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3-(Trifluoromethyl)Benzenesulfonamide

    • Product Name 3-(Trifluoromethyl)Benzenesulfonamide
    • Alias TFMSA
    • Einecs 236-774-9
    • 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

    527583

    Chemical Name 3-(Trifluoromethyl)Benzenesulfonamide
    Cas Number 353-34-8
    Molecular Formula C7H6F3NO2S
    Molecular Weight 225.19
    Appearance White to off-white solid
    Melting Point 104-108°C
    Solubility Slightly soluble in water
    Purity Typically ≥98%
    Smiles NS(=O)(=O)C1=CC(=CC=C1)C(F)(F)F
    Inchi InChI=1S/C7H6F3NO2S/c8-7(9,10)5-1-2-6(4-3-5)14(11,12)13/h1-4H, (H2,11,12,13)
    Storage Temperature Room temperature
    Synonyms m-(Trifluoromethyl)benzenesulfonamide

    As an accredited 3-(Trifluoromethyl)Benzenesulfonamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Packaging: 25 g of 3-(Trifluoromethyl)benzenesulfonamide is supplied in a sealed amber glass bottle with a tamper-evident cap.
    Shipping 3-(Trifluoromethyl)benzenesulfonamide is typically shipped in tightly sealed containers to prevent contamination and moisture exposure. It should be packaged according to chemical safety regulations, labeled appropriately, and transported in compliance with applicable local and international guidelines. Handle with care, avoiding extreme temperatures, and refer to the Safety Data Sheet (SDS) for further instructions.
    Storage Store **3-(Trifluoromethyl)benzenesulfonamide** 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 and acids. Protect from moisture and direct sunlight. Use appropriate personal protective equipment when handling. Clearly label storage containers, and follow all relevant safety protocols and local regulations.
    Application of 3-(Trifluoromethyl)Benzenesulfonamide

    Applications of 3-(Trifluoromethyl)Benzenesulfonamide in Industrial Manufacturing

    3-(Trifluoromethyl)benzenesulfonamide serves as a crucial intermediate in multiple advanced manufacturing sectors. Our facility supplies this compound at industrial scale for regulated downstream product formulations. Below are key application tracks, including compliance references, recommended proportions, process input points, and typical end products.

    1. Pharmaceutical API Synthesis (Selective Sulfonamide Building Block)

    Pharmaceutical companies utilize this intermediate for synthesizing sulfonamide-containing active pharmaceutical ingredients, particularly in the development of selective enzyme inhibitors and anti-infective agents. The unique electron-withdrawing trifluoromethyl group allows for targeted binding profiles and improves the metabolic stability of final molecules. Our QC systems support stringent batch traceability, vital in GMP-regulated supply chains.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for APIs)
    • EU Regulation (EC) No 1907/2006 (REACH)
    • United States Pharmacopeia (USP) General Chapters & Monographs
    • Japanese Pharmacopoeia (JP)

    Typical usage ratio

    • Added at 0.8%–2.5% in API stepwise synthesis by molar equivalence; ratio adjusted based on target compound and route complexity

    Downstream process integration

    • Introduced during Stage 2–3 of multi-step synthesis, after scaffold assembly; involved in direct sulfonamide coupling via nucleophilic substitution or amide bond formation

    Final product types

    • Antibacterial APIs
    • Kynurenine pathway inhibitors
    • Enzyme inhibitor drugs for oncology
    • Research-grade reference standards

    2. Agrochemical Intermediates (Sulfonylurea Herbicide Production)

    Agrochemical producers rely on this compound as a sulfonamide precursor in the manufacture of sulfonylurea-based herbicides. The trifluoromethyl substituent enhances herbicidal activity, selectivity, and environmental stability. We support full documentation and on-site audits for bulk procurement relevant to EPA-regulated markets.

    Industry compliance standards

    • US EPA Registration Regulations (40 CFR)
    • FAO/WHO Specifications for Pesticides
    • EU Plant Protection Products Regulation (EC) No 1107/2009
    • ISO 9001:2015 Quality Management System

    Typical usage ratio

    • Commonly 1.2–1.6 molar equivalents per sulfonylurea coupling reaction; adjusted by plant-specific conversion efficiency

    Downstream process integration

    • Fed into the condensation stage, where it reacts with urea derivatives under controlled temperature and pH to form the herbicide core

    Final product types

    • Mesosulfuron-methyl technical concentrate
    • Tribenuron-methyl granules
    • Finished sulfonylurea herbicide formulations (EC, WG)
    • Active ingredient intermediates for further modification

    3. Specialty Polymer Additives (Performance Modification of Engineering Plastics)

    Polymer compounders use this compound to introduce fluorinated sulfonamide groups in high-performance engineering plastics. Implementation improves flame retardancy, lowers surface energy, and optimizes dielectric properties for demanding electronic and aerospace applications. We supply detailed impurity profiles for inclusion in advanced compounding operations.

    Industry compliance standards

    • UL 94 Flammability Standards
    • RoHS Directive (2011/65/EU) for Electronics
    • ISO 10993 (parts relevant for polymer biomaterials)
    • ASTM D5138 (plastics performance testing)

    Typical usage ratio

    • Used at 0.5%–1.5% by polymer weight, depending on final application profile and required mechanical properties

    Downstream process integration

    • Added during twin-screw extrusion or melt blending stage, followed by pelletizing; dispersion monitored via FTIR and DSC analysis

    Final product types

    • Flame-retardant polyamides (PA6, PA66 compounds)
    • Dielectric polyimide films
    • Modified polyphenylene sulfide (PPS) resins
    • Aerospace-grade insulating components

    4. Medicinal Chemistry Research Reagents (Lead Optimization & Structure-Activity Studies)

    CROs and pharmaceutical innovation labs incorporate this compound during medicinal chemistry workflow, especially in the late-stage diversification of lead molecules aimed at optimizing selectivity and ADME properties. Batch-level documentation supports regulatory submission and in-house SAR documentation workflows. Supply is offered with full CoA and impurity traceability critical to preclinical development.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • FDA 21 CFR Part 58 for Nonclinical Laboratory Studies
    • ISO 17025 (laboratory competence)
    • Company-specific analytical test protocols

    Typical usage ratio

    • Solution-phase coupling reactions: 0.5–1.3 equivalents per SAR analog; optimized based on reactivity of core scaffold

    Downstream process integration

    • Employed in lead optimization by direct sulfonamide attachment or as a precursor for late-stage fluorinated modifications

    Final product types

    • SAR compound libraries
    • Preclinical drug leads
    • Analytical standards for bioassays
    • Fluorinated probe molecules

    5. Advanced Dye and Pigment Synthesis (Functional Dyestuff Intermediates)

    Producers of specialty dyes and pigments include this intermediate to modify solubility and fastness properties, particularly in applications requiring fluorination for high resistance to solvents or heat. The compound supports high purity levels required in the coloration of engineering textiles and specialty coatings, with traceable sourcing for demanding compliance audits.

    Industry compliance standards

    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) Guidelines
    • REACH Substance Evaluation (for colorants)
    • ISO 105 Series (Textile color fastness)
    • ZDHC MRSL Guidelines

    Typical usage ratio

    • Incorporated at 0.2%–1.0% by reaction mass, tuned to target solubility and lightfastness levels in final dye structure

    Downstream process integration

    • Used in the diazotization stage of azo dye synthesis, or in condensation reactions to improve molecular rigidity and UV stability

    Final product types

    • Solvent-stable disperse dyes
    • Heat-resistant pigment intermediates
    • Technical dye colorants for plastics and fibers
    • Fluorinated textile finishes
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