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4-(4-Pyridinyl)Benzaldehyde

    • Product Name 4-(4-Pyridinyl)Benzaldehyde
    • Alias 4-(4-pyridyl)benzaldehyde
    • Einecs 619-426-2
    • 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

    590562

    Chemical Name 4-(4-Pyridinyl)Benzaldehyde
    Cas Number 22137-16-4
    Molecular Formula C12H9NO
    Molecular Weight 183.21
    Appearance White to light yellow crystalline powder
    Melting Point 139-142°C
    Boiling Point 389.2°C at 760 mmHg
    Density 1.19 g/cm3
    Solubility Slightly soluble in water; soluble in organic solvents like ethanol and DMSO
    Purity Typically ≥98% (commercial grade)

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 4-(4-Pyridinyl)Benzaldehyde, labeled with chemical name, CAS number, and safety information.
    Shipping 4-(4-Pyridinyl)Benzaldehyde is shipped in tightly sealed containers to prevent moisture and contamination. The chemical is handled as a hazardous material, requiring appropriate labeling and documentation. Packages are cushioned and comply with international transport regulations, ensuring safe transit. Temperature controls are maintained according to safety data sheet recommendations to preserve product integrity.
    Storage 4-(4-Pyridinyl)benzaldehyde should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area away from sources of ignition, incompatible substances (such as strong oxidizers and acids), and direct sunlight. Ensure proper labelling and follow safety procedures for handling organic chemicals. Store at room temperature unless otherwise specified.
    Application of 4-(4-Pyridinyl)Benzaldehyde

    Applications of 4-(4-Pyridinyl)Benzaldehyde in Industrial Manufacturing

    4-(4-Pyridinyl)Benzaldehyde serves as a crucial intermediate for several advanced manufacturing sectors. Its molecular design supports demanding synthetic pathways in fields such as pharmaceuticals, agrochemicals, organic electronics, and specialty polymer industries. As a direct-production manufacturer with specialized facilities, we address market demand with controlled synthesis, precise distribution, and documented traceability for every downstream application.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    This compound is frequently utilized as a key synthon in the preparation of heterocyclic APIs, especially for anti-inflammatory and central nervous system (CNS) active agents. Its pyridine and benzaldehyde functional groups enable efficient building block insertion through controlled condensation, alkylation, or reductive amination steps. Our pharmaceutical-grade supply is GMP-validated for integration into regulated synthesis lines, supporting both investigational and commercial drug production.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • USP & EP monographs (raw materials)
    • FDA 21 CFR Part 211
    • EU EudraLex Volume 4

    Typical usage ratio

    • 0.08–0.5 molar equivalents relative to primary substrate, with ratio adjustment based on target yield and impurity profile during process optimization

    Downstream process integration

    • Charged during advanced intermediate coupling or final condensation before purification and crystallization
    • Requires inline HPLC monitoring for conversion verification

    Final product types

    • Small-molecule API (CNS modulators, kinase inhibitors)
    • Regulated intermediate for generic pharmaceuticals

    2. Agrochemical Active Ingredient Development

    This raw material is employed as a condensation partner or ring-building monomer for the synthesis of novel pesticide actives, such as pyridine-containing herbicides and fungicides. Manufacturers use it in pilot and commercial-scale production under strict process and environmental controls, ensuring consistent structural integrity and impurity management throughout multi-step organic synthesis routes.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP)
    • FAO/WHO specifications for active ingredients
    • ISO 1107 for technical material specification

    Typical usage ratio

    • 5–15% by weight relative to batch feedstock, determined by desired pesticide scaffold and optimization of reaction yield

    Downstream process integration

    • Introduced post-activation of co-monomer for cyclization or condensation stages
    • Usually followed by purification steps such as distillation or column chromatography

    Final product types

    • Technical-grade active substances (herbicides, insecticides)
    • Precursor for in-can formulation

    3. Organic Light-Emitting Diode (OLED) Material Synthesis

    In the electronics segment, this material acts as a fine chemical precursor for electron-transport and emissive layer compounds. Its integration occurs during the multi-step assembly of pyridine-based ligands or complex aromatic systems, which serve as emission-tuning functional groups in commercial OLED displays and solid-state lighting devices. Quality assurance checks include NMR, LC-MS, and photoluminescence screening.

    Industry compliance standards

    • ISO 9001 QMS for electronic materials
    • IPC-5704 for organic semiconductor materials
    • RoHS compliance (lead, heavy metal traceability)

    Typical usage ratio

    • 0.5–3% molar composition depending on the final dye or ligand loading in target OLED precursors, adjusted by electronic performance requirements

    Downstream process integration

    • Fed as a monomer during Buchwald-Hartwig amination or Suzuki-Miyaura cross-coupling for small molecule and polymer backbones
    • Final purification by preparative column chromatography or recrystallization

    Final product types

    • OLED emitter molecules
    • Electron-transporting materials for display panels

    4. Specialty Polymer and Resin Modification

    4-(4-Pyridinyl)Benzaldehyde supports custom polymer synthesis as an aromatic comonomer or functional chainstopper. It modifies surface polarity or UV-absorptivity of advanced resins, especially those based on aromatic or heterocyclic systems. End-users incorporate it during controlled solution polymerization or polycondensation, enabling property fine-tuning for optical and protective coatings.

    Industry compliance standards

    • ISO 14001 for environmental management
    • ASTM D2583 for hardness of polymer matrices
    • REACH SVHC registration (substance validation for Europe)

    Typical usage ratio

    • 0.1–2% by mass for property-modifying comonomer; higher ratios possible for chain termination or UV-absorptive enhancement

    Downstream process integration

    • Dosed into the reaction flask with other monomers during the initial mixing phase of resin synthesis
    • Followed by in-situ monitoring and viscosity control to prevent over-crosslinking

    Final product types

    • High-performance specialty coatings
    • UV-cured resins for electronics encapsulation
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    Certification & Compliance
    More Introduction

    Introducing 4-(4-Pyridinyl)Benzaldehyde: Hands-on Experience from the Manufacturer’s Bench

    A Chemical Built for Precision in Research and Synthesis

    Anyone who has spent time in a chemical plant knows quality comes down to what gets measured, tracked, and directly controlled. 4-(4-Pyridinyl)Benzaldehyde, with CAS number 939-58-2, stands out as a cornerstone compound for anyone working in advanced organic synthesis, medicinal chemistry, or the development of custom intermediates. Our teams, from raw materials handling through finished product verification, have worked closely with this aromatic aldehyde across a wide range of scales, seeing it go from bench-top synthesis to kilogram orders for research and process innovation.

    Specifications You Can Trust—Because We Make It Ourselves

    We produce this compound in both analytical and preparative grades. Typical batches test at or above 99% HPLC purity, with any trace impurities listed clearly on the accompanying COA. The material appears as a pale yellow crystalline powder. Each lot moves through our in-house spectroscopy and chromatography setups—NMR, IR, and GC-MS. Moisture content stays below 0.3%, a figure our process engineers track from solvent swaps through every crystallization stage. We keep particle size distribution within a standard micron range, as judged by sieve tests at packing, which allows researchers to dose this aldehyde precisely without suffering unexpected solubility shifts or clumping in reaction vessels.

    Purpose-Built for Robust, Reproducible Chemistry

    This isn’t the kind of aldehyde you want to cut corners on, especially if your downstream application involves multi-step transformations, heterocyclic scaffold building, or functional group manipulations sensitive to substitution patterns and residual contaminants. The para-positioned pyridine ring gives the molecule a unique electronic character. It can act as a building block in synthesizing ligands for catalysis, fluorescent markers, and diverse bioactive compounds. Our technical specialists and QC chemists check every drum, with repeated batch analyses—not random spot checks—to ensure the molecule’s performance in grilled Suzuki couplings, Knoevenagel condensations, and metal-catalyzed cross-couplings under varying conditions. Researchers won’t face unexpected byproducts caused by excess formaldehyde, oxidation fragments, or inhomogeneous batches, issues that stall progress and eat up project budgets.

    Interpretation of Real-World Production Runs

    Scaling up from lab to plant floor is never as simple as adjusting ratios on paper. The most common challenge we’ve solved involves maintaining ring integrity during the Friedel–Crafts acylation process, especially when pushing batch sizes upward. Small deviations in temperature ramp or catalyst addition can drive impurity formation—something that shows up fast under LC-MS scrutiny. By sticking to batch records and rigorous in-process controls, we repeatedly nail purity markers and yield metrics demanded by medicinal, agricultural, and specialty polymer chemists.

    Our facility’s layout—where the pyridine protection operations physically separate from aldehyde formation—has reduced cross-contamination. Temperature-sensing systems and high-shear mixers, along with a closed-cycle purification approach, ensure product consistency year-round. Logistics teams coordinate with QC so that product only clears to warehouse when the sign-off forms reach verification. The result is a benzaldehyde with predictable reactivity and structural integrity.

    Why Form and Handling Matter in the Lab

    Field experience has taught us one truth: a chemist’s time shouldn’t be wasted fighting with batches that lump, stick to glassware, or dissolve unpredictably. Raw materials shoot down productivity when they’re inconsistent from drum to drum. Our process engineers focus on granularity and flow to help researchers avoid delays. Whether you’re weighing out by spatula or running through automated powder feeders, this product remains free flowing.

    Because storage conditions vary, we seal every batch in high-barrier, tamper-evident packaging filled with low-permeability liners. This matters for anyone setting up air-and moisture-sensitive reactions. The crystalline form holds stability for at least a year under ambient storage, longer if kept under nitrogen or argon. Our own in-house studies have seen performance metrics hold steady even after weeks on the shelf—no dulling of the aldehyde signal by NMR or loss of functionality in electrophilic coupling.

    Application-Driven Feedback—From Our Lab, Not Just on Paper

    Most of our technical advances come from feedback loops between bench chemists and plant operators. We’ve worked alongside leading research teams developing kinase inhibitors, photoinitiators for advanced coatings, and molecular probes. In our Pd-catalyzed cross-coupling application reports, 4-(4-Pyridinyl)Benzaldehyde enables concise route design thanks to its reliable, clean reactivity. There’s little downtime spent troubleshooting side reactions due to unwanted methylation or decarboxylation, as can happen with less controlled starting materials.

    In actual use, researchers show appreciation for this aldehyde’s performance in step-growth polymerizations, combinatorial library synthesis, and fragment-based lead discovery. The difference: reliable lot-to-lot uniformity translates directly into fewer failed runs and cleaner purification. We consistently field technical inquiries from users wanting expanded analytical data—spectra, stability profiles, kinetic logs—which we’re able to provide from our own SOP-validated reserves. This isn’t dusty paperwork pulled from the archives; it’s current, actionable insight from today’s batches.

    Solving Pain Points Common in the Supply Chain

    Chemists in both academia and industry often tell us about delays from unreliable deliveries, supply interruptions, or subpar purity in the specialty aldehyde market. We’ve built direct shipping protocols with real-time batch tracking, so no one harried by project deadlines needs to chase down missing stock or wait for a long chain of resellers to untangle paperwork. There’s not a week that passes when someone doesn’t call about expedited delivery for time-sensitive pilot programs.

    By maintaining both made-to-order and reserve inventory structures, we can support sudden surges in demand. Our on-site logistics teams collaborate daily with the synthesis floor, ensuring communication doesn't bottleneck at the ERP stage. This has consistently translated to faster turnaround and repeatable stocking cycles for long-term partners needing scheduled deliveries or tight timelines. Our packaging design anticipates lab realities—both small-volume trial orders and multi-kilogram synthesis runs get tailored handling protocols.

    What Sets 4-(4-Pyridinyl)Benzaldehyde Apart From Other Aromatic Aldehydes

    Some might rely on off-the-shelf benzaldehydes or similar derivatives with random substituents. We’ve watched batches of lower-purity aldehydes introduce headaches during purification and stall sequence assembly. The electron-rich aromatic system and defined heterocyclic substitution here tunes reactivity and compatibility across a wide spectrum of synthetic applications. Where simple benzaldehyde or ortho-substituted analogues fall short—due to their higher propensity for polymerization or runaway side product formation—this compound preserves fidelity. Electrophilic addition and substituted ring anchoring stay smooth, even under challenging catalytic or nucleophilic protocols.

    Data from internal QC and hundreds of partner labs reflect fewer batch-to-batch inconsistencies in spectral signatures compared with similar aldehydes sourced from distributors. The specialized synthesis route—developed in-house—skips legacy contaminants like residual chlorides or N-oxides, which we’ve tracked as culprits in previous generation materials. By knowing where the pitfalls lie (because we’ve encountered and solved them ourselves), final product quality speaks to years of process optimization.

    What the Data—and Customer Experience—Reveal

    Over the years, feedback from pharmaceutical teams, specialty chemical startups, and academic researchers shapes how we troubleshoot both product and service. They value not just purity numbers but robust documentation—traceable, validated, up-to-date. Our digital COAs include not only analytical results but also batch-specific performance logs, which we store for up to five years. A recent case with a medicinal chemistry team needing gram-scale custom syntheses prompted us to revise crystallization cycles and solvent switching protocols, yielding even cleaner spectra and better thermal handling. The learning never stops, and our focus on continuous improvement means new lots roll out based on real-world feedback, not static SOPs.

    Technical support doesn’t route through generic call centers. Our chemists and engineers interface directly with users, sharing both successes and troubleshooting tips. For instance, one group using the aldehyde in a multicomponent Ugi reaction reported residual base sensitivity—our technical staff offered on-the-spot guidance, rooted in hands-on process familiarity rather than generic, copy-paste recommendations. No amount of marketing makes up for boots-on-the-ground knowledge.

    Environmental and Safety Realities

    Manufacturing specialists know regulatory compliance and operator safety require more than checklists. Our facility adheres to local and international chemical management standards, not simply to pass audits, but also to eliminate cycle time delays and unplanned shutdowns. Careful attention to air handling, material traceability, and workplace training reduces incidents tied to hazardous byproducts or waste. We integrate environmental controls into process flows, from solvent reclaim to emission controls.

    Because 4-(4-Pyridinyl)Benzaldehyde carries the safety profile typical of aromatic aldehydes, all handling, from transfer to packing, occurs in closed systems with properly rated scrubbers and ventilation. Our in-plant teams have practiced spill response, first aid, and safe storage for every batch. We run regular reviews with local safety officers and continuously update SOPs as hazard data evolves. Environmental stewardship shows in our choice of green solvents for washing operations, energy recovery systems, and waste stream monitoring. Chemists relying on us receive material that meets the current standards—not outdated norms—because our credibility and theirs both ride on keeping regulatory confidence.

    The Manufacturer’s Perspective: Why Experience Beats Hearsay

    Catalogs and datasheets only tell part of the story. In reality, understanding how a compound behaves under varied reaction conditions, how it handles during storage and transport, and what steps minimize oxidized, hydrolyzed, or otherwise degraded lots, comes only from day-to-day contact. Our leadership team started out on plant floors. Several of us have run the very reactors, written process notes, and reoptimized protection group chemistry by hand. This background filters into every part of production—from sourcing to dispatch.

    We avoid shortcuts, not from a sense of formality but because the costs of rework, customer complaints, or failed reactions impact real research time. The fact that our batches show nearly undetectable levels of common side impurities isn’t a boast—it’s a reflection of chemists who care as much about results as their customers do. Teams in pharmaceuticals, agriculture, and advanced electronics come back to us because we solve problems directly, rather than sidestepping root causes.

    Potential Solutions to Industry-Wide Issues with Specialty Intermediates

    Experts often worry about the reliability of sourcing high-value aromatic aldehydes, especially where project timelines, purity demands, or regulatory documentation create bottlenecks. Our solution revolves around direct engagement with the user—expanding production not just on schedule, but according to shared technical objectives. By investing in local warehousing linked to regional shipping hubs, shipments avoid customs stalls or climate-induced degradation. Our technical support lines remain open through regular check-ins, sharing ongoing analytics and field performance as materials integrate into early-stage or scale-up workflows.

    We see opportunity in further automating in-process controls. Installation of real-time NIR and Raman probes on several crystallization lines now produces instant, actionable data before and after unit operations, granting a degree of control that used to depend on batch-end analysis. Investment in AI-driven tracking for production anomalies continues, with missed specs flagged before reaching final QC—significantly reducing rework rates over the past year. Partnerships with packaging suppliers help us stay ahead of shifting regulations around hazardous shipments, ensuring product reaches researchers in stable, regulatory-compliant forms every order.

    Compound Insights Gained From Decades of Plant-Floor Problem Solving

    In the end, every drum of 4-(4-Pyridinyl)Benzaldehyde embodies hard-earned progress—a product of dozens of trials, revisions, and the collective practical wisdom of our manufacturing crew. We’re in constant dialogue with partners, pushing progress both in product quality and service reliability. Real progress in specialty chemical manufacturing doesn’t happen in isolation; it emerges from honest feedback, iterative optimization, and respect for the challenges faced by anyone advancing research, production, or application of target compounds. The difference between a passable grade aldehyde and one that unlocks project milestones comes down to the expertise, care, and transparency that only direct manufacturing can deliver.