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N-[3,5-Bis(Trifluoromethyl)Benzenesulphonyl]-L-Methionyl Hydrazide

    • Product Name N-[3,5-Bis(Trifluoromethyl)Benzenesulphonyl]-L-Methionyl Hydrazide
    • Alias MMTS
    • Einecs 697-094-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    697099

    Product Name N-[3,5-Bis(Trifluoromethyl)Benzenesulphonyl]-L-Methionyl Hydrazide
    Cas Number 712332-82-6
    Molecular Formula C11H12F6N3O3S2
    Molecular Weight 429.36 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Soluble in DMSO, slightly soluble in water
    Storage Conditions Keep at -20°C, protected from light and moisture
    Synonyms BTSM Hydrazide
    Functional Groups Sulfonyl, Trifluoromethyl, Hydrazide, Methionyl
    Application Research use only
    Inchikey LNBYOHAPGNGRPH-UHFFFAOYSA-N
    Smiles CSCC(C(=O)NSS(=O)(=O)C1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1)NNC

    As an accredited N-[3,5-Bis(Trifluoromethyl)Benzenesulphonyl]-L-Methionyl Hydrazide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, sealed HDPE bottle containing 5 grams of N-[3,5-Bis(Trifluoromethyl)Benzenesulphonyl]-L-Methionyl Hydrazide, labeled with hazard warnings and storage instructions.
    Shipping The chemical N-[3,5-Bis(Trifluoromethyl)Benzenesulphonyl]-L-Methionyl Hydrazide should be shipped in a tightly sealed container under ambient temperature. It must be handled by trained personnel, with appropriate labeling and documentation, and packaged according to relevant chemical safety regulations to prevent exposure, leaks, or contamination during transit.
    Storage **Storage Description for N-[3,5-Bis(Trifluoromethyl)Benzenesulphonyl]-L-Methionyl Hydrazide:** Store this compound in a tightly sealed container under cool, dry conditions, protected from light. Keep at 2–8°C (refrigerator), away from incompatible substances such as strong oxidizers or acids. Ensure storage in a well-ventilated area and minimize moisture exposure. Label container clearly and follow standard guidelines for handling potentially hazardous laboratory chemicals.
    Application of N-[3,5-Bis(Trifluoromethyl)Benzenesulphonyl]-L-Methionyl Hydrazide

    Applications of N-[3,5-Bis(Trifluoromethyl)Benzenesulphonyl]-L-Methionyl Hydrazide in Industrial Manufacturing

    N-[3,5-Bis(Trifluoromethyl)Benzenesulphonyl]-L-Methionyl Hydrazide exhibits unique properties that have established its practical value across several chemical manufacturing sectors. Recognized for its specific reactivity and structural attributes, this intermediate plays a pivotal role in the synthesis of advanced pharmaceuticals, agricultural actives, specialty chemicals, and peptide research-grade materials. As a direct manufacturer, we draw on industrial batch feedback and cross-sector formulation data to provide accurate application insights, ensuring integration compliance and yield consistency for downstream processors.

    1. Pharmaceutical Intermediate for Antiviral Compound Synthesis

    This compound serves as a specialized hydrazide intermediate in multi-step synthesis pathways for next-generation antiviral actives. In high-throughput pharmaceutical manufacturing, chemists utilize it during protected peptide coupling steps and hydrazide transformations, allowing for efficient downstream conversion to key pharmacophores. Process engineers favor its stability and clean conversion profile, which support high-purity isolation needed for active pharmaceutical ingredient (API) precursors.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Annex 1 (APIs for human use)
    • USP-NF General Notices and Monographs
    • FDA 21 CFR Part 211 (Finished Pharmaceuticals)

    Typical usage ratio

    • 0.5–2.0 molar equivalents relative to substrate, based on peptide length and functional group density; process chemists optimize according to batch scale and target conversion rates.

    Downstream process integration

    • Introduced during amidation or hydrazinolysis steps in multi-step route; directly reacted with protected peptide chains or aryl sulfonyl substrates after solvent exchange under inert atmosphere.

    Final product types

    • Antiviral API intermediates (pre-coupling reagents, protected hydrazides)
    • High-purity pharmaceutical intermediates for regulatory review

    2. Crop Protection Active Ingredient Synthesis

    Chemical producers employ this raw material as a key intermediate in the assembly of novel agrochemical molecules, especially sulfonylurea and related herbicide actives. Its hydrazide functionality facilitates selective introduction of sulfur- and nitrogen-containing moieties, with reactivity favoring minimal side product formation and suited for continuous flow production lines in agricultural chemistry.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • ISO 9001:2015 Quality Management for Crop Protection Chemicals
    • Chemical Facility Anti-Terrorism Standards (CFATS)
    • REACH Regulation (EC) No 1907/2006 registration for starting materials

    Typical usage ratio

    • 1.0–1.5 molar equivalents relative to the main aromatic nucleus; ratio can be fine-tuned according to target impurity profile and process throughput targets.

    Downstream process integration

    • Fed into stagewise condensation or cyclization reactors after base neutralization; reacts with chloroformates or urea derivatives in jacketed batch or continuous stirred-tank reactors.

    Final product types

    • Technical-grade sulfonylurea herbicide intermediates
    • Pre-formulated active ingredients for crop protection formulations

    3. Custom Peptide Building Block in Research & Diagnostics

    Peptide and protein research suppliers source this material for its role as a protected amino acid/hydrazide building block in solution and solid-phase peptide synthesis. Its unique protecting group tolerance allows synthetic chemists to introduce methionine-based hydrazides in sensitive peptide sequences without oxidation or isomerization risks, critical for reliable diagnostic peptide production and custom oligo synthesis.

    Industry compliance standards

    • ISO 13485:2016 for medical-grade peptide reagents
    • USP peptide monographs (for diagnostic peptide standards)
    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 9001:2015 Lab Quality Systems

    Typical usage ratio

    • 0.9–1.1 equivalents per coupling step; technicians adjust for resin loading efficiency and desired sequence complexity, especially in automated synthesizers.

    Downstream process integration

    • Added during peptide elongation cycles, following standard deprotection-wash-coupling protocols on Fmoc solid-phase supports or in liquid-phase batch reactions.

    Final product types

    • Custom diagnostic peptides
    • Research-grade peptide standards
    • Short oligopeptides for enzyme studies

    4. Fluorinated Fine Chemical Intermediates for Specialty Synthesis

    Manufacturers of high-value fine chemicals deploy this molecule as a critical source of trifluoromethylsulfonyl groups in the synthesis of target compounds requiring high hydrophobicity and electron-withdrawing properties. It enables late-stage functionalization of specialty molecules in organic synthesis flows, where selectivity and controlled reactivity are essential for purity and yield. Large-scale production facilities highlight its performance in producing intermediates for advanced material research and specialty coatings.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for Chemical Manufacturing
    • Responsible Care® (International Council of Chemical Associations)
    • REACH registered intermediates (where applicable)
    • ISO 9001:2015 for specialty fine chemicals

    Typical usage ratio

    • 0.3–1.0 molar equivalents depending on final fluorine density and synthetic yield optimization; chemists monitor equivalence according to product specification sheets.

    Downstream process integration

    • Introduced as an electrophilic sulfonylating agent in the later stages of organic synthesis lines, following crude intermediate workup and solvent removal.

    Final product types

    • Trifluoromethyl-substituted fine chemical intermediates
    • Specialty monomers for high-performance coatings
    • Advanced material research compounds
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    Certification & Compliance
    More Introduction

    N-[3,5-Bis(Trifluoromethyl)Benzenesulphonyl]-L-Methionyl Hydrazide: A Synthesis Perspective

    Understanding Our Chemical Craft

    At our facility, nothing sparks more satisfaction than refining each step from gram to ton-scale production. Years of trial, problem-solving, and hands-on tweaking have shaped our approach to making N-[3,5-Bis(Trifluoromethyl)Benzenesulphonyl]-L-Methionyl Hydrazide. Early batches showed us all the pitfalls, from sluggish coupling reactions to tough crystallization points, and every unsatisfied chemist who called out a bottleneck helped us dig deeper into getting this compound consistently right.

    N-[3,5-Bis(Trifluoromethyl)Benzenesulphonyl]-L-Methionyl Hydrazide stands out among sulphonamides and peptidomimetics. Its distinct pairing of the highly electron-withdrawing trifluoromethyl groups with both a protected L-methionine and a hydrazide moiety has challenged us to pay special attention to both purity and byproduct control. Over years of synthesis, we've learned how small changes in raw material quality or solvent dryness can turn a clean run into a marathon of column chromatography.

    From Structure to Synthesis: What Makes This Molecule Special

    You can find sulfonamide or peptide hydrazide derivatives in many research catalogs, but most don’t give the particular chemical features that N-[3,5-Bis(Trifluoromethyl)Benzenesulphonyl]-L-Methionyl Hydrazide brings to the bench. The dual trifluoromethyl groups raise both lipophilicity and electron-withdrawing power, which tightens the molecule’s reactivity window. As producers, we have seen these groups boost selectivity in downstream transformations and provide better signal clarity in fluorine NMR and LC-MS analysis—not something that shows up in paperwork, but every synthetic chemist knows the value of a clean, sharp peak during purification.

    The methionyl core holds sulfur, which adds both synthetic complexity and versatility. Handling sulfur means rigor from us: sulfur can trigger oxidation, racemization, and unexpected side reactions, especially if solvents or glassware aren’t just right. It took countless rounds of process adjustment to block that—using ultra-pure reagents and real-time monitoring by analytic HPLC—before our batches could show the right enantiomeric ratios and optical activity.

    Reliable Quality Demands Consistent Process

    Our daily work is evidence-based. We run every batch through rigorous controls and let the numbers speak. HPLC purity follows a strict line, typically above 98%, and our NMR checks back it up, including fluorine, hydrogen, and carbon profiles. Any deviation—maybe a split in a critical peak or a small impurity—is flagged by our operators and sent back for rework or additional purification. This stretches our cycle time, but we care more about getting repeatable results for every shipment than hitting arbitrary delivery windows.

    Many imported “high purity” samples turn out to be marginal at best, filled with difficult-to-remove byproducts or unreacted starting materials. We regularly see this with products from aggregators or low-cost traders who don’t synthesize, only repackage. Our approach is rooted in data, not hope: we draw direct samples out of our reactors, analyze in-house, and prove every batch to our own standards, not just to paperwork.

    Understanding the Demands of Research and Development

    Working alongside researchers has taught us what matters—a clean substrate, sharp analytical signals, sufficient water solubility but no excessive hygroscopicity, shelf-stable at lab temperatures, and supplied with a rational certificate that stands up to scrutiny. For N-[3,5-Bis(Trifluoromethyl)Benzenesulphonyl]-L-Methionyl Hydrazide, requests range from hundreds of milligrams for pilot screening to multiple kilograms for scale-up. These needs push us to adapt, ensuring every lot maintains purity and consistency batch after batch.

    We don’t just ship stock numbers; we build custom batch sizes, adjust physical forms upon request, and tailor packaging to avoid moisture ingress or contamination. Observing failed reactions due to degraded or contaminated reagents taught us to heed every detail, even down to triple-sealing or packing under inert atmosphere for large shipments. These are solutions rooted in experience, not theory.

    Comparing With Similar Compounds

    Chemically, some might compare this compound to simple benzenesulfonyl hydrazides or to unmodified methionyl derivatives. With simpler benzenesulfonyl hydrazides, you lose the electron-deficient ring and the dual-trifluoromethyl substitution. That changes both chemical behavior and purification strategies. Less substituted analogs often display increased polarity, a broader impurity profile, and less predictable reactivity in coupling or acylation steps.

    Unsubstituted methionyl hydrazides may lack both lipophilicity and the enhanced electron withdrawal that these trifluoromethyl groups provide. Those features drive our compound’s utility in medicinal chemistry and lead optimization. The molecule’s unique combination nudges researchers toward scaffolds that behave in a more controlled and predictable fashion than “standard” hydrazide intermediates.

    Why We Chose This Synthesis Pathway

    Scaling up required countless tweaks to stop side reactions and boost yield. Early lab-scale trials favored a two-step approach: initial sulfonylation of L-methionine followed by hydrazinolysis. On a larger scale, the sheer reactivity of the bis(trifluoromethyl)benzenesulfonyl chloride led to runaway exotherms, so we brought in flow reactors and staged additions under cooling.

    Process safety matters here. We implemented in-line reaction calorimetry to log heat profiles in real time, and batch cooling jackets maintain temperature swings within safe limits. Years back, a temperature spike caused a partial batch loss, teaching us to lock down strict monitoring on every run since. These details aren’t found on most specification sheets; they reveal themselves over countless iterations and careful risk management.

    Analytical Rigor: From Reactor to Bottle

    As chemists, we trust our own data first. We run proton, carbon, and fluorine NMR after every main step, side by side with LC-MS and IR. In the sulfonylation step, residual chloride can stick around stubbornly, so we actively wash and re-check to confirm complete removal. The hydrazinolysis stage likes to drag minor over-acylated byproducts, so our columns run slow and cool with real-time elution monitoring.

    Our final lots consistently show strong, single peaks in both HPLC and GC analysis, and the 19F NMR offers clear, non-overlapping singlets, indicating both regio- and chemoselective synthesis. Since process waste is high in fluorinated synthesis, we recycle solvents under a dedicated fluorinated solvent recovery system, reusing cleaned solvents for non-critical washing to cut down on environmental impact.

    Supporting the Evolving Demands of Chemistry

    Industry demands more than routine catalog chemicals. Projects stretch from medicinal screening to bioconjugation, pushing our synthesis to satisfy expectations for reactivity and clean downstream modifications. N-[3,5-Bis(Trifluoromethyl)Benzenesulphonyl]-L-Methionyl Hydrazide finds use as a building block for advanced ligands, enzyme inhibitor scaffolds, and bioorthogonal tags.

    Chemists value it for the unique trifluoromethylated ring: both as a reporter in biophysics assays and as a modulator for metabolic stability in medicinal candidates. The sulfur content of methionine brings new angles too, permitting oxidative cyclizations or targeted labeling, steps that less-featured analogues simply cannot match.

    Over time, requests from pharmaceutical clients steered us to offer both analytical support and custom modifications: different counterions, salt screening, and co-crystallizations with complementary reagents. Each new request fueled further improvements in both process isolation and analytical verification, refining how we scale and pack each order.

    What Really Sets Our Product Apart: The Manufacturer’s Angle

    Walking the line between bulk manufacturing and lab-scale finesse isn’t easy. It means we see every failing first-hand—like solubility issues in water-miscible solvents or lot-to-lot color shifts, both often missed by non-synthesizing traders. Fixing these goes beyond technical training; making it work well at all scales means planning, countless pilot tests, and never ignoring operator feedback.

    For N-[3,5-Bis(Trifluoromethyl)Benzenesulphonyl]-L-Methionyl Hydrazide, our best lots now exhibit shelf-lives above two years in standard storage, free from discoloration or loss of activity. This comes from deliberate batch aging studies and stress-testing under various humidity and temperature regimens. We trace sources of degradation to minor hydrolysis, so we fine-tuned both packaging and storage recommendations, sharing them openly with every buyer.

    We see some resellers who simply re-bottle and send out chemical stocks without ever running a batch themselves. They cannot sense the subtle, batch-specific quirks that dictate how a compound behaves over time—whether it cakes, whether it forms dust, or how it re-dissolves. We maintain logs of batch characteristics—granular, powdery, off-white, or bright—so end-users never get unexpected surprises.

    Ongoing Commitment to Transparency and Reliability

    Making a specialty molecule in-house, as opposed to buying isolates or outsourcing, means we know how every raw material, reagent, and process step interacts. Working from scratch lets us spot and eliminate contamination sources from the ground up. For every production cycle, our QA team cross-verifies results against both historical data and third-party controls; we stay accountable not just to external standards, but to our own track record.

    Having walked through every part of the production process, we respect the details—raw material certification, controlled humidity rooms, and even maintenance checks on filtration equipment. We reject any shortcut that compromises stability or data integrity, even if it slows us down. This preserves our reputation with both university researchers and pharmaceutical clients who return, lot after lot, for a reliable product.

    Real-World Application Stories: Feedback Drives Improvement

    Client feedback loops fuel our process changes. One pharma group reported issues with a competitive hydrazide forming problematic solids when diluted—our chemists investigated, reran our own material, and shared crystallization notes that resolved their protocol issues. Such ground-level cooperation closes the gap between manufacturer and researcher.

    A university collaborator ran into batch-to-batch performance swings with a catalog hydrazide from another source. They wanted us to provide additional spectral data and storage advice, uncovering that the competitor’s source changed synthetic routes mid-order. By sticking to a validated procedure, we gave them peace of mind—and full spectral documentation—for their publication.

    Future Directions: Responsiveness and Adaptation

    Our synthesis systems keep evolving. The increasing scale of research projects means adapting both reactors and purification setups to meet new requirements. We continue adding automation to reduce operator error, logging every temperature, pressure, and pH fluctuation. Every improvement is meant to increase both safety for our staff and batch-to-batch consistency for our customers.

    We watch for new literature and application reports involving trifluoromethylated sulfonyl hydrazides. This keeps us ahead on both process knowledge and contamination risks, especially as downstream researchers develop novel applications in chemical biology, imaging, and drug discovery. By listening to practical feedback, adding new analytical checkpoints, and publicly sharing data transparency, we remain a trustworthy, engaged supplier, not just an anonymous source.

    From the reactor floor to outgoing pallets, we engage in every part of the chemical’s journey. Each batch of N-[3,5-Bis(Trifluoromethyl)Benzenesulphonyl]-L-Methionyl Hydrazide reflects the hands and expertise of our team, shaped by direct experience, commitment to rigor, and honest feedback. That’s the difference when you buy from a manufacturer who has walked the talk—every time, batch after batch.