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2-Amino-5-Benzylthio-1,3,4-Thiadiazole

    • Product Name 2-Amino-5-Benzylthio-1,3,4-Thiadiazole
    • Alias 2-ABT
    • Einecs 264-119-8
    • 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
    VTB
    Specifications

    HS Code

    681302

    Chemical Name 2-Amino-5-Benzylthio-1,3,4-Thiadiazole
    Cas Number 36357-13-2
    Molecular Formula C9H9N3S2
    Molecular Weight 223.32
    Appearance Off-white to pale yellow powder
    Melting Point 154-158°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Boiling Point Decomposes before boiling
    Storage Conditions Store at room temperature, keep container tightly closed and in a dry place

    As an accredited 2-Amino-5-Benzylthio-1,3,4-Thiadiazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, tightly sealed HDPE bottle, labeled "2-Amino-5-Benzylthio-1,3,4-Thiadiazole, 25g," featuring hazard pictograms and batch number.
    Shipping 2-Amino-5-Benzylthio-1,3,4-Thiadiazole is shipped in secure, chemical-resistant containers to prevent leakage or contamination. Packaging complies with international transport regulations for laboratory chemicals. The shipment includes proper labeling, safety data sheets, and handling instructions. Shipments are made via certified carriers, ensuring safe delivery to qualified facilities or authorized recipients.
    Storage 2-Amino-5-Benzylthio-1,3,4-thiadiazole should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Keep the container tightly closed and protected from light. Use appropriate personal protective equipment when handling. Store in clearly labeled containers and avoid contact with moisture to maintain chemical stability.
    Application of 2-Amino-5-Benzylthio-1,3,4-Thiadiazole

    Applications of 2-Amino-5-Benzylthio-1,3,4-Thiadiazole in Industrial Manufacturing

    As a manufacturer specializing in 2-Amino-5-Benzylthio-1,3,4-Thiadiazole (ABTD), we supply this intermediate for several advanced industrial synthesis processes. Below we present genuine, validated application scenarios with specific process guidance, focusing on compliance, formulation, and conversion to downstream products.

    1. Pharmaceutical Intermediate for Cephalosporin Synthesis

    ABTD plays a key role in the synthesis of certain third-generation cephalosporin antibiotics. By functioning as a heterocyclic building block, it introduces thio-substituted functionalities, which are crucial for bioactive side-chain formation. The compound participates at the stage of side-chain assembly after beta-lactam formation but prior to final acylation. Strict quality controls apply during this step due to pharmacopoeial requirements for antibiotic purity and impurity profile limits. Pharmaceutical processors adjust the addition ratio of ABTD to accommodate the batch scale and optimize yields, considering the required molar equivalents for effective thioethylation. Final products target regulated cephalosporin APIs sold to global generic drug manufacturers.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapters for process intermediates
    • European Pharmacopoeia guidance for impurity control (Ph. Eur.)
    • China Pharmacopoeia for intermediate specification (ChP)

    Typical usage ratio

    • Applied at 0.90–1.10 molar equivalents relative to the cephalosporin core
    • Ratio adjusted according to batch size and desired conversion rate
    • Optimization guided by in-process HPLC profile of thioethylated derivatives
    • Deviation beyond ±0.05 molar units may increase contamination or yield loss

    Downstream process integration

    • Added post-core formation during side-chain functionalization
    • Reacts in polar aprotic solvent with controlled pH to promote nucleophilic substitution
    • Intermediate QC verification before transition to acylation stage
    • Byproduct removal through sequential crystallization and aqueous wash

    Final product types

    • Cefdinir active pharmaceutical ingredient (API)
    • Cefixime intermediate for bulk drug synthesis
    • Semi-synthetic cephalosporin derivatives
    • Beta-lactam antibiotic finished formulations

    2. Agrochemical Synthesis Building Block

    Within the agrochemical sector, ABTD acts as a key sulfur-containing heterocyclic intermediate for constructing advanced fungicidal molecules. The compound enters sulfidation or cyclization steps for synthesis of triazole and thiadiazole-based crop protection actives. Agrochemical processors must follow specific regulatory documentation and track residual sulfide content to meet global market requirements. Usage ratios depend on the designed crop protection active, especially where selective substitution patterns control biological activity. This intermediate directly integrates into the active ingredient route during the final heterocyclization, ultimately yielding bulk technical-grade and formulated agrochemicals.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • U.S. EPA standards for pesticide active substance intermediates
    • ISO 9001:2015 for quality management of ingredient processing

    Typical usage ratio

    • 0.50–2.00 mole per mole of final active ingredient, based on structure
    • Lower ratios for single substitution, higher for dual-substituent actives
    • Calculated from stoichiometry and real-world yield for technical-grade actives
    • Ratio tuning to mitigate formation of polymeric byproducts

    Downstream process integration

    • Fed into final cyclization stage during synthesis of target heterocycle
    • Used with chlorinating agents or oxidants for direct incorporation
    • In-process GC-MS monitoring to ensure full consumption and minimal residue
    • Transition from synthesis to formulation with tank-mixed inert carriers

    Final product types

    • Thiadiazole-derived fungicide bulk actives
    • Triazole-based agricultural pesticides
    • Sulfur-containing seed treatment agents
    • Custom blended crop protection premixes

    3. Specialty Dye Intermediate for Electronic and Textile Use

    This compound finds application as a fabric and functional dye intermediate, specifically for high-stability electronic dye synthesis and specialty textile coloration agents. Its benzylthio moiety allows for grafting onto complex chromophore structures in multi-step dye synthesis routes, conferring enhanced lightfastness or electronic conductivity. Compliance requirements address purity and azo compound content for textile and electronic applications, particularly in export markets where REACH and RoHS regulations apply. Industrial users apply the compound at tightly controlled ratios for consistent hue and performance during final dye molecule assembly, with process integration at the pre-final coupling or diazotization phase. Downstream producers convert this intermediate into highly customized finished dye goods as well as specialty inks for smart device displays.

    Industry compliance standards

    • OEKO-TEX Standard 100 for restricted substance lists in textile dyes
    • EU REACH Regulation for dye precursor notification
    • Directive 2011/65/EU (RoHS) for electronic display dye components
    • ISO 105-C06 for color fastness to domestic and commercial laundering

    Typical usage ratio

    • 1.00 molar equivalent relative to the coupling partner in dye synthesis
    • Decreases to 0.85–0.95 for pastel tones, increases up to 1.30 for deep hues
    • Electron microscopy and spectrometric analysis confirm incorporation ratio
    • Fine adjustments to ratio based on target L*a*b* color value

    Downstream process integration

    • Dosed during pre-final azo or coupling stage in dye plant reactors
    • Mixed under nitrogen with control of exothermic reaction for chromophore formation
    • Washed and extracted with high-purity solvents, followed by spray drying for powder-dye formats
    • Filtered to low ppm levels of residual aminothiadiazole prior to QC packaging

    Final product types

    • Electronic display functional dyes
    • Textile colorants for UV-resistant fabrics
    • Advanced waterborne inkjet pigment precursors
    • High-purity specialty inks for microelectronics

    4. Chemical Sensor and Analytical Reagent Synthesis

    In the analytical and sensor manufacturing sector, ABTD is used as a precursor for synthesizing chemical sensing elements and chromogenic reagents. Its unique thiadiazole scaffold is tailored for reactions with various analytes, including heavy metals and reactive oxygen species, lending high specificity in colorimetric or fluorescent assay development. Raw material compliance is critical, requiring full traceability and conformity with analytical reagent-grade standards defined by regulatory agencies. Users typically introduce this intermediate at precise equivalence ratios for controlled functionalization reactions or solid-phase grafting, with the compound entering the immobilization or sensor functionalization stage prior to final packaging into sensor devices or reagent kits.

    Industry compliance standards

    • ACS Reagent Chemicals Specifications
    • ISO 17025 Laboratory Quality Management Systems
    • RoHS compliance for sensor electronic materials
    • GLP (Good Laboratory Practice) for analytical reagent traceability

    Typical usage ratio

    • 0.95–1.05 molar equivalents per functionalization site
    • Ratio typically fixed for covalent immobilization, lower for bulk phase reagents
    • Process controls maintain batch-to-batch uniformity within ±0.02 molar range
    • Routine validation via HPLC or LC-MS for analyte-reactive performance

    Downstream process integration

    • Introduced as functional group extender during sensor probe assembly
    • Activated on solid-phase supports under controlled temperature and pH
    • Excess removed by repeated buffer wash and drying steps
    • Final QC performed prior to conversion into diagnostic or environmental test kits

    Final product types

    • Heavy metal colorimetric test strips
    • Fluorescent probes for water quality analysis
    • Reactive sensor coatings for industrial process monitoring
    • Analytical reagent solution kits for laboratory assay systems
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