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(S)-(-)-3-Butyn-2-ol

    • Product Name (S)-(-)-3-Butyn-2-ol
    • Alias (S)-(-)-Butynol
    • Einecs 211-592-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of (S)-(-)-3-Butyn-2-ol

    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 Synthesis

    Stereo-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

    • ICH Q7 Good Manufacturing Practices for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) general chapter Chiral Purity
    • European Pharmacopoeia requirements for source materials in APIs
    • FDA Process Validation Guidance for pharmaceutical intermediates

    Typical usage ratio

    • Applied at a molar ratio of 1.0–1.2 relative to the downstream ketone or aldehyde substrate, typically in the 5–15% w/w range of the overall API synthesis batch depending on the specific route and target yield.

    Downstream process integration

    • Enters at the enantioselective alkynylation step, reacting via transition-metal catalysis with carbonyl electrophiles to construct stereocenters for chiral intermediates; downstream isolation and purification adapt to maintain chiral integrity.

    Final product types

    • Enantiomerically pure pharmaceutical intermediates (e.g., protected diols and alcohol derivatives)
    • Active Pharmaceutical Ingredients for targeted chemotherapy drugs such as Epothilone analogues
    • API chiral intermediates for tyrosine kinase inhibitors

    2. Chiral Building Block in Agrochemical Intermediate Manufacture

    Producers 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

    • ISO 9001:2015 for Quality Management Systems in chemical manufacture
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • REACH registration (EC) No 1907/2006 in the EU
    • China National Standards for Pesticide Technical Material (GB/T)

    Typical usage ratio

    • Formulators utilize it at 2–10% w/w, adjusted according to the specific chiral step, substrate reactivity, and target selectivity in the product design.

    Downstream process integration

    • Used during Grignard-type addition or catalytic alkynylation steps to introduce chiral hydroxyl functions; downstream stages involve further derivatization and coupling with crop-protection active groups.

    Final product types

    • Chiral agro-intermediates for selective herbicide synthesis
    • Optically active precursors for pyrethroid insecticides
    • Building blocks for next-generation fungicidal actives

    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

    • ISO 17025 standard for laboratory analysis and certification of enantiomeric purity
    • Responsible Care® Program for fine chemical manufacturing
    • OECD guidelines for testing of new catalysts and specialty chemicals
    • REACH compliance for registered chiral specialty intermediates

    Typical usage ratio

    • Employed at 3–8% w/w in ligand synthetic schemes, with the precise level tailored to the target ligand structure or required amount for multi-step build-up in modular catalyst synthesis.

    Downstream process integration

    • Incorporated at nucleophilic addition or propargylic rearrangement steps to generate core chiral ligands, which are then purified and complexed with transition metals for catalyst development.

    Final product types

    • Bidentate and tridentate chiral ligands
    • Transition metal–chiral ligand catalyst systems for asymmetric hydrogenation, epoxidation, and cyclopropanation
    • Chiral auxiliaries for enantioselective synthesis in specialty and custom fine chemicals

    4. Chiral Component in Flavor and Fragrance Intermediate Synthesis

    In 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

    • IFRA (International Fragrance Association) Code of Practice
    • FCC (Food Chemicals Codex) guidelines for ingredients in food flavors
    • ISO 9235:2013 (Aromatic Natural Raw Materials – Nomenclature)
    • GB 30616-2014 (China National Food Safety Standard for Flavoring Substances)

    Typical usage ratio

    • Used in 1–6% w/w depending on the complexity of the aroma-building block, adjusted for volatility loss and retention in downstream distillation or formulation.

    Downstream process integration

    • Participates in Grignard, alkynylation, or Sharpless asymmetric dihydroxylation steps to construct chiral oxygenated aroma precursors; subsequent transformation yields target alcohols or aldehydes.

    Final product types

    • Chiral alcohol intermediates for fruity and floral aroma compounds
    • Enantiomerically pure building blocks for high-impact food and beverage flavors
    • Precursors for consumer fragrance and scent molecules

    5. Stereoselective Synthesis of Specialty Polymer Additives

    Chemical 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

    • ISO 14001 Environmental Management for chemical processing plants
    • ASTM D6288 (Standard Guide for Polymer Additive Manufacturing)
    • REACH Annex XVII SVHC compliance for industrial use
    • Global Automotive Supplier Quality Standards (IATF 16949), where applicable

    Typical usage ratio

    • Introduced in 0.5–3% w/w during additive synthesis and up to 10% w/w in polymer precursor stages, subject to compatibility and final property targets.

    Downstream process integration

    • Added at the stage of enantioselective functionalization or as a core building block for polymerizable monomer preparation; post-reaction, additives blend directly with base polymers during compounding or extrusion.

    Final product types

    • Chiral monomers for specialty polyesters and polycarbonates
    • Optically active polymer additives for electronic or medical packaging
    • Functional modifiers for biodegradable and high-performance plastics
    Free Quote

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    Certification & Compliance
    More Introduction

    (S)-(-)-3-Butyn-2-ol: Real-World Insights from Our Manufacturing Floor

    The Work Behind Purity and Consistency

    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.

    What Sets Our Material Apart

    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.

    Inside Our Technical Approach

    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.

    Real-World Applications: Listening to Our Customers

    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.

    Specifications Matter — More Than a Line on a Datasheet

    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.

    Comparing With Other Chiral Alcohols

    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.

    The Trade-offs Behind the Scenes

    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.

    Innovation Driven by Experience

    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.

    Challenges and Opportunities in the Years Ahead

    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.

    The Actual Value We Add

    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.

    Why Our Focus on (S)-(-)-3-Butyn-2-ol Remains Unshaken

    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.