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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 | 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. |
Applications of 3,5-Dihydroxybenzamide in Industrial Manufacturing3,5-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 SynthesisIn 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
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2. High-Performance Polymer AdditivesPolymer 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
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3. Industrial Dye and Pigment ManufacturingDyestuff 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
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4. Corrosion Inhibitor Formulations for Metal ProcessingIn 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
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