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HS Code |
795618 |
| Iupac Name | 2-amino-5-bromopyridine-4-carboxylic acid |
| Molecular Formula | C6H5BrN2O2 |
| Molecular Weight | 217.02 g/mol |
| Cas Number | 221615-75-0 |
| Appearance | Solid (white to off-white powder) |
| Solubility | Slightly soluble in water |
| Smiles | C1=CN=C(C(=C1Br)C(=O)O)N |
| Inchi | InChI=1S/C6H5BrN2O2/c7-4-1-3(9)8-2-5(4)6(10)11/h1-2H,(H2,8,9)(H,10,11) |
| Pubchem Cid | 10171141 |
As an accredited 4-pyridinecarboxylic acid, 2-amino-5-bromo- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White plastic bottle with tamper-evident seal, containing 25 grams of 4-pyridinecarboxylic acid, 2-amino-5-bromo-, labeled with hazard symbols. |
| Container Loading (20′ FCL) | Container loading (20′ FCL) for 4-pyridinecarboxylic acid, 2-amino-5-bromo-: securely packed drums, sealed, with hazardous labeling, max 13–14 MT. |
| Shipping | Shipping of 4-pyridinecarboxylic acid, 2-amino-5-bromo- requires appropriate chemical packaging to prevent leaks or contamination. The container should be clearly labeled, sealed securely, and protected from moisture and extreme temperatures. Transportation must comply with local and international regulations for hazardous chemicals to ensure safety during transit and handling. |
| Storage | 4-Pyridinecarboxylic acid, 2-amino-5-bromo- should be stored in a tightly sealed container, protected from light and moisture. Keep the chemical in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizing agents. Proper labeling is essential, and access should be limited to trained personnel. Store according to institutional and regulatory guidelines for hazardous chemicals. |
| Shelf Life | 4-Pyridinecarboxylic acid, 2-amino-5-bromo- typically has a shelf life of 2-3 years if stored in a cool, dry place. |
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Purity 98%: 4-pyridinecarboxylic acid, 2-amino-5-bromo- with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures consistent yield and reproducibility. Melting point 235°C: 4-pyridinecarboxylic acid, 2-amino-5-bromo- with a melting point of 235°C is used in high-temperature organic reactions, where thermal stability minimizes decomposition risks. Particle size <10 µm: 4-pyridinecarboxylic acid, 2-amino-5-bromo- with particle size below 10 µm is used in catalyst preparation, where fine particle distribution enhances catalytic surface area. Moisture content <0.5%: 4-pyridinecarboxylic acid, 2-amino-5-bromo- with moisture content less than 0.5% is used in solid-phase peptide synthesis, where reduced moisture prevents unwanted hydrolysis. Stability temperature 60°C: 4-pyridinecarboxylic acid, 2-amino-5-bromo- with stability temperature up to 60°C is used in storage and transport applications, where chemical integrity is maintained under moderate thermal conditions. |
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Every day in our facility, the team handles compounds that have real impact on research, technology, and finished goods. 4-pyridinecarboxylic acid, 2-amino-5-bromo- grabbed our attention years ago, not only for its interesting coordination abilities but for the solid demand from a wide spectrum of chemical innovators. With a molecular formula of C6H5BrN2O2 and a structure that brings together a carboxylic acid group with both amino and bromo substitutions on a pyridine ring, this molecule occupies a special niche that chemists know well.
You see layered utility in 2-amino-5-bromo-4-pyridinecarboxylic acid. The carboxylic acid and amino placements give targeted reactivity, while the bromo substituent brings synthetic leverage for follow-up reactions. A structure like this provides both electron-withdrawing and donating effects on the pyridine core, not just changing reactivity but opening up different branches of chemical development. That dual functionality means the compound serves as a true platform molecule, rather than a one-use specialist.
Building this compound in-house sharpens your appreciation for purity, consistency, and the importance of process control. Slight shifts in reagent ratios or temperature can affect both the product’s color and its trace impurity profile. We pay attention to solvent choice, not just for yield, but for how it affects the crystalline habit. Each small detail counts—because downstream research for our partners relies on reproducibility, not just theoretical specs.
Competition exists in the specialty chemical field, but not all lots perform the same. Some sources cut corners on drying, skip extra purification, or rely on off-the-shelf intermediates. We start with high-purity pyridine derivatives and use carefully titrated halogen sources for bromination. Full batch records trace every vessel and batch of starting material, which backs up our product integrity with solid documentation.
Experience shows a direct relationship between starting purity and the ease with which customers perform coupling reactions on the finished acid. Customers using generic material often report side product formation, especially if chlorinated or iodinated impurities slip through. Our focus on removal of these trace contaminants may not sound glamorous, but it spares researchers hours of extra clean-up or troubleshooting.
By handling this compound at scale, we learn which physical attributes matter in day-to-day laboratory and industrial handling. The solid appears as a fine off-white to beige powder, depending on exact hydration and trace byproducts. We target a melting range around 220–225°C, confirmed by internal and third-party analysis. For solubility, water and common polar organics give different results, and we provide guidance from actual dissolution trials in our lab. Excess moisture can invite clumping, so we process under low-humidity conditions before double vacuum-packing shipments.
We regularly check purity by HPLC as well as NMR, confirming content above 98 percent for typical lots shipped. Customers in pharma or biotech sometimes need further documentation, so we've adapted routine runs to provide elemental analyses and residual solvent panels. This effort pays off when projects enter preclinical or pilot scale-up, and regulators scrutinize every detail.
Demand for this molecule tracks several trends: the development of heterocyclic pharmaceuticals, the growth of agricultural chemistry, and the push for new ligands in catalysis. Medicinal chemists value the amino and bromo substitutions as anchor points for diverse functionalization, particularly in coupling or substitution reactions. The carboxylic acid group often gets transformed into esters, amides or other derivatives that end up in drug-like frameworks.
Agriculture researchers lean on the compound for preparing advanced fungicides and herbicides where selectivity comes from judicious substitution patterns. The presence of the bromo group can also boost bioactivity, depending on the final scaffold. On the materials side, the molecule’s coordination ability as a ligand sometimes enters the realm of advanced polymers and metal complexes, particularly in projects that need both robustness and adaptability. Over the years, we've witnessed many creative applications emerge—sometimes beyond what textbooks predict.
Trading houses and resellers may offer lower prices upfront, but experience shows that quality, traceability, and willingness to customize matter more as projects evolve. By dealing directly with our manufacturing team, customers steer specifications as needed. Some request altered hydration states for specific processes, or ask for co-milled blends with related pyridines. A distributor rarely delivers this flexibility or the firsthand troubleshooting advice that’s grounded in manufacturing reality.
Having dealt with hundreds of shipments, we see how shipment duration, temperature, and storage conditions impact crystallinity and flow. We hear direct feedback and constantly refine handling and packing—an attention to detail that only comes from deep involvement, not mere sales.
The specialty chemical market includes a handful of structural isomers and related pyridine acids with varying amino and bromo positions. Shifting either group on the ring—say, preparing the 3-amino or 6-bromo analog—alters both electronic character and direct reactivity. Researchers aiming for a specific substitution pattern in a target molecule often discover that changing even a single position affects coupling yields, solubility, or even safety profile.
Compared to the non-brominated 2-amino-4-pyridinecarboxylic acid, the 5-bromo analog we prepare opens new routes to cross-coupling or halogen–metal exchanges. Lab records show higher yields in Suzuki or Buchwald–Hartwig reactions when using our high-purity compound, as bromo gives better leaving group ability than chloro in most protocols. Customers occasionally test the cheaper chloro- or unsubstituted derivatives, but feedback and published data usually tip the scale back toward the bromo material for cleaner transformations and less byproduct.
Problems begin when suppliers don’t understand the link between small variations during synthesis and practical downstream effects. We encountered customers whose formulations failed to pass stability tests due to concealed batch-to-batch shifts in impurity profiles. To fix that, we standardized every key step in the process, including batch record retention and periodic cross-checks by third-party labs. Transparency builds trust; partners see we back claims with concrete data rather than vague assurances.
Lot-to-lot variation often stems from resellers blending products from multiple factories. Our policy of discrete batches and consistent upstream sources builds confidence: clients have rerun reactions using our material and reported better reproducibility against previous generic supplies. This level of standardization supports both licensing submissions and rapid troubleshooting for those scaling up.
We don’t claim perfection, but we do own every step of the substance’s journey. Some newer users face trouble dissolving or formulating the powder for certain reactions. In response, we became more transparent about solubility and offered both protocol suggestions and real-life workarounds based on process experience. Every unusual customer issue—be it color shifts, filtration residue, or unexpected odor—triggers an in-house investigation and potential process tweak. That’s how we turn customer feedback into tangible improvements.
Continual staff training and equipment upgrades form the backbone of process knowledge; in recent years, upgrading crystallizers and improving in-line monitoring has reduced deviations and boosted first-pass yield. These investments pay off not just in cost control, but in building trust with repeat clients.
With tighter environmental regulations worldwide, chemical producers can't overlook waste minimization, energy conservation, and responsible sourcing. Producing 2-amino-5-bromo-4-pyridinecarboxylic acid involves handling reactive bromine sources and organic solvents that pose both health and waste concerns if unchecked. Our operation routes spent streams into onsite recycling whenever possible, combining chemical recovery with strict emissions controls. Modern scrubbers and solid waste handling prevent offsite impacts and align us with evolving government standards.
Employees receive detailed practical training, not just once but via ongoing refreshers, reducing errors and workplace accidents. That same safety-first mindset flows into packaging and supply chain. We select shipping containers and moisture barriers robust enough to handle seasonal humidity swings or extended sea transit.
Research is a long game. The fastest, least expensive order may not always bring the best results. We maintain close communication with organizations pushing boundaries, from university labs to advanced manufacturing start-ups. Sometimes, customers discover new reactivity or process quirks and call looking for insight. We consider these conversations opportunities to both learn and share, contributing real-world experience that strengthens the entire value chain.
Many of our largest success stories start not with a catalog sale, but with a phone call or email exchange describing a novel application or challenge. Sometimes, this means customizing packaging, adjusting particle size, or even tweaking process chemistry to match a new downstream reaction. We see ourselves as true participants in others’ breakthroughs, not just raw material suppliers.
Trust builds through clear, well-organized documentation. We don’t just ship a COA—we provide the batch data, impurity scan, and even the protocols used for confirmation. Regulatory offices and project managers often ask about supply chain partners or risk assessments. We built processes to document the origin of every batch, the safety controls in place, and the route logs for each delivery.
With global shipping routes regularly disrupted, keeping accurate real-time documentation means customers can plan better and answer their own reviewers confidently. This attention to detail helps customers win grants, clear regulatory hurdles, or assure investors that supply is both secure and ethical.
The chemistry field evolves fast. Molecular frameworks that seemed niche a decade ago now anchor new families of pharmaceuticals, crop science solutions, and materials. Our 2-amino-5-bromo-4-pyridinecarboxylic acid has moved into territory we didn’t always expect—roles in diagnostic reagents, host-guest systems, and advanced optoelectronic compounds.
As technology advances, so do expectations for documentation, reproducibility, and support. We keep refining processes and training to stay ahead, and our best innovators come from listening to those using the material every day. The molecule’s ability to flex between conventional and cutting-edge chemistry will keep it central to many sectors for years to come.
Real chemical manufacturing is less about glossy pitches and more about making sure each batch does what customers need—when and how they need it. 4-pyridinecarboxylic acid, 2-amino-5-bromo- teaches that lesson with every order. Years of hands-on production, constant feedback, and a willingness to adjust puts us in a position to deliver not just a molecule but reliable outcomes. That is how we see ourselves—as partners in real-world chemical progress, not just suppliers.