2-Nitrobiphenyl

    • Product Name: 2-Nitrobiphenyl
    • Alias: 2-Nitro-1,1'-biphenyl
    • Einecs: 207-359-0
    • 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

    782960

    Cas Number 86-19-5
    Molecular Formula C12H9NO2
    Molecular Weight 199.21 g/mol
    Iupac Name 2-nitrobiphenyl
    Appearance Yellow crystalline solid
    Melting Point 71-74 °C
    Boiling Point 355 °C
    Density 1.27 g/cm3
    Solubility In Water Insoluble
    Flash Point 176 °C
    Refractive Index 1.625
    Pubchem Cid 6941

    As an accredited 2-Nitrobiphenyl factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Nitrobiphenyl is packaged in a sealed amber glass bottle, labeled with safety warnings, containing 100 grams of the chemical.
    Shipping 2-Nitrobiphenyl is shipped as a hazardous chemical under UN number 2811, class 6.1 (toxic substances). It must be packed in approved containers, clearly labeled, and transported according to national and international regulations. Ensure proper documentation, and handle with adequate personal protective equipment to prevent exposure and contamination during transit.
    Storage 2-Nitrobiphenyl should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible materials such as strong oxidizing agents. The storage area should be clearly labeled and restricted to authorized personnel. Proper precautions should be taken to prevent spills, contamination, and exposure, using suitable protective equipment.
    Application of 2-Nitrobiphenyl

    Applications of 2-Nitrobiphenyl in Industrial Manufacturing

    As a manufacturer specializing in the production of 2-nitrobiphenyl, we support a demanding marketplace with this intermediate. Below, we detail actual industrial uses, segmented by downstream sectors, compliance standards, composition details, production process stages, and typical finished product categories.

    1. Advanced Dyestuff Synthesis for Specialty Colorants

    Manufacturers of specialty azo and anthraquinone dyes use our 2-nitrobiphenyl in multi-step synthesis to achieve high-purity intermediates for textile and plastics coloring. In this sector, accurate regulation of aromatic nitro group content supports batch color consistency and lightfastness. Operators select ratio and process timing according to specific molecular targets, often integrating the product during the early stage of condensation reactions with other biphenyl derivatives. End customers produce advanced organic pigments and solvent dyes for high-performance industrial coatings, fiber coloration, and plastic mass coloration compounds.

    Industry compliance standards

    • OEKO-TEX Standard 100 (dye safety for textiles)
    • REACH Annex XVII (aromatic amine restrictions)
    • US EPA 40 CFR Part 721 (chemical use reporting)
    • ISO 9001-based QC audits for pigment manufacturing

    Typical usage ratio

    • 10-35% by mass as a primary aromatic precursor, adjusted for desired chromophore structure

    Downstream process integration

    • Introduced at aromatic coupling phase or as a nitration intermediate during pigment core formation
    • Reacted under controlled temperature and pH for stepwise reduction or diazotization

    Final product types

    • Anthraquinone dyes for polyester fibers
    • Azo solvent dyes for plastics
    • High-lightfastness pigments for automotive coatings

    2. Pharmaceutical Intermediate for Non-Steroidal Anti-inflammatory Drug (NSAID) Synthesis

    Producers of pharmaceutical APIs utilize 2-nitrobiphenyl as a controlled intermediate in manufacturing biphenyl-based NSAIDs and anti-hypertensive agents. Our material’s trace impurity profile and batch analytics support Q7 GMP compliance for regulated synthesis. The compound is introduced after initial ring synthesis, primarily for selective reduction to corresponding biphenyl amines or during halogenation steps. Downstream, this intermediate allows fine-tuned functionalization for robust molecular design of patent and off-patent pharmaceuticals.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • EDQM CEP/EP Monographs (as intermediate trace control)
    • 21 CFR Part 211 (US cGMP for finished pharmaceuticals)

    Typical usage ratio

    • 5-30% molar input relative to final API, depending on route and yield optimization

    Downstream process integration

    • Activated in mononitration to selective amination sequence
    • Reductive coupling for conversion to aminated intermediates

    Final product types

    • Biphenylcarboxylic acid NSAIDs (e.g., newer fenamate analogs)
    • Biphenyl-structured antihypertensives

    3. Fine Chemical Intermediates for Agrochemical Synthesis

    Producers of crop protection actives integrate our 2-nitrobiphenyl in the preparation of complex aromatic intermediates essential for systemic herbicide and fungicide formulas. Chemical engineers rely on controlled nitro group position for targeted halogenation or reduction. Typically, our product enters the sequence after initial core structure formation as a substrate in targeted C–N bond construction. Quality metrics and batch-to-batch reproducibility support strict agro-input formulation QC and international registration.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU Regulation (EC) No 1107/2009 (agrochemical approval)
    • ISO 17025-accredited laboratory validation

    Typical usage ratio

    • 8-20% by molar input, depending on specific agrochemical class and process yield

    Downstream process integration

    • Early aromatic substrate in multi-stage halogenation or cyanation to build active core
    • Reacted in catalytic processes for formation of complex functional groups

    Final product types

    • Selective herbicide intermediates (e.g., biphenyl-derived triazines)
    • Aromatic fungicidal precursors

    4. Monomer Synthesis for High-Performance Polymer Manufacturing

    Specialist polymer producers use 2-nitrobiphenyl as a monomer precursor for engineering resins with electrical, thermal, or photostability demands. During controlled hydrogenation, operators convert the nitro group to amine functionality, which then supports polycondensation to form aromatic polyamides or high-strength biphenyl copolymers. By managing trace metal and nitro content, manufacturers meet application-specific electrical insulation or chemical barrier requirements for industrial polymers.

    Industry compliance standards

    • ISO 9001:2015 for production QA/QC
    • UL 94 for polymer flame resistance as required downstream
    • RoHS (Restriction of Hazardous Substances) directive for electrical applications

    Typical usage ratio

    • 15-40% by mass in aromatic core material feed, adjusted for copolymer/terpolymer blend ratios and performance specification

    Downstream process integration

    • Hydrogenated to amine intermediate before polymer chain assembly
    • Included in direct polycondensation or melt blending to build backbone rigidity

    Final product types

    • Aromatic polyamides for electrical and electronic parts
    • Biphenyl copolymer resins for high-temperature components
    • Structural fiber and film materials for specialty applications

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    Certification & Compliance
    More Introduction

    2-Nitrobiphenyl: Product Insights from The Manufacturer’s Bench

    Our Chemistry—A Close Look at 2-Nitrobiphenyl

    Working every day with specialized aromatic compounds, our team often encounters requests for 2-Nitrobiphenyl. The molecule stands out because of its distinctive profile and the pivotal role it plays for professionals in pharmaceuticals, dyes, and advanced material synthesis. As chemists who handle each reaction themselves, we see how much reliability, purity, and structural consistency matter—not just for academic curiosity, but for scalable innovation and safety on the production floor.

    Composition, Model, and Specifications

    We synthesize 2-Nitrobiphenyl in dedicated reactors, closely monitoring the nitration of biphenyl to achieve high yield and selectivity at the 2-position. The resulting compound comes as a crystalline solid, typically pale yellow, with a molecular formula of C12H9NO2 and a molar mass of about 199.2 g/mol. We set standards for purity at 99% minimum by HPLC, backed with spectral (NMR, IR) and chromatographic testing, and we routinely achieve outcomes above these levels batch after batch.

    Each lot comes under strict scrutiny for traces of isomeric impurities, residual solvents, and water content. We run moisture analysis using Karl Fischer titration, always targeting less than 0.1% water content. This attention to micro-details ensures downstream users do not face unanticipated reactivity or solubility issues, especially relevant for fine chemical syntheses and sensitive pharmaceutical intermediates where every microgram of impurity may matter. Our production lines never sacrifice traceability—recordkeeping here means that any batch history can be tracked, including the origin of precursor biphenyl and even every distillation step.

    Direct Experience: Why Our 2-Nitrobiphenyl Stands Apart

    Each day in our lab, we load glass-lined reactors and manage exothermic nitration controls, steering reaction temperatures and acid ratios by hand, not just by automation. These personal checks directly influence the quality and consistency of our 2-Nitrobiphenyl. We never just rely on paperwork—we run thin-layer chromatography by ourselves, cut and analyze every band, and cross-check spectral results for each lot. That means we know the smell, hue, and physical feel of a good batch; this hands-on interaction fosters not only pride but also quick troubleshooting if anything is off-spec.

    The work doesn’t stop with synthesis. Once isolated, every batch is washed, dried, and milled under strictly controlled humidity and light, preventing deterioration or oxidation. Over the years, we’ve learned how even minor adjustments in drying cycles can alter melting point or solubility, affecting real-world application of the product. Since our clients range from academic research labs to bulk manufacturers, they need consistent melting point ranges (customarily 69–70°C) and minimal variation in bulk density. Delivering a product that behaves the same way every time saves the next chemist work and tells them their supplier actually cares.

    Uses of 2-Nitrobiphenyl

    Demand for 2-Nitrobiphenyl crosses several domains, but the most significant users come from pharmaceutical development and dye synthesis. Organic chemists recognize this compound as a key building block for high-value molecules. In drug research, it acts as a precursor for antihistamines, antipsychotics, or intermediates that benefit from biphenyl core structures. For dyes and advanced materials, the nitro functionality unlocks direct routes to amines, azos, and heterocycles, each a building block for new pigments or specialty resist materials.

    We have worked with project teams optimizing ligand scaffolds where a reliable nitro-biphenyl speeds up the hit-to-lead cycle. We’ve also supplied material for researchers developing novel colorants for LCD technology, where even faint contaminants in the starting material could alter hue, fastness, or electrical behavior downstream. Every application depends on perfect orientation of the nitro group, which is why our synthesis always targets the 2-position specifically. A small error leads to domino effects in reactivity, safety, or downstream cost.

    How 2-Nitrobiphenyl Compares to Related Products

    Aromatic nitro compounds frequently seem interchangeable in catalogs, but from the vantage of chemical synthesis and industrial scale-up, each analog behaves with individual quirks. In the biphenyl nitro series, the 2-nitro isomer differs markedly from either 3-nitro or 4-nitro biphenyl in both reactivity and application. The 2-isomer features ortho-nitro orientation, which engages in specific electrophilic substitution and palladium-catalyzed couplings. This difference directly affects product yield, byproducts, and process safety.

    In dye synthesis, for example, the position of the nitro group determines color development and fastness in the resulting pigment. The ortho-nitro effect influences reduction rates, which matters for converting the nitro group to an amine—an indispensable precursor for azo dye couplers and pharmacophores. In pharmaceutical work, this configuration affects metabolic and binding profiles, so the difference is not just academic but built into the project’s outcome. Over time, our direct production and repeated reaction monitoring have shown that the kinetics of reduction and substitution for 2-Nitrobiphenyl are distinct and require tailored conditions that we have honed by direct experience.

    Quality Assurance: What Real Integrity Looks Like

    Our production aligns with established chemical industry standards. Every batch undergoes calibration runs and internal validation, not just to mark a regulatory checkbox but to meet practical needs faced by working chemists. By stepping inside our quality labs, you would see shelf after shelf of sealed reference samples from every production year, kept for retrospective studies and any customer investigation. We run lot-to-lot reproducibility studies and retain comparison data for long-term stability tracking. Our team actively solicits feedback from users, which lets us improve even finer points: filtration protocols, solvent choices, or new containers that better survive long-haul shipment.

    We calibrate our analytics with external accredited labs, not out of obligation but to verify our numbers. So if you see a specification of “99.2% purity by HPLC,” you know direct hands—not just machines or third parties—authenticated those results with meaningful oversight. The feedback loop is constant. Unexpected shifts in melting point, unusual UV absorbance, or slight color tint prompt immediate investigation and corrective action. Sometimes it’s as simple as refining a recrystallization protocol; other times, old sample bottles are pulled and rerun to pinpoint the change.

    Addressing Challenges From The Ground Up

    Every product presents technical challenges, and 2-Nitrobiphenyl is no exception. One major issue: isomeric impurity carryover from incomplete nitration control. We have found that using precision acid addition rates, temperature clamps, and experienced operator supervision sharply cuts unwanted isomer formation. Maintaining reaction homogeneity by gradually ramping up stirring cycles further trims byproduct formation. Most off-the-shelf material we’ve benchmarked cannot compete with in-house batches where actual people, not just process control software, run reaction checks.

    Solubility presents another everyday hurdle. Some users require the product to dissolve rapidly in polar organics; for high-throughput screening, even minimal insoluble fragments can jam microplate systems. Our team learned—through trial, error, and years of hands-on troubleshooting—which crystallization or micronizing steps yield the most reliable solubility in DMF, DMSO, or ether solvents. Every time an order comes in with unusual particle size requirements or special dissolution needs, we personally engage with the chemists involved to align expectations and find the best solution.

    Sustainable Production and Worker Safety

    Handling nitration reactions brings hazards you must address outright: toxic acids, exotherms, and the risk of runaways. Our site was built considering these realities. Closed-system automation for reagent addition, exhaust monitoring, and triple-layer containment all protect not just product but the operators, whose judgment matters most for safe production. The team receives ongoing training based on real-world close calls, not just generic safety checklists. We’ve added rapid quench tanks, acid-neutralizing protocols, and double-layer PPE as knowledge from long-term staff gets folded back into operating practice.

    Our process minimizes waste. Current synthesis practices rely on efficient acid recovery, closed-loop water usage, and solvent recycling at rates above 80%. It took years to optimize for both yield and environmental stewardship, but as manufacturers, we recognize both our chemical and social responsibility. Installations such as upgraded fume scrubbing and real-time emissions monitoring were not built to please auditors but to support those who must work closest to the product.

    Packaging: Practical Insights From Day-to-Day Handling

    Solid nitro aromatics can degrade with light and moisture, so we package under argon and use UV-blocking, screw-top containers with tamper-proof seals. Years of shipping to different climates have taught us these avoid the pinkish discoloration or partial decomposition sometimes seen with less careful handling. We further double-bag every container and pack with desiccants. For bulk shipments, lining with anti-static layers prevents clumping and static discharge. Done right, each drum or bottle arrives as fresh as it left, no matter if the order ships to Helsinki or Sao Paulo.

    Regulatory, Documentation, and Traceability

    Working within international guidelines, our team tracks material all the way from bulk starting reagents to shipped end product. Every certificate of analysis is generated in-house, with direct reference to retained samples and original test chromatograms. We maintain a 7-year document archive, not to simply comply with regulation but to support our customers with any retrospective analysis or regulatory filing demands. We never reuse batch labels or relabel drums—real traceability cannot cut corners.

    We support users preparing regulatory filings or patent dossiers by providing all available spectral data, impurity profiling, and batch records on request. If an unusual impurity arises or regulatory thresholds change, our staff actively updates procedures and communicates directly, grounded in a strong relationship with the working chemists at client sites.

    Supporting Researchers and Formulators—Beyond Just Supply

    Our team frequently engages with customers as partners rather than just order processors. Researchers developing a new synthetic route or scale-up process often need more than just product; they need application data, reaction condition insights, and sometimes troubleshooting tips for downstream processing. With years of applying 2-Nitrobiphenyl in our own R&D, we can feedback practical advice—from suggested purification steps to thermal stability data—in hours instead of days.

    For customers with new regulatory or safety requirements, we assist with hazard assessment and can support risk minimization based on firsthand experience. We understand what it means to introduce a new nitro compound into an existing plant, and we stay available for consultation whether it is on storage precautions, emergency quenching, or safe scale-up. Our clients regularly say that this direct interaction saves them costly trial-and-error iterations.

    Market Perspective and Ongoing Development

    The demand profile for 2-Nitrobiphenyl is changing as pharmaceutical and material science fields grow more specialized. We see requests shifting to ever higher purity and lower impurity specifications, as well as particle customization. Clients designing highly active pharmaceutical ingredients want to eliminate even trace ppm-level contaminants. In advanced materials, minor physical differences can affect performance, so our R&D works continuously to push boundaries—tighter recrystallization, new drying techniques, and smarter packaging.

    We also monitor and anticipate changes in environmental and safety regulation. Proactive process adjustment ensures that both our staff and clients are shielded from unnecessary compliance risks. As raw material markets fluctuate—sometimes sharply due to geopolitical events—we maintain trusted sourcing channels and buffer stocks to help customers manage supply risk, ensuring research timelines and manufacturing schedules are not thrown off by unexpected shortages.

    Working at the Core: What Being a Manufacturer Means

    Direct experience at the reactor and laboratory bench translates into more than just reliable product—it shapes a supplier relationship grounded in trust, responsiveness, and deep understanding of chemical realities. Manufacturing 2-Nitrobiphenyl at a large scale isn’t just about hitting a set of numbers or ticking off a list of parameters; it is the details of precise handling, regular testing, responsiveness to customer feedback, and long-term learning that shape every kilogram we ship.

    Our practice values hands-on engagement, ongoing learning, and real partnership with scientists around the world. Over decades of work, we have seen the best results emerge not from rigid procedures but from a collaborative back-and-forth with the experts who use these building blocks in their own innovation. In every shipment, every experiment, and every challenge, our goal is to be more than a material source—to be a real partner in progress and safety in the chemical sciences.

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