|
HS Code |
960627 |
| Chemical Name | 5-bromopyridine-3-carbaldehyde |
| Molecular Formula | C6H4BrNO |
| Molecular Weight | 186.01 g/mol |
| Cas Number | 65610-71-1 |
| Appearance | Yellow to brown solid |
| Melting Point | 61-65°C |
| Solubility | Soluble in organic solvents such as DMSO and ethanol |
| Smiles | C1=CC(=CN=C1Br)C=O |
| Inchi | InChI=1S/C6H4BrNO/c7-6-1-5(4-9)2-8-3-6/h1-4H |
| Purity | Typically ≥97% (varies by supplier) |
As an accredited 5-bromopyridine-3-carbaldehyd factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 5-bromopyridine-3-carbaldehyde is supplied in a sealed 25g amber glass bottle with a tamper-evident screw cap and safety labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 5-bromopyridine-3-carbaldehyde ensures secure, moisture-free bulk chemical transport, meeting international safety and handling standards. |
| Shipping | 5-Bromopyridine-3-carbaldehyde is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. The package is clearly labeled with hazard information and handled according to regulations for hazardous goods. Transportation is done under controlled conditions, avoiding extreme temperatures and ensuring compliance with safety guidelines for chemical shipments. |
| Storage | 5-Bromopyridine-3-carbaldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. Protect from light and moisture. Ensure all handling and storage follow appropriate chemical safety protocols, including the use of suitable personal protective equipment. |
| Shelf Life | 5-Bromopyridine-3-carbaldehyde has a typical shelf life of 2–3 years when stored in a cool, dry, and tightly sealed container. |
|
Purity 98%: 5-bromopyridine-3-carbaldehyd with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal byproduct formation. Melting Point 54°C: 5-bromopyridine-3-carbaldehyd with a melting point of 54°C is used in organic synthesis reactions, where controlled phase transitions improve handling and reaction consistency. Molecular Weight 186.02 g/mol: 5-bromopyridine-3-carbaldehyd with molecular weight 186.02 g/mol is used in drug discovery research, where precise mass balance calculations facilitate accurate compound formulation. Stability Temperature 25°C: 5-bromopyridine-3-carbaldehyd with stability at 25°C is used in chemical storage applications, where it retains structural integrity over prolonged periods. Particle Size <10 µm: 5-bromopyridine-3-carbaldehyd with particle size less than 10 µm is used in catalyst preparation, where enhanced surface area promotes faster reaction rates. |
Competitive 5-bromopyridine-3-carbaldehyd prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Walk into the world of heterocyclic compounds, and you start meeting essential building blocks like 5-bromopyridine-3-carbaldehyde. The funny thing about chemistry is that the names always sound intimidating until you look at what these compounds do behind the scenes. For years, work in pharmaceutical labs, material sciences, and even agricultural research has called for intermediates that offer both reactivity and reliability. Here’s a compound that fits the bill, bridging the gap between the chemistry bench and the innovations that touch our lives.
The model here is 5-bromopyridine-3-carbaldehyde; in layman’s terms, you can picture it as a pyridine ring—imagine a hexagon of carbons with a nitrogen at its core, like the backbone of vitamin B3—with a bromine atom and an aldehyde group clinging to specified carbon positions. The way those groups sit on the ring changes how the molecule acts under different lab conditions. With a molecular formula of C6H4BrNO and a moderate molar mass, you don’t get a huge, unwieldy molecule. It’s solid at room temperature: yellowish or tan, with a scent that hints at the analytical work ahead. Most suppliers keep purity above 97%, which matters when you’re chasing specific, clean results.
Chemists trust this compound partly for its shelf stability, meaning it doesn’t throw surprises under normal lab storage. Melting points tend to cluster around the expected lab data, and it dissolves in everyday organic solvents, so it’s accessible for both seasoned researchers and those just starting to handle pyridine derivatives.
Take it from anyone who’s worked in a synthesis lab: not all pyridine carbaldehydes work the same. Placement of that bromine atom at the 5-position and the aldehyde at the 3-position changes the whole flavor of downstream chemistry. In pharmaceutical labs, 5-bromopyridine-3-carbaldehyde earns its keep as a core intermediate on the path to more complex molecules. Medicinal chemistry teams appreciate how the combination of the ‘bromo’ and ‘carbaldehyde’ groups open doors to functionalization, alkylations, and Suzuki couplings—reactions so common they’re practically household names among chemists.
It’s not just about making blockbuster drugs. This same intermediate shows up in the fine-tuning of specialty polymers. Some advanced electronics need custom-built small molecules that trace their origin to this compound. In the world of agrochemicals, minor tweaks on that pyridine ring, starting with intermediates like this one, let researchers design new herbicides or pesticides targeting specific pests while minimizing broader ecosystem impact. For those at the chemistry bench, versatility comes from that unique placement of bromine: giving chemists a solid foundation for making bonds that would be much harder—or impossible—on a ‘plain’ pyridine or a carbaldehyde missing the halogen.
You might ask, why pay attention to this one, when dozens of brominated pyridines or carbaldehyde-substituted pyridine molecules line chemical catalogs? Here’s where practical experience delivers real-world answers. Subtle changes in group position shift electron density across a molecule, changing how it reacts with nucleophiles or participates in cross-coupling. For people making organometallic complexes or constructing novel ligands for catalysis, that distinction isn’t academic—it’s the deciding factor between running a smooth reaction or wasting valuable materials on a dead-end pathway.
Older colleagues I’ve talked with have run into headaches chasing alternative molecules—some are surprisingly stubborn, requiring harsher conditions or giving up poor yields and messy purifications. The predictability of 5-bromopyridine-3-carbaldehyde brings welcome reassurance in a research space that often serves up curveballs. It can serve as a launching point for nitration, amidation, or further halogenation, each direction leading toward compounds not so easily made by other means.
My own hours in labs, and the stories of countless others, tell the same story: With enough experience, you start noticing the margin for error narrows with bulkier, more sensitive intermediates. 5-Bromopyridine-3-carbaldehyde’s consistent physical properties—clean melts, manageable volatility—take away some stress during scale-ups. Analytical chemists like its amenability to NMR, mass spectrometry, and standard characterization, which helps confirm identity and purity without repeat purification cycles.
Fewer headaches crop up during workup, too. Some aldehydes react with atmospheric oxygen or water, but keeping this one in a well-closed bottle, away from prolonged air exposure, avoids most of the common pitfalls. Given the price of reagents, especially in custom syntheses or small-batch research, reliability at every stage translates to lower costs and higher morale among team members chasing grant funding or regulatory milestones.
There’s no shortage of paperwork and legal hurdles in modern chemistry. Respecting safety isn’t optional—it’s a habit and an expectation. Compared with raw starting materials of decades past, this compound fits into existing lab protocols with no real drama. At the same time, every lab knows minor spills, inhalation risks, and skin contact causations matter. Laboratory safety sheets urge gloves, eye protection, and fresh-air hoods. Fume management and proper labeling, with quick access to emergency information, keep things running smoothly.
On the broader compliance front, handling and disposal rules follow established frameworks for halogenated organics and aromatic aldehydes. Waste storage gets managed by segregating residues, never mixing incompatible classes. Even though modern chemists have learned to reduce or recycle waste where they can, safe handling remains the responsibility of every lab member.
Demand for specific intermediates in research and industrial settings moves with the pace of innovation. As researchers target increasingly complex active ingredients and specialty chemicals, compounds like 5-bromopyridine-3-carbaldehyde draw more attention on procurement lists. Major producers put real effort into scalable, reproducible manufacturing, emphasizing traceability for buyers in regulated sectors—from pharma to agrotech to materials engineering.
Ask procurement managers or research directors which catalog compounds keep showing up, and this molecule often sits on that list. The reason is simple—chemistry is about problem-solving, and this compound opens doors that others leave closed. In some settings, the unique bromo position means a proprietary synthesis pathway comes alive, creating intellectual property or unlocking licensing advantages. People follow outcomes, and stories multiply about breakthroughs starting with the right intermediate at the right time.
No product, even a widely-used chemical intermediate, avoids criticism. Concerns often center on environmental persistence, waste stream implications, or supplier consistency. Like most halogenated aromatics, 5-bromopyridine-3-carbaldehyde isn’t biodegradable by simple routes. Thoughtful process chemistry addresses this, using controlled reactions, careful inventory management, and closed waste systems. Sophisticated labs enroll in chemical take-back programs or batch-integrated solvent recovery, routing residues away from general landfill and aiming for minimal environmental footprint.
Another running issue in chemical supply is batch-to-batch purity. Having spoken with chemists who faced assay deviations between shipments, one thing becomes clear: detailed certificates of analysis, routine third-party validation, and a willingness to verify material identity make a difference. Reputable suppliers don’t gamble with customer trust, often sharing characterization data and responding quickly to any flagged irregularities. Where smaller operations might be tempted to cut corners, established providers leverage scale to ensure consistency year after year.
In my own experience, a well-chosen intermediate acts like a lever, letting a small team tackle challenges that would otherwise call for big budgets or sprawling synthetic routes. The open-access movement in chemistry helps here. Shared protocols, published optimization data, and troubleshooting forums take away some of the historic secrecy and make newer users more confident. Online communities share tips for handling moisture-sensitive reagents or for getting strong yields from palladium-catalyzed couplings. By lowering the hurdles to safe, effective use, a next generation of researchers can work with confidence.
With 5-bromopyridine-3-carbaldehyde, the pattern repeats: collaborative troubleshooting, hands-on video tutorials, and open dialogue between suppliers and users push the field forward. This approach doesn’t only help West Coast startups chasing green energy or European biotechs building smarter sensors; it lifts every lab, including those far from the major funding hubs.
Every researcher knows the frustration of stalled projects—reactions that don’t kick off, isolations that yield nothing. Reflection and repeated lab work show the same lesson: choosing intermediates with proven reliability, like 5-bromopyridine-3-carbaldehyde, means less time solving side problems and more time inventing. Real progress happens in the space between theory and experiment, often unlocked by having the right compound ready at a critical stage.
People sometimes see chemistry as an abstract science, but day-to-day lab life tells another story. The steps from a raw intermediate to a signature molecule fill patent applications, drug filings, and product launches worldwide. Each of these steps builds on fidelity and trust—qualities shown in how a bottle performs from the first milligram to the last.
There’s no shortage of new challenges facing the world, from antibiotic resistance to the need for sustainable polymers or smarter pest control. As the problems grow more complex, the pressure rises for researchers to build on solid ground. A reliable chemical like 5-bromopyridine-3-carbaldehyde isn’t a magic solution, but it moves the baseline in the right direction. It frees up energy to focus on what’s next—whether it’s designing molecules that act faster, break down safer, or cost less to produce.
From internship experiences to stories shared by senior scientists, the message holds: research advances on the practical, well-understood tools inside every lab. Attention to quality, open communication between users and suppliers, and constant improvement in green manufacturing processes help sustain the field. A little transparency, a dash of humility in admitting what still needs work, and a sustained engagement with end-users—these support real progress.
Chemistry delivers its value step by step, with every reaction run and every product purified. In the spectrum of lab reagents, intermediates like 5-bromopyridine-3-carbaldehyde won’t often make headlines, but their impact shines through every successful experiment, patent, and published paper. For those working hard to find the next big breakthrough, picking materials with a proven track record and a network of real-world knowledge behind them marks a difference that goes way beyond the bottle.
The more we look for quality, share honest feedback, and stay open to better, safer, more sustainable approaches, the stronger the research landscape becomes. Compounds like this one will keep making life in the lab just a little easier, one reaction at a time—helping innovation reach from bench to business, from theory into the hands of people who need those discoveries most.