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HS Code |
417161 |
| Chemical Name | 2-Amino-5-pyridinecarboxylic acid |
| Molecular Formula | C6H6N2O2 |
| Molecular Weight | 138.12 g/mol |
| Cas Number | 7418-67-7 |
| Appearance | White to off-white solid |
| Melting Point | 245-250°C |
| Solubility In Water | Moderately soluble |
| Pka | 2.41 (carboxyl), 4.67 (amino) |
| Synonyms | 5-Carboxy-2-aminopyridine |
| Pubchem Cid | 200423 |
| Inchi Key | JLQDRGNNYLRJKF-UHFFFAOYSA-N |
| Smiles | C1=CC(=NC=C1C(=O)O)N |
| Storage Conditions | Store at room temperature, away from light and moisture |
As an accredited 2-Amino-5-PyridineCarboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging contains 100 grams of 2-Amino-5-Pyridinecarboxylic Acid, sealed in an amber glass bottle with detailed hazard labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 2-Amino-5-PyridineCarboxylic Acid is securely packed in 25kg drums, totaling approximately 8-10 metric tons per container. |
| Shipping | 2-Amino-5-Pyridinecarboxylic Acid should be shipped in tightly sealed containers, protected from moisture and heat. It should be labeled appropriately and transported in accordance with local and international chemical regulations. Avoid contact with incompatible substances, and follow all safety data sheet (SDS) guidelines during handling and shipping to ensure safe delivery. |
| Storage | 2-Amino-5-pyridinecarboxylic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect the chemical from moisture and direct sunlight. Keep the storage area secure and clearly labeled, following all applicable local, state, and federal regulations for chemical storage. |
| Shelf Life | 2-Amino-5-pyridinecarboxylic acid should be stored tightly sealed, in a cool, dry place; typically stable for at least two years. |
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Purity 99%: 2-Amino-5-PyridineCarboxylic Acid with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yields and minimal byproduct formation. Melting Point 273°C: 2-Amino-5-PyridineCarboxylic Acid with melting point 273°C is used in high-temperature heterocycle formation, where it maintains compound integrity during synthesis. Particle Size <10 µm: 2-Amino-5-PyridineCarboxylic Acid with particle size less than 10 µm is used in fine chemical formulation, where it promotes uniform blending and dispersion in solid mixtures. Solubility in Water 50 mg/mL: 2-Amino-5-PyridineCarboxylic Acid with water solubility of 50 mg/mL is used in aqueous solution preparation, where it allows for concentrated stock solutions in laboratory analysis. Stability Temperature up to 150°C: 2-Amino-5-PyridineCarboxylic Acid with stability up to 150°C is used in heated batch reactions, where it resists degradation and ensures consistent product quality. Molecular Weight 138.13 g/mol: 2-Amino-5-PyridineCarboxylic Acid with molecular weight 138.13 g/mol is used in analytical calibration standards, where it provides accurate quantification in instrumental assays. |
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In today’s labs and chemical supply chains, 2-Amino-5-PyridineCarboxylic Acid delivers more than just another molecule with a complicated name. With the chemical formula C6H6N2O2, it offers a unique balance between reactivity and stability. Many researchers, including those diving into pharmaceutical development and specialty materials, rely on this compound for various synthesis paths that other aminopyridine derivatives don’t quite match.
My own colleagues in the medicinal chemistry space have often pointed out how 2-Amino-5-PyridineCarboxylic Acid stands out when exploring heterocyclic structures. This acid acts as a stable building block that supports nuanced modifications, allowing for targeted adjustments and greater flexibility during complex molecule construction.
With a molecular weight of 138.13 g/mol and a solid, crystalline appearance, this compound holds up well in standard storage conditions. Chemists appreciate its slightly bitter scent because it gives a quick cue about purity levels. Unlike some relatives in the aminopyridine family, 2-amino-5-pyridinecarboxylic acid offers a high melting point, generally falling between 230°C and 234°C, which minimizes the risks associated with volatility.
Not all pyridine carboxylic acids offer the same solubility. This one dissolves well in water at moderate temperatures, allowing easier handling in both academic and commercial environments. It also shows decent compatibility with polar organic solvents. That adaptability matters when someone in the lab wants to avoid long-winded workarounds with other, more stubborn chemicals.
In pharmaceutical circles, new research methods rarely stick to cookie-cutter recipes. That's why finding a carboxylic acid that doesn’t break down easily, react uncontrollably with standard solvents, or bring unpredictable impurities into the mix matters. 2-Amino-5-PyridineCarboxylic Acid brings those strengths together, providing a backbone for synthesizing a whole class of bioactive compounds—think kinase inhibitors, potential anti-inflammatories, and candidates for CNS drugs.
Industrial researchers also see value in this molecule when looking for intermediates that don’t send process costs through the roof. Whether it’s cobalt-catalyzed coupling or Suzuki-Miyaura reactions, having a reliable pyridinecarboxylic acid keeps development timelines on track. In an age where speed from lab bench to shelf makes or breaks project budgets, every dependable building block counts.
The first time I observed 2-Amino-5-PyridineCarboxylic Acid in a real project, it was during a process development review for a small molecule pharmaceutical compound. The R&D team debated switching to a cheaper carboxylic acid to trim initial costs. Within weeks, the project circled back to this molecule because alternative routes produced either inconsistent yield or, worse, unpredictable by-products that set the team back further than anticipated.
That story plays out again and again. Too often, teams push for alternatives based solely on superficial similarities. With 2-Amino-5-PyridineCarboxylic Acid, the position of the amino and carboxylic groups unlocked a diversity of reactivity that’s simply not achievable with meta- or para-substituted relatives. It sounds technical until someone witnesses the wasted hours of troubleshooting disappear when the right substrate unlocks predictable conversions instead of experimental headaches.
Sourcing quality chemicals now isn’t just about purity on paper. The industry watches closely for sustainable processes and traceability. Suppliers offering 2-Amino-5-PyridineCarboxylic Acid with comprehensive quality control histories and transparent supply chains see increased demand. GMP-compliant batches let pharmaceutical teams move ahead with confidence during regulatory submissions. Analytical certificates go beyond a checklist; they keep everyone involved accountable, from sourcing agents to lab managers.
It helps that this compound’s synthesis typically uses safer starting materials than some of the alternatives in its class. Some modern production methods lower environmental impact by sidestepping unnecessary halogenations or oxidations. Lab teams who have seen environmental compliance issues hold up entire milestones know that saving time on regulatory review lets projects avoid expensive delays. Corporate sustainability goals now push vendors to reexamine their materials and cleaning agents, rewarding those who can provide documentation that stands up to outside audit.
It’s easy to lump all pyridine-based carboxylic acids together, but researchers benefit by understanding real differences at the molecular level. Other aminopyridinecarboxylic acids don’t deliver the same selective reactivity, especially in palladium-catalyzed couplings or amidations. Some analogues, including those with substitutions at the 3- or 4-positions, run into issues with selectivity, making purification a time-consuming slog.
Practically speaking, shifting the amino group even a single carbon away can mean the difference between a single, clean product and a spectrum of unwanted isomers. From a commercial standpoint, that inefficiency expands costs and can even force teams to abandon a route entirely. In my own work supporting medicinal chemistry programs, side products from less optimal analogues caused spectral overlap headaches in NMR and added hours to HPLC method development. With 2-Amino-5-PyridineCarboxylic Acid, that hassle shrinks, giving researchers a better chance of keeping their workloads focused on breakthroughs rather than troubleshooting.
As demand grows for innovative molecules in pharmaceutical and biotech research, so too does attention to reliable sources for specialty chemicals. Labs can’t afford last-minute surprises with key starting materials. I’ve seen project calendars slide by weeks simply because a poorly sourced batch of this acid introduced trace impurities that compromised downstream steps. Reliable suppliers provide not just an analysis report, but also documentation covering origin, transport, and handling, reducing the risk of batch-to-batch inconsistency.
For scale-up teams, reproducibility is non-negotiable. Unexpected shifts in melting point or solubility can stall an entire workflow. Over multiple projects, suppliers that fail to deliver to tight specs quickly lose favor. In contrast, companies that consistently offer high-purity 2-Amino-5-PyridineCarboxylic Acid become go-to partners due to fewer failed reactions and less time wasted on root-cause analysis. That’s not marketing fluff—it reflects years of lived reality among chemists and purchasing managers.
So many process bottlenecks begin with something as simple as the wrong building block. Upgrading inventory to include 2-Amino-5-PyridineCarboxylic Acid isn’t just a matter of having more options—it’s about unlocking smoother workflows. In projects where a narrow window for functional group transformation exists, this compound’s unique substitution pattern often acts like an all-access pass, allowing developers to bypass steps that add little but cost and time.
For newer players in the field, the best approach often involves talking directly to experienced vendors who understand project needs, rather than shopping by price tag or sticking to the most familiar catalog products. Informed conversations about assay values, byproducts, and documentation beats batch rework every time. Project leads who dedicate time to qualifying their material sources early on save days of troubleshooting and slowdowns during critical phases.
Technical teams can also benefit from direct engagement with suppliers about process changes and supply chain transparency. Environmental responsibility now sits center stage in sourcing discussions, and customers take notice of any shifts in manufacturing or handling practices. Clear documentation, open communication, and a willingness to address questions upfront stand out more than any brochure or technical data sheet.
Drug discovery, especially in small-molecule research, often resembles a patchwork of puzzle pieces that have to fit just right. 2-Amino-5-PyridineCarboxylic Acid, with its position-specific amino and carboxylic groups, gives medicinal chemists an adaptable scaffold to build next-generation therapies. Its reactivity profile falls in a sweet spot where functionalization is both manageable and reliable—not so sluggish that it requires forcing conditions, but not so reactive that it creates off-target products.
This acid’s unique setup has inspired various teams to pursue heterocycle-rich compound libraries. In one start-up lab I worked with, choosing this acid as a core intermediate boosted overall success rates across a portfolio of kinase inhibitor projects. The team attributed that improvement directly to the controlled reactivity enabled by the 2- and 5-positions, which opens doors to easy amidations, acylations, and more targeted transformations in late-stage modifications.
Computational chemists working on virtual screening see similar benefits. Using a scaffold that allows for easy computational enumeration and synthesis translates directly to faster lead optimization cycles. Stable building blocks lower the risk when moving from in-silico design to physical synthesis, and having access to robust, consistent reagents like 2-Amino-5-PyridineCarboxylic Acid reduces the likelihood of failed scale-up due to previously undetected molecular quirks.
Quality control makes or breaks any advanced chemistry operation. Most veteran chemists build a checklist for each new batch, but surprises can still pop up with off-the-shelf chemicals. Common headaches include trace inhibitors leftover from upstream processing or subtle moisture pickup during storage and transport. Labs that frequently handle 2-Amino-5-PyridineCarboxylic Acid invest in proper monitoring, not just of purity but also shelf life and packaging.
Thoughtful implementation goes beyond best practices. Storing this compound in air-tight, light-resistant containers and working under dry conditions prevent hydrolysis or other breakdown pathways. Analytical methods like HPLC and NMR serve as trusted allies for routine quality checks, but confirming supplier practices on stabilization agents and production methods provides an additional layer of assurance.
Direct feedback loops with vendors—sharing observations about solvent compatibility or minor impurities—create improvements that ripple out into wider chemist communities. My own experience working across several university-industry collaborations showed that open dialogue about practical stumbling blocks fosters innovation and smoother workflows for everyone involved.
Whether powering the next phase in drug discovery or supporting material science projects, 2-Amino-5-PyridineCarboxylic Acid builds credibility by showing up, batch after batch, with predictable performance. Bioactive compound libraries, diagnostic probe development, and emerging green chemistry applications draw from its stable core structure and selective reactivity.
Its strong roots in synthetic chemistry give start-ups and established firms a leg up without the risk of unpredictable behavior that sometimes sidelines riskier analogues. In hands-on terms, this translates to saved budgets, fewer failed experiments, and a more direct route from bench to patent application. In the relentless push to innovate, reliable chemical partners give teams space to chase real breakthroughs instead of putting out preventable fires.
The spotlight now shines on chemicals that do more than hit baseline metrics. Buyers want proactive answers about environmental impact, supply resilience, and traceability. Sourcing agents face pressure to confirm not just downstream performance but also responsible practices up the chain. Forward-thinking suppliers adapt accordingly, providing not just high-purity material but also open books on solvent use, waste treatment, and process audits.
Concrete steps help build trust. Working with partners who commit to regular third-party testing, full documentation trails, and open updates on process changes ensures continued supply of 2-Amino-5-PyridineCarboxylic Acid that matches evolving needs. As more organizations set public goals for greener chemistry, communication between vendor and client helps turn policies into best practices.
From small-scale research programs to full-scale manufacturing, the value of 2-Amino-5-PyridineCarboxylic Acid comes down to results delivered by real people solving high-stakes problems, one new compound at a time. With the right information, stewardship, and collaboration, this compound supports innovation long after its first introduction in the literature.