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4-Ethoxybenzhydrazide

    • Product Name 4-Ethoxybenzhydrazide
    • Alias 4-Ethoxybenzenecarbohydrazide
    • Einecs 252-980-2
    • 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

    170318

    Chemicalname 4-Ethoxybenzhydrazide
    Molecularformula C9H12N2O2
    Molecularweight 180.20 g/mol
    Casnumber 4547-10-4
    Appearance White to off-white powder
    Meltingpoint 120-124 °C
    Solubility Slightly soluble in water, soluble in ethanol and DMSO
    Smiles CCOC1=CC=C(C=C1)C(=O)NN
    Inchi InChI=1S/C9H12N2O2/c1-2-13-8-5-3-7(4-6-8)9(12)11-10/h3-6H,2,10H2,1H3,(H,11,12)

    As an accredited 4-Ethoxybenzhydrazide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 4-Ethoxybenzhydrazide, 25g, is supplied in a sealed amber glass bottle with a tamper-evident cap and clear labeling.
    Shipping **Shipping Description for 4-Ethoxybenzhydrazide:** 4-Ethoxybenzhydrazide is typically shipped in securely sealed containers, protected from moisture and direct sunlight. It should be transported as a stable, non-hazardous chemical at ambient temperature. Ensure packaging complies with local regulations, and material safety data sheets (MSDS) accompany the shipment for safe handling and identification upon receipt.
    Storage 4-Ethoxybenzhydrazide should be stored in a tightly sealed container in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and acids. Protect the chemical from moisture and direct sunlight. Proper labeling and handling procedures should be followed to avoid contamination and ensure safe storage conditions.
    Application of 4-Ethoxybenzhydrazide

    Applications of 4-Ethoxybenzhydrazide in Industrial Manufacturing

    As a direct manufacturer of 4-Ethoxybenzhydrazide, we support several advanced chemical processing sectors with this specialized raw material. Each application utilizes the chemical for specific, well-documented end uses where purity, traceability, and reproducible results are mandatory. Below, we outline the principal industrial scenarios, highlighting the compliance expectations, usage concentrations, integration points within downstream processes, and typical finished goods produced with our material at scale.

    1. Pharmaceutical Intermediate for API Synthesis

    Pharmaceutical companies use our product as a key intermediate for manufacturing hydrazide-based active pharmaceutical ingredients (APIs), particularly within anti-tubercular and anti-cancer drug production. The compound often enters multi-step synthesis routes that demand traceable purity profiles and validated impurity controls due to stringent regulatory oversight during API development.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • USP, Ph. Eur., and JP monograph guidance for intermediates
    • FDA 21 CFR Part 210/211 for finished pharmaceuticals
    • ISO 9001:2015 for quality management

    Typical usage ratio

    • Stoichiometric or slight excess relative to the preceding aromatic carboxylic acid starting material, typically 0.9–1.2 molar equivalents depending on reaction scale and target API

    Downstream process integration

    • Added immediately after acid chloride formation during condensation steps, followed by controlled hydrazide derivatization and purification

    Final product types

    • Pyridazine-based antituberculosis drugs
    • Hydrazine-containing anti-cancer APIs (e.g., some alkylating agents)
    • Custom synthesis intermediates for contract development and manufacturing organizations (CDMOs)

    2. Agrochemical Synthesis: Herbicide and Fungicide Formulations

    Crop protection manufacturers incorporate this hydrazide derivative in the synthesis of active ingredients for herbicidal and fungicidal products, especially for creating hydrazone linkages within proprietary formulations. Batch-to-batch consistency and defined impurity levels are critical to pass regulatory registration and environmental toxicology reviews.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals (GLP compliance where relevant)
    • EPA FIFRA requirements for technical materials
    • REACH registration (EC 1907/2006)
    • ISO 17025-certified QC laboratory requirements

    Typical usage ratio

    • Generally 1.0–1.5 weight percent of total batch mass in target active ingredient synthesis; adjusted based on agrochemical backbone structure and formulation scale

    Downstream process integration

    • Introduced post-halogenation or esterification in the hydrazide-alkylation step, then isolated and purified prior to final technical concentrate blending

    Final product types

    • Triazole and pyrazole fungicides
    • Pre-emergent herbicides containing hydrazone moieties
    • Bulk technical concentrates for subsequent formulation into wettable powders or suspension concentrates

    3. Synthesis of Specialty Dyes and Pigments

    Manufacturers within the colorant sector rely on this compound for diazo and azo-coupling reactions, where it serves as a coupling agent or intermediate in the creation of specific hydrazide-based dyes. Rigorous process control is needed to ensure color consistency and lightfastness, which are essential for downstream textile and ink producers.

    Industry compliance standards

    • EN 71-3 for the safety of toy colorants
    • REACH Annex XVII, restrictions on azodyes
    • GOTS 6.0 for textile dyes (where applicable)
    • ISO 9001 and batch traceability per customer requirement

    Typical usage ratio

    • 0.5–5.0% by weight of total monomers, depending on shade depth and pigment type; optimized following initial small-scale pilot runs

    Downstream process integration

    • Employed during the azo coupling stage after diazotization of aromatic amines, typically in water-based or solvent-based batch reactors

    Final product types

    • Hydrazide-derived azo dyes for textile applications
    • Organic pigments for high-end paints, plastics, and inkjet inks
    • Toner colorants for specialty printing

    4. Research and Development for Fine Chemical Synthesis

    Chemical R&D laboratories and pilot plants use 4-Ethoxybenzhydrazide during route scouting for novel hydrazone, hydrazide, and other heterocyclic molecule synthesis, where versatility and controlled reactivity support new compound libraries intended for material science or pharmaceutical exploration. Meticulous characterization and usability in scaled-up synthesis are key evaluation criteria.

    Industry compliance standards

    • ISO/IEC 17025 for R&D laboratory calibration and method validation
    • GLP principles for documentation and traceability (OECD or FDA)
    • In-house analytical SOPs for compound verification (NMR, MS, HPLC methods)
    • Material transfer agreement stipulations for project-specific compound delivery

    Typical usage ratio

    • Ranges from sub-stoichiometric to slight molar excess, typically 0.5–1.3 equivalents, based on exploratory synthesis conditions or targeted modification reactions

    Downstream process integration

    • Introduced at the hydrazinolysis stage during fine chemical library synthesis, then isolated via preparative chromatography or crystallization prior to structure confirmation

    Final product types

    • Building blocks for combinatorial chemistry
    • Reference standard compounds for analytical method development
    • Custom intermediates for further pharmaceutical or materials research

    5. Corrosion Inhibitor Blend Manufacturing

    Our hydrazide derivative finds targeted use in corrosion inhibitor formulation, particularly for blending into protecting solutions for oilfield, water treatment, and closed-loop cooling systems. Its role focuses on reactive nitrogen introduction, enhancing surface binding in multi-component additive systems requiring compliance documentation at every formulation step.

    Industry compliance standards

    • ASTM D1384 and D3306 for coolant corrosion inhibitors
    • API RP 932-B for oilfield water treatment
    • EU Biocidal Products Regulation (EU BPR) where applicable
    • ISO 9001:2015 for composition and release control

    Typical usage ratio

    • 0.1–1.0% by total additive formulation weight, with adjustments based on inhibitor system type and substrate material compatibility

    Downstream process integration

    • Dosed during blend-up of multi-component inhibitor concentrates, followed by recirculation homogenization and quality control for nitrogen content and solubility

    Final product types

    • Multi-metal corrosion inhibitor packages for cooling line protection
    • Closed system anti-corrosion fluids for industrial HVAC units
    • Oil and gas pipe treatment fluids
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