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3-Methylpiperidine

    • Product Name 3-Methylpiperidine
    • Alias 3-Methylazacyclohexane
    • Einecs 203-583-1
    • 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

    807059

    CAS_Number 626-56-2
    Molecular_Formula C6H13N
    Molar_Mass 99.17 g/mol
    IUPAC_Name 3-Methylpiperidine
    Appearance Colorless to yellow liquid
    Boiling_Point 132-134 °C
    Melting_Point -60 °C
    Density 0.823 g/mL at 25 °C
    Flash_Point 24 °C (closed cup)
    Refractive_Index 1.430-1.433
    Solubility_in_Water Miscible
    Odor Amine-like
    PubChem_CID 12218

    As an accredited 3-Methylpiperidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 250 mL of 3-Methylpiperidine, sealed with a screw cap, and labeled with hazard and identification information.
    Shipping 3-Methylpiperidine is shipped as a hazardous chemical, typically in tightly sealed, corrosion-resistant containers. It should be stored and transported in a cool, well-ventilated area, away from sources of ignition or incompatible substances. Proper labeling, documentation, and adherence to local regulations regarding flammable and toxic materials are required during shipping.
    Storage 3-Methylpiperidine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. It must be kept away from strong oxidizing agents, acids, and moisture. Proper labeling and secondary containment are recommended to prevent accidental release and ensure chemical compatibility in storage areas.
    Application of 3-Methylpiperidine

    Applications of 3-Methylpiperidine in Industrial Manufacturing

    As a dedicated manufacturer of 3-Methylpiperidine, we support downstream enterprises by supplying high-purity material engineered for precise applications across the pharmaceutical, agrochemical, and fine chemical sectors. Below we detail several key industrial usage scenarios, highlighting regulatory standards, dosage parameters, workflow integration points, and representative end-products used globally.

    1. API Intermediate for Antihistamine Synthesis

    3-Methylpiperidine is widely employed as a building block in the synthesis of pharmaceutical active ingredients, especially in the manufacture of second-generation antihistamines. Its tertiary amine structure facilitates targeted substitutions and ring-forming reactions during the construction of complex molecular scaffolds. Producers utilize it in batch and continuous synthesis routes to generate high-value intermediates meeting stringent medicinal standards.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Current Good Manufacturing Practice (cGMP) – 21 CFR Part 210/211 (US FDA)
    • European Pharmacopoeia (Ph. Eur) guidelines for relevant APIs
    • Chinese Pharmacopoeia (ChP) for national market supply

    Typical usage ratio

    • 0.9 – 1.2 molar equivalents relative to key acylation or alkylation step; adjusted based on specific reaction yield and purity target in multi-step synthesis

    Downstream process integration

    • Introduced during early to mid-stage condensation and cyclization stages; added to reaction vessels under controlled temperature (60–120 °C) and inert atmosphere to drive selectivity

    Final product types

    • Desloratadine, Loratadine, and related antihistamine drug substances
    • Pharmaceutical grade intermediates for further API synthesis

    2. Precursor in Agrochemical Pyridine Herbicide Manufacture

    In the agrochemical industry, 3-Methylpiperidine serves as a key intermediate for the synthesis of substituted pyridine derivatives, which ultimately become active ingredients in selective herbicides. Its controlled reactivity ensures high conversion rates and minimal impurity formation, which downstream manufacturers depend on for consistent herbicidal performance and regional regulatory compliance.

    Industry compliance standards

    • ISO 9001:2015 for chemical process management
    • FAO/WHO Specification for Pesticide Technical Material (FAO/WHO, JMPS)
    • REACH (EC) No 1907/2006 registration for substances in European markets
    • US EPA regulations on active ingredient pre-manufacture (40 CFR Part 158)

    Typical usage ratio

    • 5–9% by weight of total reaction mass, as determined by formulation pathway and targeted yield

    Downstream process integration

    • Engaged during the nucleophilic substitution and ring-closure stages of engineered synthesis lines, typically under catalytic and controlled pH conditions

    Final product types

    • Pyridine-based herbicides such as Picloram and Triclopyr technical concentrates
    • Granular and emulsifiable concentrated herbicide formulations

    3. Solvent Component for Fine Chemical Alkylation Processes

    The high boiling point and selective basicity of 3-Methylpiperidine make it an effective medium or co-solvent in fine chemical operations, particularly during specialized alkylation reactions where amine-based solvents are required to control reactivity profiles and byproduct suppression. Its use optimizes product yield while facilitating downstream purification and recovery procedures in continuous and batch reactors.

    Industry compliance standards

    • ISO 14001 Environmental Management certification for chemical manufacturing
    • OECD Guideline for Testing of Chemicals (where solvent use impacts final substance safety)
    • Internal QC protocols conforming to customer-specific procurement audits
    • National fire and occupational health safety codes for amine solvent use

    Typical usage ratio

    • 20–45% of total solvent volume, precise ratio determined by reactant solubility and catalyst compatibility

    Downstream process integration

    • Added at pre-reaction charge as primary medium for alkylation or acylation operations; monitored for residue and possible recovery at downstream distillation stage

    Final product types

    • Engineered specialty intermediates for dyes, pigments, and electronic chemicals
    • Batch-specific customized intermediates for contracted synthesis

    4. Intermediate for Synthesis of Cycloalkylamine-based Catalysts

    3-Methylpiperidine is used as a feedstock for preparing modified cycloalkylamine ligands, which downstream catalyst manufacturers employ in fine chemical and petrochemical synthesis. Its structural attributes enable controlled derivatization, resulting in catalyst systems with tailored selectivity for olefin polymerization or asymmetric synthesis.

    Industry compliance standards

    • ISO 17025 accredited analytical verification for catalyst intermediates
    • Responsible Care® Global Charter adoption for chemical handling
    • Internal QA/QC compliance for batch-to-batch consistency
    • Contractual adherence to downstream end-user technical specifications

    Typical usage ratio

    • 1:1 molar equivalent in formation of ligand backbone; adjustments made for multi-ligand system designs or specific metal coordination requirements

    Downstream process integration

    • Fed into reactor at ligand formation stage, followed by complexation with transition metals (e.g., Ni, Pd, Cu) under controlled inert atmosphere in glass-lined or stainless steel vessels

    Final product types

    • Cycloalkylamine-ligated homogeneous catalysts for fine chemical manufacture
    • Specialty catalyst packages for polymer and pharmaceutical synthesis

    5. Building Block in Organic Corrosion Inhibitor Formulations

    3-Methylpiperidine supports the development of advanced organic corrosion inhibitors for use in industrial water treatment and oilfield applications. Amines of this class enable downstream formulators to produce inhibitors that provide surface-active protective films on metal and alloy substrates, with formulation parameters engineered for local regulatory approval and performance longevity.

    Industry compliance standards

    • ASTM D2688 Standard for Corrosion Inhibitors in Industrial Water
    • National Sanitation Foundation (NSF)/ANSI 60 for drinking water chemicals (where applicable)
    • API RP 1110 for oilfield brine treatment chemicals
    • REACH compliance for European market chemical formulations

    Typical usage ratio

    • 2–8% active component in final inhibitor blend, adjusted for system pH, water hardness, and target dosage per cubic meter

    Downstream process integration

    • Introduced as part of premix phase, then subjected to blending, stabilization, and filtration processes before packaging and shipment to industrial end-users

    Final product types

    • Oilfield and pipeline corrosion inhibitor concentrates
    • Industrial cooling water treatment formulations
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    Certification & Compliance
    More Introduction

    3-Methylpiperidine: Our Perspective as a Chemical Manufacturer

    Understanding the Role of 3-Methylpiperidine in Today’s Chemical Landscape

    In our production facilities, 3-Methylpiperidine stands out as a backbone compound for both established and emerging synthesis routes. With the molecular formula C6H13N and a molecular weight of 99.17 g/mol, this clear, colorless to pale yellow liquid enters our reactors each day for one reason above all: its reliability in complex, demanding synthesis processes. Years of running batches and seeing customer applications firsthand have shown us how much depends on the consistency of our product’s purity, which must typically exceed 99% by GC analysis to meet technical and pharmaceutical standards.

    Our chemists have worked closely with our plant operators to optimize each batch so the output meets exacting specifications. 3-Methylpiperidine offers a boiling point of about 132–136°C and a melting point near −52°C. Customers often point out that the unique positioning of the methyl group at the 3-position—compared to n-methylpiperidine or 4-methylpiperidine—gives this molecule specific steric and electronic effects. These can play a key role in tuning reactivity, which is crucial for those involved in pharmaceuticals, agrochemicals, or specialty intermediates.

    Direct Production Experience: Purity, Handling, and Stability

    Daily production runs put us in direct contact with the practical realities of 3-Methylpiperidine. Material that leaves our distillation columns is colorless and features a faint, characteristic amine odor, not overpowering compared to some other aliphatic amines we manufacture. Having handled countless drums and IBCs, our team knows the importance of careful temperature controls. The compound boils lower than many other piperidines, which means storage under an inert atmosphere and tightly sealed containers. The risk of oxidation and the tendency to absorb carbon dioxide and moisture directly affect both analytical results and downstream reactions.

    We characterize each lot in-house using NMR, GC, and Karl Fischer titration to track water levels—not only to satisfy regulatory documentation but because our own synthesis teams demand it. Every error in moisture control creates real complications for catalytic and substitution reactions later down the line. Our warehouse staff monitors transfer lines for leaks and vapor buildup more strictly with 3-Methylpiperidine than with bulk base chemicals, so we retain both safety and purity.

    Applications Rooted in Real World Chemistry

    Most end-users approach us with one goal: get amines that advance their own new molecules or production processes. 3-Methylpiperidine steps into this role in a range of synthesis plans. In pharmaceutical R&D, it features in heterocycle building block strategies, making functionalized piperidine rings for diverse small molecules that often target neurological or cardiovascular pathways. We have watched several drug discovery groups select the 3-methyl derivative over its unsubstituted or N-methyl cousins specifically because of how the methyl group alters pharmacodynamics and pharmacokinetics.

    Our agrochemical customers have flagged the molecule's value as an intermediate for insecticides and herbicides. It slots neatly into multi-step processes as a base or nucleophile, where its steric profile—bulkier at the 3-position—can help modulate selectivity in addition-elimination reactions. Many years in this industry have shown us how a minor tweak like this translates into higher target yields or easier separation of byproducts. This distinction becomes clear when comparing outcomes between 3-Methylpiperidine, plain piperidine, and 4-Methylpiperidine in parallel laboratory setups.

    What Sets 3-Methylpiperidine Apart from Related Building Blocks

    Looking across our own product lineup, we notice tangible differences between 3-Methylpiperidine and more traditional piperidine derivatives. One common question from formulators and process chemists relates to how our product compares with unsubstituted piperidine. The switch to the 3-methyl variant can reduce side reactions, especially where regioselectivity or reduced basicity is necessary. In our reactors, this translates to improved yields in some Grignard reactions and condensation processes.

    For those considering alternatives like 4-Methylpiperidine, the position of the methyl group truly matters. The 3-position creates a different steric environment than the 4-position, directly influencing how the molecule binds in transition states or fits into chiral catalysts. We have seen patent literature and real process data confirm that the effects are not interchangeable, warranting a careful evaluation when route planning for active pharmaceutical ingredients or advanced intermediates. Over the years, our technical support teams have provided guidance to researchers choosing between these isomers for scale-up.

    The question of using N-methylpiperidine instead also comes up often in technical calls. Our field experience tells us the difference between an N-alkylated versus a ring-alkylated structure can determine catalyst compatibility, reactivity with acylating agents, and final end-use properties. By keeping the nitrogen un-substituted and placing the methyl at the 3-position, chemists subscribe to a completely different pattern of reactivity—something only evident through both bench-scale comparison runs and continuous customer feedback from process development trials.

    Operational Safety and Handling Lessons Learned

    In our own facility, years of practical exposure have shaped our approach to storage and safe handling. The amine odor is less sharp than with some open-chain analogues, making accidental exposure less immediately irritating, yet no less important to control. Our operators know from direct experience that even trace oxygen ingress during drum storage can lead to formation of degradation products, so we avoid long storage times and rotate stock regularly. Working with inert atmosphere blanketing and maintaining a dry, cool warehouse environment helps preserve both purity and potency—lessons learned not from sales literature but from keeping hundreds of tons moving trouble-free every year.

    Our EHS staff spends significant time training new hires on amine safety: splash risk, vapor inhalation, and correct neutralization procedures in case of spills or leaks. Even after so many batches, we take every incident report seriously. This helps us stay abreast of the latest compliance requirements for hazardous materials, and we apply voluntary best practices drawn from our global peer group. This includes regular workspace air monitoring and using closed-loop bulk transfer lines—choices rooted in practical experience rather than any regulatory minimum.

    Supporting Downstream Quality: What We Provide & Why It Matters

    We know from customer feedback that every step leading to a successful drug, pesticide, or polymer hinges on reliable raw materials. Materials shipped from our loading bays reach engineers and chemists who trust not only the purity figure but also the hands-on standards built into every drum. Impurities from oxidized amines, trace water, or extraneous amines introduce multiple headaches for subsequent synthesis: color changes, failed couplings, and regulatory documentation issues.

    Companies developing scale-up routes for APIs have explained how our documentation of traceability helps prove process history to global regulators. By tying every batch of 3-Methylpiperidine to a lot-specific COA, NMR printout, and MSDS, we let customers sleep easier—knowing they can defend their own supply chain audits. It is not uncommon for our technical support team to discuss real-world QC (quality control) troubleshooting with customers and address unexpected compatibility issues in reaction setups. Our in-lab testing and out-in-the-field experience often become a lifeline for partners looking to avoid unnecessary downtime or regulatory inspection setbacks.

    In some cases, we have supported pilot plant customers by providing alternate packaging (from drum to tanker) and variant grade options that better match end-use process requirements. For instance, pharmaceutical customers may require higher-purity, lower-metal lots compared with agricultural users. We have listened carefully and adapted, not because the market dictates it but because years of technical discussions taught us the hidden costs of underestimating end-use needs.

    Challenges & Our Approach to Continuous Improvement

    Producing 3-Methylpiperidine consistently at industrial scale has taught us to pay close attention to several process bottlenecks. Thermal control during synthesis, prevention of cross-contamination from other amines, and minimizing residual solvents all became priorities through hard-won lessons. Plant data confirmed more than once that an unstable feedstock supply chain could ruin yields or create off-spec product, so we invested in raw material qualification and redundant sourcing. On the compliance front, we keep up with REACH and GHS labeling, as we have watched regulations shift over the last decade. In some markets, end-users ask for additional certification—such as Kosher, Halal, or compliance with the latest prop 65 lists—and we work with certifying bodies where justified by customer need.

    An ongoing area for improvement comes from energy efficiency. Piperidine derivatives, including ours, are traditionally produced in processes that require significant distillation and purification steps. We have allocated R&D resources to look into alternative separation techniques—azeotropic distillation, in-situ solvent swap, and membrane filtration—to cut energy consumption. Even incremental improvements matter in both cost and carbon footprint over the long term. We assess and report key sustainability metrics like process water recycling, hazardous waste minimization, and overall emissions, not as marketing exercises but because our operations team scrutinizes energy bills and permit renewals every quarter.

    Feedback Loops: Connecting Plant Operations to Market Demands

    Through our customer-facing technical support channels, we've tracked a steady stream of new applications for 3-Methylpiperidine each year. Early interest in drug discovery has widened to specialty catalyst synthesis, custom polymer building blocks, and battery R&D. Lab-scale requests often turn into multi-ton orders for pilot or full-scale runs, and during these transitions, packing, delivery timelines, and support for analytical retesting make all the difference. The most successful collaborations happen when our production staff, commercial team, and customer’s own R&D scientists align on timelines and purity specifications. These working relationships—often stretching many years—mark the difference between transactional sales and full technical partnerships.

    As new research fields open, we adapt our manufacturing and QA workflows. Electrochemical startups, for instance, have flagged the need for trace metal analysis on all amines to avoid poisoning new battery chemistries. These learnings flow back to our plant, where we now factor ICP-MS testing into regular production batches beyond the needs of only pharma-grade customers. Such feedback loops help us spot potential failure points early and implement improvements that directly matter to those on the next step of the value chain.

    We rely on direct relationships with end-users to update our technical data packages and inform our production planning decisions. In many cases, our ongoing collaborations prompt us to run special pilot plant test batches or to adapt packaging to unusual shipping conditions. Such real-time adaptation has saved time and cost for our clients while sparing us the effort of reactive troubleshooting after issues occur. Every insight from a customer pilot plant or process chemist shapes the evolution of our own internal standards.

    Looking Ahead: Building Capacity and Resilience

    Industry demand for 3-Methylpiperidine shows no sign of slowing down. To support both legacy and new applications, our plant teams revisit capacity planning each year. Regular evaluations of production throughput, energy use, and process bottlenecks allow us to maintain high reliability even as market volumes fluctuate. In times of raw material shortage or logistics disruption, having diversified supplier relationships and in-house purification know-how has kept lines running when others suffered interruptions. We constantly refine these supply chain links, favoring local and regional sources where possible to ensure on-time delivery.

    For scale-up customers, we provide bulk options ranging from lab bottles to multi-ton ISO tanks. Our engineers work side by side with procurement teams to agree on forecasted volumes. We keep dedicated reserve capacity for strategic partners, ensuring redundancy for mission-critical rollouts in new process plants. Periodic investments in new distillation towers, recycle lines, and IT infrastructure pay off in performance and customer peace of mind.

    We track sector-wide shifts, such as changing regulatory approaches to nitrogen-containing intermediates or expanded reporting for environmental releases. By staying plugged into industry associations, academic research, and real user feedback, we future-proof not only our own plant but also customer projects that rely on just-in-time material flows and validated supply chains.

    Final Thoughts from the Production Floor

    Decades of producing 3-Methylpiperidine have taught us that excellence goes beyond a narrow focus on purity figures or generic certificates. Day in and day out, our teams test, package, and troubleshoot this amine to support a diverse landscape of process chemists, formulators, and researchers. The real difference comes from our willingness to meet each new process challenge head-on, re-invest in plant upgrades, and communicate transparently with those who trust us to deliver. The best outcomes result from hands-on operational knowledge, rigorous internal standards, and lasting relationships with the most demanding and creative users of specialty building blocks.

    At the end of each production cycle, our aim is simple: send out 3-Methylpiperidine that supports our customers’ next breakthrough—whether it is a new drug, a greener pesticide, or an advanced material. Drawing on lessons from thousands of tons shipped, hundreds of process reviews, and years of accumulated know-how, we keep our sights set on quality, safety, and partnership for the future.