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2-Methyl-3-Thiosemicarbazide

    • Product Name 2-Methyl-3-Thiosemicarbazide
    • Alias 2-Methylhydrazinecarbothioamide
    • Einecs 241-286-1
    • 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

    140709

    Productname 2-Methyl-3-Thiosemicarbazide
    Casnumber 22314-68-7
    Molecularformula C2H7N3S
    Molecularweight 105.17 g/mol
    Appearance White to off-white crystalline powder
    Meltingpoint 123-125°C
    Solubility Soluble in water and ethanol
    Purity Typically ≥98%
    Boilingpoint Decomposes before boiling
    Storageconditions Store in a cool, dry place, tightly closed
    Synonyms 2-Methylhydrazinecarbothioamide
    Smiles CC(NN=C(S)N)=N

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

    Packing & Storage
    Packing The chemical 2-Methyl-3-Thiosemicarbazide is packaged in a 25-gram amber glass bottle with a secure screw cap.
    Shipping 2-Methyl-3-Thiosemicarbazide is shipped in tightly sealed containers, protected from moisture and light. It is transported according to chemical safety regulations, typically as a non-hazardous substance. The package should be labeled clearly, handled with standard chemical precautions, and stored in a cool, dry place during transit to prevent decomposition.
    Storage Store 2-Methyl-3-thiosemicarbazide in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep it in a cool, dry, well-ventilated area, isolated from strong oxidizers and acids. Clearly label the storage area, and restrict access to trained personnel. Follow proper chemical handling protocols and local safety regulations for hazardous substance storage.
    Application of 2-Methyl-3-Thiosemicarbazide

    Applications of 2-Methyl-3-Thiosemicarbazide in Industrial Manufacturing

    As a primary manufacturer of 2-Methyl-3-Thiosemicarbazide, we supply this specialized intermediate to support production in select chemical sectors where its reactivity and functional group profile directly enhance synthesis efficiency. Deployed within tightly regulated downstream formulations, our material is adopted by leading producers for its track record in precise transformation processes. Below we detail established industrial application scenarios, corresponding compliance frameworks, recommended formulation ratios, key integration steps, and typical finished products.

    1. Active Pharmaceutical Ingredient (API) Synthesis – Thiadiazole Derivatives

    API manufacturers employ our material as a nucleophilic agent during condensation routes to construct thiadiazole nuclei, integral to a wide class of anti-inflammatory and cardiovascular therapies. Formulators consistently monitor impurity profiles and reaction yields during the hydrazinolysis and cyclization phases, with in-process controls to meet pharmaceutical quality benchmarks. The input ratio depends on both the desired API target and the stoichiometry required in semi-batch syntheses, balancing purity specifications in finished drug substances supplied to regulated markets.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • International Pharmacopoeia, USP, EP monographs (as applicable to APIs produced)
    • EMA and FDA trace impurity guidelines
    • REACH registration for import and use in pharmaceutical contexts

    Typical usage ratio

    • Usually 1.0–1.2 molar equivalents relative to target aldehyde or keto precursor; adjusted upward in multi-step reactions to ensure complete conversion, with residual content minimized prior to final purification

    Downstream process integration

    • Introduced during primary condensation or hydrazinolysis stage; followed by solvent-based workup and controlled crystallization, with in situ monitoring for complete cyclization

    Final product types

    • Anti-inflammatory APIs (thiadiazole type)
    • Cardioprotective pharmaceutical intermediates
    • Experimental CNS-active compounds for clinical pipelines

    2. Agrochemical Intermediate Production – Thiosemicarbazone Fungicides

    Industrial formulators in crop protection use this raw material as a core synthon to generate thiosemicarbazone moieties, required for the synthesis of systemic fungicides. The raw material's performance in condensation steps with various aromatic or heterocyclic aldehydes influences downstream efficacy and product shelf life. Dose optimization relates closely to the reactivity of the chosen base stock and the purity mandates for further derivatization, which are stipulated under agricultural substance regulations.

    Industry compliance standards

    • FAO/WHO pesticide specification standards
    • ISO 9001 and ISO 14001-certified production systems
    • REACH compliance for agrochemical pre-cursors
    • National agrochemical registration protocols (e.g., US EPA, EU Regulation 1107/2009)

    Typical usage ratio

    • Applied in a 0.9–1.1 molar ratio per target aldehyde, modulated by substrate-specific yields and contamination thresholds for intermediary agrochemical formulations

    Downstream process integration

    • Added at the condensation stage with temperature and pH control, followed by solvent removal and post-reaction distillation to isolate the active intermediate

    Final product types

    • Systemic fungicidal intermediates
    • Custom-built thiosemicarbazone seed treatment agents
    • Precursor compounds for new-generation plant protection products

    3. Analytical Reagent Blending – Carbonyl Compound Detection Kits

    Producers of laboratory diagnostic kits utilize the compound for its selectivity in forming hydrazone derivatives, enabling colorimetric and spectrophotometric detection of trace carbonyls in environmental and industrial samples. The formulation demands precise concentration control to eliminate matrix effects and stabilize working solutions used by accredited laboratories. Final kit assembly involves batch testing and shelf-life verification in compliance with laboratory reagent regulatory frameworks.

    Industry compliance standards

    • ISO/IEC 17025 accreditation standards (analytical laboratories)
    • EN ISO 13485 for diagnostic reagent kit production
    • Global Harmonized System (GHS) for chemical labelling and safety data
    • OECD chemical testing protocols

    Typical usage ratio

    • Incorporated at 0.5–2% w/v in buffer solutions, precisely adjusted according to assay sensitivity and method validation outcomes

    Downstream process integration

    • Dissolved into aqueous or ethanol-based reagent solutions after pH standardization, followed by sterile filtration and packaging under inert atmosphere to prevent degradation

    Final product types

    • Environmental carbonyl monitoring kits
    • Food safety hydrazone test kits
    • Sealed analytical reagent vials for QC laboratories

    4. Dye and Pigment Intermediate Manufacturing – Heterocyclic Scaffold Synthesis

    Colorant manufacturers employ the material within multi-step syntheses to introduce sulfur and nitrogen functionalities into heterocyclic pigment systems. Its intervention in ring-closure reactions plays a determinative role in color intensity and pigment stability over sustained industrial use. Sourcing consistency and additive concentration adjustments depend on end-product chromaticity and performance in targeted applications, such as industrial coatings or specialty inks.

    Industry compliance standards

    • ISO 9001 for pigment and dye production
    • ECHA guidelines for chemical hazard communication
    • APEO-free requirements and REACH substance limits
    • Specific national standards for food-contact and toy-safe pigments (if applicable)

    Typical usage ratio

    • Applied between 1.5–2.5 molar percent, calibrated against corresponding aldehyde or precursor dye intermediates to control reaction conversion and final pigment yield

    Downstream process integration

    • Fed during heterocycle assembly in staged reactions, enabling subsequent purification and calcination or grinding to meet particle size distributions demanded by downstream specialty pigment dispersions

    Final product types

    • Heterocyclic organic pigments
    • Industrial and textile dyes
    • Specialized printing inks
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