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2,3-Dichloro-Thiobenzamide

    • Product Name 2,3-Dichloro-Thiobenzamide
    • Alias 2,3-Dichlorobenzothioamide
    • Einecs 220-864-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    260427

    Product Name 2,3-Dichloro-Thiobenzamide
    Cas Number 6315-73-9
    Molecular Formula C7H5Cl2NS
    Molecular Weight 206.09 g/mol
    Appearance White to off-white solid
    Melting Point 110-113°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Structure Benzamide ring, chlorine at positions 2 and 3, thioamide group
    Synonyms 2,3-Dichlorothiobenzamide; 2,3-Dichlorobenzothioamide
    Storage Conditions Store in a cool, dry place, tightly closed container

    As an accredited 2,3-Dichloro-Thiobenzamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Packaged in a 25-gram amber glass bottle with a secure screw cap, labeled with chemical name, hazard symbols, and handling instructions.
    Shipping 2,3-Dichloro-Thiobenzamide should be shipped in tightly sealed containers, protected from moisture and light. Transport in compliance with local and international regulations for hazardous chemicals. Ensure clear labeling and provide safety data sheets. Handle with protective equipment to prevent spills, leaks, and exposure during transit. Store in a cool, dry place.
    Storage 2,3-Dichloro-Thiobenzamide should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep it separate from incompatible substances such as strong oxidizing agents. Proper labeling and secure storage conditions are essential to prevent accidental exposure or contamination. Handle with appropriate personal protective equipment.
    Application of 2,3-Dichloro-Thiobenzamide

    Applications of 2,3-Dichloro-Thiobenzamide in Industrial Manufacturing

    2,3-Dichloro-Thiobenzamide serves as a specialized intermediate in a select group of industrial sectors, with applications driven by distinct downstream process requirements. As a dedicated manufacturer, we tailor production quality, batch consistency, and regulatory documentation to support high-value end use across sectors focusing on precise formulation standards.

    1. Agrochemical Active Ingredient Synthesis

    Manufacturers in the agrochemical sector employ 2,3-Dichloro-Thiobenzamide as a building block to synthesize specific herbicide and fungicide actives, particularly for sulfur-containing aromatic products. The material participates directly in thioamide coupling and chlorination stages, enabling creation of stable pesticide precursor structures. Strict contamination controls and traceability documentation must accompany its use, especially where conversion efficiencies and purity grades influence end use registration with regulatory authorities.

    Industry compliance standards

    • REACH Annex XVII and relevant EU crop protection chemical regulations
    • US EPA registration protocols for new active substances
    • ISO 9001:2015 for production process management and batch record keeping
    • China GB 2763 Maximum Residue Limits for Pesticides

    Typical usage ratio

    • 0.5–2.0 molar equivalents, calculated against core aromatic intermediates; adjusted on basis of target molecular architecture and overall conversion yield

    Downstream process integration

    • Precursor charging stage in reaction vessels before cyclization or acylation
    • Participates in controlled temperature thionation or chlorination steps
    • Requires nitrogen atmosphere or hydrocarbon solvent base for purity maintenance

    Final product types

    • Pre-emergent herbicides containing aromatic thioamide scaffolds
    • Fungicidal spray concentrates for fruits, vegetables, or cereals
    • Intermediate compounds for further sulfenamide or imide synthesis in field crop product lines

    2. Pharmaceutical Intermediate Manufacturing

    Active pharmaceutical ingredient (API) and fine chemical producers utilize 2,3-Dichloro-Thiobenzamide to introduce protected thioamide groups at early or late synthetic stages, especially for drug candidates with benzothiazole or thiadiazole fragments. Material-grade requirements specify defined impurity profiles, rigorous lot traceability, and compliance with DMF support for QMS and cGMP standards. It is often required that the material meets compendial specifications for genotoxic impurities and aromatic residuals.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • 21 CFR Part 211—Current Good Manufacturing Practice for Finished Pharmaceuticals (US FDA)
    • EU GMP EudraLex Vol 4 for starting materials
    • USP and Ph. Eur. related monographs for intermediate quality assessment

    Typical usage ratio

    • 0.8–1.5 molar equivalents, based on lineage of synthetic route and desired pharmacophore; may be adjusted for in-process yield or in presence of labile substituents

    Downstream process integration

    • Entering as a key thioamide donor during heterocycle formation
    • Conversion steps involving substitution, protection, or cyclization under controlled pH
    • Isolated via phase separation before downstream purification and crystallization

    Final product types

    • Sulfur-containing API precursors for antimicrobial or antitumor drugs
    • Protected intermediates for custom synthesis services and CDMO outputs
    • Reference compounds for preclinical research and patent-pending NCEs

    3. Industrial Dye Intermediate Formulation

    Producers of specialty dyes and performance colorants use 2,3-Dichloro-Thiobenzamide for introduction of halogen and sulfur motifs on aromatic rings, critical for lightfastness and chemical resistance in technical dyes. Commercial-scale operations adopt this ingredient in multi-step dye molecule construction, emphasizing process stability against batch runtime variables and attention to residual chloride management. Formulators require analytical traceability, with stringent analytical controls in final chromophore design.

    Industry compliance standards

    • ISO 9001:2015 quality management for colorant manufacturing
    • OEKO-TEX® Standard 100 for restricted substance and contaminant checks
    • EU REACH Annex XVII for aromatic amines in finished dyes
    • GHS/CLP labeling for downstream handling

    Typical usage ratio

    • 1.2–3.0 weight percent relative to total dye batch mass; actual concentration based on target chromophore structure and desired shade intensity after final coupling

    Downstream process integration

    • Introduced in halogenation or sulfidation pre-polymerization reactors
    • Participates in diazo and coupling reactions for complex colorant development
    • Downstream washing and salt reduction after main reaction sequence

    Final product types

    • Reactive and disperse dyes for polyester, nylon, and cellulose fiber applications
    • Specialty colorants for digital textile printing inks and industrial plastics
    • High-performance pigments for automotive and marine coatings

    4. Rubber Vulcanization Accelerator Production

    Chemical manufacturers incorporate 2,3-Dichloro-Thiobenzamide as a sulfur donor for downstream vulcanization accelerator synthesis in tire and technical rubber industries. It enables precise introduction of sulfur containing links and modulates cure rates and crosslink structures. Production operations utilize the material in sanitized, moisture-controlled environments to protect against hydrolysis. Use aligns with environmental discharge controls and chemical hazard communication standards.

    Industry compliance standards

    • ASTM D2019 for vulcanization accelerator composition analysis
    • ISO 14001 for environmental management during chemical processing
    • SGS RoHS for restricted heavy metals and halogen content (for automotive exports)
    • OSHA HazCom 29 CFR 1910.1200 for safety data and labeling

    Typical usage ratio

    • 0.8–1.6 molar equivalents per accelerator molecule; adjusted for downstream target specifications and expected end-use application conditions

    Downstream process integration

    • Reacted with aromatic amines and sulfur donors during the synthesis of thiazole or sulfenamide type accelerators
    • Introduced under controlled mixing and refluxing conditions, often with alkaline promoters
    • Purification and moisture exclusion before packaging

    Final product types

    • Accelerators for NR, SBR, and EPDM rubber formulations in tires and conveyor belts
    • Component additives for industrial hose and sealant rubber production
    • Rubber chemicals for vibration-damping and anti-static specialty products
    Free Quote

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