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HS Code |
734533 |
| Iupac Name | 3-Hexyne |
| Molecular Formula | C6H10 |
| Molar Mass | 82.15 g/mol |
| Cas Number | 928-49-4 |
| Appearance | Colorless liquid |
| Boiling Point | 82 °C |
| Melting Point | -80 °C |
| Density | 0.75 g/cm³ |
| Refractive Index | 1.399 |
| Solubility In Water | Insoluble |
| Flash Point | -2 °C |
| Vapor Pressure | 82 mmHg (20 °C) |
As an accredited 3-Hexyne factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3-Hexyne is supplied in a 100 mL amber glass bottle with a tight-seal cap, labeled with hazard and handling instructions. |
| Shipping | 3-Hexyne is shipped in tightly sealed containers, protected from sources of ignition and stored in a cool, well-ventilated area. It should be labeled as a flammable liquid and handled according to local, national, and international regulations for hazardous chemicals. Proper protective equipment and safety measures are required during transport. |
| Storage | 3-Hexyne should be stored in a cool, dry, well-ventilated area away from sources of ignition, heat, and strong oxidizing agents. Keep containers tightly closed and properly labeled. Store in approved flammable liquid storage cabinets and away from incompatible materials. Prevent exposure to light and moisture, and avoid contact with air to minimize degradation and the formation of hazardous peroxides. |
Applications of 3-Hexyne in Industrial ManufacturingOur direct-manufactured 3-Hexyne meets the precise needs of specialized industries, serving as a high-purity intermediate and functional additive across several critical downstream sectors. The following application scenarios highlight its established deployment, compliance benchmarks, recommended dosages, integration into key processes, and the types of finished goods produced by our global industrial partners. 1. Fine Chemicals Synthesis – Cross-Coupling Intermediates3-Hexyne functions as a crucial building block in complex cross-coupling reactions, primarily Sonogashira and Cadiot-Chodkiewicz processes, enabling the formation of conjugated enynes and advanced intermediates for high-value fine chemicals. Widely adopted in facilities specializing in custom molecular design, the material’s purity and controlled reactivity support downstream synthesis at commercial scales without additional purification steps, ensuring reliable batch-to-batch quality control for active chemical development pipelines. Industry compliance standards
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2. Pharmaceutical R&D – Synthesis of Molecular ScaffoldsSpecialty active pharmaceutical ingredient (API) manufacturers utilize 3-Hexyne as a synthon in the assembly of unique carbon frameworks, supporting structure-based drug discovery and optimization. Its high reactivity in transition-metal-mediated transformations provides synthetic chemists with a reliable path to create acetylenic linkers and functionalized scaffolds. These intermediates form the backbone of next-generation lead compounds under rigorous process analytical controls, crucial for pilot and scale-up production in regulated environments. Industry compliance standards
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3. Polymer Material Modification – Functionalized PolymersProducers of specialty polymers employ 3-Hexyne to introduce pendant functional groups and modulate backbone unsaturation in block copolymers and thermoplastics. Its integration into polymer chains through controlled polymerization, alkyne metathesis, or grafting approaches enables the manufacture of high-performance materials with tailored properties, such as improved conductivity and unique surface chemistries. Strict monitoring of additive levels and residual monomers ensures downstream materials pass both regulatory and application-specific quality checks. Industry compliance standards
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4. Organic Electronic Materials – Synthesis of Conjugated Small MoleculesManufacturers in the organic electronics sector leverage 3-Hexyne for synthesizing conjugated molecular wires and electron-transporting layers. The compound’s ability to serve as an alkyne spacer allows precise engineering of π-conjugated systems, which are essential for the performance of OLED devices, photovoltaic materials, and flexible sensors. The process requires consistent feedstock purity and tight control of reaction stoichiometry to ensure device-grade product uniformity. Industry compliance standards
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5. Agrochemical Active Ingredient Synthesis3-Hexyne serves as a source of acetylenic motifs in the manufacture of active ingredients for crop protection and pest control formulations. Agrochemical companies depend on its predictable reactivity in the formation of enyne and ynone structures, elements central to the efficacy and degradability of modern herbicides and insecticides. Application occurs in tightly controlled reactor environments to minimize impurities and support full traceability for regulatory review and downstream blending into formulated products. Industry compliance standards
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Years of refining hydrocarbon chemistry have shaped our approach to producing 3-Hexyne. Every batch rolling out of our plant reflects the work and curiosity of a seasoned team, not just a compliance checklist. Today, customers in fine chemical development, pharmaceuticals, advanced materials, and research expect more than generic answers about what 3-Hexyne offers. Drawing from long-standing hands-on involvement, I’ll walk through its unmatched strengths, its place among laboratory and industrial acetylenics, its real-world quirks, and the practical guidance you only pick up at the source of production.
At its core, 3-Hexyne is an alkyne—a hydrocarbon with a distinct triple bond. What sets it apart is the centrality of that bond, flanked by two propyl chains. That C≡C stretch at the 3-position may not seem much on paper, but it carries major consequences for downstream applications. Over the years, our raw material management and distillation techniques have grown more precise because so many reactions depend on purity above 98% and minimal trace contamination. Our factory continues to invest in equipment upgrades for tighter boiling fraction control, not only to hit a spec, but to meet the ever-rising bar set by synthetic chemists.
Model designation in-house often refers to both the lot number and refinement standard. It’s tempting to gloss over those numbers, but repeat users know why that transparency is essential. A 99% pure 3-Hexyne, with less than 0.2% of its E-isomer, for example, yields predictable results in both academic and pilot-scale syntheses. That predictability lets our clients in catalysis research or polymer sciences avoid headaches from inconsistent reactivity. Simple as it sounds, purity impacts the efficiency of cross-coupling reactions, metal acetylide formation, and ring-closing steps—a difference that rarely comes through in generic product descriptions.
Very few alkynes are as frequently chosen for C–C bond formation. Many teams use our 3-Hexyne for Sonogashira coupling work, where the structure unlocks intermediate compounds used in electronic materials and drug leads. Sourcing directly from a manufacturer ensures batches arrive without polymerization inhibitors unless specifically requested, based on how the customer’s downstream chemistry runs best.
Those working in material science create conjugated systems using 3-Hexyne because the triple bond in the middle increases electronic delocalization compared to terminal alkynes. One client project involved synthesizing extended π-systems for organic electronic devices, exploiting this feature to optimize conductivity. Over the years, syntheses of intermediates for liquid crystals and pharmaceutical actives have depended on flexible availability of both high-purity and specialty-graded batches, sometimes down to gram scale for research, more often by the drum for scaling up.
Colleagues sometimes ask why a customer would choose 3-Hexyne instead of simpler alkynes such as 1-hexyne or 2-butyne. The triple bond placement is the central difference. 1-Hexyne, being terminal, shows different reactivity in metal-catalyzed coupling, where terminal alkynes favor addition chemistry. 3-Hexyne’s symmetry suppresses unwanted side reactions that crop up with terminal options, helping scale processes with fewer byproducts.
Compared to 2-butyne, which boasts greater volatility and miscibility, 3-Hexyne offers a balance between handling ease and reactivity. Semi-bulk customers have noted tighter control during storage due to lower vapor pressure, reducing losses in process environments not equipped for tight containment. The molecular weight is heavier, which can improve stability in certain protocols and reduce atmospheric contamination risks. These are not theoretical distinctions; plant operation data has shown consistently lower loss rates in standard drums compared to more volatile analogs.
Operational improvements in our own plant have taught us that for acetylenic compounds, impurities show up hardest in end-use tests, not just GC or NMR. Over the last decade, we learned that water content as low as 0.05% can derail sensitive coupling reactions. Moisture scrubbing units and micro-sieve handling cut water traces to nearly undetectable levels. Trace oxygen matters as well, so production runs always include rigorous degassing steps. These steps are not just corporate policy; we field customer calls troubleshooting failed reactions, and often, the solution comes down to the handling chain, not the chemistry itself. This kind of feedback keeps us fixing root problems, instead of just masking symptoms.
Every lot is tracked with batch records and retains care. Analysis includes gas chromatography, mass spectrometry, and headspace moisture. Inspection doesn’t end at the plant—logistics get equal attention. Packaging under dry nitrogen in PTFE-lined drums or sealed ampoules prevents minute oxidation or contamination that can throw off high-sensitivity syntheses.
Over the years, we’ve noticed that 3-Hexyne travels best under inert atmosphere, especially in bulk. Some customers request custom-textured inner linings to prevent minute polymerization or adsorption effects. Even though 3-Hexyne does not polymerize as readily as butadiene, inappropriate storage can trigger partial conversion. Old stock shows a color shift or slight viscosity increase, which is why we date-code and rotate inventory methodically. Proper venting and precise temperature control prevent container swelling—lessons learned the hard way in earlier decades before automation upgrades made oversight easier.
Spillage response on the shop floor doesn’t require exotic gear, but the sharp odor signals even a small release. Tight drum sealing and O-ring inspection remain standard best practices due to the compound’s moderate volatility. Long-term users ask for tip sheets with each order, but most find the key is storage below 25°C in a sealed, dry, shaded environment away from sources of ignition.
Many clients now run lean R&D teams, so technical partnership from a manufacturer can save time and money. We share application notes from previous collaborations, detailing unexpected byproducts or improved work-up protocols. With 3-Hexyne, teams exploring hydrofunctionalization or photochemical reactions find that detailed knowledge of minor impurity profiles can speed up new route development.
Feedback cycles from pilot plants or academic groups often push us to adjust purification schemes, especially if a new metal catalyst is involved. For instance, we adapted our drying process for custom runs destined for organometallic chemistry, resulting in a marked improvement in yield when scaled up by the client. This two-way feedback, built up through years of real projects, has led to specific process tweaks such as slowing final distillation to minimize cis-trans-isomerization.
In the present regulatory climate, supply assurance is as important as technical quality. Our own feedstock comes from established hydrocarbon facilities with chloride and sulfur controls upstream, avoiding variable contaminants that have spoiled more than one large-batch run elsewhere. Our plant logs every origin point, so if a problem arises, trace-back happens in hours, not days.
We recognize how global demand fluctuates, and the team watches market swings closely. Early on, 3-Hexyne production followed a rigid annual schedule, but demand from semiconductor precursors and specialty pharma shifted that. Today, we maintain flexible production cells, so analysts and purchasing planners can count on reliability even during commodity squeezes. Our production does not chase spot prices, since purity and safety necessitate steady process control; sacrificing this for throughput never ends well for our partners.
Plant managers expect to answer tough questions about sustainable production. With 3-Hexyne, fumeless incineration mitigates vented byproduct disposal, a necessity for keeping environmental permits in order. Over the last four years, process redesigns reduced mother liquor waste by over 30%, largely by capturing and re-processing offcuts and improving distillation reflux efficiency.
The compound demands thorough safety protocols. Staff complete air monitoring and leak drills every quarter. Acetylenic compounds, if handled with complacency, can pose ignition hazards. The plant enforces strict grounding and bonded transfer lines—and yes, we sometimes assist customers troubleshooting static charge buildup issues in their own facilities. Plant incident logs and safety meetings consistently emphasize vigilance during transfer and loading stages.
Our materials documentation traces every regulatory change affecting 3-Hexyne. International customers look for up-to-date REACH and TSCA statements, but just as crucial, they trust our firsthand records from each processing stage. Authenticity matters more here than any sales pitch; documentation reflects real labwork, real scale-up, and all the inevitable learning curves encountered.
Plenty of distributors and resellers list 3-Hexyne as another commodity on a website. In contrast, manufacturing at source opens up practical improvements that only direct experience brings. We know the tolerances of each reactor, the quirks that affect color or odor, and the subtle tweaks to packaging that impact year-over-year performance in fieldwork. This isn’t just a marketing claim—it is built out of thousands of production hours, from maintenance engineers through to technical support chemists.
A recurring customer story: an advanced materials group struggled with competing suppliers’ product turning up off-color after transit through equatorial ports. After troubleshooting together, we introduced a variant inner drum liner and a more robust nitrogen back-purge, solving the issue for shipments over 40 days. These cumulative lessons form a playbook passed down through our team, integrated into every fulfillment round. Each change, born out of hands-on involvement, makes a difference to customers who can’t afford surprises.
3-Hexyne, as a specialty alkyne, doesn’t forgive shortcuts. Drawing from decades of process improvement, raw material vetting, and collaborative troubleshooting, our product lines grow with each new challenge clients bring us. Designed for both high-throughput syntheses and niche R&D, organized around transparency and real technical support, the material we provide feeds into pharmaceuticals, coatings, electronics, and advanced composites.
No marketing gloss disguises the reality: each drum, can, or bottle that leaves our site has seen at least three quality checks, with the learning from every batch logged and used to improve the next round. For teams seeking chemical products with reliability rooted in manufacturing expertise, not just distribution efficiency, 3-Hexyne from a direct production facility can make the difference between consistent project success and costly delays.