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4-Hydroxyazobenzene

    • Product Name 4-Hydroxyazobenzene
    • Alias p-Hydroxyazobenzene
    • Einecs 202-177-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    Specifications

    HS Code

    969689

    Chemicalname 4-Hydroxyazobenzene
    Casnumber 1679-17-0
    Molecularformula C12H10N2O
    Molecularweight 198.22
    Appearance Orange-red crystals
    Meltingpoint 154-157°C
    Solubility Slightly soluble in water; soluble in ethanol and ether
    Density 1.235 g/cm3 (approximate)
    Structure C6H5N=NC6H4OH
    Synonyms p-Hydroxyazobenzene, 4-Phenylazophenol
    Iupacname 4-(Phenyldiazenyl)phenol
    Smiles C1=CC=C(C=C1)N=NC2=CC=C(C=C2)O

    As an accredited 4-Hydroxyazobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with secure screw cap, labeled “4-Hydroxyazobenzene, 25g”. Features hazard pictograms, batch number, and safety instructions.
    Shipping Shipping 4-Hydroxyazobenzene requires secure, sealed packaging, typically in tightly closed containers, to prevent leaks or contamination. It should be transported in compliance with relevant chemical transport regulations, accompanied by proper documentation and labeling. Store and ship it in a cool, dry place, away from heat, light, and incompatible substances.
    Storage 4-Hydroxyazobenzene should be stored in a tightly closed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers and strong acids. Ensure storage is secure and clearly labeled, and avoid exposure to heat, sparks, or open flames, as the compound may be sensitive to such conditions.
    Application of 4-Hydroxyazobenzene

    Purity 99%: 4-Hydroxyazobenzene with purity 99% is used in organic synthesis, where high purity ensures reproducible reaction yields.

    Molecular Weight 198.21 g/mol: 4-Hydroxyazobenzene with molecular weight 198.21 g/mol is used in dye manufacturing, where precise molecular mass allows consistent chromophore performance.

    Melting Point 153°C: 4-Hydroxyazobenzene with melting point 153°C is used in thermal processing of pigments, where stable melting behavior facilitates uniform dispersion.

    Particle Size <10 µm: 4-Hydroxyazobenzene with particle size less than 10 µm is used in inkjet ink formulations, where fine particles enhance print quality and color development.

    Stability Temperature up to 120°C: 4-Hydroxyazobenzene with stability temperature up to 120°C is used in polymer coloration, where thermal stability prevents degradation during processing.

    Solubility in Ethanol 10 g/L: 4-Hydroxyazobenzene with solubility in ethanol of 10 g/L is used in textile dyeing, where efficient solubility improves dye uptake and color uniformity.

    Absorbance Maximum 340 nm: 4-Hydroxyazobenzene with absorbance maximum at 340 nm is used in spectrophotometric calibration, where distinct absorption improves analytical accuracy.

    Photostability High: 4-Hydroxyazobenzene with high photostability is used in photoresponsive materials, where resistance to light-induced degradation maintains functional performance.

    Chemical Stability pH 4-8: 4-Hydroxyazobenzene with chemical stability between pH 4 and 8 is used in pH-sensitive sensors, where robust stability ensures long-term sensor accuracy.

    Viscosity Grade Low: 4-Hydroxyazobenzene with low viscosity grade is used in paint formulations, where low viscosity facilitates easy blending and smooth application.

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    Certification & Compliance
    More Introduction

    Introducing 4-Hydroxyazobenzene: A Practical Perspective

    What 4-Hydroxyazobenzene Brings to Everyday Chemistry

    At the intersection of research and manufacturing stands 4-Hydroxyazobenzene, a compound chemists like myself grow familiar with through years of digging into dyes, analytics, and material innovations. This bright, orange-yellow powder often catches more than the eye; it embodies both a legacy and fresh appeal in laboratories and factories alike. Unlike buzzword-heavy newcomers, 4-Hydroxyazobenzene carries a certain straightforwardness: a defined molecular structure, a proven track record, and a palette of applications where consistency actually builds trust.

    Specifications: What You Get and Why It Matters

    Looking at the model typically found in the lab, 4-Hydroxyazobenzene, or p-hydroxyazobenzene, follows the simple formula C12H10N2O. The structure features a benzene ring on each side of an azo group, with a single hydroxy group attached. This molecular arrangement translates to crystal-clear behavior during synthesis and post-processing: ease of dissolution in organic solvents, ultraviolet-visible absorption primarily centered in the 330-400 nm range, and reliable melting around 150-153°C. With a moderate polar profile, it doesn’t shy away from interactions that matter—binding, catalyzing, and shifting color with just the right chemical tweak.

    Specs like these may look routine, but real-world batches reveal subtle differences, and that’s where purity comes into play. High-performance needs drive demand for material with purity above 98%, ensuring minimal byproducts mess with intended results. Whether in pigment production or analytical work, a consistent melting point and color hue shape how easily the compound folds into the next reaction or end-use.

    Usage: Where 4-Hydroxyazobenzene Shows Its Value

    Hydroxyazobenzene makes itself useful in ways both obvious and surprisingly creative. Its most straightforward use appears in dyes and pigments—its vivid orange hues make it an anchor ingredient for coloring textiles, plastics, and sometimes inks. The color is sharp and remains stable under normal conditions, though it dances under shifts in pH, proving helpful for indicator applications in titrations and pH-sensitive products.

    Beyond color, organic synthesis often leans on 4-Hydroxyazobenzene to benchmark reactions or build more complex molecules. Researchers prefer it as a standard in thin-layer chromatography or spectrophotometric studies thanks to its absorbance profile—results stay legible and repeatable. In analytical chemistry, it slips into colorimetric tests for trace metals, riding its wave-like absorption to reveal concentrations in water, wastewater, or food matrices. Mix it with specific reagents, and you pick up shifts in color that track with the presence of nickel, cobalt, or other metals, all without fanciful apparatus or expensive kits.

    Academic uses tell only part of the story. Manufacturers who develop stabilized colorants for plastics and synthetic fibers rely on the predictable interaction between 4-Hydroxyazobenzene’s hydroxy group and various polymer matrices. This stability cuts down on fading and bleeding, which frustrates both designers and customers hoping for consistent shades. Certain medical diagnostic tests have also drawn on this compound—selective reactivity and visible color change lend themselves to rapid, on-the-spot detection methods.

    A big reason 4-Hydroxyazobenzene retains its seat at the table comes down to how it handles diverse roles: easy to produce, unlikely to break down under ambient conditions, and ready to react only when prompted. Whether you need a teaching standard or a foundation for azo dye synthesis, it keeps a promise others often overcomplicate.

    Comparing to Other Azobenzenes and Substitutes

    Experienced hands soon realize 4-Hydroxyazobenzene stands apart from unsubstituted azobenzene or its nitro- or amino- relatives. The presence of a hydroxy group doesn’t just tweak color; it reshapes both reactivity and selectivity. Take regular azobenzene: strong color, but limited solubility in water and less responsive to certain chemical triggers. By contrast, the hydroxy group in our compound opens up hydrogen bonding and greater solubility in alcohols and weak bases, expanding both lab uses and manufacturing flexibility.

    Compare it to 4-nitroazobenzene or 4-aminoazobenzene and different stories emerge. Nitro derivatives tend to tilt toward yellow-red shades and show heightened electron-withdrawing behavior. Analytical chemists prefer nitro compounds for specialized electronic studies but avoid them in contexts demanding rapid, predictable reactions with strong nucleophiles. Amino groups, on the flip side, boost solubility and chemical reactivity but complicate storage and regulatory compliance because of toxicity and environmental persistence.

    It’s not fair to call 4-Hydroxyazobenzene “safe,” since no azo dye fits that description outright, but practical experience ranks it less troublesome than many alternatives. Proper handling keeps airborne dust at bay and prevents unintended exposure, but chemical stability and relatively straightforward waste management help users in both research and industry dodge common headaches. Unlike several newer synthetic dyes, it doesn’t disassemble unpredictably during routine use. That alone makes it relevant for long-term applications where fading or structural change would cost time and credibility.

    On the issue of photostability, a critical criterion in commercial pigments and standards, the hydroxy group acts as a stabilizer under gentle light exposure. Azobenzenes without this feature darken or degrade faster, especially in outdoor or UV-intense use cases. Not perfect, but a noticeable step up from the alternatives when shelf life and shade fidelity matter.

    Market Impact and Real-World Experiences

    Global demand for dyes and colorants evolves as trends, regulations, and technology keep shifting. My own work in small-scale colorant production taught me early how batch-to-batch variation—or a sudden shortage—can disrupt operations for weeks. Reliable access to quality 4-Hydroxyazobenzene keeps projects moving in both research and light manufacturing without the price spikes associated with rarer or more regulated substances. Cost effectiveness plays in its favor, given the mature supply chain and straightforward synthetic routes available worldwide.

    Regulators have cast a sharper eye on azo dyes in recent years for good reason: concerns about breakdown products and potential carcinogenicity continue to spark research and public debate. While 4-Hydroxyazobenzene doesn’t break down into some of the riskier amines flagged in textiles, routine monitoring remains important. Companies in the EU and North America run routine analyses to assure themselves—and their clients—of compliance. Innovations in surfactants and binding agents have actually improved the environmental profile and end-use safety of finished products, reducing the environmental footprint compared to older pigment systems.

    Education and outreach often lag. I’ve seen well-meaning students and junior scientists overlook the dangers posed by fine powders or underestimate how quickly stains set. Training, good labeling, and clear safety protocols do more for safety than any amount of regulatory paperwork. I learned long ago that nothing replaces the habit of working clean, storing securely, and respecting the material. Companies willing to invest in safety gear and periodic refresher courses also see better staff retention because people feel protected.

    Seeking Solutions for Sustainable Use

    We face a fork in the road today: the drive for greener, more biocompatible colorants means products like 4-Hydroxyazobenzene will either adapt or fade behind newcomers drawn from plant sources or engineered microbes. Transitioning from petrochemicals to sustainable feedstocks isn't a quick fix, but ongoing research could allow some azo compounds to keep their foothold, provided they can deliver on lifecycle assessments and end-of-use recovery.

    A pragmatic way forward involves investing in improved capture and decomposition systems for waste materials. In both chemical plants and research labs, smart filtration techniques, advanced oxidation processes, or even microbial digestion reduce the broader environmental cost. Some groups have explored enzymatic cleavage of the azo bond, which yields less toxic breakdown products and fits within wastewater management frameworks already in place for pharmaceuticals or agricultural runoff. My hope is that with the right incentives, industry leaders will pair these high-efficiency disposal routes with reliable supply chain audits—moving from talk about green chemistry to real, enforceable action.

    Consumer end-use poses its own challenges. Those of us working with finished goods or textile applications see growing pressure for transparent labeling and tracing ingredient origins. Demanding clarity from suppliers—both for the benefit of workers and the public—goes a long way. It shouldn’t fall solely on upstream producers. Retailers and big brands must drive change by refusing shipments from non-compliant sources, rewarding vendors who document not just purity but also responsible handling and disposal.

    At the same time, new analytical technologies offer hope. Mass spectrometry, portable colorimeters, and machine-learning assisted pattern recognition speed up quality checks and root out counterfeit or subpar batches more quickly than older QC approaches. I remember sorting through faded pigment samples with nothing but a spectroscope and aging safety data sheets—far less efficient and much more open to human error. Digital transformation, responsibly applied, gives both seasoned professionals and newcomers tools to do this work better and safer.

    Outlook: Why 4-Hydroxyazobenzene Still Matters

    For all the movement in chemistry toward sustainability and the new, there’s still a need for products that keep to a steady course. 4-Hydroxyazobenzene shows that a compound’s value isn’t just in how new it feels, but in the depth of knowledge surrounding it, the consistency it offers, and its adaptability to evolving needs. In my experience, the most trusted materials are those that blend predictable science with lived-in wisdom about their risks and rewards.

    Looking back, many of today’s safe handling protocols and environmental standards were built by working day after day with established chemicals like this one. It stands as both a testament to progress and a reminder—change usually comes from improvement, not outright replacement. If you rely on reliable color metrics, spectroscopic standards, or dependable building blocks for more complex molecules, consider how 4-Hydroxyazobenzene fits in—warts and all. Its notability lies less in marketing and more in the space where chemistry meets daily practical need. That’s why, in real-world conversations, the question isn’t whether to use it, but how wisely and responsibly you choose to do so.