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HS Code |
569719 |
| Cas Number | 495-48-7 |
| Molecular Formula | C12H10N2O |
| Molar Mass | 198.22 g/mol |
| Appearance | Yellow crystalline solid |
| Melting Point | 36-38 °C |
| Boiling Point | 295 °C (decomposes) |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in ethanol, ether, chloroform |
| Density | 1.24 g/cm³ |
| Refractive Index | 1.645 |
| Iupac Name | 1,2-diphenyldiazene 1-oxide |
| Odor | Odorless |
As an accredited Azoxybenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Azoxybenzene is supplied in a 100g amber glass bottle, tightly sealed, labeled with hazard symbols and detailed chemical information. |
| Shipping | Azoxybenzene should be shipped in tightly sealed containers, protected from light and moisture. Suitable packaging materials include glass or plastic bottles, cushioned to prevent breakage. It must be labeled according to chemical safety regulations and transported as a non-hazardous material. Store and ship at ambient temperature, avoiding strong oxidizers and sources of ignition. |
| Storage | Azoxybenzene should be stored in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep the container tightly closed and clearly labeled. Store separately from incompatible substances such as strong oxidizing agents and acids. Use appropriate safety measures to prevent spills or exposure, and ensure compliance with local regulations for hazardous chemical storage. |
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Purity 99%: Azoxybenzene purity 99% is used in pharmaceutical intermediate synthesis, where high-purity ensures minimal side-product formation and consistent yield. Melting Point 36°C: Azoxybenzene melting point 36°C is used in organic electronics fabrication, where controlled melting behavior facilitates uniform thin film deposition. Molecular Weight 198.19 g/mol: Azoxybenzene molecular weight 198.19 g/mol is used in laboratory-scale mechanistic studies, where precise molecular mass allows accurate stoichiometric calculations. Particle Size <10 µm: Azoxybenzene particle size <10 µm is used in pigment dispersion processes, where fine particle distribution improves homogeneity and color intensity. Thermal Stability up to 120°C: Azoxybenzene thermal stability up to 120°C is used in polymer additive applications, where it maintains structural integrity under moderate processing temperatures. UV Absorbance λmax 320 nm: Azoxybenzene UV absorbance λmax 320 nm is used in UV-blocking coatings, where selective absorption provides enhanced photoprotection. Refractive Index 1.635: Azoxybenzene refractive index 1.635 is used in optical material formulations, where its high refractive index improves light modulation efficiency. Solubility in Ethanol 5 g/L: Azoxybenzene solubility in ethanol 5 g/L is used in dye manufacturing, where moderate solubility enables efficient mixing and uniform coloration. Viscosity Grade Low: Azoxybenzene viscosity grade low is used in inkjet printing processes, where low viscosity supports fine droplet formation and precise deposition. Purity Analytical Grade: Azoxybenzene purity analytical grade is used in chromatography reference standards, where high analytical quality ensures reliable calibration results. |
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Azoxybenzene isn't a household word, but anyone who spent time in a laboratory probably came across its sharp yellow crystals tucked into brown glass bottles. I remember seeing the label for the first time in a dusty supply room, not realizing this compound has a history in synthetic chemistry, dye manufacture, and material science that runs deeper than you might guess. Many years working with aromatic compounds taught me that not every synthesis is straightforward, and azoxybenzene often surprises with its stable structure and reliable characteristics. Unlike more volatile counterparts, azoxybenzene provides a balance between reactivity and safety, making it a frequent choice for those who need something both robust and flexible.
Azoxybenzene stands out with its distinctive yellow color, thanks to conjugation in its molecule, and its crystalline form feels solid and stable, not prone to dusting or breaking apart. Its melting point hovers around 36–38°C, so it often stays solid at room temperature, but it doesn’t resist melting for practical uses. You can detect a faint, sweet smell if you bother to get close, which is rare among aromatic intermediates. These simple sensory facts connect the chemical to real memories—an old glassware shelf, a careful hand weighing out a sample, the subtle shimmer of gold under light. To many, these are small details. For someone handling it in any meaningful volume, these features make workflows smoother and safer.
Most vendors offer azoxybenzene in grades like 98% or higher, with specification sheets highlighting purity, insoluble matter, trace metals, and residual solvents. Many of my colleagues—myself included—put a lot of faith in these numbers. Chemical synthesis relies on the certainty that what you order, you get. A poorly purified compound leads to side reactions or disappointing yields. For azoxybenzene, high purity confirms that the extraction and isolation processes worked as planned, without contamination from other aromatic compounds. The yellow color gives a quick visual check, though serious work needs a certificate of analysis. It’s always tempting to look for a deal, but in research and industrial settings, purchasing a lower-grade product leads to bigger headaches down the line.
Azoxybenzene finds its way into colorants, especially as an intermediate in azo dye synthesis. Dye chemistry captured my interest early on because of its human element: color, permanence, how materials take on meaning once dyed, painted, or printed. Azoxybenzene helps produce vivid yellows and oranges that resist fading—critical for everything from textiles to plastics. Compared to alternatives, azoxybenzene offers reliable reactivity for coupling reactions, which keeps manufacturing lines running with less variation from batch to batch. Colleagues in analytical chemistry sometimes use it as a standard reference or a test substance for instrument calibration, trusting in its purity and straightforward behavior under typical lab conditions. In academia, organic chemistry labs turn to azoxybenzene for instructive syntheses that teach students core concepts—reduction, coupling, even photochemistry. It’s approachable because it manages risks better than many volatile aromatics, promotes clear results, and introduces students to practical organic transformations. With the buzz around photovoltaic and optoelectronic materials, researchers revisit classic compounds like azoxybenzene, drawn by its unique electron structure—delocalization and its ability to donate or accept electrons under specific conditions. Not every chemical product fits such a broad range, but azoxybenzene crosses boundaries between education, industry, and innovation.
Azoxybenzene sometimes gets confused with azobenzene, but they behave differently. Azobenzene is the go-to for molecular switches because of its rapid, reversible photoisomerization. Azoxybenzene, on the other hand, resists easy flipping and holds onto its trans-configuration with a distinct stability. This difference changes the way the compound absorbs light and interacts with other chemicals. In synthesis, azoxybenzene fosters slower, often more controllable reactions. This trait saves time for chemists who want to focus on end-products instead of wrestling with runaway side reactions. Nitrobenzene or aniline derivatives may seem interchangeable at first glance, but azoxybenzene adds a layer of safety for handling and storage. Years of working with aromatic nitro compounds leave strong memories—accidents, unexpected spills, and, occasionally, hazardous decompositions. Azoxybenzene doesn’t pack the same explosive risk as some nitroaromatics. This means less stringent insurance and storage requirements, fewer nervous moments in the lab, and a product that slides more easily into university and industrial use. Another point often raised concerns downstream processing. Azoxybenzene’s higher stability streamlines purification—fewer byproducts, less time at the hotplate, less solvent wasted. It’s easier to recrystallize, and that helps reduce the amount of chemical waste. A real concern these days, with labs and factories both seeking ways to cut their environmental footprint. The ability to recover or reuse solvents, filter out crystal impurities efficiently, and avoid fiddly post-processing makes a measurable difference in long-term running costs. I’ve seen this in action: one group replaced a messier intermediate with azoxybenzene and cut solvent use by a third over the course of a year.
Digging into records from a friend’s dye plant, I noticed fewer complaints about clogs, discoloration, or inconsistent color when higher-grade azoxybenzene went into the mix. It may cost more at purchase, but the amount of time saved troubleshooting faulty batches or purifying end materials often repays the difference many times over. These small efficiencies keep production schedules tight, and they reduce staff burnout. Nobody wants to redo work because of an avoidable impurity or a slow-acting byproduct. Especially as regulatory rules tighten, having a product like azoxybenzene, with well-documented behavior and consistent quality, reduces red flags from inspectors and keeps operations smooth. Waste handling also plays a role. Lower-grade aromatic intermediates sometimes leave behind more waste, unreacted residues, or solvent-heavy broths. Azoxybenzene’s consistency translates into smaller waste streams, which in turn means fewer disposal costs and less chance of violating environmental rules. Talking to colleagues in environmental compliance, it’s clear this efficiency is more than a budget line—it’s a reputational safeguard.
No discussion about any chemical—especially one used in bulk—makes sense without acknowledging risks. Azoxybenzene doesn’t have the notoriety of some organics, but it’s not for casual use. Dust can irritate, and it shouldn’t end up down the drain. Standard lab practice—gloves, goggles, decent ventilation—handles most risks, and the compound’s stability in normal conditions helps keep incidents rare. In storage, it tolerates long stints on the shelf, which isn’t something I can say about many other aromatic intermediates. I’ve visited stockrooms where azoxybenzene sat undisturbed for years, showing little sign of decay or degradation—an asset for supply chains that sometimes run on unpredictable timelines. Safety records published over decades show that incidents linked to azoxybenzene rarely tie to explosive decompositions, which are more common with related nitro or azo compounds. Instead, the usual challenges relate to standard chemical hygiene. For any group handling aromatic compounds, this is a manageable set of risks, and azoxybenzene fits into well-established training routines.
Ask anyone working at the intersection of chemistry, manufacturing, and sustainability, and they’ll mention the shifting landscape. Fewer chemicals make it through new regulatory hurdles, and clients expect accountability from top to bottom. Azoxybenzene, with its straightforward formula and dependable performance, earns a spot by offering traceable sourcing, manageable handling, and legacy applications that don’t demand constant revision. Many compounds slide out of use simply because nobody wants to explain a messy safety or waste issue to a regulator; azoxybenzene sticks around because it avoids those stories. It’s not flashy, but it delivers. Sustainability efforts see azoxybenzene as a known quantity. Many companies now lean toward closed-loop manufacturing, where outputs from one step become feedstocks for the next. Since azoxybenzene’s synthesis, use, and cleanup all fit textbook procedures, it adapts well to greener approaches. A friend’s experience running a dye facility bears this out: after switching to a process involving azoxybenzene intermediates, they logged fewer non-compliance events, and waste output dropped below regulatory thresholds.
Materials science opens doors for new chemistry, and azoxybenzene fits in as a component in polymers, advanced coatings, and photoactive layers. Research into azoxy-based polymers gains traction in fields from smart textiles to light-sensitive electronics. While azobenzene’s fast switching action attracts headlines, azoxybenzene’s slow, persistent stability attracts those who seek durable, long-lived materials. I remember attending a conference where young researchers debated the merits of various aromatic scaffolds for solar-energy harvesting. The team working with azoxybenzene boasted low degradation rates even under extended UV exposure. Azoxybenzene’s redox properties spark interest in electronic engineering, especially where electron transfer and stability matter more than speed. Devices with azoxybenzene layers avoid performance loss due to photochemical fatigue. The slow change in conformation translates into consistent response over a device’s lifetime, ideal for long-term testing or calibration. Practical experience tells us that compounds which avoid rapid breakdown under stress stand the test of time, both in research and industry.
Buying azoxybenzene invites questions about quality, consistency, and documentation. I always advise peers to work with suppliers who provide transparent sourcing, regular quality checks, and open communication about lot-to-lot variation. Certificates of analysis matter: little numbers, but big impact. They let buyers trace every sample, catch impurities early, and verify that the yellow crystalline powder matches expectations. My experience sifting through chemical catalogs shows that price differences often hide a deeper story—cheaper options save a small amount at the checkout, but unlisted impurities surface later as extra work and greater risk. Choosing a compound like azoxybenzene involves weighing convenience against cost, history against new options, and supplier trust against the promise of a smoother workflow. My network values direct communication and support from their vendors. Emerging requirements for sustainable sourcing encourage more direct questions—where does it come from, what’s in it, and who oversaw production? The companies that can answer these questions clearly earn loyalty from research groups and factory buyers alike.
To realize the best from azoxybenzene, experienced labs and production sites emphasize prevention—preventing impurities, process upsets, and unnecessary exposure. This means regular analytical checks, control of raw material sources, and investing in equipment that encourages safe, efficient processing. Streamlined crystallization, solvent recovery, and staff training all make real impact. One plant manager I met switched over to fully vented crystallization tanks after a minor dust incident and saw a drop in both staff complaint and product loss. Waste minimization grows more important each year, with azoxybenzene-based processes seeing benefits in both waste reduction and ease of solvent recycling. Purification steps generate less secondary waste when the incoming material is relatively clean and easy to crystallize. My time working in a facility that tracked solvent use closely proved that even small efficiency gains produce meaningful reduction in cost and impact.
Not every chemical works for every process, and azoxybenzene comes with its own set of limits. For some applications, the yellow color can interfere with optical or colorless end-products. Purification adds cost for users looking for extreme clarity or requiring total absence of tints. Its melting range—while practical in most contexts—may require extra temperature controls or rapid handling to avoid liquefaction in warmer climates. People operating in high-temperature environments need awareness and proper storage protocols. Some specialists working at scale face regulatory scrutiny around aromatic intermediates, given the broad push for greener, less persistent chemicals. Azoxybenzene avoids the worst of these restrictions, but buyers and producers keep an eye on any updates, since its fate and breakdown in the environment remain under study. My own experience says this attention is a chance, not a burden: documenting safe practice, clear batch records, and effective purification will ensure ongoing acceptance.
For decades, chemists, plant operators, and educators have entrusted azoxybenzene with a role in synthesis, manufacturing, and learning. Its chemistry is neither novel nor obsolete—it roots itself in what works, offers practical advantages, and circumvents the pitfalls that bedevil flashier but riskier compounds. The lessons I’ve picked up from years in the lab are straightforward: don’t gamble with quality, don’t skimp on safety, and don’t underestimate the importance of understanding the properties underlying every scoop you weigh and every flask you charge. Azoxybenzene, for all its simplicity, rewards those approaches with consistent results and manageable risks, a rare thing in the ever-changing world of modern chemistry.
Whether you walk through a textile dye house, a college teaching lab, or a factory focused on optoelectronics, azoxybenzene turns up where thoughtful chemistry meets human needs. Its place remains secure as long as people value reliability, traceable quality, and practical results. In a world full of promises and hyperbole, sometimes the best product is the one that quietly does its job—over and over, without fuss. That’s what azoxybenzene brings to the table, and it’s why so many keep coming back to it, year after year.