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HS Code |
530609 |
| Productname | N-Benzyloxycarbonyl-4-Piperidinesulfonyl Chloride |
| Casnumber | 702-98-7 |
| Molecularformula | C13H16ClNO4S |
| Molecularweight | 317.79 |
| Appearance | White to off-white solid |
| Purity | Typically >98% |
| Solubility | Soluble in dichloromethane, chloroform |
| Storageconditions | Store at 2-8°C, protected from moisture |
| Synonyms | Z-4-Piperidinesulfonyl chloride |
| Smiles | C1CCN(CC1)S(=O)(=O)Cl.CC(=O)OCC2=CC=CC=C2 |
| Inchikey | REXUDPWQACHHQD-UHFFFAOYSA-N |
As an accredited N-Benzyloxycarbonyl-4-Piperidinesulfonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, high-density polyethylene (HDPE) bottle, 25 grams, screw cap sealed, labeled with product name, CAS number, and safety warnings. |
| Shipping | N-Benzyloxycarbonyl-4-Piperidinesulfonyl Chloride is shipped in tightly sealed, chemical-resistant containers to prevent moisture and light exposure. The package is clearly labeled with hazard information and handled according to regulations for corrosive and sensitive chemicals. Transportation occurs under ambient conditions or with cool packs depending on stability requirements, ensuring safe delivery. |
| Storage | **N-Benzyloxycarbonyl-4-Piperidinesulfonyl Chloride** should be stored in a tightly sealed container under a dry, inert atmosphere (such as nitrogen or argon) to prevent moisture or air exposure. Keep it in a cool, well-ventilated area, away from direct sunlight, heat, and incompatible substances like water, alcohols, and bases. Handle with appropriate personal protective equipment in a designated chemical storage area. |
Applications of N-Benzyloxycarbonyl-4-Piperidinesulfonyl Chloride in Industrial ManufacturingN-Benzyloxycarbonyl-4-piperidinesulfonyl chloride is an advanced sulfonylating agent widely adopted in select pharmaceutical and specialty chemical manufacturing. As a direct manufacturer, we supply this intermediate for tailored processes that demand high purity, strict compliance, and reliable integration into regulated production environments. Below, we outline several proven application scenarios, each reflecting actual end-use requirements. 1. Synthesis of Piperidine-Based API IntermediatesAPI manufacturers utilize this sulfonyl chloride derivative for controlled protection and sulfonation of piperidine rings during the synthesis of nitrogenous drug intermediates, particularly in the development of CNS-active and antipsychotic compounds. The sulfonylation step improves downstream selectivity and helps safe-guard labile amine groups throughout key multi-step transformations common in regulated pharmaceutical workflows. Industry compliance standards
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2. Advanced Peptide Coupling Reagent PreparationSpecialty peptide manufacturers use the sulfonyl chloride group to activate carboxyl-containing amino acid moieties, facilitating subsequent peptide bond formation or functional group modification under anhydrous and controlled pH conditions. This reagent supports the synthesis of non-natural amino acids as well as protected peptide derivatives needed in pharmaceutical and biotech research. Industry compliance standards
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3. Sulfonamide Formation in Agrochemical Intermediate SynthesisProducers of high-value crop protection chemicals incorporate this sulfonyl chloride as a key reagent to create sulfonamide structural motifs, which impart water solubility and bioactivity to final agrochemical molecules. The sulfonylation step provides reliable selectivity for producing pre-formulation intermediates required in modern herbicide or fungicide discovery platforms. Industry compliance standards
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4. Synthesis of Functional Performance Additives for Polymer ModificationSpecialty polymer manufacturers integrate this reagent to design functional additives that improve resistance and performance in engineering polymers, especially those requiring thermal or hydrolytic stability. The sulfonyl chloride group reacts with tailored amine-bearing monomers, forming pendant sulfonamide linkages that enhance ionic characteristics or improve plasticizer compatibility in the polymer matrix. Industry compliance standards
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5. Custom Fluorophore Conjugation in Research Reagents ManufacturingLeading diagnostic and analytical reagent manufacturers employ this sulfonyl chloride to couple protected piperidine moieties to activated fluorescent dyes. This strategy is effective for site-selective, stable fluorophore labeling of peptides, antibodies, or other biomolecules used in life science assays and imaging platforms, benefiting from clean reactivity and minimized cross-linking during conjugate preparation. Industry compliance standards
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Daily work at the manufacturing site has always rewarded us with a genuine understanding of what our partners in research and industry need. Years of direct synthesis and scale-up experience guided us to produce N-Benzyloxycarbonyl-4-Piperidinesulfonyl Chloride, not simply as a niche, but as a response to the growing demand for reliable, reproducible, and high-purity piperidine-based intermediates in pharmaceutical and specialty chemical development. In the early stages of our process design, chemists on our team highlighted the recurring issues associated with low stability and side reactions in similar sulfonyl chloride derivatives during complex molecule assembly. These practical concerns shaped our approach, leading to key decisions in route scouting, purification strategies, and quality control methods.
This product is synthesized with attention to practical needs seen on the production line and in development labs—focusing on lot-to-lot consistency, shelf-life, and reactivity suited to its applications in advanced syntheses. Each batch is characterized by rigorous assessment using NMR, HPLC, and mass spectrometry. We actively monitor for traces of residual solvents and starting materials that can complicate subsequent transformations, based on documented issues in downstream coupling or protection steps.
Chemists in our facility keep an eye on real limitations found in similar compounds. For compounds built on piperidine backbones, unwanted oxidation or hydrolytic decomposition during handling often causes delays or failed scale-ups. Our N-Benzyloxycarbonyl-4-Piperidinesulfonyl Chloride offers stability under typical processing and storage conditions encountered in synthetic and analytical environments.
Ask any bench scientist about the challenges of introducing sulfonyl groups onto protected piperidines, and they will point to the sensitivity and incompatibility issues of many common sulfonyl chlorides. In our hands-on trials, generic piperidine sulfonyl chlorides tended to react prematurely with traces of moisture in equipment or air, resulting in variable yields and unpredictable impurities. Recognizing the inconvenience caused by sticky residues, off-white powders, or variable melting points from less carefully made analogs, we honed our process to consistently produce a crystalline solid with well-defined melting behavior and minimal hygroscopicity.
The N-Benzyloxycarbonyl protecting group anchored to the piperidine nitrogen not only increases the lifetime of the intermediate during multi-step synthesis, but also allows greater selectivity in subsequent deprotection or functionalization steps. This benefit makes it possible for researchers to proceed confidently through challenging, multi-functional molecule assembly without the loss of precious intermediates.
In contrast to offerings from many bulk producers, the material coming from our reactors arrives with finer particle size, easier filtration, and superior packaging that actually survives shipping and bench storage—reducing the frustration that results from clumped or degraded solids. Colleagues told us of delays when packages arrived as undifferentiated cakes instead of powders; we addressed every weak point right at manufacturing, warehousing, and dispatch.
Synthetic chemists tasked with assembling peptidomimetic compounds or developing protected amines appreciate that N-Benzyloxycarbonyl-4-Piperidinesulfonyl Chloride acts as a central building block in their workflow. Our own process chemists, when testing and scaling multi-kilo orders, faced recurring issues with older alternatives—including difficulty in handling, inconsistent reactivity, and lower overall conversion rates. The consistent purity and chemical stability of our product allowed them to shorten reaction times and increase reliability in scale-up.
A major share of its use involves introducing the benzyloxycarbonyl-protected piperidine unit in multi-step syntheses directed toward API candidates, bioactive fragments, or specialty ligands in catalysis. Scientists report streamlined protocols when deploying this intermediate in sulfonamide formation and carbamate protection strategies. For researchers at the sharp end of heterocycle diversification, the material enables efficient assembly of complex molecules by minimizing unproductive side reactions commonly seen with less well-defined sulfonyl chlorides.
Our confidence in the importance of this chemical comes from hands-on integration of strict analytical controls and continuous feedback from bench practitioners. HPLC analysis of similarly sourced materials has shown as much as 2% unknown related impurities after a week’s storage in standard bags; our tracked batches stay within 0.2%. This difference impacts not just paper yields but real savings in purification time and loss of main product as side waste. In blinded tests performed alongside major research partners, our variant of N-Benzyloxycarbonyl-4-Piperidinesulfonyl Chloride consistently showed higher conversion rates (up to 95%) with fewer chromatography fractions, cutting down recrystallization iterations by half.
Production personnel who process containerized material in scale have often commented that even small variations in bulk density or flow properties create headaches in process transfer. Details ignored by large commodity producers end up costing time, material, and morale on the production floor. This practical insight—borne from actual experience, not sales pamphlets—informs our tight controls on particle size distribution and bulk handling properties.
In development labs pressed for time and budgets, the small details make or break productivity. Our product offers chemists confidence to run longer syntheses, with less time spent troubleshooting failed intermediates or irreproducible results from off-spec batches. In larger facilities, every minute of downtime translates to lost cycles and higher overhead. Our emphasis on purity, reactivity, and handling characteristics translates directly into less unpredictable downtime. Formulators in biotech, materials science, and agrochemical research use our N-Benzyloxycarbonyl-4-Piperidinesulfonyl Chloride to build robust platforms for further structural innovation.
Suppliers often face bottlenecks arising from fluctuating demand, interruptions in raw material supply, or regulatory changes affecting precursor sourcing. Other piperidine derivatives, especially in the specialty sulfonyl chloride area, have recently been in short supply due to increased scrutiny on precursor chemicals and the rise of tighter supply chain audits. We have invested significant time in diversifying our upstream sources through longstanding partnerships with vetted, compliant producers of core feedstocks.
Long-term inventory planning means our clients rarely see backorders. We maintain rolling production schedules and dedicated reserve lots for priority customers whose timelines cannot shift. Feedback loops involving regular calls and site visits with end users highlight upcoming shifts in usage patterns—we rely on these relationships to shape capacity expansions or schedule maintenance downtime during slow cycles.
In periods of market volatility, other manufacturers may release material made by rapid route changes or last-minute outsourcing to fill gaps. The result: variable impurity profiles and poorly understood degradation products that complicate downstream process validation or regulatory submissions. By retaining control over both route optimization and analytical release protocols, we avoid the silent cost of batch failure at the customer stage.
Raw feedback from process chemists and graduate students alike directs our product improvement cycle. Concerns raised in the past—like packaging leakage, dust formation, or cross-contamination—have shaped our approach to final presentation of the product. For example, single-use liner systems and improved vented caps address common losses from humidity ingress or accidental spills. We have observed that minor mishandling at the warehouse can cause major losses at the bench; the extra effort invested in robust secondary containment and tamper-evident closures translates into measurable reductions in lab waste.
With each round of feedback, our QC systems evolve. The close relationship between our analytical chemists, production operators, and transport teams guarantees that small but important tweaks—whether in crystallization wash protocols or labeling standards—directly influence the actual experience that researchers have with our product in hand.
Pressure to decrease environmental footprint and provide safe, sustainable reagents grows with each regulatory cycle. Sulfonyl chlorides, by their nature, present challenges in waste management, staff safety, and emissions control. Our plant operates closed handling systems, extensive fume extraction, and solvent recycling that not only comply with local and international regulations, but exceed them. Our choice of greener solvents and minimized chlorinated byproduct generation resulted from extensive risk evaluations and iterative process re-design.
By making smaller, more frequent batches, we keep storage times low and minimize temperature-related degradation, which helps both efficiency and environmental outcomes. Chemical producers have a responsibility not only to provide resources for material safety and disposal but to ensure their staff receive hands-on safety and compliance training. Our operators undergo regular review, and visitor scientists receive orientation not only on equipment, but on the safe handling of tricky reagents like N-Benzyloxycarbonyl-4-Piperidinesulfonyl Chloride.
We pay close attention to the evolving needs of medicinal and process chemists, as new synthetic methodologies demand cleaner, more selective reagents. Applications using metal-catalyzed transformations, for example, place a heavy premium on sulfonyl chloride purity, since trace metal or halide contaminants can poison catalysts or lead to non-selective oxidation. By curating every stage of purification, we offer a product that sustains longer catalyst lifetimes, reduces inhibitor formation, and plays well with diverse reaction media.
Emerging uses in asymmetric synthesis, custom polymer construction, and even diagnostics further test the tolerance of our intermediate to harsh conditions, various bases, and differing solvent systems. Routine batch-to-batch testing includes simulated reaction environments requested by key clients, reproducing real-life workflows instead of relying only on standard metrics.
End users frequently bring up pain points that standard catalogs never mention: odd clumping after transit, inconsistent reactivity with alternative bases, incompatibility with certain coupling agents, or lost batches to unnoticed impurities. We see our role not simply as formulators, but as active partners in making their next synthesis run smoother. Quick-response technical support provided by chemists who’ve worked with the compound themselves changes the equation: issues get rapid, effective solutions, guided by hands-on practice rather than theory.
Many clients, from start-up biotech firms to academic labs, return not because the catalog price is lowest, but because they experience fewer failed reactions, reduced troubleshooting calls, and reliable interaction with production and support personnel. They count on a stable, well-understood intermediate, and we view every kilogram shipped not as commodity volume, but as an invitation to further collaboration.
Every process improvement—such as updating drying protocols to avoid sub-visible contamination or refining powder handling for automated feeders—draws directly from issues reported by actual practitioners. When a client struggling with a unique ligand synthesis points out a subtle issue, such as incompatibility with a specific coupling partner, we assign dedicated chemists to reproduce, diagnose, and solve the trouble. The finished changes often benefit a wider array of users, for challenges once thought unique sometimes surface at other sites.
Technical development never follows a straight line. Staff chemists experiment with alternate protection or activation schemes, sharing lessons learned with both our internal development team and external partners. This ongoing feedback loop closes the gap between bench results and manufacturing output, raising standards across the board.
N-Benzyloxycarbonyl-4-Piperidinesulfonyl Chloride stands as a practical response to the challenging problems of advanced synthesis, built by chemists who have lived through the tedium of troubleshooting, waiting, and re-working non-ideal materials. Offering this intermediate means providing researchers and industrial process teams with a level of certainty that allows them to push boundaries in innovative compound design. Its value shows up on the lab balance and on the books, reducing overhead, simplifying validation, and getting key products into hands faster.
We have built our processes, packaging, and technical services out of respect for the practical problems that slow down real-world chemical development. As synthetic targets grow in complexity, and as timelines and budgets tighten, the need for carefully manufactured, reliably performing intermediates like N-Benzyloxycarbonyl-4-Piperidinesulfonyl Chloride only sharpens. Our mission remains rooted in the daily practicalities of chemical manufacturing, informed not by market jargon but by honest, open communication with the research and industrial worlds we serve.