|
HS Code |
125269 |
| Chemicalname | 3-Aminopyridine |
| Casnumber | 462-08-8 |
| Molecularformula | C5H6N2 |
| Molecularweight | 94.12 |
| Appearance | White to off-white crystalline powder |
| Meltingpoint | 61-63°C |
| Boilingpoint | 251°C |
| Density | 1.139 g/cm3 |
| Solubilityinwater | Soluble |
| Flashpoint | 113°C |
| Odor | Pyridine-like |
| Refractiveindex | 1.568 |
| Synonyms | 3-Pyridinamine; m-Aminopyridine |
As an accredited 3-Aminopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 3-Aminopyridine includes a 100g amber glass bottle with a tight-sealing cap, labeled with hazard and identification details. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 3-Aminopyridine: Securely packed, moisture-protected drums or bags, compliant with safety regulations, maximizing container capacity. |
| Shipping | 3-Aminopyridine is shipped in tightly sealed containers to prevent contamination and moisture absorption. It is classified as a hazardous material, requiring appropriate labeling and documentation. During transport, it must be handled according to chemical safety regulations, including protection from physical damage and storage in cool, dry conditions away from incompatible substances. |
| Storage | 3-Aminopyridine 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. Use with appropriate chemical safety precautions, ensuring the storage area has spill containment and ready access to eyewash stations and safety showers. |
| Shelf Life | 3-Aminopyridine has a shelf life of 2-3 years when stored in a cool, dry place, tightly sealed, and protected from light. |
Competitive 3-Aminopyridine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Not every chemical pulls its weight across so many fields the way 3-Aminopyridine manages to do. In laboratories and manufacturing plants alike, this compound—known in some circles by its model code 341-17-5 and its CAS number—turns heads for good reason. As someone who has seen the rush for purity and versatility firsthand, I can say straight: it pays to know what sets this one apart, especially for teams working on the edge of pharmaceutical or chemical research, or any process that asks for clean, consistent intermediates.
At the heart of this molecule is a pyridine ring with an amino group locked on at the third position. This small structural tweak brings out some unique properties compared to relatives like 2-aminopyridine or even plain pyridine. The model most commonly recognized in chemical catalogs features a fine crystalline powder that takes on a pale off-white or sometimes very light yellow color. Standard-grade material lands with a purity above 99%, which, from an R&D perspective, clears a lot of headaches linked to trace contaminants. Most batches bulk at 25 kg or 50 kg drum sizes, but smaller laboratories can usually get single-kilogram bottles that meet the same quality standards.
Some years ago, I remember comparing batches from several suppliers for a major pharma project. Analytical tests like HPLC and melting point determination (104-108°C) quickly flagged which samples met the bar for synthetic reliability. 3-Aminopyridine's water solubility isn’t just academic—dissolving it for process chemistry jobs saves time when shifting to scale-up, and the low-level volatility means safer handling. Residue on ignition checks, GC-MS impurity scans, moisture content below 0.2%—these numbers become a lifeline to regulating consistency between runs. It’s easy to underestimate how much batch failure stems from minute changes in raw material. I’ve learned not to skimp on lot-to-lot documentation, especially with a compound that steps into pharma applications.
Pyridine derivatives as a class get used everywhere, but the three-position amino group gives this one an edge, both in terms of reactivity and final product profiles. Unlike 2-aminopyridine, where the amino group cozies up to the ring nitrogen (often skewing selectivity or leading to more byproduct formation), the three-position layout cuts down complications when building heterocycles or fabricating ligands. If you’ve ever fixed a stubborn side reaction with a smart substitution, you’ll appreciate how this arrangement keeps syntheses straightforward.
Pharmaceutical developers often need intermediates that tolerate a diverse set of functional groups and mild to moderate reaction conditions. 3-Aminopyridine does the job: it processes smoothly in both aqueous and organic media, won’t burn a hole in your budget compared to more exotic amines, and passes most major regulatory checks for non-active intermediates. It’s a behind-the-scenes talent in a variety of drugs, dyes, and even specialty agrochemicals.
Most research chemists run into 3-Aminopyridine sooner or later, usually when assembling basic building blocks for antiviral compounds or skeletal muscle stimulants. It plays a key role in some treatments for neurological disorders. As a component, its stability outshines flashier, less robust reagents. During a stint in a medicinal chemistry startup, I watched teams opt for it on late-stage routes strictly because it simplified downstream purification—no messy tars, fewer byproducts, lighter colors at every cleanup step. That translates to shorter workups and quicker data when deadlines hang over a project.
In the pigment sphere, its use in synthesizing advanced dyes and specialty colorants can be the tipping point for batch quality and stability. Customers want products that last longer and show sharper color profiles, especially in coatings and plastics. The difference shows up as tighter spec sheets on shade, brightness, and material compatibility—a direct payoff from starting with reliable intermediates like 3-Aminopyridine.
Safe handling always takes center stage. 3-Aminopyridine, while less volatile than many aromatic amines, still asks for respect—gloves, lab coat, and fume hood as routine. A seasoned chemist once told me: consistency in PPE can be the difference between an easy day and a health investigation. The compound’s solid, slightly hygroscopic nature means it stores best sealed tight at room temperature, away from acids and oxidative agents. Some folks try to skimp on containment, only to battle sticky residue or unpleasant vapors. Standard glassware, polyethylene drums, or lined containers all work, as long as humidity stays in check.
Disposal protocols get more attention today than they did even a decade ago. Waste streams containing 3-Aminopyridine won’t raise red flags if treated through the usual aqueous/base decomposition or incineration methods. I’d always recommend looping in a site’s waste management lead before finalizing any synthesis run, especially on projects headed for the regulatory market.
Across the industry, consistency often slips through the cracks. Some companies sell so-called “high purity” 3-Aminopyridine, only to deliver off-spec material with subtle but stubborn impurities. These can ruin catalytic reactions or generate regulatory snags down the road. I’ve spent long hours validating raw material lots, measuring UV-vis spectra, and double-checking melting points. Supply chains have gotten better over the years; leading manufacturers back up every bottle with a full C of A and traceability reports, making it easier to troubleshoot if something reads off in QC.
Shipping and storage, while routine, still trip up teams who don’t account for long-haul environmental shifts. 3-Aminopyridine survives weeks in container ships or dusty supply rooms without much fuss, unlike more unstable reagents that degrade fast under sunlight or moist air. Still, I recommend immediate inspection on arrival, as partial lot caking or faint yellowing flags possible shelf-life issues. Returns take time, and no one likes a project setback over a $200 bottle that should have been perfect the first time.
It pays to compare what 3-Aminopyridine brings that alternatives don’t. Take 2-Aminopyridine—a staple in alkaloid synthesis and dye chemistry since the 1940s. Users betting on the two-position version sometimes hit roadblocks with selectivity, especially on extended ring-building projects or when the downstream chemistry gets picky about byproducts. As for 4-Aminopyridine, its sharp reactivity profile suits some CNS drug research, but production-scale work struggles with regulatory and storage headaches due to increased toxicity and volatility.
From my own time on both analytical QC and route scouting, 3-Aminopyridine earned its slot in procurement lists mainly by balancing ring reactivity with bench safety. Synthetic teams looking to install secondary substituents report higher yields and less tar, while scale-up researchers like its non-hazardous shipping profile. That means lower risk in both academic and commercial pipelines, from bench flask to plant reactor.
Many mid-tier manufacturers lean hard into 3-Aminopyridine precisely because of its clean reaction profile and ease of separation. I remember tracking a kilogram-scale cross-coupling route from benchtop up to multipurpose reactors. The anticipated issues—stubborn byproducts, endless washes, awkward viscosity changes—showed up much less than with bulkier amines. Filtration worked faster, crystallization brought in product with minimal color, and the isolated yield only dropped off at serious multi-ton runs.
The consistency of this compound lets teams swap reaction conditions without constantly recalibrating analytics. Some operators use ethanol or DMF as cosolvents; others go straight aqueous, relying on the free solubility to simplify workup and minimize environmental impact. This predictable behavior stands out next to trickier amines that need special conditions or generate more hazardous residues.
Industrial users in China, India, and the US keep demand steady both for export and local manufacture, proof that it remains competitive globally. Decades of process refinement give new users reliable access to documentation and robust supply—far better than dealing with obscure or regionally limited intermediates.
Today, regulatory teams play a critical role in vetting every intermediate in a pharma or specialty chemical pipeline. 3-Aminopyridine’s strong safety record makes audits and compliance reviews smoother than most. It’s not classed as a controlled substance, saves time for paperwork, and heads off concerns linked to environmental toxicity compared to nastier aromatic amines.
Continuous availability means fewer surprises during scale-up or regulatory qualification. I recall a project where a slightly altered route threatened to slip delivery schedules because the original intermediate faced raw material shortages. Swapping in 3-Aminopyridine, backed by a clear compliance record, closed the gap and let the project stay on track—proof that supply flexibility can be its own form of risk control in a volatile R&D ecosystem.
No product solves every problem. Skilled chemists and industry veterans keep a sharp eye for limits: 3-Aminopyridine works best on certain reaction types, and stubbornly resists over-alkylation or oxidative degradation. Its relatively moderate base strength can frustrate teams expecting a more aggressive amine for specific couplings or reductions. The cost, though competitive, sits just above other bulk pyridine derivatives, fueling a constant push for process optimizations and greener alternatives in large-scale work.
Green chemistry advocates argue for safer, lower-toxicity alternatives. 3-Aminopyridine meets REACH and major EPA regulations, yet teams pursuing waste minimization take extra care with byproduct and water stream management. Some newer routes focus on catalytic hydrogenation or mild oxidants, moving away from legacy methods that produce more residue or need more aggressive washing. I’ve seen lab groups publish innovative protocols that cut solvent use in half—an area always worth watching as regulations grow stricter.
The way forward depends on innovation both at the bench and the plant. Investment in tighter process controls, better raw material screening, and regular supplier audits keeps batch failures in check. Teams planning scale-up should invest in pilot runs and small-lot testing of each supplier’s product before committing to tons of material. Over and over, side-by-side tests reveal differences invisible on paper but glaring on the production floor.
Investing in better solvent recovery and improved filtration helps keep downstream work clean and environmentally responsible. Sharing analytical findings within site or corporate teams reduces duplicate failures, and honest feedback to suppliers goes a long way. The community benefits from companies who invest in R&D to further purify and stabilize the material even as supply chains globalize.
The compound’s story, after decades of use, is less about marketing and more about stamina and trust built across research and production. For every breakthrough molecule or next-gen device, countless hours of routine synthesis and method validation pave the way. 3-Aminopyridine, in the hands of dedicated teams, keeps both the ambitious and the everyday projects moving. As the landscape of chemical manufacturing keeps shifting, its reliability—backed by generations of lab and plant workers—secures its spot as a go-to intermediate for both trailblazers and workhorses in science and industry.