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4-Chloro-3,5-Diaminobenzotrifluoride

    • Product Name 4-Chloro-3,5-Diaminobenzotrifluoride
    • Alias 4-Chloro-3,5-bis(trifluoromethyl)aniline
    • Einecs 249-371-4
    • 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

    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 & Storage
    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.
    Application of 4-Chloro-3,5-Diaminobenzotrifluoride

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

    As 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 Synthesis

    Major 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

    • EN 71-3:2019 (Safety of toys – migration of certain elements)
    • ISO 9001:2015 Quality Management System for chemical process control
    • REACH (EC) No 1907/2006 registration for pigment intermediates
    • Automotive OEM environmental and non-heavy metal pigment requirements

    Typical usage ratio

    • 1.5–5.0% by mass of total pigment batch, adjusted according to targeted color index and pigment type
    • The precise dosage depends on the intended tonal strength and crystallization strategy of end pigment

    Downstream process integration

    • Nitration and cyclization reactions occur early in pigment intermediate manufacturing
    • The raw material is charged into stirred reactors before coupling or condensation under controlled temperature and pH conditions
    • In-line monitoring ensures complete conversion to designated pigment precursor

    Final product types

    • Quinacridone magenta pigments for automotive paint
    • Perylene maroon and violet pigments for industrial coatings
    • High-durability inkjet printer pigments
    • Color masterbatch for engineered plastics in outdoor applications

    2. Agrochemical Active Ingredient Synthesis

    Selective 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

    • FAO/WHO guidelines on technical material purity and trace contaminants
    • GB 2763-2023 (China MRLs for pesticides in food)
    • ISO 9001:2015 certified batch traceability
    • EU Regulation (EC) No 1107/2009—approval of active substances for plant protection

    Typical usage ratio

    • 2–4% by mass in the synthesis of target active intermediates
    • Exact input is process-controlled, set by the stoichiometry of coupling reactions and desired conversion efficiency

    Downstream process integration

    • Feeds into nucleophilic aromatic substitution and diazotization/coupling stages in herbicide or fungicide synthesis
    • Material introduced to reactors under inert atmosphere after solvent charging
    • Sample monitoring through HPLC ensures full incorporation and targeted impurity profile

    Final product types

    • Phenylurea and anilide-based herbicides
    • Systemic fungicide actives for crop protection
    • Pre-emergence weed control agents
    • Post-patent agrochemical intermediates

    3. Commercial Dye Intermediate Manufacturing

    Dye 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

    • ZDHC MRSL v3.1 (Zero Discharge of Hazardous Chemicals, Manufacturing Restricted Substances List)
    • OEKO-TEX Standard 100, Class I (textiles for babies and toddlers)
    • ISO 14001:2015 (Environmental management for dye plants)
    • EU REACH Annex XVII (Restriction of hazardous substances in textiles)

    Typical usage ratio

    • 1.0–2.8% based on the total dye formulation mass
    • Ratio determined by target dye concentration and fastness parameters specified by end-market requirements

    Downstream process integration

    • Charged into diazotization or amination sequence following sulfonation or alkylation of base aromatic core
    • Continuous-flow reactors integrate the material for high-throughput batch operations
    • Retention of trace intermediates minimized by post-reaction purification with activated carbon or ion exchange resins

    Final product types

    • Disperse dyes for polyester fiber and yarn
    • High fastness textile dyes for sportswear and outdoor apparel
    • Printing inks for synthetic fabric transfer applications
    • Reactive dye intermediates for high-performance textile finishing

    4. Advanced Polymer Additive Synthesis

    Suppliers 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

    • ISO 10993-5 (Biocompatibility testing for plastics used in electronics casings and connectors)
    • UL 94 (Flammability of plastic materials for parts in devices and appliances)
    • RoHS Directive 2011/65/EU (Restriction of hazardous substances in electrical products)
    • ISO 178 (Determination of flexural properties of plastics)

    Typical usage ratio

    • 0.3–1.2% relative to total polymer matrix, modulated according to mechanical and flammability target specifications
    • Addition above 1% may negatively influence melt flow index; formulation lab determines ideal proportion by application

    Downstream process integration

    • Material is co-polymerized or post-grafted during extrusion or batch polymerization stages
    • Feeds directly to melt-blending line or autoclave reactors for high-temperature engineering resins
    • FTIR and DSC analysis verify successful chemical incorporation into polymer backbone

    Final product types

    • Fluorinated copolymers for automotive connectors and under-hood components
    • UV- and heat-resistant plastics for solar panel housings
    • High-performance elastomer additives in vibration-damping parts
    • Printed circuit board (PCB) base materials with reduced dielectric loss

    5. Pharmaceutical Intermediate for Active Ingredient Synthesis

    Pharmaceutical 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

    • ICH Q7 GMP for Active Pharmaceutical Ingredient Manufacturing
    • US Pharmacopeia (USP) General Chapter <923> Residual Solvents
    • European Pharmacopoeia Monograph 2034 (General process requirements for synthetic aromatic intermediates)
    • FDA DMF (Drug Master File) filing for advanced intermediates

    Typical usage ratio

    • Typically 0.5–2.0% of the total molecular input for each API synthesis batch, depending on the overall synthetic sequence
    • Pharmaceutical chemists adjust input to minimize residual organohalide burden in final API lot

    Downstream process integration

    • Introduced to amidation or acylation steps following aromatic ring functionalization
    • Purification by recrystallization or preparative HPLC to meet pharmacopeial requirements
    • Lot release supported by validated analytical methods (GC-MS/LC-MS)

    Final product types

    • Advanced chemical intermediates for oncology and anti-inflammatory drugs
    • Selective kinase inhibitor active ingredients
    • Synthetic building blocks for CNS-targeted APIs
    • Patented small-molecule pharmaceutical compounds

    6. Specialty Chemical Intermediate for Liquid Crystal Materials

    Manufacturers 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

    • IEC 62474:2018 (Material declaration for electronic industry supply chains)
    • Sony Green Partner Environmental Quality Approval for LCD materials
    • RoHS and REACH compliance (for electronics and display component chemicals)
    • ISO/TS 16949 (Automotive supply chain electronics quality)

    Typical usage ratio

    • 0.8–1.5% by mass in the synthesis route for target LC compound batches
    • Ratio determined by the degree of substitution specified for each display grade LC system

    Downstream process integration

    • Charged as a nucleophile for amidation or etherification sequences in LC synthesis flow
    • Carefully integrated during pre-purification and rectification to preserve high optical anisotropy
    • Final LC mixture blending performed under nitrogen with trace water removal

    Final product types

    • Twisted nematic (TN) and in-plane switching (IPS) liquid crystal materials
    • Advanced matrix LC mixtures for 4K and 8K display resolutions
    • Custom LC formulations for automotive dashboard displays
    • High-contrast active-matrix LCD screen components
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