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1,1'-Ferrocenedicarboxylic Acid

    • Product Name 1,1'-Ferrocenedicarboxylic Acid
    • Alias 1,1'-Ferrocenediacetic acid
    • Einecs 821-442-7
    • 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
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    Specifications

    HS Code

    765705

    Chemical Name 1,1'-Ferrocenedicarboxylic Acid
    Molecular Formula C12H10FeO4
    Molecular Weight 282.06 g/mol
    Cas Number 1293-86-1
    Appearance Orange solid
    Melting Point 247-252 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Boiling Point Decomposes
    Density 1.8 g/cm3 (approximate)
    Purity Typically ≥98%
    Synonyms Ferrocene-1,1'-dicarboxylic acid
    Structure Type Sandwich compound (ferrocene derivative)
    Functional Groups Carboxylic acid
    Storage Conditions Store at room temperature, protected from moisture and light
    Ec Number 215-056-6

    As an accredited 1,1'-Ferrocenedicarboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1,1'-Ferrocenedicarboxylic Acid is supplied in a 25g amber glass bottle with a secure screw cap and clear labeling.
    Shipping **1,1'-Ferrocenedicarboxylic Acid** is shipped in tightly sealed, chemical-resistant containers to prevent moisture and air exposure. Packages are clearly labeled, handled with care, and transported in accordance with local and international regulations for chemical substances. Safety data sheets and hazard information accompany all shipments to ensure safe and compliant delivery.
    Storage Store **1,1'-Ferrocenedicarboxylic Acid** in a tightly closed container, in a cool, dry, well-ventilated area, away from sources of moisture and incompatible materials such as strong oxidizing agents. Protect from light and avoid excessive heat. Use appropriate safety precautions, including gloves and eye protection, when handling. Follow all relevant safety and environmental regulations for storage and disposal.
    Application of 1,1'-Ferrocenedicarboxylic Acid

    Applications of 1,1'-Ferrocenedicarboxylic Acid in Industrial Manufacturing

    1,1'-Ferrocenedicarboxylic Acid delivers unique redox properties and structural characteristics for professional manufacturers across advanced material science sectors. As a specialized fine chemical, it plays a critical role in precision synthesis, catalysis, and high-value-added electronics industries. The outlined applications represent established use-cases observed through customer formulation, quality management, and regulatory review.

    1. Organic Electronic Device Intermediates

    High-purity 1,1'-Ferrocenedicarboxylic Acid supports advanced manufacturing of organic field-effect transistors (OFETs) and organic photovoltaic (OPV) components. Manufacturers leverage its stable conjugated ferrocene backbone to create charge transport layers with enhanced redox activity. Integration of the material occurs during the early-stage assembly of high-mobility polymer matrices for cost-effective, scalable production of flexible electronics. Stringent trace metal and impurity controls are necessary to safeguard charge retention and electronic consistency, as specified in global electronics quality frameworks.

    Industry compliance standards

    • IPC-6012 Qualification & Performance for Rigid Printed Boards
    • IEC 60068 Environmental Testing for Electronics
    • ISO 9001:2015 Quality Management for Electronics Manufacturing
    • RoHS Directive 2011/65/EU on Hazardous Substances

    Typical usage ratio

    • 0.1–2.5 wt% in functional polymer compositions, adjusted by device thickness and targeted conductivity level

    Downstream process integration

    • Introduced during solution blending phase before spin coating or inkjet deposition; adjusted for homogeneity, followed by in-situ polymerization for film formation

    Final product types

    • OFET switches
    • Organic solar cells
    • Flexible electronic substrates
    • Printed sensors and transducer grids

    2. Redox Flow Battery Electrolyte Additive

    This ferrocene derivative acts as a stable redox mediator in the formulation of next-generation flow battery electrolytes, especially vanadium-free or hybrid organic-inorganic battery types. Manufacturers incorporate the acid for its predictable electron transfer behavior and compatibility with water or non-aqueous systems. Production requires full batch documentation, raw material traceability, and compliance with chemical storage and handling regulations. The addition point is directly into a pre-blended solution prior to cell assembly or pilot-scale up-scaling.

    Industry compliance standards

    • IEEE 1679.2 Guide for Design and Operation of Redox Flow Batteries
    • REACH (EC 1907/2006) for registration, evaluation, and safe handling
    • ISO 12405-1:2011 Requirements for Large Format Battery Systems
    • UL 9540A Battery System Thermal Runaway Testing

    Typical usage ratio

    • 1–15 mmol/L in total electrolyte composition; specific adjustments depend on desired cell voltage and compatibility with complementary catholyte/anolyte choices

    Downstream process integration

    • Dosed into solvent and mixed under inert conditions to ensure dissolution; followed by filtration and pumping to battery tanks; monitored for stability in cyclic testing protocols

    Final product types

    • Stationary energy storage modules
    • Industrial-scale redox flow battery units
    • Grid-tied backup power installations

    3. Polymer Crosslinking Catalyst in Advanced Composite Manufacturing

    Ferrocenedicarboxylic moiety aids in tailored crosslinking and copolymerization for high-performance resins and specialty thermosets demanded by aerospace and coatings sectors. Manufacturers exploit metal-organic mediation to trigger controlled chain-growth or step-growth reactions, improving mechanical strength and high-temperature stability. Inclusion at precise ratios is essential to balance polymer matrix properties, often requiring in-lab trial runs. All downstream process steps must document catalyst levels, monitor curing rates, and ensure residue compliance according to sector-specific test protocols.

    Industry compliance standards

    • ASTM D4065 Dynamic Mechanical Properties of Polymers
    • ISO 9001:2015 Manufacturing Process Control
    • NADCAP AC7130/1 Composites Manufacturing (aerospace-specific)
    • REACH (restricted substance screening in end-use composites)

    Typical usage ratio

    • 0.05–0.3 phr (parts per hundred resin), determined through rheological analysis and mechanical stress testing

    Downstream process integration

    • Incorporated during resin preparation before addition of hardener; monitored for dispersion, then processed by molding, filament winding, or lamination as per end-use specification

    Final product types

    • Aircraft structural panels
    • Composite prepregs
    • High-durability industrial coatings
    • Fiber-reinforced construction parts

    4. Ligand Intermediate for Metal-Organic Framework Synthesis

    Chemical process developers in the MOF (Metal-Organic Framework) sector utilize this dicarboxylic ferrocene for site-specific coordination and pore tuning. The symmetrical carboxyl groups form stable bonds with metals such as Zn, Cu, and Fe under hydrothermal synthesis or solvothermal methods. Purity, batch-to-batch consistency, and metal ion tolerance are essential for downstream reproducibility. Raw material addition proceeds directly into reaction vessels pre-charged with metal salts and organic solvents, monitored by pH, conductivity, and spectral analysis.

    Industry compliance standards

    • ISO 17034:2016 Reference Material Producer Certification
    • Good Laboratory Practice (GLP, OECD Principles)
    • REACH Annex VII–X analytical checks for new chemical entities
    • Specific industry end-use approval: ISO 17892-13 (MOF used in gas capture)

    Typical usage ratio

    • Stoichiometric equivalent to metal precursor (usually 1:1 molar ratio in coordination synthesis)

    Downstream process integration

    • Mixed in a one-pot process with chosen metal salt under controlled temperature and agitation; solvent selection (DMF, ethanol, water) based on specific MOF structure requirements; post-synthesis washed and activated prior to characterization

    Final product types

    • Porous adsorbent pellets
    • Selective gas capture materials
    • Catalytic supports for fine chemical production
    • Functionalized MOF powders for separation technologies

    5. Sensor Material Precursor for Analytical Instrumentation

    Producers of electrochemical sensors and biosensor chips incorporate the compound to achieve high selectivity and controlled electron exchange capabilities in detection elements. Manufacturers integrate it during electrode matrix formation or as part of immobilization protocols with other sensor-active moieties. Material documentation, traceability, and compliance with analytical instrumentation standards are mandatory. The acid’s introduction point typically follows substrate surface treatment, ensuring stable covalent attachment or physical entrapment with polymers or nanocomposites.

    Industry compliance standards

    • ISO 13485:2016 Medical Device Quality Management (for clinical diagnostics)
    • IEC 60601-1 Electrical Safety for Medical Equipment
    • ISO/IEC 17025 Laboratory Testing and Calibration
    • MIL-STD-883 (Microcircuit Testing, for military-grade instruments)

    Typical usage ratio

    • 0.05–0.8 mg/cm² on substrate, dependent on desired detection sensitivity and operational range of the sensor

    Downstream process integration

    • Deposited onto prepared electrode surfaces by drop-casting, dip-coating, or electrochemical polymerization; cured under controlled atmosphere; assembled into sensor modules for batch testing and calibration

    Final product types

    • Glucose monitoring electrodes
    • Environmental pollutant biosensors
    • Custom analytical microchips
    • Electrochemical probe assemblies
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    Certification & Compliance
    More Introduction

    1,1'-Ferrocenedicarboxylic Acid: Reliability from Source to Solution

    Understanding 1,1'-Ferrocenedicarboxylic Acid at the Source

    Every producer has their story with 1,1'-Ferrocenedicarboxylic Acid. Ours begins at the synthesis step—where chemistry meets practice. Running a chemical plant is not only about precision but also about the years spent understanding the quirks of each iron sandwich compound. It’s never enough to simply match an assay or a purity target. We look for color, grain, stability during packaging, reaction compatibility, and the way a batch holds up during application trials. It was back in the earlier days, while fine-tuning the oxidation stage, we learned the subtle cues that good ferrocenedicarboxylic acid provides, especially under different storage and process conditions.

    The specifics of our process have grown from the lessons the raw materials teach us. We rely on a consistent iron source, pay close attention to solvent reclamation, and never treat purification as an afterthought. Field reports showed us that trace contaminants in this compound can spoil it for downstream users—raising background signals in sensors, affecting electrochemical stability, or even causing trouble during workup for polymer functionalization. So, we built our analysis not just around the final product but toward what chemists in labs actually see and handle. Years spent listening to customer feedback taught us the importance of batch-to-batch sameness—a must for anyone scaling up from lab prep to pilot process.

    Composition, Appearance, and Handling

    1,1'-Ferrocenedicarboxylic acid is not some generic powder you push out the door. It’s an orange, sometimes reddish crystalline solid if you get it right and keep out photolytic or oxidative stress. The carboxylic acid groups ride on each cyclopentadienyl ring, locked to the ferrocene core with the precise geometry only a careful reaction sequence can bring. Granule size matters to anyone loading a reactor or preparing large-scale coupling reactions—too fine and it dusts, too clumpy and it resists dissolution.

    We standardize on a form that crystallizes well from aqueous media, with typical particle sizes between 100 and 500 microns. There’s a reason for this: our long-running customers in materials science prefer this range, whether they are making mixed-valence polymers or grafting carbon electrodes. It minimizes handling loss and matches their dissolution equipment, eliminating the need for unwelcome process tweaks. That’s not written down in any catalogue—it comes from years of talking directly with those who count on a stable feedstock for repeatable results.

    Purity and Impurities: More Than A Number

    No one in chemical manufacturing truly forgets their failures. Trace iron(II) or excessive oxidized byproducts once haunted us, showing up as drifting voltammograms for academic researchers or by-product peaks in analytic HPLC checks. Actual purity, checked by NMR, IR, and elemental analysis, remains above 99% in our output, but we never lean only on instruments. If a seasoned technician notices the color trend move a shade too dark, that batch gets extra scrutiny. This practice, built from failures and fixes, stops unwanted transitions in complex downstream syntheses.

    What often goes unsaid is that different end users care about different impurity tails. A sensor developer tracks voltammetric background noise; a polymer scientist sees the effect in film flexibility or dyeability. Over the years, we built our protocols to catch common problems before they head out to customers—hyrdrolytic instability, traces of iron salts, and even organic residues from side reactions. That’s the unspoken side of quality a spec sheet never quite captures. We routinely take samples from our main run and run them through stress tests, dissolutions, and secondary reactions that real-world users will perform. Truth is, it’s easier to catch a problem at the plant than field a complaint from a partner on a tight timeline.

    Functional Versatility: Applications Built on Experience

    Some customers order 1,1'-Ferrocenedicarboxylic acid to support academic curiosity—organometallic explorations and structure-property studies remain a mainstay for us. Others bring it onto the production floor. Over the last decade, we’ve seen growing demand from companies and labs working on next-generation electronic materials, such as redox-active polymers and molecular wires. The two carboxyl groups offer convenient hooks for covalent bonding, surface attachment, and further functionalization—a straightforward feature, but one that means something only when free of unknowns from upline synthesis.

    Electrochemists and sensor designers come with precise needs, notably high purity and predictable redox behavior. Some batch customers need extended stability over weeks or months, especially where device assembly cycles stretch out. We monitor our controlled storage conditions, keeping out air and moisture—any deviation leads to caking, which soon affects dispersion or surface loading in bioelectronic fabrication. We know from experience in the lab that stability in actual storage ensures that equipment calibration in end-use applications stays on point.

    Another place we see our product succeed is in smart materials programs. A customer once called to tell us that a single contaminant in their source material added weeks to their timeline, since cross-linking efficiency crashed unexpectedly. They brought us samples and asked for a breakdown. We traced the issue to a subtle by-product—another lesson in how upstream process control builds trust across the entire value chain. Since then, we regularly cross-check against the most difficult customer applications, always asking what their functional requirements demand rather than assuming that published standards are enough.

    Comparing 1,1'-Ferrocenedicarboxylic Acid to Similar Chemicals

    Any practicing chemist will notice the family of derivatives around ferrocene—monoacids, diamines, sulfonated ferrocenes, and more. Some of these behave quite differently in real-world applications. Take ferrocene dicarboxylic acid compared to its monocarboxylic sibling: the second carboxyl group doubles up opportunities to anchor to surfaces, polymers, or biological substrates. That dual functionality allows for denser packing in self-assembled monolayers and grants more robust linkage in advanced coupling reactions. In contrast, monocarboxylic ferrocene remains useful for single-point tethering, but fails to provide the stability many modern electrochemical set-ups need.

    Ferrocene diamines, another sibling, work well in polymer modifications and as building blocks in other ligands, but the acid functionality of our dicarboxylic product guarantees compatibility with esterification and amidation steps without the risk of unwanted side reactions common to amine chemistry. Experience on the plant floor confirms that acid chlorides derived from our 1,1'-Ferrocenedicarboxylic acid routinely outperform in yield and selectivity, especially in small-molecule conjugations, because we obsessively keep nitrogenous contaminants to trace levels only.

    For environmental research, some labs try using the sulfonated version. It grants water solubility, but with that comes increased hygroscopicity and more complicated downstream purification. Our customers tell us the dicarboxylic acid hits the sweet spot—enough solubility in polar media to play well with most formulations, but not so reactive as to complicate isolation or produce challenging salt mixtures. Packaging it properly, in moisture-barrier bags and under inert condition where needed, keeps it shelf-stable over long periods—a critical factor for academic users or slow-moving industrial lines.

    Quality Built Through Feedback and Adaptation

    It’s tempting to obsess over details like melt point or spectral line widths, but real feedback from the field often dictates changes in the plant. A few years ago, we faced recurring concerns about particle size consistency from several European labs running automated dispensing equipment. Rather than leaving it to chance, we adjusted our drying and grinding sequence, and shifted some crystallization conditions. Success followed—the downtime for those users dropped, and we started seeing an uptick in repeat business.

    Each adaptation, whether for packaging form, shipping size, or improved analytical testing, traces its roots to how actual people use the product. Our standard pack sizes now fit the needs of both kilo-scale researchers and bulk industrial formulators. We avoid universal solutions—no two customers build their processes the same way. Instead, we run limited pilot batches when someone approaches us with an unconventional application. Sometimes we learn something ourselves—like how trace calcium can ruin thin film transference on a research-grade carbon substrate, or how batch color uniformity predicts shelf-life in certain packaging formats.

    Every industry has its tall tales. In organometallic chemistry, one recurring thread centers on the small differences in source material—one plant’s dicarboxylic acid might play nice in a dendrimer synthesis, but prove completely incompatible for a peptide conjugation. This sharpens our focus on full traceability for every step, logging each solvent, catalyst change, and purification tweak along the way. If a customer ever calls us to chase down an unexpected result, we can walk them back through every variable—nothing is more valuable than confidence in the supply chain for innovating new molecular tools.

    Working With End Users—Real Partnerships

    We’ve always believed that manufacturing fine chemicals isn’t just shipping boxes on trucks; it’s about solving problems with people who actually use them. Beyond written feedback, we invite academics and process managers to tour our plant, share pain points, or test samples from new runs. This practice has shown us where our processes excel and where we can do better. For example, an electronics startup came to us with a requirement for nearly dust-free material for dry room processing. After working together, we modified our sieving and packing procedure, eliminating reputation-damaging returns before they could happen.

    For those scaling up from R&D to production, we walk through entire process maps together, troubleshooting solvent compatibility, waste handling, and even regulatory questions. In these sessions, we often dig up overlooked details—solvents that might carry over minor impurities, or raw material certification gaps. These collaborations often spark further improvements in both our product and client protocols, cementing a two-way trust that can’t be found in off-the-shelf commodity sales.

    Looking Ahead: Innovation with Stability

    Our investment in 1,1'-Ferrocenedicarboxylic acid is not just about the current business. We see a future where it underpins more advanced materials platforms, hybrid electronic systems, and high-value biointerfaces. Modern manufacturing means integrating digital tracking, advanced QC, and transparent reporting so customers know exactly what they receive, every time.

    We push for advances in sustainability too. Solvent recovery, minimal energy heat treatments, and greener ligands are now a regular discussion topic among our engineers. The value of this product remains as much in how it’s made as in the chemistry it enables. Environmental compliance isn’t just about ticking boxes; customers want a story—and a supply chain—they can trust for its environmental footprint and ethical production history. Our production team documents every update—down to minor tweaks in energy recovery from reaction streams—so project managers can answer difficult questions from their own oversight boards without pause.

    Lessons from the Manufacturing Floor

    No slick marketing captures the daily vigilance that true chemical manufacturing requires. Controlled humidity, careful staging of reagents, regular calibration on analytical equipment—all feed into a chain of reliability. We spend as much time training new staff on the nuances of batch differences as we do on paperwork or regulatory filings. The best batches come not from pure automation, but from an experienced operator with the eye for a telltale outlier.

    Over the years, we’ve seen customers who tried to cut corners with resellers or inconsistent sources come back after project delays or unexpected costs. It’s a reminder that, in specialty chemicals, close collaboration with the source can shield against unforeseen troubles. Feedback cycles remain open at our plant so continuous product improvement never ends up as lip service.

    Summary: Trust in Each Gram

    After decades in this business, 1,1'-Ferrocenedicarboxylic acid no longer feels like just a line item in a catalogue. Every kilogram shipped reflects years of learned precision, adaptation, and honest feedback from those who shape new science and technology. The value goes beyond a purity percent or bright orange color. It lives in deep relationships with chemists pulling late nights, engineers troubleshooting protocols, and project managers navigating regulatory pathways.

    Whenever you open a drum or a bottle from us, you’re seeing the accumulated efforts of those who care about more than specs. Quality, purity, and practicality get built upstream—to serve people with real problems to solve. Experience at the source brings not just dependable product, but also the kind of technical partnership that fuels true progress.