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1-(2-Fluorophenyl)-2-Thiourea

    • Product Name 1-(2-Fluorophenyl)-2-Thiourea
    • Alias O-(2-Fluorophenyl)thiourea
    • Einecs 252-129-2
    • 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

    828432

    Chemical Name 1-(2-Fluorophenyl)-2-thiourea
    Molecular Formula C7H7FN2S
    Molecular Weight 170.21 g/mol
    Cas Number 358-76-7
    Appearance White to off-white solid
    Melting Point 149-151°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles C1=CC=C(C(=C1)F)NC(=S)N
    Inchi InChI=1S/C7H7FN2S/c8-6-4-2-1-3-5(6)10-7(9)11/h1-4H,(H3,9,10,11)
    Synonyms 2-Fluorophenylthiourea
    Storage Store below 30°C in a dry and well-ventilated place

    As an accredited 1-(2-Fluorophenyl)-2-Thiourea 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, labeled “1-(2-Fluorophenyl)-2-Thiourea, 25g,” with hazard symbols and lot number clearly displayed.
    Shipping 1-(2-Fluorophenyl)-2-Thiourea is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. Packages are labeled in compliance with applicable regulations and handled by qualified carriers. During transit, the chemical is protected from extreme temperatures, direct sunlight, and physical damage to ensure safe and stable delivery.
    Storage Store **1-(2-Fluorophenyl)-2-thiourea** in a tightly closed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Label containers clearly, and keep away from heat sources. Use proper personal protective equipment (PPE) when handling. Follow all relevant safety guidelines and local regulations for chemical storage.
    Application of 1-(2-Fluorophenyl)-2-Thiourea

    Applications of 1-(2-Fluorophenyl)-2-Thiourea in Industrial Manufacturing

    As a direct manufacturer of 1-(2-Fluorophenyl)-2-Thiourea, we focus on high-purity supply for downstream chemical industries with stringent batch control and traceable production records. Below, we detail real industrial application areas, highlighting sector-specific compliance, composition guidelines, process integration methods, and the resulting end products adopted by our global clients.

    1. Pharmaceutical Intermediates for Thiazole and Benzothiazole Synthesis

    Our production batches serve as key thiourea building blocks for medicinal chemistry, particularly in the synthesis of thiazole and benzothiazole derivatives. These intermediates are essential in the research and manufacture of various small-molecule pharmaceuticals, where stringent trace impurity specifications and full documentation are required. The material undergoes condensation reactions under controlled pH in multi-step syntheses, followed by purification according to cGMP standards before it enters active ingredient formation.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredient Manufacturing
    • USP-NF for intermediate purity level documentation
    • EDQM Certificates of Suitability procedures
    • ISO 9001:2015 quality management

    Typical usage ratio

    • 0.8–1.3 molar equivalents relative to halogenated or nitro-benzene intermediate, adjusted based on desired conversion and batch scale

    Downstream process integration

    • Charged into reactor at initial condensation stage before cyclization
    • Monitored in-process for conversion rate by HPLC
    • Isolated in semi-pure form, then refined by recrystallization or chromatography

    Final product types

    • Anxiolytic APIs (e.g., benzothiazole analogues)
    • Antimicrobial pharmaceutical APIs
    • Seed compound libraries for lead optimization
    • Advanced research intermediates

    2. Agricultural Chemical Intermediate for Fungicides

    This compound functions as a sulfur and nitrogen donor in heterocyclic fungicide synthesis, feeding directly into industrial batch processes for commercial crop protection chemicals. Agrochemical manufacturers demand rigorous QA lot tracking, residue control, and compliance with both domestic and export regulations. Its addition affects the sulfur ring closure steps in triazole or thiadiazole formation, requiring close control of molar ratios and temperature.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH (EU) registration requirements for intermediate use
    • China GB/T 1600-2018 Pesticide Registration and Production
    • ISO 17025 analytical testing accreditation

    Typical usage ratio

    • 1.0–1.2 molar equivalents, tailored to chain length and ring closure efficiency

    Downstream process integration

    • Reacted with diketones or chloro-ketones during heterocycle assembly
    • Pre-mixed with catalysts in closed-system batch reactors
    • Monitored for residual thiourea levels in post-reaction analysis

    Final product types

    • Systemic triazole fungicides
    • Seed treatment concentrates
    • Crop-specific protective agents
    • Pre-mixed agrochemical formulations

    3. Specialty Dye and Pigment Intermediate for Organic Colors

    Manufacturers of high-purity dyes use this raw material as a nucleophilic sulfur donor in azo and sulfide-based dye synthesis, particularly for electronics, plastics, and textile markets. Its purity grade and specification sheets accompany each batch. Entry into coupling reactions must address solvent compatibility and intermediate isolation to limit cross-contamination in hypoallergenic textile dyes, anti-fade pigments, and technical application colors.

    Industry compliance standards

    • Oeko-Tex Standard 100 for restricted substance dyes
    • REACH Annex XVII pigment and dye regulations
    • ZDHC MRSL requirements for textile chemicals
    • ISO 9001 for colorant production control

    Typical usage ratio

    • 0.5–1.1 mole equivalent per dye base, adjusted for target chromophore and reaction kinetics

    Downstream process integration

    • Fed as a reactant in the azo coupling stage or for thiourea-based sulfur bridge formation
    • Process pH and temperature tightly controlled
    • Chemical recycled or neutralized as required by effluent regulation

    Final product types

    • Technical grade organic pigments for plastics
    • Hypoallergenic textile dyes
    • Printing inks for circuit boards and electronics
    • Laser printer pigments

    4. Polyurethane Catalyst Precursor for Rigid Foams

    Chemical producers use this compound as a specialized precursor for organosulfur-modified catalysts that accelerate urethane polymerization. Downstream integration requires precise catalyst synthesis conditions, including solvent selection and controlled temperature profiles to avoid degradation or impurity formation. End users in the construction and insulation sector require batch-specific technical documentation for both compliance and performance traceability.

    Industry compliance standards

    • ISO 12201 for raw material purity in foam production
    • ASTM D3574 Polyurethane Testing Protocols
    • ISO 9001 for traceability and batch control
    • EU Construction Product Regulation (CPR) for insulation foams

    Typical usage ratio

    • 1.0–2.5% by weight of total catalyst mass, optimized by polyurethane system type and curative speed

    Downstream process integration

    • Dissolved in solvent blends during catalyst preformation
    • Reacted with metal salts under inert atmosphere for active catalyst formulation
    • Monitored through batch analytics for active group concentration

    Final product types

    • Rigid foam insulation boards
    • Structural sandwich panels
    • High-resilience cold-cure foam systems
    • Refrigerator insulation foams
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