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2'-Ethoxyacetophenone

    • Product Name 2'-Ethoxyacetophenone
    • Alias 2-Acetylphenetole
    • Einecs 211-500-8
    • 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

    715278

    Name 2'-Ethoxyacetophenone
    Cas Number 4563-17-9
    Molecular Formula C10H12O2
    Molecular Weight 164.20 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 263-265 °C
    Density 1.057 g/cm3 at 25 °C
    Refractive Index 1.521-1.523
    Flash Point 121 °C
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles CCOc1ccccc1C(=O)C
    Synonyms 2'-Ethoxy-1-phenylethanone

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

    Packing & Storage
    Packing 250g of 2'-Ethoxyacetophenone is supplied in a sealed amber glass bottle with a secure screw cap and chemical labeling.
    Shipping 2'-Ethoxyacetophenone is shipped in tightly sealed containers, protected from light and moisture, and in compliance with local and international chemical transport regulations. Ensure proper labeling and safety documentation accompany the shipment. Avoid sources of ignition, and store away from incompatible materials to ensure safe handling and delivery.
    Storage 2'-Ethoxyacetophenone should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Keep the container tightly closed when not in use. Store in a chemical-resistant, labeled container to prevent leakage or contamination. Protect from light and moisture. Follow all relevant local, state, and federal regulations for chemical storage.
    Application of 2'-Ethoxyacetophenone

    Applications of 2'-Ethoxyacetophenone in Industrial Manufacturing

    As a specialized manufacturer, we supply 2'-Ethoxyacetophenone with consistent assay and process reliability to support diverse advanced industrial segments. Below are the main downstream application scenarios reflecting actual industry integration for this key aromatic ketone.

    1. UV-Curing Photoinitiators for Coatings and Inks

    Downstream formulators frequently use this raw material as a key intermediate in synthesizing photoinitiators for UV-curable coatings, varnishes, and ink systems. Its structure supports high reactivity under UV light, providing rapid polymerization and improved film properties. Process engineers often select this intermediate to modify curing speed and yellowing resistance, especially where color stability and surface hardness are critical in electronics, packaging, and automotive finishing lines.

    Industry compliance standards

    • REACH Regulation (EC) No. 1907/2006
    • ISO 9001:2015 for quality management
    • China National Standard GB18582 for interior coatings
    • Swiss Ordinance on Materials and Articles in Contact with Food (if used for packaging inks)

    Typical usage ratio

    • Intermediate is typically dosed at 10–25% molar ratio relative to total aromatic ketones in multistep synthesis of photoinitiators.
    • Actual ratio in ink or coating formulas: final photoinitiator content varies from 1–5% by weight depending on substrate and UV lamp intensity.

    Downstream process integration

    • Undergoes Friedel–Crafts acylation and etherification before condensation to target photoinitiator.
    • In blending rooms, photoinitiators are batched with monomers, oligomers, and pigments, then dispersed via high-shear mixing.
    • UV ink/varnish lines meter in the photoactive component just before packaging or filling.

    Final product types

    • UV-cured offset printing inks
    • Resilient floor coatings
    • Clear topcoats for consumer electronics
    • Instant-cure adhesives for assembly lines

    2. Fragrance and Flavors Synthesis in Fine Chemicals

    The unique aromatic and ethoxy group positioning of this ketone makes it a favored intermediate for downstream suppliers producing fragrance ketones and aldehydes. These semi-finished intermediates undergo further modification, such as reduction or methylation, then enter the compounding of specialized perfumes and food-grade flavors. Manufacturing operations control impurity profiles and adjust reaction temperatures to ensure consistent sensorial notes for the target molecules, meeting strict quality and traceability standards in the flavor and fragrance industry.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • EU Regulation (EC) No. 1334/2008 on flavorings
    • US FDA 21 CFR Part 172 (if for food contact)
    • ISO 14001:2015 for environmental management

    Typical usage ratio

    • Commonly batch-charged at 8–18% w/w in precursor blends for perfume ketone syntheses.
    • Final essence compositions: the active structural motif usually accounts for 0.1–0.3% in concentrate, before further dilution or compounding.

    Downstream process integration

    • Feeding into continuous hydrogenation and aldehyde-forming units.
    • Sublimation and crystallization refine the structure before handoff to perfumers or flavorists.
    • End-product blending with fixatives, extenders, and carriers for market-ready scents or flavoring solutions.

    Final product types

    • Eau de parfum and eau de toilette concentrates
    • Flavor additives for confectionery and beverages
    • Personal care scent compositions
    • Aromatic maskers for household cleaners

    3. Pharmaceutical Intermediate for Analgesic and Antipyretic Synthesis

    Pharmaceutical producers select this aromatic ketone as a crucial synthon in custom manufacturing active pharmaceutical ingredients (APIs), especially for certain analgesic and antipyretic agents. Chemists leverage its reactivity in Grignard reactions and aromatic substitutions, optimizing reflux conditions and pH for maximum conversion rates. During late-stage API synthesis, maintaining defined impurity limits is necessary to comply with global pharmacopoeial standards and batch release protocols. Our traceability system supports customer filings and inspections under cGMP regimes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP)
    • European Pharmacopoeia (EP)
    • 21 CFR Part 211 Current Good Manufacturing Practice for Finished Pharmaceuticals

    Typical usage ratio

    • Typically charged as 12–20% molar input in API synthesis steps for select aromatic NSAIDs and antipyretics.
    • Moles adjusted for expected target yield and impurity profile management.

    Downstream process integration

    • Batched in multi-stage synthesis routes for API core modification.
    • In-process controls monitor assay and residual solvents before intermediate isolation.
    • Final processed API sent for formulation into finished dosage forms in separate compounding areas.

    Final product types

    • Non-steroidal anti-inflammatory ingredient intermediates
    • Antipyretic API building blocks
    • Biosimilar bulk compounds for export registration
    • Reference standards for impurity profiling

    4. Agrochemical Building Block for Selective Herbicide Synthesis

    Leading crop protection manufacturers employ this aromatic ketone as a starting material in the construction of pro-herbicide core structures. It assists in enhancing the selectivity profile of active ingredients by introducing an ethoxy aromatic substitution during early catalytic coupling steps. Agrochemical process specialists monitor reaction time and solvent polarity for target molecule synthesis, ensuring the precursor matches required efficacy and environmental residue limits for specific crop registrations.

    Industry compliance standards

    • FAO/WHO Specification and Evaluations for Agricultural Pesticides
    • EU Regulation (EC) No 1107/2009 on Plant Protection Products
    • ISO 9001-certified process controls
    • China Ministry of Agriculture GB/T 1600–2010 for agrochemical actives

    Typical usage ratio

    • Added at precursor stages in 10–22% molar ratio depending on herbicide class and target selectivity spectrum.
    • Fine adjustment for downstream reactivity and formulation compatibility with adjuvants.

    Downstream process integration

    • Chlorination and etherification of the ethoxy acetophenone lead to further ring-closure reactions in active ingredient lines.
    • Combined with safeners or dispersants in preformulation batches for granules or concentrates.
    • Final herbicide formulations processed in separate plants for emulsification and packaging.

    Final product types

    • Selective herbicide technical concentrates
    • Wettable powders and suspension concentrates
    • Pre-emergence herbicide blends for row crops
    • Custom soil treatment actives for horticultural use

    5. Specialty Plasticizer Precursor in Polymer Engineering

    Polymer compounders incorporate this aromatic ketone in the synthesis of flexible, temperature-stable ester plasticizers. It acts as a functional intermediate where controlled ethoxy and carbonyl groups improve compatibility with PVC, polyurethane, and related polymers. Operators carefully meter the intermediate at the esterification reactor stage, enabling downstream formulation teams to balance flexibility, migration resistance, and processability in wire & cable jacketing and automotive interior materials.

    Industry compliance standards

    • EU Regulation (EC) No. 10/2011 on plastic materials for food contact (for relevant grades)
    • UL 94 standard for flammability performance in plastics
    • ISO 527 for polymer mechanical properties testing
    • RoHS Directive 2011/65/EU (for electronics applications)

    Typical usage ratio

    • Usually 5–16% by weight in blended plasticizer precursor batches at the polymerization stage.
    • Adjustment possible based on substrate polymer type and final durometer targets.

    Downstream process integration

    • Feeds directly into esterification reactors either via batch or continuous process streams.
    • End-use plasticizer shipped to compounding lines for incorporation with base resin and stabilizers.
    • Automatic dosing maintains consistent flexibility and melt flow in extrusion or molding units.

    Final product types

    • Flexible PVC sheathing for cables
    • Automotive dashboard polymer blends
    • PU synthetic leather for upholstery
    • Food-contact approved clingwrap materials
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