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HS Code |
325496 |
| Product Name | (S)-(-)-3-Butyn-2-ol |
| Cas Number | 20209-98-1 |
| Molecular Formula | C4H6O |
| Molar Mass | 70.09 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Specific Rotation | -45° (c= neat, CHCl3) |
| Boiling Point | 119-121°C (lit.) |
| Density | 0.939 g/mL at 25°C |
| Refractive Index | n20/D 1.439 |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C, tightly closed |
| Smiles | C#CC(C)O |
| Ec Number | 243-608-5 |
As an accredited (S)-(-)-3-Butyn-2-ol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | (S)-(-)-3-Butyn-2-ol, 25g, is supplied in an amber glass bottle with a screw cap and hazard labeling. |
| Shipping | (S)-(-)-3-Butyn-2-ol is shipped in tightly sealed containers, complying with chemical safety regulations. Packaging protects against leaks and external contamination. Recommended storage during transit is cool, dry, and well-ventilated areas, away from incompatible materials. Transport conforms to hazardous material guidelines and may require labeling as a flammable liquid, depending on the quantity. |
| Storage | (S)-(-)-3-Butyn-2-ol should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Protect from light and moisture. Store at room temperature or as specified on the manufacturer’s label. Ensure the storage area is equipped for handling flammable and hazardous chemicals. |
Applications of (S)-(-)-3-Butyn-2-ol in Industrial Manufacturing(S)-(-)-3-Butyn-2-ol plays a critical role as a chiral building block in the synthesis of a variety of advanced specialty chemicals. Our production facility supplies this material with tight enantiomeric purity controls, supporting key value chains in pharmaceutical APIs, agrochemical intermediates, optically active fine chemicals, and chiral ligands. Below we outline the main downstream industrial application scenarios with reference to manufacturing standards, practical usage ratios, integration points in customer processes, and representative end products. 1. Chiral Intermediate for Anticancer API SynthesisStereo-controlled manufacturing in the pharmaceutical sector uses (S)-(-)-3-Butyn-2-ol as a key intermediate in synthesizing chiral drug molecules, particularly anticancer agents containing propargylic alcohol motifs. Downstream pharmaceutical producers demand batch-to-batch consistency and regulatory compliance to facilitate reliable scale-up for clinical and commercial production. Industry compliance standards
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2. Chiral Building Block in Agrochemical Intermediate ManufactureProducers of advanced agrochemical actives use (S)-(-)-3-Butyn-2-ol in the asymmetric synthesis of herbicide and insecticide intermediates. Industrial-scale facilities require reliable chiral selectivity for crop-protection products, where the chiral configuration directly impacts biological performance and adherence to regional residue regulations. Industry compliance standards
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3. Chiral Ligand and Catalyst Design for Fine Chemical Synthesis(S)-(-)-3-Butyn-2-ol supports producers of chiral ligands and asymmetric catalysts, contributing directly to the development of enantioselective transformations in contract and proprietary fine chemical manufacturing. Controlled supply of this building block allows downstream partners to optimize catalytic efficiency and selectivity in custom synthesis projects. Industry compliance standards
Typical usage ratio
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4. Chiral Component in Flavor and Fragrance Intermediate SynthesisIn the flavor and fragrance sector, manufacturers employ (S)-(-)-3-Butyn-2-ol as a raw material to introduce defined chiral alcohols into high-value aroma and flavor ingredient synthesis. The enantiomeric purity along with low residual solvent content meets requirements for downstream formulation in food-contact and consumer fragrance products. Industry compliance standards
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5. Stereoselective Synthesis of Specialty Polymer AdditivesChemical manufacturers utilize (S)-(-)-3-Butyn-2-ol as a chiral modifier or precursor in syntheses that deliver optically active specialty monomers and additives for polymers. Integration of this building block permits downstream polymer companies to tailor mechanical, optical, or degradation profiles of advanced plastics and functional materials. Industry compliance standards
Typical usage ratio
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Few chemical specialties hold such quiet importance as (S)-(-)-3-Butyn-2-ol in the labs of fine chemicals, pharmaceuticals, and advanced synthesis. Our team has spent years refining the production of this chiral molecule, and in that time we have learned which variables truly shape quality. Making this compound isn’t just a matter of following textbook recipes. On the production line, reaction conditions, temperature management, and precision distillation shape both the final optical purity and the actual batch yield. Experience has shown us that a gentle ramp to reaction temperature helps control undesired side products, and skilled handling during work-up preserves enantiomeric excess.
We manufacture (S)-(-)-3-Butyn-2-ol not as a side business, but because it forms an indispensable building block in asymmetric syntheses. Customers in our sector tell us about their struggles with unreliable supply. If purity drops or the water content sneaks above spec, entire development projects grind to a halt. These conversations have guided our investments in real-time analytical controls and batch tracking. Even small changes, like improving vacuum-tight seals on distillation columns, have a big effect over thousands of liters.
Commercial (S)-(-)-3-Butyn-2-ol usually comes as a colorless or pale liquid with high optical rotation. Yet beneath these surface similarities, products can behave very differently in real applications. We focus on chiral purity and controlling trace metal content, because these factors decide if the alcohol serves well as a chiral auxiliary or intermediate. Years ago, we debated switching suppliers for some chiral catalysts—poor results from solvents led us to double down on in-house manufacture instead.
Transparency matters in this business. We share NMR, GC, optical rotation, and moisture data with partners on request, since undisclosed impurities will quickly reveal themselves in downstream reactions. Our feedback loop runs three ways: from production floor to QC, from QC to R&D, and from R&D back to the process tanks. Without this dialogue, you end up fixing someone else’s mistakes instead of building on your own strengths.
Producing (S)-(-)-3-Butyn-2-ol at scale requires setting up reactions with both selectivity and safety in mind. We use proprietary enantioselective hydrogenation of propargylic ketone, using recyclable chiral ligands that we developed together with our catalysis team. Every raw material has its own quirks—variations in supplier lots can affect catalyst performance. To account for this, our reactor team adjusts base and ligand concentrations batch by batch. Not every manufacturer takes this extra care, but our batches regularly show >99% enantiomeric excess and minimal residual metals, even before polishing.
Solvents present another challenge. Our technicians learned to avoid microbial contamination by working in jacketed stainless reactors, with direct temperature and pressure readouts. By integrating venting protocols and rapid transfer piping, we minimize contact with air and keep oxygen pickup below critical levels. Traditional glassware cannot match these controls on large scale. To ensure lower water content, we follow up distillation with nitrogen sparging, and regularly test via Karl Fischer titration.
Over time, our customers have taught us more than any textbook. Major pharmaceutical and agrochemical companies rely on (S)-(-)-3-Butyn-2-ol as a chiral synthon in production of active ingredients. In practice, a single failed resolution or metal contamination can introduce batch variability, eating into margins and creating headaches for downstream QC. Early in our manufacturing program, we tested process changes side-by-side with clients’ own pilot plants, cross-checking both yield and impurity tracking. Partners valued this openness—unexpected crystallization issues led us to unlock a faster drying regime.
Beyond large companies, smaller synthesis firms often chase ever-higher enantiomeric purity for specialty reactions. Here, trace inorganic residues or off-cut solvent peaks can decide if a project scales or stalls. Our feedback from these innovators is direct and sometimes blunt, but it has prompted us to adapt test protocols, implement upgraded column packs, and re-examine waste streams for maxima reuse and minimum cross-contamination risk. This open exchange helps us refine not just our product, but our service to the technical community.
Every batch of (S)-(-)-3-Butyn-2-ol leaves our plant with a full profile—optical rotation, GC area count, residual moisture, and heavy metal data. Demand often centers on chiral purity for enantioselective syntheses or metal content when customers plan to use sensitive catalysts further downstream. Our routine batches hit >99% enantiomeric excess, GC purity over 99%, and water typically at or below 0.05%. We stray from conventional test panels and add LC-MS on request for customers who need extra reassurance.
It pays to remember that not every grade suits every need. Some users need ultra-dry material for air/moisture-sensitive routes. We build this flexibility into our storage and drum-filling, flushing totes with argon and employing moisture-tight seals that have been tested in-house after long-haul shipping. For high-throughput pharmaceutical plants, repeatability takes precedence. Our focus on controlled packaging, side-by-side batch validation, and transparent data gives process chemists peace of mind as they scale their synthetic campaigns.
In chiral building blocks, (S)-(-)-3-Butyn-2-ol stands out for the easy accessibility of the triple bond and secondary alcohol group, which make it versatile in synthesis. Compounds like (S)-(+)-2-Butanol, or racemic 3-Butyn-2-ol, don’t offer the same combination of reactivity and selectivity. While racemates can often be resolved after initial coupling or addition reactions, we have seen this approach slow projects, waste reagents, and introduce avoidable headaches.
Chemists push for enantioselectivity from the outset, especially when downstream steps will amplify chiral errors and make purification harder. (S)-(-)-3-Butyn-2-ol allows rapid access to chiral ligands and drugs that cannot tolerate even minor racemization. We have supported synthesis groups developing kinase inhibitors, HIV antivirals, and complex agrochemicals, where a change in chirality means lost yield or regulatory hurdles.
Establishing a consistent supply of (S)-(-)-3-Butyn-2-ol is both art and science. Costs fluctuate with raw acetylene and specialty catalysts, and pressure from import controls has sometimes squeezed margins. Rather than cutting corners, we’ve built stock buffers and long-term supplier partnerships to assure reliability, even when upstream shortages spark global delays.
Logistics also matter. Not every plant can handle the specialized needs of this compound—low flash point, sensitivity to humidity, and environmental controls for waste streams. Early on, we invested in carbon-neutral disposal routes, closed-cycle vent scrubbing, and personnel training, reducing both risks and regulatory red tape. We found that upskilling our operators paid immediate dividends—fewer batch failures, less waste, and happier customers.
New synthetic methods for (S)-(-)-3-Butyn-2-ol emerge each year. Some tout one-pot processes, others champion continuous flow. We have trialed many of these in our own R&D labs. While some reduce reaction time, others introduce unknown impurities that only show up at scale. For us, experience always wins out over novelty. Our approach borrows the best from both open literature and homegrown process improvements, and always bench-tests claims before implementation. Incremental upgrades—such as next-generation stirrer designs—have made more of a difference to process throughput than many headline-grabbing methods.
Feedback from industrial partners encourages us to keep refining. Requests for lower detection limits or tighter control over filtration losses guide our investments. Adopted lean manufacturing methods and a culture of continual improvement have allowed us to strip down batch variability and keep overheads under control. Every person in our plant knows their role in this chain, and suggestions from the shop floor have led to real technical changes.
Regulatory demands continue to rise, particularly in pharma applications where trace contaminants must comply with evolving standards. We keep a close eye on changing ICH guidelines for residual metals and genotoxic impurities—because each new threshold means retesting and sometimes revisiting entire process steps. We have worked ahead with clients expecting future regulations, helping to shape robust specifications that won’t change with the next wave of policy updates.
Sustainability also shapes how we run our plant. Solvent recycling, energy recovery, and waste stream minimization are no longer optional extras—they remain essential both for environmental credibility and for cost control. Switching to closed-system processing has cut solvent loss by more than half. Zero-discharge water management impacts bottom line as much as compliance. Our team sees these adaptations not as hurdles, but as opportunities to build a more resilient manufacturing base.
Making (S)-(-)-3-Butyn-2-ol goes beyond delivering a drum to a loading bay. Years of experience have shown us that small improvements in process robustness and analytical support unlock real savings and peace of mind for chemists. We have tracked manufacturing runs right back to individual lots, recognizing patterns in impurity drift, learning from even marginal equipment failures, and acting on every anomaly, no matter how minor.
Directness shapes our approach. We don’t skate over quality issues, and our technical reports include both successes and setbacks. If a rarely observed impurity creeps in under certain raw material lots, or if seasonal changes affect batch times, we explain causes and solutions in plain language. End users, in turn, gain a stronger partner in development—one ready to adjust and support process scale-up with real data, not just sales talk.
Over the years, requests for (S)-(-)-3-Butyn-2-ol have grown, not shrunk. Customers come back because they see real value in material that performs reliably across seasons and scales. Our approach is rooted in practical chemistry, sustainable processes, and open communication—exactly the principles that build confidence and help molecules travel from research bench to final product. Each kilogram that leaves our site reflects this shared expertise. The results—robust yields, consistent optical purity, and trusted regulatory compliance—speak to the genuine care that goes into every batch.