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1H-Imidazole-4-Carboxylic Acid

    • Product Name 1H-Imidazole-4-Carboxylic Acid
    • Alias 4-Carboxyimidazole
    • Einecs 214-072-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    544142

    Chemical Name 1H-Imidazole-4-Carboxylic Acid
    Synonyms Imidazole-4-carboxylic acid
    Molecular Formula C4H4N2O2
    Molecular Weight 112.09 g/mol
    Cas Number 6946-91-6
    Appearance White to off-white powder
    Melting Point 224-228 °C
    Solubility In Water Soluble
    Pka 2.89 (carboxylic acid), 7.02 (imidazole ring)
    Storage Conditions Store at room temperature, keep container tightly closed

    As an accredited 1H-Imidazole-4-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White plastic bottle with secure screw cap, clearly labeled "1H-Imidazole-4-Carboxylic Acid, 25g", hazard and handling instructions included.
    Shipping 1H-Imidazole-4-Carboxylic Acid is shipped in tightly sealed containers to protect against moisture and contamination. It is packed according to chemical safety regulations, labeled with hazard information, and generally shipped via ground or air freight with appropriate documentation. Handle under standard laboratory chemical shipping protocols.
    Storage 1H-Imidazole-4-Carboxylic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Keep it away from sources of heat, moisture, and incompatible substances such as strong oxidizing agents. Store at room temperature and protect from light. Ensure the storage area is appropriately labeled and complies with local chemical safety regulations.
    Application of 1H-Imidazole-4-Carboxylic Acid

    Applications of 1H-Imidazole-4-Carboxylic Acid in Industrial Manufacturing

    As a specialized manufacturer, we supply 1H-Imidazole-4-Carboxylic Acid for industrial customers who require high-performance intermediates in regulated downstream applications. Our material supports production processes demanding consistent purity and documented compliance, particularly where complex synthesis or stringent quality control is essential. Below, we outline key industrial scenarios where this compound plays a well-defined role, highlighting specific standards, formulation guidelines, process integration, and targeted finished products.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Antifungal Drugs

    Pharmaceutical companies use imidazole-4-carboxylic acid as a core intermediate in the synthesis of antifungal agents such as econazole and miconazole. Its structure allows for regioselective derivatization, ensuring high yield during the formation of key imidazole rings. Production lines operating under GMP monitor every batch for residual solvents and related impurities in accordance with health authority specifications. The intermediate typically enters the multi-stage synthesis following protection and activation, contributing directly to the API’s Imidazole moiety. Final APIs undergo further purification, meeting both compendial and client-defined quality standards for use in topical or systemic antifungals.

    Industry compliance standards

    • EU GMP Part II (ICH Q7, EudraLex Vol 4)
    • USP–NF monographs relating to synthetic APIs
    • Ph. Eur. requirements for pharmaceutical intermediates
    • FDA 21 CFR 211 for finished pharmaceuticals

    Typical usage ratio

    • Ranges from 0.95–1.10 molar equivalents relative to key coupling reactants, based on target product yield and side-reaction minimization requirements

    Downstream process integration

    • Introduced during early-stage ketone/ester derivatization steps, followed by cyclization to form the core imidazole-ring structure
    • Subsequent purification through crystallization or chromatography

    Final product types

    • Pharmaceutical-grade imidazole antifungal APIs (e.g., econazole nitrate, miconazole nitrate)
    • Intermediates for prescription and OTC antifungal medications

    2. Custom Peptide Synthesis and Bioconjugation

    Contract research and biotech facilities integrate this material into the solid-phase synthesis of histidine-derivative peptides. As a carboxy-functionalized imidazole, it permits site-selective activation and amide bond formation on-resin under Fmoc/tBoc strategies. The unique ring structure allows for precise peptide folding, impacting downstream protein function in therapeutic research and drug delivery. QC teams routinely monitor amino acid purity and residual solvent content to meet international biomanufacturing requirements. Final peptides often serve as enzyme inhibitors or imaging agents after further conjugation and labeling.

    Industry compliance standards

    • ICH Q11 for Development and Manufacture of Drug Substances
    • ISO 13485 for medical device peptides
    • USP general chapters for peptide purity assessment
    • Synthetic peptide cGMP guidelines (FDA/EMA)

    Typical usage ratio

    • Standard loadings from 0.1–0.25 mmol per g resin, adjustable based on desired peptide chain length and yield optimization

    Downstream process integration

    • Loaded during side-chain or terminal modification in automated peptide synthesizers using Fmoc/tBoc chemistry
    • Followed by deprotection, cleavage, and final HPLC purification

    Final product types

    • Synthetic peptides for preclinical research
    • Peptide-drug conjugates for targeted therapies
    • Protein labeling reagents

    3. Agrochemical Intermediate for Imidazole-based Fungicides

    Major agrochemical manufacturers rely on this compound for constructing imidazole motifs present in crop protection agents. The raw material’s carboxylic acid group facilitates ring closure reactions vital to generating heterocyclic fungicide scaffolds. Processing lines closely manage contaminant levels per agricultural chemical directives. During synthesis, the compound is converted to reactive esters or amides, feeding directly into a chain of reactions leading to the desired active ingredient. Final products undergo formulation with surfactants and stabilizers for use in environmental and food-agricultural applications.

    Industry compliance standards

    • FAO/WHO specification for technical grade actives
    • REACH registration for chemical intermediates
    • ISO 9001-certified agricultural chemical production
    • National pesticide registration programs (EPA, EU/1107/2009)

    Typical usage ratio

    • 0.6–1.2 molar equivalents, tailored to the stoichiometry of multi-step coupling and closure reactions to control impurity thresholds

    Downstream process integration

    • Utilized during heterocycle ring assembly as a reactive intermediate, followed by acetylation or halogenation for product-specific modification
    • Integrated prior to final blending and formulation steps

    Final product types

    • Technical-grade imidazole fungicides (e.g., prochloraz precursors)
    • Crop protection concentrates for grain, fruit, and vegetable treatments

    4. Specialty Chemical Intermediate for Corrosion Inhibitors

    Chemical producers employ imidazole-4-carboxylic acid as a targeted building block in the synthesis of water-soluble corrosion inhibitors used in industrial cooling and process water systems. Its functionality permits efficient derivatization to ionic or amphoteric species with high affinity for metal surfaces. Production facilities validate active content and impurity profiles under specialty chemical quality schemes. The intermediate is typically transformed into quaternized derivatives or incorporated into polymeric inhibitor formulations. Downstream, it supports compounding operations for water treatment products distributed for heavy-industry clients.

    Industry compliance standards

    • ISO 9001 Quality Management for chemical manufacture
    • ANSI/NSF Standard 60 for drinking water treatment chemicals
    • Environmental Protection Agency chemical reporting (TSCA/EPA)
    • REACH Annex VII-IX for intermediate registration

    Typical usage ratio

    • 0.5–1.0 mole per mole of targeted metal-binding functional group in corrosion inhibitor synthesis, refined through pilot lot scale-ups

    Downstream process integration

    • Feeds the functionalization stage for preparation of imidazolium salts or amide derivatives
    • Co-formulated with dispersing agents or stabilizers prior to package filling

    Final product types

    • Corrosion inhibitor concentrates for industrial water circuits
    • Boiler and heat-exchanger protection formulations

    5. Diagnostic Reagent Intermediate for Imidazole-Sensitive Test Kits

    Medical device and diagnostic manufacturers integrate imidazole-4-carboxylic acid in the synthesis of chromogenic or fluorogenic reagents used in enzymatic and metal-ion detection kits. Its substitution pattern enhances chelation or signal generation properties, and formulation chemists carefully monitor metal content and pH stability. Quality teams follow ISO standards for medical reagent supply. The compound often undergoes further derivatization to generate reporter molecules, which are then immobilized on strip or microplate platforms. Final diagnostic reagents support clinical laboratories and POCT device suppliers globally.

    Industry compliance standards

    • ISO 13485 for in vitro diagnostic device manufacturing
    • IVDR (EU 2017/746) for medical diagnostics
    • USP <1225> Validation of Compendial Procedures
    • Relevant CLSI protocols for test kit development

    Typical usage ratio

    • Commonly 0.2–0.6 mmol per mmol of the reactive probe, fine-tuned for test kit batch sizes and signal sensitivity

    Downstream process integration

    • Feeds conjugation chemistry to form fluorogenic/enzyme substrates
    • Deposited or coupled onto carrier material during reagent strip assembly

    Final product types

    • Blood plasma and urine diagnostic strips for metal ions
    • Clinical chemistry test kits for hospital and laboratory use
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    Certification & Compliance
    More Introduction

    1H-Imidazole-4-Carboxylic Acid: Real-World Chemistry from the Production Floor

    Getting to Know the Backbone of Specialty Synthesis

    As a chemical manufacturer with years in the trenches, compounds like 1H-Imidazole-4-Carboxylic Acid have become a regular sight among our reactors and drying racks. Identified by its CAS number 3034-41-1, this molecule draws attention in research labs not just for its name but because of what it brings to synthetic chemistry. Our 1H-Imidazole-4-Carboxylic Acid usually appears as a white to slightly off-white crystalline powder. Chemists find themselves reaching for it more and more as synthesis protocols demand greater selectivity, higher purity, and reliable supply chains.

    Among imidazole derivatives, 1H-Imidazole-4-Carboxylic Acid stands out for a solid reason: the carboxylic acid function at the 4-position on the ring. Compared to imidazole itself, this substitution unlocks entirely new synthetic routes. While imidazole offers a versatile base scaffold, introducing the carboxyl group leads to prospects in peptide construction and as a ligand anchor for coordination chemistry. That single carboxyl group often marks the difference between a pathway that works in theory versus one that performs on the production scale.

    The Specifications We Prioritize

    Crafting 1H-Imidazole-4-Carboxylic Acid requires more than just following the literature. Our typical production run sees a purity of 98% or higher, judged by HPLC and confirmed with NMR analysis. Even the smallest impurities can complicate downstream reactions, so we keep a close eye on residual solvents, water content, and heavy metals. Moisture becomes a frequent adversary; thorough drying cycles and tightly controlled storage mean researchers aren’t left fighting mysterious reaction failures.

    Aside from chemical purity, particle size distribution has an impact on handling and dissolution. Large crystals can clog transfer lines or settle out in solution, so we often mill the batch to ensure it moves cleanly through automated feeders. A reliable melting point, usually falling between 190-195°C, signals consistent crystal structure and lot-to-lot repeatability. In our facility, we don’t expect researchers to sort through performance inconsistencies. That responsibility falls to us, as repeated pilot batches confirm solid-state properties and flow characteristics before a product ever ships.

    Bringing Utility to the Lab Bench and Beyond

    1H-Imidazole-4-Carboxylic Acid shows up in a wide range of research and industrial projects. Peptide synthesis stands out as one of its main homes, where it takes on protecting group chemistry and mediates coupling between amino acids. The carboxyl function grants this imidazole ring a dual personality. On one hand, it acts as a nucleophile or acid in coupling reactions; on the other, the ring system pitches in as a mild base. When peptide chemists describe needing orthogonal selectivity or improved yields, our product gives them a versatile handle points.

    Coordination chemistry opens another arena. 1H-Imidazole-4-Carboxylic Acid anchors itself to metal centers through both nitrogen and oxygen. This creates stable chelates and opens doors for catalyst design, enzyme modeling, and even in the assembly of metal-organic frameworks. The specific placement of that carboxylic acid lets scientists design ligands with predictable spatial orientation, something not easily achieved with unsubstituted imidazole.

    We see growing interest from the pharmaceutical and agrochemical sectors, too. Modifications at the imidazole ring can produce small-molecule drugs, enzyme inhibitors, or crop protection agents. Here, our manufacturing approach matters: any batch with trace contaminants risks introducing genotoxic impurities downstream, so every step, from raw material selection to packaging, circles back to patient and consumer safety.

    How 1H-Imidazole-4-Carboxylic Acid Stacks Up Against Similar Options

    In discussions with formulation scientists, differences between our product and standard imidazole become more than cosmetic. Imidazole-4-carboxylic acid’s extra functional group isn’t just a chemical curiosity; it plays into selectivity, solubility, and reactivity. For projects seeking simple base catalysis, standard imidazole might suffice. Once the job calls for targeted activation, complexation, or integration into large molecules, the carboxyl group in our product sets the chemistry on another track.

    Contrast this with 2-carboxylic acid imidazole derivatives, which often demonstrate altered ring electronics and poorer steric accessibility. Our experience suggests that substituents at the 4-position enable a unique, predictable interaction profile. Whether the goal is to synthesize specialized peptides or build complex organometallic scaffolds, our customers notice real performance gains when they switch from 2-carboxylic to 4-carboxylic positional isomers.

    Production Realities: Not All Compounds are Created Equal

    Every batch of 1H-Imidazole-4-Carboxylic Acid tells a story about manufacturing priorities. From experience, a seemingly minor deviation—be it in pH adjustment, solvent grade, or drying time—shows up quickly in customer feedback. Getting the purification workflow right took us multiple years and dozens of scale-up trials. We started with methods designed for small-scale laboratory work, but soon found large-scale crystallization posed new challenges, including solvent recovery and batch-to-batch reproducibility.

    Our operators train for months to read subtle signs in crystallization tanks, recognizing the texture change that signals endpoint. Routine doesn’t mean boring—troubleshooting unexpected hydrate formation or yield reductions keeps us up at night. Customers look for a powder that dissolves without drama, weighs out consistently, and fits into automated protocols. Every new order draws on data collected across hundreds of previous runs, not just a blueprint copied out of an old patent.

    Packaging may look simple, but this is another place production choices matter. The acid’s mild hygroscopicity means we double-seal in moisture-barrier bags inside rigid containers. By the time the product leaves our facility, we want it arriving in the same state it left, no matter if it crosses an ocean or endures a humid storage warehouse.

    Responsible Manufacturing and Long-Term Supply

    Sourcing raw materials has moved to the front line in recent years. We spent time auditing suppliers, demanding consistent documentation, and conducting in-house impurity scans. Our plant minimizes waste by recycling solvents when possible, using closed reactors to limit airborne releases, and routing exhaust through scrubbers. With global regulatory expectations tightening—especially when our product enters the pharma pipeline—responsibility doesn’t stop with finished goods. Traceability, documentation, and environmental controls mean our commitment doesn’t end when the drum is sealed.

    We maintain relationships with logistics partners who understand chemical sensitivities. Our job extends to ensuring material clears customs smoothly, doesn’t run afoul of changing regulations, and arrives intact. Customers regularly mention that reliable arrival sometimes matters more than absolute lowest cost—chemical delays can close down an entire research sequence. Our production planning builds in reserve stocks to give clients peace of mind during supply chain hiccups.

    Addressing the Challenges Researchers Face

    Feedback from research and production teams shapes the way we approach every batch. A decade back, many labs reported poor solubility in polar solvents—a problem that we solved with improved milling and attention to crystal habit. Stability showed up as another pain point, leading us to switch drying cycles and add real-time moisture sensing. As scientists began pushing for green chemistry and less hazardous waste, we switched from chlorinated solvents to more benign alternatives whenever possible.

    Some teams need tailored compatibility for high-throughput screens or kilo-lab supply, which prompted us to invest in modular production lines. Flexibility at the manufacturing level means one customer’s requirements for ultra-low residual metals can live side-by-side with another’s bulk commodity order. It’s not always glamorous, but weaving this kind of flexibility into our production web means projects don’t stall waiting for minor tweaks.

    Quality Control as Part of the Culture

    Every kilogram of 1H-Imidazole-4-Carboxylic Acid passes through a battery of in-process and finished-goods checks. Testing extends beyond just confirming structure. We use chromatography to track trace-level byproducts, Karl Fischer titration for water, and ICP-MS for metals. Every analytical method developed internally gets validated for accuracy across production scales. Laboratories rely on those results to green-light their own processes; we know one bad certificate can cost weeks of effort downstream.

    Instead of relegating quality control to a final hurdle, we integrate it at every stage. Operators keep logs of every step—solvent lots, batch start and end times, filtration media, dry weights. Cleaning protocols cut down on cross-contamination, and instrument calibrations occur daily. This attention creates the kind of feedback that catches an issue before it grows. For customers, that means trust is earned, not assumed.

    Cost, Scale, and Accessibility

    Balancing affordability and quality isn’t just chasing two rabbits—it defines survival in specialty chemical manufacturing. Some vendors offer rock-bottom pricing based on thin margins and little technical support. Our experience shows that research and production teams value access to technical data, rapid response to documentation needs, and honest communication when global shortages pinch the market. We meet regular requests from clients who need batch-specific support or advice, often reviewing application notes alongside the technical staff who will be running the actual experiments.

    Scaling up from bench to multi-tonne lots asks for a different mindset. The synthetic route needs to withstand persistent changes in heating and cooling rates, variable raw material lots, and the quirks of large crystallizers. We use pilot campaigns to model each transition, fine-tuning both yield and handling at every round. Investors and buyers are welcome on site, touring the shop floor and reviewing live process data. This openness underpins how we’ve secured long-term contracts with both large pharma and smaller specialty labs.

    Future Trends and Continuous Improvement

    Demand continues to shift. Increased regulatory scrutiny, push for greener process chemistry, and automation in research labs mean we constantly reevaluate synthetic routes. Each new inquiry reveals an area for improvement: lower-waste isolation, greater energy efficiency, or better batch tracking. We take lessons from every project, feeding learning back into process robustness.

    Real progress only happens by linking the insights of researchers with the practical reality of large-scale synthesis. Sometimes that means pushing equipment beyond standard limits to generate a tighter particle size; other times it means swapping an old filtration step for a membrane-based alternative. Ideas that start on the whiteboard get stress-tested in pilot reactors and, once proven, roll out across production.

    Direct Experiences from Customer Projects

    A peptide startup asked us to help troubleshoot a coupling step plagued by variable yields—analysis pointed not to their technique but to differences in material quality from suppliers. After several shared rounds of root cause analysis, we set tighter controls on our finishing and drying steps, eliminating a minor hydrate impurity. The result: yields climbed, and the customer downstream protocols switched to our material permanently.

    In another case, a multinational group needed kilogram quantities for assay development at short notice, facing delays with global shipping. Our flexible scheduling, in-house capacity, and real-time communication allowed rapid order turnaround. Engineers packed, inspected, and shipped within days, with technical teams providing documentation to satisfy import requirements in record time. This level of responsiveness wouldn’t be possible without direct control over every batch and every shipment.

    For a catalysis group developing proprietary metal complexes, switching to 1H-Imidazole-4-Carboxylic Acid with guaranteed trace-metal profiles cut down purification effort and improved final product stability. Our documentation aligned with their in-house verification, proving that the synthesis never picked up extraneous metals or polymer contaminants. Precise process control on our side reduced the validation burden on theirs.

    Honest Challenges and Real-World Solutions

    Not every project proceeds as planned. Custom derivatives and high-purity runs sometimes yield unexpected side products: shifting reaction ratios or trace residuals that only appear during scale-up. We have built-in flexibility to adapt, sometimes rerunning purification with solvent tweaks or slightly altering pH control to stabilize intermediates. Open communication with our clients means they get alerts along with proposed fixes, not just a mystery delay or unannounced deviation.

    The biggest lessons come from failures caught early. Operators and chemists swap notes during shift changes—catching a subtle impurity trend or solubility quirk before scale-up. Our culture values learning from each deviation, not hiding mistakes or blaming external factors. When tweaks solve a recurring problem in a campaign, the same fix works its way back into regular production, improving results for every batch delivered.

    Commitment to the User at Every Step

    Our drive to support the research community starts in plant design, continues through raw materials control, and finishes only when users report back success. We encourage real feedback, run joint validation studies, and look for improvement partners among our clients. This focus on mutual value means we see challenges as shared, not something to brush aside.

    With 1H-Imidazole-4-Carboxylic Acid, each new run stands on a foundation of everything learned from the last. Our motivation isn’t abstract—better chemistry means more successful research, faster milestones, and fewer project setbacks. Direct experience taught us that even a minor advantage in purity, stability, or supply brings outsized returns downstream for users. We see ourselves not as commodity suppliers, but as technical partners engaged in the daily progress of chemical science.

    Looking Forward Together

    Every improvement we make in the production and support of 1H-Imidazole-4-Carboxylic Acid emerges from a simple conviction: chemistry moves forward when researchers and manufacturers work hand in hand. We keep investing in cleaner processes, tighter controls, and faster service, always guided by what scientists at the bench are trying to accomplish. Our perspective is rooted in daily practice—not just theory—delivering one batch at a time, so researchers spend less time troubleshooting and more time advancing science.