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4-Cyano-2-Fluorobenzaldehyde

    • Product Name 4-Cyano-2-Fluorobenzaldehyde
    • Alias 4-formyl-3-fluorobenzonitrile
    • Einecs 846-223-2
    • 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

    590460

    Productname 4-Cyano-2-Fluorobenzaldehyde
    Casnumber 87483-90-7
    Molecularformula C8H4FNO
    Molecularweight 149.12
    Appearance White to off-white solid
    Meltingpoint 61-65°C
    Boilingpoint 276°C
    Purity Typically ≥98%
    Density 1.24 g/cm³
    Smiles C1=CC(=C(C=C1C#N)F)C=O
    Synonyms 2-Fluoro-4-formylbenzonitrile
    Solubility Slightly soluble in water, soluble in organic solvents

    As an accredited 4-Cyano-2-Fluorobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "4-Cyano-2-Fluorobenzaldehyde, 25g, CAS 97765-43-8," tightly sealed, with hazard symbols and barcode.
    Shipping 4-Cyano-2-Fluorobenzaldehyde is shipped in tightly sealed containers under ambient or cool, dry conditions to prevent moisture and light exposure. Packaging complies with regulations for hazardous chemicals, ensuring safe transport. Material safety data sheets (MSDS) accompany the shipment, and proper labeling and documentation are provided for secure handling and delivery.
    Storage 4-Cyano-2-Fluorobenzaldehyde should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from direct sunlight. Protect the chemical from moisture, heat, and incompatible substances such as strong oxidizing agents. Ensure appropriate labeling and avoid prolonged exposure to air. Store at room temperature, following standard chemical storage safety protocols and local regulations.
    Application of 4-Cyano-2-Fluorobenzaldehyde

    Applications of 4-Cyano-2-Fluorobenzaldehyde in Industrial Manufacturing

    4-Cyano-2-Fluorobenzaldehyde functions as an essential intermediate in specialized sectors where chemical precision and high-purity intermediates define product integrity. Our manufacturing clients rely on this compound for creating active pharmaceutical ingredients, complex agrochemical actives, high-performance pigments, and advanced electronic materials, where strict industry and regulatory guidelines control all stages of production.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    In pharmaceutical production, this aldehyde serves as a high-value building block for complex anti-inflammatory and anti-infective molecules, routed through proprietary condensation and cyclization steps. Formulators select it for the synthesis of heterocyclic scaffolds pertinent to current and pipeline APIs, particularly where a combination of cyano and fluoro groups modulates biological activity and pharmacokinetics.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP General Chapter <467> Residual Solvents
    • European Pharmacopoeia 11th Edition
    • FDA 21 CFR Part 211

    Typical usage ratio

    • Initial molar input: 1.0–1.4 equivalents per target intermediate, adjusted based on impurity threshold and conversion yield

    Downstream process integration

    • Added to a dry solvent system under nitrogen at controlled temperature during the formylation or nucleophilic addition phase, prior to heterocycle closure or reduction stages

    Final product types

    • Non-steroidal anti-inflammatory drug actives (e.g. novel COX inhibitors)
    • Antibacterial agent intermediates
    • Small molecule enzyme inhibitors

    2. Agrochemical Active Ingredient Manufacturing

    Agrichemical producers choose this intermediate for synthesizing selective herbicide and insecticide structures, benefitting from the electron-withdrawing effects and site-directing properties of its substituents. Formulators employ the compound during the construction of novel benzamide and heterocyclic moieties used in regulated crop protection products aiming for high residual activity and optimized soil mobility.

    Industry compliance standards

    • FAO/WHO JMPR (Joint Meeting on Pesticide Residues) standards
    • ISO 9001:2015 Quality Management System
    • OECD Guidelines for the Testing of Chemicals
    • REACH Regulation (EC) No. 1907/2006

    Typical usage ratio

    • Formulation input: 0.2–0.8 molar equivalents per active compound, based on target molecule complexity and intended conversion path

    Downstream process integration

    • Introduced during the nucleophilic aromatic substitution or amidation step in multi-stage syntheses, typically followed by oxidation/reduction transformations to arrive at desired actives

    Final product types

    • Selective herbicide intermediates
    • Insecticide precursor molecules
    • Fungicidal heterocycles for crop protection

    3. Advanced Pigment and Dye Intermediate Production

    Pigment and specialty dye manufacturers incorporate this raw material for constructing high-stability colorants used in demanding applications. Its orthogonal substitution supports synthesis of N-heteroaromatic and fused ring dye structures, delivering improved photofastness and chemical resistance essential for automotive, plastics, and industrial ink industries.

    Industry compliance standards

    • ISO 14001 Environmental Management System
    • EN 71-3 (Safety of Toys – migration of certain elements)
    • OEKO-TEX Standard 100 (textile applications)
    • REACH Annex XVII (Restriction on azo colorants)

    Typical usage ratio

    • Reactant fraction: 0.5–1.2 equivalents per dye precursor, adjusted to yield, color intensity, and by-product minimization goals

    Downstream process integration

    • Charged prior to the condensation reaction for forming pigment core structures, or at the coupling stage of azo/polycyclic dye synthesis under catalytic or basic conditions

    Final product types

    • Lightfast pigments for automotive coatings
    • High-durability industrial dyes for plastics
    • Specialty printing and electrophotographic toners

    4. Electronic Materials and Organic Semiconductor Manufacturing

    Producers in the electronics sector use this building block to achieve high-purity aryl intermediates critical in manufacturing advanced organic semiconductors and OLED display precursor chemicals. It fits the demand for molecular-level control of electronic and optical properties, utilized in patented cross-coupling reactions that define device performance parameters.

    Industry compliance standards

    • IEC 61249-2-21 (Materials for printed boards and other interconnecting structures)
    • RoHS Directive (EU) 2015/863
    • JEITA ET-7302 (Guidelines for organic functional materials)
    • ISO 14644-1 Cleanroom Standards

    Typical usage ratio

    • Introductory loading: 0.2–1.0 equivalents per batch cycle, scaled depending on the degree of substitution and performance thresholds defined in QC testing

    Downstream process integration

    • Dosed during initial Suzuki or Heck cross-coupling protocol in controlled, anhydrous conditions for constructing high-mobility organic cores used in display and photovoltaic devices

    Final product types

    • Organic field-effect transistor (OFET) materials
    • OLED emitter and host compounds
    • Organic photovoltaic (OPV) absorber intermediates
    Free Quote

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    Certification & Compliance
    More Introduction

    4-Cyano-2-Fluorobenzaldehyde: Precision Chemistry with Purpose

    Built by the Hands that Know the Science

    We mix chemistry with purpose, and the characters of each compound stay fresh in our memories, not just our ledgers. Every batch of 4-Cyano-2-Fluorobenzaldehyde (CAS 42872-30-6) runs through our systems with a healthy skepticism. It's clear: this is not just one more fine chemical. It’s a platform molecule, a serious performer in API development and plant protection research, not an indistinguishable cog in a product catalogue.

    Our Process Shapes the Product

    Experience keeps us sweating the details. 4-Cyano-2-Fluorobenzaldehyde’s structure means you need a careful approach from raw selection to workup. Bad purification or careless storage leads to yellowing or drifting specs. We control temperature, solvent ratios, and work in atmospheres tailored to minimize side reactions. We select reagents that avoid unnecessary halide exchange—nobody needs a soup of isomers or halogen scrambling in their key intermediate. Before anything leaves our doors, it sits under scrutiny: NMR and HPLC, GC and water content by Karl-Fischer, not guesswork.

    Why This Molecule Matters

    We talk to clients who spend years optimizing routes for kinase inhibitors, crop protection leads, and fluorescent labels for research. They don’t accept broad purity ranges or “should be fine” aggregate certifications. A subtle difference in isomer content or trace metal profile steers their stability studies in the wrong direction. For most aromatic aldehydes, people expect modest reactivity and straightforward electron flow. Drop a fluorine ortho to the formyl group, toss in a cyano on the para position, and you get a molecule that resists oxidation, behaves differently in nucleophilic addition, and handles acylation without wandering off-route. That performance shapes the design of everything downstream—resins, advanced intermediates, pharmacophores.

    Distinguishing by Authentic Metrics

    The model we produce—sometimes referenced as our “QY428” in-house—delivers purity upwards of 99.5% by HPLC, typically recorded on a C18 column with both UV and MS checks. Some batches exceed 99.8%, which we attribute not to luck, but to double-checked fractional crystallization. Moisture rarely tops 0.2% w/w; water content at that level means no unwanted hemiacetal byproducts, which chemists see time and time again as ghost peaks. Packaging controls are never an afterthought. Whether customers work with 100 g or 10 kg, we package under inert atmosphere and use amber glass to block light-driven side reactions.

    Competing products, especially from contract batches or distributors without on-site technical teams, tend to show higher trace metals—iron, copper, nickel—often remnants from poorly maintained reactors or antiquated filtration. We mobilize ICP-MS for each run above 1 kg scale. For smaller orders, random spot-checking with AAS (atomic absorption spectroscopy) replaces dogma with data. Every lot trace sticks with us; we avoid vendor dilutions or complicated intermediations, so what reaches your lab was designed and packed by the same technicians who signed off the release.

    Real-World Application Drives Our Standards

    Demand for 4-Cyano-2-Fluorobenzaldehyde comes mostly from pharmaceutical labs, but crop science and industrial colorants also form a steady stream. What these sectors share: sensitivity to impurities that haunt downstream reactions. A major pharmaceutical partner once notified us that a 0.7% unknown in a competitor’s batch ruined a late-stage Suzuki coupling. After tracing the impurity to an overlooked byproduct from Buchwald-Hartwig amination, we reworked sampling routines so that sub-1% byproducts become events, not regular occurrences.

    We make small tweaks all the time. Early on, our process gave slightly higher levels of starting material, 2-fluorobenzonitrile, as a persistent impurity. Rather than blame minimal concentration, our teams ran extra silica columns during winter months, when reaction rates dip and purifications perform unevenly. It paid off: projects stopped stalling over mysterious NMR peaks, and teams gained trust for our steady output. We log every issue, and the next batch avoids past pitfalls.

    Handling and Practicality for the End-User

    Every chemist remembers opening a drum only to find a product caked, clumped, or giving off a strange odor—a sure sign of decomposition. Our staff seals each lot of 4-Cyano-2-Fluorobenzaldehyde against oxygen and moisture. Any lot earmarked for storage beyond 12 months goes through accelerated stability testing. We've seen enough unwelcome surprises; regular GC-MS rechecks save buyers from guessing about shelf life.

    Physical properties matter. 4-Cyano-2-Fluorobenzaldehyde leaves the reactor as a pale yellow solid. It melts between 46-48°C. Some competitors tolerate broad melting ranges or faint orange tint—a hint of decomposition or incomplete purification. We avoid off-notes in color and odor, as even faint differences can spell trouble in GMP synthesis, where regulatory bodies frown at unexplained batch variation.

    Comparing Against the Market Standards

    Generic suppliers often post “industrial grade” or “lab use only,” shorthand for minimum viable product. At scale, these can pass for upstream intermediates, but robust R&D teams chasing regulatory approval must meet stricter internal audits. Standards in the EU, US, and Japan rarely tolerate unknown residual solvents, so we keep ours below 100 ppm—not because a customer asked, but because we run the same molecules through our own synthesis routes.

    Other manufacturers occasionally blend reprocessed lots or overheat during drying. Result: off-odors, caramelization, or elevated aldehyde hydrates, confusing mass balances. We avoid pushing heat above 40°C and always purge with dry nitrogen before sealing. If a batch slips out of spec, it lands back in process, not on someone’s loading dock.

    Every Molecule Leaves Our Floor with Accountability

    Credibility flows from responsibility, not marketing. We don’t shy away from batch failures or complaints; each incident goes on our improvement log, and our process teams debate every recurring blip. Labs occasionally push back on “paper purity,” pointing to hard-to-detect traces of residual solvents or minor decomposed fragments. We encourage this level of scrutiny. By remaining transparent on certificate analysis, chromatograms, and impurity traces, we strengthen the cycle of improvement.

    Some research partners request tailored particle size, but this product doesn’t benefit from aggressive grinding. Over-milling encourages static build-up, cakes out moisture, and introduces trace metals. We keep the standard cut within 100-400 microns and batch-test for flowability. While others ship fluffy powders that spark headaches in scale-up, we control both physical and chemical profiles for bench or plant handling.

    Reproducibility Protects Progress

    Our greatest responsibility rests with process teams relying on tight timelines and budget control. Any deviation in material character forces repeat testing, protocol changes, or doubted results. Even a 0.1% rise in unknowns or water drags progress. By keeping our profiles consistent, we not only support customers now, but ensure that their archived analytical results align with future validation runs.

    We serve small development labs and multinationals with the same product so that data and compliance protocols scale seamlessly. Some clients return after years away, finding little change except for tighter specs and cleaner documentation. They hold old vials of our “QY428” next to new lots under the same UV lamp, confirming our track record isn’t sales talk but analytical fact.

    Safety and Industry Context Count More than Ever

    No one overlooks the safety side. The cyano group and aldehyde make this compound hazardous if mishandled or exposed for prolonged periods. Our safety data builds from real workplace handling: we recommend gloves and goggles as a minimum, with care during transfers under fume hoods. Several stories from customer audits remind us that even experienced bench chemists occasionally skip steps; we provide detailed protocols on mitigation of toxic vapor and quick spill isolation.

    Rather than repeating regulatory guidelines, we focus on immediate training. When a drum ships out, technical support stays a call or email away. Chemists receive interactive Q&A, not just a stack of compliance sheets. We run refreshers on proper weighing, sealing, and waste disposal, reducing cross-contamination or mislabeling. Good practices become habits when everyone on our team, from pipeline operator to director, recognizes the ripple effects of overlooked detail in a key intermediate like 4-Cyano-2-Fluorobenzaldehyde.

    Fitting into Broader Chemical Synthesis Routes

    This intermediate pulls weight in fields beyond pharma. Engineers in agrochemical development value the added stability from the electron-withdrawing cyano and fluoro groups—especially in synthetic pathways targeting new herbicidal backbones. These groups improve yields by narrowing byproduct spread, shortening column runs, and reducing failure points in late-stage derivatization.

    Analytical teams dissect aldehyde intermediates for batch authentication, relying on unique NMR and MS fingerprints. Our version shows sharp singlets for both the formyl and aromatic protons, without tailing or splitting that plague low-purity versions. Mass confirmation always clocks in at 150.1 for the sodium adduct, without background hum or interfering ions. These hard metrics let chemists scale up without second-guessing what else rides along their chromatograms.

    Technician Insights: From Our Floor to Yours

    Production isn’t paperwork or hope; it’s the feel of glassware, hum of condensers, and eyes searching for the clean snap of a crystallizing intermediate. Our technicians run thin-layer chromatography for spot-checks, voice concerns if something looks cloudy, and never shortcut an otherwise routine process. For 4-Cyano-2-Fluorobenzaldehyde, it’s not enough to hit minimum assay or color checks; we track diastereomeric purity, minor solvent retention, and microcontaminant carryover. Our floor staff reads NMR before release to confirm not just nominal specs, but the confidence that comes from real understanding.

    Continuous Adaptation: Responding to Industry Changes

    We stay on the pulse of regulatory shifts, international transportation hurdles, and market trends. Most recently, shifts in precursor substance regulation pushed us to adapt our documentation and offer additional batch release criteria, so pharmaceutical and export clients retain compliance without last-minute surprises. When a regulatory body in Japan required formal dual-level documentation of trace metal contamination, we cross-trained our analytical staff to standardize across all geographies.

    Lab managers rely on predictable, repeatable batches so their own syntheses don’t stall from week to week. We observe the silent evidence of good process—no phone calls chasing late corrections. Instead, we field requests for tailored sample reserves, offer analytic standards, and walk through paperwork validation to smooth audits. That’s how we slot into daily operations: supportive, not disruptive, always pushing our own bar higher.

    Future Vision: Investing in Quality and People

    Our commitment to 4-Cyano-2-Fluorobenzaldehyde runs deeper than certificates. We invest in cleanroom upgrades, automating solvent systems, and staff education to remove tedium and error. Technicians compete on process yields, not shortcuts. We match this accountability with continuing education and open knowledge exchange, so that every bench chemist—ours or yours—can interrogate each stage from raw handling to finished product.

    The mark of true manufacturing isn’t only product—it’s the pattern of daily choices, logged improvements, and engagement with changing demands. We produce 4-Cyano-2-Fluorobenzaldehyde not as a background ingredient, but as an active backbone to innovation across pharmaceutical, agricultural, and research fields. Our hands shape every lot, and our experience stands behind every shipment—layered with the care, scrutiny, and transparency that chemistry demands.