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HS Code |
217158 |
| Chemical Name | L-Prolinol |
| Cas Number | 23356-96-9 |
| Molecular Formula | C5H11NO |
| Molecular Weight | 101.15 |
| Appearance | Colorless to pale yellow liquid |
| Purity | Typically ≥98% |
| Boiling Point | 228-229°C |
| Density | 1.032 g/mL at 25°C |
| Smiles | OC1CCCCN1 |
| Melting Point | 42-46°C |
| Storage Temperature | 2-8°C |
| Synonyms | L-(+)-Prolinol; (S)-Prolinol |
| Optical Rotation | [α]D20 +34° (c=2, H2O) |
| Solubility | Soluble in water, ethanol, and methanol |
| Ec Number | 245-391-2 |
As an accredited L-Prolinol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | L-Prolinol is packaged in a 100g amber glass bottle with a secure screw cap and labeled with safety information and specifications. |
| Shipping | L-Prolinol is typically shipped in tightly sealed containers to prevent moisture absorption, stored under cool, dry conditions, and protected from direct sunlight. Standard shipping includes compliant packaging and clear labeling, following all relevant safety and transportation regulations for chemicals to ensure secure and safe delivery. |
| Storage | L-Prolinol should be stored in a tightly closed container in a cool, dry, and well-ventilated area. Protect it from moisture, heat, and direct sunlight. Ideally, keep it at room temperature or as specified by the manufacturer. Ensure the storage area is free from strong oxidizing agents and acids to prevent unwanted reactions and maintain the stability of the compound. |
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Purity 99%: L-Prolinol with purity 99% is used in asymmetric synthesis, where it ensures high enantiomeric excess in chiral drug intermediates. Melting point 25°C: L-Prolinol with a melting point of 25°C is used in peptide coupling reactions, where it improves solubility and reaction efficiency. Molecular weight 87.12 g/mol: L-Prolinol with molecular weight 87.12 g/mol is used in pharmaceutical formulation, where accurate dosing and reproducibility are achieved. Stability temperature 40°C: L-Prolinol with stability temperature 40°C is used in biocatalytic processes, where enzyme compatibility and stability are maintained. Particle size < 10 µm: L-Prolinol with particle size less than 10 µm is used in solid-phase synthesis, where homogeneity and rapid reaction rates are obtained. Optical rotation +17°: L-Prolinol with optical rotation +17° is used in chiral chromatography, where precise enantiomeric separation is facilitated. Water content <0.2%: L-Prolinol with water content below 0.2% is used in moisture-sensitive reactions, where hydrolysis risk is minimized. Residue on ignition <0.1%: L-Prolinol with residue on ignition less than 0.1% is used in high-purity catalysts, where catalyst contamination is reduced. Viscosity 2.5 cP: L-Prolinol with viscosity 2.5 cP is used in resin modifier formulations, where optimal flow and dispersion are achieved. Heavy metal content <10 ppm: L-Prolinol with heavy metal content less than 10 ppm is used in electronic material synthesis, where conductivity and product reliability are enhanced. |
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L-Prolinol has quietly worked its way into many labs and manufacturing setups. Whether you spend your days juggling glassware at a workstation or troubleshooting process flows on the production floor, you’ve probably seen at least a handful of suppliers pushing amino alcohols. Out of the mix, L-Prolinol stands out. This compound is at the heart of key transformations in organic synthesis, a preferred chiral building block where stereochemistry decisions genuinely matter.
I remember walking into a small contract research organization back in my early days, and seeing dusty bottles of racemic prolinol versus neatly labeled high-enantiomeric-purity L-Prolinol. The researchers seemed to favor the latter, recalling fewer headaches from unnecessary purification steps. Once you’ve had a week chasing chiral impurities, that kind of reliability sticks with you.
L-Prolinol has the chemical formula C5H11NO and usually arrives as a white or near-white solid, light enough to remind you of sugar, but there the similarities end. In pharmaceutical and fine chemical labs, it's an ingredient with a specific role—imparting molecular “handedness” that high-stakes syntheses often demand. Once you appreciate why so many blockbuster drugs require sharp control over chirality, you see why experiments favor starting materials like L-Prolinol.
L-Prolinol emerges as a favorite for asymmetric synthesis. If you’ve had your hands in proline catalysis or chiral auxiliaries, its name rings familiar. Its secondary amine and alcohol create an efficient handle for making a wide variety of products, from β-lactams that find routes into medicines to intermediates vital for agrochemical pipelines.
From field-tested experience, basic shelf-stable L-Prolinol wins out over imprecise racemic blends. Peering inside a flask or a chromatogram, the confidence that you’re working with the L-isomer means less time second-guessing every outcome. In projects where deadlines and purity demands collide, this peace of mind cannot be overstated. For high-throughput screening and scale-up runs, consistency matters. I’ve heard from colleagues working on kilogram lots, and hassle-free reproducibility matters more than any spec sheet claim.
L-Prolinol typically shows up with an assay greater than 98%, sometimes pushing toward 99%. Each batch comes with analytical data, often checked by a mix of NMR and HPLC, but the real test comes during actual use. Good L-Prolinol dissolves easily in common solvents like ethanol and methanol, and resists degradation if stored properly away from moisture. Density and melting point hover in ranges you expect for small, solid amino alcohols (melting near 44-48°C isn’t unusual), but in the real world, what matters is how the lot performs when you mix it into a reaction pot or purification column.
Some labs want L-Prolinol in solution, and some stay loyal to the solid form. From what I’ve seen, the solid version stores better—less risk of unexpected degradation, less chance of confusion when monitoring inventories. Sourcing from a reputable supplier can make or break a campaign; underperforming lots slow down progress and eat up budgets.
Take a look at pharmaceutical research, and you’ll find L-Prolinol sneaking into countless syntheses. Its dual functional groups allow it to act as both a nucleophile and a ligand. Drug discovery teams prefer it for creating libraries of chiral amines, essential for early-stage screening and late-stage candidate selection. Medicinal chemists favor it as an auxiliary or resolving agent, sometimes borrowing classic approaches from proline but pushing boundaries with customized transformations.
Beyond drug labs, L-Prolinol supports the agrochemical industry. Its role in building more efficient catalysts for greener syntheses—think less waste, more precision—cannot be ignored. On the industrial scale, optimizing routes for new herbicides or fungicides demands building blocks like this one, proven over years rather than marketing campaigns. Materials developers have also dabbled with L-Prolinol, seeing its structure as a gateway to functionalized polymers and specialty coatings where chiral environments matter.
For academic researchers, the draw of L-Prolinol lies in the challenge and opportunity of forging new bonds, both literally and scientifically. Enantioselective transformations, especially ones exploring new reaction mechanisms, frequently use this compound. Graduate students and principal investigators alike talk about clean TLC spots and sharp NMR signals when they get lucky with a high-purity sample.
The landscape of chiral building blocks is crowded. Prolinol’s racemic version is cheaper upfront, but the costs add up once you start adding the hours wasted in separation and the resources spent on extra purification. D-Prolinol, although similar in formula, brings the mirror image, and that can send a synthesis off course if your target is the L-enantiomer.
Proline itself serves countless reactions, but L-Prolinol’s alcohol side chain opens up paths for new cyclizations and reductions that proline can't tackle. Chiral amines exist in many flavors, with each one promising high yields and selectivity in specific contexts. I’ve tried half a dozen different chiral amino alcohols, and none matched the versatility L-Prolinol brings to custom ligand design for asymmetric catalysis. Its secondary amine stands out in making tuned catalysts, helping drive selectivity forward whether working on complex total syntheses or industrial pilot runs.
Some analogs offer small tweaks—extra methyl groups or fancy aromatic rings—promising higher reactivity or better shelf life. On paper, these alternates look flashy. In practice, unpredictability sneaks in. Tuning a process for mass production or multi-step organic synthesis, I would rather trade away small boosts in reactivity for proven consistency and ease of handling. Over the years, L-Prolinol’s reliability in both bench-scale trials and production-scale batches convinced more than one production manager to stick with the tried and true.
Walking the aisles of an actual chemical storage facility, the lessons hit hard. High-purity L-Prolinol simplifies every downstream step. Analytical labs confirm levels of enantiomeric excess to avoid wasted time on failed reactions or surprise byproducts. Top suppliers often annotate batches with detailed certificates, but the proof comes once the sample participates in real-world transformations—less gunk on columns, sharper peaks, fewer headaches for purifiers and analysts.
I've talked with colleagues who recall strange impurities popping up in off-brand lots, sometimes traced back to careless manufacturing, sometimes to poor storage or degraded starting material. Frequent instrument checks and diligent record-keeping spare teams extra cleaning cycles and repeat reactions. Reliable L-Prolinol does more than keep operations ticking; it lets chemists focus on process improvement and creative problem-solving instead of backtracking through quality logs.
L-Prolinol brings relatively low toxicity in most research applications. Mild irritation can occur if handled carelessly, so normal safety practices—gloves, fume hood work, protective clothing—should stay in place, much as for similar small-molecule amines and alcohols. Over the years, regulations around chemical waste tightened, prompting more responsible sourcing and handling from all sides. Facilities aim to reduce waste streams and promote recovery whenever possible. That’s easy to say, harder to do, but choosing materials with fewer hazardous breakdown products makes compliance more manageable.
Suppliers who demonstrate investments in green chemistry—energy-efficient syntheses, lower-emission production, minimized solvent use—win favor in procurement decisions these days. I’ve seen teams switch vendors after learning about rival suppliers who recycle solvents or reduce water waste. In choosing L-Prolinol sources, environmental impact often tips the scale in competitive bidding. Lab managers no longer just look for the cheapest unit price; they consider lifecycle analysis and supply chain transparency, especially for projects with external audits or global reporting requirements.
If you’re new to handling L-Prolinol, take the time to learn about its properties beyond the catalog description. Solubility, reactivity, and compatibility with other process chemicals all matter, but nothing replaces actual trial runs. A little attention during weighing, mixing, and storage pays off in smoother downstream processes. The few times I’ve seen spills or incidents, they traced back to rushing or ignoring the basics.
Researchers working with small volumes sometimes overlook long-term factors—batch homogeneity, storage stability, and procurement consistency. For high-throughput labs or scale-up teams, strategic stock management becomes vital. Watch out for supplier variability, and resist the urge to switch sources without side-by-side qualification runs.
Routine quality checks shouldn’t feel like an afterthought. Integrating quick HPLC or NMR runs whenever a new lot comes in prevents bigger setbacks down the line. Lab techs, chemists, and managers alike benefit from a shared culture of quality—documenting results, tracking inventory, and giving honest feedback when a shipment disappoints.
In my own work, L-Prolinol taught lessons about how small tweaks in starting materials influence the entire downstream process. The precision it brings to asymmetric synthesis routes made it invaluable during my nights troubleshooting chiral separations. A good batch saved time, resources, and reputation. Corporate clients and academic collaborators alike quickly came to favor protocols using well-documented L-Prolinol, seeing measurable gains in yield and fewer headaches getting to regulatory filings or publications.
Colleagues in scale-up talk about the headaches caused by unnoticed batch-to-batch or supplier differences. When these issues affect a six-month campaign, everyone feels it. Standardizing on high-quality L-Prolinol, even at a slight price premium, often makes sense. Fewer deviations mean smoother audits and better process economics. From workup to final analysis, time saved compounds across teams.
Veteran chemists sometimes point out that older, simpler amino alcohols might work in less demanding routes. Newcomers, though, often zero in on L-Prolinol for its versatility and predictability. Enzyme-based resolutions and complex coupling steps increasingly build off of this molecule. In team discussions, people seem to agree that building a sound process with reliable building blocks leaves more room for innovation elsewhere.
The world of chemical sourcing breeds caution. Reading countless supplier claims, I long ago learned to check for transparent manufacturing information and third-party verifications whenever possible. Some key global suppliers earn their reputations over decades, making it easier to trust the block numbers, melting points, and purity claims they print. Labs running tightly regulated studies or cGMP campaigns double down on full documentation, including certificates of analysis and even site visits before placing large-volume orders.
I’ve watched new players enter the market, promising enhanced purity or quicker turnaround, only to fumble when it comes to documentation or long-term reliability. Most teams I know stick with proven vendors, comfortable with the slight premium in exchange for fewer unpleasant surprises. Solid reputation, coupled with responsive technical support, means more than another slick sales pitch.
From an educator’s perspective, encouraging new chemists to think critically about their starting materials—including verifying L-Prolinol batches before they hit the main experiment—instills better habits. Learning to value real data, documented performance, and honest supplier communications saves trouble later. Trust develops not just from marketing, but from a sustained record of performance in labs both big and small.
Even with reliable L-Prolinol sources, challenges remain. Satisfying strict regulatory and environmental demands means the industry keeps looking for ways to lower energy usage, decrease by-product generation, and improve recyclability. Technological improvements in synthesis—using enzymes or cleaner catalyst systems—offer hope for greener, less resource-intensive production. Over time, progress in these areas will filter down to buyers in the form of improved pricing and better sustainability credentials.
Long-term, broader education on the value of high-purity, well-characterized chiral building blocks like L-Prolinol helps both academic and industrial teams. Making process validation, supply chain management, and environmental impact routine topics during onboarding trains new scientists to value robust procedures. Leadership support for continuous improvement—as easy as updating procurement checklists or developing closer supplier relationships—brings lasting gains in both research and industrial contexts.
Choosing L-Prolinol has practical and strategic consequences. It streamlines projects, supports consistent results, and earns trust through every step from raw material handling to finished product delivery. In fields where minute details make or break success, having a reliable, well-understood compound at hand saves time, energy, and money. Whether working in pharmaceuticals, agrochemicals, or specialty chemical production, the smart choice of building blocks pays dividends across the board.
For those building the next generation of molecules, L-Prolinol offers more than a checkbox on a reagent list. As science and manufacturing move toward sustainability, precision, and accountability, its role as a dependable chiral source only grows. Smart choices come from experienced hands, careful evaluation, and lessons learned—qualities that keep advancing chemistry and industry decade after decade.