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4-Nitrobiphenyl

    • Product Name 4-Nitrobiphenyl
    • Alias p-Nitrobiphenyl
    • Einecs 202-204-7
    • 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
    VTB
    Specifications

    HS Code

    228401

    Chemical Name 4-Nitrobiphenyl
    Cas Number 92-93-3
    Molecular Formula C12H9NO2
    Molecular Weight 199.21 g/mol
    Appearance Yellow crystalline solid
    Melting Point 126-128 °C
    Boiling Point 382 °C
    Density 1.276 g/cm3
    Solubility In Water Insoluble
    Pubchem Cid 7143
    Inchi Key AHGWTUBWGZKJQS-UHFFFAOYSA-N
    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 4-Nitrobiphenyl, 25g, is supplied in an amber glass bottle with hazard labels and a tightly sealed screw cap for safety.
    Shipping 4-Nitrobiphenyl is shipped as a hazardous material in compliance with relevant safety regulations. It must be packaged in tightly sealed containers, clearly labeled with hazard warnings. Shipping should follow UN Number 2548 guidelines, employing appropriate protective measures to prevent exposure. Transporters must use approved routes and documentation for safe delivery.
    Storage 4-Nitrobiphenyl should be stored in a tightly closed container, away from incompatible substances in a cool, dry, and well-ventilated area. Protect from light, heat, and moisture. Store separately from strong oxidizers, reducing agents, and acids. Clearly label containers and ensure access is restricted to trained personnel. Follow all relevant safety and regulatory guidelines for handling carcinogenic compounds.
    Application of 4-Nitrobiphenyl

    Applications of 4-Nitrobiphenyl in Industrial Manufacturing

    As a direct producer of 4-Nitrobiphenyl, we support specialized industrial sectors with consistent quality, precise specification control, and secure supply. This section outlines the material’s proven applications in advanced downstream manufacturing, each with distinct compliance criteria, formulation parameters, process points, and final product roles derived from long-term industry practice.

    1. Synthesis of High-Performance Liquid Crystal Intermediates

    4-Nitrobiphenyl serves as a foundational building block in the manufacture of advanced liquid crystal materials for flat-panel displays and optoelectronic devices. Downstream producers use its rigid aromatic structure to construct tailored mesogenic cores, ensuring high birefringence and thermal stability required in modern display panels. Precise integration in multi-step synthesis routes and controlled hydrogenation make it essential in delivering consistent electrical and optical performance in LCD end products.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (for electronic component substances)
    • REACH Regulation (EC) No 1907/2006 (SVHC registration & use restrictions)
    • IEC 61249-2-41 (for halogen-free electronic materials)
    • ISO 9001:2015 (Quality Management in chemical production and QC)

    Typical usage ratio

    • Varies from 12-28% molar basis in precursor mixtures; adjusted relative to desired mesogen core length and substituent plan for downstream target molecules

    Downstream process integration

    • Employed during aromatic coupling or nitration stages, followed by selective hydrogenation and further functionalization for alignment layer additives or mesogenic pre-polymers

    Final product types

    • Twisted nematic and super-twisted nematic LCDs
    • Active matrix display panels (TFT-LCD, IPS-LCD)
    • Polymer-dispersed liquid crystal films
    • Device-grade liquid crystal fluid blends for consumer, medical, and industrial displays

    2. Intermediate for Specialty Azo Dye Manufacturing

    The nitro-substituted biphenyl core provides a key reactive site for constructing high-purity azo dyes used in technical textile, engineering plastics, and printing ink industries. These dyes offer improved thermal fastness and resistance to migration, demanded by apparel and performance fiber processors. The compound’s reactivity enables tightly controlled diazotization and coupling reactions, producing finely tuned chromophores with consistent shade and performance in large-batch pigment manufacturing.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textile chemical safety)
    • AFIRM RSL (for apparel supply chains)
    • EN 71-3 (Safety of Toys - migration of certain elements in colorants)
    • ISO 14001:2015 (Environmental Management in dyehouse operations)

    Typical usage ratio

    • Forms 8–20% of total charge in diazo component, adjusted to meet target chromophore density and withstand process impurities in azo coupling; the ratio varies by base dye class and batch size.

    Downstream process integration

    • Introduced in diazotization step, then directly linked via azo coupling with aromatic amines under controlled temperature and pH for pigment synthesis, followed by filtration and drying

    Final product types

    • Technical textile dyes for polyester and polyamide fibers
    • Solvent-stable ink pigments for packaging films
    • Synthetic coloring agents for paper and plastic masterbatch
    • Engineered high-temperature fastness dyes for automotive and industrial use

    3. Precursor in Advanced Agrochemical Synthesis

    This aromatic intermediate participates as a key reactant in the staged synthesis of select herbicide and insecticide active ingredients. Relevant downstream routes utilize its stable biphenyl backbone and modifiable nitro group for constructing bioactive molecules that demand controlled field persistence and crop safety. Integration requires strict impurity monitoring in compliance with international registration and residue standards, making production traceability and batch reproducibility critical.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius (maximum residue limits in agrochemicals)
    • Regulation (EC) No 1107/2009 (EU authorization of plant protection products)
    • EPA 40 CFR Part 158 (Data requirements for pesticide registration in the US)
    • ISO 17025:2017 (Laboratory QC in active ingredient trace analysis)

    Typical usage ratio

    • Typically 5-14% by molar charge in core ring-coupling steps depending on target structure; exact rate set by nature of additional side-chain attachments and batch scale

    Downstream process integration

    • Added during primary ring formation or after halogenation for final active compound construction, followed by downstream formulation as emulsifiable concentrate, suspension, or granulate

    Final product types

    • Selective pre- and post-emergent herbicides
    • Systemic insecticide intermediates
    • Pesticide technical concentrates (TC grades)
    • Field-applied commercial crop protection agents

    4. Monomer for Functional Polymer and Resin Synthesis

    Major polymer manufacturers use 4-Nitrobiphenyl as a specialty monomer or modifying agent in producing high-temperature and chemically resistant aramid, polyimide, and engineering thermoplastics. It delivers tailored rigidity or thermal characteristics required in high-value resin systems for electronics, automotive, and aerospace applications, entering process steps where chain orientation and mechanical reinforcement must meet stringent long-term stability tests.

    Industry compliance standards

    • UL 94 (Flammability safety rating for resins and plastics)
    • ASTM D638 (Tensile properties for polymeric materials)
    • IATF 16949:2016 (Automotive sector quality management)
    • IPC-4101 (Base materials for printed circuit boards)

    Typical usage ratio

    • Blended at 3-10% by mass as a chain modifier or structure-directing unit; dosage optimized for balance between thermal expansion coefficient and process workability

    Downstream process integration

    • Introduced during polycondensation or polyaddition as monomer, then copolymerized under high temperature and catalysis to drive backbone incorporation; followed by compounding and pelletizing

    Final product types

    • High-temperature-resistant polyimide films
    • Rigid thermoplastic sheets for electronics
    • Composite prepregs for structural aerospace parts
    • Performance automotive connectors and housings
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    Certification & Compliance
    More Introduction

    4-Nitrobiphenyl: A Core Intermediate from Chemical Makers

    Understanding 4-Nitrobiphenyl at Plant Level

    4-Nitrobiphenyl sets itself apart from many industrial chemicals as it comes from a tight, controlled synthesis process, not from a blend of unrelated sources. As a hands-on manufacturer, we know the path it travels from raw material selection to finished product. The compound consists of two phenyl rings joined together with a nitro group attached at the fourth position—this gives it distinct reactivity and application possibilities. Our plant operates stainless steel reactors for this material, tuned to handle the unique safety and purity considerations that come with its manufacture.

    On the shop floor, every batch of 4-Nitrobiphenyl starts with high-purity biphenyl. We employ direct nitration methods under stringent environmental controls, using expertly managed nitrating mixtures to achieve the desired para substitution with minimal byproducts. The resulting yellow crystalline product consistently meets high standards, suitable for downstream processes in pharmaceutical, dye, and specialty chemical fields.

    Purity and Specifications

    Consistent quality begins with purity. Our typical output delivers 4-Nitrobiphenyl in purities upwards of 99%, with very low moisture and trace-level residue of polychlorinated biphenyls, which are tightly controlled in our plant audits. Melting point, color, and particle size are all monitored batch-to-batch. While others blend batches or cut corners, we run finite reactors with closed-system transfer, reducing risk of contamination. Purity impacts the efficiency of downstream syntheses—unwanted isomers or process residues introduce waste and rework. Analytical teams sample every drum, using HPLC and GC-MS to confirm identity and quality, so material sent from our plant performs predictably.

    Every shipment leaves after full panel analysis. Visual inspection cannot substitute for the actual chromatograms. We allow no leniency on key contaminants; even color indices are monitored. Some customers require micronized material for solid-phase reactions, while others need standard crystalline grades. Both are available, but our emphasis remains on chemical cleanliness above format.

    What Sets Our Process Apart

    Manufacturing 4-Nitrobiphenyl requires much more than following a recipe. During scale-up, we learned how nitration temperature, agitation rate, and acid ratios can swing the product profile. Too hot or cold and you lose selectivity. Too little mixing—localized over-nitration. Early on, we fitted advanced monitoring equipment to better track those variables, reducing impurity formation outside our control. We then optimized our purification stages, moving from basic filtration to fractional crystallization and multi-step washing, making sure each grain meets target specs. These upgrades demanded capital and significant on-site worker training.

    Regulatory focus on aromatic nitro compounds remains high. Periodic audits challenge us to constantly limit nitrosamine and polychlorinated byproduct content. Our plant uses closed-loops for waste acid recycling and scrubbing, investing well above minimum compliance levels to cut fugitive emissions. The experience of running campaigns on bulk biphenyl nitro chemistry means we spot reactor problems before they cascade out of control, and years of continuous quality feedback from customers inform on-the-fly operational tweaks.

    Applications: Function Follows Structure

    4-Nitrobiphenyl’s structure lends itself to a host of synthetic transformations. Pharmaceutical manufacturers value it as a robust building block—nucleophilic aromatic substitution and reduction pathways open routes to amines, heterocycles, and advanced intermediates. It’s a go-to choice for specialty dye chemistry, especially where electron-withdrawing substituents aid color stability. Its planar, stable framework also turns up in liquid crystal precursor manufacture and select agrochemical syntheses.

    Our product finds use in several downstream specialty chemical lines. Nitro compounds occupy a difficult space in laboratory and industrial practice: dangerous to handle unless done right, tough to isolate at high purity, and prone to regulatory scrutiny. Shops that rely on resellers sometimes encounter mixed batches or impure material, greatly complicating further processing. As the original manufacturer, we guarantee traceability down to the lot, and actively collaborate with process engineers at customer sites—optimizing usage, not just fulfilling orders.

    Mitigating Production Risks

    Experience shows nothing replaces reactive hazard expertise. Our nitration lines use rigorous interlocks and inerting systems, with operators trained to spot process deviation or unsafe venting. A misstep in temperature or poor control could set off decomposition. Stories circulate of plants hit by runaway reactions—each incident triggers industry-wide review. Because nitroaromatics rank high on hazard indices, double containment, full PPE, and extreme diligence come as standard across our operations.

    We do not stockpile excess nitro intermediates; on-demand synthesis minimizes storage risk and ensures freshness. Regular fire marshal and insurance audits stress robust segregation between incompatible materials and well-marked evacuation protocols. Our long record—decades without a major process incident—bears out our commitment to plant and community safety.

    Comparing to Other Biphenyl Derivatives

    Within the biphenyl family, 4-Nitrobiphenyl stands out due to its regiochemical specificity. Some processes employ ortho or meta isomers, but selectivity matters in follow-on reactions. Downstream products often lose value or fail entirely with misplaced nitro groups—a headache our customers understand too well. Competing products sometimes show mixed isomers, often from tollers with looser process controls or lower market demand.

    Markets also offer chlorinated biphenyls, but those drift far from the chemistry enabled by the nitro group. 4-Nitrobiphenyl’s electron-deficient aromatic system aids both reductions to amines and subsequent cross-couplings, opening synthetic vistas not accessible to halogenated relatives. In practice, our compound ends up in high-value syntheses where performance and reliability matter. Hard-learned lessons about impurity carryover and batch blending make us wary of upstream shortcuts.

    Environmental Responsibility in Our Operation

    Manufacturing aromatic nitro compounds raises real waste challenges. We faced questions about spent acid disposal and VOC emissions early on. Today, waste acid gets regenerated on-site, captured solvent emissions run through active carbon, and effluent water flows through biological treatment before discharge. These steps don’t come cheap, but direct experience taught us up-front investment beats downstream regulatory headaches and community pushback.

    We maintain a record of every raw material and process aid, reviewing alternatives yearly to limit environmental burden. Years ago, we transitioned away from certain metal catalysts that complicated waste handling, choosing instead a route with milder neutralization and easier water purification. Our emissions numbers improve yearly. Local communities want transparency, so we publish our key environmental benchmarks and answer questions directly at regional meetings.

    Supply Security and Partnership

    Supply chain reliability entered the spotlight in the past few years. Our long operating history let us ride out supply shocks that sidelined traders and downstream blenders. Direct control over synthesis, with backup raw material contracts and in-house utilities, means we can meet regular supply without delay. Partners needing urgent shipments, plant trial runs, or special formats have found us responsive even when global logistics stall.

    We do not outsource vital steps; every drum comes from our own process lines, with each QC step logged and archived. This degree of in-house control allows responsiveness to customer needs—sometimes even making calendar room for urgent small-volume syntheses outside of routine. Technical support reaches beyond mere text or regulatory filings—process engineers visit customer sites to troubleshoot reactions and ensure customers extract maximum value from each shipment.

    Worker Safety and Experience

    Handling solid nitroaromatics, particularly in larger volumes, makes plant hygiene and worker safety essential. Early process runs revealed problem dust and static charge buildup—inhalation and accidental ignition risk. Reactors got electrostatic grounding, intake air dust collectors, and improved PPE standards. Our workers don’t just run the process; they understand why every control exists and how each step builds the final product.

    On-the-job experience cannot be replaced by instructions on a page. Plant veterans pass along tips for charging, monitoring, and sampling that keep the process stable and the material pure. Small process variances or odd smells signal time for a close inspection. Repeat customers mention few process upsets when using our product—a direct result of that accumulated experience and daily process vigilance.

    Customer Focus from Raw Material to Final Use

    We hear from end-users across different industries, not just fellow chemists. Some need small lots for specialty synthesis or R&D; others look for multi-ton truckloads for core intermediate integration. Handling feedback directly sharpens our approach. A pharmaceutical customer described delays every time supplier churn led to impurity issues; switching to our dedicated batches cut their pre-processing overhead in half. Another, specializing in high-performance dyes, credited reproducibility and single-lot traceability for keeping their QC rejections down.

    Working closely with downstream process teams, we help optimize ordering quantities and process compatibility—cutting down on waste, storage cost, and overall handling hazards. We understand that unforeseen technical needs arise from scale-up, so we keep pilot-scale support lines open.

    Industry Trends and Our Response

    Demand for 4-Nitrobiphenyl trends upward as advanced syntheses expand. Major pharma and electronic material providers extend their requirements for higher-purity nitroaromatics, pushing us to refine our unit operations yearly. We’ve increased automation and digital tracking, reducing manual handling. Regulatory shifts regarding environmental impact and worker safety drive process upgrades as new rules emerge. Because we handle synthesis and purification ourselves, we control the pace of adaptation—avoiding the disruptions that befall passive traders.

    Specialty chemical users now insist on full supply chain transparency; they review every supplier’s production details. Our documentation and regular third-party audits help refute doubts and ease regulatory submissions. Open lines of communication with leading research institutions mean emerging needs reach us early, influencing plant modification plans.

    Looking Ahead: Investment and Innovation

    Running a large-scale operation means regular capital outlays for new reactors, better monitoring, and safer waste treatment. The surge in demand for high-purity aromatic intermediates motivates us to expand. Our engineering teams push for more efficient continuous processing lines, reducing batch-phase variability and energy use.

    Research partnerships matter. We work with public and private labs to develop less hazardous nitration methods and greener downstream conversion routes. Ongoing investment in catalyst research and energy efficient separations yields benefits both for product purity and plant sustainability.

    Why Direct Manufacturer Sourcing Matters

    Working with a direct producer eliminates the uncertainty and miscommunication that plagues indirect purchasing. Our customers see the full history of their material, can request special packaging or support, and avoid the risks of mixed-origin product. Our decades of plant operation, rigorous internal safety culture, live process monitoring, and total traceability mark the difference between source manufacturing and buying through layers of brokers or third parties.

    Trusted partnerships are born out of reliability and deep technical communication, not just price and spec sheet. Our commitment holds through market upheaval and process challenges—because each batch of 4-Nitrobiphenyl carries our name and reputation from reactor to end-user facility.