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HS Code |
375596 |
| Chemical Name | 3-Amino-4-(Isopropylamino)Benzotrifluoride |
| Molecular Formula | C10H13F3N2 |
| Molecular Weight | 218.22 g/mol |
| Cas Number | 910232-84-7 |
| Appearance | Off-white to yellow solid |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically >98% (varies by supplier) |
| Smiles | CC(C)NC1=CC(=C(C=C1N)C(F)(F)F) |
| Storage Conditions | Store in a cool, dry, well-ventilated place |
| Synonyms | 3-Amino-4-(propan-2-ylamino)-1-(trifluoromethyl)benzene |
As an accredited 3-Amino-4-(Isopropylamino)Benzotrifluoride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 3-Amino-4-(Isopropylamino)Benzotrifluoride is packaged in a sealed amber glass bottle with a tamper-evident cap. |
| Shipping | 3-Amino-4-(Isopropylamino)Benzotrifluoride is shipped in airtight, chemically resistant containers, ensuring safety and stability during transport. Packaging complies with international regulations for hazardous chemicals, typically labeled with appropriate hazard warnings. The shipment is handled by certified carriers, and accompanied by safety data sheets (SDS) to ensure regulatory compliance and safe delivery. |
| Storage | 3-Amino-4-(Isopropylamino)benzotrifluoride should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers and acids. Store at room temperature, avoiding excessive heat. Ensure proper labeling and restrict access to trained personnel. Follow local regulations for chemical storage and safety. |
Applications of 3-Amino-4-(Isopropylamino)Benzotrifluoride in Industrial ManufacturingAs an established manufacturer of specialty aromatic amines, we supply 3-Amino-4-(Isopropylamino)Benzotrifluoride for advanced synthesis across several industries. The following application scenarios represent established use-cases within regulated and technically demanding production environments. Each application involves distinct compliance frameworks, formulation parameters, process integration steps, and final products, reflecting practical downstream requirements observed in actual manufacturing operations. 1. Agrochemical Synthesis: Herbicide IntermediateThis compound functions as a key intermediate in the multi-step synthesis of fluorinated herbicide actives, especially phenoxy and triazine derivatives. Major agrochemical manufacturers use it for introducing trifluoromethyl-aniline motifs under controlled reaction conditions, contributing to the final herbicide’s selectivity and persistence. Precise molar input ratios and purification are critical, and it must conform to rigorous trace impurity caps due to agricultural residue regulations. Industry compliance standards
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2. Pharmaceutical Intermediate for Fluorinated API SynthesisPharmaceutical synthesis routes employ this aromatic amine in building advanced fluorinated structures, particularly as a side-chain or ring substitute within small-molecule APIs. Medicinal chemistry teams require high purity, low residual solvents, and conformance to global pharmacopoeia guidelines for use in regulated final dosage forms. Integration typically involves hydrogenation or acylation steps, necessitating precise stoichiometry. Industry compliance standards
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3. Advanced Dye & Pigment IntermediateThe compound is utilized in high-value dye manufacturing for electronics and specialty textiles, serving as a key aromatic amine for introducing electronic donor-acceptor balance. Applications require precision in reactivity and chromatic control, particularly in the manufacture of disperse dyes, OLED pigments, and high-purity inkjet colorants. Downstream users focus on consistency, colorfastness, and migration, all governed by end-product claims and end-use safety. Industry compliance standards
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4. Specialty Coatings Raw Material for Fluoropolymer FinishesLeading industrial coating formulators integrate this trifluoromethyl aromatic amine as a reactive chain modifier in specialty fluoropolymer and polyurethane systems. Its introduction enhances hydrophobicity, chemical barrier properties, and UV resistance in engineered coatings. Purity, moisture content, and side-product control are critical for film formation and long-term performance, especially when coatings will be exposed to aggressive environmental factors. Industry compliance standards
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5. Electronic Chemicals: Fluorinated Etchant and Photoresist PrecursorManufacturers in the semiconductor and printed circuit board sectors utilize the compound as a precursor for high-purity etchants and photoresist specialty monomers. The product’s electron-withdrawing trifluoromethyl group imparts unique patternability and resistivity required for advanced lithography. Strict management of particulate content, ionic impurities, and residual water ensures fitness for cleanroom use and minimizes defect rates during wafer and substrate processing. Industry compliance standards
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