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2',5'-Dihydroxyacetophenone

    • Product Name 2',5'-Dihydroxyacetophenone
    • Alias 2,5-DHAP
    • Einecs 210-247-2
    • 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

    813364

    Cas Number 490-85-3
    Iupac Name 2',5'-Dihydroxyacetophenone
    Molecular Formula C8H8O3
    Molar Mass 152.15 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 146-148 °C
    Solubility In Water Slightly soluble
    Density 1.286 g/cm³
    Smiles CC(=O)C1=CC(=C(C=C1)O)O
    Pubchem Cid 68234
    Synonyms 2,5-Dihydroxyacetophenone
    Storage Conditions Store at room temperature, away from light and moisture

    As an accredited 2',5'-Dihydroxyacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for 2',5'-Dihydroxyacetophenone (25 grams) features a sealed amber glass bottle with a tamper-evident cap and clear labeling.
    Shipping 2',5'-Dihydroxyacetophenone is shipped in tightly sealed containers to prevent moisture and contamination. It should be handled with care, kept away from incompatible substances, and stored in a cool, dry place. Shipping complies with relevant regulations, and appropriate labeling and documentation are provided to ensure safe transportation.
    Storage **2',5'-Dihydroxyacetophenone** should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Keep it out of direct sunlight, heat, and moisture. Properly label the storage container and avoid prolonged exposure to air to prevent degradation or contamination of the chemical.
    Application of 2',5'-Dihydroxyacetophenone

    Applications of 2',5'-Dihydroxyacetophenone in Industrial Manufacturing

    2',5'-Dihydroxyacetophenone serves as a specialty intermediate in several focused sectors, supporting manufacturers with precise functional groups required for advanced synthesis. Below, we detail core downstream application routes and technical considerations in each industrial context based on production realities and established formulation knowledge.

    1. Pharmaceutical Intermediates: Synthesis of Antipyretic and Analgesic Drugs

    This substance functions as a key intermediate in the synthesis of certain non-steroidal anti-inflammatory and antipyretic pharmaceuticals. Many drug manufacturing processes require the precise introduction of hydroxyacetophenone structures to achieve targeted pharmacophores. Industrial synthesis employs well-defined stoichiometry and controlled reaction parameters to ensure purity and batch-to-batch consistency. Formulators strictly monitor residual levels and byproducts due to regulatory limits on impurities; validated analytical protocols ensure compliance prior to downstream formulation into active pharmaceutical ingredients (APIs).

    Industry compliance standards

    • Good Manufacturing Practice (GMP, ICH Q7)
    • Pharmacopoeias: USP, EP, JP (where applicable)
    • FDA and EMA guidelines for API intermediates
    • REACH and TSCA inventory requirements

    Typical usage ratio

    • 0.12–0.37 molar equivalents relative to final API structure, based on synthesis pathway
    • Adjustment depends on yield and purification stage efficiency

    Downstream process integration

    • Introduced in initial condensation or acylation steps for building phenolic structures
    • Followed by filtration, washing, recrystallization, and API-specific derivatization stages
    • Integrated in semi-continuous or batch production plants

    Final product types

    • Oral solid dose analgesic APIs
    • Injectable fever-reducing medicinal ingredients
    • High-purity reference standards for pharmaceutical quality control

    2. Industrial Fine Chemicals: Specialty Resin Modifiers

    Within the coatings and plastics sector, 2',5'-dihydroxyacetophenone is adopted for its phenolic hydroxyl reactivity in the synthesis of specialized resin hardeners and polymer chain modifiers. Process engineers select this intermediate to introduce precise rigid or branched sites in epoxy or urethane resins, enhancing thermal performance or chemical resistance. Ratio determination follows empirical testing, considering downstream viscosity, cure time, and crosslinking density. Manufacturers use dedicated mixing and polymerization lines with in-line monitoring to control distribution and uniformity, ensuring product stability and application consistency.

    Industry compliance standards

    • ISO 9001:2015 quality management systems for chemical synthesis
    • ASTM D1652, D4457 (epoxy and resin testing methods)
    • RoHS (Restriction of Hazardous Substances) as relevant for electronics coatings
    • REACH (Annex XVII restrictions for phenolic compounds)

    Typical usage ratio

    • 0.5–3.0% w/w of total resin weight
    • Precise dosing via gravimetric feeders, adjusted based on resin molecular weight and performance targets

    Downstream process integration

    • Charged during pre-polymer mixing or immediately post-addition of curing agents
    • Heat- or photo-initiated reaction steps monitored for exotherm and gelation endpoint
    • Final paste or liquid resin transferred to molding, coating, or casting equipment

    Final product types

    • High-durability coatings for transportation and marine equipment
    • Electronic encapsulants requiring controlled dielectric properties
    • Specialty adhesives for industrial assembly
    • Composite resin matrices for advanced construction materials

    3. Agrochemical Active Ingredient Synthesis

    2',5'-Dihydroxyacetophenone supports the synthesis of select herbicides and fungicides where the acetophenone backbone provides active moieties for plant protection. Chemical manufacturers employ the compound in staged aromatic substitution or condensation reactions, precisely controlling parameters to avoid chlorinated byproducts and maximize targeted molecule yield. Comprehensive quality checks confirm absence of unwanted isomers or process contaminants. Track-and-trace production records meet multinational crop protection regulatory submission requirements for full supply chain visibility.

    Industry compliance standards

    • Food and Agriculture Organization (FAO) and WHO specification guidelines
    • ISO 17025: Testing and calibration for active ingredient quality
    • REACH registration and safety data reporting for agrochemical intermediates
    • EPA 40 CFR part 158 for pesticide registration data

    Typical usage ratio

    • Typically 0.18–0.42 moles per target active molecule, depending on synthesis route
    • Reactant ratios empirically defined by process scale and purification efficiency

    Downstream process integration

    • Integrated in batch reactors post-alkylation/halogenation stage
    • Monitored by in-process HPLC to ensure target conversion and isolate desired product
    • Final intermediates routed to formulation and blending for field-ready agrochemical products

    Final product types

    • Pre-emergence selective herbicides
    • Fungicidal agents for horticultural applications
    • Intermediate precursors for broad-spectrum crop protection blends

    4. Fragrance and Aroma Chemicals Manufacturing

    In fragrance and aroma chemicals production, this raw material is valued for its contribution to fine-tuning aromatic ring structures, imparting unique olfactory notes required in premium finished blends. Formulators apply it during synthesis of high-value aroma intermediates, closely managing reaction conditions and purity to prevent sensory off-notes. Operations teams implement multi-stage distillation and fractional crystallization to achieve specification requirements defined by international flavor and fragrance standards. End products target high-growth segments in luxury perfumery and fine consumer goods.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards
    • FEMA (Flavor and Extract Manufacturers Association) GRAS list
    • ISO 9235: Aromatic natural raw materials vocabulary
    • Good Manufacturing Practice for Flavourings (EFSA/EU No 1334/2008)

    Typical usage ratio

    • 0.02–0.22% by total formulation mass, depending on conversion and desired aroma intensity
    • Ratio finely adjusted through iterative organoleptic testing

    Downstream process integration

    • Reacted during synthesis of core aromatic intermediates by Friedel–Crafts acylation and methylation steps
    • Processed under inert atmosphere to limit degradation during heat exposure
    • Final blending with essential oils in small-to-medium batch reactors

    Final product types

    • Fine fragrance bases
    • Aroma chemicals for luxury household products
    • Flavor modifiers in sensory analysis research
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