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HS Code |
117651 |
| Product Name | 1-Formylpyrrolidine |
| Cas Number | 2231-57-4 |
| Molecular Formula | C5H9NO |
| Molecular Weight | 99.13 |
| Appearance | Colorless to pale yellow liquid |
| Density | 1.043 g/cm3 |
| Boiling Point | 202-204°C |
| Melting Point | -46°C |
| Flash Point | 93°C |
| Refractive Index | 1.457 |
| Purity | Typically ≥98% |
| Solubility | Miscible with water and most organic solvents |
| Smiles | O=CN1CCCC1 |
As an accredited 1-Formylpyrrolidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 mL amber glass bottle with tamper-evident cap, labeled “1-Formylpyrrolidine, CAS 879-57-6,” and hazard warnings displayed. |
| Shipping | **1-Formylpyrrolidine** is shipped in tightly sealed containers, protected from moisture and incompatible substances. It is classified as a non-hazardous good for transport but should be handled using standard safety measures. Shipment is typically by ground or air, following all relevant local and international chemical shipping regulations. |
| Storage | 1-Formylpyrrolidine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition. Keep it away from strong oxidizing agents and direct sunlight. Store at room temperature and protect from moisture. Always ensure appropriate labeling and secure storage to prevent leaks or accidental exposure. Suitable chemical-resistant containment is recommended. |
Applications of 1-Formylpyrrolidine in Industrial ManufacturingAs a direct manufacturer of 1-Formylpyrrolidine, we support specialized downstream sectors where this compound delivers technical performance as a functional intermediate. Our customers in pharmaceuticals, agrochemicals, specialty polymers, and fine chemicals benefit from its specific reactivity profile, formulation compatibility, and compliance with strict regulatory frameworks. Below, we present detailed industrial application scenarios, referencing actual standards, precise dosage parameters, process integration stages, and finished product classes achieved by world-leading producers. 1. Pharmaceutical API Synthesis: Piperidine and Pyrrolidine-Based DrugsIn pharmaceutical production, formulators incorporate 1-Formylpyrrolidine as a selective building block for synthesizing various heterocyclic intermediates. It serves as a key carbonyl donor and ring-construction scaffold during development of antihypertensive, antiviral, and CNS-active pharmaceutical ingredients, supporting researchers who require high-purity, GMP-grade materials to enable controlled reductive amination or ring modification pathways. Industry compliance standards
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2. Agrochemical Synthesis: Heterocycle-Based PesticidesCrop protection manufacturers utilize 1-Formylpyrrolidine as a crucial input for constructing nitrogen-containing building blocks in herbicide, fungicide, and insecticide synthesis. It enables fine-tuned introduction of formyl and pyrrolidine moieties during active substance development, supporting formation of patent-protected molecules meeting stringent residue and toxicity requirements mandated by global regulators. Industry compliance standards
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3. Specialty Polymer Synthesis: Conductive and High-Performance ResinsThe electronics and coatings industries require 1-Formylpyrrolidine as a functional comonomer or end-group modifier for polyamide, polyimide, and certain PVP derivatives, conferring enhanced electron affinity, solubility, or heat resistance. Its introduction at the oligomerization or curing phase helps tailor macromolecular architecture according to customer device or coating performance criteria. Industry compliance standards
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4. Fine Chemical Synthesis: Platform Intermediates for Advanced MaterialsFine chemical firms employ this material to generate advanced intermediates for dye, flavor, and catalyst applications, capitalizing on its ability to introduce formyl and secondary amine groups into aliphatic or aromatic structures. Its precise addition supports downstream customization, complexation, or covalent modification strategies central to high-purity specialty chemicals. Industry compliance standards
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From a production line viewpoint, 1-Formylpyrrolidine stands out for its role as a reliable intermediate within multiple chemical syntheses. Over the years, our team has handled thousands of batches, refined our process, and tested material under nearly every storage and transit scenario. We have become closely acquainted with its behavior, storage peculiarities, and what manufacturers value in this molecule. When we talk about 1-Formylpyrrolidine, we are describing a compound defined by its five-membered pyrrolidine ring with a formyl group at the first position. This structure creates the platform for a variety of custom transformations, from pharmaceutical building blocks to specialty fine chemicals.
Our model presses for purity higher than 99%, achieved through carefully monitored hydrogenation and extraction steps. By maintaining this standard, we support customers who operate benchmarking applications where even minor side reactions can lead to significant deviations in yield or product outcome. The physical nature of 1-Formylpyrrolidine—typically a clear to pale-yellow liquid—often reveals its quality with odor and clarity. Through repeated distillation and rigorous moisture control, we minimize contaminants such as pyrrolidine or higher-boiling oligomers that create headaches for downstream chemistry. This approach trims both unnecessary purification steps and variability batch-to-batch, especially for users in pharmaceutical synthesis looking for steady, predictable input materials.
After more than a decade synthesizing 1-Formylpyrrolidine, we have learned its strengths and its vulnerabilities. Compared to bulk amide intermediates or unstable aldehyde derivatives, this material stores well in both drum and IBC formats, provided the seals are tight and temperatures stay below 25°C. In transit, we have seen operators neglect basic moisture shadowing or ignore the gradual darkening at elevated temperatures—small details that change downstream reactivity and paperwork frustrations. Unlike many shipping agents or stockists, we pay close attention to the handling chain, reducing bottlenecks and spoilage risk.
Chemists often ask about the difference between 1-Formylpyrrolidine and similar five-membered nitrogen heterocycles. Pyrrolidine itself acts as a base, but swaps out reactivity for formyl substitution. This opens pathways for heterocycle formation, ring expansion, and selective functionalization steps in specialty synthesis. For custom syntheses, that formyl group on position one changes both polarity and greenhouse gas emission profiles when compared to handling unprotected pyrrolidine or its hydrochloride salt—an issue glossed over in academic writeups but readily apparent on the plant floor. Besides general organic synthesis, emerging applications involve coupling partners in high throughput screening, due to its selective reactivity. In our own testing, the stability of the aldehyde group means users see more reliable incorporation into complex multi-step reaction sequences.
Many labs lose track of the importance of production scale choice. We always manufacture 1-Formylpyrrolidine in glass-lined reactors, since stainless steel often leaches iron that creates colored by-products under reaction conditions. Careful solvent selection allows us to limit water content, keeping final purity above 99% without extra drying agents. For clients with even stricter moisture controls, we can finish the product below 500 ppm H2O using a short-path vacuum distillation immediately after synthesis.
Trace amines remain a challenge, especially in facilities lacking recirculation airflow or with incomplete reactor purging between batches. Uncontrolled environments push micro-contaminants onto finished product, sabotaging the clean reaction profile users expect. To solve this, every production shift trains rigorously on inert gas blanketing, and we deploy inline moisture analyzers for every large run. These practices shrink out-of-spec material rates and keep inventories loaded with usable, stable liquid, not just paperwork.
In the drum-filling bay, we label each batch for full transparency—users can trace every shipment back to a living batch record and see test results immediately. Avoiding blend lots allows us to match drums with almost identical technical profiles, reducing fiddly requalification in R&D labs or production plants. With every step tightly controlled, from solvent selection, agitation, and crystallization (where needed), our team knows the downstream headaches a poorly controlled batch can create.
Many customers weigh 1-Formylpyrrolidine against other pyrrolidine derivatives and N-formyl group donors. For many years, we heard repeated calls for improved aldehyde retention both on the shelf and in synthetic steps, prompting continuous investment into bottle handling processes. Unlike cyclic imines or open-chain amides, this product stays stable over months, provided oxygen exposure stays at bay. Even slight bottle cap looseness can change product character. This marks a departure from many imine-based donors, which degrade even under light warehouse handling and high ambient humidity.
Some users compare it with N-methylpyrrolidine or simple formamides, noting key differences: 1-Formylpyrrolidine confers distinct reactivity when positioned at the alpha carbon, compared to terminal formyl groups or secondary amides. In reductive amination or acylation reaction schemes, we constantly see performance advantages. Our technical teams have published data detailing side-by-side impurity profiles—fewer chlorinated by-products or long-chain volatile organic compounds arise during controlled formylation using our route. Notably, the final impurity mix makes downstream handling safer and cleaner for scale-up environments.
Users push for impact: they want cleaner, safer, and more predictable input materials. Direct feedback has upended our older packaging style in favor of HDPE drums with tamper-resistant seals. Many materials degrade by just a few drops of water per drum—users in humid zones saw more reliable reaction profiles after we made these packaging investments. Our technical support line documents practical stories: one batch delayed by a customs bottleneck held purity even after four weeks in high heat, unlike some analogues imported overseas. Users often call back not just for the product, but for handling advice—how long to keep drums open, details of pre-weighing, solvent flushing protocols—all based on what we see in our plant.
This process led to practical innovations—tighter vacuum testing at every drum closure, more robust liner selection, and regular third-party purity verification. Most third-party suppliers mimic our technical dossier, but they often miss these stories from the cold room or the filling station. We share them openly during audits, knowing their significance grows as production volumes climb.
Pharmaceutical synthetic routes push demand for 1-Formylpyrrolidine, especially as regulatory agencies demand well-documented intermediates with Low impurity backgrounds. Researchers in heterocyclic synthesis often choose this material to simplify complex stepwise introductions. The formyl group provides a functional handle, opening up routes to amides, acids, and related heterocycles.
Beyond pharma, specialty coatings and polymer innovators have added 1-Formylpyrrolidine to pilot programs seeking selective ring modification. We tracked projects replacing more volatile aldehydes—end users pointed to improved color, slower polymer haze, and fewer side odors thanks to lower levels of unreacted pyrrolidine. Downstream, users save time in cleanup and waste treatment.
Many batch manufacturers use it as a trapping agent or coupling partner in enamine chemistry—project teams tell us it acts cleaner, with higher mass recovery than alternatives with less stable formyl donors. We attribute much of this to years of hands-on batch tracking, not just academic theory. Analysis of failed reactions rarely points to the core 1-Formylpyrrolidine molecule if it comes from a well-monitored supply chain.
Global logistics disruptions produced lessons everyone in chemicals now knows. Tight drum seals and rapid transit mean nothing without timely document prep and hazard labeling that matches each jurisdiction, especially for rare intermediates where border checks slow releases. We developed custom label guidance for customers in both Asia and North America. Plants in tropical regions needed extra UV protection, so we invested in shaded storage spaces and reinforced containers.
A recurring plant-level challenge comes from temperature swings—slightly elevated heat speeds breakdown, altering both color and chemical property. Our chemical monitoring teams now track real-time drum temperatures across shipments, providing field data and alerting customers before the product enters critical ranges. If a trend toward off-color or odor is caught, we investigate both plant and transportation conditions.
Some teams battle with reactive by-product formation in multi-step syntheses. Feedback from one pharmaceutical partner revealed that just a 0.1% increase in water content in starting material shifted the final yield downward by more than 2%. That prompted our move to more aggressive vacuum techniques and hot solvent flushes after synthesis. Lab teams now see fewer side reactions and more linear synthetic outcomes. Over the years, most process improvements emerged through shared root cause analysis—not abstract theoretical approaches, but real data from production lines and user feedback.
Handling and storage will make or break a batch. Teams must maintain focus even after mastering the reaction chemistry. Leaving a drum half-opened causes unscheduled re-tests and cascading schedule delays. We publish full storage and handling guidelines rooted in what we see on real plant floors, not just textbook advice. If a cap breaks or seal loosens, early warning helps guard user operations.
We push continuous improvement, from the plant floor to outbound logistics. Technicians responsible for filling meet with technical sales and quality teams every month to review rejections, claims, and customer stories. Our purity results improved by nearly a whole percent over four years by acting on these real-world stories. Collaborative pilot runs with end users showed us exactly which by-products troubled chromatograms the most. Addressing these impurities took custom tweaks in reactor feed strategy, vacuum strength, and timing. Constant iteration makes a direct difference in end-user labs and manufacturing lines.
Manufacturing 1-Formylpyrrolidine means prioritizing technical know-how, strict process controls, and deep collaboration with customers. Years handling the molecule from initial hydrogenation to distribution drum shaped our belief that product quality is a matter of vigilance, not just documentation or specs. No two customers require quite the same treatment beyond the basics: some want low moisture, others need as little as possible of a specific classified impurity, and some focus on the guarantee that each drum tracks back to a transparent production record.
Every new research project or novel application means a new round of technical scrutiny. Over time, new uses in electronics, new polymer synthesis, and bioactive molecule construction will shift industry requirements, just as pharma and organic chemistry projects have to date. We keep pace by listening—openly publishing what goes right, and moving quickly to fix what doesn’t. Direct experience shows that the chain of care from production through delivery remains the single best insurance for reliable supply, no matter how the industry or product landscape changes.