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N-Phenylbenzohydroxamic Acid

    • Product Name N-Phenylbenzohydroxamic Acid
    • Alias PBHA
    • Einecs 208-850-3
    • 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
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    Specifications

    HS Code

    352284

    Product Name N-Phenylbenzohydroxamic Acid
    Cas Number 1908-23-4
    Molecular Formula C13H11NO2
    Molecular Weight 213.23 g/mol
    Appearance White to pale yellow crystalline powder
    Melting Point 165-170°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Boiling Point Decomposes before boiling
    Purity Typically ≥98%
    Storage Conditions Store in a cool, dry place, away from light
    Synonyms Benzoic acid, N-phenylhydroxamic acid
    Smiles C1=CC=C(C=C1)N(C(=O)C2=CC=CC=C2)O
    Ec Number 217-609-4

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

    Packing & Storage
    Packing N-Phenylbenzohydroxamic Acid, 100g, packaged in a sealed amber glass bottle with clear labeling, safety information, and batch number.
    Shipping N-Phenylbenzohydroxamic Acid is shipped in tightly sealed containers to prevent moisture and contamination. It should be stored in a cool, dry place away from incompatible substances. Packaging is compliant with safety regulations, ensuring secure handling during transit. Proper labeling and documentation accompany the shipment according to chemical transport guidelines.
    Storage N-Phenylbenzohydroxamic Acid should be stored in a tightly sealed container under a dry, well-ventilated atmosphere, protected from light and moisture. Keep it at room temperature (15–25°C) and away from incompatible substances such as strong acids or oxidizers. Label the storage area clearly, and ensure access is restricted to trained personnel using appropriate personal protective equipment (PPE).
    Application of N-Phenylbenzohydroxamic Acid

    Applications of N-Phenylbenzohydroxamic Acid in Industrial Manufacturing

    N-Phenylbenzohydroxamic Acid serves critical roles across a select range of industrial applications, particularly where strong chelating, selective metal complexation, and reagent-specific properties are essential in downstream manufacturing. Below we detail core usage scenarios based on established industrial practice.

    1. Sulfide Mineral Flotation Collector in Non-Ferrous Metallurgy

    Downstream producers in the mining sector rely on this compound as a selective collector during the beneficiation of copper, lead, and zinc sulfide ores, especially where the rejection of iron pyrite and promotion of desirable mineral floatation is technically mandated. Its strong chelation with metal ions allows targeted separation under medium to weak alkalinity during ore processing, resulting in higher concentrate grades and minimized reagent contamination for downstream metal production.

    Industry compliance standards

    • GB/T 8197 Safety in Flotation Reagent Usage
    • EU REACH Regulations (EC 1907/2006) on chemical additives
    • ISO 9001:2015 Quality Management Systems
    • NIOSH Guidelines for Reagent Handling in Mineral Processing

    Typical usage ratio

    • 10–60 g/tonne of ore, adjusted according to ore mineralogy and gangue composition; lower dosages for ores high in target mineral, increased rates for high-slime or complex ores.

    Downstream process integration

    • Added at the conditioning stage of the flotation cell sequence following pH adjustment and before frother introduction, ensuring distribution via slurry agitation systems for full mineral contact.

    Final product types

    • Concentrates of copper, lead, or zinc
    • High-grade flotation tailings for further extraction
    • Refined non-ferrous metals after subsequent smelting
    • Blended intermediate concentrate powders for custom alloy production

    2. Metal Extraction Agent in Hydrometallurgical Processing

    Hydrometallurgy operations utilize N-Phenylbenzohydroxamic Acid as an extraction agent for selective precipitation or solvent extraction of rare and heavy metals from aqueous leachates. This reagent forms stable organometallic complexes, increasing the purity yield during solvent extraction stages for elements such as rare earths, uranium, or titanium from low-grade sources, ensuring high product specificity and reduced acid/base consumption downstream.

    Industry compliance standards

    • ASTM E1600-15 for Hydrometallurgy Test Methods
    • IEC 62769-3 for Industrial-Process Control Safety
    • ISO 14001 Environmental Management for Effluent Control
    • REACH Annex XVII for Chemical Agents

    Typical usage ratio

    • 0.05–1.2% (w/v) of aqueous solution, continuously adjusted based on feedstock concentration, leaching solution pH, and required extraction efficiency for specific metals.

    Downstream process integration

    • Dosed into counter-current extraction columns after primary leaching stage, forming strong bonds with targeted metal ions; the resulting organic phase processed via stripping and precipitation circuits.

    Final product types

    • High-purity rare earth oxide powders
    • Battery-grade cobalt or nickel salts
    • Nuclear-grade uranium dioxide intermediates
    • Refined titanium oxides for pigment or alloy feedstock

    3. Analytical Reagent for Instrumental Metal Analysis

    Chemical laboratories and industrial quality control facilities employ N-Phenylbenzohydroxamic Acid as a derivatizing and color-forming agent in spectrometric analysis, improving detection sensitivity for trace iron, copper, and thorium ions in environmental and process samples. Its high affinity for metal ions delivers consistent analytical performance in low-level sample detection, integral to regulatory and in-process controls for production environments.

    Industry compliance standards

    • ISO 17025 General Lab Competence
    • EPA 200.7 ICP-OES Metal Analysis Protocols
    • Chinese Pharmacopoeia 2025 for Reagent Purity
    • ASTM E350 Standard Test Methods for Heavy Metals

    Typical usage ratio

    • 10⁻⁴ – 10⁻² mol/L, selected based on analyte type, detection limits, and sample pretreatment matrix in manual or automated wet chemistry protocols.

    Downstream process integration

    • Mixed directly with prepared liquid samples prior to UV-Vis or AAS-analysis to induce metal-specific chromogenic complexation, measured at targeted wavelengths for quantitative or qualitative evaluation.

    Final product types

    • Certified reference materials for instrument calibration
    • Environmental monitoring reports
    • Process QC certification documents
    • Laboratory analysis data packages

    4. Organic Synthesis Intermediate for Specialty Chemical Manufacturing

    Chemical synthesis operations employ this compound as a reactive intermediate for constructing functionalized benzohydroxamic acid derivatives, which serve as building blocks in advanced pharmaceutical APIs, agrochemical agents, and photoinitiators. Its specific reactivity profile supports the production of high-purity end products, allowing modification and coupling under controlled batch or continuous flow conditions, with in-process monitoring to confirm product formation and impurity removal.

    Industry compliance standards

    • USP–NF Monographs for Starting Materials
    • ICH Q7 Good Manufacturing Practice for APIs
    • ISO 9001:2015 for Synthesis Batch Consistency
    • 21 CFR Part 211 for Traceability and Purity Control

    Typical usage ratio

    • Stoichiometric to slight excess (1.0–1.2 equiv.) according to downstream coupling partner and desired conversion yield; exact charge determined via lab-scale optimization and in-line spectrometric monitoring.

    Downstream process integration

    • Reacted in pre-heated vessels with acid chlorides or activated esters; post-reaction mixture processed via filtration, extraction, and chromatography for intermediate isolation prior to further transformation or final product formulation.

    Final product types

    • Custom benzohydroxamic acid derivatives for pharmaceutical intermediates
    • Agricultural fungicide or herbicide precursors
    • Industrial photoinitiators for polymerization systems
    • High-purity fine chemicals for research and development markets
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