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HS Code |
719549 |
| Chemicalname | 1-[4-(Dimethylamino)Phenyl]-2-Thiourea |
| Molecularformula | C9H13N3S |
| Molecularweight | 195.29 g/mol |
| Casnumber | 6107-16-6 |
| Appearance | Yellow solid |
| Meltingpoint | 187-189°C |
| Solubility | Slightly soluble in water |
| Structure | Contains a dimethylaminophenyl ring attached to thiourea |
| Smiles | CN(C)c1ccc(cc1)NC(=S)N |
| Synonyms | 4-(Dimethylamino)phenylthiourea |
As an accredited 1-[4-(Dimethylamino)Phenyl]-2-Thiourea factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle containing 25 grams of 1-[4-(Dimethylamino)phenyl]-2-thiourea, labeled with hazard warnings and batch information. |
| Shipping | 1-[4-(Dimethylamino)phenyl]-2-thiourea is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is packed according to regulatory requirements for safe transport of chemicals. Labeling includes proper chemical identification and hazard information. Shipping is conducted via approved carriers, ensuring compliance with relevant safety and environmental regulations. |
| Storage | 1-[4-(Dimethylamino)phenyl]-2-thiourea should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances, such as strong oxidizers. Protect from moisture and direct sunlight. Clearly label the container and keep it in a designated chemical storage area, accessible only to trained personnel. |
Applications of 1-[4-(Dimethylamino)Phenyl]-2-Thiourea in Industrial ManufacturingAs a direct manufacturer, we supply 1-[4-(Dimethylamino)Phenyl]-2-Thiourea for specialized industrial formulations where its unique reactivity and selectivity enable reliable process outcomes. Our material consistently supports high-value downstream operations across a tightly defined range of sectors. Detailed below are core application scenarios, including critical compliance criteria, integration methodology, and precise usage guidelines based on our field experience. 1. Metal Ion Analytical Reagents for Wet Chemical LaboratoriesThe chelating and chromogenic characteristics of this thiourea derivative drive its adoption as a diagnostic reagent in copper, iron, and other transition metal assays. Analytical laboratories in process control, materials research, and environmental testing incorporate this material to achieve colorimetric detection with high specificity. Its stable response profile helps analysts achieve quantifiable results at low detection limits, demanded for strict laboratory quality assurance programs. Industry compliance standards
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2. Photographic and Imaging Chemical ProcessingProfessional and industrial imaging facilities select this material for its function as a reducing and antifoggant agent in photographic developers and photographic emulsion stabilization. By participating in redox reactions, it improves image clarity and prevents background fog in both black-and-white and certain color photographic systems. High batch-to-batch purity ensures reproducible processing yields and consistency across different film or paper batches. Industry compliance standards
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3. Synthetic Organic Chemistry Intermediary (Research and Specialty Fine Chemicals)In advanced organic synthesis, chemists apply this compound as a building block and selective nucleophile for the preparation of thiazole derivatives, dyes, and pharmaceutical precursors. Its electron-donating amino substituent coupled with the thiourea group facilitates targeted condensation or cyclization reactions under controlled conditions, widely utilized in R&D, pilot, and small-batch specialty synthesis. Industry compliance standards
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4. Corrosion Inhibitor Additive in Industrial Water TreatmentIndustrial water treatment operators leverage the adsorption and film-forming capabilities of this thiourea-based material in closed-loop cooling and boiler circuits. It inhibits metal surface oxidation and pitting by forming a protective layer, maintaining plant asset integrity, and reducing maintenance downtime. Real-world programs value its compatibility in multi-component anti-corrosion packages with other azole and amine additives. Industry compliance standards
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5. Dyeing Auxiliary for High-Performance Textile FinishingSpecialty textile processors and dyestuff manufacturers utilize this molecule as an auxiliary component that enhances dye uptake and fastness on synthetic and blended fibers. The electron-donating and chelating features optimize dye-fiber bonding, particularly in processes targeting deep shade and color fastness. It contributes to reduced dye runoff and improved reproducibility of color shades, critical for precision textile finishing applications. Industry compliance standards
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