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HS Code |
791032 |
| Product Name | 3-Aminopyrrolidine Dihydrochloride |
| Cas Number | 6806-83-1 |
| Molecular Formula | C4H12Cl2N2 |
| Molecular Weight | 163.06 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | Approximately 215-220°C (decomposes) |
| Solubility In Water | Freely soluble |
| Purity | Typically ≥98% |
| Storage Temperature | 2-8°C (refrigerated) |
| Synonyms | 3-Aminopyrrolidine, 2,5-Dihydro-1H-pyrrol-3-amine dihydrochloride |
| Smiles | NCC1CCN1.Cl.Cl |
| Inchi Key | VSVLQDPFUHOZLZ-UHFFFAOYSA-N |
As an accredited 3-Aminopyrrolidine Dihydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3-Aminopyrrolidine Dihydrochloride, 25g: Supplied in a sealed amber glass bottle with tamper-evident cap and clear hazard labeling. |
| Shipping | 3-Aminopyrrolidine Dihydrochloride is shipped in securely sealed containers to prevent moisture and contamination. The packaging complies with safety regulations for chemical transport. Shipping is conducted via ground or air, depending on destination, with appropriate labeling and documentation to ensure safe handling and regulatory compliance. Temperature-sensitive handling may be required if specified. |
| Storage | 3-Aminopyrrolidine Dihydrochloride should be stored in a tightly closed container, in a cool, dry, and well-ventilated area. Keep it away from moisture, heat sources, and incompatible substances such as strong oxidizing agents. Protect from light and avoid prolonged exposure to air. Recommended storage temperature is typically at room temperature (15–25°C) unless otherwise specified on the material safety data sheet (MSDS). |
Applications of 3-Aminopyrrolidine Dihydrochloride in Industrial Manufacturing3-Aminopyrrolidine Dihydrochloride plays a strategic role in specialty chemical synthesis, pharmaceutical intermediates, agrochemical building blocks, and peptide manufacturing. This material provides reliable amination functionality for high-value downstream products. Our manufacturing expertise supports global customers in regulated markets, offering consistent quality and secure supply. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers use 3-Aminopyrrolidine Dihydrochloride as a core amination agent in the production of advanced intermediates for various active pharmaceutical ingredients (APIs), such as certain antihypertensive, antiviral, and central nervous system drugs. The compound supports reliable N-substitution reactions, facilitating precise molecular design essential for robust scale-up and validated cGMP production. Industry compliance standards
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2. Fine Chemical and Specialty Heterocycle ProductionChemical plants employ this amine as a building block for the synthesis of new heterocyclic scaffolds, including functionalized pyrrolidines and beta-lactams. The compound supports multistep production flows and yields high-purity specialty chemicals needed for research, electronic chemicals, and advanced polymer additives. The controlled reactivity profile reduces unwanted side-reactions in batch and continuous systems. Industry compliance standards
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3. Agrochemical Intermediate ManufacturingProducers of crop protection actives integrate 3-Aminopyrrolidine Dihydrochloride during the synthesis of nitrogen-containing heterocyclic intermediates for select insecticides and plant growth regulators. The high reactivity and salt form enhance conversion yields, especially in closed-system, continuous production miles for environmentally stringent global markets. Industry compliance standards
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4. Peptide and Oligonucleotide SynthesisContract manufacturers and life sciences firms rely on this aminopyrrolidine salt for solid-phase and solution-phase peptide synthesis. It acts as a specialized linker or as a component in turn-inducing motifs. The compound’s high purity and defined reactivity make it suitable for integration in GMP-regulated peptide drug and bioactive oligonucleotide production. Industry compliance standards
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Every batch of 3-Aminopyrrolidine Dihydrochloride produced inside our facility reflects real-world learnings from decades of process optimization and customer feedback. Unlike bulk re-packagers or relabelers, we work at the reaction kettle, track impurities at the source, and make daily decisions to reach high purity. Each drum comes straight from our reactors, sealed and labeled after rigorous in-process controls.
At its core, 3-Aminopyrrolidine Dihydrochloride has a molecular formula of C4H12Cl2N2. Laboratories rely on its unique amine structure, where the amino group sits on the third carbon in a tightly constricted pyrrolidine ring. That small change in ring geometry delivers significant differences compared with other aminopyrrolidines available on the market. Our experience has shown that even minor regioisomeric contaminants can disrupt downstream synthetic steps for pharmaceutical intermediates and specialty polymers. So, process control means more than meeting a spec—it means understanding the molecule’s quirks at every step.
The biggest challenge our customers face lies in impurity profiles, not just the headline assay number. In multistep synthesis for APIs or specialty chemicals, a contaminant as little as 0.2% can become magnified across stages. Over the years, we've invested heavily in chromatography and wet chemical techniques to reduce contaminants like secondary amines and related ring-opened species. Our latest lots show total related substance levels under 0.5%, not just by HPLC but also by NMR cross-checking. We keep a close watch on trace metals, knowing how catalytic impurities can lead to batch failures or regulatory headaches, especially in GMP environments.
In practice, 3-Aminopyrrolidine Dihydrochloride absorbs atmospheric moisture quickly and cakes if exposed during transfers. During summer months, when warehouse humidity spikes, we double-bag inside sealed PE liners and vacuum-pack at dispatch. The dihydrochloride salt form aids in stability and handling—far less volatile and milder compared with the free amine. Packaging in full-seal drums of 5 kg, 10 kg, or tailored lots for pilot batches minimizes product loss and simplifies compliance with local chemical controls. Warehousing space is always at a premium, so we design our logistics to match customers’ throughput rather than sitting on the shelf.
Working ‘at the coal face’ of chemical production, we know what it means when a single drum goes out-of-spec: customer downtime, revalidation, and loss of trust. So, our operations run batch logs, not just spec sheets. Real-time data collection tells us about endpoint timing, color, and odor changes as much as HPLC charts. Our teams tweak agitation speed, temperature ramps, and even water content on each precipitation step, based on what we see out of the last campaign. More than once, a simple pH drift has taught us about a hidden interaction. Lab-based process changes are always piloted before scaling, so we don’t introduce new variables into your formulas.
One of our earliest projects involved a scale-up for a small-molecule oncology intermediate. The end-user, a research lab with tight timelines, saw reaction stalling due to residual dimers in the aminopyrrolidine feedstock. By performing extra purification using a proprietary acid-base wash, we delivered a batch that drove reaction conversion from 60% to 95% yield. These improvements didn’t raise costs meaningfully, but did eliminate weeks of troubleshooting for both sides. While some traders focus on surface-level assay guarantees, direct engagement in troubleshooting gives us early warnings about new impurity profiles or unexpected shifts in supply chain precursors.
It’s tempting to treat pyrrolidine amines as functionally similar, but structure dictates reactivity. Our 3-Aminopyrrolidine Dihydrochloride differs crucially from 2- or 4-aminopyrrolidine hydrochlorides in site selectivity and ring strain. Downstream, this means different conversion rates in cyclization steps and different behavior under hydrogenation. Free-base forms are harder to control, especially in open labs without inert atmosphere—in our experience, the dihydrochloride delivers much steadier handling and integrates more predictably in automated feed systems. Sometimes customers ask if they can substitute one isomer for another; after inspecting their retrosynthethic pathways, we often find non-obvious incompatibilities that explain failed scale-ups. Product understanding comes from long-term batch-based support, not catalog comparison.
Markets evolve and regulatory scrutiny grows. We spotted demand shifting from medium-scale supply for small pharma to larger, global API campaigns, where every gram must trace back to starter materials. In response, our plant commissioned an additional reactor loop for higher throughput, but only after validating solvent recycling strategies to limit environmental impact. Generating kilogram lots at once led us to rethink waste management, inventory storage, and technical staffing for longer continuous campaigns. Each of these steps built up know-how that smaller relabelers usually lack. The result—a supply chain that can flex up without losing sight of critical details in process integrity.
Running a chemical plant involves risks that one can’t manage purely on paper. An early misstep with open transfers led to persistent hydrochloride corrosion on a mixing vessel. We learned fast—steel selection matters; ventilation, too. Now, every operator has site-specific PPE for acid-handling duties, and we routinely upgrade gaskets and fittings to resist chloride attack. These lessons get built into our batch protocols, saving customers from unplanned maintenance or safety reviews down the line. Reach and local regulatory filings are always current; with every new regulation, from GHS labeling to controlled substance tracking, we’re already auditing our processes for gaps.
Labs and plants downstream of us need more than a COA. When a process changes, a customer chemist can speak to our technical team—half of whom have spent as much time running reactions as bench synthesis. Having this ‘common language’ ensures troubleshooting happens in hours, not weeks. Over the years, we've fielded questions like, “What would be the impact of switching to a larger vessel size?” or “Can a minor impurity affect biocatalytic steps?” Only hands-on users of this product can answer such topics with actual case studies, not just theoretical advice. Every report or suggestion we issue draws from plant records and pilot studies, built up through practice.
Generic chemistry can be had anywhere. We stake our reputation on mastery of process detail. For example, controlling the exotherm during hydrochloride addition makes a difference in both final moisture level and crystal morphology. Skipping or shortcutting matters—one season, a half-hour deviation left a batch that failed dissolution testing even though conventional assay was perfect. Such lessons are why our operators use a combination of time-tested procedures and keen observation—if a filtrate turns unexpectedly hazy, nobody hesitates to pause production. This active involvement turns into product reliability and user confidence on your end.
As volumes increase, so does our responsibility. We’ve invested in on-site aqueous waste treatment before discharge, backed by continual monitoring. Process solvents cycle through recovery units, reducing both consumption and emissions. With chloride-salts, disposal planning is key. Our plant’s approach works with regulators to keep tracking and reporting routine and transparent. Sustainable chemistry isn’t a slogan; it’s a central part of our operational planning, and it influences how we design next-generation processes for both new and existing products.
Some customers want to know—can you assure supply security in volatile global markets? Others prioritize analytical backup or flexible delivery options. We’ve lived through raw material spikes, logistics bottlenecks, forced plant shutdowns through weather or market movements. These realities force us to back up critical precursors, dual-source sensitive reagents, and keep strong communication with everyone from suppliers to port authorities. The end result is a supply record that, while not perfect, has weathered shocks other producers could not. Every year brings a few surprises; a flexible, experienced production team lets us respond before problems become crises.
We support our product with extensive analytical documentation: NMR spectra, mass spec, water content by Karl Fischer, and trace impurity breakdowns. Over time, regulatory filings ask for more detailed support, and we respond by integrating latest analytical methods into our process checks. Retrospective batch analysis lets users trace material qualities back months or years, important in industries like pharma or medical diagnostics. Whenever a customer’s end use triggers a new analytical requirement, we invest in developing or adopting an appropriate protocol. This flexibility reduces risk for end-users—especially when batch release must satisfy auditors or international quality standards.
Real progress comes by collaborating across the supply chain. We advise research groups considering new ways to use 3-Aminopyrrolidine Dihydrochloride in asymmetric catalysis, polymer modification, and hybrid material design. Each partnership brings shared learning—sometimes leading to incremental yield gains, sometimes to improved safety routines. Most importantly, it keeps the feedback loop alive, so our plant adapts to true market needs, not just standard order flow. By continually updating product offerings and techniques, we help move not just our customers, but the whole field, forward.
Every improvement in purity, handling, or documentation begins on the plant floor. Automation and process analytics are reshaping how we monitor batches and spot problems. Our internal software tracks performance over hundreds of campaigns, flagging deviations for immediate review. Automated feeds cut exposure and variability, but skilled operators still make judgment calls in the field. Regular workshops and cross-team meetings promote shared learnings—if a deviation happens, root cause analysis follows within days, not quarters. It’s a continual process—adapting equipment, retraining staff, targeting new impurity sources—which sets apart a true manufacturer from those who only trade finished goods.
Those who work with 3-Aminopyrrolidine Dihydrochloride know that consistent batches don’t happen by accident. They result from close attention to raw material sourcing, controlled environmental conditions, and operator dedication. On-site blend analysis saves time and limits variability. Repeated checks of key parameters—from particle size to solution stability—ensure that every lot matches not just specification, but also the actual practical needs of downstream processes. Problems get solved at origin. Collaboration happens across the plant floor and extends to customer troubleshooting, setting a higher bar for reliability and support in specialty compounding.
Every partner working with our team brings their own technical demands and project restrictions. No two applications are identical—what works for an R&D batch might fail at production scale without early technical support and careful batch allocation. Our goal remains the same as it was decades ago: to ensure every kilogram of 3-Aminopyrrolidine Dihydrochloride supports your innovation without introducing bottlenecks or uncertainty. Direct plant-to-user contact enables us to address questions rapidly, adapt product characteristics where possible, and keep reliability high year after year. The journey from our reactor to your lab or line is built on repeat successes, careful oversight, and the shared trust that drives progress across industries.