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2-(4-Chloro-2-Methylphenoxy)Acetic Acid Hydrazide

    • Product Name 2-(4-Chloro-2-Methylphenoxy)Acetic Acid Hydrazide
    • Alias CMAAH
    • Einecs 410-710-5
    • 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

    732199

    Productname 2-(4-Chloro-2-Methylphenoxy)Acetic Acid Hydrazide
    Casnumber 50653-50-6
    Molecularformula C9H11ClN2O2
    Molecularweight 214.65
    Appearance White to light yellow crystalline powder
    Meltingpoint 165-170°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically >98%
    Storageconditions Store at 2-8°C, protect from light and moisture

    As an accredited 2-(4-Chloro-2-Methylphenoxy)Acetic Acid Hydrazide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White HDPE bottle labeled “2-(4-Chloro-2-Methylphenoxy)Acetic Acid Hydrazide, 25g,” with hazard symbols, lot and expiry details.
    Shipping The chemical **2-(4-Chloro-2-Methylphenoxy)Acetic Acid Hydrazide** should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Ensure labeling meets regulatory requirements and include safety information. Ship using ground transport as a non-hazardous material, unless otherwise specified by local regulations. Handle with standard precautions to avoid spillage or exposure.
    Storage Store 2-(4-Chloro-2-Methylphenoxy)Acetic Acid Hydrazide in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances like strong oxidizers and acids. Handle with appropriate protective equipment and follow all safety procedures. Store at room temperature unless otherwise specified by the manufacturer or safety data sheet.
    Application of 2-(4-Chloro-2-Methylphenoxy)Acetic Acid Hydrazide

    Applications of 2-(4-Chloro-2-Methylphenoxy)Acetic Acid Hydrazide in Industrial Manufacturing

    As a specialty manufacturer, we supply 2-(4-Chloro-2-Methylphenoxy)Acetic Acid Hydrazide for critical roles in advanced chemical synthesis and downstream processing. Our expertise ensures precise quality control and technical alignment with industrial protocols for high-value production environments. The following sections detail authentic subsectors using this compound, focusing on industrial formulation practice, compliance, processing integration, and compliant finished goods.

    1. Agrochemical Intermediate Synthesis for Herbicide Production

    This compound serves as a targeted intermediate in the synthesis of specific phenoxyacetic acid herbicides, frequently those applied in the control of broadleaf weeds. Manufacturers in the agrochemical sector utilize it at designated transformation stages where the hydrazide functionality is critical for producing active amide or hydrazone herbicidal ingredients. Strict batch testing and formulation accuracy are enforced to meet regulatory residue limits and efficacy targets for crop use registration.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Systems (Agrochemical Manufacturing)
    • REACH Regulation (European Union - herbicide intermediate listing)
    • China GB2763 Maximum Residue Limit (MRL) for Agricultural Chemicals

    Typical usage ratio

    • Usage typically ranges from 2.8% to 5.5% by mole equivalent in the condensation stage, depending on the targeted downstream herbicide structure and process yield targets.

    Downstream process integration

    • Introduced after chlorination but prior to cyclization steps in herbicide precursor assembly, often dissolved in polar aprotic solvents to maximize conversion and minimize unreacted hydrazide removal burden.

    Final product types

    • Selective post-emergent and pre-emergent herbicide technical concentrates
    • Granular and suspension concentrate herbicide formulations for agricultural application
    • Bulk active ingredient packs for further formulation

    2. Pharmaceutical Fine Chemicals—Active Pharmaceutical Ingredient (API) Synthesis

    Several pharma manufacturers incorporate this raw material within stepwise synthesis routes to produce hydrazide-containing APIs, particularly for anti-inflammatory and anti-tubercular therapeutic classes. The compound's purity and control of trace byproducts are essential due to pharmacopoeial standards. Usage requires detailed documentation of each input, with process validation according to cGMP protocols at multi-ton batch scale.

    Industry compliance standards

    • USP-NF (United States Pharmacopeia–National Formulary)
    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • China Pharmacopoeia (2020 Edition, Volume IV for Chemicals)
    • EU GMP Guidelines—Part II: Basic Requirements for Active Substances used as Starting Materials

    Typical usage ratio

    • Formulators typically add at 1.3 to 2.2 mole equivalents relative to core substrate, adjusted for API labelling requirements and impurity profile goals as established by development chemists.

    Downstream process integration

    • Hydrazide enters protected intermediate synthesis via stepwise condensation or hydrazinolysis, usually under monitored temperature and pH controls. In-process checks confirm intermediate formation prior to downstream functionalization.

    Final product types

    • Pharmaceutical-grade hydrazone and acyl hydrazide APIs
    • Bulk pharmaceutical intermediates for further derivatization and final dosage form processing
    • Research and development lots for clinical trial materials

    3. Synthesis of Specialty Dyes and Pigments (Organic Colorant Industry)

    Producers of high-performance organic dyes deploy this molecule as a coupling agent and scaffold for azo and heterocyclic pigment synthesis, especially where molecular precision is essential for shade control and lightfastness requirements. Batch pigment manufacturing lines rely on raw material traceability and detailed colorimetry to conform to international end-use standards.

    Industry compliance standards

    • EN 71-3:2019 Safety of Toys–Migration of Certain Elements (relevant to pigment end-use in toys)
    • OEKO-TEX® Standard 100 (Textile and leather chemical restrictions)
    • ISO 1248:1997 Pigments—Specifications and Methods of Test
    • US TSCA (Toxic Substances Control Act) for raw material listing

    Typical usage ratio

    • Processing plants adjust addition from 2.0% to 4.7% weight basis in coupling reactions, influenced by the desired tinctorial strength, monochromatic purity and matrix composition.

    Downstream process integration

    • Raw material introduced prior to diazotization or oxidative coupling, facilitating formation of hydrazone-based chromophores. Integrated reaction monitoring enables rapid correction for color drift.

    Final product types

    • Disperse and reactive textile dyes
    • High-resistance organic pigments for inks and coatings
    • Specialty color concentrates for plastic masterbatches

    4. Custom Synthesis of Analytical Reagents for Laboratory and Industrial QC

    Chemical reagent manufacturers select this hydrazide as a precursor for synthesizing colorimetric and spectrophotometric analytical reagents, instrumental in quantitative analysis of trace metals and hydrazones. Stringent lot-to-lot uniformity and contaminant controls underpin reliable downstream assay performance. Documentation includes batch traceability, TDS, and safety compliance registers.

    Industry compliance standards

    • ISO 17034:2016 General requirements for the competence of reference material producers
    • ISO 9001:2015 (Certification for laboratory reagent manufacturing)
    • US EPA Methods–Environmental Analytical Standards
    • ASTM D1193-06 (Specification for Reagent Water relevant to QC)

    Typical usage ratio

    • Added in a strictly controlled 0.7%–1.8% mass ratio relative to the reaction solution, calibrated for targeted reagent strength and minimizing matrix interference as specified in standard test protocols.

    Downstream process integration

    • Enters final reaction phase for analytical reagent assembly, often post-purification, then subjected to multi-stage filtration and pack-off in certified clean areas suitable for trace-level analytics.

    Final product types

    • Hydrazide-based colorimetric assay kits and reagents
    • Reference standards for environmental and food safety labs
    • Industrial laboratory titration and spectrophotometric indicators
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