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HS Code |
426639 |
| Chemical Name | 4-Chloro-3,5-Diaminobenzotrifluoride |
| Molecular Formula | C7H5ClF3N2 |
| Molecular Weight | 208.58 g/mol |
| Cas Number | 3939-09-1 |
| Appearance | Off-white to light brown solid |
| Melting Point | 128-132°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Density | 1.56 g/cm³ (approximate) |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C, keep container tightly closed |
| Synonyms | 4-Chloro-3,5-bis(aminobenzotrifluoride); 4-Chloro-3,5-diamino-α,α,α-trifluorotoluene |
| Ec Number | 223-453-8 |
| Hazard Statements | May cause skin and eye irritation |
As an accredited 4-Chloro-3,5-Diaminobenzotrifluoride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging contains 100 grams of 4-Chloro-3,5-Diaminobenzotrifluoride in a sealed amber glass bottle with a tamper-evident cap. |
| Shipping | **Shipping Description:** 4-Chloro-3,5-Diaminobenzotrifluoride should be shipped in a tightly sealed container, protected from moisture, heat, and incompatible substances. Appropriate chemical hazard labeling, documentation, and handling in accordance with local and international regulations (such as UN classification and DOT/IATA rules) are required. Use secondary containment and personal protective equipment during transport. |
| Storage | 4-Chloro-3,5-Diaminobenzotrifluoride should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from moisture and light. Label containers clearly, and avoid storing above room temperature. Ensure proper chemical hygiene, and keep away from sources of ignition. Store according to all relevant safety regulations. |
Applications of 4-Chloro-3,5-Diaminobenzotrifluoride in Industrial ManufacturingAs an advanced manufacturer of specialty aromatic chemicals, we supply 4-Chloro-3,5-Diaminobenzotrifluoride for integration in strictly regulated downstream industries. This compound’s unique structure enables high-performance intermediates, especially in fields where molecular precision, stability under harsh processing conditions, and strict compliance are essential. The following sections detail several focused industrial scenarios validated by real-world production flows and regulatory patterns. 1. High-Performance Organic Pigment SynthesisMajor pigment manufacturers utilize this compound as an essential intermediate for synthesizing quinacridone and perylene pigments, valued for their color stability in automotive and industrial paint formulations. Its electron-withdrawing trifluoromethyl group and diamino functionalities actively influence final pigment crystal morphology and shade depth, while the chlorinated aromatic ring structure supports performance under UV exposure. Industry customers precisely monitor additive concentration, as trace composition variance critically impacts batch chromaticity and dispersion. Industry compliance standards
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2. Agrochemical Active Ingredient SynthesisSelective herbicide and fungicide manufacturers rely on this intermediate to introduce substituted aniline motifs into active molecules. As a key building block, it provides strong electronic effects for improved target compound selectivity in field conditions and thermal resistance during granule processing. Chemical engineers carefully titrate addition to maximize yield while keeping residuals below agrochemical statutory limits, ensuring regulatory acceptance in restricted markets. Industry compliance standards
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3. Commercial Dye Intermediate ManufacturingDye manufacturers use this compound to obtain specific chromophores necessary for high-temperature dyeing of synthetic textiles, primarily polyester and blends. With its stable trifluoromethylated aniline backbone, it enables excellent resistance to migration and fading during garment washing. Compliance profile, purity, and process traceability remain critical due to direct application to consumer-facing end-products in regulated markets. Industry compliance standards
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4. Advanced Polymer Additive SynthesisSuppliers to the plastics and elastomers sector incorporate this specialty aromatic compound as a monomeric precursor for heat-resistant, weather-stable fluoropolymer additives. Its nucleophilic centers and halogen functionalization allow for tailored substitution on polymer side chains, enhancing thermal dimensional stability and UV resistance in engineering thermoplastics for demanding applications in automotive, electronics, and construction. Industry compliance standards
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5. Pharmaceutical Intermediate for Active Ingredient SynthesisPharmaceutical fine chemical manufacturers deploy this compound as a stepwise intermediate for synthesizing advanced small-molecule APIs featuring electron-deficient aromatic cores. The molecule’s dual amino and halogen substitutions enable regioselective derivatization, controlled via multistep reactions under cGMP protocols. Quality teams validate each lot for trace impurity profiles, as stringent pharmacopoeial requirements govern acceptable use in regulated drug markets. Industry compliance standards
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6. Specialty Chemical Intermediate for Liquid Crystal MaterialsManufacturers of advanced display technologies employ this aromatic diamine in the synthesis of side-chain functionalized liquid crystal molecules, critical for high-purity, thermally stable LC mixtures used in TFT-LCD panels. Material purity and traceability remain paramount, as even low-level contamination impacts phase transition temperature and electro-optic performance. Chemists strictly control the integration step, ensuring compliance with global electronics supply chain standards. Industry compliance standards
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