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HS Code |
607831 |
| Product Name | N-(3-Formyl-2-Pyridinyl)-2,2-Dimethylpropanamide |
| Molecular Formula | C11H14N2O2 |
| Cas Number | 1341842-45-2 |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Solubility | Soluble in DMSO, methanol |
| Storage Conditions | Store at -20°C, protected from light |
| Smiles | CC(C)(C)C(=O)Nc1c(C=O)cccn1 |
| Inchi | InChI=1S/C11H14N2O2/c1-11(2,3)10(15)13-9-8(7-14)5-4-6-12-9/h4-7H,1-3H3,(H,13,15) |
| Synonyms | 2,2-Dimethyl-N-(3-formylpyridin-2-yl)propanamide |
As an accredited N-(3-Formyl-2-Pyridinyl)-2,2-Dimethylpropanamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 1 gram, sealed with a PTFE-lined cap, labeled with chemical name, CAS, batch number, and hazard warnings. |
| Shipping | Shipping for **N-(3-Formyl-2-Pyridinyl)-2,2-Dimethylpropanamide** should comply with all applicable regulations. Ensure the chemical is securely sealed in appropriate, labeled containers. Package with protective materials inside a sturdy outer container. Ship at room temperature unless otherwise specified. Include safety data sheets (SDS) and follow all relevant transport guidelines for laboratory chemicals. |
| Storage | Store N-(3-Formyl-2-pyridinyl)-2,2-dimethylpropanamide in a tightly sealed container, protected from light and moisture. Keep in a cool, dry, and well-ventilated area, preferably at 2–8°C (refrigerator). Avoid exposure to incompatible substances such as strong oxidizing agents. Label the container clearly and handle under a fume hood using appropriate personal protective equipment. |
Applications of N-(3-Formyl-2-Pyridinyl)-2,2-Dimethylpropanamide in Industrial ManufacturingN-(3-Formyl-2-Pyridinyl)-2,2-Dimethylpropanamide serves as a pivotal intermediate in advanced organic synthesis, particularly within pharmaceutical manufacturing and specialty chemical production. As the original manufacturer, we have developed and supplied this material to downstream partners in key, technically demanding industries, where batch quality and reproducibility are critical for product integrity and regulatory approval. The following sections present verified industrial applications observed in commercial production environments, with specific details about compliance, usage ratios, process steps, and end products. 1. Pharmaceutical Active Ingredient SynthesisMedicinal chemistry groups use this compound predominantly for constructing heterocyclic frameworks and functionalized intermediates in patented small-molecule drugs. Its aldehyde and pyridine functionalities make it especially valuable in forming amide-linked scaffolds through reductive amination or multistep condensation protocols in API synthesis campaigns. Industry compliance standards
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2. Agricultural Chemical Intermediate ManufacturingManufacturers within crop protection sectors incorporate the molecule as a building block for selective herbicide and pesticide actives, benefitting from its pyridine ring and modifiable formyl group in ring-closure or hydrazone synthesis for potent agrochemical agents. Industry compliance standards
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3. Specialty Polymer Crosslinker SynthesisThis compound is employed in the synthesis of specialty crosslinkers for use in engineering polymers, leveraging the ability of its aldehyde moiety to react with multifunctional amines or hydrazides. Its role is central in generating polymer architectures with enhanced chemical resistance and specific mechanical performance targets. Industry compliance standards
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4. Fine Chemical Synthesis for Diagnostic ReagentsAnalytical and diagnostic kit producers utilize this material as a precursor for pyridine-based chromogenic and chelating agents in reagent system manufacturing. The reactivity of its formyl group supports derivatization for enzyme-labeling or ligand chelation modules in specialty chemical production. Industry compliance standards
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5. Ligand Synthesis for Homogeneous CatalysisCatalyst manufacturers select this material as a core scaffold for the preparation of bidentate and tridentate ligands, facilitating metal complexation in homogeneous catalysis systems. Its structural features enable controlled electronic effects and spatial arrangement critical for catalytic activity, especially in fine chemical and pharmaceutical process scale-up. Industry compliance standards
Typical usage ratio
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Many years of experience in chemical synthesis have shaped our approach to producing specialty compounds that consistently meet the demands of advanced research and industrial development. N-(3-Formyl-2-Pyridinyl)-2,2-dimethylpropanamide is one of those niche building blocks in our catalog, and its unique structure and purity open genuine possibilities for both research chemists and process engineers.
The backbone of N-(3-Formyl-2-Pyridinyl)-2,2-dimethylpropanamide features both a 3-formylpyridine moiety and a tert-butyl amide group. Each batch produced in our reactors reflects years of process optimization. We’ve adopted a synthetic route that offers reliable formation of the 3-formyl group and precise positioning on the pyridine ring, always keeping trace impurities under control. Quality matters not just for final yield in the lab, but also for the reliability in downstream coupling reactions and more sophisticated chemical transformations.
Our regular clientele values this molecule as an intermediate in the design of ligands, pharmaceuticals, and complex organic frameworks. The formyl group brings flexibility for further functionalization, making it a favorite for researchers exploring reductive amination, heterocyclic synthesis, or targeting new molecular scaffolds in medicinal chemistry. The 2,2-dimethylpropanamide group enhances solubility and manages steric control during multi-step synthesis, helping chemists tune polarity and reactivity in ways a simpler amide or alkyl group rarely allows.
Years spent scaling from gram-scale to pilot and then production volumes have convinced us that purity tells only part of the story. Customers often share concern about things like batch-to-batch consistency, shelf stability, and unreacted starting materials lurking in trace quantities. We run routine NMR profiles and HPLC traces for each lot, watching for even subtle impurities left from the starting 2,2-dimethylpropanamide or pyridine derivatives. Our crews work the distillation columns with an eye on fraction collection—no skipping steps, no chasing shortcuts.
Crystalline appearance, color, and moisture content also vary based on conditions during post-reaction work-up. Those details—often overlooked by resellers—matter greatly when working with moisture-sensitive transformations or maleimide coupling steps. Our trained eyes spot the difference between a well-finished product and a carelessly dried one. This compound’s pale yellow appearance and absence of off-odors give our QC staff their first sign of a clean run.
Scaling organic intermediates can challenge even veteran chemists. In the first years, we saw how quickly an uncontrolled exotherm at the formylation stage caused side reactions—no one wants unmanageable tars or over-oxidized byproducts. Controlled addition rates, jacketed vessels, and careful solvent selection made all the difference. Our team solved these headaches by investing in precise temperature monitors and automated feed pumps. Now, even as order volume grows, yields stay high and clean.
Each packing session reflects our commitment to chemical cleanroom standards. Even a hint of dust or packaging oil can show up in sensitive NMR or LC-MS analysis done down the line, so our staff handles bottles with new gloves, fresh glass, and lined containers. Storage protocols developed for this molecule take into account its mild sensitivity to strong oxidants, and exposure to prolonged sunlight—reasons why we use amber bottles and tight seals on all outgoing shipments.
Our strongest insights have come from collaborations with research groups developing new classes of pyridine-based pharmaceuticals and organometallic ligands. Many chemists who place repeat orders for N-(3-Formyl-2-Pyridinyl)-2,2-dimethylpropanamide come with feedback—from issues in solubilization to desired modification in functional group accessibility. Whether the task involves optimizing a new catalyst or building a congener library, their feedback guides our continued process upgrades.
Some projects require a push beyond standard 98% chemical grade, chasing chiral purity or the strictest metal specifications. We run analyses for trace palladium or tin, especially after catalytic formylations, and respond quickly to requests for expanded certificates of analysis. When customers face challenges in scale-up, we have sent technical support to troubleshoot on-site, reviewing reaction work-ups or helping select compatible solvents for push reactions. Those conversations spark continuous improvement in our process controls.
Chemical supply houses offer many pyridine derivatives, but few combine the selectivity profile, ease of functionalization, and stability found with N-(3-Formyl-2-Pyridinyl)-2,2-dimethylpropanamide. This molecule’s unique pairing of a formyl group at the 3-position and a branched tert-butyl amide at the 2-position creates a solid anchor for diverse organic transformations.
Colleagues in the field often share stories about close analogues. For example, 3-formylpyridine lacks the steric bulk and sterically directed electronic effects, limiting its use in crowded active sites or when building more robust complex frameworks. Simple pyridinecarboxamides fail to capture the reactivity window required in multicomponent syntheses involving nucleophilic additions or cross-couplings. The additional methyl groups on our compound’s backbone offer a blend of hydrophobicity and spatial blocking that unlocks pathways which remain inaccessible for less hindered amide analogues.
Through this experience, our process teams realize that what sets our molecule apart is both chemical and practical: easier purification, longer shelf life, and fewer ambiguities during downstream analyses. Customers report consistent spectral quality, which helps streamline library development, eliminate troubleshooting at scale, and improve overall efficiency in medicinal chemistry or fine chemical production.
Sectors as varied as medicinal chemistry, agrochemical discovery, and electronics development look for consistency above all. Researchers exploring ligand design or constructing new frameworks for molecular recognition often emphasize the importance of trace-level control over byproducts and batch uniformity. Our close relationship with some of these labs has revealed new potential for our product. Some applications involve incorporating the molecule as a key intermediate in multi-stage syntheses to build nitrogen-containing rings or as a formyl donor in one-pot reactions.
We have observed that the protection offered by the tert-butyl amide reduces unwanted side reactions compared to more labile amide analogues, meaning less troubleshooting during reaction workups and better reproducibility. In devices research, where even micrograms of a trace impurity can skew data or damage sensor function, our protocol-driven approach reduces the need for extra in-house purification. We make it easier for scientists to focus on results instead of chemical logistics.
Global supply and logistics have rarely been straightforward, with raw material shortages and evolving regulatory demands often complicating life as a chemical manufacturer. Sourcing high-purity pyridine and reliable tert-butyl reagents means working with vetted suppliers and securing recurring contracts that protect against sudden market swings. Over the years, we have expanded storage of the most sensitive reagents, investing in inert gas systems and periodic stability testing to make sure nothing compromises the critical precursor streams.
We see many distributors fall short during times of high demand, especially for specialty chemicals. Our team reduces risk for customers by scheduling regular production runs during the academic calendar and agricultural off-seasons, anticipating the year’s cyclical needs. This approach has kept our backorder rates low, even at times when sudden breakthroughs in pharmaceutical research send demand soaring.
Packaging plays its own role in overcoming shipping challenges. Since moisture control is vital to maintaining reactivity, all packaging options—from gram vials to multi-kilogram drums—come with barrier liners and humidity-absorbing sachets. Customers working in different climates routinely comment on the absence of product clumping or unexpected color changes—a testament to our control over both what goes into the bottle and how it travels the world.
To the manufacturing crew, every batch tells a story. Over the years, process engineers and QC staff have developed an internal feedback system. Any deviation, no matter how slight, gets logged and traced back through digital and paper records. Routine cross-checks with independent labs give us an outside perspective, as do batch samples sent to long-term customers for parallel evaluation. These collaborations have pointed out hidden sources of error, from minor particulate contamination during filtration up to solvent choice impacting impurity carry-over.
GMP compliance and traceability are built into our workflows. With everything tracked, from raw material batch lots to equipment maintenance intervals, we rarely lose sight of the small details that distinguish a specialty manufacturer from a generic supplier.
No intermediate gets a pass on safety or environmental impact. Our process modifications over time have replaced hazardous oxidants and reduced the use of high-boiling chlorinated solvents. Reaction byproducts see efficient neutralization in our waste treatment plant; no batch moves forward without full documentation of solvent recovery and aqueous waste handling. We take pride in minimizing our environmental impact while meeting customer demand for both safety and sustainability. The team constantly follows updates on regulatory shifts affecting use cases in different regions, collaborating with colleagues on documentation to simplify end-user compliance.
In recent dialogue with downstream processors, questions about endotoxin levels and residual metals are growing. With additional filtration and targeted scavenging at the final stage, we deliver a compound that works not just in traditional organic synthesis but increasingly in biomolecular applications or conjugation strategies. Our understanding of these market shifts has sharpened the link between continuous process vigilance and trust from our most demanding partners.
The path from bench-scale synthesis to reliable industry supply runs through many hands and minds. Every improvement in process control, packaging, and customer support shapes the confidence our clients place in us. Each research breakthrough built on our compound’s backbone reaffirms the daily care and expertise poured into every lot. Many clients order from us year after year not just because of technical specifications, but because they’ve learned to rely on direct communication and full transparency when something needs adjusting.
The daily work underpinning N-(3-Formyl-2-Pyridinyl)-2,2-dimethylpropanamide production blends chemistry with logistics, safety, and regulatory care. As the field of advanced pyridine chemistry expands, our role goes beyond the reactor and into the heart of our customers’ discoveries. Every suggestion for process improvement, every feedback call, and every shared troubleshooting story helps us fine-tune both molecule and service. We see this cycle as the real engine of excellence. Commitment to doing things right—not just according to protocol, but with an eye on future needs—defines what long-term partners come to expect.