|
HS Code |
917601 |
| Compound Name | 2-Acetamide-5-fluoropyridine |
| Molecular Formula | C7H7FN2O |
| Molecular Weight | 154.14 |
| Cas Number | 33224-20-1 |
| Appearance | White to off-white solid |
| Melting Point | 98-102°C |
| Solubility | Soluble in DMSO, slightly soluble in water |
| Smiles | CC(=O)Nc1cncc(F)c1 |
| Inchi | InChI=1S/C7H7FN2O/c1-5(11)10-7-3-2-6(8)4-9-7/h2-4H,1H3,(H,10,11) |
| Storage Conditions | Store at 2-8°C |
| Synonyms | 5-Fluoro-2-pyridineacetamide |
As an accredited 2-Acetamide-5-fluoropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle with a tamper-evident cap, labeled "2-Acetamide-5-fluoropyridine, for research use only." |
| Container Loading (20′ FCL) | 20′ FCL container loaded with securely packed drums of 2-Acetamide-5-fluoropyridine, compliant with safety and chemical transport regulations. |
| Shipping | 2-Acetamide-5-fluoropyridine is shipped in tightly sealed containers, protected from moisture and light. Packaging complies with chemical safety standards to prevent leaks or contamination. The product is labeled clearly with hazard information and handled according to applicable transport regulations for laboratory chemicals, ensuring safe delivery and preservation of chemical integrity. |
| Storage | 2-Acetamide-5-fluoropyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area. Keep away from heat, moisture, and direct sunlight. Store separately from incompatible substances such as strong oxidizing agents and acids. Proper chemical labeling and secure placement in a chemical storage cabinet are recommended to prevent accidental exposure or contamination. |
| Shelf Life | 2-Acetamide-5-fluoropyridine typically has a shelf life of 2-3 years when stored in a cool, dry, and dark place. |
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Purity 98%: 2-Acetamide-5-fluoropyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced by-product formation. Melting point 105°C: 2-Acetamide-5-fluoropyridine with a melting point of 105°C is used in solid-phase organic synthesis, where its precise transition temperature supports controlled reaction conditions. Molecular weight 154.13 g/mol: 2-Acetamide-5-fluoropyridine with molecular weight 154.13 g/mol is used in analytical standards preparation, where consistent molecular mass guarantees reliable quantification. Particle size <50 μm: 2-Acetamide-5-fluoropyridine with particle size below 50 μm is used in fine chemical formulation, where enhanced dispersion leads to uniform product quality. Stability temperature up to 120°C: 2-Acetamide-5-fluoropyridine with stability temperature up to 120°C is used in high-temperature catalytic processes, where thermal durability prevents decomposition and ensures reaction efficiency. Water content <0.5%: 2-Acetamide-5-fluoropyridine with water content below 0.5% is used in moisture-sensitive reactions, where low moisture prevents hydrolysis and increases product purity. |
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The world of chemicals often feels distant from everyday experience, but as someone who has watched the impact and reach of advanced compounds expand, I see a different story with 2-Acetamide-5-fluoropyridine. This compound, recognized for its molecular formula C7H7FN2O, emerges in laboratories and industrial spaces where precision matters. Its crystalline form, usually appearing as an off-white powder, gives a first impression that hides a lot of value beneath the surface. For those diving into organic synthesis, medicinal development, or pharmaceutical research, this molecule signals a leap toward progress.
Over the years, I’ve seen 2-Acetamide-5-fluoropyridine become a steady player in the synthetic toolbox. Pharmaceutical researchers often rely on its backbone for creating new molecules that show promise against tough diseases. The compound stands out when choosing building blocks for heterocyclic chemistry: the fluorine and amide groups both offer distinct reactivity that guides a range of transformations. Medicinal chemists appreciate how the pyridine ring, made more reactive by fluorine at the 5-position, allows for nuanced interaction with biological targets.
Lab teams seeking to create novel nitrogen-containing drugs often select this compound both for its stability and its adaptability. Its use as an intermediate bridges the gap between raw materials and complex drug candidates. Even beyond pharmaceuticals, it finds a place in materials science, contributing to the synthesis of new polymers, fine chemicals, and agrochemical leads. The diversity of its applications keeps it in steady demand.
Face it—there are many substituted pyridines out there, but not all work the same way. In my own experience, carefully comparing these products exposes subtle differences that might not seem obvious until you try to use them for real projects. The presence of the acetamide group does more than impress a chemist with its name; it directs how the molecule reacts. That's important in everything from Suzuki coupling to nucleophilic substitutions. The fluorine at position 5 isn’t just a decorative atom, either. It tailors electronic properties, influences metabolic stability, and sometimes provides just the right nudge to improve biological activity.
When lined up against other substituted pyridines or similar heterocycles, this compound has shown, time after time, a sweet spot between reactivity and manageability. Some comparables, like 2-amino-5-fluoropyridine or simple fluoro-pyridines, lack the acetamide’s shielding effect, which can leave them less versatile in downstream chemical steps. Others with different substitutions can lose out on the specific balance of solubility, stability, and reactivity that 2-Acetamide-5-fluoropyridine brings to the bench.
Anyone who’s worked in a synthesis lab knows the headache that comes from inconsistent inputs. From batch to batch, small impurities or moisture differences can derail a week’s work. This compound’s popularity grows because reputable suppliers have worked hard to standardize it. My own teams ask for certificates of analysis before starting any major project, and the best producers back up purity claims with robust HPLC, NMR, or mass spectra.
With other pyridine derivatives, the testing often shows traces of starting material or unstable side-products, particularly if storage conditions slip or timelines stretch. 2-Acetamide-5-fluoropyridine typically arrives tightly sealed, labeled for moisture precautions, and ready to jump into the next synthetic step. That sense of reliability keeps it near the top of project shopping lists.
Working closely with chemical substances over the years, I’ve come to respect the care required during handling. This molecule does not belong with hazardous heavyweights, but standard lab discipline applies. Most storage recommendations focus on cool, dry conditions, and the crystalline solid form lends itself to easy weighing and transfer. Unlike volatile substances or strong acids, there’s less risk of accidental inhalation or burns, which gives it an edge over certain alternatives in everyday research settings.
In my own experience, keeping careful records—labeling bottles with the date they are opened and closing them tightly—cuts down on degradation and waste, ensuring that the material stays potent. Dispensing a few grams at a time for benchwork reduces the risks and keeps inventories fresh.
Tracing 2-Acetamide-5-fluoropyridine through its journey in the lab, I’ve noticed repeated moments where its properties open doors that others keep closed. For teams working to build molecular complexity, this compound’s reactivity supports key transformations that might otherwise need multiple workarounds. Its amide functionality attracts interest from researchers creating enzyme inhibitors, signaling the ongoing demand for such intermediates in drug discovery.
The fluorinated nitrogen heterocycle offers unique opportunities in preparing new chemical entities. Its consistent behavior in reactions frees up more time for exploring innovative chemistry instead of revisiting process trouble spots.
With access to so many substituted pyridines, chemists make choices based on specific needs. I’ve worked with non-fluorinated analogues, and they often demand harsher conditions for the same reactions. Similarly, switching out the amide for a sulfonamide or similar group can change solubility too drastically, throwing off isolation and purification. Subtle differences in hydrogen bonding and electron flow affect the eventual outcome—sometimes making the difference between a clean product and a mixture in an impure flask.
In screening libraries for biological activity, I’ve watched as this molecule’s fluorinated ring brings a dash of extra metabolic resistance and binding specificity, compared with unsubstituted relatives. That can alter data outcomes and lead to new areas for exploration. It’s another reason why decision-makers in research settings keep 2-Acetamide-5-fluoropyridine on hand.
The real test for any specialty chemical is not just how well it performs in the manufacturer’s application notes, but how it shows up for the working scientist. Every milestone in a medicinal development program, every data point in a structure-activity relationship study, relies on consistency and predictability. Over time, I’ve talked with colleagues who mention fewer headaches and less rework when this compound, sourced from reliable channels, forms the foundation for their chemical sequences.
Predictable melting points, single-spot TLC behavior, and ease of spectral analysis give researchers more freedom to focus on the chemistry’s big questions, not the nuts and bolts of troubleshooting syntheses. It’s a luxury that pays dividends, especially as research programs scale up from milligrams to grams.
Even with so many strong points, challenges sometimes crop up. Supply chain hiccups, for example, can slow progress, particularly if worldwide production narrows to only a few suppliers. Regulatory changes occasionally squeeze import or shipment schedules, and, as with any specialized chemical, unexpected interruptions create headaches for project timelines.
Environmental questions still hang over all fluorinated chemicals. Although 2-Acetamide-5-fluoropyridine itself doesn’t fall into the persistent organic pollutant category, the broader class raises concerns about disposal and unintended release. Forward-thinking labs take care to capture waste, label residues appropriately, and use vendor take-back programs when available. Such responsibility not only satisfies environmental stewardship but also protects research investments from future regulatory surprises.
I’ve spent hours in procurement and quality meetings hammering home the value of auditing suppliers—both for ethical sourcing and environmental controls. The companies that shine in this space publicize their commitment to traceable inputs, minimized waste, and safe recycling of byproducts wherever possible. It can take extra legwork, but those steps often separate the reliable from the risky.
Switching to greener solvents, reducing unnecessary packaging, and investing in proper chemical disposal all pay off across the lifecycle of specialty products. Each of these small shifts, multiplied by hundreds or thousands of lab users, starts to change the tone of chemical manufacturing for the better.
A high-quality chemical is only as good as the people using it. My own training underscored not just technical details, but the mindset needed for careful handling and continual learning. I encourage anyone handling compounds like 2-Acetamide-5-fluoropyridine to spend time getting comfortable with data sheets—but also to keep conversations open with more experienced peers.
Bridging the gap between textbook synthesis and hands-on lab work sharpens safe technique, encourages troubleshooting, and fosters respect for the materials themselves. Mistakes happen when people rush, skip steps, or hesitate to clarify their understanding. Building a learning culture around specialized compounds keeps teams sharp and projects moving in the right direction.
All told, 2-Acetamide-5-fluoropyridine makes a strong case for itself wherever skilled hands meet challenging synthesis problems. Its chemical profile, backed by industry experience and careful testing, delivers both the creativity and reliability chemists need. By enabling streamlined transformations—and supporting ventures in pharmaceuticals, agrochemicals, and advanced materials—the compound finds a place in both everyday experiments and cutting-edge research.
Having witnessed its use across a range of studies, I keep returning to the essentials: choose quality, invest in safety, and learn from every reaction. While new molecules will always emerge, those with proven track records—like 2-Acetamide-5-fluoropyridine—tend to stick around, quietly powering innovation behind the scenes.
Chemistry never stands still. Researchers push boundaries, test new reactions, and chase after better solutions. Within that world, molecules like 2-Acetamide-5-fluoropyridine don't just fill a space—they drive progress. As teams tackle the next round of molecular puzzles, they return to reliable tools that blend advanced functionality with safe, pragmatic handling.
Investment in next-generation science involves more than clever ideas. It calls for dependable building blocks and a robust supply of specialty reagents. This product stands ready to play that role: trusted, understood, and always up for the next challenge. In labs across the globe, that's not just useful—it's essential.