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1-(3-Carboxyphenyl)-2-Thiourea

    • Product Name 1-(3-Carboxyphenyl)-2-Thiourea
    • Alias 3-Carboxyphenylthiourea
    • Einecs 697-667-2
    • 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

    325886

    Chemical Name 1-(3-Carboxyphenyl)-2-thiourea
    Molecular Formula C8H8N2O2S
    Molecular Weight 196.23 g/mol
    Cas Number 16106-43-9
    Appearance White to off-white solid
    Melting Point 235-240 °C
    Solubility Slightly soluble in water
    Boiling Point Decomposes before boiling
    Synonyms 3-Carboxyphenylthiourea
    Smiles C1=CC(=CC(=C1)C(=O)O)NC(=S)N
    Inchi InChI=1S/C8H8N2O2S/c9-8(13)10-6-3-1-2-5(4-6)7(11)12/h1-4,8H,(H3,9,10,11,12,13)
    Storage Conditions Store in a cool, dry place

    As an accredited 1-(3-Carboxyphenyl)-2-Thiourea factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with screw cap, labeled "1-(3-Carboxyphenyl)-2-Thiourea, 25g," featuring hazard symbols and handling instructions.
    Shipping 1-(3-Carboxyphenyl)-2-thiourea is shipped in tightly sealed, chemically resistant containers to prevent contamination or moisture exposure. Standard shipping complies with applicable regulations for non-hazardous laboratory chemicals. The package includes appropriate labeling and documentation. Store in a cool, dry location upon arrival and handle using proper laboratory safety protocols.
    Storage Store **1-(3-Carboxyphenyl)-2-thiourea** in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Keep it separate from strong acids, bases, and oxidizing agents. Ensure clear labeling, and restrict access to trained personnel. Use appropriate personal protective equipment (PPE) when handling. Dispose of waste according to local regulations.
    Application of 1-(3-Carboxyphenyl)-2-Thiourea

    Applications of 1-(3-Carboxyphenyl)-2-Thiourea in Industrial Manufacturing

    As a specialized manufacturer, we supply 1-(3-Carboxyphenyl)-2-Thiourea for precise downstream sectors where its unique chemical characteristics create direct operational benefits. Below, we outline the principal industrial applications, process details, and compliance standards for this raw material in mature and high-demand industrial fields.

    1. Metal Ion Chelation Agents in Electroplating Additives

    Electroplating producers rely on 1-(3-Carboxyphenyl)-2-Thiourea as a selective chelating compound, particularly for heavy metal ion complexation, which stabilizes bath composition and improves deposit uniformity. It plays a critical role in the formulation of nickel or copper electrolytes, reducing unwanted side reactions by efficiently binding with trace ionic impurities, thus extending bath life and delivering micron-level control in deposit thickness.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for Chemical Processing
    • REACH Regulation (EC) No 1907/2006 for registered use in metal finishing
    • RoHS Directive 2011/65/EU exclusion for plating chemistry
    • ASTM B322-99(2014) Standard Guide for Cleaning Metals Prior to Electroplating

    Typical usage ratio

    • 0.01–0.10 g/L in plating baths; precise level determined by metal type and operational bath load

    Downstream process integration

    • Added directly into aqueous plating electrolyte after initial composition adjustment, prior to introduction of components for metal deposition

    Final product types

    • Decorative nickel-plated fasteners
    • Copper-plated printed circuit boards
    • Corrosion-resistant machine parts
    • Electronics shielding housings

    2. Photographic Processing Stabilizer for Silver Halide Systems

    Photographic material manufacturers incorporate this raw material as a stabilizer in silver halide developing solutions where its thiourea and carboxyphenyl groups scavenge residual oxidizers. Its performance enhances image clarity and archival permanence by minimizing fogging and slowing down unwanted secondary reactions during film and paper development, which is critical for archival storage materials and high-fidelity imaging.

    Industry compliance standards

    • ISO 18902:2013 Imaging Materials Storage Standard
    • ANSI/NAPM IT9.1 for processed photographic film permanence
    • Environmental Protection Agency (EPA) 40 CFR Part 433 for wastewater from photoprocessing
    • REACH Annex XVII for use in photographic chemicals

    Typical usage ratio

    • 0.2–0.4 g/L in developer or fixing baths; adjusted per batch based on process cycle and silver content

    Downstream process integration

    • Incorporated in final formulation step before chemical filling into automated developer and fixer cartridges

    Final product types

    • Black-and-white photographic films
    • Archival-quality photographic paper
    • Instant print developer packs
    • Microfilm and X-ray image storage materials

    3. Intermediate for Specialty Agrochemical Synthesis

    Major agrochemical companies employ 1-(3-Carboxyphenyl)-2-Thiourea as a core building block for producing selective herbicides. Its molecular structure allows formation of specific thiourea-based derivatives which target key plant metabolic pathways, providing controlled weed suppression in cereal and vegetable crops. The raw material undergoes controlled condensation and functional group modification during active ingredient synthesis, supporting the development of low-residue and soil-safe formulations that meet stringent crop protection rules.

    Industry compliance standards

    • FAO/WHO Manual on Development and Use of FAO and WHO Specifications for Pesticides
    • European Regulation (EC) No 1107/2009 for Plant Protection Products
    • ISO 9001:2015 for agrochemical intermediates manufacturing
    • National or regional crop residue limits (MRLs)

    Typical usage ratio

    • By mole percentage as a precursor for synthesis, typically 0.8–1.2 equivalents versus target active compound; scale varies by synthetic route

    Downstream process integration

    • Charged into primary reactor during condensation step prior to acylation or sulfonation for downstream herbicide API development

    Final product types

    • Selective pre-emergence herbicide formulations
    • Agricultural soil amendment products
    • Ready-to-spray weed suppression agents
    • Customized granulated blends for row crops

    4. Corrosion Inhibition Additive for Industrial Cooling Water Treatments

    Producers of water treatment chemicals apply 1-(3-Carboxyphenyl)-2-Thiourea to blended corrosion inhibitor concentrates used in closed-loop and recirculating industrial cooling systems. Its dual functional groups enhance steel and copper surface passivation and reduce corrosion rates in aggressive water environments containing dissolved oxygen and mineral salts. Proven performance under dynamic system conditions supports continuous operation and asset longevity in power plants, refineries, and manufacturing facilities.

    Industry compliance standards

    • ASTM D5258-95(2015) Standard Practice for Evaluation of Corrosion Inhibitors in Cooling Water
    • ISO 9001:2015 for chemical manufacturing
    • ANSI/ASHRAE Standard 188-2021 for water system safety
    • REACH compliance for biocidal and water treatment agents

    Typical usage ratio

    • 5–20 ppm active ingredient in formulated cooling water inhibitor concentrates; calculated based on total system water volume and corrosion risk profile

    Downstream process integration

    • Blended into multi-component inhibitor packages during concentrate formulation before dilution and system dosing

    Final product types

    • Industrial cooling water treatment blends
    • Chilled water corrosion inhibitor cartridges
    • Chemical injection packs for HVAC and petrochemical cooling loops
    • Asset protection chemicals for heavy industry cooling towers

    5. Rubber Vulcanization Accelerator and Processing Aid

    Manufacturers of specialty synthetic and natural rubber compounds utilize this intermediate as a vulcanization accelerator where its structure modifies crosslinking kinetics. During sulfur curing cycles, it promotes faster and more controlled crosslinking for tires, sealing materials, or industrial hoses. Its carboxyl group enhances filler dispersion and finished elastomer properties, allowing precise adjustment of compression set, abrasion resistance, and long-term durability.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for rubber chemicals
    • ASTM D3182-21 Standard Practice for Rubber Compounding and Mixing
    • European Regulation (EU) No 2019/1021 on persistent organic pollutants (POP Regulation)
    • Compliance with PAH/REACH restrictions for automotive rubber parts

    Typical usage ratio

    • 0.3–1.2 phr (parts per hundred rubber) in rubber formulation; dosage adapted to target cure rates and mechanical property profiles

    Downstream process integration

    • Mixed into elastomer masterbatch together with sulfur and primary accelerators during initial compounding before extruding, molding, or calendering

    Final product types

    • Synthetic tire treads for commercial vehicles
    • Industrial-grade rubber gaskets and O-rings
    • Heavy-duty conveyor belts
    • Precision sealing materials for fluid hoses
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