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4-(4-Fluorophenyl)-3-Thiosemicarbazide

    • Product Name 4-(4-Fluorophenyl)-3-Thiosemicarbazide
    • Alias FTSC
    • Einecs 696-194-6
    • 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

    172548

    Product Name 4-(4-Fluorophenyl)-3-Thiosemicarbazide
    Cas Number 5397-43-1
    Molecular Formula C7H8FN3S
    Molecular Weight 185.22
    Appearance White to off-white powder
    Melting Point 168-172°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in DMSO and DMF
    Boiling Point Decomposes before boiling
    Functional Groups Thiosemicarbazide, Fluorophenyl
    Smiles C1=CC(=CC=C1C2=NN(C(=S)N2)N)F
    Storage Conditions Store in a cool, dry place, protected from light

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

    Packing & Storage
    Packing The packaging is a 25g amber glass bottle with a tight-seal cap, labeled "4-(4-Fluorophenyl)-3-Thiosemicarbazide" and safety information.
    Shipping 4-(4-Fluorophenyl)-3-Thiosemicarbazide is shipped in compliance with standard chemical safety regulations. It is securely packaged in sealed containers, protected from moisture and light. Proper labeling, including hazard and handling information, ensures safe transport. All documentation adheres to regulatory standards to facilitate smooth domestic or international shipping.
    Storage 4-(4-Fluorophenyl)-3-Thiosemicarbazide should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition, moisture, and incompatible substances such as strong oxidizers. Protect from direct sunlight and avoid prolonged exposure to air. Use proper personal protective equipment (PPE) when handling to prevent contact and inhalation. Store in accordance with local regulations.
    Application of 4-(4-Fluorophenyl)-3-Thiosemicarbazide

    Applications of 4-(4-Fluorophenyl)-3-Thiosemicarbazide in Industrial Manufacturing

    4-(4-Fluorophenyl)-3-Thiosemicarbazide serves as a critical intermediate in specialized sectors requiring stringent quality controls and reproducible performance. Our manufacturing expertise ensures this material meets the distinct processing parameters and downstream integration needs of each application. Below are primary industrial sectors where our product is consistently specified for quality-controlled operations.

    1. Pharmaceutical Intermediate Synthesis

    In regulated pharmaceutical synthesis, 4-(4-Fluorophenyl)-3-Thiosemicarbazide acts as a core intermediate for heterocyclic compound construction, frequently undergoing cyclization and subsequent derivatization steps. Large-scale production centers use this compound for synthesizing specific APIs, particularly those requiring sulfur-based functional groups to enhance biological activity and pharmacokinetics. Handling and processing must comply with cGMP as APIs progress through registered therapeutic compound pipelines.

    Industry compliance standards

    • ICH Q7 (GMP for APIs)
    • EU GMP Annex 8 (API Intermediates)
    • US FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • Chinese Pharmacopoeia, applicable API chapters

    Typical usage ratio

    • 0.12–0.25 molar equivalent relative to target heterocycle core; adjusted according to stoichiometric demand in stepwise API transformations.

    Downstream process integration

    • Charged during early-stage batch reactors, primarily in N-heterocycle ring-forming reactions before purification and salt formation; followed by continuous monitoring of reaction progress by in-process HPLC or NMR.

    Final product types

    • Active pharmaceutical ingredients (e.g., fluorinated thiohydantoin derivatives)
    • Precursor intermediates for antineoplastic and antibacterial agents
    • API-grade reference materials for QC laboratories
    • Drug substance development compounds for clinical trials

    2. Agrochemical Intermediate Development

    This compound enters agrochemical manufacturing chains as a precursor for synthesizing advanced thiosemicarbazone herbicides, seed treatment agents, and systemic fungicides. Over multiple synthesis steps, it enables precise functionalization of fluorinated aromatic backbones—required for bioactivity toward target pathogens and resistance management. Bulk processors rely on validated reaction pathways to mitigate by-product formation and maximize conversion rates under scalable conditions.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 (Quality Management in Chemical Manufacturing)
    • REACH (EC) No 1907/2006 registration for agrochemicals
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • 5–8% w/w relative to total reactant charge in multi-step active ingredient synthesis; modified by crop-specific formulation and performance testing feedback.

    Downstream process integration

    • Dosed into controlled addition reactors during the assembly of core thiosemicarbazone units; followed by acid-base work-up and solvent-removal in closed systems to ensure product purity.

    Final product types

    • Systemic fungicidal concentrates
    • Pre-emergent herbicide actives
    • Seed coating active ingredients
    • Pesticide formulation reference standards

    3. Specialty Dye and Pigment Synthesis

    In the specialty dye sector, 4-(4-Fluorophenyl)-3-Thiosemicarbazide contributes to the production of sulfur- and fluorine-modified azo and hydrazone dyes. These dyes demand exact chromophore development, usually initiated by diazotization or condensation reactions subsequent to the introduction of the thiosemicarbazide group. Industrial colorant manufacturers apply the compound in processes optimized to achieve particulate stability, colorfastness, and regulated migration under application-specific conditions.

    Industry compliance standards

    • EN 71-3 (Safety of Toys – Migration of Certain Elements, for toys and children’s products)
    • ETAD Guidelines for dye manufacturing
    • ISO 9001:2015 (Colorant Production)
    • OEKO-TEX® Standard 100 (textile dye exclusion lists)

    Typical usage ratio

    • 2–4% w/w relative to total chromophoric substrate; subject to spectral intensity and shade target adjustments in batch QC control.

    Downstream process integration

    • Introduced in the coupling stage for azo dye synthesis or applied during hydrazone formation in pigment compounders, followed by stepwise solvent exchange and precision filtration to meet demanding color spec requirements.

    Final product types

    • Technical-grade azo dyes
    • Functional textile pigment dispersions
    • Offset and packaging ink colorants
    • Plastics-compatible high-stability masterbatches

    4. Analytical Reagents and Reference Standards

    Analytical laboratories and reference material manufacturers incorporate 4-(4-Fluorophenyl)-3-Thiosemicarbazide as a highly specific derivatization agent and calibration reference in methods quantifying carbonyl and hydrazine functionalities. The compound’s reactivity profile under controlled conditions delivers stable derivatives necessary for reliable GC/MS or HPLC calibration—a critical step for method validation and routine laboratory QA/QC, particularly in pharmaceutical and environmental settings.

    Industry compliance standards

    • ISO 17034 (General requirements for the competence of reference material producers)
    • ISO/IEC 17025 (Testing and calibration laboratories)
    • USP General Chapter <232> and <233> (elemental impurities analysis)
    • Ph. Eur. (European Pharmacopoeia) Analytical Reagent specifications

    Typical usage ratio

    • Typically 0.1–0.5 mg/mL in derivatization protocols for analytical sample preparation; specific concentration optimized per method sensitivity and calibration requirements.

    Downstream process integration

    • Prepared as reagent solution or calibration mix during laboratory workflow for analyte determination (e.g., in detector calibration runs or sample pre-treatment stages), followed by documentation in QC/QA traceability systems.

    Final product types

    • Certified reference standards for analytical calibrators
    • Derivatization reagent kits for regulated laboratory use
    • Quality control calibration solutions for instrumental analysis
    • Environmental monitoring test standards
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