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HS Code |
363180 |
| Chemical Name | 1-Isopropyl-Piperidin-4-Ylamine |
| Molecular Formula | C8H18N2 |
| Molecular Weight | 142.25 g/mol |
| Cas Number | 82544-99-6 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 223-225°C |
| Density | 0.87 g/cm3 |
| Solubility In Water | Soluble |
| Purity | Typically ≥98% |
| Storage Temperature | Store at room temperature |
| Synonyms | 1-Isopropyl-4-aminopiperidine |
| Smiles | CC(C)N1CCC(CC1)N |
As an accredited 1-Isopropyl-Piperidin-4-Ylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 1-Isopropyl-Piperidin-4-Ylamine, labeled with hazard symbols, lot number, and expiry date. |
| Shipping | 1-Isopropyl-Piperidin-4-Ylamine is shipped in tightly sealed containers, compliant with chemical safety regulations. Packaging is designed to prevent leaks or contamination. The shipment includes all necessary documentation, such as safety data sheets and labeling for safe handling. Transport is typically via ground or air, depending on destination and applicable local laws. |
| Storage | 1-Isopropyl-Piperidin-4-Ylamine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers or acids. Protect it from moisture, direct sunlight, and sources of ignition. Proper labeling and secondary containment are recommended to prevent accidental contact and contamination. Always follow institutional and regulatory safety guidelines when handling and storing this chemical. |
Applications of 1-Isopropyl-Piperidin-4-Ylamine in Industrial Manufacturing1-Isopropyl-Piperidin-4-Ylamine is a specialized fine chemical serving multiple advanced manufacturing segments. As a direct manufacturer, we focus on precise quality control and traceability, supporting complex process integration and regulatory compliance for B2B partners in select pharmaceutical, agrochemical, and specialty chemical sectors. Below we detail main downstream industrial scenarios with specific technical and regulatory requirements. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisThis compound functions as a critical amination building block in the synthesis of next-generation API candidates, particularly in the development of CNS-acting agents and selective serotonin or dopamine receptor modulators. The material is incorporated in multi-stage reaction sequences, often applied after protection-deprotection cycles to introduce isopropyl-substituted piperidine rings. Medical chemists rely on its purity profile and batch-to-batch consistency to meet stringent documentation and validation during process development, especially at pilot and commercial scale. Downstream manufacturers adjust loadings based on target molecule complexity and stage yield, following strict GMP requirements. Industry compliance standards
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2. Targeted Agrochemical Synthesis (Herbicide and Fungicide Building Block)Formulators utilize this piperidinylamine during the modular synthesis of agrochemical actives, particularly as a moiety in heterocyclic pesticide scaffolds. The compound enables the introduction of specific nitrogen functionalities for molecules designed to manage resistance profiles in weed and fungal control. Process chemists rely on validated analytical data to meet agricultural purity requirements and environmental safety standards, especially as most finished products require extensive toxicological screening before market release. Industry compliance standards
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3. High-Performance Polymer Modifier in Specialty Resin FormulationThe compound acts as a polyamine modifier, mainly for the molecular engineering of specialty epoxies and urethane-linked resins. Resin manufacturers use this amine to tailor cross-link density and give rise to improved thermal and chemical stability for advanced coatings and adhesive solutions. Rigorous in-process testing ensures compliance with intermediate stage purity and downstream additive management. This approach targets electronics encapsulants and industrial-grade adhesives, where final product performance strictly relates to the incorporation point and ratio of the piperidine amine unit. Industry compliance standards
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4. Custom Fine Chemical for Biotech Research ToolsResearch reagent suppliers and life science labs use this primary amine in the preparation of labeled molecular probes and small-molecule enzyme inhibitors for screening applications. It offers a defined piperidinyl scaffold for rapid library synthesis, supporting proprietary modification of discovery-stage probes. Stringent documentation and origin traceability remain central due to regulatory audits in biomedical use, and the compound's consistency allows valid structure-activity relationship work across multiple research batches. Custom synthesis workflows often require bespoke purification protocols to suit downstream coupling technology. Industry compliance standards
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Out in the world of specialty amines, 1-Isopropyl-Piperidin-4-Ylamine takes its place as more than another niche chemical. Structurally, this compound features an isopropyl group attached to the piperidin-4-ylamine skeleton, a detail that sets up its performance chops in both synthesis and end-use scenarios. The real-world story of this molecule isn’t just about what’s on the label—it's about how its structure and properties drive outcomes in labs and on production floors.
Despite its modest size, this amine demands tight control in synthesis. Our facility builds each batch from carefully selected raw materials, keeping a relentless focus on temperature, pH, and process timing. By holding close to these parameters, we draw down on batch-to-batch deviation, aiming for purity at or above 98.5%. Trace impurities—especially secondary amines and residual solvents—stay well below industry-accepted thresholds. We use gas chromatography and NMR as daily tools, not as afterthoughts, to check the molecular integrity of everything that leaves the reactor. The dry, pale solid you see in the package speaks to these in-line controls and a team that takes accountability for every kilogram.
Too often, technical data sheets list off melting points and solubilities with no commentary on what those values actually mean in practice. 1-Isopropyl-Piperidin-4-Ylamine melts between 84 and 88°C—unlike bulkier piperidine derivatives that throw off the workflow with high-melting solids. Solubility in polar organics such as methanol, ethanol, and acetonitrile eases integration into reaction setups and downstream isolations. Moisture content runs below 0.15% because we move quickly from synthesis into vacuum drying, avoiding atmospheric uptake. To prevent cross-contamination, we clean and swab reactors and transfer lines on every cycle, and our operators document every cleaning on record, which gives us a deep history on every drum shipped. These points aren’t just numbers—they directly influence reactivity, scalability, and ease of handling over weeks and months in a warehouse or laboratory.
1-Isopropyl-Piperidin-4-Ylamine didn’t earn its place in every chemist’s inventory overnight. Researchers working on pharmaceutical intermediates appreciate the amine for its selective reactivity—coupling with acid chlorides, isocyanates, and aldehydes without kicking off a scramble of side products. In our own pilot studies, where gram-scale tedium scales up fast to the hundred-kilo level, this selectivity keeps waste down and yields up. You can chase 90% conversion on paper, but in a real reaction, side products triple your work during downstream purification. Reliable amines with steric tuning, like the isopropyl modification on this piperidine core, tilt the odds toward higher isolated yields, which makes the daily grind of workup and purification less of a headache.
In practice, 1-Isopropyl-Piperidin-4-Ylamine lands in more than one lane. Drug discovery teams blend it into combinatorial libraries, taking advantage of its ability to generate N-substituted products in fewer steps. Agricultural chemistry isn’t far behind—its alkylated amine moiety slides smoothly into synthesis pathways for fungicides and crop-boosting agents. In one recurring project, we supported a customer who scaled up a novel pesticide candidate, relying on this amine’s manageable boiling point and predictable reactivity to run their process at a larger scale without a mass of troubleshooting.
Manufacturers of specialty monomers use it to adjust the flexibility and adhesion of polymer backbones. Instead of fighting through noxious fumes from secondary amines (which we all know can reroute an entire batch due to safety incidents), the primary character here lends lower vapor risk and easier emissions control. In coatings, adhesives, or medical devices, this translates to lower operator exposure while keeping the technical specs in check, something our shopfloor team values as much as our customers do.
Side-by-side with unbranched piperidin-4-ylamine, the isopropyl variant stands out beyond the structure. That extra alkyl group crowds the nitrogen, shifting its basicity and nucleophilicity. In many hydrogenation and reductive amination reactions, this simple change allows for tighter control. Over the years, clients have come to us after rounds of failed optimization with regular piperidine derivatives, frustrated by inconsistent selectivity. Feedback circles back showing that our isopropyl model cuts down on overalkylation and keeps side reactions from taking over, which saves expensive starting materials in the process.
In screening studies for CNS-active compounds, chemists tell us that the isopropyl modification tweaks lipophilicity, opening the door for better compound penetration without the solubility snags found in bulkier, cyclic amines. This means real wins in medicinal chemistry, especially if you’re running SAR work or late-stage modifications. Our own R&D team has watched project after project shift from ordinary amines to our isopropyl-piperidine core once customers spot the short- and long-term performance benefits.
Amines carry a reputation for being stubborn in storage—yellowing, picking up water, or going off-spec after a few hot days in corrugated drums. We stock 1-Isopropyl-Piperidin-4-Ylamine in double-sealed, airtight pails with silica desiccant in every drum. It survives the four-month shuffle from reactor to client site without breaking spec as long as it stays cool and protected from air. Our in-house tests mimic everything from cold-chain logistics to sweltering non-climate-controlled warehouses. Even in sticky monsoon conditions, batches held their melting point and HPLC purity, which lets purchasing teams breathe easier about inventory sitting on hand.
Think of the difference this makes in process engineering. Less drift in raw material quality cuts down on recalibration and revalidation. Our team tracks out-of-spec reports closely—over the last 24 months, less than one drum in 500 required quarantine due to out-of-spec moisture, and most deviations traced back to accidental lid damage during inbound handling, not to synthesis itself. Keeping things right the first time means operators focus less on firefighting and more on throughput.
In all the years handling 1-Isopropyl-Piperidin-4-Ylamine, our safety culture has shaped how we make and deliver every lot. Operators work in clean zones using cartridge respirators and nitrile gloves during sampling and packing. Fume extraction and real-time air quality checks prevent exposure spikes, while every drum ships with clear labeling and hazard markings. Part of our credibility comes from owning the entire life cycle—if a drum leaves our site, we track it to installation or first use, always listening for feedback to retool our process if a safety or quality snag shows up.
Comparing the toxicity metrics, we see a much lower acute inhalation risk than with similar secondary amines, which lets our industrial buyers reduce the strictest control measures in their protocols. Shipping in solid rather than liquid form minimizes vapor and spill hazards. With less concern over stinging ammoniacal fumes, user training becomes smoother for customers scaling up handling, whether in kilo labs or full throughput environments.
Conversations with customers drive half of our process tuning. No matter how tightly controlled a product starts, downstream users expose it to conditions that no method validation ever covers. Analytical chemists in pharmaceutical pilot plants report that our crystalline, low-residual-solvent amine cuts down on background signals during HPLC and NMR analysis, freeing up more bandwidth for real research instead of troubleshooting peaks and interpreting noise.
Development teams running iterative syntheses note that higher melting point stability translates to fewer re-crystallization passes to hit the purity mark they need for regulated filings. In one story shared by a biopharma partner, access to fresh, on-spec material shaved a whole week off project timelines that used to stall while resupplying after previous supplier failures.
Shipping holds its own set of pains with specialty amines. Moisture pickup mid-transit used to spark a recall nightmare. We chased this down by overhauling sealing protocols, adopting foil laminate bags for the innermost layer, and putting humidity sensors in our logistics chain. Since these changes, out-of-spec deliveries for hygroscopic amines have dropped by more than 90%. Feedback from the field helped us tune stability for specific climate zones and storage jobs.
A recurring challenge in synthesis—especially in scale-up mode—is bleeding of color or peroxide content into downstream intermediates. Our team set up a regular peroxide assay, verifying the absence across every drum, giving medicinal chemistry and polymer teams confidence about running clean reactions. We also built tailored workup recommendations, based on our own test reactors, to help process chemists dodge filtration pitfalls and maximize time efficiency. This sort of support often goes unmentioned, but we hear from users that it is the difference between a frustrating day and a smooth campaign.
Our involvement doesn’t end once the product leaves the facility. We field technical questions on reaction compatibility, solvent selection, and even real-time process troubleshooting during kilo-scale runs. With new fields like peptide analogues and CNS-active compounds, experienced teams lean on real data—if a solubility quirk or impurity pops up, they want answers that come from hands-on experimentation, not assumptions or standard textbook notes. Everyone benefits when support matches the level of effort put into the manufacturing itself.
We run regular post-shipment surveys, calling back users at 30, 90, and 180 days after receipt, logging any shift in color, melting point, or granulation reported by the customer. Information flows both ways—details shared by one production team in southern China led us to change drying setpoints to better match tropical conditions, adding shelf-life to every subsequent drum worldwide.
Among all the moving parts of pharmaceutical and agrochemical synthesis, certain amines set a benchmark in consistency. 1-Isopropyl-Piperidin-4-Ylamine earned its place here by holding tight specifications shipment after shipment. The path from raw material bid to synthesized product isn’t always straightforward—side reactions, moisture spikes, and even packaging glitches all test the chain. We built our process to withstand these headaches, using feedback as the pressure test. Every minor deviation in crystal habit or odor prompts a review, whether or not it triggered a formal customer complaint. The point isn’t about hitting a certification—it’s about building trust, batch after batch, in dozens of global facilities.
Progress in chemical manufacturing hinges not just on technical purity but on responding to ever-tighter regulatory landscapes. With 1-Isopropyl-Piperidin-4-Ylamine, traceability comes baked in from raw input to packed drum. Analytical run data stays archived in both digital and paper form for every lot shipped, so both our auditors and our customers can access a living history of material quality.
As customers submit preclinical data or file for process patents, transparency on impurity profiles, residual solvent content, and trace metals becomes more than formality; it becomes crucial for project continuity. By publishing our analytical runs and sharing SOPs openly, we let commercial and regulatory partners work with fewer unknowns.
Chemistry doesn’t stand still, and neither do applications for 1-Isopropyl-Piperidin-4-Ylamine. Recent R&D projects target improved CNS drug analogues and lithium battery additives—places where small structural tweaks to the piperidine skeleton might unlock fresh utility or reduced toxicity. Because we run small pilot lines alongside ton-scale manufacturing, we can fine-tune batches for emerging uses, feeding back real insights to process development teams who are pushing the molecule into new territory.
Some customers seek off-spec or alternative salt forms to match new application areas—an opportunity to match formulation needs with ground-up process adjustments, such as optimized crystallization points or custom-run drying cycles. By being close to our own raw material streams and open to collaboration, we meet non-standard requests more efficiently, giving our partners an edge from the start. Chemical innovation only moves forward when suppliers help, not hinder, that push.
Every kilogram of 1-Isopropyl-Piperidin-4-Ylamine moving through our lines marks an intersection of precision, context, and care—from the operator at the reactor to the chemist drafting a new patent claim. Through all the variables—climate, shipping, changing regulatory demands, or sudden process bottlenecks—we’ve learned that technical value isn’t just about what’s in the drum; it’s about everything that keeps a batch on spec and in the hands of teams who rely on that consistency for their own advances.
In the end, 1-Isopropyl-Piperidin-4-Ylamine works as a reminder that the most important gains in specialty chemistry often come not from headline innovations, but from the daily discipline of making each batch right: clean, dry, tightly specified, and supplied with knowledge earned along the way. That’s how our team approaches this molecule, and how we continue to find new ground with every shipment delivered.