|
HS Code |
229973 |
| Productname | 2-Butynal Diethyl Acetal |
| Casnumber | 10160-04-0 |
| Molecularformula | C8H14O2 |
| Molecularweight | 142.20 |
| Appearance | Colorless to light yellow liquid |
| Boilingpoint | 155-157°C |
| Density | 0.893 g/mL at 25°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Refractiveindex | 1.431-1.433 |
| Flashpoint | 45°C |
| Purity | Typically ≥ 97% |
| Storagetemperature | 2-8°C |
| Smiles | CCOC(C#CC)OCC |
As an accredited 2-Butynal Diethyl Acetal factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 mL of 2-Butynal Diethyl Acetal is supplied in a sealed amber glass bottle with a secure screw cap for safety. |
| Shipping | **2-Butynal Diethyl Acetal** should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It must be handled as a flammable liquid, complying with all regulations for hazardous materials. Proper labeling and documentation are required, ensuring safe transit and compliance with IATA, IMDG, or DOT standards. |
| Storage | 2-Butynal Diethyl Acetal should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent moisture and air exposure. Keep it in a cool, dry, and well-ventilated area, away from heat sources, ignition sources, and incompatible materials like strong oxidizers and acids. Store in accordance with all local, state, and federal regulations. |
Applications of 2-Butynal Diethyl Acetal in Industrial ManufacturingAs a specialized manufacturer, we support multiple precision industries with high-purity 2-Butynal Diethyl Acetal, delivering quality and consistency for complex downstream applications. Our expertise enables reliable integration into high-value chemical processes, meeting stringent customer production requirements. 1. Pharmaceutical Intermediate Synthesis2-Butynal Diethyl Acetal plays a consistent role as an acetal-protected aldehyde in the synthesis of complex small-molecule APIs and advanced pharmaceutical intermediates. Medicinal chemistry teams employ it for the selective introduction of masked reactive groups during multi-step routes, particularly in constructing alkynyl-based molecular frameworks. Stringent batch traceability, impurity profiles, and documentation are critical, especially under regulatory scrutiny for in-process materials destined for clinical applications. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Active Ingredient ProductionKey agriculture chemical processors utilize 2-Butynal Diethyl Acetal for introduction of protected alkynyl aldehyde motifs in development of selective herbicides and insecticide actives. Its chemical stability enables selective functionalization and ring closure steps in pilot and full-scale manufacturing campaigns. Producers prioritize trace impurity control and adherence to global product stewardship guidelines, preparing actives for diverse registration scenarios. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Electronic Chemical Raw Material SupplyHigh-purity 2-Butynal Diethyl Acetal supports the electronics manufacturing sector, where it acts as a sensitive precursor for organic semiconductors and special functional polymers used in OLED displays and sensor technologies. End users demand electronic-grade materials free of trace metals, residual solvents, and organic contaminants, requiring rigorous in-process controls and custom documentation for every delivery batch. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Flavors and Fragrances Intermediate ManufacturingProducers of high-end aroma chemicals use 2-Butynal Diethyl Acetal as an essential protected intermediate in the controlled construction of fruity, green, and metallic aromatics. Its structure allows safe manipulation of reactive aldehyde functionalities before final deacetalization, minimizing undesired side-reactions during multi-stage syntheses. The entire process must align with food-grade production rules, including full allergen traceability, flavoring substance purity, and supply chain transparency for global brands. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Specialty Fine Chemicals for Material ScienceMaterial scientists and contract manufacturers use 2-Butynal Diethyl Acetal in synthesizing custom cross-linkers and advanced macrocycles critical for polymer modification and hybrid organic-inorganic frameworks. Producers verify purity and composition through independent audits, with performance testing in laboratory substrates and emerging commercial materials aimed at performance coatings and specialty adhesives. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2-Butynal Diethyl Acetal prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Inside the chemical industry, some molecules play quiet but indispensable roles in the background of countless syntheses. 2-Butynal Diethyl Acetal is one of them. Not everybody recognizes it by name, but chemists intent on creating highly functional intermediates in pharmaceutical and agrochemical labs ask for it by the drum and bottle. We have been working with this product day in, day out, for many years. Direct exposure to every stage of its production has given our team a practical sense of its strengths, subtle points, safety quirks, and best routes of application.
Chemically, 2-Butynal Diethyl Acetal sits at the boundary of versatility and practical stability. Its backbone—a four-carbon chain containing a triple bond and an acetal functional group—guides its reactive behavior. The model most commonly produced in our facility features a purity greater than 98%. This clarity in composition simplifies purification steps later in the process for customers working in downstream applications.
This product finds its real home in fine chemical syntheses. Acetals often serve as masked aldehydes. Here, 2-butynal diethyl acetal works well in staged synthesis where exposure to strong acids or bases cannot occur before a critical moment. Chemists who have approached us for technical guidance usually look to this product for developing complex heterocycles, specialty intermediates, or as building blocks for active pharmaceutical ingredients.
We have refined our production line to limit byproducts and impurities. The starting materials undergo strict sourcing—nothing weakens final purity like inconsistent ingredients. We lean on a controlled reaction setup, optimizing temperature and dosing rates, which—not through luck—brings the desired acetal formation over undesired polymerization or dimerization. Following this, a double column distillation step further polishes the product. In our experience, operators in our plant need to manage moisture with vigilance. Incoming water can cleave the acetal back to the aldehyde, reducing concentration of the active ingredient. Each shipment undergoes Karl Fischer titration to confirm water levels remain below 0.1%. Over years of scale-up, we have learned that excess diethyl acetal in the reaction mix does not benefit the yield. Less really is more—if the right conditions are maintained.
Every acetal has its peculiarities. 2-Butynal diethyl acetal differs in physical and chemical properties from more common acetals such as 1,1-dimethoxyethane or 2,2-dimethoxypropane. The presence of the carbon-carbon triple bond allows for further tailored chemical transformations. For example, Sonogashira couplings become accessible. Many alternative acetals lack this unsaturation, which restricts their use to simple aldehyde release in acid environments. Our clients in the fine chemical arena rely on these differences to design multi-step syntheses without costly protection and deprotection sequence detours.
2-Butynal itself is notoriously reactive, which on its own can introduce severe handling hazards and lower shelf stability. The diethyl acetal form tames that reactivity, allowing safer shipping and storage. No one in this industry ever forgets the first time a shipment of butynal arrived with a heavy odor from self-polymerization. This happens less with the acetal, all thanks to the masking effect of the ethoxy groups. For the manufacturer, this simplifies packaging and labeling compliance. For the chemist, it means setting up reactions without facing runaway byproduct formation.
At pilot and commercial scales, we have supplied 2-Butynal diethyl acetal to several pharmaceutical companies focused on targeted therapies and intermediate libraries. It typically slots into synthetic sequences as a propargyl aldehyde source, getting unmasked in a specific reaction step. Some API syntheses require strictly controlled conditions: moisture-free, oxygen-limited, and sometimes even handled inside glove boxes under nitrogen flow. Over time, those with broader experience have realized that despite being more stable than the aldehyde, 2-butynal diethyl acetal can still demand proper storage. We pack our product under inert atmosphere for good reason.
Feedback from process chemists tells us what works and what does not. Using this acetal, especially in transition-metal-catalyzed couplings, can unlock step-economical syntheses. As a manufacturer, we learned quickly how subtle batch-to-batch variations, often unmeasurable by simple GC, can throw off a pharmaceutical scale-up. Resolving these issues means continuous dialogue with clients and monitoring finer analytical parameters, not just headline purity.
Producing acetals is not without risk. Small traces of volatile organics can escape in the process stages. Our plant uses local scrubbers and emission monitoring to prevent workplace exposure and environmental release. Staff get trained not only in SOPs, but in the chemical background of why the routines exist. They see what a poorly controlled batch can yield—strong odors, product discoloration, or unwanted side products. Consistency and safety only come from respect for the unpredictable character of the alkyne-acetal mix. Regular maintenance, tight controls on feed rates, and meticulous sample retention help maintain both regulatory acceptance and our own peace of mind.
The world is shifting toward green chemistry, and the pressure is real. Acetals, being volatile organic compounds, need special care for safe transport and storage. We select drum and bottle types based on real transport challenges—pressure swings, UV exposure, condensation, or temperature excursions in shipping. Over the years, we have investigated and improved barrier coatings on our packaging, reducing both evaporation losses and incident rates during shipment. Not every acetal will behave the same under heat-stroke or cold-chain interruption: 2-butynal diethyl acetal maintains relatively stable vapor pressure until temperatures rise above typical ambient levels, but that does not grant absolute peace of mind. We have had to replace whole lots that suffered transport stress, based on nothing more than a subtle shift in product color or micro-impurity levels upon return to our lab.
Few things build trust faster than helping a chemist through an unexpected yield drop or impurity spike. One of our long-term clients ran into persistent side-product contamination. The root cause traced back to storage drums sitting just a few degrees too warm in a warehouse. We figured this out by pulling samples from retained lots in our own archives and running comparative stability studies. The fix was mundane—add a controlled cooling stage in the dispatch chain—but the knowledge came from experience gained batch after batch.
Another group needed a product variant with slightly higher purity for use in a photoactive materials program. Here, we experimented with a fractional crystallization stage post-distillation. The results proved worth the investment: client-side reaction yields jumped seven percent, cutting their downstream waste by almost half. No catalogue or technical data sheet suggests this kind of adaptation, but it happens in conversations between chemists and plant operators who know each other’s needs.
As a manufacturer, we receive frequent benchmarking requests, especially from procurement teams seeking lowest price offers. Not all 2-butynal diethyl acetals on the market are created equal. Impurities such as residual aldehyde, over-oxidized species, and color bodies can slip into final lots if process attention wavers. High-purity batches support downstream reactions without the risk of catalyst poisoning. Over many years, we have seen how substandard material leads to fouled glassware, unpredictable exotherms, or color bodies in chromatographic runs. The tighter the controls in-house, the less rework and troubleshooting the user faces later on.
We pay attention to repeated issues that surface in the industry—such as the tendency for acetals to degrade upon storage or the unseen effects of minor non-volatile impurities. Once, after fielding client complaints about slow hydrolysis in their intended deprotection step, we re-examined our own stabilizer protocols. Our QC team identified trace peroxide contaminants present in one reactor line. Adjusting the cleaning regimen resolved the problem, restoring the regular pace of their manufacturing scheme. Each minor improvement makes life easier for researchers and production managers alike.
We have found that the real challenge with 2-butynal diethyl acetal occurs in maintaining long-term shelf stability. Even in high-grade, amber glass bottles, temperature fluctuations bring about slow color shifts and possible slight changes in reactivity. Our standard procedure these days involves date-stamping each lot, maintaining back stocks in temperature-controlled rooms, and flagging material for retesting if over one year old. Product specifications sent out with each batch include analytical chromatograms, not only for end users’ peace of mind but to help diagnose issues later if needed.
Clear handling guidance often originates from factory observations. Moisture infiltration damages acetals—hands down, the quickest route to off-spec material. For labs or plants without dry-handling facilities, we commonly suggest breaking shipments into smaller containers to avoid repeated opening and closing of large drums. End users appreciate having package sizes that suit their batch sizes, not just a “one-size-fits-all” marketing approach. Cost matters of course, but experience taught us that supplying chemical solutions, not just boxed product, wins a longer customer relationship.
No chemical plant runs forever on autopilot. Each new set of regulations, updated client specification, or novel downstream application pushes the process team to evolve. With acetals like 2-butynal diethyl acetal, we look for opportunities to reduce carbon footprint. Emissions controls continue to tighten, so we invest in process intensification, seeking higher yields at lower temperature and pressure points. We monitor batch records for trends—unexpected drop-offs in productivity, slow color changes on storage—and adjust standard protocols to capture lessons learned.
A particularly active area of improvement involves reducing the energy intensity of distillation. Through pilot trials using membrane dehydration, our team has managed to lower both waste streams and utility bills. While these investments do not always produce immediate returns, they add to long-term viability. What works for petrochemical giants does not always translate well to specialty molecules like 2-butynal diethyl acetal. The movement away from broad, energy-hungry “one process fits all” lines makes us nimbler, able to tweak product specs for the niche chemistries that drive our clients’ innovations.
The wider public rarely discusses 2-butynal diethyl acetal. Yet, behind many pharmaceutical and agricultural discoveries, its intermediacy paves the way. Its acetal structure, containing a triple bond, offers unique chemical reactivity—not just another anonymous building block. We have watched companies design new catalyst systems or synthetic pathways built from its singular mix of reactivity and stability. That gives us the motivation to keep refining purity targets, stabilization systems, and production scheduling.
Its role extends beyond pharmaceuticals into specialty polymers and crop-protection agents, where flexibility of downstream modification becomes key. While larger firms sometimes default to most-easily-sourced acetals, researchers attuned to reaction nuances come back for the specific benefits: easier masking of the aldehyde, improved longevity, and access to transformations unavailable with saturated analogues.
A plant can make a molecule, but often the customer decides whether a supplier remains long-term based on real dedication to after-sales support. Our technical staff regularly answer calls about downstream problems, suggested optimization strategies, or regulatory questions. Some requests come years after a purchase: “This lot performed differently than last year’s—what’s changed?” By maintaining archives of batch data and keeping laboratory and plant teams in conversation, we pinpoint solutions quickly and transparently.
We draw on cumulative learning gained from hundreds of kilograms and thousands of batch hours. That might mean providing additional product characterization for a customer working on a patent filing, or splitting a shipment to accommodate staggered production schedules overseas. With each adaptation, our experience working directly with this compound—its quirks, sensitivities, strengths—positions us to be more than just a supplier.
Experience shapes confidence. We have seen 2-butynal diethyl acetal grow from a specialist item to a backbone intermediate in multiple chemical segments. It stands apart from other acetals because its chemical structure enables one-pot construction of challenging molecules, reduces the strain on storage and transport, and retains a manageable safety profile for trained users. Differences between this compound and simpler or non-alkynyl acetals become most visible at scale, when reaction selectivity, impurity load, or batch reproducibility matter.
We remain committed to supporting our partners who need this compound delivered to the right spec, packed the right way, and with answers ready to go for whatever new chemistry they dream up next. For every downstream breakthrough or product launch, small details in the manufacturing of building blocks like 2-butynal diethyl acetal add up, enabling progress across diverse fields.