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4-N-Butylbenzenesulfonyl Chloride

    • Product Name 4-N-Butylbenzenesulfonyl Chloride
    • Alias 4-Butylbenzenesulfonyl chloride
    • Einecs 249-642-6
    • 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
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    Specifications

    HS Code

    808142

    Chemical Name 4-N-Butylbenzenesulfonyl Chloride
    Cas Number 36506-63-9
    Molecular Formula C10H13ClO2S
    Molecular Weight 232.73
    Appearance White to off-white solid
    Melting Point 47-49°C
    Boiling Point 352.3°C at 760 mmHg
    Density 1.202 g/cm3
    Solubility Reacts with water; soluble in organic solvents
    Purity Typically ≥ 98%
    Smiles CCCCc1ccc(cc1)S(=O)(=O)Cl
    Inchi InChI=1S/C10H13ClO2S/c1-2-3-6-9-4-7-10(8-5-9)14(11,12)13/h4-5,7-8H,2-3,6H2,1H3

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

    Packing & Storage
    Packing 4-N-Butylbenzenesulfonyl Chloride is supplied in a 25g amber glass bottle, tightly sealed, labeled with hazard warnings and product details.
    Shipping 4-N-Butylbenzenesulfonyl Chloride should be shipped in tightly sealed, corrosion-resistant containers under cool, dry conditions. It must be handled by trained personnel, with appropriate labeling and documentation. Transport should comply with local and international regulations for hazardous chemicals, ensuring segregation from incompatible substances, especially water and strong bases.
    Storage 4-N-Butylbenzenesulfonyl chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture, heat, and incompatible substances such as strong bases and oxidizers. Protect from direct sunlight and avoid exposure to air, as it is moisture-sensitive and may hydrolyze. Use proper chemical storage practices to prevent accidental release or contact.
    Application of 4-N-Butylbenzenesulfonyl Chloride

    Applications of 4-N-Butylbenzenesulfonyl Chloride in Industrial Manufacturing

    As a direct producer of 4-N-Butylbenzenesulfonyl Chloride, we supply this sulfonylating agent to several sectors demanding high-purity intermediates. Below we detail its actual industrial uses, with a focus on specific downstream integrations, technical compliance, and end product profiles.

    1. Synthesis of Pharmaceutical Sulfonamides

    Pharmaceutical manufacturers use 4-N-Butylbenzenesulfonyl Chloride to synthesize sulfonamide-based APIs, especially for antibacterial agents and enzyme inhibitors. This reagent participates in targeted N-sulfonylation reactions during multi-step processing, requiring close control of residual solvents and by-products under cGMP conditions. The combination of precise input ratios and validated purification ensures consistent batch-to-batch API quality.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) Monographs for Sulfonamide APIs
    • European Pharmacopoeia (Ph. Eur.) for Sulfonylated Intermediates
    • FDA 21 CFR Part 211 cGMP requirements for finished pharmaceuticals

    Typical usage ratio

    • 1.05–1.20 molar equivalents relative to the target amine, with minor adjustment to control complete conversion and minimize impurities in the crude product

    Downstream process integration

    • Introduced during the sulfonylation step in pharmaceutical synthesis lines, often after amidation or alkylation stages; purification follows via crystallization from water-miscible solvents or selective extraction

    Final product types

    • Sulfonamide antibiotics
    • Carbonic anhydrase inhibitor APIs
    • Antidiabetic (SGLT2 inhibitor) sulfonamides
    • Intermediates for antiretroviral drugs

    2. Manufacturing of Agrochemical Intermediates

    Major crop protection formulation plants utilize this compound to prepare herbicide and pesticide intermediates, particularly for selective sulfonylureas and benzenesulfonamide motifs. Facilities prioritize high conversion and reagent recovery, using process controls to meet local environmental and chemical safety registrations before final blending and granulation.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Agrochemical Production
    • US EPA Pesticide Registration Guidelines (40 CFR Part 158)
    • REACH Regulation (EC) No 1907/2006 for European supply
    • China ICAMA certification for pesticide intermediates

    Typical usage ratio

    • 1.10–1.30 equivalents compared to nucleophilic substrate, with dosing based on analytical monitoring to maximize intermediate yield relative to solvent volume and recycle considerations

    Downstream process integration

    • Charged during the condensation or acylation steps in continuous or batch herbicide synthesis lines, followed by aqueous workup, solvent stripping, and subsequent formulation into technical concentrate or flowable dispersion

    Final product types

    • Sulfonylurea herbicide intermediates
    • Benzene-based pesticide frameworks
    • Precursor solutions for finished plant protectant formulations
    • Storable technical blends for on-site formulation

    3. Production of Polymerization Initiators and Modifiers

    Specialty polymer manufacturers deploy 4-N-Butylbenzenesulfonyl Chloride to create sulfonated initiators and functional modifying agents. These functionalities enable the design of high-performance ionomers or engineered resins with tailored ionic properties. The reagent’s reactivity and impurity profile become critical at scale, particularly for achieving reproducible sulfonation without excessive cross-linking or degradation.

    Industry compliance standards

    • ISO 14001 Environmental Management in polymer production
    • ASTM D1238 for melt flow properties
    • RoHS Directive (2011/65/EU) concerning restricted substances
    • REACH SVHC list compliance for raw material imports

    Typical usage ratio

    • 0.5–2.5% by mass, dependent on targeted degree of sulfonation and backbone reactivity of the base polymer; controlled addition under inert conditions to avoid runaway side reactions

    Downstream process integration

    • Fed to reactor vessels after polymer prepolymerization or melt-phase mixing; sulfonation step followed by neutralization and filtration before further extrusion or pelletizing

    Final product types

    • Sulfonated polystyrene resins
    • Cation exchange membranes
    • Conductive polymer films
    • Ionic functionalized engineering plastics

    4. Custom Synthesis of API Building Blocks for CDMO Operations

    Contract development and manufacturing organizations (CDMOs) employ this reagent in custom synthesis campaigns for sulfonyl-containing reference compounds, labeling reagents, and early-stage drug intermediates. Controlled sulfonylation is vital for structurally specific compound libraries, often requiring protocols validated under both GMP and ISO standards for customer submission and regulatory filings.

    Industry compliance standards

    • US FDA 21 CFR Parts 210/211 for Drug Manufacturing
    • ICH Q11 for Development and Manufacture of Drug Substances
    • ISO 13408 for aseptic processing when contract filling is involved
    • PIC/S GMP Guide for global contract organizations

    Typical usage ratio

    • Stochiometric to slight excess (1.00–1.15 equivalents) versus nucleophile; usage fine-tuned based on analytical endpoint controls for each client specification

    Downstream process integration

    • Added during late-stage functionalization or protection steps in multi-step organic synthesis; followed by rapid purification via column chromatography and solvent exchange for further derivatization or scale-up

    Final product types

    • Chemical reference standards
    • Labeling intermediates for diagnostic assays
    • Early-phase clinical trial pharmaceutical intermediates
    • Small-molecule probe libraries

    5. Preparation of Advanced Specialty Surfactants

    Producers in the surfactant and detergent sector use this molecule to introduce sulfonyl groups into hydrophobic aromatic substrates, creating precursors for customized nonionic or anionic surfactants. Control of process pH and temperature during sulfonylation ensures surface-active end products remain within safety and performance specifications for industrial and institutional applications.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals – Surfactants Biodegradability
    • ISO 9001 for Quality Management in specialty chemicals
    • EU Detergents Regulation (EC) No 648/2004
    • Relevant national chemical safety registrations (K-REACH, TSCA)

    Typical usage ratio

    • 1–3% by weight in the sulfonation reactor, adjusted by desired sulfonation degree and on-line monitoring of conversion and by-product formation

    Downstream process integration

    • Injected after pre-mixing with co-solvent into sulfonation reactor, then neutralized and spray-dried; process monitored to meet specific HLB values required in end surfactant formulation

    Final product types

    • Alkylbenzene sulfonate surfactants
    • High-foaming cleaning agent bases
    • Industrial degreasing additives
    • Special detergents for institutional use

    6. Functionalization of Aromatic Compounds in Fine Chemical Synthesis

    Fine chemical processors employ this sulfonyl chloride for introducing para-butylsulfonyl substituents to aromatic scaffolds needed in materials science and specialty reagent production. Custom protocols address reactivity, volatility, and containment, with batch records and residue traceability supporting downstream regulatory filings for specialty applications, including electronics and analytical reagents.

    Industry compliance standards

    • ISO 9001:2015 for Quality Control in Fine Chemicals
    • Responsible Care® Chemical Process Safety Management
    • REACH Regulation (EC) No 1907/2006, Annex VII-VIII
    • Chemical Safety Assessment (CSA) for specialty intermediates

    Typical usage ratio

    • 0.8–2.0 equivalents, proportional to available aromatic substrate sites; reaction control by titration or HPLC for stepwise addition and to mitigate over-reaction or dimerization

    Downstream process integration

    • Metered to aromatic substrate under controlled anhydrous conditions, followed by quenching and phase separation; resulting functionalized intermediates undergo downstream oxidation, halogenation, or coupling for variety of advanced chemical applications

    Final product types

    • Polyfunctional aromatic intermediates
    • Material science building blocks
    • Analytical derivatization agents
    • Specialty additives for niche applications
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    Certification & Compliance
    More Introduction

    4-N-Butylbenzenesulfonyl Chloride: Built on Proven Consistency, Defined by Clear Performance

    Working in chemical manufacturing for over twenty years, our commitment to reproducibility and traceable purity has grown alongside the demands from the downstream synthesis market. I have seen chemistries shift from bench-scale pilot batches to full commercial runs. Every solvent, intermediate, and reagent along the line can make or break an end product—none more notably than sulfonyl chlorides, which shape the structure and reactivity of pharmaceuticals, advanced polymers, and specialty chemicals. Among the many we prepare, 4-N-Butylbenzenesulfonyl Chloride stands out as a tried-and-tested building block, one we have made at industrial scale for well over a decade with consistent output batch after batch.

    Model and Specifications: Focusing Where It Counts

    4-N-Butylbenzenesulfonyl Chloride generally comes as a white to off-white crystalline solid, though trace color shifts can come up depending on minute process variables like reaction temperature or workup settings. Our plant has dialed in the process so that batch-to-batch variation falls below 1% for purity, running consistently above 98%. We set the actual release specifications tighter than basic catalog standards because even a slight impurity—be it residual solvent or a trace byproduct—can alter product behavior down the chain. Every drum or tote we fill has a certificate reporting purity by HPLC, melting point, and residual moisture, which matters most in scaling up into sensitive coupling reactions further downstream.

    The molecular formula of 4-N-Butylbenzenesulfonyl Chloride is C10H13ClO2S, with a molar mass that gives synthetic chemists the precision to plan out their conversions without guesswork. Chloride content, acid value, and melting point are all data points we confirm using validated lab tools; these are not just numbers on a COA but the end product of tightly managed process parameters—solvent ratios, quenching protocols, filtration timing—optimized through hands-on plant experience, not just theoretical guidelines.

    Usage: Solutions for Modern Synthesis

    I have been asked many times why purchasers seek this specific sulfonyl chloride, when the family of related compounds stretches far and wide. The butyl-substituted aromatic ring of this compound is a strategic advantage during synthesis: it serves as a stable handle for further functionalization, bringing a balance of hydrophobic and reactive character rarely matched by shorter or longer alkyl chains. Pharmaceutical manufacturers utilize it for installing the sulfonyl group onto amines and heterocycles during the assembly of small-molecule APIs, especially those where metabolic stability and tailored lipophilicity are required.

    Polymer chemists rely on this intermediate for introducing robust crosslinking sites, especially in high-performance materials where thermal stability and defined mechanical strength sit at a premium. I have also seen it used in dye manufacturing, where the butyl group supports solubility and processability in both organic solvents and blended aqueous systems. The selective reactivity of the sulfonyl chloride group lets chemists carry out predictable reactions with minimal side products. Minimizing purification steps saves time and solvent waste, a practical edge everyone appreciates on the plant floor.

    How 4-N-Butylbenzenesulfonyl Chloride Compares to Related Products

    There are dozens—if not hundreds—of sulfonyl chlorides circulating in specialty applications. Not every variant brings the balanced properties seen with the n-butyl group attached at the para position of benzene. We have compared this compound side by side with closely related analogs, such as methylbenzenesulfonyl chloride (p-toluenesulfonyl chloride) and hexyl-substituted variants, running parallel reactions in both glassware and kilo-scale reactors.

    The n-butyl version shows distinctly improved solubility in mid-polarity solvents like ethyl acetate and dichloromethane, which matters most in robust process flows that avoid phase separation or incomplete reactions. At the same time, the steric bulk of the butyl group offers a sweet spot, avoiding the sluggish reactivity of bulkier chains while providing more lipophilic character than methyl or ethyl analogs—an asset in drug design where balance between aqueous and lipid solubility drives absorption and distribution profiles. We have witnessed clients use p-toluenesulfonyl chloride in screen reactions, only to switch to our n-butyl compound after pilot-stage hurdles with volatility or inconsistent product purity. The differences are tangible in yields, in downstream filtration steps, and in easier purification runs—a fact that has converted many from generic resins and oxidizers toward our established process route.

    The Reality of Bulk Manufacturing—What Makes Our Approach Different?

    Producing sulfonyl chlorides at kilogram, multi-ton levels comes with challenges that academic synthesis does not face. Batch-to-batch reproducibility counts for everything in a regulated pharmaceutical environment. We use closed-system manufacturing in reactors lined to prevent trace metal contamination, which could easily undermine an entire production run. Our facility is designed to isolate moisture and atmospheric oxygen out of the reaction space, keeping the sulfonyl chloride from prematurely hydrolyzing—a problem that contributes to yield loss, foul odors, and hazardous waste in less controlled settings.

    The process starts with sourcing high-purity 4-n-butylbenzenesulfonic acid, going through a targeted chlorination step under chilled conditions. Temperature ramps are controlled by automated feedback loops; a deviation of even a few degrees could trigger byproducts or incomplete conversion. Our team samples every batch at key points, testing reactivity with standardized amine partners to confirm the intended chemical profile is met. This hands-on validation—witnessed in missed trigger points and micro-adjustments—connects plant operators and QC chemists in real time, not just through paperwork.

    Sustainability and Regulatory Commitment

    The sulfonyl chloride supply chain presents environmental and safety risks, especially when waste hydrochloric acid and unreacted feedstocks accumulate. We took steps long ago to neutralize waste streams and recover reusable byproducts. Our reaction workups incorporate real-time pH adjustment, closed-loop solvent recovery, and downstream scrubbing to handle volatile organochlorine emissions. Local regulators audit our waste handling every quarter, and customer audits have driven further transparency throughout our documentation and lot tracking. Every certificate is linked back not just to batch numbers, but to a chain of custody that includes solvent sources, operator logs, and in-process deviation records—an approach essential for customers complying with strict API regulatory documentation.

    Beyond compliance, manufacturing this compound with responsible waste management means safer neighborhoods and fewer unexpected toxic releases. We have adopted changes suggested by local community groups, from secondary containment berms to improved air handling units around chlorination lines, driven not by checklists but by the real risk assessments our staff conduct with regulators and independent counselors. Accidents, even minor leaks, can stop production lines and cause regulatory shutdowns—a reality anyone in the industry has faced at least once.

    Long-Term Relationships and Customer Needs

    Supplying this compound bears more responsibility than simply delivering a product at specification. The market for specialty sulfonyl chlorides remains highly relationship-driven. Many clients, especially major pharmaceutical and polymer players, have been with us for over a decade. Technical support does not end at the price quote or COA. We provide ongoing troubleshooting support, customer-specific documentation, and batch-level technical summaries for every lot shipped. Research chemists, process engineers, and plant managers alike call on us directly when troubleshooting unexpected side reactions or scale-up issues. In several instances, we have re-qualified entire supply chains after a single report of a stuck filtration, building trust by involving our technical team in root-cause analysis and corrective process changes—tasks only a hands-on manufacturer can tackle.

    On-site visits are routine for key accounts, not just for audits but for process reviews and targeted technical presentations. The value extends beyond the material cost, as clients recognize the hidden advantages of dealing with a partner who understands the nuance of chemical reactivity and scale-up logistics. By remaining involved after the sale, we continue to learn about practical hurdles our customers face, driving improvements such as shorter lead times or custom pack sizes, and providing technical data on demand for regulatory filings or process troubleshooting. Most downstream users now factor in not just the per-kilo price, but long-term stability and confidence in both material quality and technical responsiveness.

    Challenges and Solutions in Process Scale-Up

    Scaling up from lab synthesis to plant-scale production often reveals subtle hurdles. For 4-N-Butylbenzenesulfonyl Chloride, managing exotherms and side reactions during chlorination has always required careful balancing. Early in our manufacturing experience, several batches suffered reduced yield due to unanticipated temperature spikes, catalyzed by trace acids or reactor insulation faults. We solved this through a series of process upgrades, including in-line chilling, upgraded temperature probes with higher sensitivity, and increased automation in the addition of chlorinating agents. Batch records now tie together every key parameter—feedstock ratios, addition rates, agitation speed—so deviations can be caught and fixed fast.

    Working directly with end users, especially those running continuous operations, taught us that impurity profiles only become truly visible at scale. Both our lab and pilot plant keep reference samples from every production run. If a customer sees altered reactivity or product color, we can quickly trace the issue back to a particular batch and investigate what minute change may have occurred that day—anything from raw material lots to operator shift changes. This quick-response, technical-close approach prevents downtime and helps our clients identify root sources fast, saving both resources and production hours.

    Improvement by Demand—Customer Feedback Drives Us Forward

    One of our most significant improvements came from a feedback loop with a US pharmaceutical manufacturer who faced poor reactivity during a critical synthesis step. Initial testing blamed the solvent system, but cooperative sample testing with our technical team revealed trace moisture in their storage drums, not from our material but from on-site handling. We responded by adapting our packaging—deploying higher-barrier drum liners with tamper-evident seals and providing new guidelines for humidity monitoring in storage. Returns and complaints fell sharply, and the client’s overall batch yields climbed, reinforcing the value of active post-sale support.

    Every point of contact—whether a simple phone call for an MSDS update or an in-person visit during process troubleshooting—teaches us something new. Many of our procedural upgrades originated not from internal brainstorming, but direct requests from formulation chemists, plant supervisors, or regulatory staff at customer facilities. These range from requests for custom labeling with full impurity profiles, to adjusted particle size distributions that ease dissolution in specific solvent systems.

    Industry Reliability—A Direct Manufacturer’s Perspective

    In the market, traders and third-party sellers often handle dozens of lines, rarely understanding the nuances that impact a final product’s quality. Our perspective, built on manufacturing from scratch, means we deal directly with every variable—from raw material selection to the details of every reactor cleaning cycle. The integrity of 4-N-Butylbenzenesulfonyl Chloride depends on hundreds of small tasks during every shift, and a supplier standing behind both the chemistry and the logistics. We have seen clients burned by off-spec supply from opportunistic vendors, facing lost time, wasted material, and sometimes regulatory flags due to incomplete documentation or questionable batch consistency.

    Our involvement does not just protect our reputation; it safeguards the entire production process for every downstream user. Inconsistent raw materials can lead to weeks of lost work, especially in regulated synthetic pathways. Unreliable suppliers can rarely backtrack their process to answer tough technical questions or intervene urgently during process failures. Direct manufacturing, at a scale refined by years at the plant level, has built us a rapport with returning clients—who know they can trace their product’s story from sourcing all the way to application.

    Continuous Improvement and Trust Through Stability

    Each year, clients challenge us with new technical hurdles, updated regulatory demands, and evolving commercial targets. Incoming requests spur us to continually refine purification steps, cycle time, and packaging—never simply resting on an unchanged process. Our in-house development team collaborates with both R&D and production operators to translate theoretical improvements into practical plant upgrades: retooling filter trains for faster throughput, adjusting crystallization protocols for higher assay results, even introducing remote monitoring for real-time tracking of key parameters. These investments ensure the product delivered today aligns with the quality and consistency expectations set a decade or more ago.

    The market rewards trust built on repeated, successful collaborations. Our returning clients cite not only our product but our technical troubleshooting and transparent documentation as reasons for their loyalty. In the most competitive sector, the greatest asset remains mutual confidence—bolstered by proven chemistry and a willingness to adapt methods as market and client needs develop. That stability—rooted in manufacturing expertise and daily experience—means buyers can focus on innovation and production, not re-testing or troubleshooting basic intermediates.

    Clear Advantages for Downstream Applications

    Whether destined for a pharmaceutical assembly, specialty polymer chain, or high-value dye, 4-N-Butylbenzenesulfonyl Chloride performs with an edge rooted in its structure and purity. The butyl group brings flexibility and reactivity, allowing precise sulfonylation in sensitive contexts. Our clients have documented improved yields, easier workups, and fewer side products—directly attributable to high-purity starting material and steady supply. In a world where regulatory scrutiny and technical standards are only rising, being able to offer material that repeatedly passes both chemical and documentation audits gives our clients not only peace of mind but measurable operational benefits.

    Over years of experience, the real differences between sulfonyl chloride variants have become visible only at the front lines of chemical manufacturing. Researchers and process chemists who demand robust, predictable, and scalable reactivity keep returning to compounds that meet every parameter, not just the obvious price points. As the actual manufacturer, our role extends beyond material supply into a technical partnership grounded in daily experience, continued learning, and a focus on operational value generation for our partners along the chain.