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HS Code |
893595 |
| Iupac Name | (S)-3-(1-Methylpyrrolidin-2-yl)pyridine |
| Molecular Formula | C10H14N2 |
| Molecular Weight | 162.23 g/mol |
| Cas Number | 1121-89-7 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 256-258°C |
| Density | 1.04 g/cm³ |
| Solubility In Water | Slightly soluble |
| Optical Rotation | [α]D20 +85° (c=1 in ethanol) |
| Smiles | CN1CCCC1C2=CN=CC=C2 |
| Inchi | InChI=1S/C10H14N2/c1-12-6-2-3-8(12)10-5-4-7-11-9-10/h4-5,7-9H,2-3,6H2,1H3/t8-/m0/s1 |
As an accredited (S)-3-(1-Methylpyrrolidin-2-Yl)Pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 10 grams of (S)-3-(1-Methylpyrrolidin-2-yl)pyridine, securely sealed with a tamper-evident cap and labeled. |
| Shipping | (S)-3-(1-Methylpyrrolidin-2-yl)pyridine is shipped in tightly sealed, chemical-resistant containers under ambient conditions. Proper labeling, cushioning to prevent breakage, and secondary containment are used to comply with transportation regulations. Shipment is handled by certified carriers, with accompanying safety documentation (SDS) and tracking to ensure safe and compliant delivery. |
| Storage | (S)-3-(1-Methylpyrrolidin-2-yl)pyridine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Store at room temperature, avoiding extreme heat or cold. Proper labeling and secure storage are important to prevent contamination, degradation, and unauthorized access. Handle with appropriate personal protective equipment. |
Applications of (S)-3-(1-Methylpyrrolidin-2-Yl)Pyridine in Industrial ManufacturingAs the direct producer of (S)-3-(1-Methylpyrrolidin-2-Yl)Pyridine, we supply this chiral building block to global manufacturers across advanced pharmaceutical syntheses, pesticides, specialty intermediates, fine chemical synthesis, and enantioselective catalyst production. Our material is produced under strict process controls for batch consistency and traceability, supporting demanding B2B industrial applications. 1. Pharmaceutical Active Ingredient SynthesisPharmaceutical companies utilize this intermediate for manufacturing selective nicotinic acetylcholine receptor agonists and other CNS-active agents. Its chiral purity streamlines downstream enantioselective synthesis steps, especially in projects where regulatory bodies mandate high optically active component concentrations. Our material integrates directly into upstream API synthesis routes as a protected enantiopure moiety or for further functionalization. Industry compliance standards
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2. Agrochemical Intermediate ProductionAgrochemical manufacturers use this molecule to produce enantioselective insecticides and herbicides, particularly those acting on nicotinic acetylcholine receptors in target pests. It serves as a protected core scaffold for downstream halogenation and alkylation, enabling synthesis of high-value crop protection products adhering to tightening residue and purity standards. Industry compliance standards
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3. Chiral Ligand and Catalyst SynthesisSpecialty chemical companies apply this compound to synthesize enantioselective ligands and metal-organic catalysts for use in fine chemical production and asymmetric hydrogenation. The enantiopure pyrrolidine-nicotinic core enables construction of high-fidelity chiral catalytic complexes, directly supporting high-value manufacturing streams for pharmaceutical and specialty intermediates that require precision conversion and minimized racemization. Industry compliance standards
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4. Fine Chemical Intermediates for Specialty SynthesisProducers in the fine chemicals and specialty intermediates sector use it as a core chiral building block for synthesizing custom heterocyclic systems, molecular probes, and high-value lab reagents. Its optically active framework supports selective construction of advanced intermediates for research and specialty organic chemistry markets where configurational control and traceability remain essential. Industry compliance standards
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From our experience on the plant floor and in research labs, (S)-3-(1-Methylpyrrolidin-2-Yl)Pyridine stands out among synthesized chiral amines. Chemists in our plant first took a close look at this molecule because it brings the (S) stereochemistry to the pyridine scaffold with a methylpyrrolidine ring. As a manufacturer, each batch we produce must match the exacting purity levels innovators demand for advanced synthesis—and we have learned how much handling and process control matter on this compound.
The molecule may seem simple at first glance: a pyridine ring substituted by a 1-methylpyrrolidin-2-yl group, locked into the (S) configuration. But we know that stereochemistry plays a decisive role in the way our clients’ reactions unfold. Based on industry needs, we focus our production on the (S) enantiomer at chiral excesses above 99%, a threshold that ensures the downstream transformations are clean, predictable, and free from costly side-products. Our analytical chemists in the QA lab scrutinize every batch with chiral HPLC and NMR to back up the numbers.
Some off-the-shelf sources deliver racemates or cut corners in separation steps, which shows up in sluggish or faulty catalytic cycles for researchers further down the line. Long ago, we decided to use asymmetric synthesis routes rather than relying solely on resolution techniques, because we saw fewer inconsistencies and better reliability. Tight process integration lets us keep specifications sharp: moisture content no more than 0.3%, residual solvent within standard GC-MS tolerances, and the main component always over 98% area by HPLC.
The physical form matters too, especially as our customers scale up. Customers asked for material that keeps well under inert conditions and doesn’t show caking or yellowing in storage. In our experience, slight tweaks to the final purification and drying stages made a world of difference. Now, we routinely achieve a free-flowing, almost white solid that dissolves rapidly in common organic solvents.
Anyone involved in synthesis of active pharmaceutical ingredients recognizes derivatives of 3-(pyridyl)pyrrolidines as building blocks that unlock tricky routes. Our in-house team has seen this compound serve as a valuable intermediate in pipelines focused on nicotinic acetylcholine receptor modulators and other bioactive heterocycles. The (S) enantiomer frequently lays the groundwork for syntheses in neurological or pain management targets where enantioselectivity cannot be sacrificed.
Drug discovery teams want reliable chiral sources for SAR studies, and this molecule fits a unique space because of its small size, robust stability, and the way its nitrogen atoms participate in hydrogen bonding or metal coordination. On a commercial scale, we’ve seen this product used as both a direct precursor and as a scaffold for further elaboration, including N-alkylation, acylation, or Suzuki cross-coupling.
Academic users and early-stage R&D groups have different priorities. We routinely ship small packages straight from our kilo lab, and we’ve heard that the material’s solubility in polar organics accelerates purification and reaction set-up. No need for aggressive conditions or tedious extractions; the product gives clear signals in both NMR and MS, saving valuable project time. We’ve also supported groups working with radiolabeling—critical in PET tracer development—where chemical inertness and predictable reactivity under mild conditions matter.
Talking with experienced chemists, we hear it’s easy to underestimate differences between various pyridyl derivatives. Our version of (S)-3-(1-Methylpyrrolidin-2-Yl)Pyridine pulls ahead in situations where chiral purity stands as a pass/fail gate. Some alternatives arrive as mixtures or contain traces of undesired enantiomer—which leads to regulatory delays or unreliable biological results. We have prioritized a route that delivers a single, high-confidence enantiomer every time.
From a handling perspective, the structure’s additional nitrogen helps confer stability, and our research division observed resistance to oxidative degradation compared with primary or secondary amines. Unlike certain substituted pyridines that hydrolyze or demethylate under ambient humidity, this molecule has proved itself sturdy in long-term trials. We keep samples in accelerated stability chambers, and over a year’s cycle, saw no significant drop in assay or shift in color compared to competitive offerings.
Pricing always enters the conversation. We manufacture in dedicated reactors and manage solvent recovery, driving costs down as we refine scale-up parameters. Years ago, pilot batches suffered poor yields and tricky isolation, but careful tuning of crystallization steps and upgrading our purification skids resolved those growing pains. Now, our clients get reliable pricing and predictable lead times, without the sting of last-minute QC failures.
Many medicinal chemists told us about headaches caused by uneven quality from brokers or repackagers. We only produce (S)-3-(1-Methylpyrrolidin-2-Yl)Pyridine in-house, tracking every lot from raw materials through to the final drum or vial. Our traceability system connects the finished goods directly to source documentation, so collaborators in pharmaceuticals or materials labs always know the story behind the batch on their shelf.
Shipping globally means listening to what our customers observe on receipt: nobody wants clumped or yellow-stained material. By tightening moisture controls and running routine particle-size checks, we catch outliers before they ship. We swapped out traditional fiber pails for lined HDPE drums that stay inert, and let customers specify packaging volume based on intended use—whether that’s milligram samples for screening or multi-kilo orders for pilot plants.
We also learn from custom projects. Some research teams need modifications to the base molecule—different counterions, solution phase, or especially tight specifications for impurity profiles. We approach each new customization with practical input from our synthesis chemists because their shop-floor experience gives early warning of challenges. More than once, that’s meant refining a quench step or adjusting drying curves for a notoriously stubborn impurity, all before the product leaves our warehouse.
The story of (S)-3-(1-Methylpyrrolidin-2-Yl)Pyridine at our site mirrors a pattern we’ve seen elsewhere in specialty heterocycles. At the kilogram scale, consistency means more than chemical theory—each run brings nuance to crystallization behavior, and even slight temperature swings can change the profile. Our batch records show that scale-up uncovers subtle changes in exotherms or filtration efficiency, so every tech transfer involves close monitoring and rapid data sharing between shift leaders and lab analysts.
On the regulatory front, quality systems must keep pace with evolving customer expectations. We maintain full documentation for our synthetic route, impurity limits, and in-process controls, because pharmaceutical partners conduct audits that dig deep. Our team underwent annual retraining to keep up with the most current cGMP guidance, and we routinely host site visits so customers can view QA practices firsthand. Transparency through documentation builds lasting trust, both for established firms and for emerging pharma startups.
Some of our long-term partners report quicker progress in clinical development projects when their supply chain starts with our material, simply because hiccups from poorly resolved chirality or varying impurity loads no longer stall their bioassay timelines. Having direct lines to our production chemists means feedback cycles are fast: if a customer integrates our compound into a new route or formulation, we’re on hand to troubleshoot purification or propose tweaks to target tighter specs.
Our chemists constantly seek better ways to streamline the process. We use asymmetric catalysts and proprietary purification techniques developed with hands-on experience, so our route gives strong yields and sharply delineated product peaks. Batch reproducibility means our clients don’t run the risk of project delays from unexpected assay failures. This reliability attracts process chemists whose timelines demand both speed and certainty.
Facility upgrades never stop. We recently improved our effluent system by adding tailored scrubbers to handle minor amine emissions, which both complies with stricter local regulations and improves working conditions for our staff. We automate critical adjustments on the plant floor, logging temperature and pH across syntheses and routinely calibrating our instruments to lock in tight batch-to-batch consistency. Maintenance teams have highlighted the need for proactive pump and valve monitoring to prevent downtime—an insight gained only after living through the inconvenience of an unscheduled outage.
Safety training evolves as we learn from practical experience. Every chemist working with (S)-3-(1-Methylpyrrolidin-2-Yl)Pyridine completes a full hazard review, and we’ve reworked transfer protocols to cut chance of accidental exposure. Our latest procedural improvements incorporate feedback from operators, who know the material’s quirks from hand-on handling, like static buildup on certain surfaces or sensitivity to open air during extended transfers.
Sustainability starts with smart solvent use and ends with minimal waste. Our plant team invested in solvent recovery units, reclaiming and reusing process solvent in repeated cycles without sacrificing purity. We also optimize cleaning strategies, using less aggressive washes without compromising on the cleanliness needed to avoid cross-contamination.
Our raw materials team prefers sourcing from vetted, transparent partners who share audit results and prove their commitment to ethical supply. This isn’t just theory; we have seen the consequences of unreliable vendors—sudden delays, off-spec starting materials, and the need for vigilant incoming QC just to avoid headaches downstream.
Waste minimization efforts run in parallel with process optimization. We constantly review our workup protocols to keep aqueous and organic waste volumes down, teed up for treatment with minimal landfill impact. Whenever feasible, we recommend changes that ease waste handling for our customers, offering tailored documentation so disposal teams can work efficiently and in compliance with local laws. Several times, customers have called on us to support permitting or environmental submissions as they scale; we view this as part of our long-term partnership.
Every gram of (S)-3-(1-Methylpyrrolidin-2-Yl)Pyridine that leaves our site has a clear history. We don’t accept externally produced material for repackaging or reselling, because adding extra hands and opaque supply lines only increases the risk for our customers. Our inventory system links intermediate samples, analytical data, and dispatch records, giving us—and our partners—confidence in every delivery.
Chemists who come to us report frustration with layers of resellers and vanished accountability. This single-point manufacturing lets us tweak batch size, supply chain steps, and documentation bundles based on precise industry needs—no guesswork or handoff delays.
We maintain close, ongoing relationships with our client base. Technical requests don’t pass through generic customer service queues; instead, project managers loop in our production or QA lead, who can provide an answer rooted in direct manufacturing experience. Many of our process improvements and customizations stem from frank conversations with working chemists—the people putting these molecules into real products and technologies.
Our journey with (S)-3-(1-Methylpyrrolidin-2-Yl)Pyridine reflects the broader evolution of specialty chemical manufacturing. Users now expect not just product, but technical partnership backed by real-world knowledge and transparent documentation. We focus every effort on maintaining high enantiopurity and consistent physical properties, drawing on what we’ve learned from scaling up, solving downstream problems for customers, and investing in sustainable, safe, and efficient facilities.
Every improvement comes from direct dialogue—not just theory. As regulatory expectations grow and end users push for greener, safer supply chains, we keep tuning our process, open to what our partners need next. By manufacturing this product ourselves, under one roof, and refusing to cut corners or outsource quality, we offer customers across R&D, pharma, and advanced synthesis a resource they trust from the pilot stage to full production.
No matter how applications change or industries shift, our commitment remains the same: delivering (S)-3-(1-Methylpyrrolidin-2-Yl)Pyridine that exceeds the highest standards in every batch, every shipment, every time. Our story continues, shaped by each chemist, project, and innovation that makes use of this unique compound.