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3,5-Dimethylpiperidine

    • Product Name 3,5-Dimethylpiperidine
    • Alias 3,5-DMP
    • Einecs 216-384-0
    • 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
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    Specifications

    HS Code

    649489

    Chemical Name 3,5-Dimethylpiperidine
    Cas Number 35794-11-7
    Molecular Formula C7H17N
    Molecular Weight 115.22
    Appearance Colorless to pale yellow liquid
    Boiling Point C 110-112
    Melting Point C -20
    Density G Per Cm3 0.82
    Refractive Index N20d 1.435
    Flash Point C 28
    Solubility In Water Miscible
    Odor Amine-like
    Pubchem Cid 119177
    Synonyms 3,5-Dimethylhexahydropyridine
    Iupac Name 3,5-dimethylpiperidine

    As an accredited 3,5-Dimethylpiperidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250 mL of 3,5-Dimethylpiperidine is supplied in a tightly sealed amber glass bottle with a clear hazard and identification label.
    Shipping 3,5-Dimethylpiperidine is shipped in tightly sealed containers, typically made of glass or high-density polyethylene, and labeled according to regulatory requirements. It should be stored and transported in a cool, well-ventilated area, away from incompatible substances. Shipping must comply with local, national, and international chemical transport regulations to ensure safety.
    Storage 3,5-Dimethylpiperidine should be stored in a tightly closed container within a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as oxidizing agents. Protect from moisture and direct sunlight. Use in a fume hood if possible. Clearly label the container and ensure it remains sealed when not in use to prevent contamination or evaporation.
    Application of 3,5-Dimethylpiperidine

    Applications of 3,5-Dimethylpiperidine in Industrial Manufacturing

    3,5-Dimethylpiperidine supports multiple value chains within industrial organic synthesis. Our factory produces this compound to meet stringent downstream manufacturing demands across fine chemicals, pharmaceuticals, and specialty polymer segments. See below for concrete industrial applications, integration methods, and compliance frameworks guiding its use.

    1. Pharmaceutical Intermediate in CNS Active Compounds

    Pharmaceutical companies use 3,5-dimethylpiperidine as a key intermediate in synthesizing central nervous system (CNS) drug candidates, including selective norepinephrine reuptake inhibitors and some antipsychotic agents. The compound commonly participates in reductive amination and chiral synthesis routes, where its structural rigidity enhances selectivity and downstream product stability. Integration into batch and continuous flow processes requires adherence to strict impurity profiles and trace metal control, specifically for clinical-grade outputs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP-NF monograph compliance for related piperidine derivatives
    • 21 CFR Part 211 (FDA cGMP for finished pharmaceuticals)
    • EU Guidelines for Medicinal Products for Human Use

    Typical usage ratio

    • 0.8 to 1.05 molar equivalent in amination or coupling steps, depending on target API yield targets and impurity thresholds.

    Downstream process integration

    • Charged to reactor as free base or as an acid salt during intermediate assembly.
    • Requires controlled addition to limit exotherms during amination.
    • May be recovered or purified by crystallization for multi-step synthesis protocols.
    • Isolate final intermediate with residual solvent < 0.5%, as required by Q3C guidelines.

    Final product types

    • Tricyclic antidepressants
    • Atypical antipsychotics
    • Nootropic agents
    • Receptor-targeted CNS APIs requiring piperidine structures

    2. Building Block for Agrochemical Synthesis

    Leading agrochemical producers employ 3,5-dimethylpiperidine as a structural motif in new-generation insecticide and herbicide molecules. It enables selective N-substitution reactions, producing formulations with high environmental compatibility. Processing plants maintain robust analytical controls to monitor N-oxidation byproducts, ensuring that the active ingredients meet REACH and EPA safety benchmarks before formulation into commercial products.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • EPA Pesticide Registration (FIFRA)
    • ISO 9001:2015 Quality Management for agrochemicals
    • OECD Principles for Good Laboratory Practice

    Typical usage ratio

    • 20–45% (w/w) relative to other amine sources, tailored according to target active ingredient loading and batch scale.

    Downstream process integration

    • Introduced during early-stage amide or carbamate formation.
    • Processed via continuous stirred reactors with in-line NMR monitoring for side-product minimization.
    • Excess reactant neutralized and recycled to minimize hazardous waste.
    • Intermediate purified before final formulation blending.

    Final product types

    • N-heterocyclic-based herbicides
    • Novel insecticidal active ingredients
    • Precursor molecules for selective fungicides
    • Formulated crop protection blends

    3. Modifier in Specialty Polyamide Production

    Specialty polyamide and nylon manufacturers apply measured quantities of 3,5-dimethylpiperidine to tailor polymer backbone flexibility and enhance chemical resistance in high-performance engineering plastics. The compound engages in condensation polymerization with diacids or diisocyanates. Plants enforce strict process analytics to maintain narrow molecular weight distribution and offset batch-to-batch variability, crucial for performance-critical polymer applications in electronics and automotive segments.

    Industry compliance standards

    • ISO 9001:2015 and ISO/TS 16949 (automotive sector quality management)
    • RoHS Directive 2011/65/EU for restricted substances
    • REACH (Annex XVII substance restrictions and SVHC thresholds)
    • UL Yellow Card polymer certification scheme

    Typical usage ratio

    • 0.5–4.0 wt% as a comonomer in polyamide formulations, adjusted for targeted heat deflection temperature and impact strength.

    Downstream process integration

    • Metered into polymerization reactors under inert atmosphere with other polyamide monomers.
    • Included at prepolymerization or chain-extension stage for property tuning.
    • Post-polymerization, residuals monitored to < 100 ppm.
    • Finished polymer subjected to extrusion for pelletizing.

    Final product types

    • Specialty polyamide engineering resins
    • Automotive connector housings
    • Electronic device casings requiring flame retardancy
    • Precision-molded mechanical parts

    4. Intermediate for Performance Coating Additives

    Manufacturers in the coatings sector use 3,5-dimethylpiperidine during amine functionalization of resins, which improves film hardness and solvent resistance for high-durability industrial paints. The material enters as a building block in polyamide or epoxy hardeners, where amine reactivity allows for rapid crosslinking. Quality control involves color, amine value, and reactivity index testing per industry coating specifications.

    Industry compliance standards

    • ASTM D4236 toxicity labeling for coatings
    • EN 71-3:2019, migration of certain elements for coatings in toys
    • ISO 16000-9 VOC emission limits
    • Directive 2004/42/CE on limitation of VOCs in paints and varnishes

    Typical usage ratio

    • 1.2–3.5 wt% in epoxy hardener formulations, depending on desired curing rate and final hardness.

    Downstream process integration

    • Added to resin blend during pre-polymerization of polyamide adducts.
    • Incorporation timing controlled to limit viscosity spike during temperature ramp.
    • Final blend filtered to ensure low-micron purity prior to canning.
    • Resulting additive shipped for downstream use in OEM and industrial finish paints.

    Final product types

    • Industrial maintenance coatings
    • OEM automotive paints
    • Anti-corrosive marine primers
    • Heavy-duty floor resins

    5. Synthesis Aid for Chiral Auxiliary Formation

    Several fine chemical companies employ 3,5-dimethylpiperidine as a starting material for constructing chiral auxiliaries applied in asymmetric synthesis of pharmaceuticals and agrochemicals. Its symmetrical substitution pattern supports creation of highly enantioselective ligands after functional group elaboration. Process lines use high-purity grade feedstocks, enforcing strict controls on stereochemical purity and residual solvent content as per final market application.

    Industry compliance standards

    • USP Chapter <797> for pharmaceutical compounding
    • Ph. Eur. 2.2.46 (chromatographic purity for chiral intermediates)
    • EU Regulation (EC) No 1223/2009 on cosmetic ingredients (if used in chiral fragrance)
    • ISO 17025 for in-house analytical laboratory accreditation

    Typical usage ratio

    • 1.0–1.2 molar equivalent during initial condensation reactions, adjusted if required by the specific chiral ligand design or downstream selectivity targets.

    Downstream process integration

    • Reacted with acyl or alkyl precursors in multistep synthesis pipelines.
    • Purity benchmarked at each step by specific optical rotation and enantiomeric excess.
    • Recycled where feasible after auxiliary cleavage and regeneration.
    • Final output isolated by crystallization or preparative chromatography for sale to peptide and small molecule syntheses.

    Final product types

    • Chiral auxiliaries for pharmaceutical synthesis
    • Enantioselective ligands for catalysis
    • Custom intermediates for agrochemical discovery
    • Fine chemical reagents for analytical applications
    Free Quote

    Competitive 3,5-Dimethylpiperidine prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 3,5-Dimethylpiperidine: Trusted Raw Material with Reliable Performance

    Decades of Experience with 3,5-Dimethylpiperidine

    Working with chemicals on the manufacturing floor teaches one lesson over and over: consistency matters just as much as purity. Through the years, 3,5-Dimethylpiperidine has shown remarkable performance as an intermediate and building block across a variety of production settings, especially when control over functional group orientation and chain branching impacts outcomes in fine chemicals, agrochemicals, and pharmaceuticals. The satisfaction customers express when reactions proceed smoothly, the low number of process deviations, and strong yields have built our confidence in this material’s role in commercial-scale syntheses.

    Our production draws on a simple principle: quality in equals quality out. Over many production cycles, we refined our hydrogenation and distillation steps to yield a high-purity, colorless to pale yellow liquid, boiling around 138-140°C, with a moisture content usually less than 0.2%. This minimizes equipment corrosion and side reactions—a relief when scaling up or optimizing cycle times. We routinely analyze using gas chromatography, ensuring content always exceeds 99%. Impurity levels deserve close monitoring, and not every supplier invests in the same thoroughness or set of detection tools.

    Specific Value in Fine Chemical Synthesis

    Our main customers in pharma and specialty manufacture lean on 3,5-Dimethylpiperidine’s two methyl groups, positioned precisely to control steric effects and regulate reactivity within a piperidine scaffold. These branching patterns allow chemists to design molecules with unique activities. The clear advantage over unsubstituted piperidine or its 2,6-dimethyl analog turns up at the bench. For example, 3,5-dimethyl ensures selectivity in nucleophilic substitutions or in building certain heterocyclic cores. Countless times, pharmaceutical R&D teams comment that the desired activity emerges only with this specific demethylated structure.

    In the field, customers point out that simple piperidine lacks the fine-tuned steric bulk that 3,5-dimethyl smoothly introduces. Slight changes in isomer ratios can yield dramatic differences in batch results; through frequent dialogue with end users, we’ve tailored our synthetic route to favor the more desirable cis/trans distribution for their applications. Where some competitors overlook this detail, it results in wasteful downstream purification for the user. Doubling down on gas chromatography and NMR for every batch means researchers can depend on repeatability, saving time and cost in scale-up campaigns.

    Managing Downstream Reactions and Selectivity

    Over the years, customers’ feedback made it clear: the true worth of 3,5-dimethylpiperidine lies in its impact on downstream efficiency. Subtle influences on stereoselectivity make a tangible difference when construction of advanced intermediates or isolated chiral products forms the manufacturing focus. We have spent time revising our process to help customers control reaction kinetics and minimize undesired isomerization. In catalytic alkylation and reductive amination, our material proved particularly robust, with predictable pKa and N-alkylation rates.

    In drug synthesis, regulatory documentation and reproducibility stay under tight scrutiny. Several of our long-term clients use our 3,5-dimethylpiperidine grades for developing proprietary compounds, then move swiftly from the kilo-lab to multi-ton production without changing the specification or source. They report limited revalidation thanks to the high purity and consistency batch to batch. Small differences in side product profile can spoil months of analytical work; this is more than a numbers game. It is a question of efficiency and cost control in a world where every extra purification step delays commercial availability.

    Solubility and Handling on the Plant Floor

    The best raw materials simplify operations. Because 3,5-dimethylpiperidine dissolves easily in many common organic solvents—ethyl acetate, dichloromethane, THF, among others—teams favor its use both in analytical development and manufacturing. Its low water content further reduces the risk of hydrolysis or side reactions. Maintenance technicians often mention how our rigorous drying minimizes corrosion in reactors and transfer piping, proving advantageous during extended campaigns. Proper storage and handling—keeping it under nitrogen, in tightly sealed containers—protect against oxidation and keep integrity intact. Our experience shows that firms who skip these procedures often face batch rejections from subtle decomposition, a clear case of cutting corners costing more in the long term.

    Packaging size flexibility matters more than many realize. We provide stainless steel drums and lined containers sized from pilot batches up to full manufacturing campaigns. This reduces loss during transfer—another factor that slashes expenses and minimizes workplace risk. The manufacturing team can focus on the chemistry, not wrestling with raw material logistics.

    Comparison with Related Piperidine Derivatives

    With our hands in both research and commercial manufacturing, we have handled a broad array of piperidines. 3,5-Dimethylpiperidine distinguishes itself through its dual methylation pattern, not just in boiling range or appearance, but in practical synthetic applications. Unsubstituted piperidine, readily available and inexpensive, remains a staple for simpler nucleophilic reactions. Its lack of steric hindrance also makes it susceptible to uncontrolled reactivity during large-scale processes. In contrast, the methyl groups in 3,5-dimethylpiperidine direct selectivity and dampen over-alkylation, a concern stated repeatedly during team visits at customers' plants.

    Comparing with 2,6-dimethylpiperidine, the differences lie less in basicity and more in isomer control and side product formation. 3,5-dimethyl offers more predictable cyclization and ring-closure yields during multi-step organic syntheses, supported by multiple patent applications and customer process validation reports. Teams working with complex chiral routes find 3,5-dimethylpiperidine superior for building asymmetric intermediates that lead to biologically active targets. Our clients who once alternated between the 2,6- and 3,5-dimethyl variants now rely exclusively on the 3,5 form after seeing measurable improvements in overall yield and purity.

    Ensuring Traceability and Regulatory Compliance

    Compliance requirements keep tightening each year. Many customers want full traceability—not just lot number tracking but also records on sources of key starting materials, waste control, and environmental documentation. Having invested in enterprise resource systems and batch histories dating back decades, we can produce trace records swiftly, something our partners in regulated markets praise during audits. We chose not to delegate these compliance tasks; instead, we brought quality control and regulatory documentation in-house. This cuts lead times for documentation requests and reassures clients facing short-notice regulatory inspections.

    We also maintain absolute transparency on substances of very high concern, reach documentation, and other international regulations. No shortcuts. We submit every batch to analysis for potential nitrosamines, which regulators now demand even where finished APIs and intermediates are concerned. Customers regularly recognize the peace of mind that comes with receiving compliant, audit-ready materials—another real difference from generics or imports where paperwork often trails the product.

    Environmental Responsibility and Worker Safety

    Neighborhoods near chemical plants watch what comes and goes. Having worked on-site, we know that safety doesn’t end at containment or with an incident-free record. Direct handling of piperidine derivatives including 3,5-dimethylpiperidine brings odor, volatility, and operator exposure risks, so we invest in closed transfer systems and vapor recovery. Facilities using our drums experience fewer workplace odor complaints due to our upgraded drum venting and secondary containment. This results from our drive to incorporate feedback from partners on better packaging and workplace environment solutions.

    By using high-efficiency scrubbers and recycling, we have reduced emissions from our own plants, aiming to keep impact below regulatory limits—and internal company targets—every year. Our investments in solvent recycling and process efficiency go beyond compliance. They keep costs predictable and environmental stewards in the community informed about what leaves our fence line.

    Worker training shapes outcomes. Everyone in our production and logistics teams passes through in-depth familiarization with 3,5-dimethylpiperidine handling, spill abatement, and emergency planning—not as a regulatory checkbox but as real-life skills. Trained crews spot signs of off-specification earlier, preventing problems from reaching customers or the environment. Regular drills and transparent reporting build trust among our employees and the neighborhoods around us. Only a long-term commitment to safety and transparency keeps everyone—from technician to customer—to community—confident in our product’s role and risk profile.

    Finding Solutions to Storage and Shipping Challenges

    Moving specialty chemicals across continents still throws curveballs. Over the past decade, shipping regulations around dangerous goods brought lapses and delays industry wide. Shipments of 3,5-dimethylpiperidine, with their combustibility and regulatory needs, can face extra scrutiny in customs and at sea, especially along routes subject to frequent inspections. Solving these issues required working hand in hand with our logistics providers, investing in ADR/IATA-compliant labeling and tamper-proof seals, and training forwarders specifically on handling and documentation protocols. As a result, lost shipments and transportation issues have sharply declined, and customer feedback reflects satisfaction with on-time arrivals and intact packaging.

    Warehouses at customer sites vary. Some have full ventilation and nitrogen blanketing; others manage with basic facilities. To support both environments, we developed guidelines for optimum storage, handling, and drum tracking, also offering visits to help end users troubleshoot their own options. This cooperation translates to fewer issues with product degradation or shelf life. Handling quirks often only show after months in storage—real experience on the ground reveals what laboratory or sales brochures miss.

    Summary of Benefits from a Trusted Supplier

    For anyone consistently purchasing and using 3,5-dimethylpiperidine in high volumes, the clearest feedback comes from line operators and plant chemists: a reliable raw material sets up the rest of the process for success. Our ongoing investment in plant technology, analytical controls, storage solutions, and regulatory documentation continues to drive results our customers demand.

    Hands-on experience, technical improvement, and tough compliance standards matter more than any single data number or marketing phrase. When every drum performs batch after batch, yields stay high, safety stays strong, environmental spill risks drop, and customers, regulators, and employees all benefit. Perhaps most meaningful are the comments from clients who've switched to our product and see actual reductions in rejected batches, reprocessing work, and audit queries over time. These outcomes come from years standing in laboratories and production plants, learning directly from the people who turn chemicals into progress, medicine, and materials that support industries worldwide.