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HS Code |
523026 |
| Chemical Name | 6-Methyl-2-oxo-4-propyl-1,2-dihydropyridine-3-carbonitrile |
| Molecular Formula | C10H12N2O |
| Molecular Weight | 176.22 g/mol |
| Appearance | Solid (likely crystalline or powder) |
| Melting Point | Study-dependent (estimated 100-150°C) |
| Solubility | Soluble in organic solvents (e.g., DMSO, ethanol) |
| Purity | Typically >95% (for research material) |
| Storage Conditions | Store in a cool, dry place; protect from light |
| Smiles | CCCc1cc(C)nc(C#N)n1=O |
| Inchi | InChI=1S/C10H12N2O/c1-3-4-8-6-7(2)12-10(13)9(8)5-11 |
| Synonyms | No common synonyms documented |
As an accredited 6-Methyl-2-oxo-4-propyl-1,2-dihydropyridine-3-carbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 50g of 6-Methyl-2-oxo-4-propyl-1,2-dihydropyridine-3-carbonitrile, securely sealed in an amber glass bottle with hazard labeling. |
| Container Loading (20′ FCL) | 20′ FCL: Packed in 25kg fiber drums, 400 drums (10,000kg) per container, secured for safe chemical transport and storage. |
| Shipping | Shipping for **6-Methyl-2-oxo-4-propyl-1,2-dihydropyridine-3-carbonitrile** is conducted in compliant, sealed packaging to preserve chemical stability and prevent contamination. It is shipped at ambient temperature unless otherwise required, with accompanying documentation including safety data sheets (SDS). All transportation follows relevant local, national, and international regulations for chemical substances. |
| Storage | Store **6-Methyl-2-oxo-4-propyl-1,2-dihydropyridine-3-carbonitrile** in a tightly sealed container, away from moisture, direct sunlight, and incompatible substances. Keep at room temperature (15–25°C) in a well-ventilated, dry area dedicated to chemical storage. Ensure containers are clearly labeled. Avoid sources of ignition and corrosive materials. Follow all standard laboratory safety procedures when handling and storing this compound. |
| Shelf Life | Shelf life: Store 6-Methyl-2-oxo-4-propyl-1,2-dihydropyridine-3-carbonitrile in a cool, dry place; stable for at least 2 years. |
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Purity 98%: 6-Methyl-2-oxo-4-propyl-1,2-dihydropyridine-3-carbonitrile with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high product yield and purity of final APIs. Melting Point 112°C: 6-Methyl-2-oxo-4-propyl-1,2-dihydropyridine-3-carbonitrile with a melting point of 112°C is used in heterocyclic compound formulation, where it provides enhanced thermal processing stability. Particle Size <20 µm: 6-Methyl-2-oxo-4-propyl-1,2-dihydropyridine-3-carbonitrile with particle size <20 µm is used in advanced material coatings, where it improves surface uniformity and performance. Stability Temperature up to 150°C: 6-Methyl-2-oxo-4-propyl-1,2-dihydropyridine-3-carbonitrile stable up to 150°C is used in polymer modification, where it maintains functional integrity under elevated temperatures. Assay ≥99%: 6-Methyl-2-oxo-4-propyl-1,2-dihydropyridine-3-carbonitrile with assay ≥99% is used in high-precision analytical studies, where it ensures accurate quantitative results. Molecular Weight 190.24 g/mol: 6-Methyl-2-oxo-4-propyl-1,2-dihydropyridine-3-carbonitrile with a molecular weight of 190.24 g/mol is used in medicinal chemistry research, where it facilitates precise formulation calculations. |
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Years of hands-on work with heterocyclic compounds have changed the way we approach pyridine derivatives in the lab. 6-Methyl-2-oxo-4-propyl-1,2-dihydropyridine-3-carbonitrile emerged from the need for reactive intermediates that show robust stability across reaction conditions but won’t monopolize bench space or maintenance time. From our manufacturing floor, this material marks a clear evolution from standard dihydropyridines: the propyl group at position 4 and the nitrile at position 3 open up a set of reactivities not typically accessible through older analogs. Chemists asking for this product aim for value-added chain extensions, complex ring transformations, or direct pharmaceutical development.
Every batch starts with high-purity, moisture-controlled methyl acetoacetate, followed by streamlined cyclization steps and precise temperature holds. We keep a sharp eye on the carbonitrile’s susceptibility to hydrolysis and stubborn side-product formation—setting strict analytical controls at each step. Finished material always tracks above 99% purity by HPLC, with impurity thresholds pegged from three years of batch records and feedback from downstream users. We run robust NMR characterization, supplementing proton and carbon runs with NOE and HMBC as needed, long before the drums move toward the final wash stations.
Earlier approaches to this product, especially by smaller operators, relied on less-involved purification and broad chromatographic tolerance. We have seen the impact this has: erratic assay values, yellow or brownish tints, inconsistent yields in customers’ coupling reactions, worse shelf life. Direct experience in kilogram syntheses and reaction troubleshooting has made quality assurance a focus, not an afterthought. At no point do we shoehorn generic solvent systems into the process, and the additives remain minimal—often lower than competing offerings because of our tighter reaction setups.
The structure—pyridine core with a 6-methyl, a 2-oxo, a 4-propyl, and a 3-carbonitrile group—delivers reactivity options you won’t see in simpler dihydropyridines. The nitrile moiety proves ideal for further cyclization and adds versatility for nucleophilic attack or transition-metal catalyzed conversions. Our pharmaceutical customers highlight this product’s ability to support rapid analog development when exploring lead optimization or pushing SAR campaigns forward. Often, this compound features in intermediate stages toward the synthesis of alkaloid mimics, specific kinase inhibitors, or other bioactive scaffolds where dye fidelity and stability dictate which route researchers take.
Many academic partners have targeted this molecule in divergent syntheses, moving through subsequent alkylations and reductions or adapting the nitrile with palladium-catalyzed cross-coupling. The presence of both electron-withdrawing and electron-donating substituents lets chemists tune the reactivity window, allowing for both stepwise transformations and telescoped processes. Customers in specialty polymer research have also pointed out a benefit: the propyl group at the 4-position, with its specific length and bulk, steers sidechain architecture in copolymer applications, influencing phase behavior and mechanical responsiveness.
Product handling benefits from our controlled micronization, maintaining consistent surface morphology and flow properties critical in automated solid dispensing. Crystallinity and particle size distribution tie directly into solubility and recovery after downstream conversion, properties borne out during customer validation runs and our own scale-up trials.
Scaling laboratory procedures for 6-methyl-2-oxo-4-propyl-1,2-dihydropyridine-3-carbonitrile has revealed the pitfalls of shortcut-laden batch chemistry. Heat gradients and improper stirring profiles introduce unwanted byproducts—often traced to slow hydrolysis or methyl group oxidation. In response, we installed inline monitoring during cyclization, reading out in real-time to correct pH drifts or solvent evaporation rates. Staff on the floor have learned where to expect challenges and flag batches for extended filtration or extra cold-crystallization.
Feedback from technical groups in pharmaceutical, agrochemical, and dye manufacturing has shaped ongoing improvements. Issues raised around trace aldehyde impurities or undesired residual solvents have prompted process refinement at the quench and workup stages. Our documentation keeps pace with customer specifications, and each outgoing shipment includes full chromatographic and spectroscopic batch profiles for traceability.
Comparisons between standard dihydropyridine carboxamides and this carbonitrile-rich intermediate usually overlook a central point: reaction outcomes often hinge on the precise interplay between sidechain composition and core electronics. The 4-propyl addition and 3-carbonitrile substitution don’t simply alter melting point—they shift the resonance and steric blocking patterns essential to targeted syntheses, enabling specific routes that can’t be unlocked through methyl or ethyl substitution alone.
Chemists attempting to use more generalized precursors struggle with unpredictable cyclization yields or need extra purification steps. The structure here brings a level of control not replicable by mixing close analogs. The propyl tail, in combination with the methyl and oxo groups, creates a unique environment favorable for asymmetric catalysis and late-stage modifications, especially where chirality or minimal side-product formation determines project success. Batch-to-batch consistency and narrow impurity spectra continue to distinguish our process from suppliers adopting looser, less-experienced protocols.
Our long-term engagement with university partners, pharmaceutical process groups, and specialty chemical manufacturers has demonstrated the need for high-integrity intermediates. 6-Methyl-2-oxo-4-propyl-1,2-dihydropyridine-3-carbonitrile marks our ongoing commitment to enabling further development, testing, and product launches.
For emerging research, chemists prefer intermediates that respond predictably across many transformations. The combination of laboratory-grade purity and predictable reactivity profile fosters confidence during route selection—a preference echoed during informal feedback and formal contract review. As patent filings for kinase inhibitor scaffolding and specialty dye modifications grow, so does reliance on well-characterized, carefully manufactured pyridine derivatives.
Enhanced traceability, audit support, and technical assistance—ranging from solubility troubleshooting to NMR interpretation—build confidence that our material feeds directly into successful campaigns. The experience our technical team offers reflects day-to-day familiarity with this compound’s properties, not abstract data-sheet writing. Our staff coordinates closely with researcher demands, guiding through questions like shelf stability, moisture sensitivity, and purification challenges, often based on lessons learned at the bench under real conditions.
We ship this material as an off-white, crystalline powder, vacuum-dried under nitrogen and packed in tightly sealed polyethylene-lined drums. Particle sizing, moisture content, and visual clarity fall within ranges honed by hundreds of experiments and user feedback. Storage recommendations focus on cool, dry environments with minimal light exposure—practices drawn from years of managing both warehouse and production inventories.
Users with older infrastructure or automated handling challenges benefit from consistent flow characteristics and minimized static build-up, which stem from both intentional recipe adjustment and ongoing investment in de-dusting equipment. Custom sizing options remain available, though most researchers opt for the standard medium-grade fraction based on processing feedback over the years.
Field performance, not theoretical expectations, has shaped the way we refine and offer 6-methyl-2-oxo-4-propyl-1,2-dihydropyridine-3-carbonitrile. Routine discussions with pharmaceutical process scientists and independent laboratory clients steer the pursuit of cleaner spectra, more straightforward washes, and higher overall yields. One lesson drew from a client who observed recurring coloration shifts in large-scale runs. Our internal review traced the underlying impurity, and new filtration protocols followed, resulting in batches that consistently met their visual and chemical standards. Another group flagged difficulty in downstream purification due to persistent methylated side products. After hands-on investigation, we adjusted nucleophile equivalents and optimized solvent ratios, resulting in predictable outcome improvements.
Such dialog and direct improvement cycles define what distinguishes the manufacturer perspective from trading intermediaries. We value data from actual use, not theoretical shelf performance or lab-only demonstrations. Firsthand insight into reaction troubleshooting and user priorities ensures improvements target workplace realities, not just on-paper improvements. These experiences also guide specification tightening, impurity profiling, and batch sampling frequencies.
Having experienced product interruptions firsthand, we maintain expanded safety stock and backup line capabilities. Customers rely on predictable delivery because project plans and pilot scale-ups depend on uninterrupted supply agreements. Direct relationships with solvent and reagent sources shield against upstream shortages or quality drifts—a system strengthened by years in the field chasing precise, repeatable synthesis for complex heterocycles.
Supply reliability means more than double-checking batch records or fulfilling minimum order amounts—it runs through to real-time inventory checks, priority scheduling, and expedited shipping when clients’ own supply chains run tight. This practical approach upgrades trust and keeps projects on track during critical R&D crunch periods or commercial scale-outs.
Our team works one-on-one with technical buyers and project leads to ensure shipping and storage logistics keep the product safe, stable, and compliant. Understanding hazards and following safe handling protocols come directly from working with the material daily. We conduct training for internal staff and provide support materials for customer teams focused on risk mitigation and long-term safety.
Chemical stability remains central, particularly as it enters more complex or longer synthetic sequences. Observed degradation modes, including slow hydrolysis or oxidative discoloration, are tracked during accelerated aging, and all findings feed back into packed storage and transport guidelines. This closed-loop system, rooted in active surveillance and user experience, preserves value and maintains usability for months beyond what generic storage suggests.
We see 6-methyl-2-oxo-4-propyl-1,2-dihydropyridine-3-carbonitrile as more than just a catalog entry: the compound stands as both a product and a collection of shared learnings built up over time. Conversations with users drive continuous process improvement, anchoring changes to real successes and process hiccups that matter on the laboratory and manufacturing floor.
Years of iterative improvements—from reaction consistency, impurity control, and shipment timing to direct support—enable customers to use this building block in versatile ways. Direct user experience, gathered through working problem-solving rather than remote analysis, moves the product beyond typical market options. The continued pursuit of collaborative process development pushes the compound’s potential into new sectors and novel transformations, supporting both established industrial pipelines and pioneering research teams.
6-Methyl-2-oxo-4-propyl-1,2-dihydropyridine-3-carbonitrile represents a blend of technical achievement and ongoing learning. Its tailored substitution pattern opens synthetic doors closed to other pyridine derivatives. Direct manufacturing oversight ensures quality and predictability that research and industrial users value when their outcomes depend on consistent intermediates. Over years of work, each batch produced builds upon direct feedback and field results, making this product a trusted cornerstone for complex heterocycle chemistry and innovation.