Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

Propiolic Acid

    • Product Name Propiolic Acid
    • Alias 2-Propynoic acid
    • Einecs 207-835-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    317541

    Cas Number 471-25-0
    Molecular Formula C3H2O2
    Molar Mass 70.05 g/mol
    Appearance Colorless to pale yellow liquid
    Density 1.087 g/cm3
    Boiling Point 185 °C
    Melting Point -22 °C
    Solubility In Water Miscible
    Pka 1.9
    Structure HC≡C-COOH
    Iupac Name Prop-2-ynoic acid
    Odor Pungent
    Refractive Index 1.416

    As an accredited Propiolic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Propiolic Acid is packaged in a 100 mL amber glass bottle, sealed with a screw cap, and labeled with hazard warnings.
    Shipping Propiolic acid should be shipped in tightly sealed containers, protected from moisture, heat, and incompatible substances. It must be clearly labeled with hazard warnings and handled according to applicable regulations, such as DOT or IATA for hazardous materials. Ensure upright transport and secondary containment to prevent leaks or spills during transit.
    Storage Propiolic acid should be stored in a tightly closed, corrosion-resistant container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances like oxidizers and bases. Protect from moisture and direct sunlight. Use secondary containment to prevent leaks and maintain storage below room temperature if possible. Ensure proper labeling and access for trained personnel only.
    Application of Propiolic Acid

    Applications of Propiolic Acid in Industrial Manufacturing

    Propiolic acid, as a specialty alkyne carboxylic acid, enables diversified synthesis pathways across multiple precision chemical industries. Our production meets global compliance benchmarks for advanced intermediates and downstream raw materials.

    1. Agrochemical Active Ingredient Synthesis

    Leading agrochemical companies utilize this material as a reactive intermediate in producing herbicide and fungicide actives featuring triple bond functionality. Formulators introduce it at alkynylation stages to enhance bioactivity through ring closure and selectivity-modified frameworks. Downstream processes balance the input amount according to yield targets, regulatory impurity thresholds, and desired crop protection spectrum, supported by traceable material certificates during supplier audits. Primarily, it enters batch reactor systems equipped for controlled exothermicity, with in-process analytics for intermediate quality. Final products include selective contact and systemic herbicides used in regulated agricultural settings.

    Industry compliance standards

    • FAO/WHO Manual on Development and Use of FAO and WHO Specifications for Pesticides
    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015 (specifically for agrochemical manufacturing and quality management)
    • National and regional pesticide registration guidelines (e.g., EPA FIFRA in the USA, EU Plant Protection Products Regulation EC No 1107/2009)

    Typical usage ratio

    • Ranges from 0.4–1.2 molar equivalents relative to the core ring system precursor. Adjusted based on conversion rates, desired selectivity, and impurity controls.

    Downstream process integration

    • Feeds directly into alkynylation and cyclization reactions within step-growth syntheses of pesticide actives.
    • Monitored addition to batch kettle reactors with jacketed temperature control, followed by in-line removal of byproducts in semi-continuous flow where applicable.
    • Isolated, washed, and dried intermediates qualify with trace impurity (alkyne and carboxylate) analysis before formulation blending.

    Final product types

    • Phenoxy-alkynyl herbicides (e.g., propyne-based derivatives for broadleaf control)
    • Systemic triazole fungicides containing alkynyl side chains
    • Intermediate building blocks for antimetabolite crop protection agents

    2. Pharmaceutical Intermediate Manufacturing

    This acid serves as a key alkyne-carbon source for the construction of heterocyclic scaffolds and side-chain functionalization in APIs. Originating from GMP-audited synthesis lines, it enables controlled coupling, esterification, and click-chemistry expansion for medicines with specific geometric requirements. Strict material identity testing (e.g., NMR, GC-MS) and impurity profiling ensure conformity with compendial and regulatory submissions. Manufacturing plants use closed-system metering for the acid in intermediate stages, followed by in situ purification and API isolation under validated process conditions. Final API uses span oncology, anti-infective, and CNS drug categories.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP–NF (United States Pharmacopeia–National Formulary) and/or Ph.Eur. (European Pharmacopoeia)
    • FDA cGMP 21 CFR Parts 210 and 211
    • Japanese PMDA API registration requirements

    Typical usage ratio

    • 0.5–1.0 stoichiometric equivalents relative to the amine or halide reactant for C–C or C–N bond formation. Process chemists determine the scale based on impurity risk assessment and API yield targets.

    Downstream process integration

    • Charged during heterocycle formation, terminal alkyne introduction, or click chemistry modifications in multipurpose reactor trains.
    • Undergoes continuous in-line monitoring of endpoint and unreacted residue for validated cleaning procedures.
    • Impurity carryover minimized by phase-separation and chromatography pre-purification before API crystallization.

    Final product types

    • Alkynyl substituted quinolines for targeted therapy APIs
    • Nucleoside analogues with terminal triple bond sidechains
    • Diagnostic imaging tracers (PET) containing carboxyalkyne labels

    3. Polymerization and Crosslinking Additive in Resins

    Advanced polymer manufacturers incorporate this material as a crosslinker in specialty alkyne-cured thermoset resins, adhesives, and coatings. The acid’s reactive unsaturation and carboxyl group allow direct functionalization into chain-extending or crosslink-initiating roles. Engineered resin protocols dose the additive at the prepolymer mixing or curing stage, influencing mechanical properties and adhesion. Process technicians control charge rates to prevent exothermic side-reactions, coupled with FTIR validation of crosslink density. Finished resin systems target electronics, aerospace, and high-bonding industrial adhesives.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for polymer resin production
    • UL 94 Flame Retardancy (as relevant for electronics)
    • RoHS Directive (2011/65/EU, for restricted substances in end-use electronics)
    • ASTM D638 and D1002 for tensile and adhesive properties testing

    Typical usage ratio

    • 0.5–2.0 wt% depending on resin base and target crosslink density. Higher charge favored in high-performance composites, lower for general adhesives or coatings.

    Downstream process integration

    • Dosed during resin mixing, either batch or continuous-feed systems, prior to thermal or photochemical curing.
    • Reacted with anhydrides or epoxides for in-situ crosslinking under catalyzed conditions.
    • Product QC closes with DSC and gel fraction testing to confirm crosslink efficiency.

    Final product types

    • Heat-cured electronic encapsulants for microchip protection
    • High-bond industrial adhesives for electronics assembly
    • Protective coatings for aerospace structural parts

    4. Synthesis of Fine Organic Building Blocks

    Chemical processing sites leverage this acid for constructing advanced intermediates such as alkynyl esters and amides, used in custom synthesis portfolios. Its high reactivity facilitates esterification, amidation, and metal-catalyzed coupling for specialty materials in R&D, electronics, and specialty monomers. Operators implement tight charge monitoring to control exothermic reaction rates, with systems for fast downstream purification. Output purity and batch traceability comply with contract manufacturing audits. Derived intermediates flow downstream into photoresists, crosslinkers, and precision coatings.

    Industry compliance standards

    • ISO 9001:2015 for custom organics
    • Responsible Care Management System (RCMS)
    • Material identity and traceability in accordance with client QA protocols

    Typical usage ratio

    • Varies 0.7–1.5 molar equivalents, chosen according to target molecule structure and process yield optimization. Advised by pilot-scale data.

    Downstream process integration

    • Fed to multistep syntheses via automated dosing in glass-lined vessels under inert atmosphere control.
    • Paired with alcohol or amine partners for in situ formation of esters and amides, catalyzed by base or carbodiimide reagents.
    • Crude products immediately extracted, dried, then purified via distillation or chromatographic separation.

    Final product types

    • Alkynyl carboxylate esters for UV-cure photopolymerization
    • N-alkynyl amides for high-reliability electronics
    • Functionalized crosslinkers and reactive monomers for precision polymers
    Free Quote

    Competitive Propiolic Acid 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

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Propiolic Acid – Manufacturing Experience and Industry Perspective

    A Closer Look at Propiolic Acid

    Propiolic acid grabs attention in chemical synthesis. As a specialized manufacturer, we have handled this compound in full-scale production for years. Chemically, it is known as 2-propynoic acid, boasting the formula HC≡C–COOH. The triple bond in its structure tells you right away that it belongs in the acetylenic carboxylic acids family, which stands out by offering reactivity not found in its saturated or even simple unsaturated counterparts such as acrylic or propiolic derivatives.

    Experience tells us that actual production of propiolic acid requires precise control of every process stage. Trace oxygen and moisture levels matter, while temperature curves determine final purity and safety. We utilize an integrated distillation and purification setup to obtain colorless or faintly yellow liquid material, closely monitoring the acid's reactivity due to its triple bond.

    Our standard product usually contains purity upwards of 98%. Specifying the exact impurity profile always matters to our downstream partners, especially since propiolic acid will react quickly with a range of nucleophiles and electrophiles. Research customers often check by GC and NMR for propargylic impurities, while specialty polymer engineers want any residual catalyst residues below detection limits. The acid’s physical form appears as a clear to slightly yellow, mobile liquid, with a distinctive odor often described as sour or pungent—anyone who has worked with acetylenic acids in quantity recognizes it immediately.

    Manufacturing Perspective: Attention to Stability and Quality

    Much has been said about the sensitivity of propiolic acid. Acetylenic species raise red flags for safety and shelf life, so all handling processes must treat them with care. Standard packing involves amber glass or high-density polyethylene, tightly sealed, flushed with inert gas. You learn fast that storing it away from direct sunlight or higher temperatures prevents decomposition and polymerization. We regularly rotate stock to avoid prolonged storage, which has helped maintain stability and reliability for customers.

    We test every batch of propiolic acid for acidity (pKa value checks), residual solvents, and its tendency to form peroxides on standing. Our technical team focuses on minimizing residual chlorinated byproducts, since these might compromise applications in pharmaceutical or electronic synthesis. Continuous monitoring for traces of copper or other heavy metals keeps polymer chemists happy, who often require less than 1 ppm for sensitive applications.

    Unlike acetic or acrylic acid, propiolic acid is more reactive and less forgiving when handled in bulk. Even a small operational oversight can trigger undesired side reactions—polymerization, persistent gas evolution, and even violent decomposition under specific circumstances. Our long-term operators respect these hazards, and we install excess venting and rapid shutoff at every transfer point.

    Applications: Harnessing the Triple Bond

    The main appeal of propiolic acid lies in the acetylenic group. Among synthesis chemists, the triple bond and the carboxylic acid allow for pathways not available with standard carboxylic acids. In our experience supplying to R&D and pilot-scale programs, the most prominent uses span several sectors:

    Working with this acid for years has shown us how essential it has become for labs pursuing next-generation materials and medicines. The unique chemical reactivity lets chemists set up pathways unavailable by carboxylic acid substitution alone, offering innovation possibilities that saturated or even simple unsaturated acids cannot deliver.

    Comparing Propiolic Acid to Other Carboxylic Acids

    Despite structural similarities, propiolic acid differs sharply in behavior from both acrylic acid and acetic acid. Acetic acid has known stability and mildness, making it a routine industrial feedstock. Acrylic acid’s double bond grants added reactivity for polymerization and Michael additions, but does not reach the activity seen with triple-bonded systems.

    Propiolic acid, with its C≡C group, widens the window for high-value transformations. For example, it performs best when chemists need to introduce triple bonds late in synthesis or protect carboxylic acids during intricate reaction cascades. This utility defines its role in modern synthetic work, especially in high-stakes discovery projects.

    Storage and handling provide another sharp distinction. Our acetic and acrylic acid operations rarely need more than basic PPE and good ventilation. By contrast, propiolic acid prompts stricter controls—static-safe lines, constant inerting, and continuous real-time leak detection. Even experienced operators treat every transfer and supply operation with a doubled level of vigilance.

    Environmental and downstream performance rounds out the comparison. Propiolic acid generates distinct byproducts if not fully consumed; volatilization creates potential workplace and environmental hazards. Years of environmental monitoring have led us to install dedicated exhaust scrubbers and real-time acid vapor detection, since operators learn quickly how sharply this compound signals its presence, even at low ppm concentrations. Any accidental spillage or waste must go to specialist high-temperature incineration, where the triple bond ensures almost complete decomposition.

    Addressing Challenges in Manufacturing and Use

    Operational hurdles relate mainly to stability and purity. As scale increases, the risk of runaway reactions creeps up. We have shifted to semi-batch additions and interlocked pressure relief across our lines, after early pilot plants faced runaway exotherms. Our technical staff adapts process parameters for every lot; different raw material sources create slight upstream impurities that propagate through the whole cycle.

    Customers sometimes request tailor-made versions differing in impurity content, trace-element profile, or packaging. Pharmaceutical partners, for example, ask for stricter analytical reporting—volatile residuals, low water content, and regular confirmation of triple-bond integrity by IR and NMR. Our records show that customized manufacturing saves time and hassle for downstream synthesis; a single ppm-level difference in heavy metals impacts the effectiveness of a catalyst in alkynylation, which directly affects the next process step’s yield.

    Shipping and storage create further obstacles. Because its volatility sits between acetic and acrylic acid, dedicated cold storage is used for both raw product and finished batches. Only certain carriers trained in hazardous organic chemical handling will take the product, as accidental release can lead to health hazards and regulatory fines. Our logistics team tracks every container in transit and logs opening records for regulatory compliance.

    Supporting Innovation Through Direct Collaboration

    Working so closely with research and manufacturing customers opens new perspectives for product development. Many of our innovations have come from listening to the feedback of chemists who use propiolic acid in real-world, often unpredictable contexts. We work with polymerization research teams looking for improved processability by adjusting acidity or impurity profiles; pharmaceutical clients have shared early insights into how macrocyclizations or sequential click reactions could use more rigorously tested, tailored material. Every request for information or unusual packaging triggers a review rather than a brush-off—we document, produce pilot batches, and then let the customer chemist determine the outcome at their bench.

    Formulating approaches for safer handling proves essential. Staff responsible for drum transfers developed special peristaltic pumps lined with PTFE after early glass-lined steel systems suffered too much corrosion. We re-evaluated our PPE, moving to acid-resistant gloves and goggles, and we built a closed-circuit air exchange system with acid traps, which cut operator exposure and sharply reduced emission sightings. These experiences have made our approach more resilient and responsive to changing regulatory and end-use requirements.

    Offering support for small-lab synthesis as well as industrial-scale batches illustrates a theme: propreity in production leads directly to smoother research and innovation downstream. Partners tackling new molecule development often face unexpected hurdles—a misplaced trace oxidant or an impurity trending higher than the certificate of analysis allows. We have worked through hundreds of these troubleshooting cycles, rapidly running supplementary QC, then adapting feeds or retuning purification at short notice.

    Continuous Improvement and Compliance

    Lessons learned during daily production cycles build long-term improvements. Technical process improvements have reduced energy use in purification by incorporating stepwise distillation rather than single-pass, thanks to experience with thermal decomposition. Routine investment in analytical capability—high-resolution GC-MS, updated NMR—sharply reduced the rate of ambiguous impurity reports, leading to better outcomes for specialty chemical, pharmaceutical, and material science partners.

    Compliance drives many of the controls around production. New regulatory frameworks in many countries set strict limits for storage, waste handling, and transport. Full traceability now tracks every batch from raw feedstock through to delivered product. Accurate documentation supports both customer audits and national regulators, whose focus on hazardous chemical control increases yearly.

    Managing hazardous waste represents another focus area. Since improper disposal of acetylenic acids raises regulatory and environmental issues, we developed internal protocols for neutralization. After consultation with environmental partners, we built a two-stage destruction line to ensure that no active triple bond residue enters facility outflows. Operators log every transfer, and our environmental staff test run-off weekly.

    Genuine Industry Collaboration — The Heart of Reliable Chemical Supply

    Real manufacturers discover that collaboration never stops, especially with a reactive material like propiolic acid. Supporting customers means not just showing up when orders roll in, but actively following where the science, safety standards, and environmental goals move. Our own journey started with laboratory lots but scaled as new research demanded ever-stricter controls on impurity, traceability, and reliability. This industry rarely rewards shortcuts—clean, traceable product remains the best investment in everyone’s future, whether in the next great drug or the backbone of high-performance polymers.

    Daily operations bring fresh challenges. From refining a reaction sequence to improving analytical detection for an emerging impurity class, every solution feeds into a better, safer, more consistent product. By sharing data and inviting direct dialogue with customers, we avoid surprises and often lead to innovations neither laboratory nor manufacturer could reach alone. Direct feedback loops also tip us off to new trends—the demand for cleaner starting material in lithium battery technology, or more robust documentation trails for export to rapidly industrializing nations.

    The privilege of having hands-on knowledge builds trust. As markets grow and technology evolves, keeping a close loop between production team and end-user sharpens everyone’s work. We encourage our customers to share both setbacks and breakthroughs. Emerging fields like bioorthogonal chemistry, organic electronics, and polymer modification all find new uses for propiolic acid. As a manufacturer, the job does not end with loading a drum or bottling a small sample; it stretches all the way to supporting research breakthroughs and making sure every gram shipped meets expectations, reliably, every time.

    Future Outlook and Commitment

    Years of manufacturing propiolic acid and supporting its diverse applications have taught us that no batch, shipment, or application is ever quite routine. We remain committed to continuous improvement—in process, purity, safety, and sustainability. The role of propiolic acid in modern industry and research continues to grow. Synthetic chemists, materials scientists, and industrial developers are only beginning to tap its potential as new methods unfold.

    As new uses for triple-bonded acids keep emerging, both opportunity and responsibility grow. From new reaction pathways in medicinal chemistry to next-generation materials, the demands for quality and support increase. By listening closely to partners and handling every production detail with care, we keep pace with innovation. Our perspective as a manufacturer does not come just from reading market reports or following trends; it is built from the experience of every day spent refining, producing, and supporting the use of this deceptively simple, powerfully reactive chemical.

    Anyone involved in advanced organic synthesis or high-performance materials needs starting points that are not only pure but also consistent, documented, and supported by an experienced team. Our experience with propiolic acid comes from years of attention to detail, constant learning, direct feedback, and a hands-on approach that values both safety and innovation. By sharing practical know-how and backing every shipment with data and support, we help our partners realize new scientific possibilities—one batch at a time.