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HS Code |
966712 |
| Iupac Name | undec-3-yne |
| Molecular Formula | C11H20 |
| Molar Mass | 152.28 g/mol |
| Cas Number | 927-27-1 |
| Appearance | Colorless liquid |
| Density | 0.76 g/cm³ (approximate) |
| Boiling Point | 193-195 °C |
| Melting Point | -60 °C (approximate) |
| Refractive Index | 1.424 (20 °C) |
| Flash Point | 66 °C |
| Structure | CH3(CH2)7C≡CCH3 |
| Pubchem Cid | 136176 |
| Solubility In Water | Insoluble |
| Odor | Faint, hydrocarbon-like |
| Un Number | NA |
As an accredited 3-Undecyne factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 3-Undecyne is packaged in a 25 mL amber glass bottle, labeled with hazard warnings, chemical name, and concentration details. |
| Shipping | 3-Undecyne is typically shipped in tightly sealed containers under ambient conditions, away from sources of ignition, heat, and oxidizing agents. The packaging must comply with regulatory guidelines for chemicals, including proper labeling and documentation. During transport, ensure secure handling to prevent leaks or exposure, adhering to relevant safety and environmental regulations. |
| Storage | 3-Undecyne should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of heat or ignition. Keep the container tightly closed and use proper labeling. Store separately from oxidizing agents and acids. Use compatible, chemical-resistant containers. Ensure appropriate spill containment and fire safety measures are in place due to its flammability. |
Applications of 3-Undecyne in Industrial ManufacturingAs a dedicated manufacturer, we supply 3-Undecyne directly to advanced production lines where precise reactivity and purity are critical for chemical synthesis and specialty material innovation. Below we outline established industrial applications, detailing regulatory adherence, validation of usage ratios, real integration steps, and representative end products as determined by practical downstream workflows. 1. Fine Specialty Intermediates for PharmaceuticalsIn active pharmaceutical ingredient (API) and advanced pharmaceutical intermediate (API) manufacturing, our material is utilized as a key alkyne building block for carbon–carbon coupling reactions by route designers requiring high stereoselectivity. Production chemists integrate it within Sonogashira cross-coupling or related palladium-mediated synthesis to assemble complex, functionalized molecules, specifically during late-stage precursor construction for small molecule drug candidates and specialty intermediates. Material quality control adheres closely to pharmacopeial purity, heavy metal residue, and residual solvent limits, while downstream partners optimize input proportions based on target reaction pathways and yield objectives. Industry compliance standards
Typical usage ratio
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Final product types
2. Synthesis of Liquid Crystal MaterialsLiquid crystal developers rely on this C11 terminal alkyne compound for constructing non-linear aliphatic cores in high-performance mesogenic monomers. The material participates in functionalization steps, especially via alkyne–halide couplings or azide–alkyne click reactions, enabling precise tuning of electro-optical response in custom display matrix formulations. Batch material requires strict spectral and metal contaminant verification, as these factors directly affect end-use device optical clarity and dielectric stability. Additive ratios are optimized per formulation type and response uniformity in display panel applications. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. High-Purity Electronic Grade MaterialsDownstream users in microelectronics introduce this raw material into custom dielectric precursor syntheses for thin-film transistor (TFT) and organic semiconducting layer fabrication. The alkyne functionality is key for introducing cross-linkable terminal groups and non-aromatic flexibility to enhance charge mobility and reduce ion migration within fabricated circuits. All supply lots are evaluated using advanced chromatographic and trace metal testing to ensure suitability for semiconductor process environments. Adjustments in inclusion ratio, often determined by performance screening in prototype films, are tightly managed to prevent electronic property drift. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Performance Lubricant Additive SynthesisManufacturers of high-stability synthetic lubricants apply the unique triple bond functionality for targeted molecular branching in high-viscosity base oil modifiers. Precise introduction enables the design of long-chain alkynyl esters that support anti-wear and deposit-resistance properties in finished lubricants, even under sustained thermal stress or heavy mechanical load. Each batch is produced and tested per lubricant additive sector protocols, with compliance focusing on ash content and metal residue since these directly impact downstream engine or machinery performance. Usage ratio is governed by finished oil performance targets and regulatory mandates on additive content. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Agrochemical Intermediate ManufacturingAgrochemical sector formulators use this raw alkyne as a linker or functionalization point in the synthesis of selective herbicide and crop-protection active constituents. The compound allows integration of long-chain aliphatic structures, contributing to active ingredients’ soil retention and amphiphilic penetration behavior. Downstream chemical engineers manage response levels to support regulatory residue limits as well as targeted biological efficacy, integrating real-time analytical feedback when setting process input ratios and verifying output against global MRL (Maximum Residue Limits) frameworks. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Working in chemical manufacturing, we frequently handle compounds that sit on the edge of standard catalog chemistry and advanced specialty applications. 3-Undecyne often stands out in the schedule. This molecule, classified as an alkyne due to its triple bond on the third carbon of an eleven-carbon chain, brings opportunities and certain demands. CAS number 928-49-4, molecular formula C11H20, and structure CH3(CH2)7C≡CCH3 sum it up on paper, but these figures don’t tell the real story. In the plant, in the hands of chemists, and within the documentation rooms, understanding what sets 3-Undecyne apart comes from years spent managing its logistics, synthesis, purification, and packaging.
On the manufacturing floor, every run of 3-Undecyne demands attention to the details. The triple bond isn’t just a curiosity for chemists but a feature influencing reactions, stability, and processing safety. Our reactors, controls, and purification columns see a unique rhythm during its manufacture. Pure 3-Undecyne has a colorless to pale yellow appearance and a noticeable, sharp odor that operators catch long before the gas chromatograph verifies composition.
Reactions start with basic feedstocks, often long-chain bromoalkanes or terminal alkynes, channeled through carefully controlled coupling or elimination reactions. Yields depend on keeping water out, catching the right temperature, and avoiding side reactions that could lead to internal rearrangements or, worse, uncontrolled polymerization. The separation is another challenge. We rely on fractional distillation and vacuum transfer to ensure top-end purity, measured by gas chromatography and supported by NMR and infrared spectroscopy in our on-site QC lab.
Spec sheets, though important, often miss the hands-on considerations. Liquid water content, presence of unsaturated by-products, and even the way the product interacts with container linings get logged and cross-checked at batch release. We prefer glass-lined or fluoropolymer-coated equipment to limit contamination and product loss.
Our standard 3-Undecyne typically reaches above 98% purity on GC analysis, with internal documentation tracking even lower-grade fractions. Moisture and peroxide numbers are controlled below detection limits. Packing in stainless steel or PTFE-lined barrels, we arrange nitrogen blankets to minimize oxidative changes and evaporation loss. What lands on a customer’s loading dock comes with stability records, direct batch traceability, and storage guidelines tested through real-world cycles. The product holds at room temperature for over a season, but exposure to sunlight, heat, and unlined metal shortens lifespan and affects color and reactivity.
A difference becomes clear for processors who’ve tried other alkynes before. Alkynes like 1-octyne, 1-decyne, or 4-octyne have their place, but 3-Undecyne’s position of the triple bond brings distinctive reactivity. Terminal alkynes (like 1-decyne) often serve as straight acetylenic intermediates, showing higher acidity and unique coupling behaviors. Internal alkynes, especially at the 3-position, offer less polarity, different selectivity for cycloadditions, and increased resistance to certain bases and nucleophiles. That matters for cross-coupling, metathesis catalysis, or hydrofunctionalization reactions.
Take semihydrogenation: 3-Undecyne reduces cleanly to 3-undecene using Lindlar’s catalyst, with less risk of overreduction or unwanted side reactions than some terminal alkynes. Niche applications in synthetic perfumery and advanced functional materials exploit this resistance to rapid acid-base reactions and relatively stable volatility profile. Chemists focusing on new molecular scaffolds appreciate how 3-Undecyne acts as a masked diene precursor, favoring specific regioselectivity with fewer by-products.
Our experience with isomeric impurities tells us why process discipline pays off. Mismanagement during distillation or insufficient control over the feedstock purity can introduce anomalous chain branching or shift the triple bond position, showing up as tailing GC peaks or unstable baseline signals. By keeping documentation tied to retention time and using reference samples every quarter, we pin down isomer content and reduce ambiguity in analyses.
Users in labs and industrial sites come to us looking for intermediates with clear reaction footprints. 3-Undecyne stands out in transition metal-catalyzed processes. We’ve worked with pharmaceutical sites scaling new HIV medication motifs, pushing for late-stage functionalization paths based on Suzuki and Sonogashira protocols—3-Undecyne’s internal triple bond survives conditions that decompose shorter, more branched alkynes.
Custom syntheses in flavors and fragrances see 3-Undecyne stacking up as a precursor to macrocyclic musks and linear pheromone mimics. Small changes in the alkyne position impact odor profile, volatility, and long-term stability of end products. With its vapor pressure and solubility curve, our product blends well with nonpolar solvents and can be dosed straight into oligomerization or cyclization runs. Odor and evaporation rates matter for technicians preparing samples for GC-FID analysis; our consistency from batch to batch shows up as nearly superimposable chromatograms over a dozen years of retention.
Cross-linking specialist teams—manufacturers of specialty coatings or conducting polymers—seek 3-Undecyne for terminal functionalization or as a spacer in dendritic materials. Catalysis researchers mention that 3-Undecyne offers more even reactivity across the molecule’s length, reducing hot spots in the reaction mixture and delivering products with higher throughput in continuous reactors.
Even with years spent moving alkynes through tanks and reactors, 3-Undecyne still requires respect. Peroxides can build up if exposed to air or stored too long, especially at elevated temperatures. In our facility, fresh stock undergoes periodic peroxide testing—quantitative, colorimetric, not just qualitative spot checks. Both storage and shipping call for nitrogen headspace, especially in large containers or long-haul logistics.
Shipping lessons came the hard way. Early in the run, we tracked losses and minor product yellowing due to oxygen permeation through unlined drums. The switch to higher-gauge steel, tighter PTFE gaskets, and short-fill protocols (never full to the rim, always allowance for expansion) made differences that reflected in customer product claims. Even the way drums are stacked—cool, out of sunlight, away from oxidizing agents—matters more than storage instructions on a spec sheet.
Cleaning and disposal also differ. Alkynes can foul downstream incinerators with incomplete combustion, so we've adapted quenching and pre-treatment steps, ensuring legal disposal and reduced emissions. Operators receive basic but crucial training—personal monitors, chemical-resistant gloves, eye shields. Spill kits lean toward absorbent pads and neutralizing agents, since water sprays can distribute vapors instead of suppressing them. The cost and effort align with the safety and environmental responsibility we owe our communities.
As responsible manufacturers, compliance isn’t optional. 3-Undecyne fits into a mid-risk hazard class—volatile, flammable, and capable of irritating skin and mucosa. We go beyond transferring SDS documents down the supply chain. Internal drills simulate real leaks; our personnel respond within seconds, shutting valves, activating exhaust, and getting containment pillows onto any spills. No catastrophic releases in a decade, thanks to equipment upgrades and lessons written into our process management systems.
Waste management brings its own paperwork. Quarterly audits track everything from empty containers to wash solvents, with waste coding tied to official environmental standards. If a product recall comes (rare, but not impossible), our traceability systems give batch origin in seconds, allowing withdrawals and corrective steps hours before market impact. Customer requests for compliance data—RoHS, REACH, TSCA, and custom regulatory statements—land straight with our technical affairs team; we build decades of archived correspondence with regulatory authorities that prove reliability in due diligence reviews.
Partnerships with downstream users mean we advise on labeling, handling, and lab space setup for alkynes. We’ve offered on-site seminars, digital resources, and phone-in consultations—not out of obligation, but as a measure of trust. In our hands, risk is documented but also managed and, as much as possible, reduced at every stage.
Buyers fall mainly into fine chemicals companies, innovators in specialty polymers, aromas, and hybrid materials, and contract manufacturers for mid-scale pharma projects. Many first came with requests for short-term, lower volume lots, moving to annual purchase contracts only after reliability and QC matched demand. Some ask for custom blends, though 3-Undecyne as a pure substance already plays the required role in most synthetic protocols.
Key performance drivers from users: solvent compatibility, purity, storage stability, and reactivity profile. Flavors and fragrance specialists assess the product by nose and GC; coatings manufacturers look at shelf life and polymer endpoint composition; academic groups reference our published QC data to match stereochemical outcomes for studies. Our technical liaisons keep open lines for troubleshooting reaction quirks, off-odor reports, or rare out-of-spec results. This circulation between manufacturers and advanced users creates a feedback loop, keeping our own operations under constant scrutiny and improvement.
Every product line teaches lessons. Even after years, we see price pressure from shifting raw materials chains; bromoalkane sourcing ties to fluctuations in global petrochemical markets. Freight costs and container shortages add friction, especially for overseas customers. The regulatory landscape evolves—new rules on VOCs, ever-tightening transport and export declarations, and shifting customs codes all demand flexibility and a ready team. We invest in documentation systems to keep workflows nimble, avoid hold-ups, and respond with proof rather than promises.
Research requests sometimes push up against synthesis limits. Novel downstream uses call for even higher purities, or batch-to-batch analytical uniformity at uncommonly narrow tolerances. We adapt new analytical methods—2D NMR, advanced MS, and improved storage monitors—allowing us to meet those requests where possible. In-house pilot plants, faster process optimization, and ongoing safety training keep the supply chain running without major disruption, even as customer expectations rise.
3-Undecyne stays in our catalog because it brings unique chemistry to the table. Its triple bond and internal position open up specialized synthetic possibilities, especially where selectivity and mild conditions matter. A small group of customers has made it a lynchpin in their R&D, and every incremental improvement or stability extension builds that trust further.
We don’t rest on legacy procedures. Every shipping cycle, customer audit, and technical question sends us back to refine logistics, safety, and purity. Our approach—built on traceability, technical detail, and lived experience—ensures that users can plan new chemical routes with confidence, knowing that the material aligns with ambitious standards of modern synthetic chemistry.
It’s easy to see products like 3-Undecyne as mere commodities, but after decades in hands-on production, we realize how much value real experience brings. We answer not only with numbers—purity, packaging, compliance—but hard-learned details about reactivity, longevity, and end-user support. We respond to evolving needs, improving both product and process with every run. This deep involvement produces results beyond the spec sheet, building a relationship with every user who stakes synthesis and business success on our efforts.