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4-Nitrosophenol

    • Product Name 4-Nitrosophenol
    • Alias 4-Nitrosophenol
    • Einecs 210-059-8
    • 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
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    Specifications

    HS Code

    677127

    Iupac Name 4-nitrosophenol
    Molecular Formula C6H5NO2
    Molar Mass 123.11 g/mol
    Appearance Pale yellow solid
    Melting Point 70–72 °C
    Solubility In Water Moderately soluble
    Cas Number 104-91-6
    Density 1.31 g/cm³
    Pka 7.23
    Chemical Structure Nitrosophenol with nitroso group at the para position
    Pubchem Cid 7642

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

    Packing & Storage
    Packing Amber glass bottle containing 100 grams of 4-nitrosophenol, labeled with hazard symbols, chemical name, and handling instructions for laboratory use.
    Shipping 4-Nitrosophenol should be shipped in tightly sealed containers, protected from light and moisture. It must be stored and transported at ambient temperature, away from incompatible substances such as strong oxidizers. Comply with all applicable regulations for transport, labeling, and documentation, as it may be hazardous if inhaled or in contact with skin.
    Storage 4-Nitrosophenol should be stored in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers and acids. Store in a tightly closed container made of compatible materials. Clearly label the container, and avoid storing near food or drinking water. Ensure access to appropriate spill containment and emergency equipment.
    Application of 4-Nitrosophenol

    Applications of 4-Nitrosophenol in Industrial Manufacturing

    As the direct manufacturer of 4-Nitrosophenol, we supply this intermediate to global industrial partners focusing on specialty areas with proven, regulated demand. Below, we outline established commercial sectors where 4-Nitrosophenol forms a critical component of downstream processing, presenting segmented application specifics relevant to compliant, high-volume production environments.

    1. Azo Dye Intermediate for Textile and Leather Finishing

    Major dye producers incorporate 4-Nitrosophenol as a coupling component in synthesizing various mono- and di-azo dyes. Its nitroso functionality directly participates in diazotization-coupling reactions, enabling precise hue and fastness characteristics needed for advanced textile and leather goods. Downstream processors depend on its consistency and controlled dosing to stabilize tone, reduce bleed, and support industry-compliant coloration chemistry across cotton, synthetic, or hide substrates.

    Industry compliance standards

    • Oeko-Tex® Standard 100 (product class-specific limits on aromatic amine content and dye residues)
    • REACH Regulation (EC) No 1907/2006—regulation of azo dye intermediates and SVHC restrictions
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • ISO 9001:2015 quality management for textile auxiliaries and dyestuff production

    Typical usage ratio

    • Usually 0.5%–2.2% of total dye batch weight, adjusted based on target pigment structure, shade depth, and batch size

    Downstream process integration

    • Introduced during coupling reaction step in semi-batch or continuous dye synthesis line; temperature and pH are tightly controlled to ensure selective azocoupling

    Final product types

    • Disperse dyes for polyester and acetate fibers
    • Direct dyes for cellulosic textiles (cotton, viscose)
    • Azo pigments used in leather coatings and shoe finishes
    • Specialty colorants for printing inks and technical fibers

    2. Intermediate in Rubber Antioxidant Synthesis

    Chemical manufacturers utilize 4-Nitrosophenol as a selective precursor in the synthesis of certain phenolic antioxidants used to modify rubber compounds. Its controlled reactivity supports targeted coupling and subsequent reduction steps, ensuring the antioxidant's molecular structure suits high-thermal and oxidative endurance demands of automotive and industrial rubber goods. The precision of formulation is critical to achieve mandated anti-aging performance, minimize bloom, and meet prolonged service expectations.

    Industry compliance standards

    • EN ISO 8330:2014 (nomenclature and classification for rubber chemicals)
    • ASTM D4677—Standard Specification for Rubber Compounding Materials
    • China GB 3670—Rubber antioxidant quality and purity requirements
    • IATF 16949 for automotive sector quality management

    Typical usage ratio

    • Introduced at 0.8%–1.6% based on the total antioxidant batch; content may be adjusted according to the required final antioxidant activity and rubber grade

    Downstream process integration

    • Added during condensation or coupling phase of antioxidant production before downstream blending or spray-drying into ready-for-use antioxidant mixtures

    Final product types

    • Non-staining rubber antioxidants for tires and seals
    • Stabilizers for technical rubber components (hoses, belts, gaskets)
    • Protective agents for latex-modified polymers
    • Antioxidant masterbatches for custom rubber compounds

    3. Synthesis of Photographic Chemicals

    Photo-chemical manufacturers employ 4-Nitrosophenol as a critical intermediate in producing stabilizers and image-forming agents for silver-based as well as color-reversal photographic processes. The nitroso group provides reactivity needed for building specific color developer additives, enhancing grain control, and improving long-term image stability within photographic emulsions processed for archival standards and industrial imaging.

    Industry compliance standards

    • ISO 18909:2019 for imaging stability in photographic films and papers
    • ANSI/NAPM IT9.1—American standard for preservation of photographic images
    • RoHS (EU) directive—restriction of hazardous substances in imaging chemicals
    • Internal QC protocols (QA/QC per major film and photographic material manufacturers)

    Typical usage ratio

    • Applied at 0.1%–0.4%, modulated based on emulsion layer thickness and development chemistry requirements

    Downstream process integration

    • Integrated into multi-step synthesis of color developing agents or image stabilizers; introduced in controlled reactor stages prior to purification, followed by downstream formulation into dry or liquid chemical kits

    Final product types

    • Photographic developer additives for color and black-and-white films
    • Stabilizer concentrates for archival photographic papers
    • Imaging chemicals for microfilm and X-ray film processing
    • Pre-packaged kits for professional darkroom and industrial imaging use

    4. Precursor for Agricultural Chemical Ingredients

    Crop protection chemical manufacturers look to 4-Nitrosophenol as a mineralizable precursor in synthesizing select systemic fungicides and plant growth regulators. Its controlled inclusion under pins phenolic or azo-linked moieties, contributing to precise bioactivity, degradation rate, and soil adherence in final agrochemical formulations. Consistency in raw material quality is essential to ensure product registration, efficacy, and environmental compatibility required by end users and regulatory authorities worldwide.

    Industry compliance standards

    • FAO/WHO specifications for agricultural active substances
    • EPA Registration guidelines (40 CFR Part 158) for crop protection active ingredient manufacturing
    • EC Regulation 1107/2009—EU plant protection product authorizations
    • ISO 9001:2015 and ISO 14001:2015 for agrochemical manufacturing quality and environmental management

    Typical usage ratio

    • Commonly 0.3%–1.5% of total precursor charge, set by molecular conversion demand and desired synthetic yield

    Downstream process integration

    • Entered during early-stage heterocyclic or azo-coupling reactions in the synthesis plant; purified intermediates then used for downstream formulation into technical-grade actives

    Final product types

    • Systemic triazole fungicides and seed treatment agents
    • Plant growth regulators for horticultural application
    • Active intermediates for soil amendment products
    • Technical grade pesticides for further blending and commercial use

    5. Chemical Reagent for Analytical Standards Production

    Producers of laboratory and analytical reference materials integrate 4-Nitrosophenol as a stable reference for phenol/nitroso compound tests and calibration standards. Its defined chromophore and purity level deliver consistent, traceable results for analytical laboratories and QA departments in multiple industries. Primary use centers on manufacturing colorimetric test kits, proficiency standards, and QC benchmarks for assay calibration and materials validation.

    Industry compliance standards

    • ISO/IEC 17025—accreditation for testing and calibration laboratories
    • Ph. Eur. and USP reference standards guidelines for reagents
    • GLP (Good Laboratory Practice) for standard material traceability
    • ISO Guide 34—production of certified reference materials

    Typical usage ratio

    • Charged at 0.05%–0.2% in reference reagent formulations, with exact level contingent on UV-vis absorbance requirements and kit volume

    Downstream process integration

    • Salted or dissolved in base solution during compound staging, followed by drying, aliquoting, and packaging under controlled environmental conditions to prevent degradation

    Final product types

    • Colorimetric assay kits for water and food safety testing
    • Chemical calibration standards for industrial laboratory analysis
    • Certified reference materials for spectrophotometric measurement
    • Reagent-grade solutions for environmental monitoring
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    Certification & Compliance
    More Introduction

    4-Nitrosophenol: A Closer Look from the Manufacturer’s Perspective

    A Material That Shapes Research and Industry

    Producing 4-Nitrosophenol over the years has given us a close-up view of what this compound can actually do beyond the tidy lines of chemical naming. In our plant, we handle this yellow-green solid on an almost daily basis, watching it move from raw ingredient to finished powder or sometimes as a crystalline mass depending on customer preferences. Behind every packed drum, there’s the certainty of its formula: C6H5NO2. The molecule wears its structure well—a phenol ring with a nitroso group sitting at the para-position to the hydroxy group, making it chemically distinct from related phenolic compounds. Its CAS number is 104-91-6. This matters to every researcher, formulator, and technical director looking for reproducibility in synthesis, and we see the direct value this brings to labs and factories alike.

    In-House Manufacturing Experience

    For us, 4-Nitrosophenol is never a shelf product pulled out when orders come in. Batch after batch, we start from the ground up—with every lot, our crew tackles crystal clarity, impurity removal, and even the grain size, because those differences play out in customer results. Tight temperature and pressure control during synthesis matter more than any sales pitch. Color, purity, moisture level: all these details have meaning, because downstream reactions can stumble on a stray impurity or a misjudged pH. Specs found in data sheets only tell part of the story. We look at residual solvents using GC, water by Karl Fischer, and use both HPLC and UV-Vis to stay alert for side-products like 4-aminophenol or trace nitrophenols. Each release also gets tested for heavy metals and insolubles, because over time, even small variations we catch in-house have led to big differences for our industrial users.

    Purity and Consistency—Why It Matters

    One of the most discussed topics in our tech meetings isn’t just hitting a minimum purity figure; it's reducing batch-to-batch variability. That’s especially true for research institutions, dye plants, and pharma R&D departments, who want actual conversion data, not rough approximations. Some facilities ask for 98%+ GC, others want upward of 99% HPLC because the presence of 2-nitrosophenol or any ortho-isomer changes the way the molecule behaves. During production, we’ve learned the limits of standard washing with water or ethanol for removing byproducts, insisting on additional filtration when odd spikes emerge in the spectra. A lot of these decisions have come through phone calls with chemists needing a re-run or pilot-scale producers facing residue buildup. That feedback goes right back to our operators, not just into quality paperwork, which is why our batches rarely trigger unexpected customer complaints about fouling or off-colors.

    Specifications: What’s on the Label Doesn’t Tell the Whole Story

    A technical sheet lists solubility, melting point, loss on drying, and appearance—yellow to green occasional shifts, depending on storage and even the thickness of the sample. We offer common grades between 97% and 99% by HPLC, with moisture kept well below 0.3%. These numbers only matter if you’ve ever seen how subpar lots behave: discolored melting on hot plates, uneven dissolution in organic solvents, or slow yield in azo-coupling reactions. Some labs discover contamination creeping in only after byproducts cause residue in downstream distillations. That’s why we’ve focused on minimizing iron and copper levels, which can drag catalysis down or create unwanted tints in colorant manufacturing. We routinely test for sulfur and halogen impurities because certain applications—particularly antioxidant research or dye intermediates—demand much tighter controls than catalog minimums.

    Differences from Related Phenols and Nitroso Compounds

    Comparing 4-Nitrosophenol to more common phenols like resorcinol, hydroquinone, or even nitro-substituted versions reveals periodic surprises. 4-Nitrosophenol stands out for its reactive nitroso group: this changes its behavior in azo-dye formation, redox chemistry, and various condensation reactions. The ortho isomer, 2-nitrosophenol, brings different solubility and reactivity, creating trouble for those unfamiliar with handling isomeric separations. Para-nitrophenol, sometimes confused on paperwork, behaves differently in both pH-dependent solubility profiles and color changes upon reduction or acid-base reactions.

    Our process keeps 4-nitrosophenol distinct by handling the isomerization risk at every synthesis step. Because the nitroso group can act as both an electrophile and nucleophile under different reaction schemes, unintended isomerization or reduction at any stage changes not just the yield but the performance in subsequent applications. Unlike milder phenols used in solvents or coatings, 4-nitrosophenol brings a slice of unpredictability: it may shift from deep yellow to green-tinged crystals under air, especially if stored in open or slightly humid conditions. This isn’t just a visual quirk—it signals the slow formation of quinoid side products, impacting both color consistency and downstream chemical reactivity. Over the years, we’ve refined our drying and packaging to limit those changes before they show up on a customer’s bench.

    Typical Uses: Bridging Industry and Research

    In industrial and research circles, 4-nitrosophenol finds itself most often in synthesis labs and dye production—not just as a building block, but as a functional intermediate shaping the story of colorants, antioxidants, and fine chemicals. In azo coupling chemistry, this material comes into its own, reacting with aromatic amines to form intense colored compounds used in textile dyes, pigment laboratories, and even advanced imaging technology. Chemists favor 4-nitrosophenol when they want a stronger activating group than simple phenols can offer. It carves out a niche in the preparation of more complex heterocycles, not least because its electron distribution enables transformations that vanilla phenols or nitro compounds can't pull off with the same clean yields.

    Laboratories studying redox reactions use 4-Nitrosophenol as a probe or even as a substrate for new catalytic cycles, especially where selectivity for para-disubstituted aromatic compounds is needed. We’ve shipped this material to researchers working on metal-organic frameworks, enzyme mimic studies, and antioxidant evaluations. In practical terms, those orders often demand not just purity, but documentation: spectroscopic evidence of isomeric purity, no significant UV-absorbing byproducts, and sometimes even pre-dissolution in anhydrous solvents for sensitive photochemical studies. We keep these requirements at the front end of our manufacturing and testing programs, rather than treating every order as interchangeable.

    Safety, Handling, and Real-World Storage Observations

    4-Nitrosophenol comes with its own hazards, well beyond those of generic phenols. Direct handling without gloves or goggles isn’t an option, because skin absorption and inhalation risk remains real. On larger scales, dust control becomes as important as solvent selection. Our warehouse is set up with desiccation and low light in mind, reducing photodegradation and minimizing moisture pickup, which we’ve found can reactivate slow oxidation and discoloration over weeks of storage. Some customers learned the hard way that storage in clear or loosely capped containers led to sample degradation and unpredictable behavior in analytical tests. We pack smaller lots in amber bottles with nitrogen or desiccant pouches, protecting molecular structure as much as possible until the material reaches the user. Spill control and cleanup in our facility follow not just paperwork protocols but are built from patterns we’ve seen from actual incidents—ventilation, rapid isolation, and trained staff make all the difference. While the material’s toxicity profile isn’t as notorious as some nitrosoaromatics, every new batch still gets reviewed by our safety team. The rare occurrence of decomposition is usually prompted by improper storage or accidental mixing with powerful reducing or oxidizing agents, issues that plant experience taught us to anticipate long before a regulatory inspector’s checklist.

    Supporting Innovation and Problem-Solving

    The most innovative uses we’ve seen for 4-nitrosophenol often start with a phone call or email, not a standard catalog inquiry. A university lab might be mapping out radical mechanisms, or a specialty dye manufacturer could be pivoting to eco-friendlier pigment systems. In those cases, controlling trace metals or providing full impurity testing goes beyond compliance—it helps unlock better yields or more reliable analytical data. Sometimes, customers stumble upon batch-to-batch inconsistencies by the time they scale up from grams to kilograms; that feedback loop sets off internal audits of our own plant SOPs. We’ve also supported pilot lines in pharma synthesis where 4-nitrosophenol serves as a reactive handle for further derivatization. We don’t just monitor output purity but track variation in melting points or pH that might nudge downstream processes off course. Unlike high-volume commodity chemicals where minor swings get absorbed by the supply chain, the specialty nature of 4-nitrosophenol means that one batch’s small deviation can ripple into dozens of hours of troubleshooting. By maintaining regular communication with process chemists and sometimes running custom QC tests specific to their needs, we cut down on guesswork, building confidence batch after batch.

    Challenges We Face and Emerging Solutions

    Sourcing high-purity raw materials isn’t getting simpler. Supplier shifts and regulatory moves have pushed us toward more in-house analytics and supplier auditing. We devote significant time to confirming the absence of strategic impurities—not only classic contaminants like chlorides, but also trace organics invisible in standard tests. Small investments in LC-MS and advanced spectrophotometry help us catch issues before they ever leave our gates. Energy use and waste minimization have become bigger priorities, not just from a cost perspective, but due to growing scrutiny from customers and regulators. Traditional nitrosation routes arrive with their own stories of spent acid streams and waste solvents. So, a section of our R&D team focuses specifically on catalyst recycling and low-temperature process tweaks. We look for practical ways to lower emissions while still delivering reproducibly high-grade material—sometimes shifting a run from batch to semi-continuous flow to improve both yield and safety. Occasionally, we need to troubleshoot transport damage, temperature excursions, or minor contamination after shipping. Because 4-Nitrosophenol isn’t widely available off-the-shelf in consistent quality, we end up fielding direct feedback about everything from caking in storage to sample photo-instability. Each hiccup sends us back to production with concrete findings. Packaging upgrades and logistics planning just don’t happen in a vacuum—they’re informed by data from real-world use, not projections from the whiteboard. That’s a truth only years of production and close customer relationships drive home.

    What Sets Our Material Apart in a Crowded Market

    Not every supplier of 4-nitrosophenol stands on the same ground. Some rely on older, less selective synthesis that produces lots of isomers; others might skip full spectral validation, sending out product based on outdated specs. Our site runs in-line quality checks and operator logbooks sync with sample archives going back years. The insights gained from handling everything from pilot-scale runs to tons-scale orders have helped us raise the bar, offering a technical resource rather than just a commoditized batch of yellow-green powder. Repeat customers rely on more than just the advertised purity. Consistency in color, behavior in target reactions, and speed of technical response draw the line between operators who know their material and those who are only moving lots from supplier to market. Whether it’s providing impurity profiles, confirming spectral matches, or supporting custom blending for scale-up, our team works as a direct point of contact—moving beyond anonymous packaging with real answers and remediation when bumps arise. In industries where 4-nitrosophenol might account for a small cost fraction but a major role in performance—dyes, advanced materials, research reactors—compromising on quality just shifts the problem downstream. That’s why process accountability at our plant isn’t a talking point, but a lived standard, mirrored in every tested shipment.

    The Road Ahead: Responsibility, Adaptation, and Customer Partnership

    The journey of optimizing 4-nitrosophenol’s manufacture and delivery continues to evolve. Shifting regulations, new synthetic methodologies, and a growing demand for analytical data all push us to adapt and learn. We know that making high-purity 4-nitrosophenol products means more than meeting published minimums. It’s about building trust with everyone who weighs, dissolves, or transforms our product—every person counting on each detail from appearance to final residue results. By making honest improvements based on hands-on experience—tightening process control, investing in verification, and listening to what technical users face in real time—we keep moving the bar higher. Our team’s commitment to transparency and collaborative problem-solving remains at the core. This isn’t just a chemical; it’s a material that bridges innovation across fields, supported by a manufacturing partner who shares your stakes in every reaction and every result.