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HS Code |
418288 |
| Chemical Name | 4-Aminomethyl-1-N-Butylpiperidine |
| Cas Number | 7149-43-9 |
| Molecular Formula | C10H22N2 |
| Molecular Weight | 170.30 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 245-250 °C |
| Density | 0.88 g/mL at 25 °C |
| Purity | Typically ≥98% |
| Solubility | Soluble in water and most organic solvents |
| Melting Point | -70 °C |
| Flash Point | >100 °C |
| Storage Temperature | 2-8 °C |
| Refractive Index | 1.465-1.475 |
As an accredited 4-Aminomethyl-1-N-Butylpiperidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 4-Aminomethyl-1-N-Butylpiperidine is supplied in a 100g amber glass bottle, sealed with a screw cap, and clearly labeled. |
| Shipping | `4-Aminomethyl-1-N-Butylpiperidine` is shipped in airtight, chemical-resistant containers, complying with hazardous material regulations. Packaging ensures protection from moisture and physical damage. Transport is conducted via certified carriers, with appropriate labeling and documentation for safe handling. Shipment requires adult signature upon delivery and adherence to all applicable safety and legal requirements. |
| Storage | 4-Aminomethyl-1-N-Butylpiperidine should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizers and acids. Store at room temperature, and ensure the chemical is clearly labeled. Access should be limited to trained personnel following proper safety procedures. |
Applications of 4-Aminomethyl-1-N-Butylpiperidine in Industrial Manufacturing4-Aminomethyl-1-N-Butylpiperidine is a specialty intermediate with established roles in several chemical manufacturing sectors. As a direct manufacturer, we support integration of this compound into complex synthesis workflows where reactivity, selectivity, and purity critically influence end-product quality. Below are the primary industrial application scenarios, each pinpointing the unique function and compliance aspects required by downstream processors. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisThis amine intermediate plays a key function in the multi-step synthesis of specific small-molecule APIs, mainly for neurologically active compounds and certain antivirals. Custom API manufacturers rely on its high assay to initiate nucleophilic substitution or reductive amination reactions, often introducing it at critical late-stage coupling steps where structural precision impacts bioactivity and regulatory approval. Its batch traceability and low impurity profile are decisive for quality management in the pharmaceutical chain. Industry compliance standards
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2. Organic Corrosion Inhibitor Synthesis for Oilfield ApplicationsOur butylpiperidine derivative serves as a primary building block for high-performance amine-based organic corrosion inhibitors. Oilfield chemical formulators leverage its secondary and primary amine reactivity to modify alkyl chains, generating tailored molecules which adsorb strongly to metal surfaces in brine or acidic environments. It is reacted and blended during the bespoke synthesis phase for downstream field use, where formulation stability and low residual solvent content must meet explicit safety standards for environmental release and operational safety. Industry compliance standards
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3. Precursor for Polymeric Curing Agents in Epoxy SystemsAs a reactive amine, this compound forms an essential backbone component for the synthesis of higher molecular weight curing agents utilized in two-part epoxy composite production. Downstream processors exploit its flexible chain and nucleophilic properties to develop modified amine adducts, tailoring cure profile and mechanical property balance in civil engineering and electronic potting resins. Reaction control is vital as improper stoichiometry impacts pot life and end-product structural integrity. Compliance verification extends to residual amine content and amine value accuracy in the cured product. Industry compliance standards
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4. Fine Chemical Intermediate for Agrochemical SynthesisThis advanced amine intermediate directly supports the preparation of select alkylated heterocyclic agrochemical actives. Downstream formulators rely on its stable, branched structure to introduce precise nitrogen functionality in the ring-closing or condensation step, managing impurity signatures and excessive isomerization. Production of these actives operates under strict impurity profiling and contaminant elimination to ensure finished crop protection agents meet global trade and environmental standards. Volumetric dosing is critical for maintaining both target yield and regulatory compliance in active content for formulated products. Industry compliance standards
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5. Intermediate for Specialty Surfactant ManufactureThe molecule is engaged in producing tailored cationic surfactants, essential for high-performance industrial cleaning and emulsification applications. Surfactant makers value its dual amine function to introduce both hydrophobicity and pH-sensitive reactivity during key alkylation or quaternization steps. Quality-focused surfactant synthesis relies on low color and controlled amine content, as introduced during precise charging sequences in downstream reactors sourced directly from our high-purity batches. The balance between chain length and amine group location dictates the final product’s dispersant, foaming, or emulsifying effectiveness. Industry compliance standards
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Every production run for 4-Aminomethyl-1-N-Butylpiperidine comes out of hands-on process controls, not automated speculation. Our technical staff pays sharp attention to the synthesis and purification steps, not just for the yield, but also because we live close to the feedback from end-users—researchers, engineers, and chemical formulators who expect predictability, not surprises. This compound, sometimes called N-butyl-4-aminomethylpiperidine, represents a cornerstone intermediate for several high-value syntheses in pharmaceutical research and advanced materials.
We only use direct-chain butyl sources and high-purity starting piperidine to keep impurities low, and our experience says more about the value of routine proficiency testing than any marketing claim can. Molecular formula C10H22N2, a clear liquid under ambient conditions, CAS number—which you already know if you’re here—lets you track provenance on your side, but for our team, it’s about more than compliance. Every drum, no matter its batch, stands up to GC and NMR inspection long before it ever leaves our facility.
Specifications for 4-Aminomethyl-1-N-Butylpiperidine, as managed by experienced process chemists, begin with purity. Our practice doesn’t settle until each lot finishes above 99%, but the real work involves isolating potential by-products and minimizing water and peroxides, notorious for their impact in downstream steps. During producing, we don’t let up after routine distillation—random sampling checks noise levels in the nitrogen spectra, which, from long experience, closely track the compound’s readiness for tricky applications, like producing new piperidine derivatives for CNS-active drug research.
Water content remains below 0.1%, according to latest KF measurements. We log this, not as a box-ticking exercise, but because too much moisture in this secondary amine takes the reaction in directions you’d rather not see—different color development, reduced selectivity, even suboptimal catalyst interaction for those building out specialty polymers. Empirically, a reliable supply gives way to steady project timelines, and we’ve noticed that customers with tough analytical protocols come to us when they’ve been stung by inconsistent results elsewhere.
Day by day, we discover that customers expect not simply a product but guidance rooted in continuous runs and side-by-side troubleshooting. For example, formulating a substituted piperidine ring often depends on subtle aspects of the amine’s basicity profile. In our production, an extra attention goes into stripping traces of primary amines, as those alter the amination yield for certain heterocycle syntheses. Extra purification does add to cycle time, but skipping it costs more through downstream failures, as every researcher who’s dealt with side products knows.
Temperature-sensitive jobs need tips from those who’ve managed storage in various seasons. Our shipping department, familiar with the quirks of the molecule, recommends metal drums for bulk, with tighter temperature monitoring above 25°C. We seal containers under nitrogen, after our own stability tests revealed even minimal oxygen exposure during transit can affect shelf life and color stability. Most of our longtime users return, not because certificates check a box, but because lab work with our chemical saves them days they’d otherwise lose tracking batch deviations.
Our time with 4-Aminomethyl-1-N-Butylpiperidine began over ten years ago with small-lot requests from alkaloid research labs. Syntheses of antipsychotic candidates, and explorations into allosteric modulators, lean continually on reliable amine intermediates. Over the years, process chemists from different companies invited us to audit their procedures after batch failures related to amine purity and contaminant levels. Out of those collaborations came improvements in our vacuum distillation step, which we’ve maintained ever since. We’ve observed a shift toward high-throughput combinatorial chemistry, where researchers now demand kilo quantities for parallel screening. The discipline that goes into our production—tighter impurity profiles, longitudinal stability studies—doesn't just serve regulatory aims but makes real impact when each screening campaign uses grams to hundreds of grams per library. The reliability of the amine under these conditions springs from real-world feedback, not from theoretical promise.
Beyond pharma, we supply custom polymer development labs focused on fine-tuning glass transition properties using piperidine-based chain extenders. Here, monotonic reactivity and minimal color development over time means fewer failures at the extrusion line and more favorable QA stats. Those who’ve stood by the reactors at 3AM, troubleshooting a bad amine batch, use strictly defined input profiles like ours not out of habit, but hard-earned necessity.
At a glance, someone might lump all aminomethylpiperidines together. Our work, batch after batch, demonstrates otherwise. 4-Aminomethyl-1-N-Butylpiperidine should not be confused with its methyl or ethyl analogs; those differ in volatility, solubility, even basicity, making process transfer dicey. Some customers have tried swapping in N-methyl or N-ethyl alternatives to save on cost or address local procurement challenges, and their yield or selectivity suffers in subtle but consistent ways. Over multiple collaborations, we’ve helped rescue such efforts by walking back to proper use of the N-butyl variant, confirming with side-by-side pilot runs.
Even within the N-butyl family, material from different makers can surprise a formulation team with slight changes in impurity profiles. We’ve seen competitors cut corners by skipping secondary purification, which results in a noticeable backing smell—likely due to isobutylamine carryover—and darker product color over shelf life. Feedback from contract manufacturers who switched to our process, having faced challenges in direct hydrogenation steps, regularly highlights longer shelf stability and reduced batch-to-batch variability in their end-product QA results.
Real output means more than simply turning out drums for delivery. Disruptions in sourcing, weather events, and process variability must be met head-on, not glossed over with generic assurances. In this business, one learns quickly that maintenance of a reliable drying train and the right glassware seals alter not just throughput, but downstream headaches for everyone along the supply chain. Refrigerated storage, leak-tested vessels, and scheduled downtime for column re-packing may seem old-fashioned, but they directly parallel fewer field complaints and more usable “in-spec” volume per run.
We stick with lot-based documentation that traces every charge and every titration point. In practice, this drives smarter interventions when a customer calls with a performance question, as we can retrace our steps and compare to their out-turns. No substitutions for hands-on familiarity with the process—our operators routinely diagnose errors before they leave our site. For teams transitioning from academic to large-scale commercial work, these details often mean the difference between pilot success and full-scale rejection.
The chemical sector no longer has the luxury of just chasing highest conversion rates. Waste stream minimization, recoverability of solvents, and lifecycle assessment have forced every manufacturer to consider more than just per-lot performance. Our lab started switching to closed-loop solvent recovery five years ago, recapturing DMF and reducing environmental impact. Local regulations penalize improper waste handling, so we take the extra time for in-house treatment, realizing that trace organics in effluent can no longer be shunted downstream for others to fix.
Suppliers watching their image toe the green line on their websites rarely face the real costs. Only the manufacturer sees how tighter solvent recycling impacts throughput, or how footsteps of regulatory audits shape vessel-filling schedules. We invite clients to review our own records, and historically, visits from their regulatory and technical QA have led to deeper partnerships, not superficial box-checking exercises. In conversations about 4-Aminomethyl-1-N-Butylpiperidine, environmental care ranks as high as chemical purity, both because regulators insist and because downstream safety depends on it.
No certifying agency can guarantee the absence of problems in the field. Learning through years of lab mishaps, line shutdowns, and emergency conference calls, we’ve built open channels for customers to challenge us at any stage: pre-shipment, after receiving goods, or when troubleshooting their next derivative synthesis. We log every outcome, add unexpected findings to internal SOPs, and update analytics when outliers appear. We don’t treat problems as PR issues, but as evidence that real chemistry never quite matches textbook expectations.
Returning clients have told us how our packaging choices and real-time openness prevented days of lost work. Using tamper-evident drums, inert-atmosphere packaging, and custom documentation are steps our team stands behind, especially for applications demanding low unknown-impurity profiles. For us, these practices don’t just meet regulatory standards—they break the cycle of repeated QA headaches for partners who measure their own reputation on every final product batch.
Building trust comes day by day, not via catalog declarations. Many clients now expect support through pilot campaigns, IP filings, and regulatory submissions, and clear batch histories matter as much as analytical numbers. Field visits, joint lab troubleshooting, and hands-on problem solving are realities behind each shipment.
The heart of any chemical operation sits with the people who handle real product. Training doesn’t end at a single SOP reading; every member of our production crew cycles through hands-on sessions with live product, simulating every exposure risk, spills, temperature shocks, and packing issues. Years of production data inform our safety thresholds, and practical drills push us to keep one step ahead. With a secondary amine like 4-Aminomethyl-1-N-Butylpiperidine, real risks come from accidental mixing with oxidizers or high-heat handling, so controls aren’t just written, but rehearsed. Analysis reveals that the lowest incident rates come from experienced teams that view every transfer as a live risk scenario, not just a memo item. For new hires, shadowing veterans trumps computer-based modules. We observe less product waste and reduced incident reporting by maintaining this approach, and our incident logs show that proactive culture transfer results in measurable performance improvements.
Over the years, several research and process organizations have reached out after troubleshooting failed amid introducing a new supplier. In one standout case, a team working on macrocyclic compound syntheses noticed erratic yield and product color when switching from our material to a lower-priced competitor. Upon investigation, our joint analysis found that marginal increases in unknown-alcohol side products, undetected in basic analytical tests, altered catalyst performance significantly. That led us to reinforce additional GC-MS screens for alcohols in our own process, tracking these contaminants into every lot released since.
Cases like these underscore why supplier choice in amine intermediates cannot rest on price alone. Direct relationships, where manufacturers open their doors to real scrutiny, lead to mutual learning and, ultimately, to process improvements. We value every challenge brought in by customers—not as complaints, but as invitations to improve industrial practices on both sides.
Supplying 4-Aminomethyl-1-N-Butylpiperidine requires more than meeting purity specs or listing batch numbers. Real experience lands in every delivered container, every phone call troubleshooting a discolored reaction, every fix to a process upended by subtle impurity swings. Production consistency, repeat testing, record-level transparency, and direct technical engagement define our standards. The push for fairer, cleaner, more responsive chemical supply chains runs through everything we do. We care about emission records, solvent savings, people training, and know-how transfer, not just because regulations demand it, but because every research success and every smooth production run depends on us getting it right. For users who need not just a product, but a knowledgeable partner, our work speaks through every drum, every answer to a process question, and every batch history we stand ready to share.