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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 | 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. |
Applications of 2-Biphenylcarboxaldehyde in Industrial ManufacturingAs 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 Synthesis2-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
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2. Fragrance and Aroma Chemical ManufacturingThis 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
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3. Agrochemical Active Ingredient DevelopmentThe 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
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4. Polymer Additive and Modifier FormulationThis 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
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5. Dye and Pigment Intermediate Production2-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
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6. Electronic Specialty Chemical SynthesisIn 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
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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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.