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HS Code |
957606 |
| Product Name | Cis-5-Norbornene-Endo-2,3-Dicarboxylic Acid |
| Cas Number | 609-07-2 |
| Molecular Formula | C9H8O4 |
| Molar Mass | 180.16 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 210-214°C |
| Solubility In Water | Slightly soluble |
| Density | 1.5 g/cm³ (approximate) |
| Smiles | C1C2C(C1C(C2)C(=O)O)C(=O)O |
| Inchi | InChI=1S/C9H8O4/c10-8(11)6-3-1-2-5(6)4-7(12)9(6)13/h5-7H,1-4H2,(H,10,11)(H,12,13) |
| Pubchem Cid | 12771 |
| Storage Temperature | Store at room temperature, tightly closed |
As an accredited Cis-5-Norbornene-Endo-2,3-Dicarboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle with secure screw cap, labeled “Cis-5-Norbornene-Endo-2,3-Dicarboxylic Acid, 25 grams,” hazard and handling warnings displayed. |
| Shipping | Cis-5-Norbornene-Endo-2,3-Dicarboxylic Acid is shipped in tightly sealed containers, protected from moisture and extreme temperatures. Packaging complies with chemical handling regulations to prevent leaks or contamination. Ensure the container is correctly labeled and accompanied by the relevant Safety Data Sheet (SDS) for safe transportation and storage. Handle with care according to hazardous material guidelines. |
| Storage | Cis-5-Norbornene-endo-2,3-dicarboxylic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect it from moisture and direct sunlight. Store at room temperature, and follow standard laboratory chemical safety protocols to prevent contamination and maintain product stability. |
Applications of Cis-5-Norbornene-Endo-2,3-Dicarboxylic Acid in Industrial ManufacturingAs a leading producer of Cis-5-Norbornene-Endo-2,3-Dicarboxylic Acid, we support various industries that rely on its unique structure for specialized polymerization and material synthesis. Below, we detail proven downstream segments where this intermediate is integrated for advanced manufacturing, highlighting essential compliance, formulation specifications, operational steps, and delivered finished goods. 1. Cycloolefin Copolymer (COC/COP) Synthesis for Advanced PackagingCis-5-Norbornene-Endo-2,3-Dicarboxylic Acid plays a critical monomer role in COC/COP production, enhancing thermal stability and clarity for high-barrier pharmaceutical and medical packaging applications. Its bicyclic structure facilitates the ring-opening metathesis polymerization (ROMP) process, achieving elevated glass transition temperatures and minimized extractables—essential for demanding regulatory markets. Industry compliance standards
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2. Polyimide Resin Modification for Electronic SubstratesThis compound acts as a rigid dianhydride alternative or comonomer in polyimide resin formulations to increase thermal resistance and reduce dielectric constant, which is essential for next-generation flexible circuits and high-frequency PCB laminates. Its influence on chain packing and imidization chemistry leads to substrates that sustain reflow soldering and precision photolithography demands. Industry compliance standards
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3. Modifier for Unsaturated Polyester Resins in High-Performance CompositesThe dicarboxylic acid structure serves as a specialty modifier during polymerization of unsaturated polyesters, where its inclusion increases crosslink density and chemical resistance—imperative for automotive, marine, and industrial composite panels subject to corrosive conditions and loading cycles. This targeted functionalization tailors end properties beyond what phthalate or maleate systems can achieve. Industry compliance standards
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4. Crosslinking Agent in Specialty Epoxy FormulationsIn epoxy resin chemistries, the molecule functions as a multifunctional hardener or chain extender, introducing polar carboxyl groups while maintaining dimensional stability. This enables customized network structures required for potting compounds, high-voltage insulators, and structural adhesives where both rigidity and chemical impermeability are critical. Industry compliance standards
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5. Intermediate for Flame Retardant Polymeric AdditivesAs an intermediate, the compound is utilized for synthesizing advanced polycarboxylate flame retardant adducts, which improve char-forming behavior in engineering plastics. Its bicyclic architecture offers enhanced thermal decomposition pathways that complement phosphorus- or halogen-free systems in wire coatings, construction panels, and mass transit interiors facing aggressive fire performance benchmarks. Industry compliance standards
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Our team first encountered Cis-5-Norbornene-Endo-2,3-Dicarboxylic Acid as part of a series of metabolic intermediates. Chemists under our roof quickly realized the unique cycloalkene backbone this molecule offers and how its endo orientation gives researchers a different handle on reaction outcomes. We’ve produced this acid in our main plant for over a decade, seeing requests shift from traditional uses in cross-linking agents to a surge in advanced materials projects.
With the rise of precision-engineered plastics and more efficient catalyst supports, interest has only increased. Our team’s conversations with researchers and manufacturers have made one thing clear: slight differences in stereochemistry change everything. Endo-2,3-dicarboxylic acid opens up avenues that exo isomers can’t touch, and that subtlety has kept us focused on refining our own fermentation-derived routes. From the day-to-day, each batch runs through hands-on, in-house NMR checks to confirm the model: cis, not trans; endo, not exo.
Small details define the day in chemical manufacturing. The cis-fused ring structure in this norbornene acid creates a tight, strained framework, which customers have leveraged for selective reactions and advanced organics development. We’ve run side-by-side tests versus common dicarboxylic analogs. Classic glutaric or fumaric acids can’t replicate the ring strain or orientation-dependent reactivity. That explains why a number of our polymer sector clients keep this norbornene acid on recurring order—this material delivers the reactivity bump required to get specialty adhesives and polyimides over their yield thresholds.
We see requests for both fine and bulk grade. Some partners need crystalline batches with minimal trace metals for pharmaceutical research. Others prefer technical grade for resin synthesis, factoring in the heat transfer data we include from every batch. Our team’s control over particle size distribution has come from years of downstream filtration and crystallization optimization. No outsourced processes muddy the chain; everything happens under one roof, from purified starting bicyclo[2.2.1]hept-5-ene derivatives to finished acid, checked by hands in the same building each step of the way.
Chemists enjoy talking about “steric hindrance,” but real performance tells the story better. Our own process began to shine once we stopped treating cis-5-norbornene derivatives as just molecular curiosities and started listening to what bench chemists reported. That insight changed our filtration approach and our drying protocols. It became obvious the pattern of carboxyl substitution directly affects esterification speed during copolymer formation or ligand coupling in metal-organic frameworks. We document every reaction at a practical level: What does it take to get complete dissolution in different solvents? How do scale jumps affect purities?
Lifecycle studies revealed that our acid, in the cis and endo form, resists hydrolysis more effectively than its exo cousin, particularly in certain resin-casting steps where moisture is nearly impossible to control. This quality reduces batch loss and rework, helping both us and our partners save on raw input costs. We watch the trends: as more green chemistry initiatives hit the industry, customers appreciate we provide evidence from batch-level lab trials, not just summary statements.
Details like melting point and acid equivalence could fill a pamphlet, but practical experience tends to help more than tables. Our cis-5-norbornene-endo-2,3-dicarboxylic acid consistently measures a distinct melting range, tight enough to ensure batch-to-batch reproducibility but resilient to small environmental fluctuations. Overheated reactors, scale-up scorch, and solvent drag can all threaten acid integrity. We test each batch for signs of ring opening and side product formation before it gets a shipment tag. That level of attention means fewer headaches for the end-user.
Our reactors favor a catalytic process to ensure cis orientation is locked in. Years ago we retooled after noticing trace exo isomers in some competitors’ lots. Those tiny fractions derailed end uses where only the correct enantiomer unlocks a successful step. Quality isn’t an abstract pledge on a label—it’s the direct result we see in customer yields and lower process upsets.
Making this acid isn’t just a matter of following the textbook route. Over countless production runs, our operators routinely tweak reaction conditions to meet shifting project demands. Pharmaceutical research often requires crystalline, low-residual solvent lots, checked against internal GC-MS data. Advanced polymer makers request extra filtration to minimize fines and maximize compatibility in emulsion synthesis. We chart these specs in close cooperation with R&D chemists, often running split batches to deliver feedback data before the full order rolls out.
Through workshops and site visits, we’ve witnessed this acid excel where others fall short: tough copolymerization steps, difficult Diels-Alder reactions, challenging nucleophilic substitution. We support partners pushing boundaries with new block copolymer architectures, bioresorbable medical device work, and next-generation battery electrolytes. Traditional dicarboxylic acids lack the steric muscle or defined geometry required for some of these innovations. Our feedback loop with users creates better products—not in the abstract, but measured in production efficiencies and lower failure rates.
Inside cycloaddition chemistry and polymer development, subtle differences in isomer arrangement often mean the difference between industrial success and an expensive headache. We learned early on that the endo orientation—where carboxylic groups point inside the norbornene framework—changes thermal and chemical behavior, sometimes dramatically. Customers specializing in electronics or medical-grade materials depend on this reliability to meet the stringent performance benchmarks their markets demand. Feedback from these technical fields led us to deepen our own analytical tracking, monitoring batch purity at every scale-up step.
The contrast stands out most when side-by-side with the exo version. Exo-2,3-dicarboxylic acid often delivers disappointing reactivity in post-polymerization modification, especially in applications where chemical selectivity and steric control drive long-term stability. Lab partners who have switched from exo to our endo form cite fewer downstream purification cycles and a marked improvement in conversion rates for functional materials. In effect, it’s a matter of choosing the right tool for the molecular job, and our continued feedback loop with end-users ensures we hone the product that best matches those needs.
Real-world use cases highlight the acid’s versatility. In adhesives manufacturing, our acid pairs with specialty amines to yield crosslinked network polymers showing superior mechanical strength. Commercial insulation firms seek out our endo acid for new-generation polyimides, where higher glass transition temperatures are a must. In the laboratory, pharmaceutical chemists value our product for precise chiral synthesis—a role generic dicarboxylic acids can’t fill.
A memorable application came through a partner developing conductive polymers for energy storage. Their process needed a repeatable, high-yield Diels-Alder intermediate. The batch-to-batch reproducibility of our norbornene acid provided them the edge to step from lab scale into pilot line operations. We continue to compare notes on downstream modifications, documenting not just what works, but why certain isomer forms outperform others under real conditions.
Many manufacturers know the pain of off-spec delivery. Our experience taught us control of particle size and moisture absorption reduces common handling setbacks. Opening a drum at the point of use should never introduce clumping or degradation—simple steps like inert atmosphere packing and robust liner selection help us ship across climates and warehouse conditions without missing a beat. We keep logs of every batch’s logistics chain—not just for compliance, but so we can diagnose and fix root causes if challenges emerge in the field.
Stability testing simulates not only worst-case temperature and humidity, but practical lab benchtop use, frequent recapping, and container changes. Customers in both small-scale research and multi-ton commercial polymer runs rely on that confidence. By tracking feedback on caking, rehydration, and flowability, we continue iterating on both the core product and packaging methods. If batches show drift in consistency, root-cause analysis happens immediately on the same floor where synthesis takes place, not shuffled through distant third parties.
Strong partnerships come from trust, and trust starts with information. Chemists and process engineers who rely on us expect not only a reliable product, but supporting data on purity, batch analysis, and supply chain traceability. Each drum ships with detailed lot records, chromatographic fingerprints, and measured performance data relevant to key applications. Over the years, visiting partners have even walked our QC lines to watch checks unfold first hand, gaining extra confidence that our process meets evolving regulatory and application needs.
We support knowledge transfer—published case studies describe conversion yields in standout applications, and we publish bulletins on process improvements or analytical advances. By sharing both successes and obstacles, we find every production season brings a sharper approach and a closer fit between raw material and finished product.
Stringent wastewater management, closed-loop solvent recovery, and in-house hazardous emissions controls anchor our approach. As downstream clients face increasing regulatory scrutiny, we are ready with audit and compliance documentation. Close partnerships with environmental auditors help us track improvements, ensuring our norbornene acid remains a sustainable choice for partners seeking to lower their carbon and waste footprints.
Initiatives to recycle mother liquors and recover key intermediates have both cut costs and reduced environmental impact over the past years. Systems to capture VOCs and monitor chemical storage mean lost product and emissions reach minimal levels. For manufacturers in sectors sensitive to environmental oversight, our ongoing improvements and transparency create a reliable, low-risk input for challenging and tightly regulated production environments.
Each batch reflects years spent tracking down process bottlenecks and optimizing every step, from feedstock selection to final packaging. No product line stands still: chemical manufacture means living with continual challenges. Our technicians run pilot batches before any change in raw material or equipment, building institutional knowledge that lets us anticipate downstream issues before they can slow partners’ lines.
Technological improvements—better control of temperature ramps, automation of cooling and drying steps, and advanced analytics for residual solvent detection—grow from lessons learned through real missteps, not theoretical best practices. Customer issues drive our production meetings. By closing the loop with direct feedback, we build processes that withstand not just the easy cycles, but challenging runs and production scale-ups.
Problems can be signposts. Years of fulfilling demanding technical orders put us in daily touch with new analytical techniques, fresh reaction conditions, alternate blending strategies, and more. Our technical service staff operate from within the manufacturing environment, not distant offices, ensuring the lessons of each campaign inform the next ones. Problems—from solubility quirks to handling challenges—get triaged and solved by teams who run the reactors, not referenced from a manual.
That practical ownership has led us to incrementally improve the value and reliability of our cis-5-norbornene-endo-2,3-dicarboxylic acid year after year. A small solubility tweak today, an analytic check on trace byproducts tomorrow—our partners see the results in reduced rework and improved process economy. Each trouble ticket, each field trial, and every on-site customer challenge shows up in our ongoing approach to better product outcomes.
As custom synthesis becomes a bigger part of the materials market, the place for thoughtful, robust dicarboxylic acids grows. Partners in next-wave electronics, green energy, and biocompatible materials ask for tailored input acids capable of supporting ever more complex synthetic targets. We see the potential: ring-strained cycloalkenes powering new reaction pathways, fine-tuned stereochemistry driving up conversion yields, small changes rippling into major improvements on production lines.
At the core, our experience affirms that manufacturing isn’t just making molecules—it’s about listening to where those molecules create value in hard-fought processes. Each production run, each batch checked and rechecked, every question answered from the floor rather than a script—these make the cis-5-norbornene-endo-2,3-dicarboxylic acid we ship not just a reagent, but a reliable foundation for tomorrow’s breakthroughs.