|
HS Code |
453663 |
| Chemicalname | 2-Piperidylmethylamine |
| Molecularformula | C6H14N2 |
| Molarmass | 114.19 g/mol |
| Casnumber | 28236-90-4 |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 200-210°C (estimated) |
| Density | Approx. 0.96 g/cm3 (estimated) |
| Solubilityinwater | Miscible |
| Pka | Approx. 9.7 (for the amino group) |
| Smiles | NCC1CCCCN1 |
| Inchi | InChI=1S/C6H14N2/c7-5-6-3-1-2-4-8-6/h6,8H,1-5,7H2 |
| Pubchemcid | 4107742 |
| Synonyms | 2-(Aminomethyl)piperidine |
As an accredited 2-Piperidylmethylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 kg of 2-Piperidylmethylamine packaged in a sealed amber glass bottle, with hazard labeling and tamper-evident cap, for laboratory use. |
| Shipping | 2-Piperidylmethylamine is shipped in tightly sealed, chemical-resistant containers, clearly labeled with hazard and handling information. Packaging follows international and local regulations for transport of hazardous chemicals. During transit, it is protected from moisture, heat, and incompatible substances, with documentation ensuring traceability and safety compliance throughout delivery. |
| Storage | 2-Piperidylmethylamine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Keep it protected from light and moisture. Ensure the storage area is equipped with appropriate spill containment and ventilation systems, and access is restricted to trained personnel. Label containers clearly with hazard information. |
Applications of 2-Piperidylmethylamine in Industrial ManufacturingAs a manufacturer specialized in high-purity 2-Piperidylmethylamine, we support global chemical and pharmaceutical enterprises with carefully engineered intermediates. Our material meets the stringent requirements of institutional and industrial users across several core downstream sectors. Below, we detail its concrete application scenarios within real production environments, offering focused insights on regulatory adherence, technical process incorporation, and finished product development. 1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis2-Piperidylmethylamine serves as a key building block in the stepwise synthesis of central nervous system agents and select anti-Parkinsonian APIs. It reacts in the formation of complex heterocyclic intermediates during regulated multi-stage API production, requiring close compliance with drug master file submission protocols and batch traceability. End-users implement closed-reactor processing to ensure containment and reproducibility, while continuous analytical monitoring validates intermediate throughput. Downstream QC teams adjust amine input to reflect stoichiometric balances and target yield thresholds prescribed in development reports. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Intermediate ManufacturingDownstream agrochemical formulators use 2-Piperidylmethylamine as an amine-functional intermediate for selective synthesis of piperidine-based crop protection compounds. It enters key nucleophilic substitution steps, offering reactivity and steric properties required for designing herbicide and insecticide precursors. Engineers carefully control addition coefficient according to proprietary synthetic routes, while international producers align input with active ingredient access compliance and impurity management as dictated by local regulatory agencies. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Specialty Polymer Modifier ProductionProducers in the specialty plastics sector employ 2-Piperidylmethylamine to introduce amine reactivity and controlled cross-linking within engineering polymer formulations. Its addition enables tailored modification of polyimides, polyamides, and select acrylate resins, with dosage fine-tuned by viscometric and tensile test feedback loops. Integration requires adherence to advanced analytical controls and registration per environmental material directives, as downstream processors calibrate each reaction according to final application requirements in electrical, filtration, and industrial film segments. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Fine Chemical Catalyst SynthesisChemical manufacturers apply 2-Piperidylmethylamine as a ligand precursor or functionalization agent in the fabrication of advanced organic catalysts. Technical teams optimize ligand-to-metal ratios and monitor purity throughout salt formation and chelation processes. The compound's integration at controlled stages of fine chemical manufacture supports strict adherence to sector-specific GMP or quality management benchmarks, with batch-specific documentation enabling downstream catalyst end-users to meet audit and performance requirements set by major chemical processing industries. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2-Piperidylmethylamine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Producing 2-Piperidylmethylamine, also known as (2-Piperidyl)methylamine or N-(2-piperidinylmethyl)amine, means leaning into expertise and precision. Our work at the plant connects decades of experience with advancing demands from pharmaceutical and fine chemical industries. This compound, with the molecular formula C6H12N2 and CAS Number 18131-90-5, stands out due to its structure—a piperidine ring with a direct methylamine substitution at position 2. Chemists look for it when developing intermediates and forming complex molecular frameworks, especially alkaloid derivatives and active pharmaceutical ingredients.
The daily handling of this amine brings our lab and production teams into close contact with both the molecule’s physical quirks and its practical uses. Its appearance: clear, colorless to pale-yellow liquid, with a distinctive amine odor that signals its chemical purpose. The boiling point, commonly somewhere between 200°C and 210°C, gives the operator some working range during distillation and formulation. Our batch process and subsequent purification take full account of these properties, ensuring a product that meets, and often surpasses, industry benchmarks for both purity and yield.
We are often asked how 2-Piperidylmethylamine compares to other similar amines, like morpholine, 4-piperidinemethanol, or 2-pyridylmethylamine. The answer comes right from our QC lab data and customer feedback. The secondary amine group and the specific ring position give 2-Piperidylmethylamine unique nucleophilic and basicity traits. When researchers are after specific alkylation, reductive amination, or cyclization processes, switching from standard benzylamines or pyridylamines to 2-Piperidylmethylamine consistently shifts reaction selectivity and yield. For example, medicinal chemists have dialed in the use of this molecule to introduce targeted piperidine fragments onto drug scaffolds, precisely because other amines lead to higher byproducts or less stable intermediates. Each of these applications arrives in our inbox from years of collaborative research and process piloting.
Our plant teams know well that 2-Piperidylmethylamine isn’t just produced for academic curiosity; end users include pharmaceutical R&D, contract development firms, and manufacturers who need consistent lot-to-lot quality. A typical use involves building heterocyclic intermediates—often a first or second step in synthesizing antihistamines, nootropics, and enzyme inhibitors. Because our product’s purity generally runs above 99%, it supports the stringent requirements seen in preclinical and scale-up phases. Each kilogram of amine must meet low water content, minimal residual solvents, and avoid elemental impurities for these projects to stay on track.
Customers have shifted to 2-Piperidylmethylamine to overcome hurdles that show up with more common amines. One challenge: sensitivity to oxidation or acid-catalyzed decomposition in more basic amines. This compound delivers a stable backbone under most working conditions, which extends shelf life and simplifies handling during formulation. The storage recommendations we give, drawn from bench and warehouse experience, have more to do with maintaining stability and personal safety. Low humidity and tight seals keep the liquid clear, while the slight volatility means skilled technicians handle it with appropriate PPE and containment.
Commercial users benefit from direct sourcing with a manufacturer like us. Buying from the originator plant aligns production size with downstream demand, which enables both pilot batches and regular shipments for commercial synthesis to lock into the supply chain. As the only direct manufacturer in the transaction, we work face-to-face with quality teams, adjusting specs—such as particle size for salt formation or customized impurity profile—based on application data instead of marketing spin.
Scaling up 2-Piperidylmethylamine from lab to plant floor didn’t happen by accident. Early work demanded trial and error to get consistent conversion rates on the reductive amination of 2-piperidinecarboxaldehyde with methylamine, all while suppressing side reactions. The route we follow today—tested during multiple pilot runs—involves careful temperature control, slow addition of reactants, and in-process analytics to monitor the appearance of the desired secondary amine. QC teams catch off-target fractions through GC-MS and NMR before bottling, so we keep our impurity profiles both documented and transparent.
Handling waste streams responsibly sits at the core of our process. Any amine production leaves spent solvents and minor off-spec byproducts, which our site treats through established distillation and chemical neutralization units. We record all releases and actively track compliance to keep within local and international guidelines—important for those companies that assess not just cost, but also supplier sustainability records.
We routinely run kilo-scale and larger lots, always matching the needs that come in from downstream partners or new R&D clients. Each production run gets its own review and data log, which means if a customer ever needs tailored packing, purity adjustments, or batch traceability, our internal records—backed by supplied COAs—make adjustments straightforward.
Chemists often ask why they can’t swap in a cheaper or more easily available amine. Our hands-on work proves the answer. 2-Piperidylmethylamine brings together a versatile piperidine ring with a methylamine group at the right locus to open doors in medicinal chemistry. The reactivity pattern diverges from that of 4-piperidinemethanol or even linear diamines—this shows up fast in benchmarking studies and pilot projects that compare product purity and functionalization rates.
We hear from synthetic teams who thought a generic piperidine or morpholine analog might match, only to find diminished yields or downstream complications like byproduct formation. Functional groups on the 2-position of the ring steer selectivity in key reactions, including Michael additions, N-alkylation, and carbamate formation, which matters if the project goal is a conformationally restricted synthesis. The flexibility and accessibility brought by our product help chemists get the kind of control they can’t find with generic alternatives.
In comparing with 2-pyridylmethylamine, which places the amine group on a heteroaromatic ring, profound differences in reactivity and basicity emerge. Our product remains non-aromatic, which brings higher nucleophilicity under equivalent conditions and resists oxidation over long storage. The decision between these options comes down to real-world application goals: substitution chemistry, intermediate formation, or direct pharmaceutical active synthesis.
Plant chemists, formulation teams, and procurement staff have operated through enough projects to know what matters is consistent results. Our ongoing QA programs stress stability: bottle-to-bottle, year-to-year, regardless of run size. Analyses performed by in-house technicians provide details—GC for purity, Karl Fischer for water, ICP-OES for trace metals. We share these records because real-world manufacturing depends on this openness.
Sharing data and responding to feedback from customers, we have adjusted key production parameters. When feedback showed certain applications needed lower amine volatility or specific pH requirements, our process development team reconfigured distillation protocols and purification routines. This isn’t rare in chemical manufacturing—it’s routine collaboration that bridges process chemistry and end-use performance.
Differences in handling and storage compared to other amines have practical implications. Tanks, totes, or drums require proper lining and vapor containment to minimize both losses and operator exposure. Our support doesn’t stop at the factory gate; we consult on downstream safe handling, waste treatment, and emergency response as part of the direct relationship that manufacturers build with one another.
In the pharma and fine chemical worlds, every reaction step in a multi-stage project absorbs both time and budget. Choosing 2-Piperidylmethylamine often means turning a potential bottleneck into a streamlined process. Real requests include reductive amination for creating alkaloid-type structures, ring-opening reactions for targeted functionalization, or advanced coupling reactions where purity and batch consistency control final active yields.
This product supports pilot and full-scale manufacturing, from supplying milligram R&D vials up to multi-ton commercial lots. Because we synthesize and bottle at origin, we have direct input on purity specifications, packaging options—be it HDPE drums, stainless steel totes, or custom amber jugs—and logistics, which larger resellers have trouble offering without multi-tiered markups or inflexible lead times.
Our records show that contract manufacturers benefit from consistent access, alleviating issues of lot-to-lot variability that can scuttle scale-up or cause regulatory concerns. For global clients, certifiable traceability, coupled with transparent documentation, supports regulatory filings or audits, which becomes increasingly important as competition and oversight rise.
Bringing 2-Piperidylmethylamine from concept to a shipping product means ongoing adaptation. Run-to-run consistency follows from knowing the process inside out—reaction monitoring, product workup, careful distillation, and quality inspection. Training new operators involves real chemical hazards, troubleshooting, and hands-on sampling. We face recurring questions about extraction solvents, waste handling, and safe packing because each order arrives with its own technical or logistical twist.
Breaking into advanced manufacturing only succeeds when documentation and communication stay as clear as the product itself. Lab and plant teams update records with the results of every deviation or improvement. Molecule-specific hazards—amine volatility, exothermic amination stages, odor control, and vapor containment—get addressed with both engineering controls and process training.
Years in production teach two lessons: no process survives unchanged after scale-up, and every improvement rides on practical knowledge. Whether it is adjusting chiller speed for exothermic reactions or troubleshooting odor controls, the hands-on approach from experienced staff still means more than automated checklists. This attitude builds the direct relationships and trust for clients looking for both a reliable supply and technical know-how.
Rising global demand brought both supply chain scrutiny and regulatory tightening. Maintaining competitive delivery times means more than increasing reactor throughput. Each shipment—whether kilogram or multi-ton—pairs with a data trail confirming compliance with global requirements. Our internal compliance programs meet standards set not just for safety, but also for responsible sourcing and ecological disposal. Customers who audit our operations see preventative maintenance logs, batch production records, and safety training results that go beyond paper documentation.
Our past experience drove us to certify not only the finished product, but also each input, down to utilities and raw materials—efforts that minimize contamination risk and guarantee that specifications remain unchanged from lot to lot. Auditors visiting our facility focus on open access to records and visible operational controls, reflecting transparency as a manufacturing practice, not just a sales pitch.
Trust builds as a byproduct of consistency, and our partners—production chemists or downstream QA—recognize that traceable, single-origin sourcing sidesteps import hurdles, customs confusion, or unexplained variability that multistep trading sometimes introduces.
There’s a reason buyers come to us as the original producer rather than sourcing through long chains of resellers. A direct partnership means unfiltered access to technical support: from tweaking packing materials to suit a site’s environmental controls, to supporting a regulatory submission with batch-level data and access to lab notes behind each batch test.
Our ability to respond to changing project scopes—overnight increases in demand, sudden regulatory checks, or custom impurity profiling—relies on the integrated feedback loop from process development to dispatch. The same chemists and operators who scaled the product keep participating in these solutions, without barriers or lost information that arise in hands-off distributor relationships.
Keeping channels straightforward—not only for purchasing, but for feedback and improvement—means we can always adapt, whether for a new medical indication, a different solvent tolerance, or a fresh regulatory environment. Each end user builds their own process using our molecule; we match that iterative pace with both product and support.
Every round of 2-Piperidylmethylamine, from the first raw material blend to the last bottle cleaned for shipment, carries with it more than molecules—it carries the work and oversight of experienced chemists, plant engineers, and quality teams. That transforms what could be a generic intermediate into a core tool for researchers and manufacturers solving new chemical problems.
Chemistry isn’t a remote process; it is built by the same hands that solve issues as they emerge, by the same experience that teaches which adjustments keep a process smooth and a product reliable. Each inquiry and each shipment is the result of talking directly and openly, backed by a record that grows richer with every batch we manufacture. Our knowledge, our focus on traceability, and our willingness to adapt sets our 2-Piperidylmethylamine apart as more than just a product—it is the outcome of practical, real-world manufacturing done with care and pride.