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HS Code |
733237 |
| Chemical Name | 4-(2-Aminoethyl)Tetrahydropyran |
| Molecular Formula | C7H15NO |
| Molar Mass | 129.20 g/mol |
| Cas Number | 130893-03-9 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | Approx. 225-227°C |
| Density | Approx. 1.02 g/cm3 |
| Solubility In Water | Moderate |
| Functional Groups | Amino, Ether |
| Synonyms | 2-(Tetrahydropyran-4-yl)ethan-1-amine |
| Purity | Typically ≥98% |
As an accredited 4-(2-Aminoethyl)Tetrahydropyran factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed 25g amber glass bottle, labeled with chemical name, hazard symbols, lot number, and supplier details for 4-(2-Aminoethyl)Tetrahydropyran. |
| Shipping | **Shipping Description for 4-(2-Aminoethyl)Tetrahydropyran:** This chemical is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is packed to prevent leaks and damage, and is handled according to standard chemical transport regulations. Appropriate labeling and documentation are included to ensure safe and compliant delivery. Store in a cool, dry place. |
| Storage | Store **4-(2-Aminoethyl)tetrahydropyran** in a tightly sealed container in a cool, dry, and well-ventilated area. Keep away from sources of ignition, heat, and direct sunlight. Avoid contact with strong oxidizing agents and acids. Ensure proper labeling, and protect from moisture. Use proper personal protective equipment when handling to avoid skin and eye contact. |
Applications of 4-(2-Aminoethyl)Tetrahydropyran in Industrial ManufacturingAs a specialized manufacturer, we supply 4-(2-Aminoethyl)Tetrahydropyran to meet precise industrial requirements. Our experience ensures every batch meets strict quality standards for global manufacturing. Below are major application segments, each with unique specifications, dosage guidance, industrial process integration, and end-use product types. 1. Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical formula developers use this intermediate in the preparation of modified piperidine derivatives for CNS-active drugs. The rigid tetrahydropyran scaffold enables controlled side chain addition and improved molecular stability during multi-step synthesis. We deliver consistent purity for GMP environments, with batch documentation for full traceability in regulated markets. Chemists introduce our compound during key amination and cyclization steps, ensuring reaction efficiency and consistent impurity profiles. Industry compliance standards
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2. Agrochemical SynthesisProducers in the agricultural chemical sector integrate our compound to construct heterocyclic rings in novel crop protection molecules. Its unique aminoethyl-tetrahydropyran group confers bioactivity enhancements in the synthesis of certain herbicide intermediates and insecticide candidates. Formulators require high assay standards to maintain consistent crop safety profiles and regulatory acceptance. Industry compliance standards
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3. Polymer Modification AgentIndustrial polymer manufacturers employ our material as a functionalizing agent in the modification of specialty polyamides and polyurethanes. Its primary amine and cyclic ether structure enable chemical grafting, enhancing chain extension, impact resistance, and moisture barrier performance in engineered plastic blends. This additive is incorporated under controlled heat and catalyst dosage to prevent yellowing and uncontrolled crosslinking. Industry compliance standards
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4. Fine Chemical Intermediate for Specialty SurfactantsFormulators in the surfactant sector apply this raw material for constructing cationic and amphoteric surfactant frameworks aimed at industrial cleaning, anti-static additives, and corrosion inhibitors. Its unique structural motif offers tailored hydrophilic-lipophilic balance (HLB) and improved surface activity with reduced toxicity. We supply it with specification sheets suitable for regulated product development and finished goods registration. Industry compliance standards
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Every time we take up a request to synthesize a molecule like 4-(2-Aminoethyl)Tetrahydropyran, we pay close attention to the details behind its structure, reactivity, and intended application. The core of this compound—a tetrahydropyran ring with a precisely located 2-aminoethyl side chain—gives it a unique profile compared to other intermediates with simpler cyclic or straight-chain architectures. We recognized early on that the orientation of the amine group and the ring structure directly impact the compound’s utility in downstream applications.
We have spent years adjusting our production lines to respond to subtle demands in medicinal chemistry, and 4-(2-Aminoethyl)Tetrahydropyran is no exception. Handling heterocyclic compounds means accommodating extra steps—ensuring gentle environmental conditions, precise reagent addition, and attentive purification after ring formation and side-chain functionalization. Operators and QC specialists follow a routine of hands-on interventions, recognizing signals from batch color, viscosity, and pH that no automated system can fully anticipate.
Unlike more traditional amines or open-chain analogs, this compound shows less tendency for oxidation and side reactions. The cyclic ether imparts increased stability during storage. We have monitored samples through accelerated aging studies and real-world logistics; tetrahydropyran derivatives survive well in ambient conditions for months, while some acyclic analogs degrade in weeks. Control samples in transparent containers tell the story—semi-quantitative assays match visual and olfactory changes. This stability influences not just our handling in the plant but also the costs and peace of mind for our customers.
Whenever we discuss the specifications—which commonly include purity over 98% by HPLC, moisture below 0.5%, and limits for residual solvents—these aren’t just lines in a certificate. They arise from real problems we have met on the shop floor. Unreacted starting materials, leftover halosilanes, or trace metals all show up in spot tests as soon as a batch gets off track. Some years ago, a run with a leaky transfer hose gave us a chunk of inventory contaminated with mineral oil, and it took three deep distillations to bring the product back within spec. We judge “good enough” not just by hitting a number, but from hours spent tracking where impurities hide.
Logistics, too, matter. Our model for this product comes in select package sizes based on customer feedback—a lesson learned early when we ended up with a supply of 200-liter drums that nobody wanted for lab-scale research. Now, smaller vessels—amber glass bottles for high-purity research, lined containers for larger industrial quantities—fit user needs. Each package batch leaves our facility with full trace records—down to the technician who did the final cap seal. We have permanent storage logs and maintain stability samples in a dedicated vault, drawing lessons from every deviation so subsequent lots improve in reliability.
In-house teams first targeted this molecule decades ago in pursuit of building blocks for CNS-active agents. The 2-aminoethyl side chain acts as a versatile synthon for linking with other complex moieties. Drug developers prize it because it can connect with acid chlorides, activated esters, or simple aldehydes, all without too much steric hindrance or tendency to polymerize. When the synthetic route moved from gram-scale flask to full reactor, we adjusted catalyst loading, solvent swaps, and water-removal steps based on relentless feedback from QC.
We watched how lab chemists use this material as both a nucleophile (using the amine) and as a platform for further transformations—ring-opening, alkylation, and even selective oxidations. Its compact size and solubility offer advantages over bulkier ring systems or more hydrophobic cyclic ethers. For enzyme discovery and receptor-ligand modeling, the molecule slots easily into combinatorial libraries, streamlining the search for active candidates. Medicinal chemists sometimes mention the way the rigid backbone prevents unwanted conformational drift, a direct benefit when pursuing structure-activity relationships.
We have seen firsthand how a careless approach can lead to trouble, especially when dealing with low molecular weight amines. The amine group can evaporate under certain conditions, so our staff wears full-face protection during transfers, and exhaust system interlocks make sure nothing gets past a broken gasket. Every batch undergoes a full panel of safety analysis: flash point, thermal stability, vapor pressure, and, when shipping, thorough checks for container compatibility. A few years ago, a new drum supplier cut corners, and seals failed mid-transit in summer. That mishap cost us more in reputation than in rework hours. We now audit every incoming lot of packaging materials to prevent a repeat.
On the topic of standards: our lab techs run shift-long rounds with portable monitors, logging environmental exposure levels, and routinely pull up spreadsheets with five-year exposure data trends. Staff ask questions when something changes—an unusual smell, a spike in handling time—and our supervisors encourage such reports, knowing that persistent safety mindsets catch problems before they escalate.
Time in the chemical business gives a different view of product differentiation. Competitors often offer open-chain amino alcohols for related uses. We see researchers choosing those out of habit, only to find unexpected side reactions or rapid oxidation that destroys a batch of valuable intermediates. The tetrahydropyran ring in our molecule changes the game. The ether group provides stability, dampening reactivity at the adjacent carbon, and helps the amine group participate in chemistry without as much risk of self-condensation or hydrolysis.
Compared to similar six-membered heterocycles, the specific packing of this ring provides good solubility in polar and non-polar solvents—a trait borne out by the many test vials and analytics from customers returning for more. In comparison, piperidine analogs often present issues with odor and sensitivity to acid. We field questions weekly about whether a given intermediate suits their next round of synthesis, and our experience has shown this product often brings a Goldilocks balance of chemical enterprise: enough reactivity, enough stability, and enough compatibility.
Google’s principles emphasize experience and expertise for a reason. Our site-level process engineers who troubleshoot a crystallization problem at 3 a.m. know more about molecular behavior in practice than any online repository. Most optimization recipes derive from someone standing with a thermometer, counting drips and watching cloud points. Short-term efficiency or cost savings only go so far; a poorly designed process will bleed value out of every subsequent batch through rework and variable quality.
Traceability and documentation support every decision we make. Spec sheets capture a moment in time, but our real confidence comes from batch notebooks—hastily scrawled notes from a technician about color change or a pressure spike. These moments, not templated third-party assessment, ensure the next run goes without a hitch. Our senior staff study the failures as much as the wins because that’s where improvements hide. You only get consistency when people care and record everything; otherwise, you’re always one oversight away from a problem shipment.
Customers tend to approach us with specific goals—new drug scaffolds, specialty polymer design, even academic curiosity about a new class of materials. We do not see ourselves as mere suppliers, but as partners troubleshooting together. Last year a pharmaceutical startup needed a kilo-scale lot with sub-ppm metal content for a clean synthesis of a lead compound. Our bench team worked through the purification sequence, adjusting chelation and careful fractionation to protect both purity and yield. We learned through joint effort; we end up building better capacity and knowledge from every project.
Sometimes customers come in not knowing precisely what they want. We guide them on where 4-(2-Aminoethyl)Tetrahydropyran performs best—and where it doesn’t. It’s not the answer for every amination or conjugation; certain high-temperature processes can drive unwanted side reactions. Our technical advisors review customer process notes, run simulations, and prepare small lots on new solvent systems for them to validate in their own labs. This cycle informs our data and upgrades the whole industry’s comfort with more nuanced synthons.
Scaling a molecule from grams to multi-ton runs brings issues not visible at small scale. We watch solvent consumption, energy usage, cumulative waste, and emissions. A few years ago, we switched to a more efficient hydrogenation catalyst that dropped both run times and waste levels for this product. The change took weeks of plant trials and small-scale validations, but tracking annual utility consumption showed measurable improvements. Sustainability audits now form part of every internal process review; production teams brainstorm at every quarterly meeting about upstream waste minimization, even if regulatory targets haven’t changed yet.
Waste minimization matters not only for our conscience, but for cost and safety. Water separation, solvent recovery, and byproduct tracing each make a real difference to product margin. These gains don’t always get headlines, but by tuning every aspect of our process, from how quickly a quench runs to how we reclaim spent solvent, we keep both the process and the finished product competitive and safe.
Customer requirements evolve with every inquiry. Few buyers need the same set of criteria: bioconjugation groups emphasize purity and trace impurity removal; fine chemical producers prioritize reliability of supply and consistent batch-to-batch performance; academic labs sometimes have niche needs, such as isotope labeling or specific salt forms. We accept the challenge. In the last few years, more customers have asked about custom derivatives—protected amine versions, salt forms, and even radiolabeled analogs. We refine our production line to accommodate as many tweaks as feasible, tracking every parameter along the way.
Working directly with those who use the molecule in practice reveals what analytical metrics really matter. HPLC area normalization or NMR purity capture technical details, but the core experience comes from a researcher opening a vial—if crystallinity, solution clarity, or odor diverges from expectation, user trust suffers. We maintain a customer feedback loop, not just at the level of sales staff, but including lab staff, who test retention samples, check documentation, and compare notes with buyers' internal analyst teams. This direct interface gives us a sharper edge than competitors who farm out their manufacturing or rely on resellers for client interaction.
Adaptability underpins our ability to deliver reliable specialty chemicals. Regulatory trends keep changing, whether it’s new REACH directives, stricter local emissions codes, or evolving expectations about product origin and traceability. We respond by building solid documentation, upskilling staff, and continually reviewing process safety and environmental data. The world expects more than simple compliance: buyers and collaborators look for proof of ethical manufacturing, data transparency, and continuous improvement.
Respect for chemists and plant operators—those who live with each molecule and its risks day by day—forms the culture we protect. Anyone can buy a jar of an intermediate, but trust builds only from open books, honest sharing of pitfalls, and willingness to help users find the right fit for their goal. Open communication reduces misunderstandings, keeps shipments running smoothly, and builds a stronger foundation for the next generation of chemical development.
Having authority over every step from raw material sourcing to product shipment makes a visible difference in the chemical supply chain. We don’t rely on a cascade of intermediaries diluting accountability. Our people operate the reactors, validate the cleanings, execute every control sample, and sign off at dispatch. There’s no substitute for firsthand oversight of every variable that could affect performance, stability, or safety.
Key differences set direct manufacturers apart from traders. Some companies outsource production, then repackage materials under their own label. We’ve cleaned up behind some of those middlemen, receiving panic calls when a batch failed due to mishandled temperature or storage. The more hands a product passes through, the more chance for slip-ups or quality drift. By managing everything ourselves, we keep our own high standards and respond instantly to issues, rather than tracing backward through a web of third-party vendors.
The needs around 4-(2-Aminoethyl)Tetrahydropyran today are not the same as even five years ago. Some customers now explore the tetrahydropyran scaffold for new biologically active agents, conjugates for diagnostics, or innovative polymer links. We dive into literature, collaborate with leading researchers, and sometimes bring in outside consultants to expand our knowledge base about emergent uses. Product management in this climate requires both humility and curiosity; you cannot predict which property will matter most next year, so you prepare for the widest range of possibilities without drifting from your core manufacturing strengths.
We encourage internal experimentation. Lab techs regularly synthesize new analogs, test alternative salts, and review process improvements even outside direct commercial orders. This flexible, data-driven culture produces both solutions for client challenges and avenues for our next strategic investments.
From conception to completion, the journey of 4-(2-Aminoethyl)Tetrahydropyran mirrors the ethos of good manufacturing—real-world knowledge, careful process, direct engagement with users, and respect for the molecule and people at every step. The peculiarities of this compound, the rigorous handling standards, and the lessons learned over years of synthesis make it both a practical choice for advanced chemistry and a testament to the value of being close to the tools and the craft.
Every bottle leaving our site bears the mark of hands-on attention and continuous improvement. We learn not just from textbooks or spreadsheets, but from every late-night reaction monitoring session, every customer phone call, and every batch that passes or fails QC. This focus provides assurance and clarity for those relying on our materials to build something new and valuable in their industries.