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HS Code |
467092 |
| Chemicalname | 2-Amino-5-carboxypyridine |
| Molecularformula | C6H6N2O2 |
| Molecularweight | 138.13 g/mol |
| Casnumber | 3430-14-6 |
| Appearance | White to off-white solid |
| Meltingpoint | 285-288°C |
| Solubility | Soluble in water |
| Pka | 2.0 (carboxylic acid), 4.5 (amino group, approximate) |
| Smiles | C1=CC(=NC=C1C(=O)O)N |
| Inchi | InChI=1S/C6H6N2O2/c7-5-2-1-4(6(9)10)3-8-5/h1-3H,(H2,7,8)(H,9,10) |
As an accredited 2-Amino-5-carboxypyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100-gram 2-Amino-5-carboxypyridine is packaged in a sealed, amber glass bottle with a tamper-evident screw cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-Amino-5-carboxypyridine: securely packed in sealed drums or bags, efficiently loaded and optimized for transport. |
| Shipping | 2-Amino-5-carboxypyridine is shipped in tightly sealed containers to prevent moisture absorption and contamination. It should be transported under ambient temperature, complying with standard chemical handling regulations. Ensure labeling for hazardous material as appropriate. Store and ship away from incompatible substances, and follow all local and international shipping guidelines for laboratory chemicals. |
| Storage | 2-Amino-5-carboxypyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Protect it from moisture and direct sunlight. Store at room temperature, and ensure the storage area is clearly labeled and only accessible to trained personnel. Always follow standard safety and handling practices. |
| Shelf Life | 2-Amino-5-carboxypyridine typically has a shelf life of at least 2 years when stored in a cool, dry, tightly sealed container. |
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Purity 98%: 2-Amino-5-carboxypyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high product yield and minimal impurities. Melting point 249°C: 2-Amino-5-carboxypyridine of melting point 249°C is used in heat-stable dye formulations, where it provides consistent thermal stability during processing. Particle size <10 µm: 2-Amino-5-carboxypyridine with particle size below 10 µm is used in catalyst manufacturing, where it improves surface area and catalytic efficiency. Aqueous solubility 30 mg/mL: 2-Amino-5-carboxypyridine featuring aqueous solubility of 30 mg/mL is used in injectable drug design, where it enhances bioavailability and drug delivery. Stability temperature up to 120°C: 2-Amino-5-carboxypyridine stable up to 120°C is used in high-temperature reaction environments, where it maintains structural integrity and consistent reactivity. UV absorbance (λmax 275 nm): 2-Amino-5-carboxypyridine with UV absorbance at λmax 275 nm is used in analytical reference standards, where it provides reliable calibration for spectrophotometric analysis. Moisture content <0.5%: 2-Amino-5-carboxypyridine with moisture content less than 0.5% is used in electronics chemical processing, where it prevents hydrolysis-related degradation and prolongs shelf life. |
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It's easy to browse through chemical catalogs and spot a dozen pyridine derivatives, but 2-Amino-5-carboxypyridine speaks up for itself through its composition and functional group arrangement. With an amino group at position 2 and a carboxylic acid at position 5, this compound offers unique reactivity that’s tough to find in generic substitutes. The structure isn’t just a trivial detail for chemists either — each functional group means a new route for derivatization, which appeals whether you’re planning to synthesize pharmaceuticals, explore new catalysts, or develop research reagents. The molecular formula, C6H6N2O2, seems simple, but its backbone shapes plenty of outcomes in a lab setting.
Even after years in the lab, the feeling you get when a stubborn reaction finally comes together thanks to just the right scaffold never gets old. I’ve found 2-Amino-5-carboxypyridine’s dual functional groups open up some genuinely flexible routes for synthetic transformations. For example, coupling the para-positioned acid group offers more selective amidation or esterification than you’d get with compounds where reactive moieties sit next to each other. That nuance in positioning helps during stepwise synthesis — you can dodge common byproduct headaches and gain more control over reaction sequences.
One practical project involved piecing together a heterocyclic drug lead candidate. Many intermediates just didn’t offer the kind of selective access or mild reaction conditions that 2-Amino-5-carboxypyridine provided. Instead of juggling awkward protecting group steps, this model allowed straightforward peptide coupling, clean ring closures, and easy purification. Simple functional group interplay can sound dull until you experience the hours saved — and a cleaner NMR spectrum the next morning. Anyone who works at the bench recognizes how small molecular differences spare afternoons filled with column chromatography and troubleshooting.
In academic or industrial settings, finding a solid starting point for new analogs puts you ahead of the game. This compound’s combination of hydrophilic and nucleophilic centers expands not just synthetic options, but also potential biological activity — crucial for teams screening new leads or fine-tuning active ingredients. Its carboxylic group easily forms salts or esters, which allows for ready solubility adjustments and increased pathway flexibility compared to mono-functionalized pyridines. That opens up new lanes in pharmaceutical and agrochemical research, where solubility and absorbency often bottleneck progress.
Contrast that with other pyridine derivatives. 2-Aminopyridine misses the versatility added by a carboxy group. 2-Carboxypyridine, on the other hand, restricts possibilities by only offering one active handle. Working with 2-Amino-5-carboxypyridine reminds you how much added value a second, properly positioned group brings for building complexity or branching out into libraries of analogs. The ability to vary reaction order lets researchers dial in on optimal synthetic strategies rather than being locked to a rigid path.
It’s tempting to get lost in the specifics, but in daily practice, this compound supports advances in drug discovery, dye manufacturing, and specialty material synthesis. Researchers chasing new antibacterial agents or chelating ligands often reach for this molecule to scaffold diverse libraries. The amino group can take up acyl, sulfonyl, or alkyl substituents, while the acid end enables easy linkage to other moieties. In advanced pharmaceutical synthesis, these coupling options support both hit identification and optimization, since medicinal chemists must balance potency, solubility, and metabolic stability all at once.
I’ve seen small biotech teams gravitate to this model during the early hit-to-lead phase, where structure-activity relationships hinge on the flexibility of chemical modifications. That comes into sharper focus when competing platforms offer little customization. Even high-throughput screening robots still need compounds that qualify for simple, robust SAR studies. Some production labs leverage its reactivity to develop new fluorescent probes for diagnostic kits, or as intermediates for specialty polymers that anchor protein binding domains. In all those cases, the dual functional nature easily saves steps and reduces isolation hassles.
Not every supplier meets the stringent demands of pharmaceutical or analytical grade research. Contaminants or poor batch consistency can tank a synthetic route or throw data reliability into question. Most widely used forms hover around 97–99 percent purity, though higher is available for more sensitive applications. The crystalline solid dissolves well in water and common organic solvents, which is convenient for preparation and workup steps. Handling is straightforward, avoiding some of the volatility or scent issues found in similar pyridine compounds. Still, moisture sensitivity remains, especially during storage, making well-sealed containers and dry conditions a must for maintaining shelf stability.
Availability ranges from laboratory gram-scale packaging to multi-kilogram orders for industrial synthesis. Teams developing scale-up processes quickly notice the difference between a compound they can order off-the-shelf in robust supply, and niche species that force custom syntheses and unpredictable lead times. Efficient cost and reliable logistics have real impact — especially for companies running dozens or hundreds of analog syntheses each quarter.
Working with fine chemicals always nudges one to consider both human health and environmental risks. 2-Amino-5-carboxypyridine avoids the harsh volatility of lower-weight pyridine analogs, making inhalation less of a worry, but skin and eye contact risks remain standard. Gloves and eye protection form the baseline for any good lab safety protocol. Environmental breakdown studies show moderate persistence, but wastewater steps should rely on activated carbon or advanced oxidation for best-practice remediation. Compared to some multi-halogenated or heavily nitrated pyridine derivatives, this compound presents a less toxic profile and a reduced ecological hazard, supporting safer research and manufacturing environments.
Compliance with modern chemical policy — whether REACH, TSCA, or local safety standards — counts more each year. Downstream users increasingly ask for assurance on both workplace exposure limits and environmental fate. This compound offers a solid track record, but documentation from reliable suppliers remains key to keeping regulators satisfied. Assessing product traceability and audit trails has become part and parcel of even mid-size research operations.
Chemical procurement choices impact both cost and research success. While the upfront price matters, hidden costs lurk in unreliable shipping, sketchy certificates of analysis, or unpredictable purity. In comparing 2-Amino-5-carboxypyridine options, it pays to look at supplier reputation, established batch history, and quality assurance protocols. In some markets, sellers emphasize “low price” without supporting claims. Time wasted validating a subpar batch or adjusting synthetic steps after a surprise impurity profile adds more headaches — and expenses — than most purchasing agents anticipate.
I’ve run scale-ups where a subtle contaminant, not declared on the supplier’s certificate, stalled everything. We traced the batch back to a source with lax QC and ended up paying more in time and repeat orders to fix the problem than if we’d picked a premium vendor to start. That lesson — buy from verified, transparent sources — stuck with me. Down the line, this extra scrutiny means avoiding the frustration of seeing odd signals spike in your analytics, or — worse — losing months on a project that won’t replicate due to impurity-driven artifacts.
Every field pushes for more sustainable, cost-effective synthetic routes. 2-Amino-5-carboxypyridine supports green chemistry by reducing multi-step protection protocols, which translates to fewer solvents and reagents spent in each run. As pharmaceutical research leans harder into process sustainability, molecules that merge two independently functionalized groups deliver more with less. Researchers aiming for API (active pharmaceutical ingredient) candidates can more easily avoid non-compliant intermediates or excessive byproducts.
Not every team focuses on the same endpoints. Diagnostics benefit from the building block’s reactivity, enabling the attachment of marker groups or signal molecules under mild conditions. Material science groups experiment with its scaffolding potential in custom polymers or next-gen ligands for targeted delivery or novel sensing platforms. On the regulatory front, the clear molecular map — with an established usage history — helps expedite registration and avoids the traps of newly-minted “designer” compounds whose endpoints remain unknown.
Globalization has filled warehouses with a dizzying range of specialty building blocks, but recent disruptions made supply chain security a boardroom issue again. For researchers and manufacturers, a reliable stream of intermediates like 2-Amino-5-carboxypyridine allows steady progress, rather than waiting out shipping or customs lags. In some sectors, switching to local or regionally sourced material builds resilience. Savvy buyers look for suppliers with documented quality control, backup production sites, and rapid order fulfillment.
Firms under tight timelines — startups chasing regulatory milestones or pharmaceutical majors scaling a new drug — benefit from partnering with vendors who understand not only the chemistry but the project’s urgency. Delays can cost millions or tip the balance on back-to-back development programs, underlining the real-world value of thoughtful sourcing. This isn’t about a single product’s spec sheet, but about integrating supply-side thinking with R&D planning, so ideas travel smoothly from design to delivered product.
Decisions rarely rest on technical details alone. Global regulatory trends, pushback against hazardous processing, pressure to show greener methods, all shape procurement. Lab directors need proof of full traceability and credible documentation, not just a bottle dropped at their door. For teams navigating regulatory approval, paperwork and raw material sourcing have become nearly as important as chemical reactivity itself.
The product’s positioning in chemical catalogs reflects a long-standing record as a go-to intermediate for both new drug entities and established product pipelines. In some review articles and patent databases, 2-Amino-5-carboxypyridine appears as an essential building block for kinase inhibitors and metal chelators, two classes of compounds on the front line of modern therapeutics and diagnostics. These examples show how practical utility fits hand-in-glove with regulatory approval pathways.
Research chemists routinely weigh the tradeoffs between single- and dual-functionalized pyridines. 2-Amino-5-carboxypyridine outpaces mono-functional analogs by streamlining synthetic planning and supporting denser functionalization. Though some options offer similar base frameworks, few present as much opportunity for selective substitution and coupling under mild conditions. Even more exotic analogs, festooned with halogens or rings, often bring new headaches — toxicity, expensive raw materials, or limited reactivity.
This cost-benefit balance guides both big pharma and academic labs. In the chase for new molecules, researchers hunt for scaffolds that grow with their project’s needs, not ones that close off directions. Scalability, safety, and multipurpose chemistry keep 2-Amino-5-carboxypyridine in play amid a tide of more complicated, less tractable specialty chemicals.
Despite the advantages, risk lies in every chemical supply chain. Poor documentation, inconsistent batches, or low-grade material slip into the market, especially for high-demand intermediates. One solution: build direct relationships with reputable suppliers, request comprehensive batch analysis, and invest in periodic third-party verification. Internal professional development — keeping scientists up-to-date on both regulatory trends and analytical verification — helps organizations anticipate and sidestep these pitfalls.
In terms of laboratory safety, routine training doubles as a solution to many common mishaps. Regular refreshers on handling corrosive agents, understanding MSDS sheets, and disposal protocols reduce the odds of accidental exposure or downstream environmental issues. Investment here pays off, since insurance and regulatory compliance almost always cost less up front than after an incident.
The best R&D programs tap not only into chemistry, but also a community of practice. Ask any working chemist, and a chain of mentors, colleagues, and vetted suppliers stands behind projects that nail both the science and the logistics. With 2-Amino-5-carboxypyridine, deep domain knowledge — from optimal coupling conditions to regulatory documentation — supports safe, predictable, and successful research. New graduates or techs can come up to speed quickly when they’re handed a well-characterized product with a legacy of diverse usage.
Encouraging a culture of information sharing, open data reporting, and knowledge transfer stands out as an everyday solution to many of the industry’s headaches. Labs that bookmark not just publications but real-world process notes build stronger, more resilient programs. That’s how incremental change leads to real organizational expertise and accelerates scientific discovery.
If you walk through the history of modern organic synthesis, the progress always belongs to those who combine solid basics with smart innovation. 2-Amino-5-carboxypyridine exemplifies this blend: foundational in its reliable chemistry, flexible in the hands of creative researchers, and proven across diverse sectors. The real power of this compound lies not in novelty, but in the connectivity and expanded options its structure offers.
Whether the goal is reliable production for an established process, inventive new routes for novel targets, or a safer, greener workflow, the right building block makes a difference. Choice matters — both in the molecules added to the toolbox and the teams assembled for the journey. As I look back on projects where the smart selection of key intermediates unlocked new opportunity, the lesson is clear. The compounds that survive changing trends and tough regulations are those that balance versatility, safety, and practical value.
So, for those planning their next synthesis or mapping out multi-step production, this model deserves a place at the top of the shortlist. Experience tells me that with every experiment and every step toward greater safety or innovation, the choice of the right chemical tool can mean the difference between frustration and discovery.