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2-Nitrobiphenyl

    • Product Name 2-Nitrobiphenyl
    • Alias 2-Nitro-1,1'-biphenyl
    • Einecs 210-324-1
    • 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
    VTB
    Specifications

    HS Code

    787439

    Cas Number 86-19-5
    Iupac Name 2-Nitrobiphenyl
    Molecular Formula C12H9NO2
    Molecular Weight 199.21 g/mol
    Appearance Yellow crystalline solid
    Melting Point 68-71 °C
    Boiling Point 333 °C
    Density 1.273 g/cm³
    Solubility In Water Insoluble
    Flash Point 175 °C
    Smiles C1=CC=C(C=C1)C2=CC=CC=N2(=O)
    Pubchem Cid 7047

    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 Amber glass bottle with screw cap, labeled "2-Nitrobiphenyl, 25g," hazard symbols, CAS number, supplier logo, and safety precautions.
    Shipping 2-Nitrobiphenyl is shipped according to hazardous chemical regulations. It should be transported in tightly sealed, labeled containers, protected from physical damage, moisture, and incompatible substances. Shipping must comply with applicable local and international dangerous goods guidelines (UN 2811, Toxic Solid, Organic, n.o.s.). Proper documentation and appropriate hazard communication labels are required.
    Storage 2-Nitrobiphenyl should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of heat, sparks, or open flames. Keep it away from incompatible materials such as strong oxidizing agents and bases. Store under conditions that prevent contamination and moisture ingress. Properly label the container, and restrict access to qualified personnel only.
    Application of 2-Nitrobiphenyl

    Applications of 2-Nitrobiphenyl in Industrial Manufacturing

    2-Nitrobiphenyl serves as a key intermediate in several specialized industrial production chains, where its unique aromatic structure and nitro functional group enable transformation into high-value chemicals. As a direct manufacturer, we facilitate downstream integration of this raw material for consistent quality and regulatory alignment. Below, we highlight major application domains where 2-Nitrobiphenyl demonstrates established utility.

    1. Pharmaceutical Intermediate Synthesis

    In the pharmaceutical sector, 2-Nitrobiphenyl acts as a building block for the synthesis of complex heterocyclic compounds, particularly for molecules containing biphenyl or phenyl group-based pharmacophores. Its incorporation occurs predominantly in the stepwise construction of APIs such as sartans (angiotensin receptor blockers) and certain nonsteroidal anti-inflammatory drugs. Downstream producers utilize our high-purity batches to maintain consistency with strict pharmacopeial monograph specifications and ensure downstream traceability throughout validation and scale-up.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Chinese Pharmacopoeia, European Pharmacopoeia, USP (API impurity profiles)
    • ISO 9001:2015 for quality management systems
    • REACH Regulation (EC) No 1907/2006 registration and handling

    Typical usage ratio

    • Formula integration varies between 5–25% by molar ratio, adjusted according to target API structure and desired yield optimization; batch records document adjustments per product line.

    Downstream process integration

    • Entry as an electrophilic aromatic substitution reactant or nucleophilic coupling precursor in multi-step organic synthesis, especially Suzuki-Miyaura cross-coupling and subsequent reduction/amidation pathways.

    Final product types

    • Losartan, Valsartan, biphenyl-based NSAIDs, and specialty generic API intermediates.

    2. Dye and Pigment Manufacturing

    2-Nitrobiphenyl is a critical feedstock for formulating benzidine-derived and biphenyl-type azo dyes, where its chemical structure allows for stepwise conversion into high color-fastness pigments. Downstream blending requires stringent quality checks to prevent trace impurities that could impact chromatic properties or fastness ratings demanded by the textile, leather, and plastics sectors.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (exclusion of carcinogenic amines and safe dye composition)
    • EU REACH Annex XVII—Restricted Substances List for dyes
    • ISO 105 (Textile color fastness standards)
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) guidance

    Typical usage ratio

    • Loading typically ranges from 8–18% based on pigment or dye molecular weight calculations; adjustment per target absorption spectrum and binding efficiency on substrate.

    Downstream process integration

    • Employed in nitro reduction and subsequent diazotization, progressing to final coupling reactions for azo dye synthesis; introduced upstream in slurry blending or sodium dithionite reduction lines.

    Final product types

    • Benzidine yellow, biphenyl azo pigments, textile dyes for synthetic and natural fibers, ink colorants for industrial printing systems.

    3. Agrochemical Active Ingredient Precursor

    2-Nitrobiphenyl functions as a foundational intermediate for several biphenyl-based herbicide and fungicide actives, especially in the synthesis of selective agents for cereal and fruit crops. Agrochemical manufacturers require feedstock with defined nitro purity levels and controlled contaminant limits to meet agrotoxicity and residue standards.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides (JMPR)
    • ISO 9001:2015 quality documentation
    • European Union Regulation (EC) No 1107/2009 for plant protection product registration
    • U.S. EPA Active Ingredient Review Guidelines

    Typical usage ratio

    • Used in 3–10% proportions relative to total mole balance in precursor blends, with process engineers adjusting based on electronic effects required in final actives.

    Downstream process integration

    • Introduced at aromatic nitration or halogenation stages, followed by catalytic hydrogenation, condensation, and cyclization in the construction of fungicide or herbicide cores.

    Final product types

    • Biphenyl-based fungicides (e.g., phenylcarbamate types), selective herbicides, plant disease control agents, grain and post-harvest fruit preservatives.

    4. Polymer Additive and High-Performance Material Synthesis

    In the advanced polymer sector, 2-Nitrobiphenyl is applied as a monomer precursor for functionalized polyarylenes and as a modifying agent in specialty engineering plastics. Its biphenyl core imparts rigidity, chemical resistance, and thermal stability to polyimide films and other aromatic polymers, relevant for high-temperature and electrical insulation applications. Producers depend on narrow purity tolerances to secure polymer chain integrity and repeatable physical properties in the finished goods.

    Industry compliance standards

    • UL 94 (Flammability of Plastic Materials for Parts in Devices and Appliances)
    • RoHS Directive (2011/65/EU) for hazardous substance limits in electrical/electronic equipment
    • ISO 9001:2015 process quality
    • ASTM D5207 for high-temperature electrical insulation materials

    Typical usage ratio

    • Monomer-loading ratios typically from 2–7% in specialty blend formulations, with precise adjustment based on targeted glass transition temperature and desired dielectric properties.

    Downstream process integration

    • Fed as a comonomer into polycondensation or polyimide synthesis reactors; integrated during controlled-temperature melt blending or solvent casting for specialty film production.

    Final product types

    • High-performance polyimide films, thermoset resin components, advanced insulation tapes, and electrical/electronic encapsulation materials.

    5. Specialty Chemical Synthesis for Analytical Reagents

    2-Nitrobiphenyl is also utilized as a precursor in the synthesis of analytical standards and specialty reagents, particularly in the development of biphenyl-based calibration compounds used in chromatography and spectrophotometry. Precision in purity and batch-to-batch traceability is essential, as these downstream products underpin laboratory QA/QC workflows and reference standard production.

    Industry compliance standards

    • ISO/IEC 17025 for laboratory competence
    • USP Reference Standard guidelines
    • ISO Guide 34 (Reference Material Producers)
    • Good Laboratory Practice (GLP) regulations

    Typical usage ratio

    • Conversion sources use 2–12% by reagent feedstock mass, tailored to compound synthesis yield and purity requirements.

    Downstream process integration

    • Engaged as an arylating agent or reduction source, entering precursor conversion reactors or direct reagent synthesis lines; followed by precision-splitting and purification workflows for analytical compound isolation.

    Final product types

    • Chromatographic calibration standards, biphenyl-based analytical reagents, quality assurance kit contents, and laboratory test reference materials.
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    Certification & Compliance
    More Introduction

    2-Nitrobiphenyl: Purpose, Purity, and Practical Insights from the Factory Floor

    Experience with 2-Nitrobiphenyl Production

    Every search for reliability in the chemical lab comes back to the actual source. In our own lines, 2-nitrobiphenyl always presents itself as a material that demands close attention from raw input to final drum, and customers looking for consistency care about how things come off the line. Our daily production routines involve close calibration of conditions, knowing that the purity and color of the nitro compound reflect the care taken in every stage—ultra-narrow column operation, monitored stirring, temperature tracking, and downstream refinement. The precise reaction between biphenyl and nitrating mix does more than produce a pale yellow crystalline solid; it sets in motion a chain of trust with synthetic chemists counting on that purity for downstream efficiency.

    What True Consistency Means for Specifications

    In the world of aromatic nitro compounds, precision goes beyond meeting a certificate. Our in-house labs check for limiting impurities every day. The melting point for technical or high-purity 2-nitrobiphenyl typically lands near 80–83°C, and we maintain tight control on isomer proportions, looking for less than 0.5% ortho contaminant. Even a small spike in impurities can complicate subsequent synthesis, especially when the end goal involves pharmaceuticals or specialty intermediates.

    For a color developer or agrochemical precursor, uneven batches with specks of brown byproducts signal risk for downstream reactions; they simply will not do. We see how subpar products elsewhere lead to unnecessary rechecks, failed reactions, or costly purification steps. Bringing specifications beyond a printed “minimum 98%” into real-world dependability takes everyday vigilance.

    End Uses: Why the Details Matter

    Among all biphenyl nitro derivatives, 2-nitrobiphenyl stakes out applications in dyestuff synthesis, intermediate production for pharmaceuticals, and specialty color formulating. As a building block, its position supports the classic Borsche–Drechsel cyclization, allowing for carbazole manufacture, plus pages of patents detail its use in anti-inflammatory and anti-cancer research. This is not an abstract exercise: our technical support team has worked with colorant innovators seeking tight batch results because a single off-spec shipment can spoil weeks of work downstream.

    In contrast, 4-nitrobiphenyl or 4,4′-dinitrobiphenyl target other synthesis flows with different reactivity and spatial demand; the ortho-nitro variant uniquely positions itself for constructing ring-fused structures or acting as a precise scaffolding point. It’s these subtle but essential differences from the para-isomer that explain why some reaction protocols just don’t cooperate unless the ortho isomer performs without extra isomeric drag.

    What Sets Factory-Made 2-Nitrobiphenyl Apart

    The difference between a manufacturer’s product and a generic resold lot often emerges in crystal clarity and batch repeatability. Handling 2-nitrobiphenyl isn’t just pouring a bottle into a box. Our operations run hot and cold, quite literally, and purity depends on attention at every step: fresh, stabilized acids; newly distilled biphenyl; scrupulously controlled glassware; careful product separation.

    People involved at each workbench know why each variable matters—dry air lines curb oxidation, line filtration prevents dust pickup, and prompt cooling prevents side-products that turn the whole drum a disappointing brown. That experience shows up in what leaves the factory: a clear pale yellow solid, fine-grained and easily transferred, usually in low-dust crystalline form that chemists appreciate for its reliable transfer and reproducibility.

    Practical Considerations from Synthesis to Sale

    Ask anyone who has dealt with triggered exotherms in large-scale nitrations: lab-scale preparation does not tell the whole story. Industrial-scale reliability requires not just the right reactants but also careful temperature and stoichiometry control. Mistakes at this step generate not just off-color product but also safety and yield issues. Our staff guard against over-nitration through continuous monitoring; endpoint detection combines in-line sensor feedback with batchwise sample checks—a practice that’s saved thousands in avoided downtime and reworking over the years.

    Once crystal nucleation starts, growth conditions need close oversight. Too rapid cooling forms dust; too slow leads to larger, irregular crystals that complicate downstream handling. Controlled drying and transfer into drums matter as much as the initial synthesis, since humidity or off-gassing paves the way to shipment headaches: stuck powders, caking, or strange odors that complicate end-user storage. Foresight and meticulous recordkeeping mean that regular customers get batches that slot smoothly into their own production lines with fewer surprises.

    Observations from Customer Feedback and Industry Use

    Chemists expect intermediates like ours to perform predictably. Several times, a formulation customer has sent us test results flagging even small batch-to-batch variations, asking for explanation or advice on purification profiles. Trace metal content can affect specific catalyst runs—so we maintain routine checks, using validated ICP analysis and documentation that tracks each lot’s journey from start to finish.

    In pharmaceutical R&D, researchers look for clean melting, rapid solubilization, and robust, documented GC profiles. Each customer order provides feedback, and over time their shared insights have continually shaped our technical support materials and posting of analytical protocols, saving everyone time and keeping their projects moving. For dye makers, high absorbance and clear spectrum are only possible with batches free from yellow-brown tar contaminants formed by secondary oxidation, which factory-level oversight addresses daily.

    Comparing 2-Nitrobiphenyl to Other Nitro Compounds

    On the surface, nitrobiphenyls of all isomers can look similar. Experience on the shop floor makes their practical differences feel obvious. The ortho arrangement in 2-nitrobiphenyl creates a kink in the molecular shape. This alters how it stacks, melts, and reacts—to the point where certain fold-in reactions just do not occur reliably with para or meta isomers.

    As a result, chemists needing a nitro group next to a ring junction find 2-nitrobiphenyl offers reactivity that 4-nitrobiphenyl lacks. Likewise, 2-nitrobiphenyl’s solid state stability and relatively mild odor—so long as drying is complete—mean easier shelf storage, though care is still needed to avoid excess warmth or moisture, both of which can degrade product purity and handling.

    In contrast, dinitro and halogen-substituted biphenyls, though vital for specialized syntheses, introduce greater health and environmental risks, higher fuming, and lower yields on account of their reactivity. Our ongoing investments in vent systems and waste treatment reflect these realities, and regulatory audits keep us honest on compliance, worker protection, and batch documentation.

    Environmental and Safety Observations

    Years of manufacturing 2-nitrobiphenyl have underlined how factory-level attention to waste management, air handling, and exposure risks outpaces what many outside observers imagine. While nitroaromatics demand careful respect for health and safety, our workflow includes full-time air monitoring and closed transfer systems. The feedstock’s nip of odor never leaves the factory. Our on-site waste streams undergo neutralization before leaving, and every staff member receives updated training based on actual shop-floor experiences—like how quickly a few spilled grams can lead to hazmat protocols.

    From the production line to the dock, controlling dust and vapors means real investment in high-performance filters and design tweaks to batch rooms. Our policy of assigning a named team with clear lot responsibility puts accountability in every hand, which reduces mixed-batch errors and supports clean reporting all the way through the final product.

    Technical Support Born from Direct Use

    Work in a factory reveals questions that might never arise in a reseller’s catalog. Customers call about solvent compatibility—our own tests show 2-nitrobiphenyl dissolves well in acetone and hot ethanol but resists water and low-grade hexane. Feedback about storage translates into direct guidelines: tightly closed HDPE containers in cool, dry, ventilated locations keep the solid free-flowing for over a year.

    Analytical needs often mean custom GC or HPLC protocols. We provide these from our own method development records, not just literature pulls. Sometimes this means showing a process chemist how to tweak separation runs if trace biphenyl remains, or swapping column conditions to dodge co-elution with ortho contaminants. Our technical support crew spends as much time coaching on practical runs as filling paperwork.

    The Real-World Cost of Quality Failures

    Hundreds of syntheses in pharma and colorant labs depend on predictable reactions, so a weak batch crowds error bars and erodes confidence down the line. Over-dry, under-dried, or misfiltered crystals all provoke the same headaches: variable color, slow response to solvents, or poor mixing. It’s not just a theoretical risk; we’ve processed more than a few emergency returns after third-party drums failed a customer’s incoming QC, while ours passed sequential spot checks and long-term shelf tests.

    Mistakes in nitration methods, incorrect drying, or contamination not only ruin single batches but can cascade through a production line. Our strict error-reporting framework ensures that such incidents get swift root-cause analysis and revised SOPs, sparing future batches from repeat pitfalls. Experienced hands know factory-quality 2-nitrobiphenyl means not hunting for clean lots among inconsistent drums.

    Logistic and Documentation Practices from the Source

    Shipping thousands of kilograms each year with exacting batch tagging and documented analysis turns into a quiet point of pride. By keeping both digital and handwritten batch logs, we provide traceability unmatched by third parties. Over decades, this approach has allowed us to resolve shipping delays or QC hold-ups quickly, since a signed record follows every lot from vessel to drum.

    Customs or border queries often come down to clear documentation, and our experience has helped more than a few customers avoid costly clearance holds thanks to properly formatted and translated certificates and test reports. Rather than generic “meets spec” stickers, our labels and MSDS sheets reference actual production runs, so customers know what they have.

    Listening to the Chemists: Collaborating for Tomorrow’s Formulations

    Handling 2-nitrobiphenyl year in and year out keeps the lessons fresh—stability remains paramount, and method consistency forms the backbone for every project downstream. Regular meetings with academic partners and manufacturing customers highlight both the routine and novel ways the compound appears in patents or process tweaks, with direct feedback shaping our internal priorities for next quarter’s manufacturing improvements.

    Even as new derivatives emerge and regulatory standards tighten, the day-to-day work of maintaining a reliable, safe, and clean 2-nitrobiphenyl supply supports all the innovation at the end of the chain. No matter how the recipe evolves, robust quality comes from direct responsibility, deep batch records, and a healthy respect for the realities of factory chemistry.