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2-(Trifluoromethoxy)Benzenesulfonamide

    • Product Name 2-(Trifluoromethoxy)Benzenesulfonamide
    • Alias 2-(Trifluoromethoxy)benzenesulfonamide
    • Einecs 676-890-1
    • 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

    957835

    Chemical Name 2-(Trifluoromethoxy)Benzenesulfonamide
    Cas Number 61272-80-0
    Molecular Formula C7H6F3NO3S
    Molecular Weight 241.19 g/mol
    Appearance White to off-white solid
    Melting Point 97-101 °C
    Solubility Soluble in DMSO, methanol
    Purity Typically ≥98%
    Smiles NS(=O)(=O)C1=CC=CC=C1OC(F)(F)F
    Inchi InChI=1S/C7H6F3NO3S/c8-7(9,10)15-6-4-2-1-3-5(6)14(11,12)13/h1-4H,(H2,11,12,13)
    Synonyms 2-(Trifluoromethoxy)benzenesulphonamide
    Storage Conditions Store at room temperature, protected from moisture and light

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

    Packing & Storage
    Packing Sealed amber glass bottle, 25 grams, with tamper-evident cap, labeled with chemical name, purity, hazard symbols, and handling instructions.
    Shipping 2-(Trifluoromethoxy)benzenesulfonamide is shipped in tightly sealed, chemical-resistant containers to prevent leakage or contamination. It is transported under ambient conditions, avoiding excessive heat or direct sunlight. The package is clearly labeled with hazard information and handled according to regulations for non-flammable, non-corrosive organic chemicals. Safety data accompanies each shipment.
    Storage **2-(Trifluoromethoxy)benzenesulfonamide** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Avoid exposure to moisture. Store at room temperature, protected from direct sunlight. Label the container clearly, and ensure access is limited to trained personnel using appropriate personal protective equipment (PPE).
    Application of 2-(Trifluoromethoxy)Benzenesulfonamide

    Applications of 2-(Trifluoromethoxy)Benzenesulfonamide in Industrial Manufacturing

    2-(Trifluoromethoxy)Benzenesulfonamide is an advanced building block widely adopted across several chemical manufacturing sectors. As the direct manufacturer, we support demanding integration by providing consistent quality, technical documentation, and full regulatory traceability for industrial partners. Below, we detail its primary downstream uses, each with unique compliance standards, process routes, and product outcomes.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical companies incorporate this compound as a key intermediate in synthesizing specific sulfonamide-containing drug candidates, such as certain kinase inhibitors and anti-inflammatory molecules. The strict control over its purity and traceability enable efficient reaction steps in multi-stage organic synthesis. Researchers and process chemists utilize this intermediate to access target molecules with trifluoromethoxy functional groups, which can improve metabolic stability and bioavailability in the final active pharmaceutical ingredients (APIs).

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP-NF and Ph. Eur. residual solvent and impurity controls
    • FDA 21 CFR Part 210/211 (for API manufacturing)
    • REACH registration for import and safe handling

    Typical usage ratio

    • 0.05–0.3 molar equivalents relative to primary API target
    • Ratio adjusted according to synthesis pathway and substrate reactivity

    Downstream process integration

    • Enters directly after initial aromatic substitution or amidation step
    • Used in coupling reactions involving sulfonamide formation
    • Handled in inert atmosphere for high-value batch synthesis

    Final product types

    • Small molecule APIs containing trifluoromethoxyphenyl motifs
    • Clinical trial candidate molecules
    • Patented kinase and enzyme inhibitors
    • Pharmaceutical process intermediates for further derivatization

    2. Agrochemical Research and Production

    Leading agrochemical innovators use this material to introduce fluorinated sulfonamide groups within selective herbicide and fungicide development projects. It serves as a structural motif to enhance product stability, soil persistence, and environmental profile while reducing toxicity in target applications. Synthetically, it reacts under controlled conditions to produce trial compounds evaluated for biological activity and regulatory submissions.

    Industry compliance standards

    • OECD GLP for R&D and batch traceability
    • FAO/WHO Guidelines on acceptable daily intake for pesticide residues
    • ISO 9001:2015 quality management for agrochemical manufacture
    • EU Regulation (EC) No 1107/2009 on plant protection products

    Typical usage ratio

    • 1–10% w/w in pilot batch synthesis (for new actives screening)
    • Lower ratios for field trial formulations

    Downstream process integration

    • Enters in the heterocycle-forming stage for new herbicide scaffolds
    • Employed during late-stage derivatization and purification
    • Used in R&D labs and pilot-scale kilo-labs for candidate selection

    Final product types

    • Novel pre- and post-emergent herbicides
    • Experimental fungicides for broadacre and specialty crops
    • Patent-protected crop-protection agents
    • Agrochemical process intermediates for further scale-up

    3. Advanced Material and Polymer Modification

    Materials science companies incorporate this compound as a specialty modifier in high-performance polymer formulations. The trifluoromethoxy and sulfonamide functional groups introduce enhanced thermal stability, reduced flammability, and increased chemical resistance for end-use applications in electronics, membranes, and specialty coatings. Engineers blend the compound at specific ratios during polymerization to impart target physicochemical properties.

    Industry compliance standards

    • ASTM D4329 (accelerated ageing for polymer stability)
    • RoHS 2.0 Directive for hazardous substances in electronic materials
    • ISO 10993 for biocompatible materials (for membrane/contact applications)
    • REACH SVHC screening for non-listed substances

    Typical usage ratio

    • 0.1–2% by weight in advanced polymer formulations
    • Ratio optimized based on desired performance metrics and matrix compatibility

    Downstream process integration

    • Added during pre-polymerization blend for specialty resin manufacturing
    • Post-reacted or end-capped into existing polymer chains
    • Processed under controlled temperature and mixing protocols for uniform dispersion

    Final product types

    • Electronic circuit board coatings for high-temperature use
    • Membrane materials for filtration and gas separation
    • Low-flammability engineering plastics
    • Specialty films for industrial and medical device applications

    4. Organic Synthesis Reagent for Fluorinated Compound Manufacture

    Specialty chemical producers use 2-(Trifluoromethoxy)Benzenesulfonamide as a reagent in preparing diverse fluorinated compounds for further applications in flavors, fragrances, and specialty fine chemicals. It participates in selective transformations, such as sulfonamidation and nucleophilic aromatic substitution, adding value due to its electron-withdrawing and hydrophobic properties. Process chemists design multi-step reactions where its structure enables unique substitution patterns not accessible from other sulfonamides.

    Industry compliance standards

    • ISO 9001:2015 quality management for specialty chemicals
    • Hazardous chemical registration and safe handling under GHS/CLP
    • GMP Part II (for food-contact or pharma-adjacent intermediates)
    • Local environmental and waste disposal regulations (e.g., US EPA)

    Typical usage ratio

    • Stoichiometric to slight excess (1.0–1.2 molar equivalents) in preparative reactions
    • Optimization based on nucleophile/electrophile reactivity and scale

    Downstream process integration

    • Used in early-to-mid-stage synthetic transformations for fluorinated side-chains
    • Combined in automated flow and batch reactors
    • Reaction monitored using HPLC/GC for product quality control

    Final product types

    • Fluorinated intermediates for fine chemicals
    • Precursors for fragrance and flavor formulation
    • Custom reagents for contract synthesis partners
    • Halogenated specialty ingredients for downstream industry use
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    Certification & Compliance
    More Introduction

    Introducing 2-(Trifluoromethoxy)Benzenesulfonamide: A Manufacturer’s Perspective

    Understanding 2-(Trifluoromethoxy)Benzenesulfonamide

    The story of 2-(Trifluoromethoxy)Benzenesulfonamide starts on the shop floor, where chemistry and engineering meet to create a versatile compound valued in research and development. In the production environment, familiar scents from sulfonamide reactions linger as operators monitor each vessel for signs of complete conversion and purity standards. Decades of hands-on experience have taught us that not all benzenesulfonamides behave the same, especially once the trifluoromethoxy group attaches itself to the aromatic ring. That simple change brings a world of difference to the final product’s reactivity and application potential.

    This molecule offers a unique profile: a trifluoromethoxy group situated at the ortho position of the aromatic ring, paired with a sulfonamide function para to it. With a molecular formula of C7H6F3NO3S and relative molecular mass in the mid-200s, 2-(Trifluoromethoxy)Benzenesulfonamide stands apart from simpler sulfonamides in both behavior and processability, which has made it a favorite among those engaged in medicinal chemistry discovery and agrochemical synthesis.

    From Reactor to Finished Material: What We Know About Synthesis

    Manufacturing this compound brings its own set of challenges. Each stage from raw material selection, handling aggressive reagents, temperature controls, agitation speeds, and even filtration methods influences final quality. Beginning with substituted anilines and progressing through selective trifluoromethoxylation and sulfonamidation steps, we maintain strict environmental safeguards and monitor every batch for trace byproducts. The trifluoromethoxy group tests our engineering know-how; managing pressure and heat is critical. We’ve refined our protocols for years, using GC-MS and NMR to assure consistency, so that customers get a reproducible compound every shipment.

    Every operator on our lines knows that poor heat transfer, improper washing, or skipping QC checks can ruin an entire batch. Instead, we’ve built a culture around vigilance and pride in our craft. Only those who stand on the front lines, hour after hour, appreciate the stubborn impurities that this chemistry can yield if equipment fouls or temperatures drift. So we invest in batchwise process analysis and routine cleaning cycles, saving countless hours in troubleshooting and waste remediation.

    Purity and Specifications: Standards That Shape Research Progress

    Our product typically leaves the drying oven as a white to off-white solid, matched to published literature for appearance and melting point. Purity consistently exceeds 98% by HPLC and NMR standards. We track water content using KF titration and residual solvents via headspace GC, preventing issues in downstream formulation or catalysis applications. Appearance can tell an experienced operator plenty about in-batch contamination: a subtle hue shift warns of incomplete washing or excess byproduct retention, cues missed by less practiced eyes.

    We maintain a straightforward specification set, honed over decades in the industry. Purity thresholds are based on our own kinetic and thermodynamic process experience, sensitive to even trace color bodies. Physical consistency—granular, free-flowing, with minimal dust—reflects hours of hands-on labor in drying and packaging cycles. The close relationship between our plant staff and technical team means concerns move from laboratory bench to kilogram-scale reactors without delay.

    Application Insights: Why Trifluoromethoxy Changes Everything

    The trifluoromethoxy group isn’t just a decorative substituent for synthetic chemists; it tunes the electron density on the aromatic ring and influences how the molecule interacts in biological or catalytic systems. In medicinal chemistry, researchers depend on this exact substitution to improve metabolic stability of a drug candidate, minimize off-target activity, or enhance blood-brain barrier penetration. Our QC chemists talk to customer labs every year, learning how formulation tweaks with our 2-(Trifluoromethoxy)Benzenesulfonamide feed into patent filings and clinical progress. This feedback loops back into how we control trace impurities and lot-to-lot color.

    In agrochemical circles, the perfomance of the trifluoromethoxy group brings advantages in pest- or weed-resistance studies. Sulfonamide linkages, known for their flexibility, let agrochemical researchers adjust molecular scaffolds rapidly, then optimize for activity and persistence. Our product stands out because we make it at industrial-scale, while still maintaining tight controls that minimize minor side products—critical for research translation, regulatory submission, and field trial success. Customers gravitate towards this particular compound over simpler benzenesulfonamides, noting the consistent performance in their syntheses and down-the-line biological outcomes.

    Comparing to Other Benzenesulfonamides: Nuanced Differences in Use

    Experience teaches us that benzenesulfonamides as a class cover a range of behaviors, depending on what functional groups are installed and where. The trifluoromethoxy modification at the ortho position brings unique electronic properties, impacting both physical handling and reactivity. Unsubstituted benzenesulfonamides or those carrying alkoxy groups at other positions generally exhibit improved water solubility but lack the metabolic resilience of our product. On the production floor, the trifluoromethoxy group increases volatility of side fragments, raising the stakes for safe containment and waste management.

    Reactions using 2-(Trifluoromethoxy)Benzenesulfonamide tend to complete under milder conditions than those employing heavily substituted analogs. The electron-withdrawing trifluoromethoxy group both activates the ring for certain coupling reactions and modifies acid-base balance during sulfonyl chloride activation. Customers mention that downstream purification becomes more straightforward thanks to reduced byproduct formation, shortening time to assay and formulation. That difference means less turnaround time for delivery, greater batch reproducibility, and lowered risk of scale-up issues.

    Smaller producers or those who work through third parties often struggle to balance purity with volume, which can lead to inconsistency from lot to lot. By having all synthesis and purification steps under our roof, we control the entire chain and respond instantly if a test result falls below the line. That’s particularly important for unique fluorinated aromatics like 2-(Trifluoromethoxy)Benzenesulfonamide, where resin and solvent carryover can create subtle but costly contamination.

    Our Experience and Continuous Improvement in Manufacturing

    As a manufacturer, we learn most from problems and unexpected outcomes. Years ago, an unexpected crystal habit formed during scale-up caused blockages nearly every cycle. Addressing this meant re-investigating raw solvent choices, seed crystal maturity, and temperature ramp rates—steps often ignored in basic protocols. Colleagues with better instincts for manual sampling outperformed heuristics software, catching issues earlier and saving substantial batches. Our best process improvements come from a blend of chemistry fundamentals and the day-to-day experience that comes from making this compound hundreds of times per year.

    Trace metal contamination was another key concern. Early batches picking up unexpected palladium or copper forced us to refine filtration regimes and source new gaskets, lines, and reactor coatings. The learning curve reinforced the value in regular in-house equipment audits and weekly analytical checks, which have now become standard. None of these things surface in textbooks or vendor recommendations but matter hugely for delivering material that passes even the most demanding research compliance screens.

    A Trusted Tool in Discovery and Development

    We see our customers use 2-(Trifluoromethoxy)Benzenesulfonamide as a building block in both discovery-stage chemistry and in later-stage candidate optimization. Some prefer its clean conversion in Pd- or Cu-catalyzed cross-coupling reactions. Others mention how the trifluoromethoxy substitution assists in late-stage functionalization of complex scaffolds—a job poorly suited to analogues lacking both the electron-withdrawing strength and the unique steric effects of the group. Our technical team often collaborates on troubleshooting tricky routes, advising on temperature windows or solvent compatibility from the perspective of scale manufacturing.

    Feedback from medicinal chemistry teams points out accelerated SAR cycles and increased throughput in screening campaigns. In an industry where every week saved can advance a patent or publication, dependable supply and quality make a real-world difference. Our decades spent perfecting this product mean fewer unpleasant surprises for researchers confronting aggressive timelines and moving targets.

    Quality Assurance Born from Experience

    Every vessel we clean and batch we test reinforces the importance of process integrity. Poor containment once led to batch cross-contamination, forcing us to halt operations and track the problem to a leaking gasket. These hard lessons build a culture of accountability and respect for standard operating procedures, from raw material reception through in-process monitoring, polishing, and final packaging. Unlike anonymous commodity traders, we stake our reputation on each drum and kilo. Instrumental verification comes alongside bench chemists’ inspection; both matter.

    Customers want transparency—clear impurity profiles, direct lines for feedback, and openness about unusual results. Having every step under one roof lets us trace any issue back and prevent recurrence. Regulatory compliance is not an afterthought; it comes from everyday diligence and repeated investment in both equipment and people.

    Addressing the Real-World Challenges: Waste, Safety, and Environmental Responsibility

    Those who handle trifluoromethylation know the unique hazards involved. Our people manage not just the chemistry but also the safety systems that keep hazardous byproducts out of the environment and our operators out of harm’s way. We’ve invested in scalable scrubber technology and solvent recovery lines, minimizing emissions and reducing waste going to incineration. Quarterly reviews of all air and water outflow data keep us ahead of evolving regulations, not just compliant but committed to being responsible stewards of our chemical know-how.

    Service teams track process incidents and operational data, comparing performance year-to-year and between lines. That kind of learning keeps us nimble and ahead of shifts in market demand or government oversight. Operators run mock-drills and keep emergency gear on hand, moving safety from paperwork into day-to-day action.

    Building Enduring Relationships with Customers and Partners

    Long-term reliability speaks for itself. Our history of dependable supply during volatile global conditions proves the value of integrated, local production. Customers have contacted us when other suppliers fell short or when variable import quality threatened research progress. Our entire process chain—from raw material procurement to final QA approval—remains transparent and open to audit.

    We’ve worked side-by-side with R&D labs and process engineers in establishing new routes, troubleshooting failed reactions, and researching novel end-uses for trifluoromethoxy aromatics. Our technical teams stay plugged into current literature and patent landscapes, anticipating customer needs. Rather than just shipping product, we commit to supporting clients through experimental setbacks and scale-up pain points.

    Why 2-(Trifluoromethoxy)Benzenesulfonamide Represents a Step Forward

    Nearly every advance in specialty chemistry reflects trust between makers and users. With 2-(Trifluoromethoxy)Benzenesulfonamide, we bring together deep process experience, attention to material handling, and unbroken feedback cycles with end users—turning a specialized molecule into a foundation for innovation in modern chemistry.

    The trifluoromethoxy group gives researchers a new lever for fine-tuning molecular properties, an option less accessible even just a decade ago for many organizations. Our internal benchmarks, refined through hundreds of batches and direct customer dialogue, reflect the importance of rigorous standards and close relationships spanning years. We keep listening, adapt our equipment, adjust our SOPs, and train our people, always with an eye toward getting the best possible material into scientists’ hands.

    Every advance in product quality or environmental performance traces back to honest, careful effort. We wake up every morning to the same challenges as our customers—demand for purity, pressure for consistency, unpredictability in research priorities and regulatory realities. Our role as a producer means continual self-assessment and visible investment in the next level of technical and service excellence. For those exploring new chemical frontiers or streamlining their operations, our product stands ready to support the journey.