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HS Code |
397227 |
| Chemical Name | 1-Phenacylpyridinium Bromide |
| Cas Number | 6286-30-2 |
| Molecular Formula | C13H12BrNO |
| Molecular Weight | 294.15 |
| Appearance | White to off-white crystalline powder |
| Melting Point | 182-185 °C |
| Solubility | Soluble in water, methanol, ethanol |
| Storage Conditions | Store at room temperature, keep container tightly closed |
| Pubchem Cid | 13939 |
| Synonyms | N-Phenacylpyridinium bromide |
| Boiling Point | Decomposes before boiling |
| Inchi Key | QMHZRLZARWCRLL-UHFFFAOYSA-M |
| Smiles | C1=CC=CC(=C1)C(=O)C2=CC=CC=N2.[Br-] |
As an accredited 1-Phenacylpyridinium Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1-Phenacylpyridinium Bromide is packaged in a 25g amber glass bottle with a secure screw cap and appropriate hazard labeling. |
| Shipping | **Shipping Description (approx. 50 words):** 1-Phenacylpyridinium Bromide should be shipped in tightly sealed containers, protected from moisture and light. It is typically classified as a hazardous material due to its potential health hazards. Ensure compliance with local regulations, including labeling and documentation. Use appropriate secondary packaging to prevent breakage and leakage during transit. Store at room temperature. |
| Storage | 1-Phenacylpyridinium Bromide should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. Keep it at room temperature, avoiding sources of moisture and heat. Proper labeling and secure shelving are recommended to prevent accidental spillage or contamination. Always follow institutional and safety guidelines. |
Applications of 1-Phenacylpyridinium Bromide in Industrial ManufacturingAs a direct manufacturer of 1-Phenacylpyridinium Bromide, we deliver specialized grades that support key synthetic processes demanding precision and regulatory compliance. The material’s ionic properties and photochemical reactivity enable its integration into select downstream production chains. The following application scenarios highlight areas where industrial processors consistently employ our product to meet the needs of high-value finished goods and regulatory standards. 1. Photoinitiators for UV-Cured Coatings and InksIndustrial UV-curable coating and printing ink manufacturers utilize our product as a quaternary ammonium photoinitiator component, targeting high-efficiency cationic polymerization for electronics, packaging, and functional surface finishing. Compatibility with state-of-the-art UV equipment, combined with predictable initiation rates, supports rapid industrial-scale runs. Because downstream processors must meet global restrictions on extractables and ensure indoor air safety in end-use, they precisely control the photoinitiator ratio and integrate the compound at strictly specified process steps for batch consistency. Industry compliance standards
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2. Synthesis of Pyridinium-Tagged Intermediates in Organic Fine ChemicalsPharmaceutical and agrochemical firms use our material as a key building block for pyridinium-functionalized intermediates, supporting research and commercial synthesis where reversible ionic tags or photolabile leaving groups are needed. Process chemists rely on the compound’s controlled reactivity to introduce pyridinium moieties for application in high-value molecule development, maintaining traceability and batch homogeneity under regulated GMP conditions. Industry compliance standards
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3. Analytical Reagents in Chromatographic and Mass Spectrometric Sample PreparationAnalytical reagent manufacturers select this specialty compound for its role in derivatization protocols that increase sensitivity and selectivity in chromatographic and MS workflows. The compound’s effectiveness in rendering functional groups detectable at low concentrations supports stringent QA/QC environments in pharmaceutical and environmental laboratories, ensuring reproducible results in regulated fields where validated methodology is mandatory. Industry compliance standards
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4. Synthetic Photochemistry for Specialty Surfactant ProductionProducers of advanced surfactants for semiconductor processing and electronics assembly leverage our material as a phase transfer catalyst and photoreactive template. Its ability to mediate controlled quaternization reactions and enhance photochemical efficiency supports precise surface modification protocols. Downstream plants regulate dosage carefully to balance phase transfer kinetics against photoinitiator decomposition in multi-step surfactant synthesis, aligning output with rigorous electronics-grade purity demands. Industry compliance standards
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Every chemist working with pyridine derivatives comes across points in synthesis where straightforward, reliable reagents are a must. Over decades producing fine organic chemicals, we've seen how specialty salts like 1-Phenacylpyridinium Bromide fit into high-value work across pharmaceuticals, analytical chemistry, and synthetic development. Unlike commodity reagents that flood the market and trade through countless hands, making this compound in-house allows us to test, adjust, and meet research needs that off-the-shelf material simply can’t address.
The structure of 1-Phenacylpyridinium Bromide offers both the reactivity of a pyridinium cation and a phenacyl group, presenting a balance between nucleophilic and electrophilic behavior. This peculiar intersection of chemical traits opens the door to creative syntheses that regular pyridinium salts cannot match. Chemists use it for generating diphenylacetylene, pushing forward chalcone chemistry, and facilitating N-alkylation routes that other pyridinium salts can’t unlock as easily. Over years making and using this compound, we’ve come to appreciate its nuanced roles that tend to get lost under sterile catalog numbers.
1-Phenacylpyridinium Bromide isn’t a product anyone can whip up in a generic plant environment. Sourcing reliable benzyl bromide, controlling the exact stoichiometry, and minding temperature gradients make all the difference in purity. In-house synthesis gives direct oversight. We see batch differences firsthand, isolate impurities ourselves, and tighten up processes when we spot minor color or yield shifts. Each lot can be traced back to the starting materials and trial runs. If we pick up hints of brown tinge or oily residues, we tweak purification steps on the spot.
We have repeatedly observed research clients discovering that off-color or poorly crystalline product from resellers leads to low yields, unexpected byproducts, or trouble scaling reactions from milligrams to grams. It doesn’t always show up in a routine HPLC scan. A decade of hands-on production has taught us that you only get the full sharpness of 1-Phenacylpyridinium Bromide’s reactivity profile with material made, handled, and reviewed in-house. Commercial checks aren’t always enough — you need someone who cares about the work, not just the sale.
Our approach involves keeping reaction times precise, water activity low, and finishing with cycle after cycle of crystallization and drying. It takes more effort and cost upfront, but the difference shows when customers achieve consistent melting points and full conversion in their critical steps. Product that feels right, smells right, and gives the bright white or faintly cream appearance it’s known for gives chemists the confidence to move fast.
1-Phenacylpyridinium Bromide (sometimes called pyridinium phenacyl bromide) comes together through a condensation of pyridine and phenacyl bromide. On paper, this reaction may look straightforward, but real-world operation reveals challenges — exotherms can run away fast, side products may stick if temperature isn’t watched closely, and the product must precipitate cleanly. Anyone cutting corners or scaling with crude solvents risks persistent yellow impurities or, worse, batch-to-batch variability that forces customers to revalidate every time.
From our experience, solvent quality shapes every yield. Trace moisture or oxidized pyridine turns clean crystallization into a greasy mess. If a customer’s downstream reaction relies on that batch, they end up troubleshooting longer than necessary. We've responded over years by batch-distilling both pyridine and phenacyl bromide, filtering every feed for fine particulates, and using fresh desiccants. Such detail keeps each lot ready for direct-to-reactor use.
Our product carries its full molecular identity: C13H12BrNO. Importantly, it melts dependably in the range described by the literature, settling quietly between 149–151°C. We test this with every run to keep drift in check. Analytical checks, right down to specific rotation and NMR, answer tricky calls from academics and industrial partners who need absolute certainty before a scale-up. We also avoid relying solely on certificates or general QC claims. The real measure happens in our glassware, our vacuum lines, our ability to see a fine, rapid precipitation and know it will perform at your bench just as it has at ours.
Application drives every formulation we perfect. Laboratories turn to this product for selective N-benzylation — an operation that underpins synthesis of heterocycles, alkaloids, and advanced intermediates. In real research, speed and reliability mean everything. If a batch of 1-Phenacylpyridinium Bromide underdelivers, a whole week’s work can unravel by the time yields drop or byproducts show up.
It’s not just a matter of pushing through reaction steps either. Analytical chemists use it for fluorimetric determination of thiols, targeting sensitive samples where most reagents would add fluorescent outliers. Professionals in peptide modification value its reactivity under mild conditions; reactions go forward with low excess and the product can be worked up without harsh quenching. This control over reaction progress has led several groups to publish on chalcone, flavonoid, and even azine skeleton formation. In each case, feedback filters straight back to the factory floor, guiding tweaks in the purification or drying sequences.
Scale brings distinct challenges. In multigram or pilot runs, big exotherms or incomplete vacuum drying stall progress. By having seen the impact on our own plant, we aim to ship batches that deliver on every scale, not just in academic vials. We mark, label, and test more than required by regulation because catching the few “off” bottles can make the difference between a productive week and hours lost chasing a ghost in the results. Experience also tells us that certain suppliers get complacent — cutting drying times, throwing everything through a single filter medium, or skipping small residue checks. Our hands-on approach has proven that production of sensitive reagents needs tight oversight from a team that understands why details matter.
You could try using generic pyridinium bromides — they cost less, ship from dozens of vendors, and claim the same backbone structure. But you’ll miss the point if you skip 1-Phenacylpyridinium Bromide’s specific properties. The phenacyl group dramatically shifts electron density at the nitrogen, making substitution easier and opening up reactions with a broader set of nucleophiles. These subtleties allow for chemoselectivity that simply doesn’t show up with unsubstituted or differently functionalized pyridinium salts.
Direct competitors like 4-Phenacylpyridinium Bromide, or even N-benzylpyridinium bromides, lack the same performance profile. The conjugated phenyl ring plus carbonyl group push reactivity further — reactions that stall or trail off with other salts move rapidly with our product. Chemists who struggle to alkylate sensitive molecules often switch to our compound after repeated setbacks elsewhere. Factually, greater electron withdrawal produces more complete conversion, sharper product peaks, and easier isolation in complicated research setups.
While off-brand options saturate the market with uncertain provenance, we stick to small-lot production. Each kilogram walks through solvent washes and vacuum trays under a trained eye. We test for residual free bromide and confirm that decomposition remains below measurable thresholds for at least six months in a well-sealed, low-humidity environment. Only this approach gives end users peace of mind when pushing projects past deadline pressure or into regulatory reviews.
We regularly field calls from researchers chasing purity percentages for their next protocol. Real-world work isn’t about chasing an extra decimal — it’s about knowing whether a small impurity will flatten a yield or ghost through the process unspotted. Because we produce 1-Phenacylpyridinium Bromide ourselves, we back up every bottle with the ability to answer technical questions from practical experience. Who else will tell you straight up that over-drying at high vacuum can collapse the product’s fine crystal structure, making it a challenge to dissolve? Instead of hiding behind vague answers, we respond based on hundreds of crystallizations and run corrections on the fly where necessary.
We treated one client’s quality issue by changing to fresh pyridine and triple-wash solvent systems after troubleshooting their feedback in discussion with our plant team. After a string of low conversions in their synthesis, they tried our suggested method, and reaction times fell in half. These stories keep us sharp and remind us why chemical production needs more than just a balance and a batch log.
Years of feedback say that the smallest process details — whether it’s glass surface choice, the angle of stirring, or how cold a unit gets during precipitation — leave as big an impact as the grade and purity specs on a sheet. Customers turning to our product for the first time often start by comparing it kilogram for kilogram against competitor brands, then switch after consistent results in pilot labs. The switch involves knowing what cycles create the sharpest particle size, which solvents preserve the delicate balance of dryness without producing overdried, dust-prone crystals, and how to spot telltale moisture levels before they twist yields. Only through direct experience can a supplier fine-tune these variables, translating bench tricks into large-batch reliability.
There’s talk in the market about the value of chemical traceability, but unless you’ve run full-lot syntheses and stood by to see what doesn’t work, it’s theory. We’ve spent years controlling every parameter, from raw material sourcing to solvent selection and the timing of final packaging. Only a manufacturer can size up lot numbers and blend minor inconsistent batches to maximize uniformity across the shipment. Customers rely on this handshake-level trust, not because the certificate claims everything checks out, but because the background story supports it.
We build continuous feedback into the offer — if a batch doesn’t dissolve as fast or isn’t as free from color as in past orders, chemists can call back and speak straight to the technician who was there at the reactor. That rarely happens with material traded half a dozen times across suppliers. In-house oversight gives us resources to halt questionable reaction runs, scrap inconsistent crystallization batches, and make up the difference in subsequent production. It’s not unusual for us to pour extra man-hours into meeting a challenging custom order or adjusting to scale because ultimately, reproducibility defines whether the research advances or stalls.
Several years ago, we sharpened our protocols for particularly moisture-sensitive clients, who ran high-precision analytical methods on each order. We learned firsthand that, under some humidity, shipping even sealed bottles can cause sub-ppm bromide drift — tiny on paper, but significant for high-sensitivity HPLC. In response, we implemented a double-sealing order for every gram of 1-Phenacylpyridinium Bromide leaving our site. It cost a little more, but by cutting down on customer troubleshooting, we saw more repeat business and stronger relationships over time.
As research pushes further into sustainable chemistry and green methodologies, we’ve adapted the 1-Phenacylpyridinium Bromide process as well. Early protocols for this compound favored heavy solvents and open atmospheres. Today’s demands look for lower residual solvents, greener purification, and traceability down to the starting batch. We’ve refitted plant equipment in the last five years, replacing legacy solvent tanks with low-emission alternatives and updating crystallization chambers to cool using non-halogenated refrigerants. Our product now matches and, in many cases, exceeds expectations set by major research initiatives aiming to cut down on toxic byproduct release.
Actual production records and feedback tell a story that is impossible to see from the outside. While competitors in emerging markets sometimes shave cycles off for speed, these shortcuts show up in tests after scale-up. Subtle side products that never appeared in a basic TLC scan can crash advanced synthetic runs or contaminate follow-up reactions multiple steps later. We pay regular visits to university labs and industry meetings to learn what issues show up down the line so our internal controls evolve in real time.
Growing global scrutiny over chemical provenance shows no signs of slowing. We keep direct audit trails for each batch of phenacylpyridinium bromide, which means any research group working in regulated spaces (pharma or government labs) has instant access to origin details that distributors or secondary handlers struggle to provide. As end uses diverge — from targeted anticancer agent protocols to fluorescent tagging — we map out which production tweaks matter and which trade-offs introduce risk.
Across all product grades, the ultimate challenge for chemists stays the same: how to trust your reagents so you can push experiments to the bleeding edge. Having produced 1-Phenacylpyridinium Bromide in our own facility for years, we’ve seen labs struggle with inconsistent reactivity, background impurities, or similar salts that can’t deliver the selectivity needed. By keeping every stage hands-on, from purification to packing, we close the knowledge gap between benchwork and bulk synthesis. This partnership with end users doesn’t stop at the shipment — we listen to follow-up issues, log every success and setback, and tailor adjustments for tomorrow’s batches.
Looking ahead, as research branches into cutting-edge domains such as photoinitiated synthesis and advanced heterocycle design, the nuances of reagents like 1-Phenacylpyridinium Bromide gain even more value. We adapt by studying the latest literature, collaborating with key users, and investing in equipment upgrades that bring ever tighter control over moisture, residual halides, and crystalline form. Demand for reproducibility won’t ease in high-value spaces, especially in regulated industries, so the only answer is to pair real-world feedback with relentless process improvement. This is what keeps chemists at the forefront and ensures every batch sent out into the world stands up to scrutiny.
We believe the time invested perfecting 1-Phenacylpyridinium Bromide translates directly into better research outcomes. By sticking to these standards, sharing insights from our own operation, and staying open to improvement, we will keep helping our customers step out confidently into the next phase of discovery. The best chemistry doesn’t happen alone — it depends on every hand that shapes a product from raw idea to shipment-ready bottle. We’re proud to be part of that process, every step of the way.