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1-[(4-Methylphenyl)Sulfonyl]-4-Piperidinecarboxylic Acid

    • Product Name 1-[(4-Methylphenyl)Sulfonyl]-4-Piperidinecarboxylic Acid
    • Alias Tosylpiperidine-4-carboxylic acid
    • Einecs 696-198-0
    • 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

    152518

    Iupac Name 1-[(4-Methylphenyl)sulfonyl]-4-piperidinecarboxylic acid
    Molecular Formula C13H17NO4S
    Molecular Weight 283.35 g/mol
    Cas Number 151585-53-2
    Appearance White to off-white solid
    Melting Point Approx. 180-185°C
    Solubility Soluble in DMSO, slightly soluble in water
    Purity Typically >98%
    Storage Conditions Store at 2-8°C, keep container tightly closed
    Synonyms 4-Piperidinecarboxylic acid, 1-(4-methylphenylsulfonyl)-
    Smiles CC1=CC=C(C=C1)S(=O)(=O)N2CCC(CC2)C(=O)O

    As an accredited 1-[(4-Methylphenyl)Sulfonyl]-4-Piperidinecarboxylic Acid 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 labeled “1-[(4-Methylphenyl)Sulfonyl]-4-Piperidinecarboxylic Acid, 25g,” with hazard symbols and lot number.
    Shipping 1-[(4-Methylphenyl)sulfonyl]-4-piperidinecarboxylic acid should be shipped in tightly sealed containers, protected from moisture and light. Transport under controlled temperatures, avoiding extremes, and comply with relevant chemical and hazardous materials regulations. Ensure proper labeling and include safety documentation. Handle with care to prevent spills and exposure during transit.
    Storage **Storage:** Store 1-[(4-Methylphenyl)sulfonyl]-4-piperidinecarboxylic acid in a tightly sealed container, protected from moisture and direct sunlight. Keep in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers or bases. Ensure proper chemical labeling and store at room temperature or as directed by the manufacturer’s safety datasheet.
    Application of 1-[(4-Methylphenyl)Sulfonyl]-4-Piperidinecarboxylic Acid

    Applications of 1-[(4-Methylphenyl)Sulfonyl]-4-Piperidinecarboxylic Acid in Industrial Manufacturing

    1-[(4-Methylphenyl)Sulfonyl]-4-Piperidinecarboxylic Acid finds specialized applications across several regulated industries. The following sections describe common downstream uses based on real-world manufacturing experience in active pharmaceutical intermediates, agrochemical synthesis, specialty polymer modification, and advanced material research. Each segment details industry-specific standards, material inclusion ratios, integration steps, and end product outputs.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Manufacturers utilize this compound as a critical intermediate during the multi-step synthesis of certain piperidine-based APIs, particularly those targeting neuropharmacological therapy. The presence of the sulfonyl group enhances intermediate stability and functional group selectivity in N-alkylation and carboxylation reactions. Production follows stringent GMP guidelines, with thorough monitoring of starting material quality and in-process control. Material addition occurs immediately after the core piperidine ring construction to facilitate coupling or protection/deprotection stages.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) Monographs for chemical starting materials
    • US FDA 21 CFR Part 210/211 for pharmaceutical production
    • Japanese Pharmacopoeia (JP) for import/export requirements

    Typical usage ratio

    • Batch syntheses range from 0.2 mol to 1.2 mol per mol of target API precursor, depending on target molecular substitutions and purification strategy

    Downstream process integration

    • Material reacts in protected stages after initial piperidine core formation
    • Used in amidation, N-alkylation, and bifunctional linker coupling steps for CNS-active drugs
    • Integrated in semi-continuous reactors for scale-up
    • Residuals removed via SPE or preparative HPLC

    Final product types

    • Finished API intermediates for anti-psychotic drugs
    • Precursors for anti-depressant actives
    • Biosimilar R&D compounds for generic producers
    • Pilot-scale API validation batches

    2. Agrochemical Acaricide and Insecticide Precursor

    Leading agrochemical formulators select this compound during the synthesis of piperidine-derived acaricides and specialized systemic insecticides. The benzylsulfonyl motif is essential for tuning target specificity and breakdown profile in soil environments. Formulation engineers adjust the inclusion ratio based on the desired active loading and local regulatory maximum residue levels (MRLs). Integration occurs during the coupling phase after key backbone construction, before final side-chain modification and formulation.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) process controls
    • REACH Annex VI chemical safety assessment (EU market)
    • ISO 9001:2015 for agrochemical production
    • China GB 2763-2021 MRL for pesticides in food

    Typical usage ratio

    • 0.8 to 1.3 molar equivalents per agrochemical scaffold, depending on ring substitution and downstream derivatization requirements

    Downstream process integration

    • Added during intermediate formation and backbone chain extension in batch reactor or flow systems
    • Precedes purification and esterification/amide coupling for final active formulation
    • Material monitored by LC-MS throughout processing to ensure full conversion
    • Residuals controlled below 0.5 ppm in technical concentrate

    Final product types

    • Technical grade acaricides for commercial agricultural applications
    • Systemic insecticide intermediates for seed coating
    • Export-ready active materials for pesticide formulation plants
    • Evaluation samples for international regulatory submission dossiers

    3. Functionalized Monomer for Specialty Polymer Synthesis

    Producers of high-performance specialty polymers incorporate this compound as a chain modifier or monomer subunit in piperidine-containing resins and ion-exchange membranes. The unique sulfonyl group enhances ion conductivity and mechanical durability in harsh operational environments. Processing engineers test multiple usage ratios at pilot scale to meet target performance for membrane selectivity or resin crosslink density. The raw material enters the polymerization stage, either as a comonomer or via a post-functionalization grafting process.

    Industry compliance standards

    • ISO 9001:2015 quality management system for polymer manufacturing
    • UL 94 flammability for polymer products used in electronics
    • IEC 61340-5-1 for antistatic material in electronics
    • RoHS Directive for heavy metal content in finished goods

    Typical usage ratio

    • 5–15% by weight of functional monomer to total monomer charge; modified according to molecular weight and end-use specification

    Downstream process integration

    • Charged to bulk copolymerization reactors as a co-monomer or modified via post-polymerization grafting
    • Functionalized after initial backbone polymerization for surface treatment applications
    • Polymer blend compounded with additives during extrusion
    • Analytical QC by FTIR and GPC after each batch

    Final product types

    • High-performance ion-exchange membranes for industrial water treatment
    • Electrolyte polymer films for lithium batteries
    • Crosslinked resins for specialty filtration
    • Antistatic coatings for precision electronics packaging

    4. Ligand Precursor in Advanced Material Research

    Academic and commercial R&D labs utilize 1-[(4-Methylphenyl)Sulfonyl]-4-Piperidinecarboxylic Acid to synthesize custom ligand structures for use in metal-ion complexation and organometallic catalysis studies. The molecule’s simultaneous carboxyl and sulfonyl functionalities allow multi-point attachment, crucial for creating chelating agents or durable molecular frameworks. Chemists determine specific loading based on target coordination chemistry and substrate compatibility. Introduction takes place after initial ligand backbone assembly, with subsequent purification and analytical verification according to institutional protocols.

    Industry compliance standards

    • OECD Guidelines for Testing of Chemicals (for published research)
    • ISO/IEC 17025 for chemical analysis during academic R&D
    • Environmental Health and Safety protocols for chemical handling (lab-specific)
    • GHS labeling and documentation for laboratory chemicals

    Typical usage ratio

    • 0.1–0.5 molar equivalents per metal center in model studies, adjusted based on ligand field requirements

    Downstream process integration

    • Ligand assembly via condensation with pre-formed aromatic or heterocyclic frameworks
    • Introduced prior to final metal complexation or as post-functionalization agent
    • Purified by column chromatography or preparative HPLC before screening
    • Characterization by NMR, MS, and X-ray crystallography

    Final product types

    • Chelating ligands for catalysis development
    • Model organometallic complexes for academic publication
    • Custom coordination polymers
    • Reference standards for analytical method development
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    Certification & Compliance
    More Introduction

    1-[(4-Methylphenyl)Sulfonyl]-4-Piperidinecarboxylic Acid: An In-Depth View From a Chemical Manufacturer

    Knowing Our Chemistry: An Eye for Consistency and Quality

    Every batch of 1-[(4-Methylphenyl)Sulfonyl]-4-Piperidinecarboxylic Acid leaving our reactor reflects lessons from years in organic synthesis. Running a plant means facing day-to-day technical realities that academic papers don’t talk about. Process consistency anchors everything; even a small drift in sulfonation temperature, or a trace of water sneaking into the isolation step, can shift the purity, color, or even the final texture of the product. Our operators, some with decades on the floor, know the hazards of condensation lines, blocked filters, and the persistent weight of quality checks. No shortcuts make the cut.

    The story behind each lot runs deeper than a case label. At our site, we train new hires to respect how every variable, from cycle time in the piperidine carboxylation to how quickly a batch cools before filtration, feeds directly into finished specifications. Technical staff track these details for a reason: pharmaceutical researchers and advanced material chemists depend on batch-to-batch sameness, and so do we.

    The Substance at Hand: Unique Features and Actual Applications

    This molecule, built on the backbone of piperidine and decorated with a 4-methylphenylsulfonyl group, stands out for real reasons. We select only high-grade starting material; our 4-methylbenzenesulfonyl chloride stock gets incoming batch confirmation before tank transfer, and the piperidine derivative’s quality determines yields, not just residual impurities.

    Every time the acid hits the application stage, it shows its value—particularly in medicinal chemistry. Called on as an intermediate or protecting agent, it offers a balance between reactivity and selectivity across a range of coupling and derivatization reactions. Unlike basic carboxylic acids that might hydrolyze under extended storage, this compound maintains its integrity, letting chemists push further in catalyst screening or scaffold modification.

    There’s a demand for piperidine sulfonyl derivatives whenever a project moves from early screening to process development. Our partners in pharmaceutical R&D come to us not just for a supplier relationship, but for technical troubleshooting—because they know that variations in melting point or trace metal content can alter downstream yields or even regulatory submissions.

    Unpacking Our Specifications: What Sets Our Process Apart

    Often, customers new to this compound ask what sets our 1-[(4-Methylphenyl)Sulfonyl]-4-Piperidinecarboxylic Acid apart from other offerings. The difference starts at process controls. We keep typical purity over 99 percent by HPLC, with single impurity specs under 0.2 percent. This is not advertising bravado—analytical sheets trace back to batches pulled directly by plant supervisors, put under GC-MS and LC-MS by our own analytical team.

    Physical form also matters, so we don’t just run automated drying cycles and ship ‘as is.’ Our product leaves the dryer as a free-flowing white solid, not a clumped, faintly yellow cake. This means users in kilo-scale synthesis or formulation labs don’t spend hours breaking down lumps or filtering residues. Moisture content stays below 0.2 percent by KF titration; too much residual solvent can cause issues in sensitive transformations. Some labs skip even this check, but that overlooks repeated problems on their end.

    Particle size makes a difference, though customers rarely ask until they’ve dealt with poor solubility elsewhere. With our controlled crystallization, nearly every lot falls within a narrow size range, so it dissolves and reacts predictably. This gives researchers freedom to work at higher concentrations, with fewer adjustments between runs.

    Stability in storage and shipping rounds out our difference. Reactive functional groups can taint results if not stabilized. We pack in inert lined drums under controlled humidity, which avoids sporadic oxidation seen in loosely packaged acids. Our repeat customers point out the trouble-free processability of our material, not just its certificates.

    End Use: Why Synthetic Chemists Value This Molecule

    Chemistry teams don’t choose intermediates in isolation. They need to balance cost, reactivity, safety, and downstream compatibility. The structure of 1-[(4-Methylphenyl)Sulfonyl]-4-Piperidinecarboxylic Acid builds flexibility into synthetic schemes. Its bulky sulfonyl group blocks reactions at certain sites, guiding transformations to more accessible positions, which helps when constructing complex scaffolds.

    Medicinal chemists rely on predictable protection and deprotection behavior. This compound fits the bill. The sulfonyl cap is tough enough to stand up to tough conditions, like strong bases or mild reduction, yet it can be removed without damaging other fragile groups. In peptide synthesis, for instance, selective removal after chain elongation keeps the rest of the structure intact.

    Material scientists have found value in the unique hydrophilic-lipophilic balance this molecule offers. Its dual nature makes it particularly useful in surfactant development or as an anchor in adaptive coatings. Graduate students and manufacturing engineers both want intermediates that deliver reliable chemical behavior, not theoretical promise.

    Differences from Similar Products: Practical & Technical Dimensions

    The chemical marketplace isn’t short on piperidine derivatives, and many catalog houses list structurally related acids. In practice, not all meet expectations on purity, stability, and consistency. Some traders repackage or source from multiple unknown sites, making it a riskier choice for regulated industries. As the manufacturer, we know exactly which vessel made which drum, and we can trace impurity profiles back months or years.

    Sulfonyl-piperidine acids of other substitution patterns often fail to combine reactivity and selectivity at the right levels. For example, switching to a non-methylated sulfonyl group makes it less hydrophobic, changing its compatibility in organic solvents; an unsubstituted piperidine changes the basicity, which in turn alters coupling outcomes. These subtleties matter once you’re scaling reactions, not just pipetting milligrams.

    We’ve compared notes with project managers frustrated by inconsistent acid numbers or the presence of minor byproducts, such as unreacted sulfonyl chloride or over-oxidized species. Our dedicated purification and QA processes address such concerns head-on. No customer has ever benefited from discovering these variables late in a scale-up run.

    Actual Uses: Industry Voices and Demands

    Beyond academic curiosity, the reality is that 1-[(4-Methylphenyl)Sulfonyl]-4-Piperidinecarboxylic Acid has found persistent demand in the development of small molecule APIs (active pharmaceutical ingredients), peptidomimetics, and specialized polymer additives. Some customers use it as a coupling partner in convergent synthesis, benefiting from the precise functional arrangement; others exploit the sulfonyl group as a means to tune activity or block undesired reactivity in their lead series.

    Process engineers looking to avoid side-product formation appreciate the structural clarity of this compound. Several industry partners have chosen us after failed experiences with unstable or polymorph-prone alternatives elsewhere. Our own technical support, on call with actual lab records, has helped parametrize their procedures, reducing failed batches and long washouts.

    We see steady requests from contract research outfits in Europe and North America, who integrate this intermediate at pilot or production scale. In recent years, regulations and strict audit requirements have raised the bar on documentation and control, especially for intermediates destined for regulated drug development. Our operation has geared QA and batch release procedures specifically to meet these higher demands, routinely sending full analytical packages upon request. We see the difference in long-term repeat orders.

    Manufacturing Challenges: Crafting Reliable Chemistry

    Producing complex intermediates on an industrial scale demands expertise and vigilance. The organic process for sulfonylation requires exacting control of reagents and temperatures; runaway reactions risk not only low yields but also operator safety. We have invested in process automation and robust monitoring tools to minimize any chance of over-sulfonation or thermal excursions.

    Purification, often treated as an afterthought by limited-scale vendors, gets no shortcuts here. Removing process residues and color bodies while retaining optimal yields takes precise solvent choices and operator feel for separation cues. The finished material’s brightness isn’t just for appearance. Persistent trace impurities can poison catalysts or complicate downstream assays. Our QA techs routinely grind and sample from different layers of each drum; any batch that falls outside agreed limits gets full investigation, not excused as “within commercial range.”

    Each campaign brings new challenges—pump downtime, spike in raw material cost, or unplanned customer audits. Our plant management team stays focused on long-term reliability, not just quarterly targets. Customers benefit from running their own chemistry with fewer headaches and surprises along the way.

    Being the manufacturer, rather than a middleman, means we answer for every drum—good or bad. Feedback goes straight to the chemists and engineers in charge, bypassing layers of sales bureaucracy. That’s how technical improvements actually reach the shop floor and the customer bench.

    Focusing on Real-World Solutions

    Industry partnerships make it clear: flexibility and communication win over set-and-forget supply. We maintain an open line for technical questions, whether about reactivity in a novel coupling method, or safe handling advice during a scale-up. We share best practices learned in the plant—avoid moisture in open vessels, dissolve slowly under nitrogen, control temperature ramps to avoid side reactions.

    Some customers request specific packaging options or additional impurity checks to align with QA protocols. We accommodate custom needs with the same rigor as any standard spec; our QA systems are built to manage traceability and documentation, so regulated users can qualify our material for any critical path.

    Problems happen in research and manufacturing, and solutions come from direct dialogue with users. We share troubleshooting notes and alternative workups, informed by our years at the bench and in the control room. That builds reciprocal trust—a factor you can’t import from a catalog.

    Weighing Importance in Evolving Markets

    As new regulations, environmental goals, and customer audits reshape the fine chemicals industry, our experience producing 1-[(4-Methylphenyl)Sulfonyl]-4-Piperidinecarboxylic Acid takes on renewed relevance. European and North American regulatory shifts have tightened documentation and traceability. Our long-term investment in real-time analytical monitoring and secure batch records allows us to meet higher customer expectations without scrambling to catch up.

    We continue to advise partners on sustainability efforts, offering greener process alternatives or solvent recycling strategies where possible. Our product isn’t just about a clean analytical trace; it reflects broader priorities in worker safety, environmental responsibility, and lifecycle reporting. Our technical staff participate in industry working groups and customer audits, improving our process every year.

    The lessons learned from tracking every batch through our reactors play out in the end user’s lab. Predictability, open communication, and genuine support can’t be improvised. Being the source of record for 1-[(4-Methylphenyl)Sulfonyl]-4-Piperidinecarboxylic Acid, we commit to improvements informed by lived realities, not sales hype.

    Where catalog companies disappear after the invoice, we remain an active technical stakeholder, standing behind every drum shipped and every conversation had. Researchers, production chemists, and project managers deserve that commitment, and it’s what keeps us pushing for better with each campaign.