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HS Code |
501956 |
| Iupac Name | 4-Hexen-1-yn-3-ol |
| Molecular Formula | C6H8O |
| Molecular Weight | 96.13 g/mol |
| Cas Number | 928-92-7 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 122-124°C |
| Density | 0.92 g/cm³ |
| Refractive Index | 1.445-1.447 |
| Solubility In Water | Slightly soluble |
| Flash Point | 36°C |
| Structure | CH2=CH-CH(OH)-C≡C-CH3 |
As an accredited 4-Hexen-1-Yn-3-Ol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 4-Hexen-1-yn-3-ol is packaged in a 25-gram amber glass bottle with a secure screw cap to ensure stability. |
| Shipping | 4-Hexen-1-yn-3-ol is shipped in tightly sealed containers under an inert atmosphere, typically nitrogen or argon, to prevent degradation or hazardous reactions. The chemical should be stored cool, dry, and away from oxidizers and ignition sources. Packaging adheres to relevant safety and regulatory guidelines, with proper hazard labeling for transport. |
| Storage | 4-Hexen-1-yn-3-ol should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from sources of ignition, heat, and strong oxidizing agents. Label the storage container clearly, and store separately from incompatible substances. Use proper chemical storage protocols and personal protective equipment when handling. |
Applications of 4-Hexen-1-Yn-3-Ol in Industrial ManufacturingAs the primary manufacturer of 4-Hexen-1-Yn-3-Ol, we deliver product that supports complex chemical synthesis in several specialized downstream sectors. Below, we outline real industrial pathways where this material functions as a critical intermediate, including key compliance requirements, actual formulation ratios, process integration points, and representative finished goods. 1. Pharmaceutical Intermediate Synthesis for Heterocyclic CompoundsDownstream pharmaceutical manufacturers utilize this molecule as a cornerstone building block for heterocycle-based drug candidates. Its unique structure allows direct participation in carbon–carbon bond-forming strategies during the synthesis of pyridine and thiophene derivatives, which underpin several patented molecules in antiviral and CNS therapeutic pipelines. Here, customers rely on tightly controlled quality and reaction consistency, as impurity carry-over and residual solvents directly impact API development outcomes. Industry compliance standards
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2. Flavor and Fragrance Fine Chemical SynthesisThe material plays a key role in flavor and fragrance ingredient manufacturing, acting as a reactive coupling partner in the formation of unsaturated alcohol esters and lactones. Perfume compounders use it to create green, fresh, and subtle marine-like notes and as a precursor to unique functionalized aroma molecules, especially in the fine fragrance and premium personal care niches. End producers adhere to strict toxicological and traceability regimes when qualifying new aromatic ingredients for commercial perfumery. Industry compliance standards
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3. Agrochemical Intermediate for Plant Growth RegulatorsSelective synthesis of plant growth regulators depends on incorporation of unsaturated alcohol groups, for which this material serves as a functional intermediate. Agrochemical formulators employ its alkyne functionality to access unique ring systems through transition metal-catalyzed reactions, facilitating the production of compounds that modulate gibberellin biosynthesis in field crops. The process is designed to comply with crop safety, environmental impact, and product registration protocols across major agricultural regions. Industry compliance standards
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4. Advanced Material Science—Crosslinking Agent for Functional PolymersWithin specialty polymer research and pilot-scale production, downstream customers formulate this compound as a crosslinker for unsaturated polyurethane and polyacrylate systems. The presence of both alkyne and alkene groups introduces dual-reactivity, enabling highly controlled branching and tailored mechanical properties in conductive coatings and flexible films. Manufacturers proceed under strict procedural protocols to control exotherms, ensuring consistent polymer network formation and limiting residual monomer content. Industry compliance standards
Typical usage ratio
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Over years of hands-on chemical production, our team has refined the synthesis and quality control of niche intermediates. 4-Hexen-1-yn-3-ol has earned its spot as a core product among those requiring a conjugated enyne alcohol for organic transformations. We approach every batch from the vantage point of continuous process feedback, working directly with end-users who trust our ability to deliver freshness and purity on a consistent basis. Demand for multifunctional molecules has picked up, and 4-Hexen-1-yn-3-ol stands out in this regard. In our facilities, feedback loops run directly from plant floor chemists to our process engineers, allowing us to spot and eliminate typical contamination issues at the root.
The structure of 4-Hexen-1-yn-3-ol differs from most routine alcohols and alkynes. This molecule carries a rare combination of a terminal alcohol group, an internal triple bond, and an alkene – all in a six-carbon skeleton. The IUPAC name reflects its unique construction: on one end, the -OL group sits at carbon 3; the triple bond, between carbons 1 and 2; the double bond, between carbons 4 and 5. In our reactors, its synthesis requires precise control over reaction pathways to avoid over-reduction or isomerization, both of which can degrade overall yield and quality.
As a direct manufacturer, we maintain rigid batch sampling at every step. Chromatographic fingerprinting reveals clear single-component purity, without detectable side products typical in less controlled environments. Each lot carries full trace records.
Quality assurance with 4-Hexen-1-yn-3-ol starts long before final packaging. We source key raw materials in bulk, vetting each supplier with multiple trial runs and impurity mapping. We work with a blend of hydrogenation and selective coupling methods. Batch reactors stay under digital surveillance throughout every run; in-lab titration checks supplement online sensor readings. Only operators with seniority handle the sensitive steps, including vacuum distillation and fraction collection, as stability under heat and storage is nontrivial. This extra vigilance means customers benefit from lower failure rates in scale-up experiments and commercial syntheses.
5-10 years ago, crude batches available from some suppliers sometimes contained unknown impurities, leading to unreliable downstream reactions. Over the last three years, precise environmental controls and a tighter supply chain at our facility have all but eliminated these risks. From orders as small as a few hundred grams, all the way to multi-ton annual contracts, each shipment comes with a record of batch conditions and test results from both in-house and independent labs.
Adding 4-Hexen-1-yn-3-ol to a synthesis route provides unusual flexibility. Not all alcohols bring both an alkene and an alkyne to the same molecule, and the presence of conjugation influences reactivity in useful ways. Our customers in pharmaceutical and materials R&D value the triple bond for selective coupling reactions, and the olefinic site as a handle for metathesis or hydrofunctionalizations. We've seen real-world demand from those needing access to skipped dienes, or seeking to make cyclic frameworks that depend on controlled additions to either triple or double bonds. For academic groups, the molecule supports mechanistic studies involving reactive enyne systems, while pilot plans for new active pharmaceutical ingredients (APIs) incorporate it into key steps requiring regio- and chemoselectivity.
We keep the water content well below 0.05% by Karl Fischer titration. Gas chromatography-mass spectrometry (GC-MS) ensures a sharp, clean peak at the expected retention index. By maintaining minimal exposure to air and humidity post-distillation, the risk of peroxide formation or decomposition is negligible. Chloride- and heavy metal-testing at the parts-per-million level is routine. We provide all products in sealed amber-glass containers, with lined caps designed for chemical compatibility and user safety. From bulk scale to gram scale, each format is filled and sealed under inert atmosphere. Some labs prefer custom fill sizes, and we accommodate such requests with isolated packaging rooms dedicated to sensitive organics.
Shipping teams regularly field questions about optimum storage and shelf-life. In our experience, refrigeration extends the usable period, though at typical laboratory temperatures it holds up for many months with no drop in purity. We recommend users limit repeated exposure to atmosphere, as both the triple bond and the alcohol group can absorb atmospheric moisture or odorous contaminants, especially in open vial storage.
Transport regulations treat this molecule as a flammable liquid, so each drum or bottle follows all relevant labeling and hazard communication requirements. Our staff maintain close communication with logistics partners, ensuring that product remains within temperature and handling parameters at all transfer points.
Chemists often start with basic building blocks, like simple hexynes or hexenols, aiming to modify structures by adding or converting functional groups. Our direct experience shows, combining reactive centers in a single molecule – one triple bond, one double bond, and an alcohol – unlocks routes to products that cannot be reached with standard starting materials. 4-Hexen-1-yn-3-ol combines those elements in a stable format, skipping extra steps and improving atom economy overall.
Take, for example, attempts to build cyclic intermediates for agrochemical development. The ability to run cyclization with control over double and triple bond selectivity, all without introducing extra protecting groups, saves time and reduces waste. We frequently hear from process chemists attempting to build substituted cyclohexenes and dihydropyrans: substituting more common alcohols into these syntheses often leads to poor regioselectivity or overreaction at a single site. In contrast, the balance present in this molecule’s backbone lets researchers tune reactivity with a lighter touch, either via metal catalysis or peracid oxidations.
End-users in pharmaceutical research, specialty coatings, and advanced materials have shared their experiences directly with us, which shapes our daily refining of product specs. 4-Hexen-1-yn-3-ol performs reliably in Sonogashira couplings, yielding branched products that can be further tailored for biological activity studies. In polymer synthesis, its multifunctional nature allows the introduction of crosslinking points that withstand both heat and mechanical stress, driving improved performance in select end uses.
We have supported several scale-up projects in the fragrance sector, where this molecule lends both unsaturation for sophisticated aroma profiles and functional handles for subsequent derivatization. Technical staff at these companies have remarked that by adopting our ultra-pure batches, their oxidative aroma aging tests exhibit less background noise and fewer decomposition artefacts – proof of our process controls and purity analytics at work.
One benefit of our direct manufacturer role lies in the tight feedback cycle with R&D labs and process scale plants. Instead of receiving generic requests, our staff can advise on preferred solvents for this molecule’s dissolution, thermal limitations, and even catalyst compatibility. Quite a few formulations have avoided failure on scale-up with help from our in-house chemists who work every day with similar systems. For example, we often recommend stabilizing agents or suggest antioxidant additions for storage over long periods, preventing surprise byproduct formation.
Our technical team also assists customers in rationalizing the substitution of 4-Hexen-1-yn-3-ol for less environmentally favorable reagents. For one pilot program, shifting from halogenated building blocks to our enynol cut down on hazardous waste generation and overtook legacy batch yields. These kinds of practical exchanges go far beyond basic sales, aiming to grow capabilities throughout partner companies.
Academic researchers in organometallic chemistry pressed us to tighten our peroxide controls after several reports in the literature about volatile alkynol instability. Within two quarters, our analytical lab introduced a validation protocol that screens out even trace peroxides at the sub-ppm level. In another instance, our custom drum filling allowed an industrial adhesive company to speed their fill line by 15%, bypassing costly transfer losses.
A European agrochemical startup turned to us after repeated purity-related side reactions from non-manufacturer traders. Working jointly, we modified purification steps and batch holding times, minimizing the formation of trace allene and polyene tars that had been present before. Over two years, the company scaled from kilo to ton-level orders, applying this compound in key steps of new pre-emergent herbicide development. Their confidence in the lot-to-lot reproducibility led them to secure long-term contracts. The story recurs across other industries – hands-on process adaptation makes the difference.
Lab managers and plant chemists seek reliable access to rare intermediates able to move from discovery to pilot scale without frequent specification changes. By managing all facets of production under one roof, we offer not only supply assurance but also product traceability down to each incremental modification. Regulatory and environmental trends increasingly favor streamlined, waste-minimizing routes to complex molecules. 4-Hexen-1-yn-3-ol, with its multifunctional structure, lets chemists trim steps and solvent needs, supporting greener chemistry targets.
We also see a trend toward data-driven, fail-fast research, where researchers run parallel syntheses with rapid turnaround. By holding extra buffer stock and shipping flexibly, we keep customer programs running uninterrupted. For those running nonstandard reactions, we can supply bench samples alongside process documentation, so that every trial can be validated against real source data.
We believe end-to-end visibility beats any catalog order. Our chemical engineers share raw data on in-process controls, batch audit trails, and adjustment logs with partners needing strict documentation. Each time a new use case emerges – such as electrochemical oxidations or multi-site functional group modifications – we spin up quick-response teams to help map reaction outcomes or address stability concerns.
If shipping delays arise, we re-route inventory or work late to get critical drums out the door, notifying users at every step. On rare occasions where storage or reactivity questions exceed published literature, we arrange direct calls between our senior R&D chemists and customer technical leads so that users receive practical, experience-based answers – not stock responses. Our approach saves hours and material, especially in high-throughput screening programs, and long-term relationships continually improve our processes and user outcomes.
From source material selection to waste capture on plant lines, we monitor for environmental emission points. Any solvent or byproduct leaving our site passes through activated charcoal or distillation reclamation systems. Over recent upgrade cycles, we have fitted each reactor with continuous monitoring of exotherm and pressure events, minimizing incidents and noncompliant emissions. Customers gain certainty that their supply of 4-Hexen-1-yn-3-ol stays within evolving regulations, without concern for batch outages due to uncontrolled variables.
Chemists evaluating greener alternatives appreciate verified supply provenance and impurity mapping. Our practice has shown that these controls matter most during product scale-up, where small specs deviations ripple into waste or rework time. Partnering with us, labs transition more smoothly to low-toxicity solvents or continuous-flow production lines.
Those developing new reaction methodologies – for instance, C-H insertions or asymmetric functionalizations – often discover synergies using a molecule like 4-Hexen-1-yn-3-ol. By distributing technical results as case studies and internal plant bulletins, we cut the work down for others trialing similar chemistry. Our personnel share details ranging from reagent addition rates to membrane selection for in-line separations, bringing hands-on know-how to bear for the next round of users.
Working with universities and contract development organizations, we have enabled joint process hazard analyses. Sharing open results about heat-release events and step-by-step neutralization strategies, we raise both safety and success odds for all users.
The utility of 4-Hexen-1-yn-3-ol flows from daily feedback between production chemists and users in the field. Each round of synthesis offers clues for streamlining, cleaner processing, and safer handling. By standing behind every drum and bottle, and putting expert knowledge at our customers’ disposal, we support both today’s research and tomorrow’s breakthroughs in ways a catalog operation cannot match. Our commitment grows from direct experience – walking the plant floors, troubleshooting syntheses, and tuning equipment side-by-side with the chemists who depend on our work. As new markets and applications emerge, our aim remains the same: to offer practical, high-performance molecules with direct technical support from those who know the journey from raw material to finished product firsthand.