|
HS Code |
405524 |
| Chemical Name | 2-Pyridinecarboxylic acid, 6-methyl-5-nitro- |
| Molecular Formula | C7H6N2O4 |
| Molecular Weight | 182.13 g/mol |
| Cas Number | 64056-48-0 |
| Appearance | Yellow solid |
| Melting Point | 234-238°C |
| Solubility | Slightly soluble in water |
| Smiles | Cc1ccc([N+](=O)[O-])nc1C(=O)O |
| Inchi | InChI=1S/C7H6N2O4/c1-4-2-5(9(12)13)3-8-6(4)7(10)11/h2-3H,1H3,(H,10,11) |
| Pubchem Cid | 2764620 |
| Synonyms | 6-Methyl-5-nitropicolinic acid |
As an accredited 2-Pyridinecarboxylic acid, 6-methyl-5-nitro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, tightly sealed with screw cap, labeled with chemical name and hazard symbols. Contains 25 grams of 2-Pyridinecarboxylic acid, 6-methyl-5-nitro-. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-Pyridinecarboxylic acid, 6-methyl-5-nitro-: Typically packed in fiber drums, 8-10 MT per 20′ FCL. |
| Shipping | **Shipping Description:** 2-Pyridinecarboxylic acid, 6-methyl-5-nitro- should be shipped in tightly sealed containers, away from heat, moisture, and incompatible substances. Use appropriate labeling according to chemical hazard classifications. Ensure cushioning and secondary containment to prevent leaks and spills. Ship according to local and international transport regulations for hazardous chemicals. |
| Storage | Store 2-Pyridinecarboxylic acid, 6-methyl-5-nitro- in a cool, dry, well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizing or reducing agents. Keep container tightly closed and clearly labeled. Avoid moisture and sources of ignition. Use secondary containment to prevent spills. Ensure appropriate chemical segregation and access for authorized personnel only. Store at recommended temperature as indicated on the product label. |
| Shelf Life | 2-Pyridinecarboxylic acid, 6-methyl-5-nitro- typically has a shelf life of 2–3 years when stored in cool, dry conditions. |
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Purity 98%: 2-Pyridinecarboxylic acid, 6-methyl-5-nitro- with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal side-reactions during coupling processes. Melting point 206°C: 2-Pyridinecarboxylic acid, 6-methyl-5-nitro- with a melting point of 206°C is used in organic electronics manufacturing, where elevated thermal stability allows for precise fabrication conditions. Particle size <10 µm: 2-Pyridinecarboxylic acid, 6-methyl-5-nitro- with particle size under 10 µm is used in formulation of fine chemicals, where uniform particle distribution facilitates consistent compound dissolution rates. Moisture content <0.5%: 2-Pyridinecarboxylic acid, 6-methyl-5-nitro- with moisture content less than 0.5% is used in solid-state synthesis, where low moisture enhances reproducibility and product shelf-life. Stability temperature 180°C: 2-Pyridinecarboxylic acid, 6-methyl-5-nitro- with a stability temperature of 180°C is used in advanced material research, where thermal robustness ensures integrity during high-temperature reactions. |
Competitive 2-Pyridinecarboxylic acid, 6-methyl-5-nitro- prices that fit your budget—flexible terms and customized quotes for every order.
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At our plant, this compound never arrives as a mystery. We produce 2-Pyridinecarboxylic acid, 6-methyl-5-nitro- from start to finish, watching every reaction, confirming every purity, and knowing exactly the challenge this molecule can present. Over the last decade, customers have come to us with varying requirements, but the consistency of this material keeps demands high, especially from research and intermediate synthesis sectors.
The structure of 2-pyridinecarboxylic acid, with substituted methyl and nitro groups at the 6 and 5 positions, brings a set of properties quite distinct from other pyridinecarboxylic acids. Run this batch side by side with an unsubstituted picolinic acid, and you will see clear performance differences in downstream chemistry. The nitro group, especially at position 5, adds reactivity not seen in more common carboxylated pyridines. This is what many of our partners look for—the ability to unlock further substitution, couple reactively with amine or alcohol intermediates, or test new derivatives in early-stage pharmaceutical research.
From a technical viewpoint, this compound comes off the still as a pale crystalline solid, usually near 98% purity out of the reactor. Drying and micronization control particle size. Over the years, we standardized fineness according to customer needs, though the most common batch size hovers around the kilogram scale rather than the dozens of tons typical with agricultural intermediates. This product almost always heads out in small drums or lined pails, kept under nitrogen for long-distance freight.
We take pride in not relying on external sources for this compound. Outsourcing brings wild swings in purity and yield. Instead, we control every step: starting with high-grade alkylpyridines, setting up clean nitration in jacketed reactors, and following with careful acidification. Our teams see every batch pass through in-line HPLC checks before release, since trace isomers and unreacted starting material bring headaches for researchers and scale-up chemists alike. More than once we’ve had clients switch to our lot after weeks lost to “off-spec” deliveries from brokers outside the supply chain.
The most practical lesson we learned: even a fraction of a percent in nitro group misplacement or unsalvaged methylated impurities can show up as ghost peaks in a client’s analytical workup. This is one place where small differences in synthesis show up in real application problems. We worked directly with several research teams who confirmed chromatograms from our batches fit their validation requirements. With direct sourcing, batch records are transparent and questions get answered quickly.
Chemists seek out 2-pyridinecarboxylic acid, 6-methyl-5-nitro- for applications that go well beyond textbook curiosity. In pharmaceutical R&D, it often acts as a building block for more complicated nitrogen heterocycles. Many experimental antiviral and anticancer candidates take a pyridine scaffold, then add substitutions at 5 and 6 to probe for changes in bioactivity—a demand we hear repeatedly. The pattern of reactivity unlocked by our nitro-methyl mix has also drawn attention from agrochemical teams investigating new chelating agents and micronutrient solutions.
Some clients come to us looking to derivatize at the acid group, taking advantage of the electron-withdrawing effect of the ring substitutions. We’ve supported synthetic teams converting this acid to esters, hydrazides or amides. The reaction conditions are tunable: lower temperatures and controlled solvent choice allow selective modification without breaking the sensitive nitro or methyl groups. Our history of direct communication with customers provided case after case where even a minor tweak in drying or storage media kept a lab’s project on track.
Occasionally, we are approached by electronics research groups, drawn to the redox properties offered by the aromatic nitro. Applications here usually seek to leverage electron-deficient pyridine in metal complexation for film or catalyst work. While such orders are rare, this has provided a window into niche applications, especially as teams look to blend organic synthesis with materials science.
It’s easy to overlook differences between similar-looking pyridinecarboxylic acids until time is wasted on unexpected reactions or inconsistent results. We have seen customers buy a “6-nitro” or “6-methyl” substituted acid, only to realize placements matter; a misplaced methyl or nitro leads to an entirely different reactivity profile. More common picolinic acid derivatives do not carry the dual substitution, so their ability to participate in certain coupling or cyclization steps is sharply reduced.
By producing all our derivatives under one roof, we quickly respond to requests for combinatorial samples or closely related analogs, comparing analytical data directly. If someone uses a regular 2-pyridinecarboxylic acid as a precursor, the absence of a nitro at 5 and methyl at 6 positions often forces them into multistep synthesis, driving up reagent and labor costs. Our product cuts out time and effort in this respect, letting synthetic teams focus on their main work instead of troubleshooting upstream intermediates.
We have tested and refined our packaging over countless shipments. Extended transit or long storage without inert conditions risks browning or degradation, especially in high-humidity climates. Our sealing process maintains tight control over moisture and oxygen exposure. On rare occasion, when a drum arrives with slight caking due to temperature swings, it is always traceable to a break in shipment chain integrity—never from our production or packaging end. Long-term storage studies at our site show stable color, flow, and purity over two years, which matches most laboratories’ consumption timelines.
Direct conversation with chemists in the field taught us that even seasoned buyers sometimes confuse this compound with a similar methyl or nitro derivative until they see substantive differences in reaction rates and yields. From graduate students in academic labs to production chemists in contract research, requests for detailed lot histories and full chromatograms became standard over the last five years. In several cases, a customer’s project stalled using lower-purity material, turning around after switching to our verified batches. This speaks not just to purity, but the subtle impact of trace impurities and isomers unique to this synthesis.
One university researcher brought our team into a project after failing scale-up runs with a commercial lot from a catalog supplier. By switching to our product, which tracked impurity profiles down to the hundredths of a percent, the group saw reproducible coupling reactions and successful downstream modifications. This reinforced our decision to invest in high-throughput HPLC and NMR verification on every batch, even if it pushed our QC costs higher. The chemical market often underestimates the real-world costs of low-quality intermediates.
We treat safety as part of routine, not an afterthought. Nitro-aromatic compounds require specific handling, so operators in our plant rely on closed-loop transfer, up-to-date protective gear, and regular training. Additionally, our environmental controls allow us to recover solvents and neutralize waste streams. Nothing leaves our site untreated or unchecked. While these standards may go unsung, our clients depend on this reliability to avoid regulatory surprises.
We keep detailed batch records and can provide full traceability upon request—a must for customers gathering documentation for regulatory filings or audits. This isn’t window dressing; researchers and procurement specialists pushed for this level of traceability as projects moved from small scale to pilot or commercial production. Our own process audits prepared us to deliver not only a pure reagent but the paper trail proving it.
Most of the time, synthetic chemists find their greatest challenges involve bottlenecks at the intermediate level. During customer visits and technical troubleshooting sessions, two issues came up again and again: inconsistent purity and unpredictable conversion rates. For complex molecules like this one, the solution comes from a tight relationship between synthetic process control and end-user feedback. We have adapted our synthesis conditions, refined drying procedures, and standardized storage protocols based on these discussions. Every adjustment improved not only our own process but helped chemists outside our walls trust the material.
A university spinout group once described a key project stalling due to a single bad shipment of a similar nitro-methylpyridine. After joining our supply, their conversion efficiency improved and product isolation became more reliable. The process lessons gained from these interactions have often made their way back into our own manufacturing documentation, closing the loop between producer and end user.
We have seen that the market for this compound values true transparency—batch purity, real traceability, and honest communication outweigh glossy catalog promises or low pricing unsupported by manufacturing depth. Our knowledge draws not from abstract market theories but from practical, day-to-day synthesis, optimization, and customer feedback. The value we offer rests not just in what leaves the drum, but in how closely we work with our customers to close gaps between raw material supply and finished product success.
By bringing 2-pyridinecarboxylic acid, 6-methyl-5-nitro- to market with complete in-house control, verified purity, and honest technical support, we’ve created material that meets the actual demands of synthetic chemists and R&D teams across industries. Whether the goal is a pharmaceutical intermediate, a metallorganic study, or a new agrochemical lead, our experience has taught us that every batch and every conversation brings new lessons. This attitude has carried us for years, and will continue to guide our work as the needs and applications of this versatile molecule continue to evolve.