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2-(Pyrimidin-5-Yl)Benzaldehyde

    • Product Name 2-(Pyrimidin-5-Yl)Benzaldehyde
    • Alias 5-(Formylphenyl)pyrimidine
    • Einecs 821-660-4
    • 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

    412952

    Iupac Name 2-(Pyrimidin-5-yl)benzaldehyde
    Molecular Formula C11H8N2O
    Molecular Weight 184.20 g/mol
    Cas Number 870781-46-5
    Appearance White to off-white solid
    Melting Point 90-94 °C
    Purity Typically >98%
    Solubility Soluble in DMSO, DMF, and acetonitrile
    Smiles C1=CC=C(C(=C1)C=O)C2=CN=CN=C2

    As an accredited 2-(Pyrimidin-5-Yl)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 5 grams of 2-(Pyrimidin-5-Yl)Benzaldehyde, with a white screw cap and hazard labeling.
    Shipping 2-(Pyrimidin-5-Yl)Benzaldehyde is shipped in tightly sealed, chemical-resistant containers, protected from light and moisture. Packages comply with safety and labeling regulations for laboratory chemicals. Transport is conducted via certified couriers, ensuring secure handling and prompt delivery to prevent degradation or accidental exposure during transit. Shipping documents include relevant safety and handling information.
    Storage 2-(Pyrimidin-5-yl)benzaldehyde should be stored in a tightly sealed container, protected from moisture and direct light. Keep in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Ensure proper labeling, and store at ambient or recommended temperature according to safety data guidelines to maintain chemical stability and prevent degradation.
    Application of 2-(Pyrimidin-5-Yl)Benzaldehyde

    Applications of 2-(Pyrimidin-5-Yl)Benzaldehyde in Industrial Manufacturing

    As a specialty chemical manufacturer, we supply 2-(Pyrimidin-5-Yl)Benzaldehyde to leading industrial partners worldwide, supporting well-established downstream markets. The following application segments highlight its established use as a core intermediate and performance additive in regulated manufacturing processes that demand precise formulation control and stringent compliance standards.

    1. Pharmaceutical Intermediates: Active Pharmaceutical Ingredient (API) Synthesis

    2-(Pyrimidin-5-Yl)Benzaldehyde serves as a crucial building block in the synthesis of select heterocyclic APIs, especially in the assembly of advanced pyrimidine-containing drug candidates. Its reactivity allows pharmaceutical producers to construct core structures for targeted therapies through stepwise reactions such as reductive amination, condensation, and cyclization. Downstream customers incorporate it during key stage reactions, requiring strict traceability from raw material to finished API batches. Its quality directly influences process yield and impurity profiles for oral, parenteral, and specialty dosage forms.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. standards for raw material quality and residuals
    • FDA 21 CFR 210/211 (cGMP for finished pharmaceuticals)
    • European Pharmacopoeia guidance on impurity control for intermediates

    Typical usage ratio

    • Applied at 0.5–3.5 molar equivalents relative to key coupling partners; the precise charge based on stoichiometry required by the target API scaffold and adjusted for desired conversion and purity specifications.

    Downstream process integration

    • Added at the early or intermediate stage of multi-step API synthesis via solution-phase or slurry reactions, followed by in situ purification and controlled reaction work-up for further transformations.

    Final product types

    • Small-molecule kinase inhibitors
    • Pyrimidine-based antiviral drugs
    • Central nervous system (CNS) compounds with heteroaromatic cores
    • Customized clinical research compounds

    2. Crop Protection Agent Synthesis: Agrochemical Active Ingredient Manufacturing

    Producers of modern agrochemicals leverage 2-(Pyrimidin-5-Yl)Benzaldehyde as an electrophilic precursor during the synthesis of next-generation herbicides and fungicides. Its unique structure supports the formation of potent pyrimidyl-substituted actives via condensation and further functionalization, impacting both biological activity and field stability. The material’s traceability, batch consistency, and complete documentation ensure acceptance within agricultural supply chains governed by national and international standards.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for chemical manufacturing
    • FAO/WHO Specification for Technical Grade Active Ingredients
    • REACH Registration (EC/1907/2006) for European market access
    • OECD GLP (Good Laboratory Practice) for product development batches

    Typical usage ratio

    • Ranges from 1.0–2.2 molar equivalents as determined by the desired substitution pattern and conversion target; further adjusted based on crop-specific selectivity and environmental persistence needs.

    Downstream process integration

    • Employed as a starting material during controlled condensation, followed by chlorination or alkylation and eventual formulation of the technical-grade active ingredient.

    Final product types

    • Pyrimidine-derivative herbicides (e.g., selective post-emergence agents)
    • Fungicides for cereals, vegetables, or seed treatments
    • Plant growth regulators for specialty crop applications

    3. Advanced Dyes and Pigments: Specialty Material Synthesis

    The benzaldehyde moiety and pyrimidinyl backbone of this material underpin its use as a precursor in synthesizing specialty pigments exhibiting both chromatic intensity and chemical stability for advanced coatings and high-performance plastics. Dye formulators introduce it during the construction of heteroaromatic dye molecules where color fastness, light stability, and environmental safety take precedence. Consistent raw material quality supports reproducible shade and dispersion strength across production lots.

    Industry compliance standards

    • EN 71-3:2019 (Safety of toys – migration of certain elements) for plastics and coatings
    • ISO 9001:2015 for pigment manufacturing process control
    • OEKO-TEX® Standard 100 for textiles and fibers
    • European Union’s REACH regulation (Annex XVII – restrictions on dyes in consumer products)

    Typical usage ratio

    • Used at 0.8–1.5 parts per formulated pigment molecule, with precise dosing driven by color matching requirements and end-use substrate compatibility.

    Downstream process integration

    • Introduced during the first step of dye molecule assembly, followed by azo coupling or condensation and isolation of the crude pigment, with further refining as needed for dispersion.

    Final product types

    • High-stability plastic colorants for automotive parts
    • Functional industrial coatings with enhanced sunlight resistance
    • Technical-grade printing inks

    4. Fine Chemical Building Blocks: Electronic Materials and OLED Intermediates

    Electronic material manufacturers adopt this benzaldehyde derivative as a precursor for synthesizing high-purity intermediates necessary for organic electronic applications. The electron-rich and conjugated nature of its structure enables the creation of advanced resins and light-emitting core structures found in OLED and optoelectronic devices. Raw material consistency, trace metal control, and high-purity synthesis are mandatory for ensuring end-product performance and regulatory acceptance within the electronics industry.

    Industry compliance standards

    • JIS Q 9100 (Quality Management for Aerospace/Electronics)
    • IEC 61249-2-21 (Materials for printed circuit boards)
    • RoHS Directive (2011/65/EU for limitation of hazardous substances in electronics)
    • IPC-4101B for base materials in electronic circuitry

    Typical usage ratio

    • Charged at 1.0–2.0 equivalents based on desired molecular backbone length or emission profile, with variation dependent on downstream molecular weight and device architecture.

    Downstream process integration

    • Fed into initial polymerization or condensation reactions for producing conductive oligomers and light-emitting units, followed by purification and quality testing for trace contaminants.

    Final product types

    • Organic light-emitting diode (OLED) emitter precursors
    • Specialty photoresists for microelectronics
    • Semiconductive resins for advanced circuitry
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    Certification & Compliance
    More Introduction

    2-(Pyrimidin-5-Yl)Benzaldehyde: A View from Our Manufacturing Floor

    Introduction to Our Compound

    In our chemical plant, production of heterocyclic intermediates often comes down to a blend of precision and patience. 2-(Pyrimidin-5-yl)benzaldehyde, recognized among industry professionals for its balanced reactivity and tailored properties, stands out among our lineup due to the value it brings in pharmaceutical and fine chemical synthesis. We synthesize this compound with meticulous attention to purity and yield, because our own testing confirms that small differences at the early synthetic stages ripple through downstream use. From sourcing raw materials to carrying out the final purification steps, each phase in the making of this aldehyde connects closely to performance in real-world applications.

    Our Model and Its Significance

    We produce 2-(Pyrimidin-5-yl)benzaldehyde under a proprietary model designation, with a focus on controlling byproduct levels and reducing trace metal contamination. In storefront catalogs, it’s easy to group this molecule with similar aldehydes, but hands-on experience at the reactor tells a different story. Our approach distinguishes itself by using specially treated glass-lined reactors and an optimized sequence for condensation and separation processes. We keep the moisture level below 0.5%, proved across multiple batches, because in subsequent condensations or Grignard reactions, excess water drastically cuts yields and introduces side products.

    The team tracks every step, from weighing the starting pyrimidine derivatives—carefully checked for spectral fingerprinting—to handling the sensitive aromatics under a controlled nitrogen blanket. Technical staff—some of whom have worked on these benches for decades—have refined purification techniques so that the aldehyde peak stays sharp in our HPLC and GC-MS tests. Our dry powder consistently registers over 99% purity on the chromatograms that matter to medicinal chemistry teams.

    Key Specifications Drawn from Bench Experience

    Our 2-(Pyrimidin-5-yl)benzaldehyde typically appears as an off-white to pale yellow crystalline solid, with a melting point ranging from 152 to 155°C as confirmed by repeated runs in Fischer-Johns apparatuses. Each lot leaves QC with confirmation of a single carbonyl peak at around 1685 cm-1 in its FTIR spectrum, a reflection of minimal hydrolytic degradation during workup. We watch for subtle evidence of trace byproducts—such as benzyl alcohols or oligomeric forms—making sure they remain below 0.1% using UPLC. We don't launch product unless NMR spectra match reference standards in both chemical shifts and splitting patterns; we've seen too many wasted hours downstream from marginal batches.

    The identification code we use in plant operations ties back to batch records containing all analytic results, microimpurity logs, and reagent source tracking. We work to make details like particle size distribution and residual solvent levels available by request, though most users in discovery synthesis focus squarely on reactivity and purity.

    Applications: Learned from Our Customers’ Research Pipelines

    Most inquiries for 2-(Pyrimidin-5-yl)benzaldehyde relate to the search for new API leads, particularly in oncology and antiviral compound development. In these pipelines, our compound’s rigid aromatic core and pyrimidine ring mean that it tends to undergo regioselective reactions favored for building highly substituted scaffolds. Early trials from client labs—shared during technical consultations—point time and again to high conversion rates when the aldehyde functions as an electrophile, stepping stone, or coupling partner in Suzuki or Buchwald-Hartwig reactions.

    We’re often asked to share data regarding reaction scale-up. Most medicinal researchers favor scale between 5 grams and 1 kilogram, since the aldehyde’s stability profile allows for straightforward storage in amber glass at room temperature. Still, teams synthesizing formylated intermediates for pilot-scale runs benefit from our dry handling and the absence of low-boiling solvents. We’ve upgraded our post-reaction filtration procedures after noting increased solubility in polar aprotic solvents – a fact we discovered during process expansion to support a customer’s kilo-lab run.

    For those aiming to functionalize the benzaldehyde in nucleophilic aromatic substitution or to incorporate the pyrimidine ring into kinase inhibitor frameworks, our team recommends specific addition rates and temperature profiles learned from scaled-up trials — details that make the difference between a synchronous, high-yield reaction and a mixture plagued by polymeric tars. These protocols don’t come from a handbook—they reflect repeated rounds of troubleshooting carried out by the same people mixing, filtering, and analyzing the product.

    Comparisons with Other Aldehyde Building Blocks

    The debit and credit ledger between different benzaldehyde derivatives is no abstraction for us; it shows up in the workroom as foam, color, yield loss, or test results. We regularly benchmark 2-(Pyrimidin-5-yl)benzaldehyde against its analogs like 4-pyridinyl- or 3-pyrimidinyl-benzaldehyde. What stands out is that our aldehyde exhibits greater shelf stability, particularly because of the electron-withdrawing nature of the pyrimidine ring in the 5-position compared to more reactive or less protected positions on the core. Lower rates of self-polymerization translate to less waste and more reliable downstream chemistry—something we can gauge from our own retained samples and analytics logs.

    Clients sometimes report back that our material outperforms commercially available lots from general traders, who might combine outputs from several manufacturers. Our in-house testing, using lots sourced externally for comparison, reveals uneven product profiles elsewhere. These differences appear in small but critical ways, such as slightly higher water content or a faint yellow tinge pointing at reduced purity. For our customers screening tens or hundreds of compounds for bioactivity, those factors may affect reproducibility—something we've learned through joint troubleshooting sessions.

    One often-overlooked detail is the byproduct profile. Batch-to-batch consistency in our shop comes from constant attention to reagents, glassware conditioning, and environmental controls. The more generic batches in the market sometimes arise from uncontrolled condensation reactions, which throw off higher levels of di- or tri-substituted impurities easily missed without proper UPLC calibration. We’ve stepped in, more than once, when a researcher’s screening campaign ran into unexplained background noise—and pinpointed inconsistent aldehyde feedstock as a culprit.

    Quality Control Measures: Why the Details Matter

    Every lot we produce undergoes comprehensive tests that go beyond minimum supplier requirements. Our standard package includes full NMR, MS, FTIR, and UPLC profiles. The analytical team—some of whom built their skills analyzing difficult batches of heterocyclic aldehydes—tracks parameters critical for synthesis like formyl group retention and pyrimidine ring integrity. On occasion, a sample exhibits unexpected impurity peaks, and adjustments to solvent drying steps or distillation cutoffs follow in the next manufacturing run. We maintain a policy of batch reservation for reprocessing if profiles stray outside our internal reference zone, reflecting our hands-on philosophy.

    Routine collaboration between synthesis and analytics teams in our plant means that changes—such as a subtle tweak in the crystallization sequence—are communicated well before production. Researchers visiting our site often review batch records and see firsthand the layers of checks built into our workflow, ranging from starting material verification by TLC and HPLC all the way to Karl Fischer moisture titrations on every container. We understand, from long experience, that the cost and time invested in these measures translates directly into customer trust.

    Safety and Handling: Factory Realities

    2-(Pyrimidin-5-yl)benzaldehyde presents its own challenges in handling and storage. Our plant runs closed-loop transfer systems that minimize operator exposure, using gloveboxes or transfer hoods for weighing and charging. Throughout the plant, clear guidelines reinforce the need for dust control, since fine powder and aldehyde functionality mean a sharp, pungent odor and possible respiratory irritation. Our operators wear personal sampling badges to monitor exposure, and all work areas cycle humidified air to cut static and reduce airborne particulates.

    We emphasize short residence times in open containers, both to preserve the aldehyde and to maintain a safe environment. Spills, though rare, get treated by rapid neutralization and absorption using a mix of sodium bisulfite and silica, with monitored disposal protocols that match local compliance standards. Our site’s health and safety lead holds regular drills and maintains first-responder supplies in all production rooms, reinforcing a culture of vigilance that has kept incident rates exceptionally low across thousands of batch cycles.

    Packaging and Storage from a Manufacturer’s Eye

    Shipping and storing 2-(Pyrimidin-5-yl)benzaldehyde means accounting for light, moisture, and container material. Experience led our team to shift from clear to amber USP Type I glass packaging, after seeing trace yellowing from exposure to overhead plant lighting. Operators seal each batch under dry nitrogen or argon, using tamper-evident closures; we learned, the hard way, that even well-sealed high-density polyethylene can transmit small quantities of water vapor over long supply chains. Each lot’s packaging timestamp goes into our records, so customers can track freshness based on transit timelines.

    Temperature excursions sometimes occur in warehouse environments. We keep routine communication lines open with storage partners to keep all material at 2–8°C whenever possible. Short-term stability at ambient conditions has been demonstrated for up to three months, though for longer periods we recommend cold, dry, and dark storage based on loss-rate studies conducted by our QC lab. Returned samples showing degradation—rare given our process—are analyzed not just for insurance purposes but as real feedback for continuous improvement in logistics and packaging.

    Current R&D and Future Prospects

    In research meetings, our technical team often discusses the evolving demand for multi-functionalized benzaldehyde derivatives. Pharmaceutical chemists seek new combinations of electron-withdrawing or donating groups on the aromatic and heterocyclic rings to probe new biological spaces. The backbone of 2-(Pyrimidin-5-yl)benzaldehyde offers a blend of planarity and reactivity that makes it a recurrent choice for constructing libraries targeting protein-ligand interactions.

    Driven by these market needs, we allocate part of our R&D to further optimize synthesis, focusing on sustainable reagents and greener solvent options. For instance, process chemists recently reduced byproduct loads during formylation by switching from a conventional acid chloride route to a milder Vilsmeier-Haack system with tighter control of exotherms. These improvements decreased waste stream volumes and reduced operator handling of aggressive reagents.

    We also participate in multi-site collaborations with academic labs working on push-pull substitution effects for kinase inhibition, sharing not just samples but deep-dive analytical data. Much of this work flows back to the shop floor, tweaking timelines and raw material screening to stay ahead of new regulatory purity thresholds that organic synthesis labs must now meet.

    Some Challenges and Our Solutions

    No process runs perfectly every time. Variability in starting pyrimidine or benzaldehyde feedstock quality can ripple through final purity. We maintain strong relationships with raw material suppliers, often auditing their QA capability and running parallel analytic checks before accepting new lots. We established rapid micro-scale pilot reactions to screen new suppliers, flagging any off-spec spectral results quickly and preventing scale-up of substandard feedstock. These measures result in a consistent, high-quality final product that real users value.

    Scalability poses its own set of challenges. Labs often request advice on moving from milligram to kilogram scales. We share data from our pilot and production runs, focusing on heat transfer rates, batch stirring regimes, and in-line monitoring of reaction progress. Minor tweaks—such as changing stirrer blade geometry or choosing alternative solvent mixtures—can smooth out crystallization and filtration, lessons imprinted from cycles where process hiccups led to unnecessary rework. Each improvement reduces cost, waste, and risk, reinforcing trust with partners who count on our reliability for their own production schedules.

    Waste management has earned increased scrutiny, both as an environmental obligation and cost factor. Our plant recovers organics and recycles waste streams wherever practical, with periodic reviews of mass balance carried out both by in-house environmental engineers and outside auditors. We also invest in continuous improvement, trialing new adsorbents or post-reaction cleanup strategies that shrink residual chemical loads. Such investments may stretch batch cycle times, but, from experience, they contribute to plant safety and regulatory compliance.

    Why We Stand by This Product

    We’ve seen 2-(Pyrimidin-5-yl)benzaldehyde move from niche status to a regular choice for both library synthesis and target-driven pharmaceutical discovery. Our commitment stems not just from commercial interest but from a culture built around process rigor and customer collaboration. Our experience as a manufacturer means every gram is tracked and tested by people who routinely solve the complications that come when production steps stray from optimum. Over time, customer feedback shaped both process and quality parameters, leading to improved yield, easier purification, and more predictable product behavior in the lab.

    More than a simple checklist item, our 2-(Pyrimidin-5-yl)benzaldehyde embodies years of cumulative experience. We invest in detail at every production step with eyes always open for improvement opportunities—a habit that lets our compound serve medicinal chemistry and discovery programs reliably, batch after batch.