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3-Chloro-4,5-Diaminobenzotrifluoride

    • Product Name 3-Chloro-4,5-Diaminobenzotrifluoride
    • Alias 4,5-Diamino-3-chlorobenzotrifluoride
    • Einecs 253-953-2
    • 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
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    Specifications

    HS Code

    318359

    Chemical Name 3-Chloro-4,5-Diaminobenzotrifluoride
    Cas Number 26163-09-3
    Molecular Formula C6H5ClF3N2
    Molecular Weight 196.57
    Appearance Light tan to brown solid
    Melting Point 133-138°C
    Solubility Slightly soluble in water
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, keep container tightly closed, protect from moisture
    Synonyms 3-Chloro-4,5-diamino-α,α,α-trifluorotoluene
    Inchi Key NWDKOSZVTKZVGF-UHFFFAOYSA-N

    As an accredited 3-Chloro-4,5-Diaminobenzotrifluoride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g package contains 3-Chloro-4,5-Diaminobenzotrifluoride in a sealed, amber glass bottle, labeled with hazard and safety information.
    Shipping 3-Chloro-4,5-Diaminobenzotrifluoride is shipped in tightly sealed containers, protected from light and moisture. The chemical is packed and labeled according to international transport regulations for hazardous materials, with clear hazard identification and handling instructions. Transport is typically by ground or air freight, requiring appropriate documentation and safety measures.
    Storage **3-Chloro-4,5-diaminobenzotrifluoride** should be stored in a tightly closed container, in a cool, dry, well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Use appropriate personal protective equipment when handling, and ensure the storage area is equipped for spill containment and proper chemical labeling.
    Application of 3-Chloro-4,5-Diaminobenzotrifluoride

    Applications of 3-Chloro-4,5-Diaminobenzotrifluoride in Industrial Manufacturing

    3-Chloro-4,5-Diaminobenzotrifluoride serves as a highly specialized building block within several fine chemical value chains. Our production integrates stringent quality management to support downstream users in demanding sectors. Below, we provide a detailed overview of core industrial application scenarios, each illustrated with industrial benchmarks for compliance, dosage, process use, and final products.

    1. High-Performance Agrochemical Synthesis

    Leading agrochemical companies use this compound as a key diamine intermediate in selective herbicide and fungicide active ingredient synthesis. During scale-up production, it provides controlled reactivity and consistent halogen content to meet complex formulation requirements for crop protection agents with strict impurity profiles.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides and Formulations
    • ISO 9001:2015 quality management for agrochemical intermediates
    • REACH Regulation (EC) No 1907/2006 for substance registration and safety
    • EPA Registration Standards for Technical Grade Active Ingredients

    Typical usage ratio

    • 4%–7% by mass within multi-step synthesis, adjusted for specific target molecule yield and by-product minimization

    Downstream process integration

    • Enters the reaction during nitroaromatic coupling prior to triazine or pyridine ring closure, followed by purification and isolation under nitrogen atmosphere

    Final product types

    • Herbicide actives based on substituted phenyl urea or triazine chemistry
    • Active intermediates for strobilurin-class fungicides

    2. Advanced Pharmaceutical Intermediate Manufacturing

    Regulated API producers employ this compound for constructing fluorinated aromatic frameworks in antineoplastic and central nervous system drug intermediates. The precise substitution pattern offered improves selectivity profiles during multi-step synthesis campaigns under GMP guidance in validated facilities.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • USP–NF, Ph. Eur., and JP Compendial Monographs for starting materials (when applicable)
    • 21 CFR Part 211 (US FDA) for finished pharmaceutical quality systems
    • Chinese Pharmacopoeia standards for key pharmaceutical intermediates

    Typical usage ratio

    • 0.9–2.3 equivalents in relation to the target coupling reagent, variable according to the API synthesis stage and reaction efficiency

    Downstream process integration

    • Charged after initial halogenation in amidation or Buchwald–Hartwig amination, usually at controlled temperature and pH endpoints

    Final product types

    • Fluorinated aniline intermediates for anticancer drug manufacture
    • Precursor blocks for neuroprotective small molecule APIs

    3. Colorant Intermediate in High-Performance Dye Production

    Dye manufacturers integrating high stability and lightfastness in textile printing colorants utilize this material for making complex azo and anthraquinone dye precursors. Its electron-withdrawing trifluoromethyl and chloro substitutions enhance reactivity control for shades requiring precision in hue consistency and migration resistance.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile chemical inputs
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 14001 Environmental Management for colorant waste management
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) guidelines

    Typical usage ratio

    • 2.5%–5% by molar percentage, tailored in relation to diazotization or coupling partners for targeted chroma saturation

    Downstream process integration

    • Introduced post-sulfonation step for diazo coupling with stabilized aromatic partners, followed by filtration and spray-drying processes

    Final product types

    • Reactive azo dyes for synthetic and natural fiber printing
    • Anthraquinone-based blue and violet dyes for technical textiles

    4. Fluorinated Polymer Additive Manufacturing

    Leading polymer compounders utilize this molecule as a chain-modifying additive to impart chemical resistance in specialty polyimide and polyamide resin systems. Its reactivity and substitution pattern enhance polymer backbones during high-temperature polycondensation, improving solvent and UV stability in mission-critical end-use applications.

    Industry compliance standards

    • ISO 1043-1 designation for fluorinated aromatic polymers
    • UL 94 Flammability Standards for plastic materials
    • RoHS Directive 2011/65/EU for restricted substances
    • EN ISO 9001:2015 for compound manufacturing quality management

    Typical usage ratio

    • 0.5%–1.2% by weight within the polymer matrix, fine-tuned per application for mechanical property retention

    Downstream process integration

    • Dosed in the monomer feed before high-temperature melt polycondensation, then pelletized and compounded for downstream molding

    Final product types

    • High-end electrical insulation films for mobile devices
    • Engineered polymer housings for chemical process equipment

    5. Electronic Materials Precursor for Photoresist Synthesis

    Semiconductor material suppliers leverage this compound in the formulation of advanced aromatic diamine building blocks designed for high-selectivity positive-tone photoresists. Its unique substitution delivers critical resolution and line-edge stability in lithographic patterning processes essential for device miniaturization under cleanroom conditions.

    Industry compliance standards

    • IATF 16949:2016 for electronics materials supply chain management
    • SEMI C57 standard for photoresist raw materials
    • IPC-4101E for supportive laminate compatibility
    • ISO 14644-1 classification for cleanroom integration

    Typical usage ratio

    • 0.7–1.5% by mass of total matrix monomer, dependent on targeted molecular weight and resist patterning characteristics

    Downstream process integration

    • Blended during polycondensation with formaldehyde or aromatic diacid co-monomers, followed by purification and formulation into liquid resist systems

    Final product types

    • Positive-tone photoresists for advanced integrated circuit fabrication
    • Coating precursor resins for flat panel display manufacturing
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