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2-Bromo-2'-Hydroxyacetophenone

    • Product Name 2-Bromo-2'-Hydroxyacetophenone
    • Einecs 229-865-4
    • 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

    955033

    Chemical Name 2-Bromo-2'-Hydroxyacetophenone
    Molecular Formula C8H7BrO2
    Molecular Weight 215.05 g/mol
    Cas Number 24715-06-2
    Appearance White to off-white solid
    Melting Point 70-74 °C
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles CC(=O)C1=CC=CC=C1OBr
    Iupac Name 1-(2-Bromo-2-hydroxyphenyl)ethan-1-one
    Storage Conditions Store at 2-8°C, dry, well-ventilated area

    As an accredited 2-Bromo-2'-Hydroxyacetophenone 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-Bromo-2'-Hydroxyacetophenone, sealed with a screw cap and labeled with hazard warnings.
    Shipping 2-Bromo-2'-Hydroxyacetophenone is shipped in tightly sealed containers, protected from light and moisture. It is handled as a hazardous chemical, following DOT, IATA, or IMDG regulations. Packaging is in accordance with safety standards, with clear hazard labeling. Temperature and ventilation controls are maintained to avoid decomposition or hazardous reactions during transit.
    Storage Store 2-Bromo-2'-Hydroxyacetophenone in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from light and moisture. Clearly label the container and ensure access is limited to trained personnel. Follow all applicable safety and handling guidelines for hazardous chemicals.
    Application of 2-Bromo-2'-Hydroxyacetophenone

    Applications of 2-Bromo-2'-Hydroxyacetophenone in Industrial Manufacturing

    2-Bromo-2'-Hydroxyacetophenone is a specialized chemical intermediate widely adopted in targeted segments of pharmaceuticals, fine chemicals, and advanced material manufacturing. As the original producer, we prioritize precise integration of this material in highly controlled production chains, ensuring each usage matches critical regulatory and performance demands. Below are core application scenarios in which this substance contributes essential reactivity and structural features for advanced derivatives.

    1. Pharmaceutical Intermediates for API Synthesis

    This compound serves as a crucial building block in the synthesis of pharmaceutical active ingredients, especially for selective kinase inhibitors and related heterocyclic drug molecules. Manufacturers utilize its bromine and hydroxy groups to achieve regioselective modifications, allowing reliable introduction of targeted moieties in multi-step flow or batch synthesis routes. Product consistency and traceability remain focal points throughout all stages of handling and formulation, as end use connects directly to regulated finished pharmaceuticals.

    Industry compliance standards

    • Good Manufacturing Practice (GMP) for APIs (ICH Q7, EudraLex Volume 4)
    • US FDA 21 CFR Part 211 (Finished Pharmaceuticals)
    • European Pharmacopoeia Monograph 5.2.2 (Impurity Control)
    • Chinese Pharmacopoeia (ChP) General Chapters on intermediates

    Typical usage ratio

    • Introduced at 0.5–5.0 mol% relative to core API precursor; actual ratio tailored by downstream substitution pattern requirements and specific route yield optimization.

    Downstream process integration

    • Reacted in early or mid-stage steps (such as C–C or C–N coupling) via metal-catalyzed or nucleophilic substitution, followed by purification and transfer to subsequent elaboration steps under closed reactor or continuous flow conditions.

    Final product types

    • Kinase inhibitors
    • Anti-inflammatory agent molecules
    • Oncology drug precursors
    • Custom research APIs for clinical development

    2. Light Stabilizer Intermediate for UV Absorbers

    Chemical manufacturers incorporate this raw material in the targeted synthesis of benzotriazole and salicylate-based UV absorbers, used extensively in plastics, coatings, and inks requiring protection against photodegradation. The hydroxy and bromo functionalities enable efficient coupling with triazoles and other aromatic platforms, conferring strong UV-shielding properties after ring closure and downstream derivatization.

    Industry compliance standards

    • REACH Registration (EC 1907/2006) for UV absorber substances
    • ISO 9001:2015 for quality management in additive manufacturing
    • OECD Testing Guidelines 301 (Biodegradability) and 406 (Sensitization)
    • EU Plastics Regulation (EU) No 10/2011 for food contact plastics

    Typical usage ratio

    • Used at 1.0–6.0 wt% of targeted additive batches; concentration varies based on desired UV spectrum and compatibility in polymer matrix.

    Downstream process integration

    • Undergoes nucleophilic aromatic substitution and cyclization with amines or triazoles in solvent-based reactors, followed by isolation and microfiltration, then transferred into masterbatch extrusion or varnish blending units.

    Final product types

    • UV stabilizer masterbatches for polyolefins
    • Light-stabilizing additives for automotive coatings
    • Anti-yellowing agents for flexible packaging films
    • UV-blocking inks for security printing

    3. Fine Chemical Intermediate for Agrochemical Synthesis

    In crop protection chemical development, this material plays a role as a precursor in the elaboration of benzoxazole and related heterocyclic cores found in specific fungicidal and herbicidal actives. The brominated acetophenone structure is exploited for regioselective ring closure and further halide displacement reactions, enabling scalable, cost-effective introduction of essential biological motifs in protected environments.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications (FAO/WHO Joint Meeting)
    • OECD Good Laboratory Practice (GLP) Principles
    • Chemical Control Order regulations for intermediate handling
    • ECHA CLP Regulation (EC) No 1272/2008—classification and labeling for transport and worker safety

    Typical usage ratio

    • Charged at 2.5–8.0 mol% depending on desired batch size, reaction throughput, and precursor:product conversion efficiency.

    Downstream process integration

    • Engaged in cyclization and substitution steps over base or acid catalysts, followed by organic workup, aqueous extraction, and subsequent formulation into technical-grade agrochemicals via solvent spraying or granulation units.

    Final product types

    • Benzoxazole-based fungicide intermediates
    • Herbicidal actives
    • Technical-grade pesticide bases

    4. Component for High-Performance Photoinitiators

    Producers of UV-curable resins and inks employ this compound as a structural intermediate to introduce advanced benzoyl moieties in specialty photoinitiators. The material’s functional group profile facilitates controlled acylation or etherification, yielding modified photoinitiators with precise activation wavelengths and surface compatibility, supporting fast polymerization in 3D printing and industrial coatings.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for chemical process plants
    • GreenScreen® Certified for chemical hazard assessment (where relevant)
    • RoHS Directive 2011/65/EU for electrical and electronic products using UV coatings
    • SWISS Ordinance on Materials and Articles in Contact with Food (SR 817.023.21) for UV-curable coatings in packaging

    Typical usage ratio

    • Added at 0.2–3.0 mol% of targeted photoinitiator synthesis batches; adjusted by downstream wavelength match and end-use polymer matrix.

    Downstream process integration

    • Reacted with aromatic acid chlorides or substituted phenols under phase-transfer conditions, isolated by crystallization, then milled and standardized for direct blending into pre-polymer resin systems or pigment concentrates.

    Final product types

    • UV photoinitiator blends for inkjet printing
    • Photoactive resin additives for stereolithography (3D printing)
    • Fast-cure wood coatings
    • UV-functionalized adhesives for electronics assembly
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