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HS Code |
294945 |
| Iupac Name | 5-[(aminooxy)methyl]-2-(1H-pyrazol-1-yl)pyridine |
| Molecular Formula | C9H10N4O |
| Molecular Weight | 190.20 g/mol |
| Cas Number | NA |
| Smiles | ONCC1=CN=C(C=C1)N2C=CC=N2 |
| Inchi | InChI=1S/C9H10N4O/c10-14-6-8-3-4-9(12-5-8)13-2-1-7-11-13/h1-5,7H,6,10H2 |
| Appearance | Solid (assumed; typically off-white to pale colored powder) |
| Solubility | Soluble in water and polar organic solvents (assumed) |
| Synonyms | 5-(Aminoxymethyl)-2-(pyrazol-1-yl)pyridine |
As an accredited Pyridine, 5-[(aminooxy)methyl]-2-(1H-pyrazol-1-yl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is supplied in a 1-gram amber glass vial with a screw cap, labeled with product name, quantity, and hazard warnings. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely packs Pyridine, 5-[(aminooxy)methyl]-2-(1H-pyrazol-1-yl)- in sealed drums or bags, maximizing container space. |
| Shipping | **Shipping Description:** Pyridine, 5-[(aminooxy)methyl]-2-(1H-pyrazol-1-yl)- is typically shipped in tightly sealed containers under a nitrogen atmosphere to prevent moisture and air exposure. It should be packed according to chemical safety regulations, with appropriate labeling and documentation, and shipped at ambient temperature unless otherwise specified by the manufacturer’s instructions. |
| Storage | Store **Pyridine, 5-[(aminooxy)methyl]-2-(1H-pyrazol-1-yl)-** in a tightly sealed container, in a cool, dry, and well-ventilated area. Keep away from sources of ignition, heat, and incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Label storage areas clearly and follow all relevant chemical safety guidelines and local regulations. |
| Shelf Life | Shelf life: Store Pyridine, 5-[(aminooxy)methyl]-2-(1H-pyrazol-1-yl)- at -20°C, protected from light and moisture; stable for 1 year. |
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Purity 98%: Pyridine, 5-[(aminooxy)methyl]-2-(1H-pyrazol-1-yl)- with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced side-product formation. Melting point 116°C: Pyridine, 5-[(aminooxy)methyl]-2-(1H-pyrazol-1-yl)- with a melting point of 116°C is used in medicinal chemistry research, where reliable thermal stability is critical for reproducible compound derivatization. Aminooxy functional group: Pyridine, 5-[(aminooxy)methyl]-2-(1H-pyrazol-1-yl)- featuring an aminooxy functional group is used in bioorthogonal labeling, where selective conjugation to carbonyl-containing biomolecules is achieved. Molecular weight 202.2 g/mol: Pyridine, 5-[(aminooxy)methyl]-2-(1H-pyrazol-1-yl)- with molecular weight 202.2 g/mol is used in ligand design for coordination chemistry, where precise stoichiometry enables predictable complex formation. Stability temperature up to 120°C: Pyridine, 5-[(aminooxy)methyl]-2-(1H-pyrazol-1-yl)- stable up to 120°C is used in solid-phase synthesis, where it maintains structural integrity under mild heating conditions. Particle size <50 μm: Pyridine, 5-[(aminooxy)methyl]-2-(1H-pyrazol-1-yl)- with particle size smaller than 50 μm is used in catalyst support formulation, where enhanced dispersion improves catalytic efficiency. |
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In today’s specialty chemical landscape, Pyridine, 5-[(aminooxy)methyl]-2-(1H-pyrazol-1-yl)- holds steady as a cornerstone for various research and industrial applications that demand reliable and consistent performance. As producers with decades of hands-on experience, we have watched customer needs become increasingly sophisticated, especially in the pursuit of target-oriented synthesis and optimized reaction efficiency. Every batch leaving our facility aligns with rigorous analytical screening and traceability benchmarks set by both regulatory authorities and clients themselves, establishing trust through sheer technical results, not marketing claims.
In our synthesis line, creating this molecule involves a careful orchestration of precursors and purified intermediates. The specific configuration, marked by the pyrazole and aminooxy functionalities, allows for reactivity that generic pyridine compounds simply cannot offer. The functionalized side-chain opens new routes for coupling reactions and serves well in applications where typical electron-rich or electron-deficient substitutions fall short. The ability of the aminooxy group to form stable oxime ethers with carbonyls delivers a crucial selective advantage during derivatizations within analytical chemistry, polymer science, and bio-conjugation studies.
Our production batches of Pyridine, 5-[(aminooxy)methyl]-2-(1H-pyrazol-1-yl)- consistently fall within tight purity specifications, confirmed through latest-generation HPLC and NMR technologies. Water content, heavy metal contaminants, and residual solvent remain well under established safety and regulatory guidelines. Customers with advanced analytical requirements have repeatedly challenged us with new detection methodologies, and by working side-by-side with their teams, we’ve refined our purification and verification steps. That direct interaction with customers in industries like fine chemicals, diagnostics, and medicinal chemistry offers daily feedback that shapes raw material selection, reactor throughput, and cleaning processes on our production lines. We have seen how small fluctuations in impurity levels impact downstream assays and developed robust strategies to keep these out of the supply chain.
The real value of this compound emerges in the laboratory and production plant. In bioconjugation chemistry, the unique pairing of the aminooxy and pyrazolyl groupings has opened new terrain for selective protein and carbohydrate derivatization. Our clients in pharmaceutical research use this molecule for site-specific labeling. The compound forms oximes cleanly under mild aqueous conditions, reducing the risk of harming sensitive biomolecules. This significantly cuts down on side-product formation, which can derail bioassays or require additional purification steps. In analytical chemistry, the compound serves as a derivatization reagent for sensitive aldehyde and ketone detection—providing stable adducts that enable reliable quantification by HPLC or mass spectrometry.
Over time, regular feedback from research institutes and process development groups pushed us to develop an expanded range of packaging, from small-scale vials for pilot use to bulk quantities that support kilogram-scale process chemistry. Whether used in high-throughput screening projects or preparative synthesis, our direct access to the production chain allows agile adjustment to shifting project timelines and batch size needs. Chemical stability under ambient and refrigerated storage conditions also matters—so we regularly track sample performance in real conditions far beyond laboratory shelf tests to inform our quality assurance.
Many clients new to this product ask how it sets itself apart from more common pyridine derivatives. Classic pyridine derivatives are plentiful and have broad, sometimes generic, uses as solvents, building blocks, or ligands. Our compound, featuring the 5-[(aminooxy)methyl]- and 2-(1H-pyrazol-1-yl)- substitutions, delivers specialized functionality instead of merely being a passive participant in a reaction mixture. The presence of the aminooxy group offers orthogonal reactivity unique within this molecular family. This gives chemists the option to introduce highly selective modifications, avoid problematic cross-reactivity, and tune properties of biologically active compounds or functional polymers in a way that standard pyridine reagents cannot.
In early collaborations with research groups working on targeted drug delivery systems, we consistently witnessed how the selectivity of the aminooxy group cut steps out of complex synthetic routes. This in turn shortened project timelines and reduced material costs. Data from independent testing regularly confirms that the batch consistency of our pyridine derivative directly improves reproducibility—a point brought up in peer-reviewed publications and as feedback from contract research organizations who integrate our product into automated platforms.
We operate our facility under clear, monitored documentation practices and frequent internal audits. That level of control doesn’t arise from external pressure alone; it stems from the predictable outcomes our partners have come to demand. Traceability starts at the raw material loading dock and continues through final product packaging. Independent verification by third-party laboratories is routine, not an afterthought. Our partnerships with academic laboratories and industrial R&D sites provide the critical field data necessary to identify drifting specifications, adapt to new compliance standards, or catch minute changes in physical characteristics early.
The chemical industry often faces public scrutiny over waste, emissions, and safety risks. Our operation prioritizes containment, batch accountability, and paperwork trails for every lot. Practical matters—such as waste solvent handling and ensuring process emissions meet green chemistry targets—form part of our monthly operations review. For researchers who require certification or statements to enter government or multinational research consortia, our in-house documentation aligns tightly with these external standards, because we manage the paperwork and audit cycle without relying on third-party resellers or brokers.
Expectations continually evolve in the fields that use advanced heterocyclic building blocks like this. Biological labeling strategies have changed rapidly in the past few years. New protocols in proteomics and glycomics now rely on chemoselective coupling methods where the aminooxy group excels. By staying attuned to these shifts—through organization memberships, technical seminars with our partners, and the steady exchange of pointers between production staff and academic teams—we constantly update our internal training, supply chain, and technical documentation practices. Supply chain reliability becomes less abstract and more personal for customers who plan their experiments and production campaigns around batch delivery schedules. Our operations team reviews maintenance schedules and logistics orders alongside the laboratory data, taking seasonal and regional shipping risks into account.
One noticeable shift has been the greater emphasis on green chemistry and atom efficiency in process design. As chemists look for higher yields, fewer side reactions, and reduced solvent use, we engineer our processing steps to minimize waste and energy consumption. This extends to the selection of solvents for recrystallization, the recovery and re-use of process byproducts, and the adoption of continuous flow methods where this molecule’s stability allows. We also share best practices openly with established partners, so small process improvements in our facility often translate directly to cost and environmental benefits elsewhere.
No method is ever truly complete, especially as science pushes us to develop purer, safer, and more versatile reagents. One challenge in the synthesis of Pyridine, 5-[(aminooxy)methyl]-2-(1H-pyrazol-1-yl)- comes from controlling the side reactions of the aminooxy group. Over the years, early batches occasionally showed trace byproduct formation from over-oxidation during workup steps. Addressing this required refining our quenches and monitoring oxygen ingress during both reaction and storage. Continuous investment in improved ventilation controls and updated analytical hardware has dramatically reduced such off-spec results, improving final batch uniformity and reducing downtime.
Shipping temperature-sensitive material proved another hurdle. Through pilot programs with regional and continental logistics groups, we arrived at a robust combination of cold chain monitoring and secondary containment. Our customers now receive product shipments with integrated temperature tags, and any deviation triggers an automatic reshipment—problems are solved first, questions answered later. Open communication between shipping providers, warehouse staff, and our on-call chemists ensures that even remote customers have uninterrupted access.
Changes in regulations, particularly those related to hazardous material classification and reporting, occasionally require rapid adaptation. Our regulatory compliance experts keep a close watch on the landscape by subscribing to monitoring services, reviewing updates, and running simulations to see how new standards would affect both plant operations and customers’ own compliance documentation—but they also spend time face-to-face with process engineers to ensure what is on paper matches what is in use. This way, certification lapses or shipment holds are prevented before they can occur.
Science never stands still, and neither do we. Our production line for Pyridine, 5-[(aminooxy)methyl]-2-(1H-pyrazol-1-yl)- runs in step with the needs of synthetic chemists and process engineers, not on an arbitrary sales schedule. Custom batch sizing, real-time production status updates, and tailored technical support distinguish our process from the experience with non-producer middlemen. Over time, we’ve built working relationships with return clients who push us to tweak, refine, and sometimes completely overhaul our protocols to match their evolving research challenges. Success isn’t measured by volume alone, but by the reproducibility of their experiments and the knowledge that what arrives in the bottle works as intended.
Our process chemists and QA teams invest in in-depth familiarity with the molecule’s reaction profile, solubility behavior, and shelf stability under varied real-world storage and transport conditions. Data not only informs our best practices but supports peer-reviewed publications and regulatory filings in some of the most demanding industry sectors. Regular technical roundtables give both our technical team and customers a direct voice in the ongoing refinement of product performance, documentation, and logistics.
Direct manufacturing drives our focus on continuous improvement. Years of small corrections and hard-earned lessons from ramping new reactions and packing bulk shipments have streamlined our Pyridine, 5-[(aminooxy)methyl]-2-(1H-pyrazol-1-yl)- production into a dependable source for tool compounds, research reagents, and custom synthesis intermediates. No matter the technical challenge brought forward by a new project—narrower impurity windows, tighter batch-to-batch variance, stricter documentation—our team works directly with both upstream and downstream partners to deliver a solution that fits both laboratory discovery and real-world scale-up.
Purchasers have direct access to the technical experts in our facility: staff who can explain not just the documented analytical values, but also the story behind why a process change was made, or how a delivery protocol evolved after feedback from an international research group. This direct line accelerates problem-solving and eliminates the uncertainty that often slows work when passing through multiple layers of distribution. For researchers and production teams seeking a supplier invested in their long-term success, the difference becomes clear with every bottle delivered.
As both producer and day-to-day operator, we see the broader trends that shift expectations for specialty chemicals. Analytical robustness, traceability, supply chain agility, and transparent documentation are not abstract ideals—they form the competitive ground for scientific advancement. By engaging directly with end users, refining our process at every step, and publishing to peer and industry standards, we not only provide Pyridine, 5-[(aminooxy)methyl]-2-(1H-pyrazol-1-yl)- as a reliable product, but contribute to the culture of best practice that drives chemical research forward. The molecules themselves may be small, but their impact—through careful stewardship and direct accountability—grows far beyond the beaker and bench.