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N-Ethyl-N-Methylpiperidinium Iodide

    • Product Name N-Ethyl-N-Methylpiperidinium Iodide
    • Alias EMPy·I
    • Einecs 632-171-5
    • 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

    142104

    Chemical Name N-Ethyl-N-Methylpiperidinium Iodide
    Cas Number 27005-28-1
    Molecular Formula C8H18IN
    Molecular Weight 255.14 g/mol
    Appearance White to off-white solid
    Melting Point 175-178°C
    Solubility In Water Soluble
    Storage Conditions Store at room temperature, in a tightly sealed container
    Synonyms 1-Ethyl-1-methylpiperidinium iodide
    Pubchem Cid 2821500
    Iupac Name 1-ethyl-1-methylpiperidin-1-ium iodide

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

    Packing & Storage
    Packing A 25g quantity of N-Ethyl-N-Methylpiperidinium Iodide is packaged in a tightly sealed, amber glass bottle with safety labeling.
    Shipping N-Ethyl-N-Methylpiperidinium Iodide should be shipped in a tightly sealed container, protected from moisture and light. Ensure compliance with local and international chemical transport regulations. Label the package as hazardous if applicable, and include the appropriate Safety Data Sheet (SDS). Transport should be via a reputable chemical courier or carrier.
    Storage **N-Ethyl-N-Methylpiperidinium Iodide** should be stored in a tightly sealed container, protected from light and moisture, and kept at room temperature (15–25°C). Store in a dry, well-ventilated area, away from incompatible substances such as strong oxidizers. Proper labeling and containment will help prevent contamination and ensure safe handling. Always follow local safety regulations for chemical storage.
    Application of N-Ethyl-N-Methylpiperidinium Iodide

    Applications of N-Ethyl-N-Methylpiperidinium Iodide in Industrial Manufacturing

    As a primary manufacturer, we supply N-Ethyl-N-Methylpiperidinium Iodide to key downstream sectors that require unmatched batch consistency and traceable quality in specialty applications. Below, we outline the leading industries that utilize this material, specifying industry standards, dosage guidelines, integration steps, and resulting end-use products.

    1. Electrolytes for High-Performance Dye-Sensitized Solar Cells (DSSC)

    Developers of third-generation photovoltaic modules incorporate our quaternary ammonium iodide as a high-stability ionic conductor within DSSC electrolyte blends. Formulators reference device-specific standards for stability and photoconversion efficiency. End users value iodide salts for their consistent electrochemical activity and batch reproducibility in mass production environments.

    Industry compliance standards

    • IEC 62688 (Photovoltaics - Design qualification of DSSC modules)
    • Electrochemical Society ECS Standard Methods for DSSC analysis
    • In-house QC protocols for impurity and ionic mobility

    Typical usage ratio

    • 0.05–0.2 M in final liquid electrolyte solution, with specific concentration adjusted based on target ionic conductivity and device scaling requirements

    Downstream process integration

    • Dissolved into the prepared organic solvent matrix (acetonitrile, methoxypropionitrile, or similar) following the addition of the redox mediator; batch mixing performed during the final electrolyte formulation stage immediately before cell injection and sealing

    Final product types

    • Dye-sensitized solar module panels
    • Indoor photovoltaic arrays for IoT power sources
    • Flexible solar film sheets

    2. Electrochemical Supercapacitor Electrolytes

    Supercapacitor manufacturers select our piperidinium iodide compound for applications in high-energy density symmetric and asymmetric devices, especially where thermal endurance and ionic mobility under cycling are critical. The raw material enters the blending phase, supporting high-rate charge/discharge across extended operational lifespans.

    Industry compliance standards

    • IEC 62391 (Fixed electric double-layer capacitors for use in electronic equipment)
    • RoHS Directive 2011/65/EU for heavy metals and halide components
    • UL 810A (Electrochemical Capacitors Safety Standard)

    Typical usage ratio

    • 0.01–0.1 mol/L, tuned to optimize operating voltage window and ESR (Equivalent Series Resistance) within device-specific electrolyte formulations

    Downstream process integration

    • Combined with supporting electrolyte salts and solvents in controlled reactors during the liquid or gel-phase electrolyte compounding step; introduced prior to the automated assembly of capacitor cell stacks

    Final product types

    • Supercapacitor cells for energy storage modules
    • Backup power units for consumer electronics and grid applications
    • Hybrid electric vehicle boost modules

    3. Phase-Transfer Catalyst in API Synthesis

    Pharmaceutical manufacturers employ N-Ethyl-N-Methylpiperidinium Iodide as a selective phase-transfer catalyst during the alkylation and nucleophilic substitution reactions for certain small-molecule active pharmaceutical ingredients (APIs). Its high purity and controlled impurity profile support batch-to-batch reproducibility mandated by regulatory filings.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • US Pharmacopeia (USP) for residual solvents and impurities
    • EU GMP Annex 8 for starting materials

    Typical usage ratio

    • 0.5–2 mol% relative to the limiting reagent in the synthetic route; adjusted to drive complete phase transfer and minimize side reactions during scale-up

    Downstream process integration

    • Added to the reaction vessel at the interphase of aqueous/organic boundaries, promoting the migration of reactive anions into the organic phase to accelerate coupling or functionalization steps in API construction

    Final product types

    • Regulatory-submitted small-molecule APIs
    • Pharmaceutical intermediates for further synthesis or direct formulation
    • Contract-manufactured drug substances

    4. Quaternary Ammonium Salt for Ionic Liquid Engineering

    Chemical processing firms and specialty chemical labs deploy our iodide salt as a core building block in custom ionic liquid synthesis, targeting applications that require wide electrochemical windows and precise viscosity ranges. Ionic liquid formulators value product traceability and consistent ion structure.

    Industry compliance standards

    • ISO 9001:2015 (Quality management systems for specialty chemicals)
    • REACH Regulation (EC) No 1907/2006 for chemical registration and use
    • In-house analytical protocols for ion purity and water content

    Typical usage ratio

    • 0.1–1 molar equivalent in custom ionic liquid formulations, reflecting desired melting point and solvation properties; major ratio adjustments based on final engineered liquid specification

    Downstream process integration

    • Charged to glass or inert-lined vessels during the cation/anion exchange sequence, commonly under anhydrous and oxygen-free conditions, before downstream ionic separations and purification

    Final product types

    • Ionic liquids for battery electrolyte R&D
    • Solvents for advanced organic synthesis
    • Specialty catalysts and extraction agents
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    Certification & Compliance
    More Introduction

    N-Ethyl-N-Methylpiperidinium Iodide: Manufacturer Commentary

    Crafting Quality Compounds for Real-World Needs

    As a direct manufacturer with years behind reactors and purification columns, I understand how a specialty chemical shapes the work of researchers and product formulators. N-Ethyl-N-Methylpiperidinium Iodide stands out among quaternary ammonium salts. This compound, formed by functionalizing a piperidine ring with ethyl and methyl groups, then pairing it with iodide, brings consistent results in both academic and industrial settings.

    Understanding the Chemistry

    The backbone of this molecule comes from the six-membered piperidine ring, a structure well appreciated for its stability and solubility across multiple solvent systems. Adding ethyl and methyl groups changes the electronic and steric profile, affecting both reactivity and handling. Pairing the cation with iodide instead of more common halide anions such as chloride or bromide, changes not just solubility but also downstream compatibility in catalyst systems and organic synthesis.

    From Bench-Scale to Bulk Synthesis: Scaling for Consistency

    When we produce N-Ethyl-N-Methylpiperidinium Iodide, every stage from raw material screening to final isolation receives careful attention. The process isn’t just about following a recipe; variation in temperature, choice of solvents, and timing of quaternization matter deeply. Inconsistent procedures risk off-color product, issues with hygroscopicity, or difficulties downstream.

    Technical demands ask for a product that dissolves fast, without cloudiness or particulates. Experience during synthesis and post-synthesis purification plays a big role here. Too much residual starting material or incorrect reaction conditions bring NMR-detectable impurities and affect downstream reactivity. Consistent melting point and confirmed purity by HPLC or titration ensure that our compound supports sensitive projects in catalysis, phase-transfer systems, or advanced analytical tasks.

    Common Uses in Today’s Labs and Plants

    Colleagues across organic synthesis and pharmaceutical research trust N-Ethyl-N-Methylpiperidinium Iodide for phase-transfer catalysis and as a supporting electrolyte in select electrochemical applications. In my own experience, its symmetrical structure compared to other substituted piperidinium salts leads to better reproducibility in multi-step reactions that require cationic transport. Iodide’s larger ionic radius and polarizability, compared to chloride or bromide, provides a softer interaction that is often the difference in yields and selectivity, especially for those scaling up for pilot or production batches.

    Conductivity and solubility remain central for those using it as an electrolyte. The iodide anion supports specific needs in redox chemistry, where performance falls short with smaller or harder halides. Over years of feedback from application chemists, the demand for high-purity piperidinium salts with tailored ion-pairing properties has grown, strongly driving how we design our production runs.

    Model, Purity, and Handling: Why Our Product Delivers

    We keep specifications grounded in end-use, not just arbitrary numbers. A reliable melting range, high assay by titration, and absence of darkening under ambient storage—those qualities matter more to most users than an ultra-narrow particle size, since this compound is usually dissolved before use. Attention to lot-to-lot reproducibility means academic teams can repeat protocols without chasing new variables each time.

    Handling characteristics such as caking resistance and free-flowing crystals are results of process design and controlled drying conditions. A compound may look fine at first, but within a month unwanted moisture absorption or discoloration can creep in. Running our plant's vacuum drying and packaging cycles according to humidity and season keeps the product ready for immediate incorporation into target processes.

    Comparing to Other Quaternary Ammonium Salts

    Many users ask why not choose a simpler salt, such as N-Methylpiperidinium Chloride or Tetraethylammonium Iodide. For work that involves stubborn organic or biphasic reactions, the unique balance of hydrophobic and hydrophilic character in N-Ethyl-N-Methylpiperidinium Iodide can tip the scales. Its structure allows it to move reactants across phase boundaries better in certain solvents than a bulkier or smaller cation.

    Against common tetraalkylammonium salts, our compound carries a piperidine backbone, which affects the compound’s profile in complex mixture separations or as a phase-transfer agent. In our testing, and in reports from users, side-reactions or background interferences are lower compared with less structurally rigid ammonium salts. The ability to tailor ionic strength without excessive foaming or precipitation, especially in concentrated systems, sets it apart during scale-up.

    Operating With the Research Community in Mind

    Unpredictable availability or fluctuating quality from intermediaries often frustrates both bench chemists and process engineers. Manufacturing N-Ethyl-N-Methylpiperidinium Iodide in-house rather than relying on repackagers gives us control over every raw material batch, reactor cleanout, and packing method. Direct accountability translates to consistent supply and a willingness to discuss custom tweaks to composition, within regulatory and logistical limits.

    We invest in analytical testing beyond routine checks. Final lots receive multinuclear NMR, moisture determination, and purity assessment by ion chromatography or titration. Our plant experience has shown that extra diligence during batch record keeping and sample archiving pays off. When collaborators need a detailed impurity profile or trace element scan, historical analytical records from our own runs facilitate regulatory filings or publication requirements.

    The Impact of Supply Chain Choices

    Sourcing secondary or tertiary amines for quaternization isn’t a trivial matter. Problems with trace metal contamination, varied amine quality, or unexpected peroxide formation in raw materials can end up spoiling the final salt’s properties. We build raw material qualification programs by tracking in-house and outside laboratory certificates, and we revisit supplier audits.

    Shipping piperidinium salts may pose sensitivity to light, heat, or humidity. Our packaging solutions, such as laminated foil packs and rigid containers with desiccant liners, reflect years of shipping both domestically and internationally. We’ve learned that a product that looks fine at the dock may degrade in transit if labeling, closure torque, or pallet stack height is neglected.

    Taking Feedback Seriously

    Users in the organic research and analytical community often reach out after using N-Ethyl-N-Methylpiperidinium Iodide in unexpected experiments. Their input about solubility in less common solvents, unexpected reactivity in complex matrices, or challenges in scaling up gram- to kilogram-scale reactions prompts us to adjust, improve, or clarify our recommendations. For example, process reviews led us to adjust drying protocols to minimize trace water that complicates anhydrous applications.

    Reports of performance under UV or thermal stress led us to modify work-up and packaging steps. New regulatory interpretations about handling iodine compounds sometimes require more detailed traceability and documented GMP controls. As a primary source, we take that responsibility seriously, conducting process changes, additional operator training, and regular updates to data sheets and shipment documentation.

    Maintaining Product Stability and Longevity

    Over the years in manufacturing, product stability isn’t a box to check—it’s an ongoing process. We continually review data from retained samples, tracking discoloration rates, agglomeration, or caking hazards under controlled storage. By maintaining a library of real-time and accelerated stability samples, we catch shifts in product attributes before they reach end users.

    Monitoring for loss of free flow or crystal integrity after months in storage exposed us to the importance of container selection and secondary overwraps. Users storing product for extended periods avoid unwanted surprises from moisture uptake or subtle iodine loss, a lesson learned by scrutinizing both our storage rooms and those of large customers.

    Supporting Safety and Sustainability

    As a manufacturer, safety during both synthesis and downstream use guides facility upgrades and operator training. Handling of quaternary salts—especially those containing iodide—demands respect for proper ventilation, personal protective equipment, and contamination controls. Waste minimization and responsible iodide disposal form part of our standard protocols, and we use data-driven methods to track loss rates and solvent recovery.

    Regulatory expectations continue to evolve. We track updates in chemical registration, transport safety rules, and disposal guidelines. By adjusting plant practices and documentation ahead of time, we help customers avoid project delays or regulatory snags. Third-party audits and environmental reviews push us to keep improving. Sustainable sourcing of both piperidine and iodide components supports the long-term reliability of our product lines.

    Clear Advantages Over Generic Stocks

    Anyone working directly with N-Ethyl-N-Methylpiperidinium Iodide quickly notes that off-the-shelf formulations from traders bring inconsistency in appearance, solids content, or shipping stability. Time and again, customers report batch-to-batch variation from brokers or multi-brand distributors, learning that purity, handling, and appearance affect both research outcomes and regulatory documentation.

    Our direct control—from synthetic planning to filling and labeling—lets users plan confidently for medium or large-scale needs. Whether supporting a long-term synthetic sequence, or scaling up a promising route to commercial scale, a steady supply of reliable, well-documented product removes an often-overlooked bottleneck.

    Working With Specialty Applications and Innovations

    Several new research areas drive rising demand for quaternary piperidinium salts with specific substituents and anions. Fine-tuning the cation’s structure shifts reactivity in transition metal catalysis, supporting innovations in cross-coupling chemistry and new organic materials. For those developing advanced batteries or sensors, the right balance of conductivity and stability opens up new device architectures.

    In my own involvement with early-stage research partners, direct technical dialogue with our chemists shortens the path from laboratory-scale proof-of-concept to kilo- or multi-kilogram evaluation. This also brings out unique needs, like adapting drying steps or adjusting purity for high-precision analytical applications. We treat these not as custom orders of the month, but as opportunities to evolve our process and product suite to stay aligned with real science.

    Final Thoughts as a Manufacturer

    Producing N-Ethyl-N-Methylpiperidinium Iodide from the ground up means something different than simply repackaging or relabeling. Each reaction, filtration, drying step, and packaging run builds on the lessons of previous batches. As chemistry projects continue to deepen in complexity and scale, consistent supply and direct technical communication matter more than ever. Whether the work is on the bench or the pilot plant floor, a truly reliable specialty chemical is an asset, not a variable.

    Committing to direct manufacturing gives users a clear edge. They gain not only a product made to tight and relevant standards, but direct access to those who know how and why it was made. We listen closely, improve steadily, and always produce with both the science and the end user top of mind.