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2-Biphenylcarboxaldehyde

    • Product Name 2-Biphenylcarboxaldehyde
    • Alias Biphenyl-2-carbaldehyde
    • Einecs 207-419-9
    • 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

    155131

    Chemical Name 2-Biphenylcarboxaldehyde
    Synonyms o-Biphenylcarboxaldehyde, 2-Formylbiphenyl
    Molecular Formula C13H10O
    Molar Mass 182.22 g/mol
    Cas Number 3218-36-8
    Appearance White to off-white solid
    Melting Point 63-66 °C
    Boiling Point 227-229 °C at 19 mmHg
    Density 1.11 g/cm³
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=CC=C(C=C1)C2=CC=CC=C2C=O
    Inchi InChI=1S/C13H10O/c14-9-11-7-3-5-10-6-1-2-8-12(10)13(11)4-7/h1-9H
    Pubchem Cid 18757

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

    Packing & Storage
    Packing A 100-gram amber glass bottle with a secure screw cap, labeled "2-Biphenylcarboxaldehyde," hazard symbols, and handling instructions.
    Shipping 2-Biphenylcarboxaldehyde is typically shipped in sealed, chemical-resistant containers, protected from light, moisture, and incompatible substances. Packaging adheres to hazardous material regulations, often with cushioning and secondary containment to prevent leaks. All shipments include appropriate hazard labeling, documentation, and compliance with local and international transport regulations for chemicals.
    Storage 2-Biphenylcarboxaldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. Keep it away from oxidizing agents and acids. Store under an inert atmosphere, such as nitrogen, if possible. Ensure proper labeling and keep out of reach of incompatible substances and unauthorized personnel.
    Application of 2-Biphenylcarboxaldehyde

    Applications of 2-Biphenylcarboxaldehyde in Industrial Manufacturing

    As a direct manufacturer of high-purity 2-Biphenylcarboxaldehyde, we enable downstream industries to enhance product performance and process reliability through careful integration of our material. Below, we detail the primary industrial application segments where this aromatic aldehyde delivers unique technical advantages, meeting stringent compliance and supporting specialized processing routes.

    1. Pharmaceutical Intermediate Synthesis

    2-Biphenylcarboxaldehyde functions as a key intermediate in the synthesis of various active pharmaceutical ingredients, particularly for anti-inflammatory and anticonvulsant compounds, where selective functional group transformations and high-purity profiles remain crucial. Its introduction supports Grignard reactions and cyclization steps in multi-step manufacturing routes, contributing to molecule scaffolding in regulated pharmaceutical environments.

    Industry compliance standards

    • United States Pharmacopeia (USP)
    • European Pharmacopeia (Ph. Eur.)
    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 211

    Typical usage ratio

    • Batch formulations use 0.2-1.2 molar equivalents depending on the targeted intermediate; precise ratio determined by reaction pathway and output yield requirements.

    Downstream process integration

    • Material is introduced during the condensation or coupling stage of API intermediate synthesis—often preceding cyclization or reduction steps, with strict controlled addition to avoid overreaction or impurity formation.

    Final product types

    • Anti-inflammatory API intermediates
    • Anticonvulsant drug precursors
    • Specialty drug scaffold molecules

    2. Fragrance and Aroma Chemical Manufacturing

    This aldehyde finds established use in the construction of high-value aroma chemicals, particularly those serving as building blocks for musky, woody, and floral notes in fine fragrance formulations. Its ability to participate in Schiff base and acetal formation reactions gives rise to unique olfactory properties demanded by perfumery and premium personal care product manufacturers.

    Industry compliance standards

    • IFRA Code of Practice (International Fragrance Association)
    • EU Regulation (EC) No 1223/2009 for Cosmetics
    • ISO 9235 for natural aromatic raw materials (when used in semi-synthetic blends)
    • REACH Regulation (EC) No 1907/2006

    Typical usage ratio

    • 0.05–0.5% (w/w) in concentrate blends; amount adjusted for target fragrance intensity, volatility modulation, and regulatory restrictions on aldehyde content.

    Downstream process integration

    • Raw material is charged during initial mixing with alcohols or ketones in the creation of Schiff bases, followed by solvent removal and purification for use in complex fragrance compounds or fine aroma blends.

    Final product types

    • Fine fragrance bases
    • Personal care aroma concentrates
    • Home fragrance diffusers

    3. Agrochemical Active Ingredient Development

    The compound serves as a starter framework for the formation of biphenyl-derived agricultural actives, including fungicides and plant growth regulators. Its reactivity as an aldehyde allows precise transformation with hydrazines, amines, or other nucleophiles during synthetic route development, supporting the production of molecularly targeted crop protection agents that comply with strict residue and toxicological standards.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius for pesticide residues
    • US EPA Title 40—Protection of Environment
    • European Union Regulation (EC) No 1107/2009 concerning plant protection products
    • ISO 9001 for quality management during synthesis

    Typical usage ratio

    • Prepared at 0.3–1.5 molar equivalents depending on the functional group transformations and end-use agrochemical structure; ratio adapted to the efficiency of the downstream coupling or condensation reaction.

    Downstream process integration

    • Raw material added to reactor during the synthesis of biphenyl-based core structures, integrated prior to heterocycle formation or halogenation steps necessary for the final active ingredient profile.

    Final product types

    • Biphenyl-system fungicides
    • Plant growth regulation agents
    • Precursor intermediates for crop protection R&D

    4. Polymer Additive and Modifier Formulation

    This aromatic aldehyde supports functionalization in polymer chemistry, especially for the synthesis of chain-terminated or crosslinked polymers used in specialty coatings and advanced engineering plastics. Its inclusion provides rigidity and chemical stability, required for performance plastics under heat or mechanical stress. Material selection follows guidelines to minimize extractables and assure compatibility with food-contact or electronic-grade polymers.

    Industry compliance standards

    • US FDA 21 CFR 177 (Polymers for Food Contact)
    • ISO 9001:2015 for polymer production
    • UL 94 (Flammability of Plastic Materials)
    • EU Regulation (EU) No 10/2011 (Plastic materials and articles intended to come into contact with food)

    Typical usage ratio

    • 0.1–1.0% by weight during polymer modification; dosage determined by required degree of crosslinking or terminal functionalization for targeted resin performance.

    Downstream process integration

    • Introduced in the compounding or reactive extrusion phase, often together with catalysts, followed by curing or post-polymerization to achieve the designed molecular architecture.

    Final product types

    • High-performance engineering plastics
    • Functionalized polymer coatings
    • Chemically resistant resin modifiers

    5. Dye and Pigment Intermediate Production

    2-Biphenylcarboxaldehyde acts as a precursor for the synthesis of sophisticated dyes and pigments, especially those requiring extended conjugation for color stability and intensity. Producers leverage its controlled condensation behavior in the creation of azo, benzylidene, and isoindoline chromophores. Its application enables fine-tuning of colorfastness and chemical resistance for industrial textile and printing systems.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (textile safety)
    • EU REACH Regulation (Annex XVII, Restrictions on the manufacture and use of certain hazardous substances)
    • ISO 105 (Textiles—Tests for colour fastness)
    • CEN/TS 14234 (Dyes and pigments for ink formulation)

    Typical usage ratio

    • 0.25–1.8 molar equivalents in pigment precursor synthesis; the applied amount is defined by the desired chromophore system and process throughput for colorant yields.

    Downstream process integration

    • Raw material supplied to the reaction vessel for condensation or coupling with amines and diazonium salts, typically preceding oxidation or cyclization steps needed for pigment particle crystallization.

    Final product types

    • Synthetic azo dyes
    • Color-stable textile pigments
    • Inks for industrial digital printers

    6. Electronic Specialty Chemical Synthesis

    In the electronics sector, 2-Biphenylcarboxaldehyde supports the synthesis of specialty materials for organic semiconductors, OLED intermediates, and advanced liquid crystal components. Its rigid biphenyl structure and reactivity permit targeted molecular engineering for charge transport enhancement, stability improvement, and oxidation resistance in display materials and electronic interfaces.

    Industry compliance standards

    • JEDEC J-STD-033 (Handling and Process Guidelines for Moisture/Reflow Sensitive Devices)
    • RoHS Directive (EU) 2011/65/EU on the Restriction of Hazardous Substances
    • ISO 14001 (Environmental management applicable to electronics manufacturing)
    • IPC-4101 (Specification for Base Materials for Rigid and Multilayer Printed Boards)

    Typical usage ratio

    • 0.02–0.3 molar equivalents per batch, with precise levels determined by the required degree of functionalization or the synthesis step for the final electronic material.

    Downstream process integration

    • Material added in the functional group modification or core-building step of intermediate synthesis for organic optoelectronic layers, usually in sealed, moisture-controlled reactors for purity and performance assurance.

    Final product types

    • OLED intermediate materials
    • Advanced liquid crystal additives
    • Semiconductor organic compounds
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    Certification & Compliance
    More Introduction

    2-Biphenylcarboxaldehyde: Chemical Insight from the Manufacturer's Perspective

    Experience in Manufacturing 2-Biphenylcarboxaldehyde

    Over the years, our team has seen the role of 2-Biphenylcarboxaldehyde grow throughout many industrial workflows. Developing this compound has shaped the way we look at aromatic aldehydes and their downstream applications. We notice requests for biphenyl intermediates have ticked upward, especially as the world leans more on high-value fine chemicals for pharmaceutical, agrochemical, and specialty material synthesis. From process design to batch control, each step we take aims to deliver a product hitting tight purity standards, equipped to handle both research and upscaled production.

    Product Model and Physical Characteristics

    2-Biphenylcarboxaldehyde offers a balance of molecular rigidity and functional reactivity. As manufacturers, we pay close attention to physical form—pure batches yield clear, pale-yellow crystalline solids with a faint aromatic scent. Each production run gets analyzed for its melting point range, appearance, and chemical stability, since even subtle changes steer upstream and downstream yields. We focus on producing consistent purities, often exceeding 98%, with tightly managed moisture and trace impurities, knowing too well how trace water or phenolic contaminants can hinder performance for sensitive synthetic routes.

    Packing and Handling Practices

    Delivering this compound means managing more than just the molecule—it’s about logistics, protection, and usability at the receiving end. Real-world storage needs call for moisture-resistant, opaque containers, especially since minor exposure can prompt slow degradation or yellowing. Teams handling packing keep direct contact minimal using closed-system transfers and antistatic liners. These measures reduce the risk of contamination or unwanted exposure. Even the choice of drum lining material matters; changing from metal to high-density polyethylene brought improvements in shelf life on extended shipments.

    Practical Uses in industry Applications

    Applications of 2-Biphenylcarboxaldehyde draw mostly from its role as an intermediate for synthesizing complex organic molecules. During our scale up of this product, we support customers who supply liquid crystals, homologated biphenyl aldehydes, and agrochemical actives. Fine chemical routes leverage its reactivity at the formyl group; we see frequent modifications toward making biphenyl acetic acids, alcohols, or heterocyclic scaffolds. Researchers in academic settings often reach out because it serves as a convenient substrate for Suzuki coupling studies, especially when exploring substitution patterns or structure-activity relationships.

    Our technical support team regularly consults with process leads in pharmaceutical companies who harness this compound for access to arylated building blocks, often toward anti-inflammatory agents, antihistamines, or synthetic intermediates not easily accessed through other means. Its unique placement on the biphenyl backbone—formyl at the ortho-position—shapes how it reacts with nucleophiles, making it distinctly more useful in migrations, cyclizations, or controlled condensations compared to non-ortho isomers.

    How 2-Biphenylcarboxaldehyde Stands Out from Related Products

    From a synthetic chemist’s viewpoint, not all biphenyl aldehydes behave the same. During pilot studies, we compared 2-Biphenylcarboxaldehyde to its para- and meta- analogues. The ortho-formyl group introduces distinct steric effects, which can tweak chemoselectivity in Grignard additions or Wittig reactions. Down the line, this property leads to more predictable cyclizations, higher regioselectivity, and less unwanted oligomerization—matters that often determine batch success or failure.

    Contrast this to, say, simple benzaldehyde or 4-biphenylcarboxaldehyde: the former lacks the extended biphenyl structure and fails to deliver the same breadth of π-system conjugation, while the latter doesn’t bring the same directed reactivity owing to its spatial arrangement. Customers mention achieving greater yields or reduced by-products when using the ortho variant for core-forming steps, especially when assembling molecules for high-purity demand areas like OLED materials or archaeological reagent kits.

    Challenges and Solutions in Production

    Producing aromatic aldehydes always stirs debate over air sensitivity and potential oxidation. Having run dozens of scale-ups, we found that ambient moisture and tiny leaks in process lines build up benzaldehyde or carboxylic acid impurities, eroding consistency. To address this, our operations team revamped drying protocols and strengthened nitrogen blanketing throughout classifier stages. These subtle process improvements led to cleaner product with longer stability windows on the shelf.

    Occasionally, trace metal catalysts left behind from coupling reactions creep into the final material. Analytical teams use ICP-OES and strict wash sequences to lower these levels. Those small details shape not only analytical readings, but downstream catalytic hydrogenation or biotransformations, which can become unreliable otherwise. In addition, we implemented real-time chromatographic monitoring, so every lot ships after confirming tight retention time, ensuring research labs and scale-up sites receive what their procedures expect.

    Real-World Feedback from Industrial Users

    Users in the pharmaceutical development field report fewer bottlenecks during late-stage functionalization of biphenyl motifs. One feedback loop led us to refine drying and packaging, prompted by difficulties encountered in multi-step synthetic campaigns. By keeping the aldehyde uncompromised from day one, researchers reduce their purification steps. Material scientists comment on reliable consistency across lots, which helps with reproducibility in the lab, especially when developing new organic electronic materials or catalytic screens.

    Agrochemical processors express that the ortho-substituted nature lines up better for some herbicide intermediates; the reactivity allows for clean transformations without excessive side-product formation, streamlining production timelines. We also hear from academic research groups who use the compound as a substrate to model biphenyl migration, working through mechanistic pathways in new reaction classes. With well-defined purity and transparency in analytical results, labs avoid guesswork, expediting fundamental discoveries.

    Safety and Environmental Considerations

    Handling aromatic aldehydes requires care. Though less volatile than simple benzaldehyde, 2-Biphenylcarboxaldehyde still demands good air handling and storage away from oxidants. Early on, we transitioned to stronger local exhaust and enforced sealed systems to limit airborne concentrations. Proper labeling, training, and restricted access in work areas all stem from lessons learned on actual exposure case reviews. Bulk users request documentation on residual solvents, so we maintain open reporting and proactive batch analysis.

    Waste minimization starts at process design. We target closed-loop distillation for solvent recovery and send spent process solutions through on-site treatment. Our team worked with environmental partners to lower chemical oxygen demand (COD) in effluent streams, much of it originating from biphenyl intermediates. For any off-spec or aged material, we provide take-back programs, so waste is remediated or recycled where possible.

    Continuous Improvement and Technical Support

    Feedback channels shape how we improve this product. Customer calls, technical visits, and shared troubleshooting efforts contribute to ongoing optimizations in process efficiency and product reliability. Chemists at scale have highlighted trace impurity trends linked to seasonal temperature swings; integrating more rigorous environmental controls reduced outliers and enhanced reproducibility, which matters most for users qualifying for regulatory submissions or large-scale batch upticks.

    One successful collaboration with a contractor highlighted the benefit of real-time analytics. Chromatographic fingerprinting across longer runs allowed not just early-out specifications, but detection of sluggish side formation before it accumulated. Shared learning pushes us to invest in more analytical horsepower—from routine GC and HPLC to advanced NMR and mass spectrometry. End users see value in transparent, fully-documented spectra, leading to smoother project audits and fewer sourcing headaches.

    Broadening Use Cases through Application Experience

    2-Biphenylcarboxaldehyde carries a unique blend of aromatic stability and formyl reactivity. We’ve worked with bioprocess engineers who adapted this chemistry for biosynthetic pathway research, testing new enzyme candidates for aromatic ring functionalization. The compound’s well-defined structure provided a controllable target that aided in improving biocatalyst selectivity, paving the way for greener synthesis options.

    Polymer chemists also report on its use as a monomer precursor for specialty resins or advanced materials that rely on tailored biphenyl motifs. The ortho position leaves sufficient space for further substitution, matching design needs for high-performance coatings or thin-film applications. This adaptability has prompted new requests for collaborative scale-up, focused on controlled substitutions suited for specific end-use cases—each iteration supported with batch-specific analytical packages so research teams can hit the ground running.

    Manufacturing Challenges in a Fast-Changing Market

    The steady rise in fine chemical demand means evolving process efficiencies and capacities. Our facility responds to rapid order swings, all while guarding product consistency. We undertook capital investment in reactor upgrades, adding better thermal management and automated dose systems, because the exothermic nature of formylation exaggerates impurity formation at uncontrolled heat spikes. Increased throughput testing improved turnaround and created room for small pilot projects, where rapid test cycles help synthetic researchers scale ideas into reality.

    Supply chain interruptions, such as delays in base phenyl starting materials or solvent constraints, required shifts toward localized vendor relationships and buffer inventories. The unpredictability of upstream materials has led us to pre-qualify multiple suppliers and validate their material through our own labs. This redundancy supports customer planning for both long-term projects and sudden surges prompted by research discoveries.

    Comparing to Traditional Aromatic Aldehydes in the Lab and Plant

    In research settings, the difference between standard and ortho-substituted biphenylcarboxaldehydes shows up in both reactivity and end product properties. Direct feedback from synthetic chemists working with diverse arylaldehydes underscores the value of the ortho format: lower by-products, higher selectivity, and reliability when stepping into multistep syntheses. We observe clear opportunities for exploring more complex transformations, especially for users focused on developing patentable routes or proprietary intermediates.

    In plant settings, stability on storage and minimal degradation during processing offer practical benefits. Our continual sampling and batch tracking pointed out that prolonged storage above recommended temperatures prompted trace acid formation—a lesson that steered us toward refrigerated warehousing and batch size adjustments. This practice led to fewer rejected lots and more predictable in-line performance during scale-up.

    Partnerships and Future Development

    Working closely with industrial partners, research collaborators, and contract manufacturers, we seek out opportunities for co-innovating on process improvements and new applications. Demand for biphenyl derivatives in next-generation electronic materials, advanced pharmaceuticals, and green chemistry routes drives our investment into application-focused R&D. We sponsor joint studies under confidentiality, offering access to detailed analytical data, smaller test lots, and process documentation so teams can quickly enter feasibility and pilot stages with minimal risk.

    Current projects include developing formulations tailored for solid-state reaction conditions, pursuing both improved handling properties and compatibility with automation. We’re evaluating continuous production options, leveraging flow chemistry to boost both safety and batch reliability, and extend shelf life for global shipping. Customers participating in these pilots know they have a say in process adjustments, because every feedback cycle shapes future runs for both existing and emerging applications.

    Looking Ahead: The Value of Direct Manufacturer Relationships

    From the manufacturing floor to technical support, direct engagement with users means we stay attuned to evolving needs—whether in fine chemical synthesis, advanced material development, or new research frontiers. Our experience with 2-Biphenylcarboxaldehyde reflects more than just molecule production. Each step, from raw material control through to tailored logistics, adds value that end users appreciate, especially as demands for transparency, reliability, and high-quality documentation become industry standard. As applications evolve and research pushes forward, we remain committed to refining production, nurturing collaboration, and supporting innovation that starts with dependable, well-characterized starting materials.