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HS Code |
333634 |
| Iupac Name | 5-amino-1H-imidazole-4-carboxamide |
| Molecular Formula | C4H6N4O |
| Molar Mass | 126.12 g/mol |
| Cas Number | 3031-94-5 |
| Appearance | White to off-white crystalline powder |
| Melting Point | 245-250°C (dec.) |
| Solubility In Water | Soluble |
| Pka | 8.68 (amino), 9.71 (carboxamide) |
| Boiling Point | Decomposes before boiling |
| Synonyms | AICA, 5-amino-1H-imidazole-4-carboxamide |
| Structure Type | Heterocyclic organic compound |
| Storage Conditions | Store at 2-8°C, tightly closed, dry place |
| Pubchem Cid | 1078 |
| Smiles | C1=NC(=C(N1)N)C(=O)N |
| Inchi | InChI=1S/C4H6N4O/c5-3-2(4(6)10)7-1-8-3/h1H,(H4,5,6,7,8,10) |
As an accredited 5-Aminoimidazole-4-Carboxamide (AICA) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 5-Aminoimidazole-4-Carboxamide (AICA) is packaged in a 25g amber glass bottle with a tamper-evident screw cap and clear labeling. |
| Shipping | 5-Aminoimidazole-4-Carboxamide (AICA) is shipped in tightly sealed, chemical-resistant containers, protected from light, moisture, and extreme temperatures. The packaging complies with safety regulations for laboratory chemicals. Transport is typically via ground or air freight, following established protocols for hazardous or sensitive substances to ensure integrity and safety during delivery. |
| Storage | 5-Aminoimidazole-4-carboxamide (AICA) should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry place, ideally at 2–8°C (refrigerator temperature). Avoid exposure to excessive heat, humidity, and incompatibles like oxidizing agents. Ensure proper labeling and store away from food and incompatible substances to maintain chemical stability and safety. |
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Purity 98%: 5-Aminoimidazole-4-Carboxamide (AICA) with a purity of 98% is used in nucleotide biosynthesis research, where high purity ensures reliable experimental results. Molecular Weight 111.10 g/mol: 5-Aminoimidazole-4-Carboxamide (AICA) featuring a molecular weight of 111.10 g/mol is utilized in metabolic pathway analysis, where precise dosing is critical for consistent bioactivity. Water Solubility 50 mg/mL: 5-Aminoimidazole-4-Carboxamide (AICA) with water solubility of 50 mg/mL is used in pharmaceutical formulation development, where enhanced solubility facilitates improved compound delivery. Stability Temperature up to 25°C: 5-Aminoimidazole-4-Carboxamide (AICA) stable up to 25°C is employed in enzyme activation assays, where stability at room temperature maintains reagent integrity. Particle Size <10 µm: 5-Aminoimidazole-4-Carboxamide (AICA) with particle size below 10 µm is incorporated in cell culture studies, where small particle size ensures uniform distribution in media. Melting Point 245°C: 5-Aminoimidazole-4-Carboxamide (AICA) with a melting point of 245°C is used in thermal stress testing, where high melting point allows for assessment under elevated temperatures. UV Absorbance λmax 262 nm: 5-Aminoimidazole-4-Carboxamide (AICA) exhibiting UV absorbance at λmax 262 nm is utilized in quantitative HPLC analysis, where distinct absorbance enables precise detection. |
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5-Aminoimidazole-4-Carboxamide, more commonly identified as AICA, represents a unique foundation in the landscape of fine chemicals. This compound, recognized for its purity and stability, holds a noteworthy position, especially where the synthesis of nucleotides and nucleosides comes into play. Unlike generic intermediates, AICA brings depth to chemical research and development, supporting both academic inquiry and real-world pharmaceutical innovation.
My experience in chemical analysis has taught me that purity makes a world of difference. Labs depend on fine-detail accuracy, much like a chef depends on fresh ingredients. The quality and reproducibility of results often hang on sourcing reliable intermediates. AICA, with well-defined structure and minimal contaminants, keeps reactions consistent. Its formula, C4H5N3O1, offers a firm platform for high-level synthesis tasks, particularly where the fine-tuning of DNA precursors or the development of enzyme inhibitors is involved.
Looking at real-world use, AICA typically comes in powder or crystalline form. The melting point, solubility profile, and spectral data shape how it performs in the lab. Experts usually check these properties by running HPLC, NMR, and mass spectrometry to confirm not only the presence of AICA but also its suitability for advanced synthesis. A high assay—usually over 98%, in my experience—sets the gold standard for serious lab work. Moisture content often falls in the single digits, ensuring material doesn’t degrade or clump.
I’ve noticed solubility stands out most when choosing between similar compounds. AICA dissolves nicely in water and most polar solvents, which speeds up experimental timelines. This trait becomes valuable for research teams under pressure to deliver results on a tight schedule. Workflows run smoother because less time gets lost to trial-and-error dissolutions or the frustration of undissolved solids.
Researchers frequently use AICA as a precursor in the creation of nucleoside analogues. Its imidazole ring, adorned with the right functional groups, acts as a bridge in nucleotide biosyntheses, particularly for analogues that mimic adenosine or guanine bases. In the pharmaceutical world, AICA helps assemble the backbones for drugs that modulate enzyme activity—especially those involved in metabolic diseases and immune response.
One striking difference between AICA and other intermediates is the role it plays in AMP-activated protein kinase (AMPK) research. AICA is famous for forming the basis of AICAR (5-aminoimidazole-4-carboxamide ribonucleotide), a compound celebrated for its ability to trigger AMPK pathways. This property has made it a standard tool for scientists exploring diabetes, energy metabolism, and exercise physiology. It’s rare for a chemical intermediate to influence such a wide span of scientific and medical fields, and I’ve seen researchers move seamlessly from basic synthesis to in vivo testing because they could trust the starting material.
On the supply side, AICA’s value lies less in sheer volume than in its consistent chemistry. Batch-to-batch variability can turn any promising synthetic route into a headache. The answer always circles back to reputable sourcing and trust in chemical certification. Whether running a small pilot study or ramping up for larger-scale manufacturing, reproducibility remains key. I’ve heard too many stories—some of my own—where projects faltered because someone gambled on a cheaper, inconsistent supply of an intermediate.
AICA’s production typically involves multi-step processes using specific protecting and deprotecting groups, ensuring that the desired five-membered ring structure forms cleanly. Each manufacturer holds its own secrets when it comes to yield optimization. Unlike some chemicals prone to racemization or unpredictable impurities, AICA generally arrives as a single, well-defined species. Stability on the shelf and during reactions stands out, making it easy to store and to weigh out for both one-off syntheses and automated work.
For anyone comparing AICA with other imidazole derivatives or nucleotide intermediates, the small details make all the difference. Many imidazoles lack the carboxamide function at position four, which can limit their downstream modification options. In practice, AICA’s functional groups lend themselves to a wide variety of substitution reactions, important when chemists want to introduce tailored modifications for specific targets. Some related compounds might suffer from lower aqueous solubility or can generate side-products more easily in standard coupling reactions, increasing purification steps and labor costs.
In my work, I’ve watched teams waste valuable days—sometimes weeks—chasing impurities caused by less selective intermediates. AICA’s defined reactivity and clean profile help avoid those detours. This alone makes it not just another building block on the shelf, but a trusted mainstay for anyone looking to avoid surprises. The result is more predictable reaction yields and a true reduction in troubleshooting.
Researchers across reputable institutions place a premium on traceability and documented quality. Certificates of analysis back up each lot of AICA with hard numbers for purity, heavy metal content, and residual solvents. This drives confidence not only in published results, but also in regulatory submissions and patent filings. My experience suggests that careful attention to supply-chain documentation can save labs from costly recalls or failed audits, keeping the focus on real discovery instead of paperwork disasters.
Stability also plays into safe handling. Unlike volatile solvents or unstable organometallics, AICA generally rests easy in the storeroom—provided containers stay dry and tightly closed. Standard precautions for fine powders—avoid inhalation, limit skin contact, and clean up spills promptly—apply as with most research chemicals. Supply partners help fill in these safety gaps by providing transparent safety data and updates on best handling practices, but day-to-day safety relies on habits built in the lab.
AICA enables more than just chemical transformations. Its most profound value emerges in biological studies, where AICAR—its ribonucleotide form—acts as a functional mimic for AMP. I’ve witnessed how this property jumpstarts studies of metabolic disease models, aging, and muscle physiology. AICAR clears a path for mapping out previously murky metabolic pathways, laying the groundwork for next-generation treatments. The credibility of such research ties directly to the confidence scientists place in the starting material, making the integrity of AICA supply a matter of more than just convenience.
The chemistry supporting AICA’s transformation into AICAR runs deceptively simple on paper: glycosylation, protection, and deprotection schemes. Yet tiny differences in the starting carboxamide intermediate create outsize effects downstream, impacting both product purity and biological activity. My own efforts at scaling up nucleoside analog synthesis taught me not to underestimate this fact. Sourcing from reliable suppliers, confirming clean analytical spectra before each new batch—these small steps shield teams from missed milestones later.
Scaling up for pharmaceutical pipelines introduces a new layer of scrutiny. Sourcing from reputable chemical companies, checking for ISO and GMP compliance, and demanding third-party analytical confirmation all build a buffer against poor outcomes. For operations outside big pharma, shared knowledge—peer-reviewed records, published analytical profiles, and cross-lab validations—help keep standards high across the industry.
Transportation presents its own challenges. AICA’s solid, non-volatile nature makes shipping straightforward, avoiding the tight restrictions placed on corrosive liquids or controlled substances. Still, suppliers who pay close attention to packaging—multi-layer, moisture-proof bags, for example—cut down on waste or accidental exposure. The future of chemical logistics may see more real-time tracking and integrated chain-of-custody platforms; every missed shipment or unexplained delay costs scientists both productivity and peace of mind.
From a research angle, AICA functions as more than a stepping stone to test tubes and technical papers. Its predictable behavior in both bench-scale and pilot-scale reactions encourages researchers to take bold approaches without worrying that the basics will let them down. Students on their first organic synthesis project, veteran chemists troubleshooting a metabolic pathway—all benefit from the reliability AICA brings.
AICA also offers an empowering force for small-batch and specialty API manufacturers. Where off-the-shelf building blocks falter, a well-characterized intermediate like AICA enables faster product development cycles. Combined with the explosion of automated synthesis and robotic platforms, AICA keeps pace with both traditional hands-on chemistry and the next wave of digital-led manufacturing.
AICA’s use doesn’t stop at the reaction vessel. Labs committed to sustainability take special care in minimizing chemical waste—recovering excess materials, tracking solvents, and applying greener disposal methods. The limited toxicity and straightforward handling of AICA align nicely with these efforts. Manufacturers focused on environmental responsibility optimize their production routes to cut down on hazardous by-products, conserve water, and use energy more efficiently.
Community knowledge-sharing helps expand responsible use outside single research labs. Publishing best practices for AICA’s integration into both basic and clinical research builds a foundation for smarter science. Regular review of literature, honest reporting of synthesis pitfalls, and open access to data amplify the impact of a compound that, despite its small footprint, shapes some of the biggest breakthroughs in drug discovery and molecular biology.
As scientific knowledge deepens, more projects gravitate to sophisticated nucleotide and nucleoside analogues. Robust, reproducible intermediates like AICA will only grow in importance. Advances in process chemistry may push for even tighter purity standards and greener production methods. With AI reaching into synthetic route discovery, automated quality monitoring, and logistics, the boundaries of AICA’s impact will likely expand.
Transparency, peer validation, and a commitment to quality provide the guardrails for safe, sustainable innovation. Both established enterprises and younger startups invest in traceability, digital recordkeeping, and responsive supply-chain partnerships to deliver AICA where and when it matters most. I’ve seen that team spirit, in the end, lifts all researchers. A solid intermediate brings out the best in collaborative problem-solving, helping transform raw scientific curiosity into new treatments and discoveries for tomorrow.
AICA’s lasting value comes from more than just its role in the reaction flask. It represents a legacy of rigorous standards, collective learning, and ongoing stewardship. Scientists and suppliers alike share the responsibility for safeguarding both quality and transparency. Each test for purity, each documented procedure, and every honest report of successes—and failures—strengthens the chain of trust that lets the next scientific leap forward land on solid ground.
Every time a researcher uncaps a bottle of AICA, there’s a silent acknowledgment that precision and care matter as much as inspiration. Thoughtful sourcing, open communication, and persistent attention to detail keep experiments on track and ideas moving forward. The success stories built on this compound belong not just to those behind the bench, but to the broader communities they aim to serve.
Across the spectrum of drug discovery, metabolic research, and materials chemistry, 5-Aminoimidazole-4-Carboxamide plays an outsized role in enabling innovation. Its proven performance, clean handling, and scientific trustworthiness support projects from early brainstorming to finished application. As challenges in health and technology grow more complex, having foundational resources that perform without guesswork matters more than ever.
Researchers face enough unknowns; building on a base as solid as AICA means fewer distractions, more focused creativity, and results that stand up to both peer scrutiny and the pressures of translation from lab bench to real-world problem solving. By investing in quality, transparency, and the best science available, both suppliers and users of AICA lay the groundwork for the next era of discoveries—turning today’s questions into tomorrow’s answers.