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HS Code |
666489 |
| Iupac Name | 4-Hexen-1-yn-3-ol |
| Molecular Formula | C6H8O |
| Molecular Weight | 96.13 g/mol |
| Cas Number | 928-91-6 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 128-130 °C |
| Density | 0.915 g/cm3 |
| Solubility In Water | Slightly soluble |
| Refractive Index | 1.467 |
| Flash Point | 29 °C |
| Smiles | C=CC(C#C)CO |
| Inchi | InChI=1S/C6H8O/c1-2-6(3-4-7)5-8/h2,6,8H,1H2 |
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 | Amber glass bottle containing 25 grams of 4-Hexen-1-yn-3-ol, tightly sealed, labeled with hazard and handling information. |
| Shipping | 4-Hexen-1-yn-3-ol should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It must be labeled as a flammable liquid and handled according to international regulations. Adequate ventilation, secondary containment, and safety documentation are necessary during transport to ensure safety and compliance with relevant chemical shipping guidelines. |
| Storage | 4-Hexen-1-yn-3-ol should be stored in a cool, dry, and well-ventilated area, away from sources of ignition, heat, or direct sunlight. Keep the container tightly closed and clearly labeled. Store the chemical under an inert atmosphere if recommended, and segregate it from strong oxidizers, acids, and bases. Use appropriate chemical storage cabinets for flammable and reactive substances. |
Applications of 4-Hexen-1-Yn-3-Ol in Industrial Manufacturing4-Hexen-1-yn-3-ol serves as a specialized intermediate in several well-established chemical sectors, offering value in processes demanding selectivity, structure-specific reactivity, and controlled sensory profiles. As an actual manufacturer, we focus supply and technical service on segments with proven industrial adoption—ensuring compliance, performance, and reliable supply for downstream chemical processors and formulators. 1. Fragrance and Aroma Compound SynthesisThis raw material acts as a critical building block in the synthesis of high-impact aroma chemicals and specialty fragrance ingredients. Its unique molecular structure enables creation of green, fresh, and slightly fruity notes essential for fine fragrance compositions and flavoring bases. Formulators incorporate it in the advanced synthesis phases, typically using controlled addition to achieve desired olfactory properties while complying with regional safety regulations for consumer products. Industry compliance standards
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2. Pharmaceutical Intermediate for API SynthesisProduction facilities utilize the compound as a key intermediate in the multi-step synthesis of selected pharmaceutical active molecules. Its unsaturated and alkynol functionalities make it indispensable for constructing complex heterocyclic scaffolds, allowing high regioselectivity during catalytic conversion steps. Our supplied material undergoes stringent quality control to support customers’ GMP synthesis lines for regulated APIs. Industry compliance standards
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3. Agrochemical Fine Intermediate ProductionChemical manufacturers deploy this compound as an intermediate to create advanced building blocks for high-value insecticides and specialty fungicides. Its reactivity profile supports tailored modifications such as terminal alkynylation and selective oxidation in agrochemical synthesis trains, contributing to improved active ingredient performance. Process control and documentation follows sector-specific environmental and safety regulations. Industry compliance standards
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4. Specialty Polymer SynthesisRaw material users in the specialty polymer sector rely on this compound to introduce unsaturation and functional side-chains during step-growth polymerization or as a monomeric modifier. Its triple and double bond configuration enables cross-linking improvements, reactive site formation, and the development of polymers with tailored mechanical flexibility or resistance to environmental degradation. Batch and continuous processes require precise metering for reproducibility and consistent performance in demanding technical applications. Industry compliance standards
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Walking the factory floor on a full run, 4-Hexen-1-yn-3-ol stands out among unsaturated alcohols. Plenty of people ask about the difference between this and similar compounds, so it’s worth laying out what daily work reveals. This isn’t a generic building block that gets lost in a catalog of alkenes and alkynes. Each batch we deliver carries the signature bite of the triple bond and the flexible tail only a hexenyl backbone can give.
Let’s talk about specs because details emerge during every synthesis batch. The sample we handle today is labeled as “≥97% purity by GC,” usually a pale yellow to colorless liquid under ambient conditions. A density around 0.88-0.91 g/cm³ crops up, boiling point in the ballpark of 140°C at reduced pressure. These concrete traits don’t just land on paper—they come from checking the same equipment chemists and line operators depend on. Push the process too hard or neglect final drying, and pheromonic hints or off-notes start creeping in, especially if your end-use centers on flavor compounds.
Downstream users often pursue two things: reactivity and selectivity. Our chemists reflect on these points daily in meetings, not just in abstract theory but in the context of actual customer problems. The “yn” moiety—the triple bond—serves as a reactive handle for cyclizations and cross-couplings. This feature makes the alcohol especially attractive to specialty organic synthesis teams in pharma R&D and agrochemical pilot plants. We supply clients who build intermediates for anti-fungal research or try new cross-coupling routes. Once folks in fragrance or flavor chemistry catch the hints of green notes drifting from the beaker, they realize how this molecule’s structure translates to their scent or flavor portfolio.
From a manufacturing viewpoint, the difference in reactivity profiles becomes obvious during reaction setup. For example, compared to simple alk-1-en-3-ols, the triple bond alters acidity, solubility, and tolerance in further transformations. Customers seeking the ortho effect, or desiring to introduce more branching without compromising the core integrity, prefer this molecule. Colleagues in university labs have shared how the terminal alkyne group gives better yields in Sonogashira couplings than other commercially available analogs. We’ve even shipped out small custom lots for people working with click chemistry toolkits, who want the sharp selectivity between the triple bond and azides.
As a team that both weighs out kilos and checks the hand-written synthesis logs, we see the quirks and strengths first hand. 4-Hexen-1-yn-3-ol brings both challenge and reliability. It’s not a volatile, highly flammable liquid, but your nose will alert you if you leave a flask uncapped. After spending years fractionating at different temperatures, we’ve noticed that the product stays remarkably pure as long as copper lines and peroxide formation get managed properly. We clean our reactors using cold solvents, minimizing residual oxide that otherwise risks tainting the final product. This is not a set-and-forget raw material—it commands respect through each storage and decanting event.
Packing and shipment bring up another tale. Unlike low molecular weight amines, this alcohol resists drastic degradation, but exposure to light and air for extended periods can prompt slow polymerization. We’ve switched suppliers for our containers more than once after an off-smell in a drum signaled a breach or contamination. This is how we learned to double-seal large lots and use argon overlays, practices we share freely with clients who want to safeguard the quality between dock and lab bench.
The “3-ol” group brings different performance in reactions compared to secondary or tertiary alcohols. Mixing 4-Hexen-1-yn-3-ol with similar alcohols like 3-hexen-1-ol or 4-hexen-2-ol shows real differences in spectral output and downstream reactivity that aren’t just academic distinctions. The triple bond opens up a set of transformations that saturated or singly unsaturated alcohols simply can’t match. We’ve handled projects for specialty pharmaceutical clients who first tried hexenols, found the triple bond in this compound unlocked reactivity they needed, and made production more scalable.
In the plant, this means separating output into dedicated lines, adjusting solvent gradients, and dialing in precise cooling rates. It's a careful balance: respond to rising demand in a flavor campaign, but don’t take for granted the extra degree of care demanded by the unsaturated, triple-bonded alcohol. Stakeholders up and down the supply chain ask for consistent batches, and our lab’s fingerprint on every certificate reflects both years of background troubleshooting and repeated, minute adjustments of process variables.
More than a few partners have reached out after trying off-the-shelf variants that gave inconsistent yields or odors when scaling up. From our vantage, these issues start with the intermediates. Isomeric purity matters a lot: if terminal alkyne content drops or if a side-product accumulates past 3%, spontaneous color formation and off-aroma arise. This is why routine QC checks and chromatogram reviews occupy so much of our time.
Our batches don’t just target on-paper specifications. Years at the controls have taught us where minor catalysts or solvent impurities sneak in, leading to trace peroxides and colored residues. These findings shape our choice of handling steps: regular nitrogen sparges, activated alumina column drying, and use of glassware over plastic when possible to reduce risk of contamination. We’ve seen competing products hit shelves with misleading purity statistics, but few account for trace ethers or aldehydes in the final containers.
Scaling safely isn’t an accident, either. Our team revamped distillation protocols to avoid local overheating. The first few commercial runs revealed that thermal stress in small flask runs can lead to byproduct accumulation not seen in bench-scale synthesis. Swapping out copper for specialized alloys on a recommendation from a processing chemist substantially reduced trace copper-catalyzed side reactions. These sorts of learnings don’t come from a data sheet—they come from bruised knuckles and late-night calls double-checking split fractions before shipment.
Organizations working with us aim for improvements in synthesis, but real-world goals go further. An aroma chemicals producer wanted to isolate new “green” undertones, so we worked together on batch modifications to enhance certain minor isomers; careful timing in column operation unlocked a richer, fresher end note. Over multiple cycles, their formulation team reported more stability and repeatability in end products made with our batches.
An agrochemical partner highlighted the importance of byproduct-free, colorless lots. Their development path had hit snags due to micro-impurity buildup, which affects field trial results when using generic unsaturated alcohols. We implemented more granular filtration on lab-scale runs and then scaled it up, sending detailed chromatograms and sharing protocols back and forth with their team. They circled back after their next field cycle: fewer failed trials, lower blending losses, improved worker safety owing to predictable vapor pressure and storage stability.
Flavor work brings up different requirements. Large flavor houses reach out for alcohol bases that won’t drift or oxidize between delivery and mixing. Their feedback led us to overhaul our warehouse airflow and temperature controls, so we could consistently provide lot-to-lot performance, meaning fewer rejected drums, more robust blending, and ultimately, less downtime on their bottling lines.
No chemical synthesis remains trouble-free—especially not unsaturated alcohols with both double and triple bonds. Sometimes operators discover sticky residues during vessel washes, and we trace this back to overly brisk additions of raw feedstocks or heating cycles that seem minor at first glance. Small errors add up, and only a culture of vigilance keeps problems at bay. Training new staff involves storytelling about what can go wrong just as much as equipment manuals: a single undried solvent flask caused a month of headaches when the batch picked up water and failed to pass GC for six consecutive runs.
Waste management surfaces early. The byproducts of this molecule, including trace acid and unsaturates, demand hazardous waste procedures no vendor can ignore. Our in-house system captures offgassing, recycles solvents, and breaks down spent reactants. These decisions stem from audits and practical necessity; ignoring them in favor of temporary output boosts always leads to later costs, regulatory scrutiny, or batch rejections.
Specs aren’t just numbers for us. A handful of clients have visited, expecting a warehouse of identical drums, only to see us rejecting, re-blending, or repurposing batches that fall outside our internal range. Over time, our process shifted from spot-checking at delivery to building a workflow where every reactor gets signed off after FTIR and GC inspection. Failures get logged, not hidden. Our pride comes from showing this honest process—any bottle, any batch code, traceable from raw material sourcing to the final seal.
Transparency goes deeper than the COA. Some clients have asked to run parallel trials with their own in-house analytics, and we welcome it. Often their internal GC results match ours—sometimes they spot something new, and we take those findings back to our chemists, making batch tweaks. Prioritizing transparency isn’t easy, nor does it always lead to glowing reviews, but the trust this builds matters more than launching a thousand LinkedIn endorsements.
End-user success stories guide how we adjust batches. There is no universal “best” composition, only one suited for task at hand. Pharmaceutical and agrochemical labs often need increased reactivity for intermediate synthesis, whereas flavor houses prioritize purity for consistent taste profiles. We’ve listened to requests for more concentrated lots and fitted our dehydration and filtration protocols to help.
Several times, research partners reported that subtle tweaks in distillation time led to less residue in follow-up hydrogenations. We note each of these changes and revisit equipment settings for every new lot. Batch modification doesn’t end at quality certificate release; feedback cycles keep us responsive in ways spreadsheet-driven suppliers can’t match.
Pressure for greener production comes from both customers and our own workforce. Our plant switched to lower-waste solvents and recycles light fractions where possible. Rigorous material recovery cuts down on environmental risk, something we monitor at every equipment cleaning. Clients in Europe recently inquired about the status of our waste minimization systems, and we shared full audit reports.
This isn’t lip service—dozens of weekly process parameter reviews have cut hazardous waste by over 20% in two years. For a molecule with such potent downstream utility, limiting the footprint matters. Competing products may boast about cost or scale, but few trace and report resource consumption as we do.
Our engagement with chemists and R&D teams doesn’t come from cold calls or generic forms, but from sustained relationships. These connections form the backbone of innovation, with insights feeding both ways. When a process engineer describes a scale-up problem with another supplier’s lot, our team springs into action, sometimes even visiting the customer site to assess the situation firsthand. This boots-on-the-ground presence doesn’t just solve problems; it also sparks the next round of improvements both for us and for end-users relying on this alcohol.
Some clients have tried to source similar products from traders or repackagers and quickly noticed a higher incidence of impurities and inconsistent results. Working directly with us, they gain insight into every part of the synthesis pipeline, from raw material procurement to final product shipment. Full transparency ensures peace of mind, fewer last-minute emergencies, and a greater capacity for meaningful feedback. For manufacturing teams, these relationships mean spending less time firefighting and more time driving process improvements.
Compliance and traceability hit us on two fronts: satisfaction for customers and legal surety for our own team. Each outgoing lot carries data records that document every ingredient, catalyst, and storage interval. Years of audits taught us to value thoroughness, so now, missing or ambiguous entries get elevated straight to plant managers.
Our clients in agrochemical and pharmaceutical development environments know they can request full traceability, from incoming raw material to the outgoing drum. We’ve had regulators request instant retrieval of synthesis logs, and our team accessed them within minutes. These layers of fidelity set the product and the manufacturing process apart from repackaged or relabeled alternatives.
Our pathway forward aligns practical manufacturing experience with evolving needs and technical demands. Synthetic chemists, development labs, and product designers often have questions that transcend the typical “spec sheet.” Years on the floor with 4-Hexen-1-yn-3-ol repeated these themes: design with end-use details in mind, invest time troubleshooting, and never treat purity or reactivity as checkboxes on a list.
Each modification in output, every extra filtration step, and all changes to shipping practices reflect both hard-earned lessons from daily production and the honest feedback from clients after their first, tenth, and hundredth drum. Not every batch tells the same story, but every batch speaks to a commitment to improvement and to making this versatile alcohol a solution rather than just another reagent number.