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HS Code |
729879 |
| Cas Number | 101-81-5 |
| Molecular Formula | C7H10N2 |
| Molecular Weight | 122.17 |
| Iupac Name | 2-(2-pyridyl)ethanamine |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 256-257 °C |
| Melting Point | -9 °C |
| Density | 1.067 g/cm³ |
| Solubility In Water | Miscible |
| Flash Point | 112 °C |
| Refractive Index | 1.581 |
| Pubchem Cid | 7681 |
As an accredited 2-Pyridylethylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Pyridylethylamine is supplied in a 100g amber glass bottle with a tight-sealed cap and hazard labeling for chemical safety. |
| Shipping | 2-Pyridylethylamine is shipped in tightly sealed containers to prevent moisture and contamination. It should be handled with care and transported according to relevant chemical safety regulations. Packages are labeled with appropriate hazard information. During shipping, keep away from heat, ignition sources, and incompatible substances to ensure safe delivery. |
| Storage | 2-Pyridylethylamine should be stored in a tightly sealed container, away from light, heat, and sources of ignition. Keep it in a cool, dry, well-ventilated area and segregate from incompatible substances such as strong oxidizers. Ensure proper labeling and handling in accordance with safety guidelines to prevent accidental exposure or environmental contamination. |
Applications of 2-Pyridylethylamine in Industrial Manufacturing2-Pyridylethylamine is a specialty organic intermediate that finds industrial adoption in select fine chemical, pharmaceutical, and agrochemical sectors. Below we present verified downstream application scenarios with a focus on technical standards, process roles, and finished product types. 1. Pharmaceutical Intermediate for Antihistamine APIsIn pharmaceutical synthesis, 2-Pyridylethylamine functions as a critical precursor during active pharmaceutical ingredient (API) production, particularly for second-generation antihistamine compounds. QC teams monitor incoming material for purity and specific trace impurity profiles that could impact downstream synthesis yields. R&D labs optimize the ratio within multi-step manufacture to minimize side reactions and reduce purification requirements. The primary value lies in delivering consistent reactivity for scale-up batches, with process engineers controlling time and temperature during amidation or alkylation steps where this intermediate is introduced. Downstream, the final APIs require precise chromatographic validation against pharmacopeial standards before tableting or encapsulation lines proceed. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Synthesis — Pyridine-Based Herbicide Intermediates2-Pyridylethylamine serves as a building block for agrochemical manufacturers producing selective pyridine-ring herbicides. Formulation chemists integrate this intermediate during the N-alkylation step to construct key ligands which determine herbicidal mode of action. Process engineers dose the ingredient precisely to avoid over-alkylation, monitoring residue and reaction completeness via HPLC. The application ensures regulatory traceability for ingredient origin, supporting product registrations with global authorities. Agrochemical products using these synthetic routes then undergo biological screening before bulk formulation and packaging as commercial crop protection inputs. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Specialty Corrosion Inhibitor Agent in Oilfield Additive ProductionOilfield chemical producers incorporate 2-Pyridylethylamine into proprietary blends for corrosion inhibitor concentrates targeting pipelines and extraction infrastructure. The amine group anchors the compound’s effectiveness as a film-forming agent, bonding to steel surfaces to reduce hydrogen sulfide and CO2-induced corrosion. During blending, quality assurance enforces batch uniformity by closely monitoring active content and amine purity, which influences overall inhibitor performance. Operators adjust concentration in line with projected field deployment rates, considering crude composition and anticipated downhole temperatures. Final concentrates are validated to ensure compliance with regional oilfield chemical regulations before shipment for field mixing or direct injection. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Rubber Accelerator Manufacturing for Specialty ElastomersProducers of high-performance elastomers select 2-Pyridylethylamine as an accelerator intermediate for the controlled vulcanization of specialized rubber compounds used in technical seals and hoses. Incorporation of this compound occurs after primary fillers are blended but before crosslinking occurs, allowing for targeted modulation of cure rates and final mechanical properties. QC personnel rigorously control the input ratios to match formulation specifications established in development, with variations based on the target crosslink density for the application sector. The result is rubber goods demonstrating stable elasticity and resistance to chemical aging, delivered according to OEM and export quality standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Decades of focused chemical synthesis have honed our approach toward products like 2-Pyridylethylamine. Whenever we handle this compound, its practical value shines in both research and industrial setups. At its core, 2-Pyridylethylamine (commonly recognized due to its ethylamine group attached to a pyridine ring) delivers unique chemistry: it brings together nucleophilic reactivity with a stable pyridine backbone. Years of continuous process optimization remind us that behind each drum lies much more than a CAS number. There is a daily routine of purity checks, controlled moisture, and unrelenting attention to batch traceability.
Our typical offering centers on the model with at least 98% purity, popular with labs and larger-scale formulators. Over the years, clients push us higher—every decimal point in assay matters for critical synthesis in pharmaceuticals or advanced materials. Most orders specify a colorless liquid or pale-yellow oil, and this consistency builds confidence. You see, batch testing never becomes a checkbox exercise; staff have caught subtle shifts in UV spectra or faint side product peaks, which shows why transparency and discipline become habits, not promises.
A difference emerges in the care taken from the earliest reaction stage. Pyridine derivatives demand handling that prevents atmospheric moisture and avoids contamination. Over time, our teams have invested in closed-loop process controls since trace impurities—often invisible to a casual glance—can skew sensitive downstream reactions. Bottling the product fresh, under inert gas, and using low-permeability packaging shows dedication to a process. We minimize exposure to air and ambient light. This comes from past lessons: even a partial day in improper storage can tip a marginal sample over the acceptable limit for key end users.
Other companies sometimes opt for expedited processing where cycle time trumps detail. The results speak for themselves. Less stringent protocols leave behind trace water, halides, or secondary amines, which catalyze unwanted side reactions in high-value applications. Our teams still rely on hands-on rotary evaporation. Even though automation tempts with speed and efficiency, nothing replaces the sound of the solvent line or the tactile sweep of the pipette as residue leaves the flask.
For formulation scientists, 2-Pyridylethylamine delivers more than just a building block. Chemists recognize the N-ethylpyridinium core for cross-coupling, activation, and as a stepping-stone to many bioactive molecules. Having a reliable source translates into fewer headaches chasing impurities and less time wasted repeating purification. The amine group’s reactivity supports wide adoption in pharmaceutical intermediate synthesis, dye chemistry, and ligands for catalysis. In our experience, only a handful of similar compounds offer the same balance of basicity and manageable volatility, which broadens its laboratory uses.
We have observed researchers trust 2-Pyridylethylamine for histamine receptor studies and analytical calibration. Its handling familiarity—moderate odor, low vapor pressure, quick aqueous solubility—helps ease training for new graduates or production staff. Most critical applications run side-by-side with stringent purity requirements, and the ability to ship consistent lots eliminates requalification nightmares.
Clients shifting from alternative brands often notice differences beyond nominal assay figures. Trace metal content can make or break metal-catalyzed reactions. Our manufacturing standards enforce background checks—raw materials never slide by without analysis for heavy metals, nitrates, or halides. Chromatograms get archived not because of regulatory obligation, but as proof the chemistry stays robust year in, year out.
Some manufacturers focus more on throughput, leading to inconsistency in haze, color, or off-notes detected by sensitive noses in quality control. Reactions in glass-lined vessels reduce the downstream work in color correction and removal of micro-impurities. Solvent washes and sequential distillation steps come from hard lessons during scale-up runs—where even ppm-range contamination in pyridines or ethylamines can later turn into sticky silica columns and hours lost to reprocessing.
We focus on the demands from pharmaceutical synthesis and agrochemical screening projects. They need clean, well-documented batches—no shortcuts. We retain detailed records for every production lot: raw materials’ source, employee sign-off, chromatography, and stability data extending sometimes longer than regulatory requirements demand.
The main contrasts arise from how we treat purity and versatility. Take benzylamine, often used in similar coupling chemistry. Its volatility can complicate handling, and it features different nucleophilicity and reactivity profiles when compared to 2-Pyridylethylamine. In several custom syntheses, we observed successful substitution and activation steps thanks to the latter’s unique balance of properties. Subtle as it seems, the presence of the pyridine ring alters both electron density and aromatic stabilization; product yields and reactivity frequently shift in side-by-side experiments.
Other pyridine-based amines, such as 3-pyridylethylamine or 4-pyridylethylamine, diverge in both reactivity and basicity due to positional differences. Only the 2- derivative regularly produces the yields, selectivity, and solubility our customers rely on for high-throughput chemical screening and medicinal chemistry pipelines. In catalysis research, several project teams reported cleaner ligand exchange with our 2-Pyridylethylamine, noting reduced byproduct profiles in final products. The downstream purification savings become evident after the first few runs—column fractions clear up, and NMR spectra show fewer rogue peaks.
Production-scale chemists rely on adaptability from product to product. With 2-Pyridylethylamine, the real-world difference comes in tolerance under a range of reaction temperatures and solvents: it partners well with both polar and nonpolar systems. Over years of supporting custom syntheses, we’ve witnessed clients run arylation, alkylation, and reductive amination projects without adjusting conditions just to accommodate product stability or reactivity. The robustness of the amine group (paired to a pyridine ring that resists excessive oxidation) grants operators a wider safety margin.
The storage characteristics matter as well—most competitive products require specialized refrigeration or desiccation. Consistent drying protocols and secure packaging mean fewer surprises during inventory—in our case, unopened drums remain stable on standard warehouse racks, marked only for physical separation from strong acids or oxidants. Our material profiles display sharp, reliable melting range and boiling point, so distillation-based processes never require excess caution or overdesign.
Some older literature mentions concerns over shipping volatility or oxidation. Our upgrades to packaging—moving from standard HDPE to lined aluminum and nitrogen-purged containers—lengthened effective shelf life and has all but eliminated off-putting odors or clouding, even in multi-month logistical chains. Such tweaks stem from lived experience. If you have ever opened a drum only to find yellowing or strange floating solids, you understand the frustration of re-qualifying entire inventories.
Biotech startups request smaller drums for combinatorial chemistry, where every reaction well needs dependability. Bulk pharmaceuticals prefer intermediate quantity, focusing on maximizing throughput without risky excess stock. In both scenarios, 2-Pyridylethylamine forms the backbone for selective alkylations and amination protocols. Our work with scale-up groups often features custom packing—weighing under inert atmosphere on demand so that final users never struggle to split kilo-amounts in a glovebox or airlock.
We have supplied advanced materials labs investigating new electronics applications of pyridine derivatives, where a stray anion or iron contaminant would skew dielectric properties or contact resistance. Clean, low-metal content becomes non-negotiable. Meanwhile, in specialty dye intermediates, even negligible haze or yellowing can ruin an entire synthesis batch. Each return customer shows which small details matter: stability in color, thermal performance, and absence of tars or polymeric residue.
With specialty chemicals, tangible metrics matter, but so does underlying repeatability. We stick by regular retesting: IR, NMR, and elemental analysis run on every major lot. Teams review historical data for shifts that could hint at subtle process drift. Over time, this guards against both outright defects and creeping impurity buildup. Unlike generic offerings, our 2-Pyridylethylamine frequently passes secondary checks: low UV absorbance, no extraneous baseline humps, sharp 1H-NMR resonances. These features explain lower failure or dispute rates for our customers and fewer out-of-spec rejections across our lifetime supply record.
We learn most from vocal customers; even minor complaints receive extensive internal discussion. Someone reporting a faint greenish tinge might trigger a week-long review of distillation logs, condenser temperatures, or glassware checks. The chain of accountability stretches from senior chemists to warehouse team leads. One takeaway: nothing stays static. Every improvement, such as solvent quality upgrades or process automation, depends on linking real-world problems with targeted solutions. We maintain flexibility: if a researcher needs a unique grade or packaging, our short batch cycle can often address the need within a week, not months. No tally of monthly output means much without confirming the outcome—low variance, clean spectra, zero residue, and satisfied partners.
Maintaining purity demands constant vigilance. Analytical techniques have evolved—what looked pure to yesterday’s GC can now show minor, reactive byproducts under HRMS. This discovery, far from a setback, sparks process intensification. Now, our post-reaction purification step includes not just distillation, but column checks and pre-package impurity scans using advanced spectrometers. Every adopted enhancement comes from a frustration solved, not simply following trends.
Platform upgrades only prove their worth if they show up in the customer’s hands. For example, years back, a run of corked containers absorbed too much warehouse odor. Old style seals got swapped out for fresher, more chemically resistant liners. Now, trace odor incidents virtually disappear. Similarly, wider-bore bottle necks cut dispensing accidents in fast-paced environments, where minutes spent pouring add risk or downtime.
Working with the actual manufacturer shortens the information gap. End-users get answers from the people who make the chemicals, not from intermediaries relaying unknown stories. Questions on reaction scale, solvent compatibility, or packaging for specific instrumentation reach our technical group, not a help desk. If a customer needs modifications—larger capacity flasks, trace impurity tests, evidence of full metal screening—these requests become real options, not paperwork shuffled between offices. Few understand the complexities of isolation at every scale, from sub-liter to hundreds of kilos.
Through dozens of long-term partnerships, one lesson never fades: transparency and responsiveness carry more weight than standard spec sheets. Researchers want to see clear, robust answers regarding lot traceability, impurity breakdown, and batch stability. By controlling the full production chain, each point of contact reassures the end user that what arrives will work in the bench reaction, pilot plant, or industrial process—without surprise drift in yield or color, no arguments over ambiguous labeling, and no guessing about the true age of inventory.
2-Pyridylethylamine, viewed from the lens of honest manufacturing, turns into more than just a catalogue entry. It arises from hundreds of daily choices—raw sourcing, attention to reaction conditions, careful packaging, patient batch testing. It sits at the intersection of multiple professional communities: from academic advanced materials teams to industrial formulators aiming for cost-effective consistency.
By keeping our processes visible and flexible, even as we scale, we respond to real concerns. Material that passes our quality control matches up to client expectations not because certification demands it, but because repeat relationships depend on it. The open feedback loop between production, quality assurance, and end users forms a practical partnership—each informed customer input sparks another round of internal review. From improved product purity to safer packaging, every enhancement finds its origin in solving a practical problem.
Tested, proven 2-Pyridylethylamine enables smoother, more predictable research and production outcomes. The value goes beyond a line on a budget request; the material itself, and the means by which it is made, shapes downstream discoveries and new product launches. Skilled hands, trained eyes, and honest chemistry make this possible. The reward comes in loyal users who trust each shipment will do its job, every time—and who reach out with fresh challenges, knowing that those will be met with diligence, pride, and practical skill born of long experience in chemical manufacturing.