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3,5-Dihydroxybenzamide

    • Product Name 3,5-Dihydroxybenzamide
    • Alias 3,5-Benzenediamide
    • Einecs 207-568-9
    • 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

    951558

    Cas Number 2164-48-1
    Molecular Formula C7H7NO3
    Molecular Weight 153.14 g/mol
    Iupac Name 3,5-dihydroxybenzamide
    Appearance White to off-white crystalline powder
    Melting Point 207-211 °C
    Solubility In Water Slightly soluble
    Smiles C1=C(C=C(C=C1O)O)C(=O)N
    Pubchem Cid 24224
    Synonyms M3,5-dihydroxybenzamide; Resorcylamide
    Logp 0.12
    Pka 8.95

    As an accredited 3,5-Dihydroxybenzamide 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 3,5-Dihydroxybenzamide; labeled with product name, purity, safety warnings, and manufacturer details.
    Shipping 3,5-Dihydroxybenzamide is shipped in tightly sealed containers, protected from light and moisture. It is packed according to chemical safety guidelines to prevent contamination and spillage. The package is labeled with hazard information, handled by trained personnel, and transported following local, national, and international regulations for safe chemical transit.
    Storage 3,5-Dihydroxybenzamide should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, well-ventilated area, ideally at room temperature. Avoid exposure to heat, incompatible substances, and sources of ignition. Clearly label the container and store it away from food, drink, and incompatible chemicals such as strong oxidizing agents.
    Application of 3,5-Dihydroxybenzamide

    Applications of 3,5-Dihydroxybenzamide in Industrial Manufacturing

    3,5-Dihydroxybenzamide serves critical functions across several specialty industrial sectors, supporting advanced material and chemical synthesis. As a dedicated manufacturer, we supply this intermediate exclusively for established downstream applications that leverage its unique diaryl amide structure and hydroxy functionality for targeted process advantages. Below, we detail major industrial implementations with relevant compliance, formulation, integration, and end-product insights.

    1. Specialty Pharmaceutical Intermediate Synthesis

    In the pharmaceutical sector, 3,5-Dihydroxybenzamide plays a precise role as an intermediate during the production of certain benzamide-derivative APIs, including inhibitors and non-steroidal drug scaffolds. Its dual hydroxy functionalization facilitates regioselective acylation and subsequent ring modification, especially in multi-step synthesis where fine control of ortho/para substitution is necessary. Downstream users leverage it in controlled batch and continuous reactor systems, maintaining compliance with drug master file referencing and cGMP requirements for active intermediate handling.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Parts 210 and 211
    • European Pharmacopoeia monographs for applicable APIs
    • China Pharmacopoeia when exporting to domestic market

    Typical usage ratio

    • Depends on target molecule, typically 0.8–1.5 molar equivalents relative to coupling reactant
    • Adjusted for stoichiometry in protected intermediate synthesis and oxidative coupling steps

    Downstream process integration

    • Charged at the initial condensation or amidation step in multi-step batch synthesis
    • Subjected to controlled heating, solvent swaps, and phase transfers in sealed systems
    • Product traced with in-process HPLC and LC-MS analytics for regulatory documentation

    Final product types

    • Benzamide-based APIs for anticancer, antihistamine, or psychotropic drugs
    • Key intermediates for further heterocycle formation
    • Fine chemicals certified for finished pharmaceutical production

    2. High-Performance Polymer Additives

    Polymer formulators in the high-performance plastics sector utilize 3,5-Dihydroxybenzamide as a chain-modifying additive and cross-linking agent. Its ortho-dihydroxy arrangement provides exceptional compatibility with polyamide and polyimide resin streams, supporting improvements in thermal stability, glass transition temperature, and adhesion properties for specialty engineering plastics. Polymer process engineers introduce the material during solution or bulk polymerization where tight control of monomer ratio and residence time is essential for quality assurance and downstream compliance.

    Industry compliance standards

    • EU REACH Regulation (EC) No 1907/2006
    • DIN EN ISO 9001 for polymer quality systems
    • ASTM D256, D638 mechanical and safety testing protocols
    • RoHS 2011/65/EU for restricted substances

    Typical usage ratio

    • 0.1–2% by total monomer mass, depending on required crosslink density and specification
    • Adjusted up to 3% for specialty high-heat formulations targeting >250°C

    Downstream process integration

    • Added at pre-polymer formation stage in batch or continuous reactors
    • Melt-processed under nitrogen atmosphere to preserve hydroxy integrity
    • Monitored by rheology and FTIR for degree of incorporation

    Final product types

    • Polyimide and polyamide specialty resins (films, fibers, injection-molded parts)
    • Electrical encapsulant compounds for high-temperature electronics
    • Co-extruded multilayer engineering plastics for automotive and aerospace use

    3. Industrial Dye and Pigment Manufacturing

    Dyestuff and pigment producers employ 3,5-Dihydroxybenzamide as a core coupling component in synthesis of azo, anthraquinone, and reactive dyes with improved tinctorial strength and brightness. Its functional group pattern promotes controlled diazotization and extended conjugation during pigment molecule construction. Downstream operational teams typically handle the raw material under carefully controlled pH and temperature to avoid premature hydrolysis or byproduct formation, and integrate documented QC measures under sector-specific standards.

    Industry compliance standards

    • ISO 9001:2015 for pigment and dye manufacture
    • OEKO-TEX® Standard 100 for textiles dyes
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • EU Ecolabel criteria for printing and textile dyes

    Typical usage ratio

    • 1–5% weight/weight based on total aromatic diazo component
    • Lower end for tracer dyes, higher end in highly substituted pigment syntheses

    Downstream process integration

    • Added during main azo-coupling or anthraquinone cyclization stage
    • Reacts under alkaline or acidic conditions based on process route
    • Yields monitored for color index and purity, pre- and post-filtration

    Final product types

    • Disperse and reactive dyes for polyester and cellulose fibers
    • Pigments for high-value printing inks and plastics
    • Specialty colorants for coatings and electronic displays

    4. Corrosion Inhibitor Formulations for Metal Processing

    In advanced metal treatment and water system maintenance, formulators select 3,5-Dihydroxybenzamide as a chelating base and passivation aid for corrosion inhibitor blends. Its molecular geometry enables stable surface complexes with iron, zinc, and aluminum, supporting reduced oxidation and scale formation in harsh industrial conditions. Manufacturing engineers dose the material directly into aqueous or glycol-based inhibitor concentrates, with subsequent process lines monitoring for compliance and performance per strict regulatory and technical benchmarks.

    Industry compliance standards

    • ASTM G31-21 for corrosion inhibitor performance
    • EU CLP Regulation (EC) No 1272/2008 for chemical safety classification
    • ISO 8044 for corrosion terminology and practice
    • US EPA Guidelines for water treatment chemical use

    Typical usage ratio

    • 0.02–0.1% by total inhibitor mass for standard steel and iron systems
    • Adjusted according to metals present and system pH

    Downstream process integration

    • Mixed into corrosion inhibitor concentrate during final blending
    • Dosed into recirculating water, pickling, or metal washing lines
    • Performance verified via ICP-OES and corrosion coupon analysis

    Final product types

    • Chemical inhibitors for industrial water treatment
    • Inhibitor packages for cooling circuits and heat exchangers
    • Metal surface treatment fluids for automotive and industrial components
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