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2-Hydroxyacetophenone

    • Product Name 2-Hydroxyacetophenone
    • Einecs 202-593-7
    • 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

    351369

    Chemical Name 2-Hydroxyacetophenone
    Synonyms o-Hydroxyacetophenone
    Molecular Formula C8H8O2
    Molar Mass 136.15 g/mol
    Appearance White to pale yellow crystalline solid
    Melting Point 82-86 °C
    Boiling Point 286 °C
    Density 1.168 g/cm3
    Solubility In Water Slightly soluble
    Cas Number 118-93-4
    Smiles CC(=O)C1=CC=CC=C1O
    Pubchem Cid 8800
    Inchi InChI=1S/C8H8O2/c1-6(9)7-4-2-3-5-8(7)10/h2-5,10H,1H3

    As an accredited 2-Hydroxyacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2-Hydroxyacetophenone is packaged in a 100g amber glass bottle with a secure screw cap, labeled with hazard warnings.
    Shipping 2-Hydroxyacetophenone is shipped in tightly sealed containers, protected from moisture and light. It is transported in compliance with relevant chemical safety regulations, ensuring correct labeling and documentation. During transit, measures are taken to avoid exposure, leaks, and damage, ensuring safe delivery to laboratories or industrial users.
    Storage 2-Hydroxyacetophenone should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers. The storage area should be free from moisture and protected from direct sunlight. Proper labeling and compliance with relevant safety regulations are essential to prevent accidental exposure or contamination.
    Application of 2-Hydroxyacetophenone

    Applications of 2-Hydroxyacetophenone in Industrial Manufacturing

    With decades of technical expertise in aromatic ketone synthesis and controlled batch production, we supply 2-Hydroxyacetophenone for specialized downstream segments where its properties support both functional performance and regulatory compliance. Below, we detail the principal sectors and specific industrial processes where our material integrates as a critical intermediate or additive, built on verified application experience and customer manufacturing feedback.

    1. Pharmaceutical Intermediate for API Synthesis

    As a strategic intermediate, 2-Hydroxyacetophenone enters pharmaceutical manufacturing routes for developing a range of APIs, particularly anticonvulsants, non-steroidal anti-inflammatory drugs, and select anti-infectives. Our customers employ this material during multi-step organic synthesis, relying on its stability and purity to meet stringent output quality. Integration occurs in the early or middle stage condensation or cyclization reactions that form core heteroaromatic systems, always under validated GMP controls and tight impurity monitoring.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) guidelines per WHO, US FDA, and EudraLex Volume 4
    • Relevant pharmacopoeia monographs (USP, Ph. Eur., JP) for recognized intermediates
    • ICH Q3A/B impurity and residual solvent controls
    • REACH registration and toxicological reporting

    Typical usage ratio

    • 0.2 – 1.5 molar equivalents relative to next reaction partner in synthetic sequence; adjusted based on targeted batch size and required final yield

    Downstream process integration

    • Charged into the reaction vessel post-initial solvent charging and pre-catalyst addition, often under inert nitrogen atmosphere, followed by temperature-controlled condensation or cyclization with in-process HPLC monitoring

    Final product types

    • Generic and branded pharmaceutical APIs such as antiepileptics (e.g., clonazepam intermediates), anti-inflammatory agents, and wide-spectrum antibacterials

    2. Fragrance Ingredient and Stabilizer in Fine Chemical Formulations

    Perfume compounders and flavor manufacturers utilize 2-Hydroxyacetophenone for its warm, floral, and slightly balsamic note, as well as its stabilizing effect on other aromatic ingredients. Industrial blending balances its olfactory contribution with product safety, especially for leave-on skin-contact formulations. Our material enters the blending step post-dilution, co-dissolving with alcohol and essential oils before aging and QC by gas chromatography.

    Industry compliance standards

    • International Fragrance Association (IFRA) Amendment recommendations
    • ISO 9235:2013 guidance for aroma chemical origin and purity
    • Cosmetic Regulation (EC) No 1223/2009 for EU markets
    • Food and Drug Administration (FDA) 21 CFR, as applicable for indirect flavorant uses

    Typical usage ratio

    • Fragrance bases: 0.05–0.25% w/w of total concentrate, with upper limits guided by IFRA usage restrictions for certain product categories

    Downstream process integration

    • Added during perfume concentrate compounding, after dilution of other oil-soluble ingredients, with mixing under controlled temperature and subsequent solvent addition, followed by standing/aging to develop scent profile

    Final product types

    • Luxury and consumer-grade perfumes
    • Personal care fragrances (e.g., lotions, deodorants)
    • Functional fragrances for household cleaning and laundry products

    3. Resin Crosslinking Agent in UV-Curing Systems

    In the field of photopolymer coatings, inks, and adhesives, 2-Hydroxyacetophenone functions as an efficient photoinitiator or crosslinking co-agent, driving fast, uniform polymerization under UV radiation. Our customers integrate this material during masterbatch preparation, where its solubility in acrylate and urethane oligomers ensures rapid curing, minimal yellowing, and optimal mechanical properties for industrial coatings and specialty inkjet formulations.

    Industry compliance standards

    • ISO 9001:2015 (quality management for coatings/inks)
    • EN 71-3 for toy coatings and children’s goods
    • REACH Annex XVII for photoinitiator substances
    • AgBB evaluation (for VOC contribution in construction/living spaces, where relevant)

    Typical usage ratio

    • 0.3–1.2% w/w total formulation solids, determined by resin type, film thickness, exposure equipment, and desired cure speed

    Downstream process integration

    • Dosed directly into preweighed resin blend prior to pigment or additive dispersion; solubilized thoroughly before filtration and automated UV curing

    Final product types

    • UV-curable wood and plastic coatings
    • Inkjet and screen printing inks for packaging
    • Pressure-sensitive and industrial adhesives

    4. Synthesis Intermediate for Agrochemical Actives

    Through precise batch synthesis, agrochemical manufacturers incorporate 2-Hydroxyacetophenone as a building block for herbicide and fungicide actives, specifically compounds requiring aromatic ketone or hydroxybenzyl motifs. The material proceeds via controlled acylation, condensation, or etherification, feeding into further steps like halogenation or heterocycle closure for high-performance crop protection agents. Our strict lot traceability supports formulated product approval and field demonstration requirements.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Plant Protection Products
    • OECD Principles of Good Laboratory Practice (GLP) for environmental fate and toxicology
    • ISO 17025 certified testing for analytical batch release
    • REACH substance notification and classification, with focus on agro-use

    Typical usage ratio

    • 0.5–2.0 molar equivalents, depending on the complexity of the downstream active structure and specific crop formulation strategy

    Downstream process integration

    • Reacted during the initial chain-building stage, typically via Friedel–Crafts or Mannich reactions, before subsequent derivatization, crystallization, and formulation as a suspension concentrate or water-dispersible granule

    Final product types

    • Systemic herbicide actives (e.g., those based on acetanilide or imidazolinone backbones)
    • Protective fungicides/formulated chemical crop protection products

    5. Corrosion Inhibitor Booster in Metalworking Fluids

    Precision machining and metal treatment manufacturers integrate 2-Hydroxyacetophenone into high-stability water-miscible cutting fluids as a chelating and corrosion inhibition enhancer. Our technical practice infuses the additive during the final blending phase with other amines and neutralizing agents, aiming for strong film-forming ability and reduced oxidative wear of ferrous parts, especially in aerospace and automotive machining under high-load conditions.

    Industry compliance standards

    • ASTM D4627 for evaluating corrosion inhibition in metalworking fluids
    • ISO 6743/7 (classification of lubricants for metalworking)
    • European Chemical Agency (ECHA) notification for use in mixture products
    • SAR/TSCA compliance for US export and import

    Typical usage ratio

    • 0.05–0.12% w/w of finished fluid, optimized by laboratory salt spray and break point tests for specific alloy systems

    Downstream process integration

    • Incorporated during the late-stage compound blending, after base oil solubilization and preceding pH balancing, then homogenized and filtered prior to final QC

    Final product types

    • Multi-metal cutting fluids for precision machining
    • Temporary indoor anti-rust fluids
    • Machinery coolants for demanding industrial sectors
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