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5-Amino-1H-Imidazole-4-Carboxamide Hydrate

    • Product Name 5-Amino-1H-Imidazole-4-Carboxamide Hydrate
    • Alias AICAR Hydrate
    • Einecs 629-349-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    359606

    Chemical Name 5-Amino-1H-Imidazole-4-Carboxamide Hydrate
    Synonyms AICAR hydrate, 4-Carboxamido-5-aminoimidazole hydrate
    Cas Number 3387-68-2
    Molecular Formula C4H6N4O·xH2O
    Molecular Weight 130.12 g/mol (anhydrous base)
    Appearance White to off-white powder
    Solubility Soluble in water, slightly soluble in ethanol
    Melting Point Exceeds 300 °C (decomposes)
    Storage Temperature 2-8 °C
    Purity Typically ≥98%

    As an accredited 5-Amino-1H-Imidazole-4-Carboxamide Hydrate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g quantity of 5-Amino-1H-Imidazole-4-Carboxamide Hydrate comes in a sealed, amber glass bottle with detailed labeling.
    Shipping 5-Amino-1H-Imidazole-4-Carboxamide Hydrate is shipped in tightly sealed containers to protect from moisture and contamination. The chemical is typically transported at room temperature, following standard safety protocols. Proper labeling and documentation ensure compliance with regulations. Handle with care, using gloves and protective equipment during receipt and storage.
    Storage 5-Amino-1H-Imidazole-4-Carboxamide Hydrate should be stored in a tightly closed container, in a dry and well-ventilated place. Keep it at room temperature, away from sources of moisture and incompatible substances. Protect from light and excessive heat. Store in accordance with standard laboratory chemical storage guidelines to ensure stability and safety.
    Application of 5-Amino-1H-Imidazole-4-Carboxamide Hydrate

    Applications of 5-Amino-1H-Imidazole-4-Carboxamide Hydrate in Industrial Manufacturing

    Our facility supplies high-purity 5-Amino-1H-Imidazole-4-Carboxamide Hydrate for advanced industrial applications. Below, we detail the principal manufacturing sectors utilizing this intermediate, focusing on compliant integration, specific dosage, process steps, and finished product outcomes.

    1. Pharmaceutical API Intermediate for Purine Synthesis

    This compound serves as a critical building block in the synthesis of purine-based active pharmaceutical ingredients, most notably for antineoplastic and antiviral drugs. Downstream manufacturers employ it in the multi-step production of key APIs such as Acyclovir and related nucleoside analogs, where its amide and amino groups facilitate target-specific cyclization and incorporation. Controlled batch addition occurs after initial pyrimidine derivatization but prior to final ring closure and purification steps in GMP-validated environments.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP-NF monographs (API-specific as applicable)
    • EDQM CEP (for APIs exported to EU)
    • CFR 21 Part 211 guidelines (US FDA)

    Typical usage ratio

    • 0.18 – 0.46 molar equivalents per target API batch, adjusted based on nucleoside analog type and yield optimization studies

    Downstream process integration

    • Added during the purine ring assembly step via controlled dissolution and pH adjustment
    • Reacted with formylating or alkylating agents under nitrogen protection for purity
    • Followed by filtration, washing, and crystallization specific to API route
    • Monitoring for residuals under validated analytical protocols (HPLC, GC-MS)

    Final product types

    • Antiviral drugs (e.g., acyclovir, ganciclovir)
    • Cytostatic agents
    • Diagnostic reagents for in-vitro test kits
    • Pharmaceutical grade intermediates for global API export

    2. Veterinary Pharmaceutical Synthesis

    In veterinary API manufacturing, this raw material is utilized for assembling nucleoside structures central to antiparasitic and immune-enhancing formulations targeting livestock and companion animals. Integration occurs post-initial cyclization but ahead of esterification, requiring careful control of aqueous-organic interface conditions and real-time monitoring for regulatory specifications relevant to animal health products. Batch records must capture all traceability from lot to finished doseform.

    Industry compliance standards

    • VICH GL24 guidelines (Good Manufacturing Practice for Active Substances)
    • European Pharmacopoeia (Ph. Eur.) Veterinary monographs
    • US Pharmacopeia Veterinary Requirements
    • ISO 9001:2015 for Quality Management Systems in veterinary manufacturing

    Typical usage ratio

    • Typically 0.22 – 0.32 molar equivalents per batch, adjusted based on formulation strength and regional veterinary formulation limits

    Downstream process integration

    • Charged to synthesis vessel during precursor modification pre-final conversion
    • Mixing with protective ligands to ensure stability in subsequent esterification
    • Temperature adjusted between 20-35°C to minimize degradant formation
    • Material balance confirmed before transfer to the final formulation line

    Final product types

    • Injectable veterinary medicines
    • Oral immunostimulant APIs
    • Final bulk intermediates for licensed veterinary preparations
    • Custom reference standards for regulatory submissions

    3. Custom Synthesis of Nucleotide Biochemicals

    Manufacturers supplying laboratory and biomedical research markets incorporate our compound into custom syntheses of nucleotide and nucleoside biosubstrates, including 13C- and 15N-labeled analogs. Careful stoichiometric control and isotopic purity are essential here, with the compound introduced as a nucleophilic amine resource during ring closure under inert atmosphere conditions. Strict in-process testing guarantees minimal side-product formation and high target substrate yield, critical for downstream genomics and diagnostic manufacturers.

    Industry compliance standards

    • ISO 13485 for medical device and diagnostic raw materials
    • CFR 42 Part 493 CLIA for clinical laboratory reagents
    • Internal Standard Operating Procedures (SOPs) for research chemicals
    • REACH (EC 1907/2006) for laboratory chemical supply in Europe

    Typical usage ratio

    • Ratio varies from 0.19 – 0.25 mole per equivalent of labeled precursor, adjusted for specific isotopic protocol and substrate complexity

    Downstream process integration

    • Dosed into stirred-reactor after preparation of unlabeled or labeled ribose precursors
    • Process maintained at low temperature to preserve isotopic labeling fidelity
    • Intermediate purified by ion-exchange chromatography before final product synthesis
    • Each run tracked for isotopic enrichment QC

    Final product types

    • Standard nucleotide triphosphates for sequencing kits
    • Isotopically labeled nucleosides for NMR studies
    • Custom oligonucleotide building blocks
    • Reference materials for molecular biology research

    4. Fine Chemical Production for Analytical Standards

    Within the fine chemical sector, the hydrate functions as a precursor during high-purity synthesis of imidazole-based analytical standards. Downstream integrators demand this material for use in trace analysis calibration, method validation, and QC protocols for regulated industries. Precision in both mass addition and timing ensures batch-to-batch reproducibility and consistency of final analytical calibrators, especially those entering pharmaceutical and pesticide residue laboratories.

    Industry compliance standards

    • ISO/IEC 17025:2017 for testing and calibration laboratories
    • AOAC analytical methods for reference standards
    • USP Reference Standard protocols for identity and purity
    • Sigma-Aldrich CertiPro standard verification

    Typical usage ratio

    • 0.48 – 0.61 gram-atom equivalent per target molecule synthesis, adapted according to analyte response and detection requirements in calibration matrix

    Downstream process integration

    • Mixed with specific aldehyde or acid under controlled pH for fine chemical pathway
    • Isolated via slow precipitation and purified through repeated recrystallization
    • Filtered and dried in vacuum chambers to achieve reference-grade purity
    • Batch tested using chromatographic and spectrometric techniques

    Final product types

    • Official pharmaceutical analytical standards
    • Environmental monitoring calibrators
    • Pesticide residue detection reference substances
    • Stability test benchmark compounds for regulated industries
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    Certification & Compliance
    More Introduction

    5-Amino-1H-Imidazole-4-Carboxamide Hydrate: Bringing Precision to Research and Development

    Understanding a Key Ingredient in Modern Science

    Some compounds take on a bigger role in life sciences simply because they work. 5-Amino-1H-Imidazole-4-Carboxamide Hydrate—better known to many in the scientific community as AICAR hydrate—has been steering important changes in how labs approach biochemical studies. The unique structure of this molecule, with both amino and carboxamide groups hanging off the imidazole ring, explains much of its behavior and why research teams keep it stocked on their shelves.

    The model that reaches most laboratories features a white, water-soluble crystalline powder, usually packed with high purity above 98%. Industries that place trust in their outcomes, such as biotech startups or academic labs, look at every decimal of purity before deciding what lands inside their test tubes. With AICAR hydrate, the quality difference translates straight into the confidence researchers hold in their data. A low impurity count means less “background noise”—a factor anyone who’s ever run a spectrophotometer or enzyme assay understands immediately.

    AICAR hydrate has built up years of credibility in AMP-activated protein kinase (AMPK) research. I remember the first project I took part in where it became the centerpiece—a metabolic desk experiment tracking how muscle cells react to stress. What stuck with me then, and sticks with a lot of biochemists now, is that it’s not another ‘just-for-show’ reagent gathering dust on the shelf. Because of its role as an AMP analog, this compound can essentially flip on AMPK pathways. Turning them on lets people see what happens during metabolic shifts, such as energy shortages or exercise. Teams interested in diabetes, obesity, and cellular aging have relied on this effect to figure out real-life puzzles.

    Why Purity Puts Everything on the Line

    If you walk into any active research lab, experiment failure is more than a headache—it throws off timelines, eats budgets, and sometimes puts whole publications in question. This is why technical grade AICAR hydrate doesn't make the cut for anything beyond quick screening tests. The model tailored for analytical accuracy usually comes in forms meeting trace-metal and residual solvent standards suitable for pharmaceutical or academic studies.

    I’ve seen the difference up close. Next to generic or lower-grade chemical options, higher-quality AICAR hydrate draws a clear line in experimental control. With weaker grades, unexpected peaks may show up in HPLC runs. Down the line, those tiny impurities can block enzymes or interfere with receptor binding, hiding the actual effects a team is looking for.

    AICAR hydrate’s molecular formula, C4H6N4O·xH2O, shapes both its strength and its behavior in application. The hydrate form carries defined amounts of water, which adds weight but can also change the way the compound interacts inside reactions. For teams recalibrating for consistent dosing, this matters—even a fraction of a milligram can change outcome trends in sensitive bioassays. Those who have spent hours tracking unpredictable data shifts recognize how crucial it is to factor in the hydrate weight and moisture percentage.

    Distinctiveness: Not All Imidazoles Work the Same Way

    Comparing AICAR hydrate to other imidazole derivatives, the differences matter more than the similarities. Having run head-to-head trials, I’ve found that other analogs, despite having the same core ring, may lack either the carboxamide or amino modification. These little changes derail how the molecule fits into enzymes and cellular machinery. While many imidazole-based products are common in chemical synthesis (buffers, heterocycle building blocks, or even pharmaceuticals), only AICAR’s specific arrangement activates AMPK in a predictable way. Replacing it with cheaper or more abundant cousins in a biological protocol usually ends with discouraging results, as the pathways just don’t turn on.

    Choice between hydrates and anhydrous versions also impacts hands-on results. The hydrate form, which retains water molecules within its structure, can dissolve more smoothly and avoid static issues. It rarely clumps, so weighing out doses for tissue culture or animal testing becomes much simpler. Some labs stick to the anhydrous form when they need the absolute lowest molecular weight for dose calculation. From experience, the hydrate is usually the go-to because of its stability and easier handling, especially in high-volume, repetitive testing settings where speed and reliability matter every day.

    Practical Use in Daily Lab Work

    Product handling might seem trivial, but every seasoned researcher learns how minor inconveniences—difficult solubility, sticky powders, inconsistent reactivity—lead to costly lapses in data collection. AICAR hydrate’s powder form often dissolves in water or cell-culture medium at concentrations commonly used for enzyme assays or cell signaling experiments. Sterility, a big concern for cell culture and animal work, stays manageable with filtration through standard 0.22-micron filters. Researchers aiming for the tightest error bars appreciate that the compound holds up under freeze-thaw cycles and resists light degradation, features that aren’t always true for every alternate AMP analog or nucleotide mimic.

    The compound’s shelf stability lets labs plan multi-week protocols without fear of breakdown or contaminant buildup. This was brought home to me during a series of high-throughput screens where sample prep spanned days. Materials left out of the fridge for hours—often unavoidable during busy benchwork—still measured as stable, thanks to the predictable hydrate structure.

    AICAR Hydrate’s Place in Future-Forward Research

    Interest keeps rising in metabolic syndrome, insulin resistance, and even exercise mimetics that recreate some benefits of movement without actual physical training. Academia and pharma companies both invest in AICAR hydrate to test new ideas about how cells sense and respond to energy deprivation. One fact stands out: compared to other chemicals, AICAR hydrate’s capability to selectively activate AMPK without widespread off-target activity gives clearer, more clinically relevant insights.

    Unlike broader metabolic modifiers, such as metformin or compound C, which introduce plenty of unknowns into cell models, AICAR hydrate sticks closely to one known route. Its utility shows up in published data all over the world, with thousands of articles discussing how this compound reveals the adjustment of gene expression, mitochondrial dynamics, or autophagy. All attempts to substitute it with other nucleoside analogs miss its knack for tuning the very signal that researchers care about: energy homeostasis.

    On my own old project teams, attempts at using closer “imitators” without the amide structure resulted in partial activation or, worse, complete pathway silence. This single point of difference—a hydrogen bond here, a methyl group there—translates directly to millions saved or lost as drug screens move through the preclinical pipeline.

    Why Regulatory Trust Begins with Raw Materials

    Any time a drug candidate moves from early-stage discovery to animal studies, the question of origin, specification, and prior use comes up. Regulatory agencies don’t negotiate around impurity spikes or ambiguous hydration states. Companies with an eye on downstream FDA or EMA submission demand lot traceability and validated purity for everything, starting with routine reagents. AICAR hydrate that meets published pharmacopeia or ACS requirements grants project leads the confidence to press forward.

    Batch-to-batch consistency protects experimental design against one of the oldest headaches in science: irreproducibility. Having seen colleagues scramble after an outlier batch crippled months of results, I understand why purchasing managers and principal investigators prefer higher-grade reagents—even when budget constraints weigh heavy. The cost, when distributed over an entire project, often means little compared with the risk of having to re-run an animal study or restart an entire thesis year.

    For those of us who spend hours at the bench, there’s also a peace of mind that comes from trusting a single supplier and a validated lot. Knowing that a stalk of powder won’t bring any unexpected surprises lowers stress during report write-ups and peer review. It also means fewer headaches explaining curious outliers to supervisors or co-authors.

    Eco-Consciousness and Safe Use: Factors that Matter More Today

    Labs now face fresh scrutiny about every chemical they bring in, from procurement teams to scientific oversight boards. Concerns include the environmental load of manufacturing, responsible disposal, and personal safety. AICAR hydrate, produced under green chemistry standards, means less waste in synthesis and fewer pollutants downstream. Some suppliers use solvent recovery or energy-efficient crystallization, which sits better with sustainability targets—a shift I’ve seen firsthand in grant award requirements and internal audits.

    Handling also shifts with improved product consistency. Labs that run daily pipetting and weighing routines want powders that leave little residue, avoid airborne particulates, and reduce awkward cleaning or protective measures. Years ago, accidents caused by careless handling of impure or unstable imidazoles sent more than one researcher to medical checkups. Quality production of AICAR hydrate—free of avoidable irritants—lowers these risks. This shy, nearly silent but life-saving detail hits home for any researcher after a long week in the lab.

    Looking for Answers: The Compound as a Scientific Compass

    Some debates about AICAR hydrate always come up—mostly about whether alternative AMPK activators or mimetics exist that offer the same reliability at a lower cost or with greater shelf stability. Over years of literature reviews and method comparisons, most groups return to the original for its track record. While newer options exist, these either warp the data with off-pathway actions or spiral into rapid breakdown under typical storage conditions.

    One might ask: could future advances produce a next-generation AMPK activator that combines the cost and safety advantages of AICAR hydrate with simple, bioisosteric tweaks? Possibly. But after fielding protocols handed down from senior grad students, I’ve learned this: results beat novelty every time in a clinical research cycle. Teams prize hard-won experience, so as of now, AICAR hydrate keeps its crown.

    This isn’t about holding tradition for tradition’s sake. The compound adapts—newer synthetic routes increase batch yields while reducing environmental load. Improved documentation lets researchers troubleshoot down to the microgram, just by scanning a QR code or pulling lot records from the cloud, a far cry from the early days of paper batch sheets and hand-written archives. Some may scoff, but having a known starting point and traceability lifts a huge psychological and regulatory burden.

    Addressing Access and Cost Challenges

    Pricing remains an issue, especially for cash-strapped university labs or small contract research organizations. Open-access repositories and group-buying programs present ways to lower costs per gram. Many junior researchers share their leftover stocks within university networks, stretching budgets and materials—though this calls for careful labeling and storage to avoid cross-contamination or misdosage. On a practical level, leadership often negotiates bulk orders with suppliers who provide certificates of analysis and comprehensive technical support, making the compound more accessible for early-career teams.

    Some institutions have tried synthesizing AICAR hydrate in-house, but this usually brings more hassle than savings—impurities, variability, even hazardous byproducts. Unless a bench chemist has strong credentials and analytical backup, commercial sources give the needed reliability and save on wasted effort. The efficiency, safety, and regulatory compliance pay off in time and money, especially during major grant reviews or regulatory submissions.

    Solutions: Making a Critical Chemical Stand the Test of Time

    While rising costs and tight budgets shadow research projects everywhere, clear options for cutting corners often appear more dangerous than wise. For AICAR hydrate, alternative solutions include developing local partnerships with trusted distributors, joining research consortiums to leverage collective bargaining, and keeping tight records of use per experiment. These steps help justify purchases to both supervisors and grant reviewers.

    Another route involves closer attention to experimental design. By prioritizing dose-response studies, minimizing batch preparation losses, and tightening up documentation, research teams get more from every milligram. Years of troubleshooting have taught me that careful pipetting and proper sealing of vials during storage can double shelf life and prevent waste.

    An overlooked but effective solution is to share best practices across research teams. Informal talks, lab rotations, and peer mentorship make a difference—especially when they focus on the tiny hands-on tips that keep AICAR hydrate working as expected. Whether it’s a suggestion about dissolving the powder in ethanol before adding to water, or reminders to check the hydration percent on each new batch, community learning counts for more than any instruction manual.

    Final Thoughts

    AICAR hydrate doesn’t get flashy write-ups or trade show billboards, but it drives quiet revolutions in cell metabolism, pharmacology, and disease modeling. Its reputation comes from years of reliable performance, clear documentation, and a safety profile that fits the way scientific research works today: precise, cost-conscious, and always moving toward answers that matter. Every graduate student who’s run a Western blot on an AMPK pathway, or tracked metabolic flux in live tissue, knows this compound’s name. The work behind the scenes gets easier when trust begins with what’s inside the bottle—and that trust puts 5-Amino-1H-Imidazole-4-Carboxamide Hydrate in a class of its own.