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HS Code |
766677 |
| Iupac Name | 2-amino-6-methylpyridine-3-carbonitrile |
| Molecular Formula | C7H7N3 |
| Molecular Weight | 133.15 g/mol |
| Cas Number | 23056-36-8 |
| Appearance | Off-white to pale yellow solid |
| Melting Point | 143-146 °C |
| Solubility | Moderately soluble in water, soluble in common organic solvents |
| Smiles | CC1=NC(=CN=C1N)C#N |
| Pubchem Cid | 24642351 |
| Synonyms | 2-Amino-6-methyl-3-cyanopyridine |
| Storage Conditions | Store in a cool, dry place, tightly closed |
As an accredited 3-Pyridinecarbonitrile, 2-amino-6-methyl- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 3-Pyridinecarbonitrile, 2-amino-6-methyl-, 25 grams, features an amber glass bottle with safety labeling and hazard warnings. |
| Container Loading (20′ FCL) | 20′ FCL: 16 MT net weight packed in 640 fiber drums (25 kg each) on pallets, suitable for chemical export. |
| Shipping | Shipping of 3-Pyridinecarbonitrile, 2-amino-6-methyl- should comply with all applicable regulations. The chemical must be packed in secure, leak-proof containers, clearly labeled, and accompanied by the appropriate safety data sheet (SDS). Handle with caution, avoiding contact with incompatible materials, and ship only via authorized carriers with proper documentation. |
| Storage | **3-Pyridinecarbonitrile, 2-amino-6-methyl-** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Proper chemical labeling and secondary containment are recommended to prevent leaks or accidental exposure. Ensure access to safety data sheets and appropriate personal protective equipment. |
| Shelf Life | The shelf life of 3-Pyridinecarbonitrile, 2-amino-6-methyl- is typically 2–3 years when stored tightly sealed in a cool, dry place. |
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Purity 98%: 3-Pyridinecarbonitrile, 2-amino-6-methyl- with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures consistent yield and product quality. Melting Point 123°C: 3-Pyridinecarbonitrile, 2-amino-6-methyl- with a melting point of 123°C is used in organic crystalline engineering, where precise melting behavior facilitates reproducible crystal formation. Molecular Weight 133.15 g/mol: 3-Pyridinecarbonitrile, 2-amino-6-methyl- with a molecular weight of 133.15 g/mol is used in ligand design for coordination chemistry, where accurate molecular mass supports stoichiometric calculations. Stability Temperature up to 80°C: 3-Pyridinecarbonitrile, 2-amino-6-methyl- stable up to 80°C is used in high-temperature reaction conditions, where thermal stability minimizes degradation during processing. Particle Size < 20 µm: 3-Pyridinecarbonitrile, 2-amino-6-methyl- with particle size less than 20 µm is used in fine chemical blending, where small particle size allows uniform dispersion in composite formulations. |
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After years standing over glass reactors and fielding calls from bench chemists and procurement teams, I’ve seen the steady shift in demand for specialty intermediates like 3-Pyridinecarbonitrile, 2-amino-6-methyl-. Few outside our plant appreciate how tightly controlled each batch must be. Suppliers sometimes present an array of similar-sounding pyridine nitriles, often differing slightly in their methyl or amino positions. In practice, these details decide everything from reaction yield to downstream product viability. This isn’t marketing nuance – it’s the difference between a process hitting target and a week of wasted time.
3-Pyridinecarbonitrile, 2-amino-6-methyl- draws interest thanks to its specific substitution pattern. The combination of a nitrile at the pyridine 3-position, an amino group at the 2-position, and a methyl at the 6-position opens up avenues for heterocyclic synthesis not accessible with more typical isomers. Our work shows how the orientation of the methyl group influences both solubility and nucleophilic reactivity at the nitrogen. Direct feedback from R&D teams reinforces that, in some target molecules, this particular layout outperforms precursors where the methyl sits elsewhere.
When our process engineers look for materials that minimize side products, the benefits of this configuration become clear. The 3-cyano position aligns with common cross-coupling protocols in medicinal chemistry. We see regular orders from labs developing kinase inhibitors and agrochemical scaffolds where a clean pyridine backbone is essential. In our experience, buyers often learn the hard way that switching among pyridinecarbonitrile isomers disrupts both yield and isolation, despite what theoretical papers sometimes promise.
On our floor, each batch follows a protocol that we’ve refined by actually running kilograms, not just talking in the break room. We know the raw input cost changes month to month, but so does the sensitivity of downstream reactions to even minor impurities or residual solvents. Avoiding trace diketones and halide byproducts at this scale takes more than generic “routine control” – it means working directly with analytical chemists to not only test but adjust real-time purification. We tweak flow rates and column loads, favoring actual yields over theoretical throughput. Most customers never see this stage, though they usually notice when a compound “suddenly” works better in their project.
We don’t chase minimum spec to win line items. Material that doesn’t meet our cutoff for melting range or visible clarity doesn’t leave the loading dock. The truth is: real-world applications punish inconsistency. It’s too common to see other products labeled with wide assay windows, hiding batch-to-batch variability under “typical” numbers. Our quality checks extend to monitoring the ratio of E/Z isomers, even when buyers haven’t requested them. Painful lessons taught us that even those fractions, once ignored, disrupt subsequent heterocycle closure or trigger unexpected side reactions—things that cost time and reputation for both of us.
The bulk of requests come from pharmaceutical and agrochemical innovators. This molecule acts as a tightly defined building block; it’s the starting point for active pharmaceutical ingredients with fused ring systems or for fine-tuning plant growth regulators that major brands incorporate into their portfolios. We’ve shipped material for both large-scale route scouting and focused SAR studies. Researchers often emphasize not just overall purity but also how well the product dissolves in polar solvents and its response to reduction. Our observations match these reports: the substituted pyridine ring offers just the right balance of electronic effects when constructing more complex nitrogen heterocycles.
One repeated trend from our partners: several complain that other suppliers’ analogous compounds break down more quickly once exposed to ambient humidity. In side-by-side comparisons, our batches regularly demonstrate improved stability, both during storage and in-handling on their benches. There’s no magic here – control comes from real attention to residual water and a packaging protocol that seals out air at the point of fill, not after bulk transfer in a distant warehouse. A stable intermediate doesn’t just mean fewer headaches for us as the manufacturer – it translates to fewer failed syntheses at the customer’s lab. That’s a win for everyone, especially project managers working against unforgiving timelines.
Experience proves that many so-called equivalent products aren’t direct substitutes. Changing the methyl or amino location – or leaving them out altogether – shifts both chemical reactivity and regulatory acceptance for an entire synthetic route. Several of the earlier projects we supported involved extensive troubleshooting when clients attempted to swap in a 4-methyl or 5-amino variant, thinking the core pyridine skeleton would behave the same. They learned quickly that small digital tweaks on paper turn into major headaches on the bench. The 2-amino group, coupled with the 6-methyl, sets up specific hydrogen-bonding interactions and electronic fields that downstream steps rely on. We’ve mapped this with both analytical and hands-on feedback.
These differences matter even for seemingly minor applications. Take ligand synthesis for transition-metal catalysis: slightly shifting a substituent alters both the binding strength and the resulting selectivity in the final application. Several chemical catalogs lump together the “pyridinecarbonitrile” class, glossing over what matters at the project scale. Our line focuses tightly on the 3-pyridinecarbonitrile, 2-amino-6-methyl- due to consistent requests for high-control syntheses that struggle when substitutions drift from this exact configuration. As a result, our repeat customers know what arrives in the drum or vial won’t force a round of back-and-forth with their analytical team.
After dozens of shipments under wildly different weather, we’ve gathered more than a few stories about what can go wrong. 3-Pyridinecarbonitrile, 2-amino-6-methyl- won’t tolerate rough handling or poorly controlled storage for long. Once, a client stored our product near an open dock door and watched it draw enough atmospheric moisture to affect dissolution properties. Applications that depend on sensitive next steps found their conversion efficiency undercut by what looked like a minor handling error. It highlighted for us why every drum leaves here sealed and tagged for traceability, with clear guidance for storage away from light and damp environments.
Transport partners sometimes underestimate how critical consistent temperature and dryness really are. We’ve fielded calls from downstream plants wondering about slight shifts in melting behavior following transit during summer months. Each time, we retrace the supply chain with the transportation partners to close those gaps. We’ve invested in improved liners and fast-turn logistics to pare down time in uncontrolled environments. Regular feedback loops with receiving labs let us fine-tune both the packaging and the advice we provide on early-stage sampling – often saving days of troubleshooting for busy end users.
As manufacturers, we respond directly to what we see in our own batches and hear from buyers. Trends in the regulatory environment, especially for pharmaceutical intermediates, keep shifting. ICH guidelines grow stricter, driving expectations for trace metals, residual solvents, and even chiral purity in what used to be regarded as simple intermediates. In reaction, we’ve updated analytical platforms, adding LC-MS and GC headspace to check critical markers every time. Our process operators run in-house training on each analytical parameter, so questions or failures get flagged before material starts its journey to you.
The expectation now isn’t just “pure enough” for today’s project. Customers need leap-frogging quality to avoid redoing analytical work six months or a year down the line, when regulatory review or process upscaling comes knocking. We run retain samples well past the current shelf life and test them periodically against fresh batches, tracking subtle changes that could signal either process drift or packaging flaws. Acting early on these lessons staves off the worst-case scenario: expensive do-overs for large-scale customers. If a problem emerges, we don’t hide it or pass the blame; after all, we want to catch issues before they become bigger headaches out in the field.
Anyone watching global chemicals in recent years knows disruptions don’t stay confined to logistics. Regulatory shifts, feedstock shortages, even climate-driven production losses in upstream plants ripple down to intermediates like this. Early last year we saw key precursor prices spike with little warning, shaking expectations for both cost and lead time. We kept material flowing by building buffer stock and lining up alternative routes for critical input chemicals. This costs more up front, but those who waited for generic imports often faced unpredictable delays.
As the folks who live with these realities, we believe transparency with our partners matters more than claiming just-in-time perfection. Updates on upstream shifts, honest lead time forecasting, and a willingness to hold committed stock separate us from brokers who simply change their promises with the market. Our long-term customers keep returning for that reliability. They know we’ll raise the alarm early if something affects a scheduled delivery, and adjust plans or source alternates before a project timeline slips. The push-and-pull of real manufacturing never stays static, so we stay ready for new supply chain swings.
The best insights often come not from a conference hall, but from the troubleshooting calls that follow a product launch or a new process. We keep a close eye on material performance in customer hands, documenting how each lot holds up in their syntheses, what turns up under chromatography, or how long it really lasts in storage. This relationship means more than the initial sale. Detailed feedback drives our next round of tweaks, and we often build small, trial-based lots for critical partners refining their routes.
The applied knowledge that distinguishes a specialty chemical manufacturer rests on the real outcomes seen in the field, not in theoretical best-case projections. Running a plant means weathering both planned process upgrades and unexpected equipment hiccups, all while holding to promises made on quality and delivery. That’s what defines long-term trust in this sector. 3-Pyridinecarbonitrile, 2-amino-6-methyl- isn’t simply another entry in a database. For process engineers and scientists alike, its value shows up in reliable reactivity, solid shelf life, and a track record of meeting project targets. We share these insights openly, not to boast, but to help the next round of users make informed choices and push their own chemistry forward with confidence.
In this field, every intermediate comes with a backstory of trial, adjustment, and real-world application. It’s easy to overlook the subtleties that come from batch experience and continuous customer feedback. Generating 3-Pyridinecarbonitrile, 2-amino-6-methyl- at scale means managing reaction kinetics that shift with weather, raw purity, and slight catalyst tweaks. We’ve discarded plenty of what “should” have worked on paper, learning instead to follow the data after scale-up. Each rejection, rerun, and improvement goes back into the process, creating a cycle of refinements that builds not just a product, but a platform for other applications as well.
Our customers push us with their evolving needs. Some want faster delivery for pilot runs; others request tighter impurity control for registration batches. Years of fielding requests for tailored parameter sets means we’ve gotten comfortable balancing these demands without losing core quality. Instead of promising the impossible, we collaborate on achievable goals with every engagement, flagging real constraints openly. This trust-building exercise serves both sides best, cutting down project delays and letting the science lead.
Manufacturing chemicals at this level isn’t a closed-loop – it’s a continual process of adaptation fed by new challenges, client questions, and the reality-check of scaled-up projects. 3-Pyridinecarbonitrile, 2-amino-6-methyl- is just one example of how attentive process control, steady communication up and down the chain, and a willingness to pivot build resilience for everyone involved. Robust supply, practical advice, and an insistence on repeatable results set the groundwork for both current projects and those yet to be imagined. That’s the path forward, both in today’s lab and tomorrow’s.