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HS Code |
146434 |
| Product Name | 3-Amino-5-bromo-2-chloropyridine |
| Cas Number | 61373-33-5 |
| Molecular Formula | C5H4BrClN2 |
| Molecular Weight | 207.46 g/mol |
| Appearance | Light yellow to yellow crystalline powder |
| Melting Point | 78-82°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water |
| Smiles | Nc1cncc(Br)c1Cl |
| Inchi | InChI=1S/C5H4BrClN2/c6-3-1-4(8)9-2-5(3)7/h1-2H,(H2,8,9) |
| Storage Condition | Store at room temperature, keep container tightly closed |
| Synonyms | 3-Amino-5-bromo-2-chloropyridine |
As an accredited 3-Amino-5-bromo-2-chloropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3-Amino-5-bromo-2-chloropyridine, 25g, is supplied in a tightly sealed amber glass bottle with a printed hazard label. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Standard 20-foot container, packed with securely sealed drums or bags of 3-Amino-5-bromo-2-chloropyridine, ensuring safe transport. |
| Shipping | 3-Amino-5-bromo-2-chloropyridine is shipped in tightly sealed containers, packaged to prevent moisture and contamination. It should be stored in a cool, dry environment, away from incompatible substances. Ensure compliance with all local, national, and international regulations regarding the transport of hazardous chemicals, including proper labeling and documentation. |
| Storage | **3-Amino-5-bromo-2-chloropyridine** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. Avoid exposure to moisture and humidity. Store the chemical at room temperature and ensure that proper chemical labeling is present. Handle with appropriate personal protective equipment to avoid inhalation or skin contact. |
| Shelf Life | 3-Amino-5-bromo-2-chloropyridine is stable under recommended storage conditions; shelf life is typically 2–3 years in a cool, dry place. |
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Purity 98%: 3-Amino-5-bromo-2-chloropyridine with a purity of 98% is used in pharmaceutical intermediate synthesis, where high purity ensures optimal reaction yields and minimal side product formation. Melting Point 94-98°C: 3-Amino-5-bromo-2-chloropyridine with a melting point of 94-98°C is used in agrochemical research, where defined thermal properties support process stability during formulation. Molecular Weight 223.44 g/mol: 3-Amino-5-bromo-2-chloropyridine with a molecular weight of 223.44 g/mol is used in heterocyclic compound production, where precise stoichiometry improves end product consistency. Stability Temperature up to 80°C: 3-Amino-5-bromo-2-chloropyridine stable up to 80°C is used in dye manufacturing, where resistance to decomposition under processing conditions enhances pigment quality. Particle Size <50 µm: 3-Amino-5-bromo-2-chloropyridine with particle size below 50 µm is used in catalytic applications, where increased surface area improves catalytic efficiency and reaction rate. |
Competitive 3-Amino-5-bromo-2-chloropyridine prices that fit your budget—flexible terms and customized quotes for every order.
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In the world of chemical manufacturing and drug development, precision determines outcomes. One compound standing out in the toolkit of medicinal chemists and industrial researchers is 3-Amino-5-bromo-2-chloropyridine—model number 3A5B2CPY. Its introduction broadens what’s possible for companies looking to scale up custom molecules. From my years working with custom synthesis projects and fine chemical distribution, this compound sparks interest because it doesn’t just extend the pyridine family; it brings key advantages for both bench-scale innovation and larger, pilot-scale demands.
Looking at the name, each part unlocks information for a chemist. A pyridine backbone signals aromatic stability and a familiar foundation for many critical reactions. The three substituents—an amino group at the third position, a bromo at the fifth, and a chloro at the second position—do more than decorate the ring. They direct how the molecule interacts with other reagents and give clear options for further modification. Its molecular weight, around 224.45 g/mol, and its white to off-white color in pure powder form provide physical cues that help chemists ensure they are handling the correct substance.
More than once, I have seen colleagues appreciate the way its moderate melting point and manageable solubility profile streamline both handling and purification. Accurate records report a melting point in the region of 100-103°C. Its consistent batch-to-batch quality reflects real care in synthesis—something partners in downstream research learn to value.
What sets 3-Amino-5-bromo-2-chloropyridine apart is the thoughtful combination of electron-donating and electron-withdrawing groups on a compact aromatic system. Many pyridines used on the bench either skew toward simple halogen substituents or feature basic amino modifications. When you add both to the same ring—especially in a pattern like this—unique reactivity emerges. For those who synthesize complex pharmaceuticals or explore structure-activity relationships, this means fewer steps and higher chances of success.
During one contract synthesis, my team debated between using a mono-halogenated pyridine and a dual-substituted approach. The amino-bromo-chloro pattern proved decisive, delivering easier access to arylation and cross-coupling strategies. Halogen atoms anchor the molecule as solid handles for Suzuki or Buchwald-Hartwig couplings, while the amino group opens the door to diazotization or amide formation. Others on the market either offer less selectivity or force chemists through more purification.
Bringing a versatile intermediate onto the shelf reshapes what medicinal chemists and agrochemical companies attempt in their pipelines. I often see this compound bridging gaps in oncology drug discovery, where time-to-lead and molecular variation can make or break a project. Research groups value it for fragment-based approaches, using it to quickly assemble candidate molecules with highly tailored properties. The regulatory pressures these labs face make reliability and traceability non-negotiable—traits where this pyridine scores consistently well.
Small- and medium-scale manufacturing units also get tangible benefits from adopting such intermediates. The fine chemical sector, especially across East Asia and the US, relies on predictable quality, manageable storage conditions, and regulatory compliance. Various reports confirm that 3-Amino-5-bromo-2-chloropyridine can survive moderate periods of storage without significant degradation—a relief for teams that must stock multiple intermediates and juggle unpredictable timelines.
Drug development doesn’t just advance by inspiration; it results from smart planning and efficient use of intermediates. Working closely with regulatory consultants and pharmaceutical partners has shown me that a compound like this one delivers significant timesaving. Its halogenated positions allow versatile late-stage modifications, and chemists can introduce functional groups with accuracy no simple mono-substituted pyridine matches. These options help teams respond quickly to new biological data and change directions without losing weeks to repeated synthesis.
Many new kinase inhibitors and central nervous system (CNS) agents start with pyridine cores. Divergent synthesis routes, especially those involving cross-coupling or acylation, depend on molecules offering both chemical resilience and tunable reactivity. The layout of amino, bromo, and chloro on this structure suits microwave-assisted reactions and batch production lines. It has helped several groups publish new active pharmaceutical ingredient (API) analogs while cutting unnecessary synthetic steps. This efficiency reflects a wider industry move towards greener synthesis: using fewer solvents, cutting waste, and improving the environmental footprint per kilo.
Some years ago, a mid-size pharma client asked for a new anti-inflammatory lead with a unique profile. Their team mapped out routes involving traditional 3-aminopyridine, but the selectivity stalled under certain conditions. Swapping in 3-Amino-5-bromo-2-chloropyridine, yields jumped by almost twenty percent, and the process avoided tedious chromatographic separation. Similar feedback came from agricultural research, where analogues inspired by this intermediate improved the spectrum of antifungal agents. Its robust purity suited both discovery and pilot-scale batches. This experience, echoed by trusted suppliers and peer-reviewed literature, cements its status among research-driven labs.
Specifications matter more than marketing. Buyers expect a content purity of 98% or higher, backed by NMR and HPLC certificates. Trace metal contamination can short-circuit a research campaign, so reliable vendors ensure heavy metal content falls well below accepted industry thresholds. Moisture control ranks as another challenge—packing it in light- and air-tight vessels prevents caking and preserves reactivity. I have learned the hard way that improper sealing, even in temperate climates, can shave weeks off shelf life. The best labs check each new bottle and store it away from sunlight, at ambient or sub-ambient temperatures.
Laboratory stewardship extends to safe storage and transparent labeling. SDS data confirms this pyridine presents moderate risks typical of many halogenated amines. Those handling it use gloves, goggles, and lab coats as a matter of routine. While its acute toxicity numbers stay within manageable ranges, accidental inhalation or prolonged skin contact prompts quick action and thorough washing. Responsible supply chains keep safety data up to date, reflecting best practices for regulatory compliance and employee protection.
Legal teams and regulatory officers care about documentation. Each shipment needs to track batch origin and analytical confirmation. Border crossings and customs clearances accelerate when all paperwork is in order, and investing early in traceability avoids downstream headache. Pharmaceutical manufacturers already juggling global supply must navigate complex frameworks—this intermediate, supplied with transparent records, fits into these rigorous logistics.
Looking across the major catalogs, other pyridines either lack the specific substitution pattern or cost more per gram for similar purity. I often see competitors push 3-bromo-2-chloropyridine as an alternative. While useful for certain coupling reactions, it lacks the amino group’s ability to unlock further pathways, leaving some projects stuck or requiring additional steps. Mono-halogenated amines exist, but dual-halide versions like this one give buyers extra leverage for next-generation drugs and specialty materials.
The difference shows up not just on the benchtop, but in the broader context of sourcing. Pricing fluctuates, but buyers prioritizing stability and consistency risk delays with less common derivatives. My experience tells me that professional circles rely on a short list of proven intermediates—and 3-Amino-5-bromo-2-chloropyridine consistently ranks among them for both small lab runs and scale-up batches.
Trust grows from facts and transparency, not branding alone. Leading suppliers provide full certificates of analysis, share real-time updates on stock status, and respond quickly to technical questions. Labs facing inspection or audits lean on traceable, well-documented supplies. International markets shift constantly, but sourcing from partners who emphasize expertise, reliability, and clear communication pays off. Companies known for transparent sourcing contribute to the credibility of the entire supply chain.
I recall plenty of cases where labs rejected intermediates for missing paperwork or unexplained odor variations. Labs routinely turn away shipments lacking proper integrity seals, labeling, or reference spectra. Reputation grows for those who include photographic documentation of the batch, spectroscopic data, and shipping condition reports. For 3-Amino-5-bromo-2-chloropyridine, such attention to detail means fewer surprises and higher satisfaction—all essential for labs who can’t afford uncertainty during tight project cycles.
Chemists cite storage and purity drift as main hurdles. Moisture absorption can lead to clumping and lower yield. I recommend keeping stocks tightly capped and opening new containers only shortly before planned use. Some clients consider nitrogen-purged storage, depending on local humidity and volume. Large buyers often arrange for regular shipments in smaller quantities rather than warehouse huge reserves that risk spoilage.
Pricing remains another flashpoint, especially during periods of global supply chain instability. Forming relationships with proven partners—who offer both stable prices and quick delivery—can smooth the process. Some companies sign framework agreements, locking in rates for recurring shipments, while others diversify their sourcing. Working closely with procurement and quality assurance officers pays long-term dividends.
The chemistry sector faces rising calls for sustainable operations. Waste minimization and eco-friendly disposal stay on every agenda. Halogenated pyridines, while useful, must be handled with attention to end-of-life processing. Years of consulting with environmental health teams reinforce the value of reliable waste collection and clear documentation. Most labs now coordinate with certified disposal partners, ensuring solvent and solids leave the facility under strict supervision.
Some research teams investigate greener synthesis routes, using alternative reagents or less energy-intensive processes to produce intermediates like 3-Amino-5-bromo-2-chloropyridine. This shift may shorten or reconfigure some synthetic schemes, demanding flexibility from staff and suppliers. Over time, embracing best practices in green chemistry promises not just compliance but cost savings—both from lowered waste fees and from bolstered company reputation in sustainability reviews.
As drug discovery accelerates and specialties like material science step up demands on custom intermediates, transparent knowledge exchange grows more critical. Peer-reviewed journals, webinars, and technical user groups amplify both successful syntheses and lessons from failed approaches. During my years supporting contract research and development organizations, the most innovative breakthroughs came from groups sharing both analytical challenges and solution strategies. For 3-Amino-5-bromo-2-chloropyridine, community insight helps identify contaminants faster and optimize purification techniques.
Open communication with suppliers supports better process development. Teams discussing challenges up front—like adjusting to new solvents or updating purification—receive more relevant technical support. Over time, these dialogues improve both product quality and end-user confidence. While large firms often run their own internal quality audits, partnering with external experts strengthens adaptability during industry shifts. The compound becomes more than a reagent; it becomes a touchpoint in a broader collaboration among buyers, sellers, and regulators.
The story of 3-Amino-5-bromo-2-chloropyridine only partly centers on molecular structure. Its strength lies in enabling rapid, flexible exploration across pharmaceuticals, agriculture, and new material development. Stakeholders from bench scientists to supply chain managers build their projects on reliable access, predictable performance, and transparent documentation. Having spent years shepherding products from early discovery through scale-up and commercial launch, I have seen how one reliable intermediate can pivot an entire campaign from delay to success.
Continuing to invest in trusted sourcing, sharing performance feedback, and holding suppliers to the highest standards delivers long-term value. As demands in chemical and pharmaceutical manufacturing evolve, staying aware of both the unique properties of intermediates and the broader context of ethical, sustainable supply unlocks next-generation discoveries. 3-Amino-5-bromo-2-chloropyridine remains a standout example of how combining technical reliability with transparent, expert-driven partnerships moves both industry and science forward.