|
HS Code |
430521 |
| Chemical Name | Bromohexadecyl pyridine |
| Molecular Formula | C21H36BrN |
| Molecular Weight | 382.42 g/mol |
| Cas Number | 1122-89-6 |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents (e.g., chloroform, methanol) |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Synonyms | 1-Bromohexadecylpyridinium |
| Smiles | C16CCCCCCCCCCCCCCBr.N1=CC=CC=C1 |
| Inchi Key | FELXKYJRDWSSIF-UHFFFAOYSA-N |
As an accredited Bromohexadecyl pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Bromohexadecyl pyridine, 10g, supplied in a sealed amber glass bottle with a secure screw cap and chemical hazard labeling. |
| Container Loading (20′ FCL) | 20′ FCL typically holds Bromohexadecyl pyridine in 160–200 tightly sealed drums, ensuring safe, moisture-free bulk transport. |
| Shipping | Bromohexadecyl pyridine should be shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. It is classified as a hazardous chemical and must comply with relevant transportation regulations. Proper labeling, safety documentation, and secondary containment are required to ensure safe handling and prevent leaks during transit. |
| Storage | Bromohexadecyl pyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect it from heat, light, and moisture. Ensure proper labeling and handling procedures to minimize exposure. Store in accordance with all relevant local, state, and federal regulations for hazardous chemicals. |
| Shelf Life | Bromohexadecyl pyridine typically has a shelf life of two years when stored in a cool, dry, and tightly sealed container. |
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Purity 98%: Bromohexadecyl pyridine with 98% purity is used in organic synthesis, where it ensures high reaction yield and minimal byproduct formation. Molecular weight 381.41 g/mol: Bromohexadecyl pyridine at 381.41 g/mol is used in surfactant formulation, where it enables optimal micelle stability and uniform dispersion. Melting point 52°C: Bromohexadecyl pyridine with a melting point of 52°C is used in pharmaceutical intermediate production, where it allows consistent processing and controlled dissolution rates. Hydrophobicity index 7.1: Bromohexadecyl pyridine with a hydrophobicity index of 7.1 is used in membrane coating applications, where it improves barrier properties and chemical resistance. Stability temperature up to 120°C: Bromohexadecyl pyridine stable up to 120°C is used in high-temperature catalysis, where it maintains structural integrity and catalytic efficiency. Particle size <10 μm: Bromohexadecyl pyridine with particle size less than 10 μm is used in nanoparticle surface modification, where it provides uniform surface coverage and enhanced functionalization. Viscosity grade low: Bromohexadecyl pyridine with low viscosity grade is used in liquid crystal formulation, where it promotes rapid alignment and stable phase transitions. Solubility in ethanol: Bromohexadecyl pyridine soluble in ethanol is used in reagent preparation, where it achieves homogeneous mixtures and predictable reagent performance. |
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Bromohexadecyl pyridine stands out a bit in the growing library of modern chemical agents. I’ve followed its development for a few years, watching the way this single molecule has carved out a niche for itself in both research labs and industrial workbenches. Much of the enthusiasm around it comes from a simple fact: it brings together a long, saturated alkyl chain and a bromine atom attached to a pyridine ring, all in one tidy package. It might sound technical, but this structure lets scientists and product designers push into some useful applications that older reagents just can’t quite manage. Clean innovation often means pulling ahead in material science and production without lending your process a stronger smell or corrosive touch. Bromohexadecyl pyridine tends to get noticed because it seems to sidestep some of the headaches caused by comparable surfactants and alkyl halides.
The key here isn’t just novelty but function. Bromohexadecyl pyridine (I’ll call it BHP for short) shows up in areas where both stability and controlled reactivity matter—especially when you need a longer-chain alkyl group and a halogen leaving group, all bound to a nitrogen-containing ring system. Its direct competitors sometimes leave scientists making tradeoffs: shorter chains may boost solubility, but they don’t build the same hydrophobic profiles needed for more advanced micelle or vesicle construction in biochemistry. Drop the pyridine ring, and you often lose some of the selectivity seen in organic transformations, as the ring nitrogen gives extra direction in coupling reactions.
BHP’s long alkyl arm, measuring in at sixteen carbons, brings more than length. Longer chains alter partition coefficients in organic syntheses, changing how a molecule interacts at phase interfaces. That’s crucial in extraction work or when building synthetic membranes—areas where the action rides on subtle chemistry, not just bulk mixing. If you’re working in pharmaceuticals or advanced surfactant design, you’ve probably seen this firsthand. Pyridine as a base has long enjoyed its reputation in catalysis and nucleophilic substitution. Drop a bromine on the end of that carbon chain and you tap into a blend of leaving group reactivity (thanks to bromide) and the guidance of the pyridine ring. In use, this lets you build custom-tuned intermediates for alkylation, quaternization, and even surface modification without depending on short-lived or overly volatile alternatives. Compared to plain hexadecyl bromide, BHP’s ring means reactions often head toward a more predictable set of products—extremely valuable if you’re running a tight lab schedule.
Having worked under a few mentors in both academic and industry settings, I’ve watched BHP make early inroads into the fields of advanced surfactants and tailoring of surface-active agents. Think of work in materials science where the drive toward bio-compatibility or chemical specificity can push a whole project either toward a breakthrough or a frustrating dead end. Scientists in membrane protein isolation, for example, often need surfactants that not only disrupt lipid bilayers at just the right concentration but can also offer a leaving group for further functionalization. BHP specifically supplies a rare design feature: its pyridine core keeps it from folding up into micellar aggregates too soon, carrying out its duties without clogging up analytical columns or interfering with protein structure.
Then there’s its value in organic synthesis. If you’re after a controlled quaternization, the compound plays well with other building blocks and opens up quaternary pyridinium intermediates that can anchor catalytically active phases. In practice, that often means sharper yields and cleaner separation, especially where highly polar or highly nonpolar phases need to stay distinct in a reaction flask. I've seen chemists swap out less predictable alkyl halides for BHP and walk away with fewer headaches over unwanted side reactions—a testament to both planning and sheer molecular design.
BHP usually arrives as a white to off-white crystalline solid, with a molecular weight just north of 400 g/mol. Its melting point sits higher than some of its smaller cousins, often in the range of 60 to 80°C, giving it a versatility that suits both room-temperature and slightly elevated operations. Solubility patterns matter: BHP tends to dissolve better in organic solvents like chloroform, dichloromethane, and certain ethers, though it can exhibit some amphiphilic tendencies due to its lengthy hydrocarbon tail. Water solubility, while not its strongest suit, shouldn’t be dismissed outright in mixed solvent systems.
Most commercially available grades of BHP focus on purity, typically boasting levels above 98 percent. Trace impurities, such as mono-brominated or oxidized side products, get flagged immediately in reputable labs, as they can impact downstream functions—especially in pharmaceuticals. Assessing a batch means checking for these trace contaminants via NMR or HPLC; even small deviations can spell trouble in rigorous applications. If you’ve ever been burned by poor-quality reagents, you understand why these checks matter. The consistency of a well-made grade often distinguishes BHP in long-term research studies where a single bad lot could derail months of careful planning.
BHP carves out its space most clearly when judged against both classic alkyl bromides and common long-chain surfactants. Standard alkyl bromides, such as hexadecyl bromide (cetyl bromide), bring reactivity but lack the added utility of a heterocyclic base. You can toss a pyridine ring into the mix but combining it with a lengthy, brominated alkyl chain isn’t always straightforward. Some reagents give you halogen flexibility—like the choice between bromide or chloride—but often at the cost of the chain’s length or ring structure, narrowing how they fit into a larger synthetic pathway.
The kind of selectivity that BHP offers means less time spent cleaning up reaction mixtures and less risk of introducing undesired byproducts. In my own lab work, I’ve noticed how subtle changes to the leaving group and alkyl chain can tip the balance between a scalable, reliable process and a day wasted sorting through chromatography columns. Longer alkyl chains frequently help build amphiphilic agents, crucial in detergents or liquid crystal work. Still, only specific ring systems can shepherd reactivity in the right direction. Toss that all together, and BHP doesn't just compete—it often leapfrogs comparable reagents, particularly if you’re pushing for innovation in drug delivery systems or functional coatings.
Sourcing quality chemicals today means knowing both the origins and the batch histories of your raw materials. The science community has seen what happens when chemicals are cut with excess impurities, leading to unexpected side effects or failed reactions. In Europe, recent REACH guidelines put a premium on transparency, with researchers now asking for full traceability down the supply chain. BHP fares well under these conditions because reputable producers supply solid certification packages—COAs backed by chromatographic and spectroscopic analysis. No one wants to gamble budget and reputation on uncertain input materials.
At the bench, ease of handling matters, too. BHP, despite its reactivity, doesn’t present the same acute risks as shorter, highly volatile alkyl halides. With proper gloves and ventilation, spills get contained quickly, and any fumes tend to be manageable compared to some lower-weight analogs. Most working labs keep it in cool, dry storage under nitrogen just to prevent slow oxidation or hydrolysis, lessons learned over decades of organic work. My experience watching lab techs, pharmacists, and chemical engineers approach BHP is that they treat it as they would a fine tool—respecting its power without fearing the hazards seen with less stable halides.
Chemical agents don’t just stay put in research journals—they move into manufacturing, into products we see and touch every day. The blend of long-chain hydrophobicity and a reactive bromide offers a rare double act, tempting designers and creative chemists beyond standard surfactant and alkylation roles. Advanced coatings, crosslinked polymers, and drug carriers benefit from the resilience and controlled reactivity that BHP supplies. A decade ago, you’d see only the bravest teams venturing into these applications. Now, as more materials science programs weave together organics and inorganic frameworks, this compound’s hybrid nature invites broader use.
I’ve seen teams use BHP in nanostructure formation for catalysis, where its amphiphilic segment sorts itself across interfaces, and its bromine handle offers chemoselectivity for anchoring catalysts. Some early reports from biomedical engineering circles suggest potential in crafting responsive coatings for implantable devices—think drug-eluting stents or biosensors that need a smart surface, able to bind biomolecules one moment and shed them the next. Achieving these kinds of results depends on tight quality control and deep chemical understanding, but BHP’s structure keeps showing up as one formula with more flexibility than most.
No commentary on lab or industrial chemicals should ignore environmental stewardship. While BHP doesn’t share the acute aquatic toxicity of some short-chain surfactants, its breakdown products do deserve attention. Responsible labs collect and handle BHP waste under standard solvent and halide protocols, making no assumptions about downstream impacts. Good ventilation helps, and teams log all spills and decompositions as part of their environmental accountability plans. Over the years, I’ve seen environmental profiles for comparable agents get re-written as government guidelines shift, especially with respect to persistent organic pollutants. Prudent users of BHP stay ahead of regulation by reviewing disposal routes and by avoiding routine dumping into commercial drains.
On the workplace safety front, gloves and eye protection score high on any checklist. Bromo compounds can be strong alkylators—the very property that makes BHP useful as a synthetic handle—so minimizing skin exposure keeps staff out of harm’s way. Fume hoods clear lingering vapors well before they pose inhalation risks. Continuous training builds habits that protect both workers and the products they help create. In my own experience, regular check-ins and safety drills allow staff to act quickly and calmly, whether responding to smoke, minor spills, or an accidental splash.
BHP’s full potential hasn’t been charted yet, in part because many labs tend to reach for more established long-chain surfactants or pyridine derivatives. Still, creative teams in medicinal chemistry and advanced materials keep nudging boundaries. As researchers convert BHP into quaternary salts or couple it to other heterocycles, new pathways open in catalysis and bioactive compound development. The challenge comes in translating bench-scale success into industrial reliability, keeping purity high and costs controlled. This matters most where regulatory approval hangs in the balance, as in pharmaceutical synthesis or medical device manufacturing. Most advances here depend on open sharing—peer-reviewed validation, real-world batch testing, and transparent error reporting. The more this community leans into best practices, the more we’ll see BHP’s strengths used where they matter most.
Limitations persist, especially around water compatibility and the cost associated with high-purity supply chains. The company chemist worried about an already-stretched budget will notice that BHP, while often outperforming conventional agents, can tip a project into the red if not managed wisely. In some setups, older, less functionalized bromides still earn their keep due to lower up-front costs. The game then becomes picking BHP when its unique blend of reactivity and specificity justifies the investment, not as a catch-all solution. Familiarity and long-term real-world feedback help set the boundaries around its use, making for a smarter, more reliable buildout in production lines.
One of the lessons I’ve drawn from working across research and production is that responsible innovation rests on two core ideas: clarity in purpose and transparency in process. BHP embodies both, provided users respect its power and limits while sharing their results with peers. As regulatory frameworks get tougher and end-users pay closer attention to raw material sourcing, compounds like BHP will perform best where communication is active, QA protocols are robust, and environmental impact gets baked into project design.
The coming years will likely see BHP move from specialty research tool to a backbone ingredient in more high-value applications—especially as surface chemistry, molecular recognition, and sustainable synthesis all gain ground. By choosing chemicals with both functional and ethical advantages, the industry stands a better chance of building products that work not just on paper, but in messy, real-world conditions, too.
Addressing lingering issues means acting on a few simple strategies. For supply quality, maintaining deep partnerships with reputable chemical vendors pays off. Responsible buyers verify certificates, demand transparent data, and keep records that outlast a single batch run. For labs struggling with solubility concerns, mixed solvent systems and custom surfactant blends can nudge BHP into the right setting without forcing expensive reformulation. Where cost poses a problem, pooled purchasing and coordinated use across multiple research groups or production sites can stretch supply budgets. Many research consortia now share stock and purchase agreements, reducing overhead while increasing quality assurance steps.
Those setting up new applications can also learn from peer failures and successes. Talking openly about purification hiccups or unexpected side-products pushes everyone forward, strengthening the case for BHP adoption in fields far outside surface chemistry or classic organic synthesis. As younger scientists and engineers enter the field, they bring both a fresh view and a demand for greater transparency—qualities that favor compounds like BHP when companies or research teams are willing to share honest feedback.
In short, bromohexadecyl pyridine may have started out as a specialized, highly technical agent, but it now finds itself at the crossroads of innovation, responsibility, and practical science. Its journey shows what happens when chemistry, careful stewardship, and an appetite for applied learning all come together in one package. The story isn’t finished, but so far, the results look promising: a balanced blend of performance, control, and opportunity across multiple sectors that rely on smarter chemistry every day.