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4-(Pyridin-3-Yl)Benzaldehyde

    • Product Name 4-(Pyridin-3-Yl)Benzaldehyde
    • Alias 3-PyBA
    • Einecs 629-685-9
    • 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

    396869

    Productname 4-(Pyridin-3-Yl)Benzaldehyde
    Casnumber 871012-41-6
    Molecularformula C12H9NO
    Molecularweight 183.21
    Appearance White to off-white solid
    Meltingpoint 98-102°C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as DMSO, methanol
    Smiles C1=CC(=CC=C1C=O)C2=CN=CC=C2
    Inchikey NIKXBCXSNYIPGE-UHFFFAOYSA-N
    Storagetemperature Store at 2-8°C
    Synonyms 4-(3-Pyridyl)benzaldehyde

    As an accredited 4-(Pyridin-3-Yl)Benzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 4-(Pyridin-3-Yl)Benzaldehyde is supplied in a sealed amber glass bottle with a secure screw cap and label.
    Shipping Shipping of **4-(Pyridin-3-yl)benzaldehyde** is conducted in compliance with chemical transport regulations. The compound is securely packaged in sealed, inert containers, clearly labeled with hazard information. It is shipped via regulated carriers to prevent exposure, contamination, and degradation, with all accompanying documentation as per safety and regulatory requirements.
    Storage Store 4-(Pyridin-3-yl)benzaldehyde in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers. Keep container tightly closed when not in use. Avoid exposure to moisture. Use suitable personal protective equipment when handling, and follow standard laboratory safety protocols for aldehydes and aromatic compounds.
    Application of 4-(Pyridin-3-Yl)Benzaldehyde

    Applications of 4-(Pyridin-3-Yl)Benzaldehyde in Industrial Manufacturing

    4-(Pyridin-3-Yl)Benzaldehyde serves as a key intermediate in various specialty chemical synthesis lines. Our technical team supports downstream manufacturers in pharmaceuticals, advanced materials, and electronic chemical sectors. By integrating this intermediate, operators gain consistent processability and direct compatibility with large-scale industrial workflows.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    Our 4-(Pyridin-3-Yl)Benzaldehyde is a reliable building block in the synthesis of pyridine-containing API molecules, such as kinase inhibitors and cardiovascular agents. Formulation chemists use this aldehyde in key condensation and cyclization reactions. This enables production of high-purity API precursors meeting current regulatory and quality requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF Monographs on intermediates
    • European Pharmacopoeia (EP) API intermediate guidelines
    • 21 CFR Part 211 US FDA cGMP for finished pharmaceuticals

    Typical usage ratio

    • 0.12–0.63 molar equivalents per step, adjusted according to target API yield and reaction selectivity; process chemists determine ratio after pilot studies

    Downstream process integration

    • Introduced during the early-stage condensation or coupling reaction as a key functionalized aromatic aldehyde, typically in a nitrogen-inerted reactor, followed by downstream quenching and extractive purification

    Final product types

    • Pyridine-substituted anti-cancer drug intermediates
    • Novel cardiovascular agent scaffolds
    • Research-grade pharmaceutical research compounds
    • Generic small-molecule API precursors

    2. OLED and Organic Semiconductors Synthesis

    Chemical engineers in the optoelectronic sector employ this material in the fabrication of custom aryl-pyridine ligands for metal-based emitters and charge transport layers. The aldehyde group enables controlled Suzuki or Heck coupling, delivering consistent substrate performance for large-area device deposition. Our batch records support stringent trace impurity controls required for electronics processing.

    Industry compliance standards

    • JEITA (Japan Electronics and Information Technology Industries Association) Material Qualification Protocols
    • RoHS Directive (2011/65/EU) for restriction of hazardous substances
    • REACH Regulation (EC 1907/2006) pre-registration of substances
    • IEC 61249-2-21 flame retardants exclusion in electronics

    Typical usage ratio

    • 3–10% by weight in ligand precursor batch, determined by device architecture and emitter loading in downstream formulations

    Downstream process integration

    • Used as a functional aldehyde in palladium-catalyzed cross-coupling to form biaryl ligands for phosphorescent emitter synthesis; processed under cleanroom-grade solvent conditions for electronic-grade purity

    Final product types

    • OLED blue and green emitter cores
    • Charge transport material intermediates
    • P-type and N-type organic layer precursors
    • Photoactive compounds for OLED panel production

    3. Agrochemical Heterocycle Building Block

    In the crop protection industry, our material supports synthesis of substituted pyridine-benzaldehyde cores, which form the basis for innovative herbicide and fungicide actives. Reaction steps utilize the functional aldehyde selectively for Schiff-base formation and subsequent ring closure. Detailed analytical certificates ensure the absence of controlled impurities for regulatory submission batches.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • ISO 9001:2015 Quality Management for Agrochemical Production
    • Controlled Substance Regulations (as applicable by region)
    • Directive 2009/128/EC on Sustainable Use of Pesticides

    Typical usage ratio

    • Typically 0.2–0.9 equivalents, with ratio set according to downstream heterocycle yield and process scalability studies in pilot plants

    Downstream process integration

    • Added to the first-stage reactor during synthesis of active heterocyclic intermediates, followed by stepwise condensation and protective group manipulations under monitored temperature control

    Final product types

    • Precursor to selective herbicide actives
    • Fungicide active scaffolds for broadleaf crops
    • Pyrazole and imidazole agrochemical intermediates
    • Testing samples for residue and tox studies

    4. Specialty Polymer Modification

    Specialty polymer firms use our aromatic aldehyde in targeted functionalization of engineering plastics and resins. The molecule’s reactive formyl and heteroaromatic ring support controlled grafting onto preformed polymer chains to enhance mechanical or optoelectronic properties. Quality compliance documentation supports downstream validation for regulated applications, including some medical and electronic grades.

    Industry compliance standards

    • ISO 10993-5 (Cytotoxicity for polymeric biomaterials, when intended for medical applications)
    • ASTM D638 Mechanical Properties Test for Plastics
    • RoHS Compliance for plastics in electronics
    • FDA 21 CFR 177.2600 (if components are intended for limited food contact silicone elastomers)

    Typical usage ratio

    • 0.5–2.3% by mass relative to base polymer chain, controlled to maintain polymer chain integrity and functional group distribution across batches

    Downstream process integration

    • Dispersed during solution polymerization, or reacted post-polymerization via grafting/coupling step using acid catalysis, typically followed by washing and extrusion for pellet or film formation

    Final product types

    • Optical-grade resins for display films
    • Functionalized engineering plastics for automotive applications
    • Biocompatible elastomers in limited-use medical devices
    • High-Q dielectric polymer films for circuit boards

    5. Analytical Reagent and Fine Chemical Synthesis

    Laboratories and chemical suppliers integrate this compound into synthesis of calibration standards, derivatization agents, and specialty ligands for analytical chemistry. Chemists adapt the reactivity of the aldehyde to introduce pyridine motifs selectively for research and quality control reference substances. Our batch release data include extended purity and trace metal analysis as demanded by advanced labs.

    Industry compliance standards

    • ISO 17034:2016 Reference Material Producers
    • ISO/IEC 17025:2017 General Requirements for Testing and Calibration Laboratories
    • ASTM E2877-13 for analytical reagent qualification
    • Internal trace photon/metal benchmarks for LC-MS/GC laboratories

    Typical usage ratio

    • 5–20 mg per 100 mL standard solution, or as specified by analytical protocol for derivatization reagent synthesis

    Downstream process integration

    • Weighing and direct dissolution for analytical reference solution, or condensation with hydrazine/amine group to form stable labeling compounds prior to instrument calibration

    Final product types

    • Certified reference standards for UV/Vis and HPLC
    • Stabilized analytical grade derivatization agents
    • Ligand libraries for academic and industrial screening
    • Quality control markers for research and contract testing labs
    Free Quote

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    Certification & Compliance
    More Introduction

    4-(Pyridin-3-Yl)Benzaldehyde: Experience from the Manufacturer’s Floor

    Understanding 4-(Pyridin-3-Yl)Benzaldehyde Through Day-to-Day Manufacturing

    Every new order for 4-(Pyridin-3-yl)benzaldehyde reminds us that the market for pyridine derivatives continues to grow in both scale and diversity. Decades of hands-on synthesis and customer feedback have shaped not only our production methods but also our understanding of what makes this molecule valuable on both technical and economic fronts. The backbone of this compound—melding a pyridine ring with a benzaldehyde group—serves unique purposes in pharmaceuticals, agrochemical research, dye intermediates, and beyond. The implications of its use go well beyond academic curiosity, impacting real commercial and therapeutic pipelines.

    Getting Precise with Our Process

    The process behind each batch doesn’t rely on vague formulae. From the first minute, purity targets direct every operational choice. The yield and color can shift with subtle tweaks in temperature, pressure, and reagent concentration, making it essential to manage each stage with vigilance. Our veteran operators understand that even minor variations influence not only HPLC purity but also shelf life and stability. Lab notebooks filled over many cycles of optimization reveal patterns—for example, an elongated drying phase at reduced pressure preserves the aldehyde group and prevents discoloration. That difference decides whether the finished product meets the high standards expected by peptide and custom synthesis partners or leads to costly rework.

    Main Specifications: No Room for Shortcuts

    Purity levels always draw the most attention. We routinely see specifications calling for 98% minimum by HPLC, though some projects, particularly where the molecule will serve as a building block in drug research, demand 99% and above. It’s not just about pushing the number up; it’s about knowing how to weed out residual solvents, isomers, and related impurities at trace levels. Moisture content demands close monitoring since a complex moisture profile alters reactivity and crystallization. Color is assessed visually and using spectrophotometric reading—years ago, we learned slight amber tints point to side reactions, offering a warning signal to the QC team.

    Tracking Down What Sets It Apart

    Many chemicals serve as building blocks—benzaldehydes and pyridine derivatives each have long lists of analogs. Blending the two into 4-(pyridin-3-yl)benzaldehyde gives a hybrid platform. Chemists gained a toolkit for Suzuki couplings and C–H functionalizations, as the electron-donating and withdrawing capacity splits across the two rings. The formyl function anchoring onto the benzene ring means ligands can easily be developed for catalytic systems or new chemical entity development, while the pyridine has always excelled in chelating applications or as a nucleophilic partner.

    In practice, projects requiring selective reactivity or compatibility with both aromatic and nitrogen-containing frameworks gravitate toward this aldehyde. Its reactivity profile sets it apart from classic benzaldehyde or pyridinecarboxaldehyde. These differences are not theoretical; they show up as smoother reaction monitoring in cross-couplings, less interference in downstream processing, and higher yields in final API syntheses. Customer project teams have reported cleaner chromatograms and better throughput thanks to this compound’s favorable balance of electronic and steric properties.

    Purity Battles: What We See Daily

    Our journey with this molecule has never followed a straight line. On some days, we pull off a run that hits target purity in just two crystallizations and column passes. Other days, minor contamination from a feedstock or solvent batch means extra cleanup—trust gets built in these moments of problem-solving. Adjustments during synthesis, pressure cycles, or workup conditions create lessons; everyone in the crew remembers moments they caught a faint off-aroma during distillation or found a yellow tint after extended stirring. Only granular experience allows us to judge when to discard a batch early to avoid a downstream headache, as opposed to improvising a recovery technique and salvaging valuable material.

    Customers who rely on this aldehyde appreciate direct communication about batch variation or unexpected hold-ups. We log and track every batch against its GC, NMR, IR, and HPLC profiles, learning over time which tweaks consistently close the gap between ‘spec-compliant’ and ‘ideal for synthesis’. Working this way allows us to reduce wasted inputs and pass those savings back in consistent pricing offers, not just in words but in market-verified contracts.

    Where Customers Take It Next

    Some clients use 4-(pyridin-3-yl)benzaldehyde as a key intermediate in medicinal chemistry—specifically, drug discovery programs that assemble heterocyclic scaffolds. Others bring it into the world of OLEDs and specialty materials, where electron distribution across the rings yields better performance in device prototypes. We have tracked it into research streams around photopolymerization and dyes, especially when target molecules require blendable electronic properties. Spin-off uses in agrochemical labs show up every year or two, almost always aiming at new pest management or plant protection platforms. The litmus test is repeat business: feedback often points to straightforward integration into reaction regimes with lower by-product burden.

    Handling and Logistics: Lab Realities Feed Into the Factory

    Raw material management remains the unsung hero in quality output. From pyridine and substituted benzaldehyde starting points, the path demands full traceability. Secure containers and on-site checking of solids and liquids help prevent contamination—particularly by moisture or poorly cleaned lines. Trace levels of metal or acid contaminants can permanently compromise a run. Training every new shift in the avoidance of cross-contamination spells fewer troubled nights for the quality manager and a proven lower defect rate over hundreds of large- and medium-scale batches.

    Finished 4-(pyridin-3-yl)benzaldehyde, once packed and sealed and labeled with all the analytical data, makes its way into custom-fitted drums or bags. We mark every lot down to kilo, batch, and production date. Purity, moisture, and residual solvent data travel with it. It’s a product line built for real-life research and production demands—not just compliance on paper, but a long track record of safe packaging, reliable transit, and fewer surprises on customer arrival. Our delivery teams have learned lessons in temperature management; extreme heat or cold during shipping nudges batches toward degradation. Experience on the ground means batches are prepared for local as well as international standards.

    Supporting Fact-Driven Innovation

    Manufacturing always evolves with customer expectation and research advances. We’ve seen big changes over the years—early on, orders came mostly from bench-scale academic groups, with gram requirements. Today’s production leans toward pilot and semi-commercial scales, occasionally running into multi-hundred-kilogram loads for customers aiming to scale up their own work. We prepare for new needs by following not only the scientific literature but also firsthand input from long-term clients who share tactical insights after running dozens of their own reactions.

    As chemistry evolves, certain features trend in and out of favor—sometimes it’s the need for faster delivery, sometimes requests come for adjusted particle size or alternative solvents. These practical discussions drive real changes in our workflow, from reengineering drying ovens for gentler evaporation to adding post-synthesis particle checks. Having our own analytical suite onsite has been essential. Every batch receives the same depth of scrutiny, regardless of size or destination, ensuring there’s no dilution of quality with increased scale.

    Looking Across the Synthetic Landscape

    It’s common for researchers to compare this molecule with close relatives—substituted benzaldehydes, pyridinecarboxaldehydes, and similar aromatic heterocycles. Some products prove too unstable for prolonged storage, or their electronic properties don’t match the application’s needs. The dual functionality in 4-(pyridin-3-yl)benzaldehyde fills a niche that bridges both reactivity and ease of functionalization. Drawing from many customer discussions and in-house comparative syntheses, our team has verified fewer unexpected by-products in alkylation and condensation reactions carried out with this material, compared with single-ring alternatives. The difference can mean the success or failure of a project upstream—reduced masking or side chain reactions pay off in both purity and overall yield downstream.

    Small distinctions like boiling point or solubility curve change the outcome during isolation and purification. Teams handling kilo-scale reactions favor materials with consistent handling properties. 4-(Pyridin-3-yl)benzaldehyde shows good stability under nitrogen and a reasonable melting point, so packaging and storage don’t require major process changes in modern production settings. Its mean particle size per batch remains uniform, owing to long-refined crystallization methods and storage controls, reducing the risk of compaction or “cake” formation during storage.

    Upholding Quality Without Shortcuts

    In many industries, cost-cutting translates to batch-to-batch variability, inconsistent impurity profiles, or even compromised yields. It’s tempting to chase lower production costs by reducing purification cycles or sidestepping long-term analytical controls. We have resisted calls to relax QA; every step from the raw incoming material to shipment gets documented and trailed, and each operator knows the value of stopping a run at the slightest red flag—quality makes its mark in the end results, not just in statistics. The investment in quality protocols means that synthesis partners, whether small startup labs or established process houses, count on a consistent product that won’t derail downstream processing or require last-minute project changes.

    Beyond customer-facing controls, we see responsibility measured in how waste streams are managed and how all by-products are treated—we log and handle all hazardous and non-hazardous materials through strict procedures that align with the latest regulatory demands. On-site treatment plants and partnerships with certified handlers complete the picture. Adapting these protocols over time keeps both our crews and end users safe, which draws repeat business from companies and labs that can’t tolerate risk or scandal tied to poor chemical stewardship.

    Reflections from Years on the Production Line

    The story of every successful product package starts long before an inquiry lands in the sales mailbox. Layered in every kilogram of 4-(pyridin-3-yl)benzaldehyde is a record of trial, error, success, and refinement. Only by keeping production and troubleshooting close can a team spot a subtle slip in color, odor, or solubility, and pivot in time to ensure the lot never leaves the factory floor in substandard shape. This mindset of obsessive tracking—batch journals, analytic reports, daily meetings, operator insight—produces not only a chemical but a record of trust and reliability that research teams come to depend on.

    Longstanding experience tells us which factory conditions bring out the best crystal form and which bits of local water supply must be pretreated for traces of iron or microcontaminants. Teams that stay in close touch with projects using our material feed vital feedback into every operational cycle. Once, a recurring issue in a partner lab’s chromatography routine led to a process tweak on our end—a single distillation protocol adjustment improved chromatogram clarity at their site without impacting cost structure or throughput. That direct line from bench chemist to manufacturing manager suddenly pushed our product into preferred-supplier status for a whole network of discovery labs.

    Preparing for What’s Next

    Markets and technologies shift quickly, but some fundamentals remain the same: the need for transparency, high purity, reliable delivery, and open communication through every step of the procurement journey. Teams in R&D need confidence that their supplier understands the technical context of their work, not only the transactional aspect. With 4-(pyridin-3-yl)benzaldehyde, the work never stops—new projects raise nuanced questions about particle morphology, long-term storage stability, and tolerance to different solvents or reagents encountered in scale-up. Each request or data point provides clues for future improvements.

    The confidence built through decades as a direct manufacturer shapes how we develop and deliver this molecule. Even as competitors come and go, customers return because they can count on the lived experience, detailed record-keeping, and consistent innovation we bring to the table. 4-(pyridin-3-yl)benzaldehyde has earned its place in chemists’ toolkits; the expertise behind every lot ensures it continues to serve that role far into the future.