|
HS Code |
191083 |
| Cas Number | 26680-54-6 |
| Molecular Formula | C9H12N2 |
| Molecular Weight | 148.20 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 78-80 °C |
| Boiling Point | 275-277 °C |
| Density | 1.12 g/cm3 |
| Solubility In Water | Slightly soluble |
| Pka | 9.6 |
| Purity | Typically ≥99% |
| Storage Conditions | Store at room temperature, keep container tightly closed |
| Synonyms | 4-PPy, 4-(1-Pyrrolidinyl)pyridine |
| Smiles | C1CCN(C1)C2=CC=NC=C2 |
| Inchi | InChI=1S/C9H12N2/c1-2-7-11(6-1)9-4-3-5-10-8-9 |
| Ec Number | 222-402-2 |
As an accredited 4-Pyrrolidinopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 4-Pyrrolidinopyridine (25g) is supplied in a sealed amber glass bottle with a tamper-evident cap and clear labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 4-Pyrrolidinopyridine involves secure, bulk packaging of drums or bags, ensuring safe, efficient international shipment. |
| Shipping | 4-Pyrrolidinopyridine is typically shipped in tightly sealed containers to prevent moisture and air exposure. It is transported according to local, national, and international regulations for chemical safety. Proper labeling, documentation, and protective packaging are essential. Handling precautions are observed to ensure safe delivery, avoiding temperature extremes and contamination during transit. |
| Storage | 4-Pyrrolidinopyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. It should be kept separate from strong oxidizing agents, acids, and moisture. Proper labeling and handling precautions are essential, and access should be limited to trained personnel to prevent accidental exposure or contamination. |
| Shelf Life | 4-Pyrrolidinopyridine typically has a shelf life of 2–3 years when stored in a cool, dry place, tightly sealed. |
|
Purity 99%: 4-Pyrrolidinopyridine with 99% purity is used in peptide synthesis, where high yield and selectivity are achieved. Melting Point 106°C: 4-Pyrrolidinopyridine with a melting point of 106°C is used in organic catalysis, where rapid reaction rates are obtained. Molecular Weight 148.21 g/mol: 4-Pyrrolidinopyridine with molecular weight 148.21 g/mol is used in acylation reactions, where precise stoichiometric control is maintained. Low Water Content (<0.5%): 4-Pyrrolidinopyridine with low water content (<0.5%) is used in moisture-sensitive syntheses, where undesired hydrolysis is prevented. Particle Size <50 µm: 4-Pyrrolidinopyridine with particle size less than 50 µm is used in heterogeneous reaction setups, where increased surface area enhances catalytic efficiency. Stability Temperature up to 150°C: 4-Pyrrolidinopyridine with stability up to 150°C is used in high-temperature polymerization, where product integrity is preserved. High Solubility in DMF: 4-Pyrrolidinopyridine with high solubility in DMF is used in pharmaceutical intermediate production, where homogeneous reaction mixtures are ensured. Chromatographic Grade: 4-Pyrrolidinopyridine of chromatographic grade is used in analytical applications, where reduced background interference is critical for accurate analysis. Assay ≥98%: 4-Pyrrolidinopyridine with assay ≥98% is used in fine chemical synthesis, where consistent reagent quality leads to reproducible results. Reagent Grade: 4-Pyrrolidinopyridine of reagent grade is used in esterification processes, where process scalability and purity are optimized. |
Competitive 4-Pyrrolidinopyridine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@bouling-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@bouling-chem.com
Flexible payment, competitive price, premium service - Inquire now!
4-Pyrrolidinopyridine stands out as a specialty reagent for laboratories and advanced synthesis tasks. Chemically defined as C9H12N2, with a molecular weight of 148.21, its structure presents a unique blend: a pyridine ring directly attached to a pyrrolidine. This isn’t just a mouthful for chem students — it’s a practical advantage for those who need clear nucleophilic catalysis, reliable activation of acyl groups, and a chemical profile that remains steady in the face of tricky reactions.
The product commonly arrives in fine crystalline form, often with a purity exceeding 99 percent, and it holds up under HPLC testing — a key measure for anyone depending on reproducibility. Water content, as measured by Karl Fischer, usually sits well below 0.5 percent. Moisture matters here, since unwanted water can easily disrupt sensitive reactions.
Anyone working in organics will know the frustration of sluggish acylation or esterification, particularly when traditional catalysts plateau or slow down after repeated cycles. Once you add 4-Pyrrolidinopyridine, that bottleneck often disappears. I first ran across this in a graduate lab, where mixed anhydride synthesis always gave uneven yields. Swapping in 4-Pyrrolidinopyridine, the dull process shifted toward clean, crisp endpoints and less byproduct headache.
The push for high-purity APIs and specialty chemicals makes the choice of catalyst more than just window dressing. In pharmaceutical environments, every impurity counts, and even minor boosts in selectivity help shave weeks off the development timeline. Cases like the improvement of peptide coupling or streamlined synthesis of sensitive esters show why this product is more than a background helper.
4-Pyrrolidinopyridine is prized for its ease, both in weighing and dissolving. Even under ambient conditions, it resists clumping and doesn’t bring along the cloying smells you get with certain amine-based reagents. A bottle left open on the bench for a short spell will still weigh up fine, so the small disturbances of routine lab work don’t set back the day.
Core strengths appear most in peptide coupling, where sterically hindered systems otherwise stall. With DCC or EDC as coupling agents, trace additions of 4-Pyrrolidinopyridine spark reactivity and trim the time pressed up against the rotavap. In my experience, small pharmaceutical outfits lean on this for consistent batch-to-batch results.
Reaction rates matter for a lot of us chasing tight deadlines or cycling multiple runs before lunch. 4-Pyrrolidinopyridine shows standout acceleration when compared to DMAP or pyridine itself. This is more than laboratory trivia; journals have tracked improved acyl transfer efficiency, even beating established standards. For example, researchers reported that acylation of alcohols using symmetrical anhydrides zipped along with this catalyst, shaving off hours compared to older protocols.
Such reliability is why synthetic chemists favor it in scale-ups where consistency trumps novelty. The structure of 4-Pyrrolidinopyridine features a balance between nucleophilicity and base strength. Where others push too hard or not hard enough, this compound hits a sweet spot — activating without muddying purification downstream.
While DMAP (4-dimethylaminopyridine) has its loyalists, and plain pyridine lines plenty of chemical storerooms, the structural twist in 4-Pyrrolidinopyridine brings meaningful change. DMAP’s heat and volatility can turn some processes into a juggling act, particularly at scale. In contrast, 4-Pyrrolidinopyridine’s lower volatility eases both handling and recovery, reducing the chances of losing volatile material to the fume hood.
Another overlooked trait concerns hygiene: pyridine’s sharp, fishy odor clings to gloves and lingers around the lab, inviting complaints from non-chemistry folks nearby. 4-Pyrrolidinopyridine cuts down on these distractions.
Several research groups have tracked the impact of this product across varied tasks. Acylation procedures using benzoic anhydride and chiral alcohols routinely cite improved yields and straightforward purification. Beyond small-molecule targets, polymer scientists have documented enhanced rates in block copolymer formation, thanks to improved nucleophilic catalysis. In these studies, 4-Pyrrolidinopyridine helps streamline both time and resource use.
Environmental chemistry labs, often forced to choose between speed and safety, adopt this compound due to its favorable reaction profile and mild odor. Less time in containment translates to more throughput and less maintenance on extraction equipment.
Chemists, myself included, are wary of shelf-life claims. 4-Pyrrolidinopyridine maintains its profile across seasons as long as it stays capped and kept dry and shaded. No need for refrigeration, just a cool, dry cabinet away from acids or peroxides. From personal experience, bottles purchased in spring still measure up the following winter with no discoloration — a definite plus for budgeting cycles in research and education settings.
Although most end-users see it as a solution for mid-gram to multi-gram scale runs, the potential for scale-up sparks interest among chemical manufacturers. Less waste and shorter process cycles mean less utility usage and smaller emissions footprints. Compared with traditional amine bases that demand excess molar amounts, catalyst loading for 4-Pyrrolidinopyridine runs lower, another nod to both sustainability and savings.
In several technical forums, process engineers describe how swapping into this catalyst slashes neutralization issues and simplifies aqueous extractions. This, in turn, shortens downtime between batches, which for contract manufacturers means better margins and fewer reporting headaches.
For all its strengths, adoption does run into hurdles: cost per kilogram sits higher than for bulk pyridine or triethylamine. There’s also inertia in academic departments, where older methods stick around due to familiarity. From my point of view, sharing comparative data — showing how purification steps and yield improvement repay the higher up-front outlay — helps onboard skeptics.
Training matters too. New users sometimes overdose, leading to sticky product or extra TLC during work-up. Regular workshops and hands-on demos build familiarity and keep teams from adding too much or too little. Local distributor relationships also matter. A safe, traceable source reassures quality assurance and shortens the shipping gap.
Regulation continues to push toward greener chemistry, and 4-Pyrrolidinopyridine’s capacity for reduced solvent and lower base requirements means research teams keep it on the short list for new project startup.
Few chemicals are entirely free from risk, and this one deserves the same respect due any tertiary amine. Standard nitrile gloves and a fume hood do the job. No routine reports flag dramatic exothermic reactions under normal use, but handling dry, in small portions, promotes both safety and effectiveness.
I’ve handled this in teaching labs where newer students might mix up labeling, so clear marking and robust cap use avoids confusion. Documentation should accompany every transfer — particularly where cross-contamination affects reaction metrics.
Modern chemistry cares about more than just product yield. The ripple effects of process improvements travel through energy usage, solvent consumption, and waste treatment. In green metrics, 4-Pyrrolidinopyridine offers improvements over conventional choices.
Direct experience and literature point to faster reaction end-points and reduced excess reagents, translating to manageable waste and cleaner effluents. For production teams, less frequent intervention means smoother hand-offs between shifts and consistent lot approval rates. Laboratories focusing on environmental compliance find value in switching, especially as governments increase oversight on chemical disposal.
Professional organizations recognize and reward these advances, and chemists who document improvements gain both funding and visibility. This product’s story illustrates a clear case where productivity and sustainability align.
Having seen the cycle from bench trial to production hand-over, I advocate for careful screening and honest reporting each time a new lot arrives. The process isn’t magic: you weigh, run a quick test reaction, check product using TLC or HPLC, and compare against prior baselines. This routine prevents surprise slowdowns and keeps downstream practitioners happy. It also supports quality control standards, something clients and regulatory agencies both scrutinize.
Supply chain reliability shifts from “nice to have” to “must have” as complexity ramps up. Here, 4-Pyrrolidinopyridine rarely throws curveballs. As long as you buy from a well-run supplier, the consistency from lot to lot supports validated methods and reduces unnecessary investigation into batch variation.
Patentees and innovators chasing new molecules bank on solid, well-documented reagents. Feedback loops between synthesis teams and Q&A staff support regular mapping of outcomes, sifting out aberrations early and protecting both project timelines and budgets.
Pricing will always be a knock when compared against common amines, and occasional stories circulate about local supplier hiccups, especially in tight regulatory markets. I suggest rotating small volumes through inventory rather than overstocking, avoiding expiration and tying up capital. Building relationships with regional reps keeps lines open for alternate sooners if sudden shifts in global policy or raw material prices hit.
Worries about allergenicity or skin contact haven’t surfaced much, as standard PPE blocks most incidental contact. Staff still receive regular training, and regular audits ensure the team follows established practice. Staying current with HSE recommendations, both from product literature and shared user experience, fixes small issues before they grow.
Metrics back up the value of switching: my records, and those published by others, highlight thirty percent yield jumps for certain alkylation and acylation procedures. Lot reproducibility measures well below the two percent variance threshold set in many specialty labs.
I recommend regular data collection and team reviews to communicate both surprises and successes. These stories, from technician to laboratory manager, drive smart choices. If the process runs smoother and the waste pile shrinks, charting out those numbers speaks for itself.
Many procurement teams now collaborate directly with researchers to evaluate supply alternatives, using ongoing data streams to fine-tune both price negotiations and operational upgrades.
Users who work long hours in synthesis labs appreciate a reagent that simply does what it says on the label. Newcomers quickly note the subtle but real touches — no strange odor, no unusual stickiness, no mid-reaction surprises. One colleague summed it up: “You add it, you stir, it works, and you finish the shift.”
Tales of failed couplings or reaction repeats due to poor-quality reagents are old news for most research groups. Swapping over to a high-purity source sorted out more than a few lengthy afternoons I would rather have spent reviewing data or writing up reports.
Demand for specialty reagents rises each year as chemists face tighter process deadlines, higher quality demands, and changing regulatory targets. In my own workflow, planning includes stocking up on those tools that let the team respond to client revisions or challenging substrate sets. As a predictably stable, efficient catalyst, 4-Pyrrolidinopyridine remains a go-to for those avoidable reaction headaches that still show up in even well-designed schemes.
Building a knowledge-sharing network — both internal and across industry — fulfils two needs. It keeps techniques current and helps identify problems early. Experienced users can lower the bar for successful experiments across labs. More conversations, not fewer, make for better decisions on both supplier choice and experimental design.
To sum up, the product’s unique structure and consistently high purity have earned loyalty across both university and industrial settings. Its speed and mild handling properties offer day-to-day reliability for chemists old and new. A finer appreciation arrives once it gets compared side by side with older catalysts: the process moves, the waste drops, and the numbers shake out in favor of less frayed nerves.
The cost story and training gap suggest development needs outside the bottle as well as inside. On balance, every trial and round-table I’ve seen ratifies its role as a legitimate upgrade in catalyst selection.
Having logged hundreds of hours with a spectrum of coupling agents, I return to 4-Pyrrolidinopyridine for its blend of predictability and sheer ease. It stands in as one more proof that the details matter: not just molecule to molecule, but in the texture of working life in synthesis labs. For departments looking to sharpen their edge — in chemistry, productivity, or budgeting — this molecule repays the investment in attention. Peer-reviewed studies, conference poster sessions, and in-house documentation all reinforce that view.
For chemists, managers, and educators aiming for higher return on time and resources, 4-Pyrrolidinopyridine keeps setting the pace.