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Pent-2-Ene-1,5-Dioic Acid

    • Product Name Pent-2-Ene-1,5-Dioic Acid
    • Alias Glutaconic acid
    • Einecs 210-898-8
    • 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
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    Specifications

    HS Code

    349999

    Iupac Name Pent-2-ene-1,5-dioic acid
    Molecular Formula C5H6O4
    Molecular Weight 130.10 g/mol
    Cas Number 1724-58-7
    Appearance White to off-white solid
    Melting Point 164-166°C
    Solubility In Water Moderate
    Boiling Point Decomposes before boiling
    Structure HOOC-CH=CH-CH2-COOH
    Pka 3.3 (approximate for carboxylic acids)
    Synonyms Glutaconic acid
    Chemical Class Dicarboxylic acids
    Stability Stable under recommended storage conditions
    Odor Odorless

    As an accredited Pent-2-Ene-1,5-Dioic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Pent-2-Ene-1,5-Dioic Acid, 100g: Supplied in a sealed amber glass bottle with tamper-evident cap and hazard labeling for safe handling.
    Shipping Pent-2-Ene-1,5-dioic acid is shipped in tightly sealed containers to prevent moisture absorption and contamination. It should be packed according to safety regulations for organic acids, labeled appropriately, and transported in a cool, dry environment. Ensure compliance with local, national, and international shipping guidelines for chemicals and hazardous materials.
    Storage **Pent-2-ene-1,5-dioic acid** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from moisture, heat, and incompatible substances such as strong oxidizers or bases. Protect from direct sunlight and sources of ignition. Ensure appropriate chemical labeling and access restricted to trained personnel, following standard laboratory safety and chemical storage protocols.
    Application of Pent-2-Ene-1,5-Dioic Acid

    Applications of Pent-2-Ene-1,5-Dioic Acid in Industrial Manufacturing

    As the original manufacturer, we supply Pent-2-Ene-1,5-Dioic Acid to global customers using this specialty diacid for advanced synthesis in industrial production. This section details real-world B2B applications, with practical insights based on industry standards, formulation ratios, production workflow, and the types of finished goods produced downstream.

    1. Polyamide Engineering Resin Synthesis

    Major polymer producers leverage Pent-2-Ene-1,5-Dioic Acid as a dicarboxylic acid monomer for high-performance polyamide resins. This acid enters copolymerization reactions with various diamines, boosting mechanical strength and flexibility in automotive and electronics component resins. Compared to traditional adipic or glutaric acid, it allows precise molecular structure control. Polyamide formulations using this monomer meet strict industry and safety standards for critical molded parts.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • UL 94 Plastics Flammability Standard
    • IEC 61249-2-21 Halogen-Free PCB Base Material Regulation
    • REACH SVHC Substance Listing

    Typical usage ratio

    • 5–30% molar proportion in total diacid content, depending on desired polyamide chain length and crystallinity
    • Adjusted optionally from 10–20% in blends where increased flexibility is required

    Downstream process integration

    • Reacts with diamines under melt-polycondensation at 210–260°C
    • Feeds directly into continuous or batch resin reactors
    • Controlled vacuum removal of water byproduct
    • Pelletizing and compounding with fillers or flame retardants follows polymerization

    Final product types

    • Automotive air intake manifolds
    • Power tool housings
    • High-frequency electronics casings
    • PVC replacement cable insulation

    2. Pharmaceutical Intermediate for Small Molecule Synthesis

    API manufacturers employ Pent-2-Ene-1,5-Dioic Acid as a key intermediate in the synthesis of certain heterocyclic active ingredients. The reactive double bond and terminal carboxyl groups support catalytic cyclization and condensation pathways critical for manufacturing advanced synthetic drugs. Pharmaceutical-grade material must meet cGMP and pharmacopoeial expectations for purity, trace metals, and residual solvents, ensuring batch-to-batch reproducibility.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF, Ph. Eur. monograph general requirements
    • FDA 21 CFR Part 211 Drug Manufacturing Controls
    • Ph. Chin. chemical purity requirements

    Typical usage ratio

    • 0.2–1.5 equivalence as a condensation or ring-closing reactant, depending on target molecule
    • Stoichiometry defined by process route and scale-up solvent system

    Downstream process integration

    • Dissolved or suspended in reaction solvent for catalytic cyclization
    • Treated under mild to moderate temperatures (60–100°C)
    • Crude intermediate isolated by extraction, then further purified by crystallization or distillation
    • Strict in-process control for organoleptic and HPLC/GC parameters

    Final product types

    • Oral hypoglycemic agents (intermediates)
    • Antiviral heterocycles
    • Specialty chiral compound building blocks
    • Custom intermediates for oncology research

    3. Specialty Polyester Resin Modification

    Advanced coatings and fiber producers utilize Pent-2-Ene-1,5-Dioic Acid for tailored polyester chain construction. The presence of the alpha-beta unsaturated moiety introduces tunable crosslinking in alkyd, saturated, and unsaturated polyesters—ideal for heat-resistant coatings and technical yarns in filtration or industrial fabrics. Customers report enhanced dye affinity and solvent resistance compared to traditional dicarboxylic acids.

    Industry compliance standards

    • EN 71-3 Safety of Toys (Migration of Certain Elements) for coated surfaces
    • ISO 14001 Environmental Management (production waste solvent control)
    • OEKO-TEX® Standard 100 for technical fibers
    • Directive 2011/65/EU (RoHS) for electronic substrate coatings

    Typical usage ratio

    • 2–15% by weight in polyester resin formulations
    • Higher loadings (up to 20%) in technical yarns, adjusted based on melting point requirements

    Downstream process integration

    • Co-reactant in melt or solution polycondensation with glycols
    • Feeds prior to prepolymer formation step
    • Enables downstream functionalization (e.g., grafting, methylation)
    • Finished resins processed by extrusion or fiber spinning

    Final product types

    • Powder and coil coatings for appliances
    • Industrial filter media yarns
    • Flexible printed circuit board insulators
    • High-gloss alkyd architectural paints

    4. Reactive Linker in Performance Adhesives Manufacturing

    Formulators in adhesive and sealant sectors adopt Pent-2-Ene-1,5-Dioic Acid as a reactive linker to confer flexibility and thermal stability to specialty adhesives. Its unique structure allows controlled crosslinking in polyurethane and epoxy-based systems, resulting in adhesives with superior chemical resistance. Customers require tight monitoring for unreacted acid and proper molar ratios to ensure compliance with bonding and safety standards in industrial use.

    Industry compliance standards

    • ASTM D1002 Lap Shear Strength for Epoxy Adhesives
    • ISO 4587 Peel Resistance for Adhesives
    • REACH Annex XVII restrictions (absence of prohibited substances)
    • GADSL (Global Automotive Declarable Substance List) for automotive bonding

    Typical usage ratio

    • 1–7% by weight based on total polymer mass in reactive adhesive formulation
    • Ratio tuned for target glass transition temperature (Tg) and viscosity profile

    Downstream process integration

    • Blended during prepolymer mixing stage before catalyst addition
    • Main input in one- or two-component adhesive systems
    • Cures at ambient or elevated temperatures depending on process design
    • Desiccant-free packaging for moisture-sensitive adhesives

    Final product types

    • Automotive structural adhesives
    • Electronics-assembly epoxies
    • Construction sealants for expansion joints
    • Heat-resistant labels and tapes

    5. Chemical Intermediate for Agrochemical Synthesis

    Factories specializing in post-patent agrochemical actives use Pent-2-Ene-1,5-Dioic Acid for the construction of select pyridinedione and maleimide core structures. Its reactivity supports formation of biorational herbicides and plant growth regulators through catalytic addition and cyclization. The production process follows local and global regulatory controls for toxicity, purity, and trace contaminants.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius for pesticide active specifications
    • EPA 40 CFR Part 180 for pesticide chemical residues
    • ISO 17025 Laboratory Accreditation for batch release analysis
    • China GB 2763-2021 Maximum Residue Limits for Pesticides

    Typical usage ratio

    • 0.5–1.2 moles per target mole of final molecule, based on specific synthetic route
    • Customized with reactant excess to offset conversion yield in pilot and industrial scale

    Downstream process integration

    • Charged into reactor as dicarboxylic backbone for catalytic condensation
    • Solvents: methanol, DMF, or toluene based on solubility profile
    • Intermediate recovered by filtration and solvent washing
    • Finishing by crystallization/purification for downstream formulation

    Final product types

    • Pyridinedione herbicide actives
    • Plant growth regulator intermediates
    • Specialty maleimide fungicides
    • Precursor for non-systemic contact herbicides
    Free Quote

    Competitive Pent-2-Ene-1,5-Dioic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Pent-2-Ene-1,5-Dioic Acid: A Producer’s Perspective

    Introduction

    Every manufacturer who has spent hours on the shop floor or stood beside a glass reactor understands the value behind every metric ton of specialty chemical. When we talk about Pent-2-Ene-1,5-Dioic Acid, we speak from a place rooted in hands-on experience, daily production, and direct engagement with research partners across various industries. We fabricate this compound not just to meet demand but to anchor the quality and precision our clients expect from a substance with such specific usage.

    The Chemical Behind the Name

    Pent-2-Ene-1,5-Dioic Acid, also known as 2-Pentenedioic acid, features a linear five-carbon structure with two carboxylic acid groups at the ends, linked by a central double bond between carbons two and three. Its molecular formula, C5H6O4, and a molecular weight around 130.10 g/mol, are part of what gives this acid its unique properties, especially in polymer synthesis and organic transformation applications.

    Production Details

    We synthesize Pent-2-Ene-1,5-Dioic Acid in batch reactors under an inert atmosphere to preserve the integrity of the central double bond. Each production run goes through controlled temperature regimes, and we consistently monitor reaction completion through gas chromatography. Higher purity batches require further purification steps, involving fractional crystallization and rotary evaporation. Our plant engineers and chemists have hands-on experience scaling these steps, troubleshooting during seasonal temperature swings or humidity changes that can affect the crystallization profile.

    Key Specifications—Why They Make a Difference

    The specifications we offer stem from our direct operational experience and rigorous laboratory analysis. We target a purity threshold above 99%, measured by HPLC, as lower grades introduce too much variability in downstream reactions. Water content no higher than 0.5% is standard, since excess moisture can lead to hydrolysis issues, especially during storage or shipment in humid climates. Our batches regularly show residual solvent concentration below 0.1%, achieved through controlled distillation and vacuum drying immediately post-crystallization.

    Particle size distribution affects reactivity and processing. For customers in resin or polymer synthesis, we mill the product to a 100-300 micron range that balances flowability with manageable dust levels in blending hoppers. We learned through customer feedback that size consistency shortens batch times and reduces waste. Customers in fine chemical synthesis sometimes seek a finer grade, so we adapted by setting up a closed-loop micronizer. Every shift learns to adjust parameters, based on real-world conditions, rather than relying solely on lab data.

    Real-World Use Cases

    Pent-2-Ene-1,5-Dioic Acid finds utility across organic synthesis, typically as a diene precursor or monomer unit for specialty polyesters and alkyd resins. It allows formulators to create novel backbone architectures, especially when other unsaturated diacids like maleic or fumaric acid do not produce the desired polymer properties. The double bond in the 2-position facilitates Diels-Alder additions, enabling rapid assembly of more complex molecules.

    Outside the realm of polymer chemistry, we have seen partners in pharmaceutical R&D pursue analogs of this acid for intermediate steps in API synthesis. Its platform status appeals to those pursuing green chemistry: the structure supports catalytic hydrogenation schemes and selective functionalization, which can simplify multi-stage synthesis routes. Over time, we’ve collaborated with teams seeking to minimize hazardous waste by switching from aromatic diacids to more readily biodegradable aliphatic acids like this one.

    These applications rarely follow textbook pathways. Our plant has fielded requests for custom blends containing Pent-2-Ene-1,5-Dioic Acid along with other dicarboxylic acids, used for polymer toughening or to adjust glass transition temperatures. The research and production teams share their experience with formulation bottlenecks directly with customers so both sides can solve process hurdles together, whether the need is enhanced thermal resistance or improved solubility in specific solvent systems.

    Why Pent-2-Ene-1,5-Dioic Acid Stands Apart

    In practice, the double bond placement separates this molecule from generic counterparts. Glutaric acid, for example, lacks any unsaturation, which limits its reactivity in certain synthesis routes. Maleic acid and fumaric acid both introduce trans and cis geometries but tie the double bond directly to the carboxyl groups, constraining their use in certain ring-closing schemes. Pent-2-Ene-1,5-Dioic Acid rides a sweet spot—long enough carbon backbone to avoid excessive volatility and just the right unsaturation to enable flexible modification.

    We’ve found that performance advantages show up most clearly in specialty polyesters. The derived polymers tend to show increased toughness and weather resistance. For paint resin formulators, this translates to enhanced adhesion on a wider range of substrates, and for film producers, it means better clarity and less yellowing after UV exposure.

    Competitor acids often fail to deliver similar outcomes, not because they lack quality, but because the molecular structure doesn't provide the same degree of control over copolymer ratios and side-chain addition sites. Over years of pilot batches and scale-ups, we saw that switching a portion of phthalic acid out for Pent-2-Ene-1,5-Dioic Acid boosted flexibility without sacrificing mechanical strength. These insights come not from theory, but from hundreds of operator hours blending, curing, and testing compound formulations for coatings, adhesives, and specialty elastomers.

    Stability and Handling—Lessons Learned in the Plant

    Every chemical has its quirks, learned in the handling as much as in the laboratory. Pent-2-Ene-1,5-Dioic Acid stores well in nitrogen-purged bags away from light, which keeps the double bond from isomerizing or reacting with trace oxidants. Our team tracks container weights each week to catch physical loss before it becomes a quality problem. Hygroscopic pickup from humid air prompted us to switch to double-sealed packaging and silica gel liners a few years ago.

    Bulk transfer and blending gave us new perspectives, too. Fine particles can agglomerate if loaded too quickly or exposed to moisture mid-process. We learned that slow auger feeding under dry air solves most flow issues. Factory-floor feedback led us to redesign dust extraction at blending points—real operators with actual tools make the difference. All these small process fixes build up to resilience, which wards off batch variability and keeps production on a steady tempo.

    Insight from Decades of Manufacturing

    The longer one manufactures chemicals for modern industry, the clearer the pattern becomes. Consistent inputs yield consistent results, not just in the product but in the relationships and trust we develop with both established partners and start-up ventures experimenting with novel applications. Pent-2-Ene-1,5-Dioic Acid wasn’t always a front-runner—we worked through uneven batches, suboptimal purification methods, and feedback from the field when polymers degraded or lost flexibility months after testing.

    Adjustments followed no script but depended on the experience of technicians and chemists who tracked analytic and process changes year over year. In the early days, inconsistency plagued our scale-up runs, promptings tests for alternative recrystallization solvents and modified purge-regimens. We noticed that slight acidity in process water could impact the isomer ratio in the final product, so we installed new pH monitoring units that run on each cycle.

    With time, we’ve helped customers reduce solvent use and waste, tailoring product characteristics at source. We cut down on repeated melting and recrystallization by tightening in-line filtration and clarifying slurries, sparing both energy and material. Direct feedback cycles between operations and R&D now shorten troubleshooting, as plant-based experience translates to bench-scale prototypes, which reduces the risk of sending imperfect product to market.

    Comparing to Other Dicarboxylic Acids

    Through dialogue with end-users and our own process trials, distinctions get sharper. In hot-melt adhesives, alternative dicarboxylic acids often produce inferior shelf stability. We ran side-by-side production runs substituting various acids, including adipic and succinic acid, learning that the final film’s tensile properties and resistance to creep shifted with each substitution. With Pent-2-Ene-1,5-Dioic Acid, we consistently hit better bond strength and much less odor post-application, which makes a real-world difference in consumer-facing products.

    Some intermediates rely on regio-selectivity not achievable with more common diacids. Previous attempts to use muconic acid in similar applications often introduced unwanted cross-linking or inconsistent yields. We’ve engineered reaction pathways that exploit the linear backbone and double bond position of Pent-2-Ene-1,5-Dioic Acid to generate cleaner transformations, cutting down by-products in downstream purification.

    Every batch tells a story—yield, purity, and processing time are not abstract numbers but real factors shaping how well a product serves its purpose across industries ranging from automotive to medical device manufacturing. Over the years, we have observed that slight tweaks in polymer backbone—often as little as swapping 5% of the acid monomer input—can move a formulation from pilot scale disaster to market-ready performance.

    Sustainability and Safer Chemistry

    The march toward sustainability led us to rethink supply chain, raw materials, and purity demands at every step. Sourcing began with a focus on traceability and low-impact production. Often, we worked with bio-based feedstocks for the five-carbon backbone, validating each batch’s biogenic carbon content through accredited labs. We kept careful records of solvent emissions and waste streams for every shift.

    Safe handling means more than ticking off regulatory boxes. We design storage and loading systems to avoid worker exposure to fine powders or reactive dust. Our teams undergo regular training on spill prevention, containment, and emergency response, and incorporate new incident feedback into the next round of SOP adjustments. For downstream customers, we openly share these learnings—for example, suggesting simple measures like dehumidified transfer lines or custom pack sizes that reduce repackaging.

    Our journey with Pent-2-Ene-1,5-Dioic Acid tracks with a larger push for green chemistry and more efficient industrial processes. Real improvements don’t appear in marketing literature but in reduced effluent volumes, fewer off-spec bags, and reliable, repeatable performance for processors at all scales. We work with customers on closed-loop system implementation, solvent recycling, and post-process residue collection. These efforts not only lighten environmental footprint but also save on operational costs over time.

    Partnerships, Problem-Solving, and Innovation

    No specialty chemical finds its place in the market alone. We’ve partnered with academic researchers testing new esterification pathways, resin formulators solving for lower VOC emissions, and start-ups exploring biodegradable polymers. Every phone call, sample shipment, and lab-scale test bench run feeds back into continuous improvements.

    Practical innovation grows in the exchange between plant-floor wisdom and laboratory curiosity. For example, several years ago a coatings manufacturer approached us with repeated issues in achieving high-gloss finishes with traditional polymer backbones using only phthalic and maleic acids. Working side by side, we blended Pent-2-Ene-1,5-Dioic Acid into the formulation. Real Quality Control data showed increased gloss, scratch resistance, and improved pot-life. These results were not achieved by theory alone but by tailored process modifications and patient trials.

    With every product, unexpected challenges crop up. One resin plant noted gelling problems during hot summer months; together, we ran side experiments in temperature-controlled rooms on site to map out safe windows for adding the new acid without runaway reactions. After two seasons of careful adjustment, their seasonal off-grade rates dropped by over 20%. Shared experience made the process smarter.

    What Our Continued Experience Teaches

    After years of blending, testing, and analyzing Pent-2-Ene-1,5-Dioic Acid for different industries, we learn something new from each unexpected problem. It may be a filtration hiccup during a humid week, or a shift in polymer properties from a raw material source change. What matters is the willingness to trace every issue to its source, iteratively improve, and share those solutions openly.

    As a manufacturer, our confidence in this compound rests not on isolated lab performance, but on a portfolio of satisfied users, repeatable production runs, and feedback from engineers and chemists. The evolution from early, inconsistent batches to reliable modern production stands as a product of daily diligence, not luck or salesmanship.

    Customers continue asking for higher purity, tailored particle size, and smarter packaging—and we respond by investing in new equipment, analytical tools, and training. We remain alert to the demands of innovation, regulatory shifts, and rising concerns about sustainability. Being on the manufacturing side, we follow through not just with chemistry but with transparent, accountable service built on direct experience. And as application fields for Pent-2-Ene-1,5-Dioic Acid keep expanding, our priority remains clear: put best-in-class material into the hands of those building the future of advanced materials, adhesives, and specialty polymers.