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HS Code |
515705 |
| Iupac Name | N-(1-cyclopenten-1-yl)morpholine |
| Molecular Formula | C9H15NO |
| Molecular Weight | 153.22 g/mol |
| Cas Number | 946714-85-8 |
| Appearance | Colorless to pale yellow liquid |
| Solubility | Soluble in organic solvents |
| Purity | Typically ≥97% (as available commercially) |
| Smiles | C1CCC(=C1)N2CCOCC2 |
As an accredited N-(1-Cyclopenten-1-Yl)Morpholine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of N-(1-Cyclopenten-1-Yl)Morpholine is supplied in a tightly sealed amber glass bottle with a tamper-evident cap. |
| Shipping | **Shipping Description:** N-(1-Cyclopenten-1-Yl)morpholine should be shipped in tightly sealed containers, protected from moisture and light. It must be handled according to standard chemical safety procedures, labeled appropriately, and accompanied by relevant safety data sheets. Transportation should comply with local and international regulations for non-hazardous organic chemicals. Avoid extreme temperatures. |
| Storage | N-(1-Cyclopenten-1-yl)morpholine should be stored in a cool, dry, and well-ventilated area, away from heat, open flames, and direct sunlight. Keep the container tightly closed when not in use, and store it away from strong oxidizing agents and acids. Ensure appropriate chemical storage labeling and comply with local, state, and federal storage regulations for hazardous materials. |
Applications of N-(1-Cyclopenten-1-Yl)Morpholine in Industrial ManufacturingAs a committed manufacturer of advanced chemical building blocks, we supply N-(1-Cyclopenten-1-yl)morpholine to support core innovations in demanding industrial sectors. This high-purity intermediate enables precise molecular modifications and functionalization steps in several downstream fields, always meeting critical requirements for compliance, process efficiency, and reliable formulation performance. Below, we present key application scenarios based on documented, established industry adoption. 1. Active Pharmaceutical Ingredient (API) SynthesisOur material plays a role as an intermediate in the synthesis routes of several APIs, supporting medicinal chemistry programs targeting complex small molecules. Its unique cyclopentenyl structure allows for regioselective derivatization within complex heterocycle assembly, which is essential for medicinal value creation in cardiovascular, anti-infective, and CNS drug candidates. Customers engage this intermediate during the late-stage route optimization for clinical and commercial supply, demanding trace impurity control and comprehensive batch traceability. Industry compliance standards
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2. Agrochemical Synthesis and Crop Protection FormulationsN-(1-Cyclopenten-1-yl)morpholine helps formulate advanced active ingredients and key intermediates for selective herbicides and fungicides. Industrial users leverage its cyclopentenyl-morpholine backbone to create molecular scaffolds with improved land persistence and target specificity. Our material is commissioned for batch and continuous production cycles that require close attention to residual levels and field use compliance, supporting downstream integration into both technical-grade and formulated pesticide products. Industry compliance standards
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3. Specialty Polymer Performance AdditivesThe cyclopentenyl-morpholine moiety acts as a specialty functionalizing agent in the production of advanced polymers, mainly for engineering plastics with tailored thermal, dielectric, or mechanical properties. Polymer compounders and resin manufactories introduce this raw material in functional monomer or end-capping steps to impart hydrophilic-lipophilic balance or modulate cross-link density, particularly in polyamides, specialty polyurethanes, and thermoset resins utilized in electronics, automotive parts, and insulation applications. Industry compliance standards
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4. Fine Chemical Intermediate for Fragrance and Flavor SynthesisFlavor and fragrance manufacturers utilize this intermediate to construct building blocks for complex aroma compounds, targeting cyclic lactones and morpholine-derivatives central to premium olfactory profiles. Specialist synthesis routes employ the cyclopentenyl group to facilitate ring expansion and unique substituent introduction necessary for natural-identical and artificial aroma formulations. High-purity, low-odor grades are essential to downstream blending and quality management, with particular concern for allergen and solvent residual regulation in consumer products. Industry compliance standards
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5. Organic Electronics and Functional Materials SynthesisWithin organic electronics, this intermediate enables the construction of complex conjugated molecules with tailored electron-donating properties, crucial for developing organic light-emitting diodes (OLEDs), organic photovoltaics (OPV), and related functional coatings. R&D and pilot lines in materials science introduce the morpholine-cyclopentenyl motif to fine-tune exciton behavior, solubility, and stability during high-purity organic layer deposition. Precise control of structural regularity, contamination, and process reproducibility drive adoption in this high-spec sector. Industry compliance standards
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Competitive N-(1-Cyclopenten-1-Yl)Morpholine prices that fit your budget—flexible terms and customized quotes for every order.
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Chemical manufacturing brings with it a steady stream of challenges, from raw material sourcing to customer demand for reliability and performance. In the last decade, we have seen specialty amines like N-(1-Cyclopenten-1-Yl)Morpholine rise in popularity across both pharmaceutical and agrochemical research sectors, driven by evolving synthetic needs and the limitations of conventional reagents. As a manufacturer, we set out to answer these challenges with careful process development and a commitment to reproducibility.
Producing N-(1-Cyclopenten-1-Yl)Morpholine requires exacting controls at every step. We have designed our process so every batch meets stringent purity and composition standards before it leaves our synthesis plant. Each run starts with cyclopentene and morpholine of established grades. Rigorous in-process testing keeps by-products in check, especially allylation side reactions that compromise downstream yields for our customers. Our team has learned the nuances that can derail this compound’s synthesis, including temperature drifts close to cyclopentene’s boiling point or atmospheric moisture that skews amine quality. Experience has taught us to review every detail of the batch record before we approve any shipment.
Quality matters in specialty chemistry. We maintain a typical purity above 98%, verified by GC and supported with NMR results. Customers rely on our transparent approach to certificate and supporting data. Draw samples are archived, letting us revisit batch analytics whenever questions arise years down the line.
Demand varies depending on the research utility for N-(1-Cyclopenten-1-Yl)Morpholine. Some customers ask for multi-kilo lots where even trace catalyst residues must be checked down to low ppm. Others, especially universities or early-stage companies, want smaller bottles for screening. To support this, we offer several packaging formats and flexible minimum order quantities that cut down delays for smaller developers. All product leaves our site in HDPE containers with tamper-evident seals. Each container receives its own tracking code, so its path from synthesis to shipment stays auditable.
We approach packaging size as a technical conversation, not a marketing decision. Bulk customers who need bespoke drum sizes for automated dispense can call our process engineers directly; these conversations often spark tweaks in our delivery bottling, reducing batch-batch cross contamination risk. Looking at the requests over the past year, research groups tend to start with 25g or 100g units before scaling to kilo orders—flexibility at this early stage keeps their projects moving.
Morpholine derivatives have played classic roles as solvents, stabilizers, and intermediates. Introducing a cyclopentenyl group creates new chemical opportunities for synthesis. Unlike simple alkyl morpholines, this cyclopentene ring brings rigidity, a feature valued in medicinal chemistry scaffolding. Medicinal chemists often mention how the cyclopentenyl morpholine reduces rotational freedom in precursor steps—helpful for fine-tuning activity or metabolic attributes in their candidate molecules. The five-membered ring holds up better than open-chain analogs when subjected to oxidation or strong bases during later synthetic steps.
Researchers have told us that switching from a linear N-alkyl morpholine to this cyclopentenyl version often cuts down unwanted side reactions in complex transformations. Where a typical benzylmorpholine brings concerns with electrophilic aromatic substitution or excessive lipophilicity, N-(1-Cyclopenten-1-Yl)Morpholine treads a balance between accessibility and reaction control. The combination improves cuprous or palladium-catalyzed cross couplings, an area we've tracked for some time based on customer feedback.
Pharma research groups tell us they use N-(1-Cyclopenten-1-Yl)Morpholine as a small-molecule intermediate in lead optimization. The cyclopentenyl moiety enables access to functionalized ketones and amides that straightforward morpholine can’t produce due to overalkylation or competing enamine formation. Scale-up groups have tested our product under both anhydrous and mixed-solvent systems; here, our low residual water content means consistent reaction predictability, key for process reproducibility.
In agrochemical synthesis, compound libraries benefit from morpholine derivatives for their unique SAR profiles. When companies push for new crop protection molecules, the cyclopentene group helps tune bioavailability in vivo. Unlike some larger-ring morpholines or simple methyl cyclopentyl amines, N-(1-Cyclopenten-1-Yl)Morpholine enters ring-closing transformations with better selectivity due to the electron-donating nature of morpholine’s nitrogen. One customer’s feedback led to our internal study on enantioselective additions with this product, and those results are now guiding others in catalytic reaction development.
We keep learning from the bench experience of synthetic chemists. Some have reported success in late-stage diversification, using this compound for aziridine formation and as an intermediate in chiral ligand synthesis. The rigidity granted by cyclopentene becomes a tool, unlocking routes closed off by more flexible structures. In our own R&D lab, we’ve documented stability in protic solvent series up to reflux, supporting purifications through aqueous workups without hydrolysis.
Years of customer dialogue have taught us what “quality” means beyond a printed spectra. Repeat users know batch-to-batch consistency saves days on their project timelines. For this morpholine, we run every lot against a defined specification: appearance, GC purity, water content (Karl Fischer), and heavy metal screening. Analytical standards are purchased from ISO-verified suppliers, and we keep records open to external audits. Each batch leaves our QC lab only after three analysts sign off, a practice that started following a customer’s in-house rejection more than a decade ago.
Some users need expanded analytical data for regulatory or compliance filings, especially in pharma pathways. Our in-house team offers HPLC, LC-MS, and elemental analysis upon request. We have noticed a rising trend in customers requesting orthogonal analysis before submission to national health authorities—faster access to these reports lets their regulatory teams cut down waiting times. Keeping this testing in-house also reduces the risk of product tampering or mix-ups in transit.
Researchers are rightfully cautious about chemical safety. N-(1-Cyclopenten-1-Yl)Morpholine benefits from morpholine’s relatively low acute toxicity, but the presence of the cyclopentene group calls for established protocols. Manufacturing teams wear splash-resistant gloves, run containment ventilation during distillation, and keep containers sealed outside the glovebox. Each drum ships with a tested seal; transport follows ADR or DOT guidelines for hazardous shipments, and customers often request supporting paperwork for air or sea cargo. Our technical staff keeps current on international shipping codes, and we have a habit of updating safety documentation annually based on the latest published data.
We find regulatory clarity gives our partners peace of mind. Our product meets the purity needs for research, but we are careful to flag batches intended for human or animal studies. Early on, one company bypassed standard QC review, resulting in rework and delay—since then, we have made it standard to review every application’s compliance risk with the end user. This transparency protects both our partners and our own process reputation in crowded regulatory environments.
Supply chains in fine chemicals move at a different rhythm compared to commodity products. The past few years’ disruptions have made that even more obvious. We keep material planning nimble, routinely switching between European and Asian raw material suppliers to avoid single-source risk. Whenever a global disruption looms, we add safety stock at key intermediates, sometimes keeping 3–4 months’ worth onsite. The investment pays off: larger customers never face lengthy backorders, even at the peak of market volatility.
Process logistics for morpholine derivatives require cool, dry storage. We run all warehouses at controlled ambient humidity. During heat waves, backup generators hold container temperatures below the product’s safe storage threshold. Every delivery follows a validated chain-of-custody process. Our tracking system logs timestamps and receiver signatures, rerouting in the event of transport delays or customs checks.
Running a chemical plant means shouldering responsibility for more than just profit and loss. Solvent choice, waste minimization, and energy efficiency each play their part in sustainable operations. Our shift to high-boiling, recyclable solvents during morpholine synthesis has halved annual waste volumes for this product line in the past three years. Distillation residues get sent to a licensed facility for recovery, not open disposal.
Energy use has dropped since reworking our heating protocols for cyclopentene reactions. Upgrading reactors with modern insulation trims gas demand, and removing a night shift during low-volume months has slashed overnight lighting and auxillary losses. As manufacturer, we prefer these investments over carbon offsets—they provide direct impact we can measure alongside production output.
Customers are asking more about green credentials. We stay transparent by sharing energy use statistics, waste volume disclosures, and the lifecycle footprint of major solvent stocks. Every improvement is tracked against internal goals; our hope is that others take the same accountability approach in their custom synthesis.
Our technical support lines stay open well after shipment. Research partners troubleshooting a stubborn reaction can call with questions about solubility, reactivity under odd conditions, or best storage practices. Experienced chemists, not just sales agents, pick up the phone to talk. This has led to practical problem solving—like suggesting co-solvents that can dissolve particularly challenging intermediates or sharing observations from our own catalysis projects that parallel the user’s reaction route.
We shape our product line based on user input. Synthetic feedback sometimes inspires us to tweak production—tightening impurity controls, developing new purification columns, or modifying packaging to better fit automated platforms. Our engineers regularly reach out for user reviews, inviting onsite audits or visits to see the manufacturing process in person. This level of transparency fosters trust and keeps our team grounded in the real needs of research chemistry.
Not all morpholine derivatives act equally in the lab. Where typical N-alkyl morpholines face issues with over-alkylation or instability during storage, N-(1-Cyclopenten-1-Yl)Morpholine remains robust under a range of synthetic conditions. The introduction of the cyclopentene scaffold creates new reactivity, letting researchers attempt transformations that otherwise stall with linear analogs. The rigid structure adds selectivity, especially in conjugate addition, cycloaddition, and late-stage heterocycle formation.
There are cases where a project team switched from a simple N-allyl or N-benzyl morpholine to our product and ended up raising final yield or cutting purification steps. This morpholine’s unique balance between electron density and structural bulk helps mask reactive sites during tough reactions, letting researchers overcome bottlenecks in complex synthesis. These subtle differences, picked up through practical experience, continue to shape our approach to process improvement and customer education.
Our history with N-(1-Cyclopenten-1-Yl)Morpholine has shown that the right niche intermediate enables much broader innovation than a standardized set of reagents. Direct collaboration, deep process knowledge, and commitment to transparency keep us flexible, responsive, and trusted among those taking on ambitious new syntheses.