards in chromatographic and colorimetric testing. The compound’s defined structure and spectral properties meet the stringent requirements of chemical and pharmaceutical laboratories, supporting trace analysis, system suitability testing, and method validation.

    Industry compliance standards

    • ISO 17034:2016 General requirements for reference material producers
    • USP Reference Standards protocols
    • Ph. Eur General Chapter 2.7.2 for analytical standards
    • ISO/IEC 17025 testing laboratory accreditation

    Typical usage ratio

    • Analytical standards use from 1 mg/mL up to 100 mg/mL solution, depending on method sensitivity and detection limits. Calibration kits adjust quantity precisely based on instrument make, analysis range, and matrix complexity.

    Downstream process integration

    • Reagent manufacturers dissolve the material in high-purity solvents, filter, and aliquot reference solutions during kit assembly. Quality control tests each batch with high-resolution mass spectrometry and NMR to certify identity and purity before packaging for laboratory supply networks.

    Final product types

    • HPLC/GC reference standards
    • Routine pharmaceutical testing kits
    • Colorimetric determination kits for research labs
    • Pesticide and contaminant analysis controls
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