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2-Fluorobenzenesulfonamide

    • Product Name 2-Fluorobenzenesulfonamide
    • Alias 2-Fluorobenzenesulfonamide
    • Einecs 243-125-4
    • 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
    VTB
    Specifications

    HS Code

    324307

    Product Name 2-Fluorobenzenesulfonamide
    Cas Number 456-17-7
    Molecular Formula C6H6FNO2S
    Molecular Weight 175.18 g/mol
    Appearance White to off-white solid
    Melting Point 98-102 °C
    Purity Typically ≥98%
    Solubility Soluble in DMSO, slightly soluble in water
    Smiles C1=CC=C(C(=C1)F)S(=O)(=O)N
    Inchi InChI=1S/C6H6FNO2S/c7-5-3-1-2-4-6(5)11(8,9)10/h1-4H,8H2
    Synonyms 2-Fluorobenzenesulphonamide; o-Fluorobenzenesulfonamide
    Storage Conditions Store at room temperature, keep container tightly closed

    As an accredited 2-Fluorobenzenesulfonamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Fluorobenzenesulfonamide is packaged in a 25g amber glass bottle, with a tamper-evident cap and safety labeling.
    Shipping 2-Fluorobenzenesulfonamide is shipped in tightly sealed containers to prevent moisture exposure and contamination. The chemical is classified as non-hazardous for transport but should be secured and clearly labeled. It is shipped at ambient temperature, following standard regulations for chemical substances, with proper documentation and safety data included.
    Storage 2-Fluorobenzenesulfonamide should be stored 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. Protect it from moisture and direct sunlight. Ensure proper labeling and secure storage to prevent accidental release. Always follow local regulations and laboratory safety protocols for chemical storage.
    Application of 2-Fluorobenzenesulfonamide

    Applications of 2-Fluorobenzenesulfonamide in Industrial Manufacturing

    As an established manufacturer of 2-Fluorobenzenesulfonamide, we supply this specialty intermediate to a concentrated range of value-added industrial sectors. Our experience underlines its application in pharmaceutical active synthesis, agrochemical production, performance dyeing agents, and polymer additive modification. The following scenarios detail specific integration methods, safety and quality requirements, technical inclusion rates, and downstream product categories adopted by our global business partners.

    1. Pharmaceutical Active Ingredient Synthesis

    Pharmaceutical manufacturers integrate 2-Fluorobenzenesulfonamide as a sulfonamide group donor in the synthesis of select N-heterocyclic structures, specifically for non-steroidal anti-inflammatory drugs (NSAIDs) and certain anti-microbial APIs. Its fluorinated moiety allows for targeted receptor interaction and favorable drug metabolism profiles, given stringent regulatory and impurity controls in pharmaceutical applications. Synthetic protocols incorporate the material at the stage of sulfonamidation, forming key intermediates before subsequent cyclization or acylation steps.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice (GMP) Guide for Active Pharmaceutical Ingredients
    • USP General Chapters <467> (Residual Solvents)
    • European Pharmacopoeia (Ph. Eur.) individual monographs guidance for related substances
    • 21 CFR Part 211 (US FDA CGMP for finished pharmaceuticals)

    Typical usage ratio

    • Input at 0.15–0.25 molar equivalents relative to the primary amine component; precise ratio adjusted based on targeted yield and downstream impurity profiles required by the finished API specification.

    Downstream process integration

    • Introduced during sulfonamidation step under nitrogen at 60–80°C in polar aprotic solvents, followed by aqueous work-up and purification, prior to heterocycle formation or further functional group modification.

    Final product types

    • Non-steroidal anti-inflammatory API intermediates
    • Antimicrobial drug candidates (preclinical and clinical)
    • Sulfonamide-based intermediate compounds for secondary functionalization

    2. Agrochemical Intermediate Production

    Major crop protection manufacturers utilize 2-Fluorobenzenesulfonamide in the multi-step synthesis of selective herbicides and fungicide actives. Its stable sulfonamide unit and aromatic fluorine substitution offer selective bioactivity when incorporated into heteroaromatic scaffolds. This compound enters the process during active ingredient construction, before cyclization and formulation of technical material, ensuring compliant impurity levels and batch consistency under agrochemical quality standards.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management Systems
    • Regulation (EC) No 1907/2006 (REACH) for chemical substance registration
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • Active ingredient assembly step: 2–7% w/w based on the molar equivalent of the primary precursor; actual consumption rate determined by the selectivity and by-product minimization parameters set by each own plant protocol.

    Downstream process integration

    • Charged to sulfonamidation reactors prior to coupling with pyridine or triazine bases, conducted under controlled temperature and monitored for unreacted starting materials; isolated intermediates progress to technical active formulation.

    Final product types

    • Selective triazine and pyridine herbicides
    • Fungicidal active intermediates for cereals and oilseeds
    • Custom sulfonamide building blocks for new pesticide candidate molecules

    3. Performance Dye and Pigment Formulation

    Leading colorant producers add 2-Fluorobenzenesulfonamide during the synthesis of high-performance azo and anthraquinone dyes. By modifying diazonium intermediates, it imparts increased solvent resistance and stability in textile and plastics applications. The sulfonamide linkage forms part of the chromogenic system, especially for technical dyes requiring durable coloration performance on synthetic fibers and polyolefins. Batch formulation and quality checks align with international dye standards, and the compound is precisely dosed to minimize waste and optimize chroma and lightfastness.

    Industry compliance standards

    • ISO 105-C06:2010 (Textiles — Tests for color fastness)
    • Oeko-Tex Standard 100 (Textile ecotoxicology)
    • EN 71-3:2019 (Migration of certain elements — Safety requirements for toys)
    • REACH Annex XVII (Restriction of certain hazardous substances in dyes/pigments)

    Typical usage ratio

    • 1.2–2.5% w/w relative to the diazotized aromatic amine precursor; rate varied by desired shade depth, substrate compatibility, and endpoint application requirements set by each customer’s color formulation.

    Downstream process integration

    • Reacted with pre-formed diazonium salts in aqueous acid phase, typically at 0–5°C, followed by coupling, filtration, and washing; end-use pigment formulation further dispersed with resin or polymer matrices as required for the specific industrial route.

    Final product types

    • Solvent- and lightfast textile dyes (polyester/acrylic fibers)
    • Plastic pigments for automotive parts and masterbatch
    • Specialty ultramarine and violet technical colorants for industrial coatings

    4. Polymer Modifier Additive Manufacturing

    Producers of specialty polymers incorporate 2-Fluorobenzenesulfonamide as a functional additive to modify thermal and electrical profiles of engineering plastics. The compound reacts with polymer chains or acts as a chain terminator, introducing controlled sulfonamide groups to tailor dielectric properties, flame resistance, or surface hydrophobicity. Addition occurs inline during melt-kneading or solution polymerization and requires quality assurance measures to comply with electrical and mechanical industry norms.

    Industry compliance standards

    • UL 94 (Tests for flammability of plastic materials)
    • ASTM D638 (Standard Test Method for Tensile Properties of Plastics)
    • IEC 60243-1 (Electric strength of insulating materials)
    • ISO 9001:2015 (Polymer manufacturing quality systems)

    Typical usage ratio

    • 0.05–0.2% w/w as a processing additive or modifier; optimized in pilot batches according to targeted improvement in dielectric breakdown voltage or flame retardancy rating for the specific engineering resin system.

    Downstream process integration

    • Fed into the polymer melt at compounding stage, homogenized via twin-screw extruder or high-shear solution batch; additive dispersal monitored by spectroscopy or chromatographic analysis to ensure uniformity prior to final shaping or granulation.

    Final product types

    • High-performance electrical insulating films
    • Flame-retarded engineering polymer pellets for automotive and electronics
    • Antistatic and hydrophobic masterbatch compounds
    Free Quote

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    Certification & Compliance