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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 | 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. |
Applications of 1-(3-Carboxyphenyl)-2-Thiourea in Industrial ManufacturingAs 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 AdditivesElectroplating 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
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2. Photographic Processing Stabilizer for Silver Halide SystemsPhotographic 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
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3. Intermediate for Specialty Agrochemical SynthesisMajor 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
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4. Corrosion Inhibition Additive for Industrial Cooling Water TreatmentsProducers 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
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5. Rubber Vulcanization Accelerator and Processing AidManufacturers 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
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