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2-Butynyl 4-Methylbenzenesulfonate

    • Product Name 2-Butynyl 4-Methylbenzenesulfonate
    • Alias 4-Methylbenzenesulfonic acid 2-butynyl ester
    • Einecs EINECS 253-002-0
    • 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

    611181

    Chemicalname 2-Butynyl 4-Methylbenzenesulfonate
    Casnumber 54014-36-9
    Molecularformula C11H12O3S
    Molecularweight 224.28 g/mol
    Appearance Colorless to pale yellow liquid
    Boilingpoint 110-112°C at 2 mmHg
    Density 1.18 g/cm³
    Smiles CC#CCOS(=O)(=O)C1=CC=C(C)C=C1
    Storageconditions Store at 2-8°C, dry and well-ventilated place
    Solubility Soluble in organic solvents such as dichloromethane and ether

    As an accredited 2-Butynyl 4-Methylbenzenesulfonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g of 2-Butynyl 4-Methylbenzenesulfonate is packaged in a sealed amber glass bottle with a chemical-resistant screw cap.
    Shipping 2-Butynyl 4-Methylbenzenesulfonate is shipped in sealed, chemically-resistant containers to prevent leakage and contamination. It is transported as a hazardous material, in compliance with relevant local and international regulations. Proper labeling and documentation accompany each shipment, ensuring safe handling and storage during transit. Store away from heat, sparks, and incompatible substances.
    Storage 2-Butynyl 4-Methylbenzenesulfonate should be stored in a cool, dry, and well-ventilated area, away from sources of heat and ignition. Keep the container tightly closed and protect it from moisture and light. Store separately from incompatible substances such as strong oxidizing agents and bases. Use appropriate chemical storage cabinets designed for flammable or reactive organic compounds.
    Application of 2-Butynyl 4-Methylbenzenesulfonate

    Applications of 2-Butynyl 4-Methylbenzenesulfonate in Industrial Manufacturing

    2-Butynyl 4-Methylbenzenesulfonate serves as a specialized intermediate in fine chemical synthesis, enabling precision modification in complex organic molecules. Our expertise as a manufacturer ensures precise control of quality critical for downstream applications, spanning from pharmaceutical synthesis to advanced material creation. Below are the major industrial sectors utilizing this compound, with technical integration points and compliance references for each application.

    1. Active Pharmaceutical Ingredient (API) Synthesis — Alkynylation Reagent

    This sulfonate functions as a potent alkynylation agent in the development of small-molecule APIs, especially those utilizing terminal alkyne moieties for molecular diversification. It supports nucleophilic substitution steps during late-stage synthesis, enhancing route efficiency while maintaining strict impurity profiles according to ICH and pharmacopeia requirements. Process chemists depend on its predictable reactivity for scalable, reproducible operations in both pilot and industrial volumes.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP and Ph. Eur. monographs for final API compounds
    • 21 CFR Part 211 (US FDA GMP for finished pharmaceuticals)
    • EU GMP Vol 4 (for production and quality management)

    Typical usage ratio

    • 0.8–1.1 molar equivalents to target nucleophile (reaction-specific, adjusted for yield optimization and impurity control)

    Downstream process integration

    • Alkylation or alkynylation steps in multi-step organic synthesis, typically following initial functional group activation and prior to purification or cyclization

    Final product types

    • Branded and generic APIs incorporating alkynyl side chains (e.g., anti-cancer, anti-inflammatory pharmaceuticals)
    • Key intermediates for peptide and heterocycle modification

    2. Specialty Agrochemical Intermediate — Selective Herbicide Synthesis

    In herbicide active compound manufacturing, 2-Butynyl 4-Methylbenzenesulfonate is used to introduce alkynyl groups into aromatic frameworks, promoting mode-of-action diversity. It participates in nucleophilic substitution protocols, which demand high selectivity and minimal by-products. Facilities governed by global agrochemical stewardship policies favor this approach for its precision and efficiency in constructing target molecules under controlled batch or continuous processing.

    Industry compliance standards

    • FAO/WHO specifications for pesticide production
    • ISO 9001:2015 Quality Management System
    • REACH regulation (EU Registration, Evaluation, Authorisation, and Restriction of Chemicals)

    Typical usage ratio

    • 0.9–1.2 equivalents relative to the base substrate, optimized per process development and impurity specification set by regulatory submission dossiers

    Downstream process integration

    • Employed after initial core structure assembly, within the alkynyl functionalization stage, preceding target site-selective derivatization or esterification

    Final product types

    • Herbicide active ingredients featuring alkynyl phenyl motifs
    • Intermediates for synthesis of crop protection products

    3. Advanced Electronic Materials — Organic Semiconductor Precursor

    This compound contributes alkynyl-sulfonate moieties during organic semiconductor precursor syntheses, especially for developing π-conjugated frameworks. Electronic material manufacturers leverage its high chemical purity to ensure defect-free polymer backbones, critical for performance in thin-film transistors, OLEDs, and organic photovoltaic cells. Precise dosage and process sequencing reduce batch-to-batch variation in electronic applications subject to strict defect tolerance.

    Industry compliance standards

    • IEC 60068 (Environmental Testing for Electronic Components)
    • UL 746C (Polymeric Materials – Short Term Property Evaluations)
    • ISO 9001:2015 for manufacturing traceability and QC

    Typical usage ratio

    • 0.5–1.0 equivalents per mol functional monomer, optimized to device performance criteria and carrier mobility studies

    Downstream process integration

    • Engaged in step-growth polymerization or Stille/Sonogashira cross-coupling, prior to film-casting or device fabrication

    Final product types

    • Organic semiconducting polymers for OLED and OPV applications
    • Electronic ink dispersions
    • Charge transport layer materials

    4. Fine Chemical Synthesis — Custom Synthesis Building Block

    Custom synthesis providers and contract development organizations integrate this sulfonate as a building block for bespoke molecules, including diagnostic reagents and research tools. Its selectivity in coupling reactions, especially with heteroaromatic or aliphatic nucleophiles, supports streamlined synthetic route design and robust scale-up. GMP or non-GMP settings utilize its reliable composition for time-sensitive projects requiring close analytical tracking and batch documentation for traceability.

    Industry compliance standards

    • ISO 9001:2015 for quality management in custom synthesis
    • Sigma-Aldrich standards for fine chemical quality (internal QC references)
    • Accreditation as per customer-specific protocols for cGMP projects

    Typical usage ratio

    • 0.7–1.5 equivalents dependent on complexity of target molecule, adjusted according to desired site-selectivity and reactivity of starting materials

    Downstream process integration

    • Used in nucleophilic displacement reactions, notably after protective group removal or prior to terminal functionalization, under inert atmospheric conditions

    Final product types

    • Custom analytical reagents
    • Building blocks for molecular diagnostics
    • Non-clinical research compounds
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    More Introduction

    2-Butynyl 4-Methylbenzenesulfonate: Practical Insights from the Manufacturer

    Understanding 2-Butynyl 4-Methylbenzenesulfonate in the Lab and on the Plant Floor

    Over years of fine chemical production, we’ve learned that reliable access to specialty reagents makes or breaks research timelines and process scale-up for our clients. Among the compounds we synthesize, 2-Butynyl 4-Methylbenzenesulfonate stands out as a go-to substrate when selectivity and efficiency matter. Chemists come to us for this molecule when they need the clean coupling and manageable reactivity that other alkyne-based sulfonates can’t match. From pilot to production, we see this compound fill a unique role in modern synthesis.

    We observe that researchers reach for 2-Butynyl 4-Methylbenzenesulfonate not simply because of its structure, but for the margin of safety and predictability it brings to end-stage transformations. The butynyl group, while reactive, brings fewer impurities compared to longer-chain analogs or more sterically hindered sulfonates. With a clean 4-methylbenzenesulfonyl leaving group, this compound lets skilled chemists control alkynylation reactions with a clarity of outcome not always possible using bulkier or less volatile substituents. Through constant collaboration with both academic and industrial users, we’ve tailored our process to keep batch consistency high and side-product contamination low.

    Product Model, Purity, and Our Hands-on Approach

    Years ago, before we introduced routine micro-scale column analytics, purification yields from phenyl sulfonate-based alkynes sometimes suffered from trace polymer formation. By refining our crystallization and drying steps, we consistently deliver 2-Butynyl 4-Methylbenzenesulfonate to meet the high specifications researchers expect: clean NMR spectra, trace water content, and sharp melting behavior, every drum and bottle. Our typical model, referenced internally as BMBS201, is processed under argon and packaged with desiccant to guarantee freshness and minimize hydrolysis—details born out of repeated direct feedback from customers scaling up their reactions who saw subtle differences degrade performance.

    We’ve watched trends shift toward more sustainability-conscious protocols, so we’ve put effort into reducing chlorinated solvents and offering solventless processing on request. By tracking every variable, from sulfonyl chloride purity to final bottle headspace, we’ve pushed reproducibility to a level where formulators can run parallel trials with trustworthy input materials and convert those results directly to pilot or manufacturing scale.

    Real-World Usage and End-User Experience

    Chemists buy 2-Butynyl 4-Methylbenzenesulfonate from us primarily for its robust performance in Sonogashira cross-coupling, alkyne-ether formation, and as an intermediate for more complex molecular scaffolds. Medicinal chemistry groups often report that having such a clean, crystalline precursor speeds up their SAR studies by allowing direct use in downstream transformations. Some firms attempting higher-step synthesis told us about the headaches from minor isomer formation using less refined sulfonate esters. After switching to our compound, several teams noted fewer chromatographic separations and tighter isolation of their targets.

    Many smaller labs want not only assurance of purity but also guidance on scale-up. We’ve collaborated with process engineers who tell us about the “unknown unknowns” — the impurities that only show up at the multi-kilogram stage. Reworking a failed batch of complex pharmaceuticals because the leaving group broke down is costly and avoidable. Through regular conversations and technical feedback loops, we refine our batches and transparently share analytics with every shipment. For critical reactions—such as selective monoalkynylation or the preparation of conjugated enynes—consistent supply at narrow batch-to-batch variation is key. From grams in the R&D stage to drums for early clinical campaigns, customers come to us expecting this level of traceability.

    Why the Difference Matters to Chemists and Manufacturers

    We’ve tested a range of related compounds—propargyl, butynyl, pentynyl sulfonates—from other suppliers. Variable reactivity, unwanted side reactions, and batch inconsistency were common pain points reported by users. Some generic sources yield products with solvent residues or moisture levels that quietly sabotage downstream yields. By comparison, our 2-Butynyl 4-Methylbenzenesulfonate batches show narrow melting points, robust storage stability, and documentation on every lot. One project leader remarked that the biggest commercial risk outside the chemistry was “what you don’t know about where your reagents came from.”

    In the market, you’ll find cheaper or higher-throughput options for some alkynyl sulfonates. Price alone doesn’t tell the productivity story. Teams running high-value transformations want to avoid heterogenous impurities and uncharacterized minor byproducts. We designed our process to emphasize traceability. Every drum carries a manufacturing record and complete spectral trace. Sometimes clients bring samples bought elsewhere for comparison, pointing out unclear NMR peaks or unexplained loss on drying. We analyze, troubleshoot, and routinely demonstrate—side by side—where the differences lie in reactivity, color, and impurity profiles.

    Supporting Breakthroughs from Academic Labs to Full-Scale Reactors

    Recent years have shown increased demand for small- and medium-scale customization. Contract research organizations (CROs) often start with a few grams, validating yield and reactivity before scaling up. We tailor batch sizes for pilot-scale projects, leveraging mid-sized reactors and agile logistics that enable customers to move from benchtop to process chemistry in weeks, not months. Groups working on complex syntheses—polycycles, bioactive scaffolds, new electronic materials—need flexibility and technical support. Our in-house analytical team can adapt release criteria and provide detailed impurity profiling as needed for regulatory submissions.

    Feedback from a specialty API program highlighted how important reaction reliability becomes at scale. The chemists reported formation of less than 0.05% sulfonic acid byproduct at a kilogram batch size—well within process thresholds and simple to remove by aqueous wash. By working directly with client QC teams, we can troubleshoot any deviations before they become bottlenecks. Clarity in specifications improves productivity, reduces need for repeated purification, and shortens time to delivery of final products.

    Learning from the Industry and Investing in Consistency

    As direct manufacturers, we bear the responsibility for every gram shipped. We’ve seen more automation in analytical validation, with NMR, LC/MS, and Karl Fischer titration coming online in tandem. This allows our teams to catch deviations at milligram levels, before they can affect larger vessels and supply chains. We invest in continuous training and automation not for the sake of buzzwords, but because every hour saved in QA is an hour that can be spent on synthesis and troubleshooting for our clients.

    A few years ago, a customer encountered persistent microcontaminant issues using another vendor’s butynyl sulfonate. Cross-reactivity with other sulfur-based additives in their protocol led to unreliable endpoint tests. We worked alongside their team to adapt the sulfonyl chloride sourcing and raised purity, leading to a batch-to-batch reliability that saved both teams material and time. With our logistics and transparent documentation, labs now can cross-check our analyses with their in-house capabilities, reinforcing trust, and opening room for process optimization.

    Safety, Handling, and Storage—From Lab Reality

    2-Butynyl 4-Methylbenzenesulfonate doesn’t cause the same headaches as some more volatile or thermally unstable reagents, yet it still warrants practice in careful handling. In our experience, shelf life tracks cleanly with moisture exclusion and inert packaging. More than a few times we’ve helped process teams recover material after accidental air exposure—having seen how minor hydrolysis or partial oxidation sets back a synthesis campaign. By keeping critical inventory under argon and away from atmospheric moisture, failures traced to starting material degrade significantly. Hand-to-hand relay from dry room to shipping means users receive shipment without unpleasant surprises in their prep.

    On the practical side, waste management considerations factor into most production decisions. Residual traces can be handled by standard organic solvent and aqueous waste protocols—something important to scale-up and kilo-lab operations aiming for compliance. Over time, firsthand discussions with environmental health and safety officers helped us standardize our labeling and storage recommendations. Storing the sulfonate in amber bottles, packed in secondary containers with desiccant, became our routine because of clear improvements in both quality and user satisfaction.

    What Chemists Say: Field Notes from the Usual and the Unusual

    We derive much of our practical knowledge from stories clients bring us. One early adopter, focused on alkynylation of heterocycles, reported side-by-side comparisons across a dozen leaving groups. Frequent purification steps, loss in yield, and capricious crystallizations motivated their switch to our 2-Butynyl 4-Methylbenzenesulfonate. According to their bench notes, reproducibility improved, and troubleshooting time dropped. Another client, developing a scale-up for an advanced material, found our batch to provide lot-to-lot uniform peak area in HPLC analyses, saving weeks in analytical method validation.

    Instrumental data only tells part of the story. Our technical staff spend time on the phone with buyers asking about details like odor profile, handling ease, and visual color—from nearly water-white to pale straw. This real-world, hands-on exchange feeds directly into our process improvement cycles. Field inquiries pushed us to tighten filtration, adapt packaging size, and refine documentation.

    Drivers for Ongoing Process Improvement

    Learning doesn’t end at shipping. Customers increasingly ask for new analytical data, trace element reporting, and in some cases, green chemistry certification. By focusing on direct synthesis rather than repackaging, we stay ahead of most regulatory and market trends. Over the last year, we’ve improved solvent recycling, reduced use of halogenated organics, and implemented in-situ FT-IR monitoring for key steps. These changes have lowered waste and made our process leaner, which clients appreciate in their own sustainability reporting.

    We’re asked regularly about scale-up and continuous flow. Our engineering team has piloted several projects converting old batch recipes to flow reactors. Customers running hundreds of grams per week appreciate the reliability—productivity goes up, side reactions drop, and the narrow residence time window almost eliminates overreaction or under-reaction. This transition didn’t happen overnight; we trialed small runs, analyzed deviations, then invested in stainless reactors particularly suited to the sulfonate’s solubility and heat-sensitive profile. This kind of incremental learning, guided by both successes and failures, makes the difference between off-the-shelf materials and those built around end-user needs.

    Patent, Regulatory, and Global Sourcing Considerations

    Because of the growing importance of patent-clear supply chains, we track every raw material lot back through our vendors and regularly audit for compliance. Many clients need to file regulatory documents downstream; they want complete confidence in every step from feedstock to finished material. By handling synthesis and purification in-house, we eliminate uncertainty and can rapidly respond to patent queries, lot trace requests, or sudden demand spikes brought on by new filings.

    Global supply issues frequently push buyers to seek new vendors, but direct manufacturing close to end-users insulates both sides against market volatility. Shipments don’t face unexpected customs challenges or month-long delays from offshore sourcing. Our process, built in partnership with client timeline demands, closes many of the gaps and delays seen by those sourcing through multiple middlemen or cross-border traders.

    Challenges and Solutions from the Shop Floor to the Research Bench

    Every specialty chemical has idiosyncrasies. Trace impurities sometimes arise from small changes in process water or batch temperature. By maintaining steady-state parameters, we cut out variability that can cause issues at both lab and plant scale. We’ve learned to anticipate questions about reactivity—especially from teams looking to use the compound outside standard coupling chemistry. Transparency and open real-time feedback with process chemists help address new challenges quickly, from unanticipated color changes to variable reactivity in unconventional solvents.

    On rare occasions, a project has run into scale-up problems unrelated to our raw material—such as unexpected glassware fouling or incompatible catalysts. Our technical support team keeps communication lines open, troubleshooting alongside partners rather than sending generic advice. This collaborative, responsive mode of operation developed organically over years, after seeing the costs of disconnected support in both time and material waste.

    Looking Ahead: Responding to Research and Market Evolution

    As research trends migrate toward more complex and functionalized alkynes, the need increases for materials like 2-Butynyl 4-Methylbenzenesulfonate, where balance between manageable reactivity and synthetic versatility matters. We expect rising inquiry volumes from teams exploring new therapeutic and material science frontiers. Early-stage access to high-quality, well-characterized intermediates allows innovators to bypass the frustrations of uncertain starting points and move straight into creative, value-added steps.

    A reliable supply chain, robust analytics, and transparency—these grow from daily habits at the plant, not headlines. Our experience shows the best results come from proactive partnership with working chemists, open exchange of process details, fast feedback on real problems, and relentless drive to improve. The right reagents—made carefully, handled with respect for end-use, and delivered with complete analytics—support breakthroughs, keep projects on time, and let scientists focus on advancing the science, not compensating for avoidable error. For all of us shaping tomorrow’s chemistry, these details add up.