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2-(3,4-Dichlorophenyl)-1-Hydrazinecarbothioamide

    • Product Name 2-(3,4-Dichlorophenyl)-1-Hydrazinecarbothioamide
    • Alias ZINC000001551941
    • Einecs 259-486-8
    • 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

    364493

    Chemicalname 2-(3,4-Dichlorophenyl)-1-Hydrazinecarbothioamide
    Molecularformula C7H7Cl2N3S
    Molecularweight 236.13
    Casnumber 29980-61-0
    Appearance White to off-white solid
    Meltingpoint 174-176°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically >98%
    Boilingpoint Decomposes before boiling
    Storagetemperature Store at 2-8°C
    Smiles C1=CC(=C(C=C1Cl)Cl)NNC(=S)N
    Synonyms 3,4-Dichlorophenylthiosemicarbazide

    As an accredited 2-(3,4-Dichlorophenyl)-1-Hydrazinecarbothioamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass bottle containing 25 grams of 2-(3,4-Dichlorophenyl)-1-Hydrazinecarbothioamide, labeled with hazard warnings and handling instructions.
    Shipping 2-(3,4-Dichlorophenyl)-1-Hydrazinecarbothioamide is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Standard shipping is via ground or air, compliant with relevant chemical transport regulations. Proper labeling and documentation are provided to ensure safe handling during transit and upon delivery to laboratory or industrial destinations.
    Storage 2-(3,4-Dichlorophenyl)-1-hydrazinecarbothioamide should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible materials such as strong oxidizing agents. Store at room temperature and handle with appropriate personal protective equipment, ensuring safe practices to minimize exposure and degradation.
    Application of 2-(3,4-Dichlorophenyl)-1-Hydrazinecarbothioamide

    Applications of 2-(3,4-Dichlorophenyl)-1-Hydrazinecarbothioamide in Industrial Manufacturing

    2-(3,4-Dichlorophenyl)-1-Hydrazinecarbothioamide serves as a specialized intermediate and functional agent across multiple industrial synthesis channels. As the actual producer, we document several authentic downstream sectors, covering process integration, compliance standards, recommended dosing, and finished output types. The following subsections outline practical applications based on customer formulation needs, technical specifications, and established industrial flows.

    1. Agrochemical Intermediate for Herbicide Synthesis

    This raw material acts as a key building block in the synthesis of specific thiosemicarbazone-based herbicides. Agrochemical formulators employ it for selective targeting of broadleaf weeds in cereal and vegetable crops. Process engineers frequently introduce it during early-stage coupling reactions, ensuring chemical stability and purity for downstream performance. Its dichlorophenyl functionality enhances target binding in active agrochemical agents.

    Industry compliance standards

    • GMP Guidelines (ISO 22716:2007) for agrochemical manufacturing
    • FAO/WHO Specification for Plant Protection Products
    • EU Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market
    • REACH Registration for precursor substances

    Typical usage ratio

    • Generally 0.15–0.25 molar equivalents relative to core ring reactant; formulation scientists adjust based on targeted end-activity and impurity profile requirements.

    Downstream process integration

    • Added directly to the initial condensation phase in multi-step herbicide synthesis as a nucleophilic reactant.
    • Integrated in batch or semi-continuous reactors under controlled pH and temperature for consistent yield.

    Final product types

    • Selective thiosemicarbazone herbicides (e.g., triazolethione derivatives)
    • Pre-emergent herbicide concentrates for cereal crops
    • Water-dispersible granule formulations
    • EC (emulsifiable concentrate) active ingredient blends

    2. Pharmaceutical API Precursor in Antitubercular Drug Synthesis

    This compound is a trusted intermediate in the synthesis of certain active pharmaceutical ingredients (APIs) aimed at treating tuberculosis and related mycobacterial infections. Medicinal chemists utilize its hydrazinecarbothioamide core to drive cyclization reactions. The compound enters the process at the API’s core heterocycle formation stage, facilitating high conversion and product stability needed for later pharmacological stages.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapter 1083
    • WHO Technical Report Series, Guidelines for the manufacture of pharmaceutical starting materials
    • EudraLex Volume 4 GMP requirements for pharmaceutical production

    Typical usage ratio

    • Typically 1.0 molar equivalent per resultant API core; adjustment occurs according to specific API synthesis yield and downstream impurity control strategies.

    Downstream process integration

    • Charged into the closed-loop condensation reaction sequence for the thiosemicarbazone ring closure, with strict environmental control to avoid hydrazine emission risks.
    • Used pre-crystallization for API isolation and purification steps.

    Final product types

    • Antitubercular pharmaceutical actives (e.g., certain thiosemicarbazone analogs)
    • Oral dosage form precursors (e.g., tablets, capsules)
    • Parenteral formulation bulk APIs
    • Reference standards for pharmacological research

    3. Intermediate for Synthesis of Specialty Dyes

    In the dye and pigment sector, this compound acts as an essential precursor for the production of complex thiosemicarbazone-azo dyes. Dye chemists value its distinct dichlorophenyl group, which permits novel coloration properties and high color-fastness in textile applications. The material directly participates in diazotization and coupling reactions, creating final chromophores for textile, paper, and leather coloration.

    Industry compliance standards

    • Oeko-Tex Standard 100 for eco-friendly dye components
    • ZDHC MRSL v3.0 (Zero Discharge of Hazardous Chemicals)
    • EU REACH Annex XVII restrictions on azo dyes
    • ISO 9001:2015 for dye production quality management

    Typical usage ratio

    • Ranges between 0.10–0.35 molar equivalents dependent on desired shade intensity and substrate compatibility.

    Downstream process integration

    • Introduced during the azo-coupling stage for pigment synthesis, under controlled pH and agitation.
    • Employed as a final step reactant in high-performance pigment condensation for high-end printing inks.

    Final product types

    • Reactive and direct textile dyes with enhanced wash resistance
    • High-performance pigments for technical printing inks
    • Custom-formulated dyes for leather finishing applications
    • Paper colorant additives

    4. Corrosion Inhibitors Manufacturing for Industrial Fluids

    The material finds use as an intermediate in the production of organothio corrosion inhibitors, especially in coolant and industrial process fluid formulations. Its thioamide functionality helps final inhibitors form protective films on metal surfaces. Chemical engineers dose it in multi-step syntheses to generate molecules targeting specific corrosion pathways seen in oil & gas and water treatment sectors.

    Industry compliance standards

    • ASTM D6107 Standard Test Method for Compositional Analysis of Corrosion Inhibitors
    • API RP 552 standards for process fluid inhibitors
    • EU Directive 2010/75/EU (Industrial Emissions) for chemical emissions
    • ISO 9001:2015 Quality Management Systems for specialty chemicals

    Typical usage ratio

    • Employed at 0.10–0.25 mol fractions relative to base amine or carboxyl precursor, to achieve the desired inhibitor molecular structure.

    Downstream process integration

    • Blended into intermediate condensation steps during organic corrosion inhibitor synthesis.
    • Utilized in continuous stirred-tank reactors for reliable molecular weight control.

    Final product types

    • Oilfield corrosion inhibitor concentrates
    • Water-soluble industrial antifreeze additives
    • Closed-circuit cooling water treatment inhibitors
    • Corrosion-protective coatings for infrastructure piping

    5. Polymer Crosslinking Agent for Performance Resins

    This hydrazinecarbothioamide serves as a block for synthesizing crosslinking agents in performance polymers, particularly in specialty resin and adhesive markets. Formulation chemists use it to introduce thioamide linkages for improved flexibility, adhesion, and chemical resistance. The compound enters as a functional crosslinker at the pre-polymer stage and supports molecular customization for tailored end-use properties.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for polymer production
    • RoHS Directive 2011/65/EU for electronic adhesives
    • REACH compliance for polymer additives
    • EN 923:2015 for adhesive terminology and definitions

    Typical usage ratio

    • Commonly 1–4% w/w based on polymer solid content, determined by crosslinking density and desired thermal/chemical resistance targets.

    Downstream process integration

    • Introduced to the pre-polymerization batch as a chain-extending and crosslinking agent.
    • Formulated into resin mixtures before curing or film formation in adhesive compound blending.

    Final product types

    • Chemically resistant epoxy adhesives for electronics
    • Flexible polyurethane foam binders
    • High-durability acrylate performance coatings
    • Specialty thermosetting resins
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