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5-Norbornene-2-Endo,3-Exo-Dicarboxylic Acid

    • Product Name 5-Norbornene-2-Endo,3-Exo-Dicarboxylic Acid
    • Alias cis-5-Norbornene-exo-2,3-dicarboxylic acid
    • Einecs 208-863-7
    • 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

    394120

    Chemical Name 5-Norbornene-2-endo,3-exo-dicarboxylic acid
    Molecular Formula C9H8O4
    Molecular Weight 180.16 g/mol
    Cas Number 872-36-6
    Appearance White to off-white powder
    Melting Point 182-185°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Boiling Point Decomposes before boiling
    Density 1.46 g/cm³ (approximate)
    Smiles OC(=O)[C@H]1[C@H]2C=CC[C@@]2(C(=O)O)C1

    As an accredited 5-Norbornene-2-Endo,3-Exo-Dicarboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "5-Norbornene-2-endo,3-exo-dicarboxylic acid, 25g," with safety warnings, chemical structure, and lot number.
    Shipping 5-Norbornene-2-endo,3-exo-dicarboxylic acid is shipped in tightly sealed, chemical-resistant containers, protected from moisture and direct sunlight. The packaging complies with local and international regulations for the transport of laboratory chemicals, ensuring safety and stability during transit. Appropriate labeling and documentation accompany each shipment for hazard identification and safe handling.
    Storage 5-Norbornene-2-endo,3-exo-dicarboxylic acid should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers and bases. Store at room temperature and ensure proper labeling to prevent accidental misuse. Handle with appropriate personal protective equipment to avoid skin or eye contact.
    Application of 5-Norbornene-2-Endo,3-Exo-Dicarboxylic Acid

    Applications of 5-Norbornene-2-Endo,3-Exo-Dicarboxylic Acid in Industrial Manufacturing

    5-Norbornene-2-endo,3-exo-dicarboxylic acid serves as a key intermediate in several advanced downstream production fields, where its bicyclic structure and dicarboxylic functionality drive performance in specialty polymers, adhesives, resins, and fine chemicals. As a direct manufacturer, we provide industrial customers with high-purity material meeting strict specification demands for regulated production environments.

    1. High-Performance Polyimide Resin Production

    Polyimide resin manufacturers use this dicarboxylic acid as a dianhydride precursor, allowing for controlled imide ring formation and rigidity in high-temperature insulation and films. The molecular structure introduces specific chain stiffening, required in aerospace, semiconductor fabrication, and flexible circuit applications that must withstand extreme conditions for extended periods. Each production batch relies on consistent raw acid quality to assure reproducible polymer characteristics and to meet global safety and performance regulations.

    Industry compliance standards

    • IEC 61249-2-12 (Polyimide materials for printed circuit boards)
    • UL 94 V-0 (Flame-retardancy of plastic materials)
    • IPC-4101 (Specification for base materials for rigid and multilayer boards)
    • REACH Regulation (EC) No 1907/2006 compliance

    Typical usage ratio

    • Monomer loading typically ranges from 20–35 mol% of total tetracarboxylic acid content for targeted polymer architecture; adjustment depends on imidization control and desired glass transition temperature.

    Downstream process integration

    • The acid enters the polyamic acid synthesis step, reacting with aromatic diamines under nitrogen at low to moderate temperatures, followed by thermal or chemical imidization to yield the final polyimide chain structure.

    Final product types

    • Flexible polyimide films
    • High-temperature resistant fibers
    • Microelectronic thin film substrates
    • Coatings for circuit boards and aerospace insulation

    2. Thermosetting Epoxy Modifier Synthesis

    Manufacturers of advanced thermoset epoxies incorporate this bicyclic dicarboxylic acid into formulations to enhance chemical resistance, dimensional stability, and toughness by introducing rigid structural units at the curing phase. The acid’s carboxyl groups react with epoxide groups during cross-linking, leading to improved heat resistance and minimized shrinkage in electronics casting compounds and structural adhesives, critical for long-term reliability in electrical and automotive environments.

    Industry compliance standards

    • IPC-4104 (Spec for multilayer rigid and flexible substrate materials)
    • RoHS Directive 2011/65/EU
    • ASTM D1652 (Test methods for epoxy content)
    • IEC 60695-11-10 (Fire hazard testing)

    Typical usage ratio

    • Common addition levels: 2–8 phr (parts per hundred resin) based on target network density and required mechanical modulus; ratios tailored to user-defined performance windows.

    Downstream process integration

    • The acid is blended into the epoxy resin prior to curing, where it participates in the cross-linking reaction—either through pre-reaction to create modified epoxy or as a co-curing agent in the primary formulation tank.

    Final product types

    • Encapsulation compounds for semiconductor devices
    • Printed circuit board prepregs
    • Structural adhesives in automotive assembly
    • High-temperature potting resins

    3. Unsaturated Polyester Resin Modifier

    Composite manufacturers utilize this bicyclic dicarboxylic acid to achieve higher rigidity and dimensional stability in unsaturated polyester resin (UPR) formulations. By introducing non-linear, sterically hindered carboxyl units, formulators improve cross-link density and thermal distortion thresholds, essential for demanding applications such as corrosion-resistant pipe systems, tank linings, and protective composite panels.

    Industry compliance standards

    • ASTM D638 (Standard Test Method for Tensile Properties of Plastics)
    • EN 13121 (GRP tanks and vessels for use above ground)
    • ISO 9001:2015 certified manufacturing procedures
    • REACH Annex XVII for restricted substances

    Typical usage ratio

    • Incorporation rate typically set between 0.5–3.0 wt% as a co-monomer or modifier, depending on reactivity ratio with maleic anhydride and desired end-use properties.

    Downstream process integration

    • Added during polyesterification together with primary diacids and glycols, or as a post-polymerization modification to adjust resin viscosity and cross-linking behavior.

    Final product types

    • Chemical-resistant fiberglass pipes
    • Industrial storage tank linings
    • Marine composite panels
    • Thermoset molded housings

    4. Functional Dianhydride Building Block for Specialty Coatings

    In specialty coating intermediates, this compound serves as a precursor for synthesizing functional dianhydrides, utilized by paint and varnish formulators aiming for improved solvent resistance and adhesion on metals and engineered plastics. The precise control over ring structure ensures defined curing kinetics and surface hardness, valuable in the manufacture of anti-corrosion primers and protective coatings for demanding industrial and marine settings.

    Industry compliance standards

    • ISO 12944-6 (Paints and varnishes - corrosion protection)
    • ASTM D3359 (Standard Test Methods for Adhesion by Tape Test)
    • Directive 2004/42/EC (VOC content in paints)
    • GMP for coatings under FDA Title 21 CFR 175.300 (Food contact surfaces)

    Typical usage ratio

    • The precursor forms up to 15–40 mol% of total dianhydride used in advanced polyamic acid preparations for subsequent conversion to imide-containing coatings.

    Downstream process integration

    • Synthesized dianhydride intermediate is first prepared from this acid, then dissolved in appropriate solvents alongside diamines and curing agents before film deposition by spray, dip or blade-coating.

    Final product types

    • Anti-corrosive primers for metal structures
    • Solvent-resistant varnishes for plastic housings
    • Engineered coatings for offshore equipment
    • Electrical insulation coatings for transformers

    5. Pharmaceutical Fine Chemical Intermediate

    The molecular rigidity and bifunctional carboxylic moieties make this acid suitable for synthesis of specialty fine chemical building blocks used in active pharmaceutical ingredient (API) manufacturing. Chemical development teams integrate it for ring closure steps, linker introduction, or as a scaffold in the formation of advanced intermediates, contributing to patent-protected synthesis routes and chiral API development programs.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) under ICH Q7 (Active pharmaceutical ingredients)
    • USP/NF monographs for intermediates (where applicable)
    • European Pharmacopoeia (Ph. Eur.) requirements for fine chemicals
    • FDA 21 CFR Part 210/211 (Pharmaceutical manufacturing)

    Typical usage ratio

    • Applied in stoichiometric quantities as dictated by targeted step yield; typically 1.0–1.2 mol equivalents based on desired conversion rates and purification criteria.

    Downstream process integration

    • Charged as a starting acid or as a coupling partner for condensation reactions, undergoing further transformations including esterification, amidation, or cyclization, sequenced per validated batch and continuous processes.

    Final product types

    • Chiral building blocks for drug synthesis
    • Key scaffolds in heterocyclic pharmaceutical intermediates
    • Precursor units for oncology API programs
    • Modular linkers for antibody-drug conjugate development
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    Certification & Compliance
    More Introduction

    5-Norbornene-2-Endo,3-Exo-Dicarboxylic Acid: Beyond the Basics in Synthesis

    Pushing the Limits of Dicarboxylic Acid Utility

    Over decades of hands-on production, we’ve observed a good number of organic acids drift through laboratories and industrial plants—phthalic, succinic, you name it. 5-Norbornene-2-Endo,3-Exo-Dicarboxylic Acid stands apart each time the question of synthetic versatility comes up. We make this material onsite, starting with high-pressure Diels-Alder techniques rather than relying on generic intermediates. This choice turns out to be more than a technicality; it shows in both the purity and the physical consistency of every batch.

    This molecule isn’t just a two-headed carboxylic acid. Its rigid norbornene skeleton brings a unique reactivity that chemists still regularly exploit for niche polymer backbones and catalyst frameworks. Unlike more linear or symmetrical dicarboxylic acids, the norbornene core keeps the carboxyl groups locked in an orientation that opens new doors in molecular design. In our experience, this spatial arrangement has proven crucial for high-performance materials development, particularly in scenarios demanding well-defined cross-linking points or where the polymer backbone itself needs an added level of chemical resistance.

    Naming, Models, and Why Structure Always Matters

    Ask any synthetic chemist why structure makes a difference, especially with norbornene derivatives, and you’ll see a familiar smirk. The 2-endo,3-exo configuration isn’t just nomenclature—it dictates the way this acid enters reactions. For decades, we have refined our control over the endo and exo isomers, keeping a close eye on the downstream properties in whatever field customers are working: biomedical devices, smart membranes, or next-generation resins. The exo-oriented carboxyl group is more accessible in many transformations, and the endo group often modifies reactivity in subtle but important ways.

    Complex syntheses involving 5-Norbornene-2-Endo,3-Exo-Dicarboxylic Acid rarely unfold the same way as when using maleic or fumaric acid. The norbornene ring shifts stereochemistry and electron density, making it an exceptional candidate for ring-opening metathesis polymerization (ROMP). Every time a client arrives aiming to build advanced photoresists or robust ion-exchange resins, they recognize pretty quickly that the norbornene core doesn’t behave like the more pedestrian aromatic dicarboxylic acids.

    Real-World Use: From Trial Reactions to Full Scale Manufacturing

    We have spent years learning what works with this compound and how it can fall short when used with certain catalysts or under harsh conditions. Our on-site quality control ensures batch-to-batch consistency, especially because even slight differences in crystalline habit or trace byproducts can throw off large-scale applications. The acid finds its way into demanding synthesis steps, often as a bridge to highly functionalized intermediates or polymers.

    Chemical manufacturers want reliability—a trait developed through years of seeing what fails in actual production, not just in a theoretical data sheet. If you plan to use 5-Norbornene-2-Endo,3-Exo-Dicarboxylic Acid for ROMP, our experience backs up the need for minimal unsaturation impurities and tightly controlled particle size. We have proven, through plenty of iterative process improvements, that careful purification after the Diels-Alder step and subsequent hydrolysis pays dividends in both activity and color stability, particularly when final users are aiming at high-end electronics or medical-grade plastics.

    Our application chemists always remind collaborators that this acid produces polymers with significantly higher glass transition temperatures compared to what you get from open-chain dicarboxylic acid-based monomers. That alone has made it a preferred choice in membranes designed for aggressive filtration, where dimensional stability and long-term resistance to solvents separate successful products from those that fall apart or leak after just a few cycles.

    Comparison With Other Dicarboxylic Acids

    Many industries still rely on more accessible dicarboxylic acids—adipic, maleic, even simple phthalic acids—for standard polyesters or copolymers. Those compounds serve their purpose if mechanical strength and temperature performance aren’t pushed to the limit. In contrast, 5-Norbornene-2-Endo,3-Exo-Dicarboxylic Acid reliably provides rigidity and strain tolerance you cannot engineer into simple linear or aromatic acids. This distinction matters most for specialty applications: aerospace, high-end composites, and demanding electronics.

    Aromatic dicarboxylic acids tend to impart chemical resistance but lack the backbone flexibility for certain modern uses, while aliphatic ones give softness but can’t handle heat or stress. Norbornene-based acids deliver the sweet spot of rigidity with slight molecular flexibility—especially beneficial in engineering polymers needing both shape retention and some wiggle room at a molecular level.

    Specifications That Actually Shape Performance

    Across our batches, we consistently aim for acid purities above 98 percent, with water and ash content held to tightly defined thresholds. Real-world application doesn’t leave much room for error, so we’ve invested in full-spectrum NMR analysis and chromatographic profiling directly onsite. Methods like single-crystal X-ray confirmation have let us assure structure for research users requiring traceability all the way down to the stereochemical level.

    From a handling perspective, our material enters the market in fine crystalline powder, never agglomerated bulk. Chemists working at the bench or moving to pilot plant appreciate this finer sizing—not only for easier weighing and dissolution but also for steady feedstock behavior in automated mixing and extrusion systems. The fine particle habit allows for accurate dosing in multistep processes—especially essential in continuous-flow synthesis setups, where blockages and flow variability can drag down plant uptime fast.

    Role in Next-Generation Polymer Design

    Speak with any synthetic chemist developing specialty polymers for batteries or tailored coatings, and their requirements often hang on how well the monomer resists outgassing or hydrolysis. Hydrogen-bonding capability and backbone stiffness determine everything from operating temperature to reactivity sequence during polymerization. Years of application trials have confirmed what literature hinted at: 5-Norbornene-2-Endo,3-Exo-Dicarboxylic Acid forms backbones that outperform many traditional dicarboxylic acids, especially under heat or in aggressive chemical environments.

    At the manufacturing level, this translates directly to fewer lot-to-lot failures and more consistent end product dimensions. We’ve collaborated with electronics firms that demand patternable, photosensitive polymers free from migration or yellowing. Our norbornene-based acid has proven up to the job each time, where more flexible dicarboxylic acids have failed to deliver the necessary chemical rigidity.

    Traditional dicarboxylic acids tend to show their weaknesses at the edges of performance: poor edge retention, stress whitening, creeping at elevated temperatures. Polymers derived from norbornene-2-endo,3-exo-dicarboxylic acid, in contrast, maintain crisp dimension lines and reliable electronic properties across repeated thermal cycles. Our internal accelerated aging tests back up what end users see in automotive and precision component settings: parts come out looking the same after weeks in the heat as they did on day one.

    How We Improve Supplier-Customer Transparency

    Too many suppliers stop at the minimum bar for purity claims or physical descriptions. Our materials scientists won’t accept vague traceability; each lot carries verified analyses with impurity profiles that don’t just list ‘unknowns’ but specify them by retention time, NMR pattern, and—if needed—mass spectral signature. This approach isn’t about glossing up a certificate but making sure formulators can troubleshoot any downstream hiccup using robust data, not guesses.

    Working as the original manufacturer, we understand how earlier steps influence later performance. Over the years, we’ve invested in both instrumentation and team training to spot problems early. Our QC lab routinely fields requests from application partners to recheck compatibility or spot-check aging samples, offering deeper insight than what a generic spec sheet could provide. This creates a feedback loop where practical issues—static buildup, flow irregularities, or discoloration—get solved at the source, often with a tweak in the crystallization profile or drying parameters.

    Meeting Regulatory and End-Market Demands

    Being a manufacturer means more than just hitting technical targets; it requires keeping up with shifting regulatory landscapes, especially on residual solvent thresholds and trace impurity profiles. Across every batch, we track and minimize small-molecule byproducts using gas and liquid chromatography—crucial trust factors for medical or food-contact candidates, where compliance audits come unannounced and certification hinges on quantitative contaminant tracking.

    Late-stage product qualification usually reveals whether a raw material supplier has lived up to their statements. We provide not only standard GC/HPLC analysis but also method validation documents for clients pursuing complex registrations or certifications. By sharing our methodologies openly, we enable formulation changes or regulatory submissions to progress without surprises.

    Troubleshooting and Problem Solving in Real Applications

    Our technical contacts often walk formulation teams through issues that rarely show up in the literature: sticky mixing behavior at certain concentrations, unexpected shifts in viscosity during scale-up, or color changes under UV curing conditions. These practical problems trace directly to minor impurities or batch-inhomogeneity. We understand these pain points from having faced them ourselves in full-scale reactors, not simply at the lab bench.

    One specific area where we’ve made a difference lies in predicting when storage humidity or low-level metallic contamination will affect subsequent polymerization rates. For customers producing critical coatings or precision-molded segments, the slightest deviation in impurity profile risks a failed lot. In one memorable project, a tight window for moisture uptake meant revising both our drying and packaging protocols. Only with direct feedback from end users and our own pilot lines did we lock down the process, ensuring problem-free runtime no matter the season or warehouse conditions.

    Why Our Team Cares About Process Traceability

    Working at scale means embracing challenges others leave to chance. Every critical parameter in our own Diels-Alder reactors—temperature ramp profiles, pressure cycling, catalyst concentrations—traces directly to the reproducibility of the endo/exo product ratio. This matters for catalysis clients optimizing reaction sites and for polymer formulators relying on predictable melt flow and glass transition points.

    Our process engineers have learned through troubleshooting that seemingly minor adjustments in reaction time can nudge the exo content higher, tilting polymer characteristics toward improved mechanical resilience or altered cure rates. Achieving this degree of control takes years and a willingness to backtrack, document, and sometimes rebuild an entire reactor setup. Distributors rarely see this day-to-day grind, but customers down the line benefit with materials that do their job every run, not just in ideal lab conditions.

    Building Relationships Through Real Applications

    Over the years, we have worked side-by-side with polymer chemists, analytical R&D teams, and production engineers facing setbacks from less predictable suppliers. Direct access to the minds behind the process—chemists who developed the scale-up protocols and QA staff who fine-tuned the impurity clean-up—not only saves time, it forges trust. Our clients know they aren’t just another name in a database; they get clear answers, tailored advice, and a straight path between their own challenges and possible solutions.

    These connections go beyond transactions. If a membrane fabricator runs into an issue with filtration cutoff drift, or an electronics developer notices dielectric loss increases after field aging, they often loop back to us for troubleshooting. In each case, a solution usually lies in deeper process understanding, not just a tighter spec.

    Supporting Innovation Through Steady Supply

    In industries ranging from aerospace to water purification, disruptive products have emerged from patient reformulation based on the unique properties of norbornene-derived dicarboxylic acids. The ability to guarantee long-term supply continuity stands at the core of these efforts. Customers focusing on product launches or multi-step scale-up projects need confidence that not only does today’s batch deliver, but tomorrow’s run will match it, down to the byproduct fingerprint.

    Changeover planning, scale-up validation, and end-use claim support depend on shared data and processes. We continue to encourage developers working with 5-Norbornene-2-Endo,3-Exo-Dicarboxylic Acid to communicate both ambitions and setbacks; real progress emerges from honest talk and willingness to adapt.

    Charting the Next Steps in Norbornene Chemistry

    No one in the chemical industry stands still. As advanced composites and functional materials move forward, the tools—both molecules and processes—must keep pace. Every improvement we’ve made in purity, batch reliability, and application support has come from direct engagement with innovators and everyday production teams. By producing 5-Norbornene-2-Endo,3-Exo-Dicarboxylic Acid with unwavering attention to real-world utility, we aim to keep chemists and engineers at the forefront of their fields, helping them achieve things previously out of reach for classical dicarboxylic acids.

    In this environment, practical knowledge matters as much as technical specs. Our commitment comes from years of listening, testing, retooling, and learning from failures. That ethos guides everything from how we optimize reactors to how we write impurity reports and plan customer support.

    As chemical tools grow more sophisticated, the foundational molecules behind innovation can’t lag behind. We’re dedicated as practical partners—not just raw materials vendors—to keeping norbornene-based dicarboxylic acids ahead of the curve, backed by real experience and a clear record of success in the toughest applications the industry has to offer.