4-Nitrobiphenyl

    • Product Name: 4-Nitrobiphenyl
    • Alias: p-Nitrobiphenyl
    • Einecs: 202-204-7
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    948824

    Chemical Name 4-Nitrobiphenyl
    Cas Number 92-93-3
    Molecular Formula C12H9NO2
    Molecular Weight 199.21 g/mol
    Appearance Yellow crystalline powder
    Melting Point 126-129 °C
    Boiling Point 358 °C
    Density 1.27 g/cm3
    Solubility In Water Insoluble
    Flash Point 163 °C
    Pubchem Cid 7096
    Smiles C1=CC=C(C=C1)C2=CC=C(C=C2)[N+](=O)[O-]

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

    Packing & Storage
    Packing The 4-Nitrobiphenyl is packaged in a 100-gram amber glass bottle, featuring a secure screw cap and detailed hazard labeling.
    Shipping 4-Nitrobiphenyl is shipped as a hazardous chemical and must be securely packed in appropriate, sealed containers. It should be clearly labeled and accompanied by safety data sheets. Transport requires compliance with local, national, and international regulations, typically under Class 6.1 (toxic substances), and stored away from incompatible materials, heat, and ignition sources.
    Storage 4-Nitrobiphenyl should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area, away from heat, sparks, open flames, and strong oxidizing agents. Store away from incompatible materials such as reducing agents. Proper labeling and secure access are essential to prevent accidental exposure, as 4-Nitrobiphenyl is a hazardous and potentially carcinogenic substance.
    Application of 4-Nitrobiphenyl

    Applications of 4-Nitrobiphenyl in Industrial Manufacturing

    As a primary manufacturer of 4-Nitrobiphenyl, we serve specialized industrial sectors where this compound’s precise chemical profile is essential in advanced synthesis processes. Below we outline key application scenarios, detailing integration details and operational standards for professionals in chemical production and procurement.

    1. Synthesis of High-Performance Organic Dyes

    Downstream dye manufacturers employ 4-Nitrobiphenyl as a coupling component in the synthesis of disperse and solvent dyes for fibers and plastics, leveraging its aromatic structure for increased color stability and intensity. Its consistency ensures batch-to-batch reproducibility required for demanding textile and plastic coloration processes, where trace impurities can cause significant color deviations or fastness issues. Through controlled nitration and subsequent reduction, dye producers integrate this intermediate to achieve advanced chromophores with improved light and wash fastness, meeting both fashion and technical textile needs.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for finished dye content in textiles)
    • REACH Regulation (EC) No 1907/2006 Annex XVII
    • ZDHC MRSL (Version 3.1 permissible limits for dye raw materials)
    • ISO 105-C06 for color fastness in end-use clusters

    Typical usage ratio

    • 2–7% weight by weight relative to total dye batch, adjusted based on molecular weight of target dye conjugates and color depth requirements; higher loadings used for synthesis of deep-shade dyes

    Downstream process integration

    • Acts as an electrophilic aromatic substrate in diazotization and coupling stages of azo dye synthesis
    • Introduced post-nitration in the preparation of biphenylamines, enabling subsequent reduction and condensation reactions
    • Directly consumed in coupling with diazonium salts to yield specialized disperse and solvent dye variants

    Final product types

    • Disperse dyes for polyester fiber coloring
    • Solvent-based plastic dyes
    • Specialty textile pigment concentrates for industrial yarn
    • Technical dye intermediates for further modification

    2. Manufacturing of Advanced Liquid Crystal Display (LCD) Compounds

    Producers of liquid crystal monomers and display-grade chemical intermediates rely on the rigid, planar structure of 4-Nitrobiphenyl to synthesize biphenyl-based mesogens. The material supports development of key components that impart alignment, thermal stability, and electro-optical properties critical for modern LCD applications. Stringent process controls during the Friedel-Crafts and subsequent reductions integrate this raw material into liquid crystalline core structures, satisfying the purity and polymorphism specifications for high-resolution display manufacturing.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) on hazardous substances for display materials
    • IPC-4101B (base materials for printed electronics)
    • ISO 9001:2015 certified manufacturing protocols for electronic-grade chemicals
    • IEC 62321 analysis for impurity and heavy metals control

    Typical usage ratio

    • 0.5–3% of the total monomer feed in liquid crystalline precursor batches; adjusted depending on the targeted mesogen chain length and orientation properties

    Downstream process integration

    • Nitrated biphenyl is reduced and incorporated into subsequent alkylation, acylation, or esterification stages to build liquid crystal monomers
    • Introduced in the initial organic synthesis stage for fine-tuning melting point and phase transition behavior
    • Directly linked to functional groups (e.g., cyano, alkoxy) through cross-coupling processes to yield the final liquid crystalline molecules

    Final product types

    • Twisted nematic (TN) and Super Twisted Nematic (STN) liquid crystal mixtures
    • Active-matrix TFT-LCD panel formulations
    • OLED display precursor chemicals
    • High-purity liquid crystal intermediates for further mesogen engineering

    3. Production of Polyaryl Polymer Engineering Plastics

    4-Nitrobiphenyl serves as an essential arylation building block during the synthesis of targeted polyaryl engineering plastics, including poly(aryl ether ketone) and related high-performance resins. Polymer engineers exploit its molecular rigidity to achieve polymers offering high thermal resistance and dimensional stability for critical electrical and mechanical applications. Controlled reduction and subsequent polymerization steps make use of the material’s biphenyl core, enabling scale-up of specialty polymers for aviation, electronics, and energy technologies.

    Industry compliance standards

    • UL 94-V0 (flammability for engineering plastics)
    • ASTM D6262 for polyaryletherketone product quality
    • IEC 60695 (test methods for plastics used in electrical equipment)
    • REACH SVHC compliance on starting monomers and polymer units

    Typical usage ratio

    • 5–15% by mole in monomer feed for step-growth polymerizations, modulated for chain rigidity and target molecular weight

    Downstream process integration

    • Inserted in the arylation phase as a backbone-building monomer before reduction and polymer condensation
    • Integrated as a chain-stiffening agent to modulate glass transition and melting temperature in polymer backbone construction
    • Blended in multi-step synthesis with dihalides or dicarboxylates for high-molecular-weight polymer production

    Final product types

    • Poly(aryl ether ketone) (PAEK) engineering resins
    • High-performance electrical insulation sheets
    • Components for aerospace and automotive electrical systems
    • Heat-resistant injection-molded parts

    4. Intermediate for Pharmaceutical Synthesis Pathways

    Chemical synthesis groups in pharmaceutical manufacturing use 4-Nitrobiphenyl as a specialized intermediate for the development of select antihypertensive and anti-inflammatory agents, exploiting its biphenyl framework for pharmacophore construction in API research pipelines. Stringent traceability in compliance with GMP protocols governs every stage, from controlled reduction to biaryl coupling. The compound’s stability and reactivity make it a reliable precursor for advanced multi-step synthetic routes, frequently serving as a protected aryl fragment en route to the assembly of bioactive molecules.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) for relevant precursors
    • European Pharmacopoeia (Ph. Eur.) General Monographs
    • 21 CFR Part 211 (US FDA cGMP for finished pharmaceuticals)

    Typical usage ratio

    • 0.3–2.5 molar equivalents relative to the target intermediate, depending on pathway selection and desired yield of final API

    Downstream process integration

    • Enters as a protected or unprotected biphenyl intermediate in cross-coupling reactions such as Suzuki, Stille, or Buchwald–Hartwig amidations
    • Used as a nitro-substituted aryl donor for further conversion to amino or alkyl biphenyls in preparative organic synthesis
    • Subjected to hydrogenation and refined for use in scaffold construction before final derivatization

    Final product types

    • Advanced pharmaceutical intermediates
    • Biphenyl-based antihypertensive and anti-inflammatory drug candidates
    • Active pharmaceutical ingredient (API) scaffolds
    • Research-stage biaryl building blocks for medicinal chemistry

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    Certification & Compliance
    More Introduction

    4-Nitrobiphenyl: Practical Insights From the Manufacturer’s Bench

    Stepping Into the World of 4-Nitrobiphenyl

    At the production floor, 4-nitrobiphenyl isn’t just a line item—it’s a compound that demands attention and care from raw material sourcing through every last crystallization. We’d like to share a genuine, clear-eyed look at this specialty chemical: its manufacturing quirks, uses that steer research and industry, and small but crucial factors that split it from the herd.

    A Look at the Model and Specifications

    4-Nitrobiphenyl carries the molecular formula C12H9NO2 and a CAS number that lab professionals recognize at a glance. Typical batches roll off the line with a pale yellow appearance and a sharp melting point near 126°C. We track impurities closely, as trace contaminants can sideline entire syntheses. Analysts at our site use HPLC and GC methods that pull apart even minor side products and byproducts, ensuring purity usually reaches over 99%.

    Density rounds out at around 1.26 g/cm3 in pure, dry solid. Moisture control matters—not just for shelf life, but to avoid packing issues and static, both of which can gum up automated feed hoppers. Our process team regularly audits packaging to guard against aggregation and accidental trace water absorption, since both tend to cause trouble downstream.

    What Sets 4-Nitrobiphenyl Apart?

    Not every biphenyl derivative acts the same. The nitro group on the fourth position does more than just decorate the molecular structure. It sharply alters its electronic character, changing how it interacts with metals, acids, and reducing agents. Lab chemists lean into these properties when they assemble dyes, specialty organics, and advanced intermediates that form the backbone of electronic components.

    The crystalline form and consistent particle sizing smooth out later handling. Clumping has cost us shipments before, so we invested in sieving and flow control. Our R&D team also keeps a watchful eye on isomer formation—runaway isomers can confuse purification or generate dangerous byproducts. We’ve honed separation steps that increase the selectivity for 4-nitro substitution over 2-nitro or 3-nitro analogs. This sets our finished material apart from standard mixed-nitro biphenyls that come from less controlled reactions.

    Customization is not an afterthought. Our synthesis team adjusts protocols on customer request, optimizing for lower residue solvents or specific crystalline sizes, because these subtle differences influence processing yields later on. The point isn’t making bulk grades but creating a reliable, traceable material tailored for repeatable industrial or research outcomes.

    Uses Drawing From Real-World Experience

    Over the years, we’ve shipped 4-nitrobiphenyl to plants focused on specialty dyes, liquid crystals, and precursor molecules for higher-level synthesis. It isn’t a commodity chemical. Each order usually begins with a discussion about what the chemist plans to do—whether that’s coupling reactions, reducing it to 4-aminobiphenyl, or deploying it as a probe in photochemical work.

    In dye and pigment manufacture, you need consistent starting materials. If you’re optimizing color yields or crystalline purity in advanced pigments, minor impurities can nudge the hue or fade resistance. Customers in the electronics industry drive a different set of requirements, asking for extra process controls around trace metal content and organic impurities from our side. We source base biphenyls with rigorous upstream vetting to prevent cross-contamination from halogenated feedstocks. This came out of feedback we picked up from one customer whose microelectronics failed QA due to ppt-level halides.

    Imagine custom OLED development or exotic ligand synthesis—there, even minor residue from chloride or sulfur reagents can throw off the entire device. That’s where experienced manufacturing counts. We switched to sealed, inert-atmosphere purification for certain lots, shaving off parts-per-million contamination levels that used to return as technical complaints. Tracking every material batch, including cleaning solvents and process reagents, isn’t just for our records; it’s what customers rely on when troubleshooting or scaling up.

    Factory-Led Focus: Production Challenges and Lessons Learned

    Anyone running nitro group chemistry knows that safety beats every other concern. We remember a time when one pilot-scale lot overheated during nitration. That single event led us to invest heavily in process monitoring and real-time exotherm detection. In thirty years of operation, making benzene derivatives is never routine. Every batch faces its own quirks—sudden color shifts, foaming, or deviations in reaction time that can signal process drift or hidden contamination. We’ve trained our techs to recognize these early so nobody’s caught off-guard.

    Quality isn’t something you inspect in afterward; it starts at the reactor. For the nitro step, we use only stabilized nitrating mixtures—no exceptions. Off-specification material never makes it into downstream blending. We grind, sieve, and repack freshly made 4-nitrobiphenyl in controlled atmosphere rooms. Our in-house scientists work directly on the manufacturing floor, not in distant offices. This keeps communication tight, production nimble, and unplanned events rare.

    Sustainability features more now than it did a decade ago. Waste acid recycling, improved solvent recovery, and water usage reductions entered our standard operating plans after tightening global rules and watching profit margins squeezed by waste disposal costs. There have been times when the waste stream nearly outweighed the usable product. Solutions came not from wishful thinking but operator-driven improvements—tailoring reactor additions, temperature ramps, and post-reaction workups. Our approach never chases zero risk but aims for accountability, traceability, and consistent improvement over each campaign.

    How We See the Role of 4-Nitrobiphenyl Today

    In a developed plant, 4-nitrobiphenyl finds less use in consumer products and more as a building block for those who manufacture the products that touch everyday lives. Think about the dye in a technical textile or the charge-transport material in a next-generation display. The people who order from us are scientists and engineers chasing both classic reactions and experimental work. That puts more pressure on robust documentation, lot-to-lot reproducibility, and detailed technical dialog.

    Many new clients arrive after previous suppliers fell short on documentation or traceability. One international order was held at customs for weeks due to misclassification and incomplete records. We now over-document each batch, tying every kilo to safety data, certificates of analysis, and COAs signed by technical staff who actually made the material, not just the QA team. We believe in open communication with our partners—rarely does a large order finalize without several technical calls or even a physical sample evaluation phase. Mistakes are expensive, so clarity up front pays back in operational confidence.

    Technical support stands as a core piece of what we offer. Unlike generic resellers, our production chemists field questions in real time. If a customer from the pharmaceutical sector reports an unexpected impurity profile downstream, we do more than just apologize. We dig back into batch logs and even rerun analytical comparisons to help pin down root causes, even when the source lies outside our gates. Knowledge isn’t just transferred; it shapes each new campaign and batch record.

    Practical Differences from Alternative Aromatics and Nitrobiphenyls

    4-Nitrobiphenyl doesn’t behave like its more volatile or less substituted cousins. Compared to 2-nitrobiphenyl or unsubstituted biphenyl, its higher melting point means less dusting, less inhalation risk, and easier containment. Its reactivity targets fewer side reactions, translating into higher purity and yields for those downstream transformations in established organic syntheses.

    For applications seeking substituted aminobiphenyls, reduction from the 4-nitro position leads to single, predictable isomeric products—unlike ortho- or meta-nitros, where the position muddles downstream routes or impacts physical properties. Its crystalline nature also brings lower static risk and ease of handling for automated dosing and feeding systems. These differences become apparent only after repeated commercial-scale runs. New entrants to the market may overlook these points, but experienced technologists know how night-and-day even minor chemical shifts can be in commercial plants.

    Comparing it to 4-aminobiphenyl is instructive. While both can act as intermediates, the nitro derivative often serves as the upstream protected form, carrying less risk in terms of ambient toxicity and requiring simpler handling protocols. Once reduced, amine analogs require more aggressive containment and waste stream treatment—a strong argument for sticking to the nitro counterpart as long as reaction schemes allow.

    Environmental, Health, and Regulatory Considerations

    Legislation has grown tighter around aromatic nitro compounds. We track and comply with REACH requirements, US TSCA eligibility, and country-specific rules covering both transport and workplace exposure. Our site uses closed transfer for bulk handling, rigorous ventilation, and real-time monitoring for fugitive emissions. Shelving and long-term stores take place in fire-resistant, temperature-steady structures—nobody wants an avoidable incident triggering months of regulatory review.

    Training runs deep, not just for operators but anyone handling packaging, loading, or shipment documentation. Exposure controls and response procedures are standard—each line worker learns to recognize nitro compound symptoms and emergency decontamination methods. We’ve refined spill response through drills and live scenario training, building expertise into the workflow rather than tacking it on after an incident.

    Waste routines matter. The spent acid residue and filter cake from nitration, if managed poorly, pose both environmental liability and real risk to staff. We treat all mother liquors, scrutinize spent filters, and segregate containers for trace nitro organics as hazardous until analytical confirmation. It slows operations, but after a single over-the-limit discharge over a decade ago, we learned that cleanup is costlier than prevention. Our compliance costs increased, but so did our customers’ trust in proven safety records—a non-negotiable in today’s market.

    The Road Ahead: Collaboration, Quality, and Value

    Industrial chemistry rewards those who listen to end users and adapt to changing needs. We take each new inquiry about 4-nitrobiphenyl as a test—can we not just match a spec, but help our partners exceed their historical benchmarks? This means more than selling molecules; it requires delivering support, open communication, and continual process upgrades backed by firsthand operational insight.

    New trends point to growing demand for traceable, ESG-forward chemical supply chains. We see customers asking for not just COAs, but environmental impact statements and evidence of reduced carbon footprints. Our facility has responded by auditing solvent recovery rates, switching to lower-emission transport partners, and publishing broader environmental disclosures. Large clients with global footprints feel pressure from their end markets to prove responsible sourcing—and every chemical we ship now carries that story.

    Feedback guides us. A client in Asia once flagged a recurring packaging abrasion that, left unchecked, threatened to contaminate sensitive feedlines. Solving that didn’t just protect a sale; it deepened trust and kicked off refits on our own in-house conveyors. Similar improvements happen whenever a client calls with a technical question, whether it centers on reaction kinetics, shelf stability, or safe transport.

    Real-world production teaches more lessons than any spec sheet or catalog entry ever will. In the grind of daily operations, we’ve learned that attention to detail, clear documentation, and a willingness to open the plant for audits and technical reviews matter just as much as the molecular formula. If a problem shows up in the field, we track it back—always ready to make adjustments and share what we’ve discovered.

    4-nitrobiphenyl demands that kind of rigor, partnership, and trust. In our view, this is what separates manufacturers who treat each drum as a commodity from those committed to advancing chemical craft and long-term reliability. We stand alongside our customers, delivering not just product, but the experience and insight that come from decades spent working with complex aromatic compounds.

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