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HS Code |
808833 |
| Iupac Name | pyridine-3-carbohydrazide |
| Molecular Formula | C6H7N3O |
| Molecular Weight | 137.14 g/mol |
| Cas Number | 59-88-1 |
| Synonyms | 3-Pyridinecarboxylic acid hydrazide, Nicotinic acid hydrazide, Isonicotinic acid hydrazide |
| Appearance | White to off-white solid |
| Melting Point | 182-184°C |
| Solubility In Water | Soluble |
| Boiling Point | Decomposes before boiling |
| Pubchem Cid | 8761 |
| Smiles | C1=CC(=CN=C1)C(=O)NN |
| Inchi | InChI=1S/C6H7N3O/c7-9-6(10)5-2-1-3-8-4-5/h1-4H,(H2,7,9,10) |
| Density | 1.315 g/cm³ |
| Storage Conditions | Store at room temperature, protected from light and moisture |
As an accredited pyridine-3-carbohydrazide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, opaque plastic bottle containing 100 grams of pyridine-3-carbohydrazide, labeled with hazard symbols, product details, and safety instructions. |
| Container Loading (20′ FCL) | **Container Loading (20′ FCL):** Pyridine-3-carbohydrazide is securely packed in 20' FCLs, maximizing space, ensuring safety, and compliant with shipping standards. |
| Shipping | Pyridine-3-carbohydrazide should be shipped in tightly sealed containers, protected from moisture and light. It must be clearly labeled and handled according to chemical safety regulations. During transit, it should be accompanied by appropriate safety documents and kept at room temperature to prevent any decomposition or hazardous reactions. |
| Storage | Pyridine-3-carbohydrazide should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Keep it protected from moisture and direct sunlight. Ensure proper labeling and secure storage to prevent accidental release. Follow all relevant safety guidelines and local regulations for chemical storage and handling. |
| Shelf Life | Pyridine-3-carbohydrazide is stable under recommended storage conditions and typically has a shelf life of at least two years. |
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Purity 99%: Pyridine-3-carbohydrazide with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high product yield and reproducibility. Melting point 205°C: Pyridine-3-carbohydrazide with a melting point of 205°C is used in solid-state formulation development, where it offers enhanced thermal stability during processing. Molecular weight 137.14 g/mol: Pyridine-3-carbohydrazide with molecular weight 137.14 g/mol is used in medicinal chemistry research, where it allows precise dosage calculations and formulation scaling. Particle size <100 µm: Pyridine-3-carbohydrazide with particle size less than 100 µm is used in fine chemical synthesis, where it improves dissolution rates and reaction efficiency. Stability temperature up to 150°C: Pyridine-3-carbohydrazide with stability temperature up to 150°C is used in heated reaction systems, where it maintains structural integrity and consistent performance. |
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Stepping into a modern lab, stacks of vial bottles line the shelves, each carrying a code with its own backstory in the massive world of chemical synthesis. Pyridine-3-carbohydrazide carved out its place here long ago, but its story is still building. Seasoned chemists recognize it straight away, not just for its straightforward structure—derived from the robust pyridine core—but because it reliably supports so many syntheses and transformations. Different from mainstream reagents that show up in almost every lab drawer, this molecule tunes its reactivity just right for a variety of projects, bridging the worlds of pharmaceuticals, agrochemicals, and specialty organics.
Chemists know pyridine rings stand tough under pressure, but attach a hydrazide group at the 3-position and the whole game changes. That little tweak unlocks amide bonds and introduces a strong nucleophilic site. In practice, pyridine-3-carbohydrazide becomes a quiet powerhouse—offering the building block qualities of a classic amide with the versatility chemists look for. I’ve watched researchers reach for it during the scramble to design a more effective pharmaceutical scaffold, since it builds bridges for functionalization yet holds firm during tricky reaction conditions. No wonder so many patent filings in recent years call for its structure.
Walking through competing shelves of chemical reagents, you won’t mistake pyridine-3-carbohydrazide for more familiar hydrazines, nor for common substituted pyridines. Structurally, it stands apart due to the careful interplay of its hydrazide’s reactivity and the aromatic stability of pyridine. Other similar hydrazides might break down, or react uncontrollably when things heat up. Unlike straight pyridine derivatives, it smoothly accommodates additional modifications because its amide handle tames the wild side of hydrazine, allowing for better selectivity in reactions.
Many years ago, a benchmate handed me a bottle during a late-night synthesis and said, "Use this over the others—you’ll thank me when you purify." He was right. Compared with the likes of isonicotinic hydrazide or unsubstituted hydrazides, this molecule gave me fewer headaches at the workup and cleaner yields when it counted. Turns out, the difference isn’t just luck: the 3-position substitution limits certain side reactions that bedevil close analogues, making it friendlier for forming key intermediates, especially for those after specificity in condensation or cyclization steps.
Every year, new academic papers and patent filings remind us that pyridine-3-carbohydrazide has legs far beyond its structure. In the medicinal chemistry field, this molecule frequently forms the backbone for anti-tuberculosis agents, among other bioactive compounds. Drug developers reached for it when searching for isoniazid alternatives, benefiting from its tweakable chemical profile and improved pharmacokinetics in candidate molecules. In my own collaborations with pharmacologists, I saw this firsthand when our hits using alternative hydrazides faltered in metabolic stability tests—yet the 3-carbohydrazide analogues persisted, sometimes lasting twice as long in vitro.
Out in agricultural chemistry, its robust backbone lends itself to designing safer fungicides and pesticide intermediates. I’ve seen a push for greener chemistry recently, driving demand for pyridine-based hydrazides that don’t break down into toxic byproducts. Pyridine-3-carbohydrazide checks that box more reliably than less-stable analogues, particularly when end-users demand products whose traces don’t linger in soil or water. It turns out, for the teams racing to meet new regulatory demands, this niche hydrazide often tips the balance.
In the open marketplace, pyridine-3-carbohydrazide isn’t just another white powder bagged by the kilo. Most reputable suppliers offer it with purity pushing 98 percent or higher, reassuring those of us in synthesis or screening that there’s little risk of reaction variability from batch to batch. I’ve come to rely on suppliers who provide infrared and NMR spectra for every lot, because small differences in purity matter when you’re trying to tease out subtle biological effects. Stability across months at room temperature lets labs avoid the headaches of degeneration or dangerous decomposition—you can leave a bottle uncapped longer than you'd like to admit, and not lose your investment.
Most research teams appreciate how pyrogenic tests tend to show low toxicity in handling, especially compared with some related hydrazines, though obviously gloves and hoods stay part of daily protocol. In weighing up safety versus utility for frequent handling, many chemists I know agree: there are much riskier compounds in the average synthetic pipeline.
Pyridine-3-carbohydrazide slips into roles beyond the drug discovery sphere. Material scientists sometimes tap it for constructing organic dyes, complex ligands, and as a precursor for more elaborate electronic or photonic molecules. It’s the sort of platform candidate that doesn’t steal the limelight, but quietly supports innovation—especially valuable for teams focused on tuning nucleophilic properties or introducing controlled redox activity. I’ve worked with teams using it at the base of metal-organic frameworks designed for catalytic applications, appreciating the extra stability during high-temperature reactions that would easily break lesser hydrazides apart.
Let’s not forget the analytical chemists looking for new derivatization agents. Pyridine-3-carbohydrazide, thanks to its nucleophilicity and amide functionality, makes an effective tag for certain spectrometric assays. The selectivity of its reactions—even when other nucleophiles hang around in solution—makes it a favorite in the toolkit, shedding light on tricky molecular identities or helping quantify traces of environmental pollutants. Compared to standard tagging reagents, I’ve noticed fewer side products clogging up the spectra, shortening analysis cycles and saving precious sample time.
On the bench, chemists love predictability. Pyridine-3-carbohydrazide delivers in this arena. It joins condensation reactions with aldehydes or ketones, giving stable hydrazones that crystallize without drama. If you’re after five- or six-membered rings with nitrogen in just the right spot, this molecule steps up as an intermediate. It’s no surprise to find its fingerprints all over routes to fused heterocycles or pyridazinone derivatives. I’ve learned to appreciate that dependable reactivity, especially when organic purification can eat up days—fewer impurities and higher selectivity shrink the grind of isolation and rental of column time.
Beyond the bread-and-butter coupling chemistry, pyridine-3-carbohydrazide takes on role as an anchor for further functional group manipulations. You can protect the hydrazide for later transformations, tack on acyl or sulfonyl groups, or use selective reductions to explore different oxidation states. That’s critical for those chasing analogues with slightly altered profiles, hoping for a new activity or lower toxicity. Many times over, chemists turn to this molecule when other amides fall short—its isomer placement and lower steric hindrance improve downstream results, and in conversations with process chemists, I’ve heard praise for its ability to simplify work flows at scale.
The hunt for the right chemical often focuses on purity—not just to meet regulatory standards but to keep experiments credible. More than once I’ve seen projects stall because early results turned out to be artifacts from low-grade feedstock. Pyridine-3-carbohydrazide brings relief there. Most suppliers now offer certificates of analysis verified by third-party labs, including impurity profiles and breakdown products. Repeated tests support that batches sourced from established producers remain remarkably consistent, easing the worry for those who can’t afford repeats or wasted time.
With supply chains stretched in many fields, reliable access has become an issue. I know several research managers who keep a backup supply locked away, mindful that delays in receiving an order could halt months of work. Unlike designer compounds or rare specialty intermediates, pyridine-3-carbohydrazide generally avoids wild price swings thanks to broad manufacturing capacity worldwide. That’s a relief as budgets tighten in both academic and industrial settings. Even as global logistics fluctuate, this molecule rides out bumps in the road better than the competition.
Every chemist’s storybook includes cautionary tales of mishandled reagents. With pyridine-3-carbohydrazide, daily safety protocols can be straightforward without causing anxiety. Short exposures in the open air rarely cause problems unless dust is kicked up, a big plus compared to more volatile or fuming amines. Labs sticking to standard operating procedures—gloves, eye protection, proper waste disposal—usually report no more incidents than you’d expect from any powdered organic. On the rare occasion an accident does happen, outcomes tend to be less severe than with potent irritants or neurotoxic hydrazines. That’s reflected in published safety data: irritation is possible, but the compound doesn’t easily volatilize or jump into the air, helping to protect both chemistry veterans and newcomers during high-traffic bench work.
It’s hard to overstate the importance of predictable safety, especially in teaching labs. No one wants headlines about a mishap derailing a budding scientist’s passion. So when faculty and lab supervisors recommend this over more hazardous alternatives, it’s worth listening. The extra peace of mind translates into more engaged experimentation, letting curious minds focus on discovery rather than dread cleanup.
Even the most trusted chemicals require vigilance. For pyridine-3-carbohydrazide, concerns sometimes surface around long-term storage or the fate of minor impurities. Occasional batches turn up with traces of unreacted starting materials or byproducts, underscoring the need for supplier transparency and routine in-lab purity checks. Investing in routine NMR and HPLC scans, even if redundant, guards hard-won results from doubt. A good analytical suite pays for itself as soon as one project avoids a derailment.
A subtler challenge comes from the push for greener chemistry. Though pyridine-3-carbohydrazide itself breaks down less harmfully than related hydrazides, solvents and auxiliary reagents still leave footprints. Several labs (my own included) have experimented with aqueous and solvent-free methods for key condensation steps, trimming both toxic waste and cost. Some success stories point to microwave-assisted synthesis as a means to lower energy consumption and shrink reaction times—a clear upgrade for any operation worried about throughput and emissions. It’s this kind of innovation that shifts reputations, turning a middle-tier commodity into a trusted component of sustainable chemical manufacturing.
Looking back, pyridine-3-carbohydrazide’s real value lies in its ability to serve as a dependable springboard. It empowers chemists to build smarter, safer, and sometimes greener molecules, whether the endgame lies in new drugs, cleaner pesticides, or advanced materials. Its straightforward handling and flexible reactivity have earned it loyalty across disciplines. Importantly, it bridges practical lab work with responsible innovation, addressing the dual need for reliable supply and responsible stewardship.
As the demand for tailored molecules grows, especially with regulations tightening around both safety and environmental fallout, the search for alternative intermediates intensifies. Pyridine-3-carbohydrazide, with its proven track record and adaptable chemistry, stands ready to meet those demands. For those new to the field, investing in good supply pays dividends in long-term project stability. For those of us who’ve been in the trenches, this molecule represents the best kind of research partner: quiet, capable, and always ready for the next challenge.