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2'-Hydroxy-5'-Nitroacetophenone

    • Product Name 2'-Hydroxy-5'-Nitroacetophenone
    • Alias 5-Nitrosalicylaldehyde
    • Einecs 244-555-3
    • 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

    867549

    Iupac Name 1-(2-hydroxy-5-nitrophenyl)ethan-1-one
    Molecular Formula C8H7NO4
    Molecular Weight 181.15 g/mol
    Cas Number 2660-70-6
    Appearance Yellow solid
    Melting Point 122-125°C
    Solubility In Water Slightly soluble
    Smiles CC(=O)C1=C(C=CC(=C1)N(=O)=O)O

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

    Packing & Storage
    Packing Amber glass bottle, 25g, tightly sealed with screw cap, labeled with chemical name, formula, hazard symbols, and manufacturer details.
    Shipping 2'-Hydroxy-5'-Nitroacetophenone is shipped in tightly sealed containers to prevent contamination and moisture absorption. It should be transported as a chemical substance under standard chemical shipping regulations, with appropriate labeling and documentation. Store in a cool, dry place, away from incompatible materials, and handle using suitable protective equipment during transit.
    Storage 2'-Hydroxy-5'-Nitroacetophenone should be stored in a tightly closed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Store at room temperature and avoid exposure to excessive heat. Properly label the storage area and follow all local regulatory guidelines for chemical storage.
    Application of 2'-Hydroxy-5'-Nitroacetophenone

    Applications of 2'-Hydroxy-5'-Nitroacetophenone in Industrial Manufacturing

    Our facility produces 2'-Hydroxy-5'-Nitroacetophenone to exacting quality standards, supporting key downstream industries where its functional properties contribute directly to advanced end formulations. This section details concrete industrial sectors where this specialty intermediate delivers precise value, addressing regulatory expectations, recommended formulation ranges, established integration methods, and the range of commercial end products our partners manufacture.

    1. UV Stabilizer Intermediate Manufacturing for Polymer Additives

    Major polymer additive producers utilize our product as a building block in the synthesis of benzophenone-based UV absorbers, which are critical in protecting plastics from discoloration and brittleness under prolonged sunlight exposure. The material enters the core condensation stage with specific dihydroxybenzene derivatives, providing the key nitro and hydroxy moieties essential for subsequent transformations under controlled hydrogenation and nucleophilic substitution sequences.

    Industry compliance standards

    • REACH (EC No. 1907/2006) Registration and Compliance
    • ISO 9001:2015 Certified Production
    • RoHS Directive (EU) 2015/863 for absence of restricted substances in additives
    • Applicable under FDA 21 CFR 177.1520 for polymers used in food contact (as finished additive component of listed stabilizers)

    Typical usage ratio

    • Reaction charge: 0.5–1.2 mol per mol of dihydroxybenzene co-reactant, adjusted for final UV stabilizer yield and target molecular structure

    Downstream process integration

    • Input at the etherification or acylation step in UV stabilizer manufacturing, followed by reduction and further functional group modification; in-process sampling for purity and conversion monitoring

    Final product types

    • UV-absorbing additives for PP, PE, and PVC masterbatches
    • Light-stabilizing formulations for automotive and outdoor polymer parts
    • Protective films and coatings for packaging materials
    • Specialty technical compounding agents for electronic device enclosures

    2. Pharmaceutical Intermediate in Antifungal Active Ingredient Synthesis

    In the synthesis of specific antifungal agents, this raw material contributes to the production of heterocyclic compounds containing benzophenone backbone modifications. API manufacturers employ the compound during the early-stage diketone formation, setting the reactive framework that supports further amination, cyclization, and nitro group reduction steps necessary to achieve pharmacologically active structures.

    Industry compliance standards

    • Good Manufacturing Practice (EU GMP, Part II: Basic Requirements for Active Substances)
    • ICH Q7 Guideline for API production
    • USP/NF General Chapter <1078> Good Manufacturing Practices for Bulk Pharmaceutical Excipients
    • Environmental, Health, and Safety requirements for nitro-aromatic handling (OSHA 29 CFR 1910.1200)

    Typical usage ratio

    • Reactant in diketone stage: 0.8–1.1 equivalents per desired yield, modulated by yield optimization analyses and target impurity profiles

    Downstream process integration

    • Charged during the diketone or ketone-nitro precursor step, processed in jacketed vessels with temperature control; integrated in-line quality checks for residual starting material

    Final product types

    • Active pharmaceutical ingredient (API) intermediates for topical and systemic antifungals
    • Bulk intermediates for finished OTC and prescription antifungal medications
    • Building blocks for secondary amine derivatives and pro-drug development

    3. Synthesis of High-Performance Pigment Precursors

    Pigment manufacturers incorporate this chemical when producing azo and nitroaromatic pigment intermediates, valued for their intense yellow to orange chromaticity and strong lightfastness. The raw material participates in the diazotization or coupling reactions with anilines, where its functional groups ensure high reactivity and selectivity during pigment core construction. This drives the formation of high-purity intermediates suitable for advanced pigment dispersion.

    Industry compliance standards

    • EN 71-3:2019 Migration of Certain Elements for toy applications
    • ECO PASSPORT by OEKO-TEX® for textile pigment inputs
    • ISO 14001:2015 Environmental Management for pigment plants
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) guidance

    Typical usage ratio

    • Coupling component: 0.7–1.3 mol per mol diazonium salt, optimized for color yield and purity; fine-tuned for specific hue and fastness requirements

    Downstream process integration

    • Mixed in the pigment precursor reaction vessel after pH adjustment; monitored for coupling completion before further dye extraction or precipitation

    Final product types

    • Disperse azo pigments for plastic, fiber, and ink coloration
    • Organic pigment intermediates for paints and industrial coatings
    • High-color-strength powder pigments for polyester fiber dyeing

    4. Intermediate for Agrochemical Active Ingredient Synthesis

    Our manufacturing partners in the agrochemical sector use this compound for constructing select nitro- and hydroxy-containing heterocycles, which function as critical groups in the final formulation of herbicides and seed coatings. During the key condensation or substitution process, the chemical introduces necessary electronic properties to enhance binding and biological activity in soil or foliar application products.

    Industry compliance standards

    • FAO/WHO Code of Conduct on Pesticide Management
    • ISO 9001:2015 Quality Management for agrochemical production
    • EU Plant Protection Products Regulation (EC) No 1107/2009
    • China GB 4839-2009 Safety Standards for Agrochemical Raw Materials

    Typical usage ratio

    • Core intermediate charge: 0.8–1.0 equivalents relative to co-reactant, adjusted based on desired agrochemical load and environmental fate studies

    Downstream process integration

    • Loaded into primary condensation reactors; process staged for precise timing with alkylation or amination, followed by neutralization and pre-crystallization filtration

    Final product types

    • Active ingredients for pre-emergent and post-emergent herbicides
    • Seed treatment compounds
    • Intermediate bases for further agrochemical diversification (e.g., fungicides, insecticides)
    Free Quote

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    Tel: +8615371019725

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