Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

4-Fluoro-3-Nitrobenzaldehyde

    • Product Name 4-Fluoro-3-Nitrobenzaldehyde
    • Alias 4-fluoro-3-nitrobenzaldehyde
    • Einecs 697-805-4
    • 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

    830957

    Productname 4-Fluoro-3-Nitrobenzaldehyde
    Casnumber 446-84-6
    Molecularformula C7H4FNO3
    Molecularweight 169.11
    Appearance Yellow to orange solid
    Meltingpoint 42-46°C
    Density 1.49 g/cm3
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=CC(=C(C=C1F)[N+](=O)[O-])C=O
    Inchi InChI=1S/C7H4FNO3/c8-6-2-1-5(4-10)7(3-6)9(11)12/h1-4H

    As an accredited 4-Fluoro-3-Nitrobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, screw cap, chemical label with hazard symbols; contains 25 grams of 4-Fluoro-3-Nitrobenzaldehyde, stored securely.
    Shipping 4-Fluoro-3-Nitrobenzaldehyde is shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. Packages comply with regulatory requirements for hazardous chemicals. Proper labeling ensures safe handling and transport. Shipping is conducted by authorized carriers specializing in chemical logistics, maintaining appropriate temperature and safety protocols to prevent spills, leaks, or degradation during transit.
    Storage 4-Fluoro-3-nitrobenzaldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents and strong bases. Protect from light and moisture. Proper chemical labeling and secondary containment are recommended to prevent leaks or spills. Wear appropriate personal protective equipment when handling.
    Application of 4-Fluoro-3-Nitrobenzaldehyde

    Applications of 4-Fluoro-3-Nitrobenzaldehyde in Industrial Manufacturing

    4-Fluoro-3-Nitrobenzaldehyde serves as a critical intermediate in several high-value chemical transformations across pharmaceutical, agrochemical, and specialty material industries. As the original manufacturer, we ensure material purity, documentation, and batch consistency for demanding downstream synthesis environments.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers typically select 4-Fluoro-3-Nitrobenzaldehyde as a starting material for the synthesis of fluorinated heterocycles and substituted aniline derivatives, supporting the production of advanced active pharmaceutical ingredients. The nitro and fluoro substituents facilitate regioselective reactions, especially in Suzuki, Heck, and reductive amination processes, with precise documentation for DMF filings and GMP batches. Our material supports validated multi-step campaigns under controlled cGMP environments, where traceability and impurity profile critically affect the final drug registration. Integration usually occurs at the early-stage functionalization step, where both electronic and steric effects are exploited to control downstream selectivity and purity. Analytical support ensures compliance with monograph requirements and ICH Q3A thresholds for genotoxic impurities.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211: Finished Pharmaceuticals
    • Ph. Eur. and USP specification adherence for intermediates
    • Controlled Substances Precursors—national regulations as applicable

    Typical usage ratio

    • 0.8–1.2 mole equivalents for stepwise condensations
    • Adjusted according to target yield and process mass intensity (PMI)
    • Verified by HPLC and NMR to maintain sub-ppm residual levels in final APIs
    • Variability driven by process scale-up and batch-to-batch revalidation

    Downstream process integration

    • Introduced during Grignard or nucleophilic aromatic substitution stages
    • Participates directly in reductive aminations and fluorinated building block assembly
    • Controlled via in-process analytical technology (PAT) at reaction and work-up
    • Impurity carry-over managed through phase separation and solvent extraction protocols

    Final product types

    • Quinolone antibiotics (fluorinated analogs)
    • Antiviral small molecule actives
    • Pyridine and imidazole-based kinase inhibitors
    • Pilot-scale clinical intermediates and registered starting materials

    2. Agrochemical Active Ingredient Production

    Leading crop protection companies rely on this raw material to build prefunctionalized benzaldehyde scaffolds for selective herbicides and insecticides. The electron-withdrawing nitro and fluoro groups support fine-tuning of biological activity and target selectivity, crucial in the synthesis of nitroaniline and benzoxazole derivatives often found in novel agrochemical actives. Manufacturing lines integrate this intermediate in early-stage coupling, where process engineers monitor solubility and reactivity to prevent by-product formation. Compliance with local and multinational chemical registries ensures that the end molecules meet regulatory audits for field trials and global registrations.

    Industry compliance standards

    • FAO/WHO Technical Specifications for Plant Protection Products
    • REACH registration (EC No. 1907/2006, EU)
    • US EPA Pesticide Registration requirements
    • ISO 9001 certified quality management systems

    Typical usage ratio

    • 10–20% molar excess in nucleophilic aromatic substitutions for target scaffold generation
    • Ratio tuned by process chemists based on downstream conversion to benzoxazole and pyridyl groups
    • Higher percentages applied in pilot-scale runs for impurity mapping
    • Adjusted as per impurity control during scale transfer

    Downstream process integration

    • Used as the primary aromatic aldehyde in condensation with amines/amide derivatives
    • Highly monitored in flow chemistry modules to maintain uniform batch profile
    • Integrated into automated batch reactors for continuous processing of agro intermediates
    • Final purification accomplished via crystallization or liquid-liquid extraction

    Final product types

    • Benzoxazole-based herbicides
    • Nitroaniline-derived insecticides
    • Seed treatment chemicals
    • Soil-active fungicidal intermediates

    3. Dye and Pigment Intermediate Manufacturing

    Industrial dye manufacturers incorporate this benzaldehyde derivative to synthesize specialty azo and anthraquinone dyes, especially those requiring tailored absorption spectra for high-performance textile or ink applications. The material enters key condensation or coupling processes, imparting both electron-deficient character and enhanced photostability to the resulting chromophores. Our process experts support downstream partners with purity guidance to minimize color impurities. In continuous dye production, consistency and predictable reactivity are essential for reproducible batch color metrics and resistance properties.

    Industry compliance standards

    • Oeko-Tex Standard 100—chemical input control
    • ETAD (Ecological and Toxicological Association of Dyes and Pigments Manufacturers) guidelines
    • ISO 9001 process documentation
    • REACH substance registration for pigments

    Typical usage ratio

    • Varies from 2–10% by mass in condensation feeds based on target chromophore structure
    • Adjusted according to molar balance for chromogenic depth and purity
    • Optimization based on colorimetric QC for L*a*b* value consistency
    • Final ratio controlled upstream to limit residual impurity impact

    Downstream process integration

    • Feedstock in diazonium salt coupling to form azo linkages
    • Precursor in Friedel–Crafts acylation or nucleophilic aromatic substitution stages
    • Metered addition in continuous stirred tank reactors (CSTRs)
    • Purified via liquid chromatography before blending into dye or pigment formulations

    Final product types

    • Fluorinated azo dyes for synthetic fiber coloration
    • Inkjet printer pigment dispersions
    • High-fastness textile dyes
    • Photo-stable plastic colorants

    4. Specialty Fluorinated Polymer Additive Formulation

    Producers of high-performance polymers and specialty materials use this compound to introduce polar and fluorinated groups during the synthesis of advanced resin or copolymer additives. Often, the aldehyde serves as a functionalizing agent for post-polymerization modification, imparting improved solvent resistance or unique dielectric properties to engineering plastics. The chemical handles enable grafting onto polymer backbones or cross-linking in situ, where formulating chemists adjust the lading to control end-use performance, such as adhesion, thermal stability, or fluorine content.

    Industry compliance standards

    • RoHS 2011/65/EU compliance for electronics plastics
    • UL 94 standards for flame retardancy
    • ISO 14001: Environmental management in chemical processing
    • NIOSH and OSHA standards for in-plant safety

    Typical usage ratio

    • Typically 1–5% by mass in resin modification stages, dependant on target F-content
    • Process engineers may increase up to 8% for specialty dielectric or barrier formulations
    • Dosage optimized to limit effect on polymer mechanical properties
    • Ranges smaller for end-use in automotive or electronics insulation compounds

    Downstream process integration

    • Employed in batch or continuous solution polymerization
    • Incorporated during in situ functionalization of acrylate or epoxy resins
    • Grafted onto chains via aldehyde-amine or aldehyde-hydrazide chemistry
    • End-use polymers pelletized and functionalized before extrusion or molding

    Final product types

    • Fluorinated polyester and epoxy materials for electronics
    • Surface-modified films for technical membranes
    • Custom fluoropolymer masterbatches
    • Flexible cable jackets with enhanced thermal and solvent resistance

    5. Fine Chemical Building Block Production

    Custom synthesis firms and fine chemical manufacturers use this aldehyde as a key building block in the development of reference standards, analytical probes, and development-stage small molecules for research use. The unique substitution pattern supports the assembly of complex aromatic systems, where product managers specify physical and spectral specifications to match high-purity requirements for analytical and scale-up work. Process chemists depend on lot-to-lot consistency to support structure–activity relationship studies, where any impurity or batch variation distorts target screening data. We provide batch-level support and additional purification on request to meet the grade required by analytical, development, and preclinical environments.

    Industry compliance standards

    • ISO 17034: General requirements for the competence of reference material producers
    • GLP (Good Laboratory Practice) for research intermediates
    • Analytical method validation guidelines (ICH Q2)
    • REACH substance tracking requirements

    Typical usage ratio

    • Variable, typically 0.5–5 mmole scale for analytical reference preparation
    • Up to 20 mmoles for pilot research campaigns
    • Final usage defined by stoichiometric needs of model compound or standard synthesis
    • Controlled both gravimetrically for accuracy and analytically for traceability

    Downstream process integration

    • Serves in initial coupling or derivatization for analytical standard preparation
    • Applied in multistep routes for tool compound library synthesis
    • Sampling and aliquoting supported by full COA and spectral documentation
    • Enters custom purification pipelines prior to customer shipment

    Final product types

    • Spectroscopic and chromatographic reference standards
    • Structural analogs for assay calibration
    • Intermediate for model compounds in SAR studies
    • Preclinical probe molecules
    Free Quote

    Competitive 4-Fluoro-3-Nitrobenzaldehyde prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    4-Fluoro-3-Nitrobenzaldehyde: Precision Chemistry From the Manufacturing Floor

    Introduction to 4-Fluoro-3-Nitrobenzaldehyde

    Every batch that leaves our plant tells the story of methodical synthesis and years of accumulated technical learning. 4-Fluoro-3-Nitrobenzaldehyde, recognized by chemists for its nuanced reactivity, comes from a process designed for reliability on the bench and at scale. We know its chemical structure — a fluoro group at the para-position and nitro at meta — shapes its applications and gives it an edge over simple benzaldehydes. Years of process tweaks taught us small impurities or instability can stall a whole campaign. Even basic chlorination or nitration steps look easy until you’re running them on hundreds of kilograms. That’s a lesson you only have to learn once.

    Specifications and Model: Practical Choices that matter

    In our line-up, 4-Fluoro-3-Nitrobenzaldehyde (CAS 348-98-5) sits in the basket of highly functionalized benzaldehydes. Typical batches run at a minimum purity of 99 percent by GC, with water routinely below 0.2 percent. In practice, we often see an even tighter spread — our regular customers know to expect testing sheets clipped to every drum. This transparency isn’t for show; it follows from real pushback years ago, when a single contaminated batch nearly wiped out a partner’s development run. We learned the hard way that consistency trumps maximum theoretical yield. Trace residuals, such as 3-nitrobenzaldehyde or unreacted 4-fluorobenzaldehyde, don’t simply go away; even low ppm will show up in downstream coupling steps or post-reaction purification.

    We never just weigh and ship this compound. Drying methods, container choice, and in-house logistics matter as much as synthesis. The pale yellow solid ships in HDPE drums or glass bottles from our main site. Technicians keep the packing line dry to minimize caking, which some clients in humid regions reported long ago. Months spent working with autoclaves and batch reactors taught us bulk containers always find a way to let in moisture, so we run moisture control checks twice — once at packing, once at dispatch. Often, chemists ask for custom mesh or particle sizing, but for 4-Fluoro-3-Nitrobenzaldehyde, sticking to a fine crystalline powder works best, based on feedback from both HPLC and synthetic chemists.

    Why Purity and Handling Mean More than a Spec Sheet

    Academic papers focus on yields and selectivity, glossing over how a production batch can misbehave. In the plant, we watched hot, aggressive reaction conditions convert traces of aldehyde back to starting materials, or in the worst cases, yellow-brown decomposition products that sour an analytical report. Years of dialling in pH, solvent volumes, and order of addition mean fewer side reactions and more robust final product. We run GC, HPLC, and NMR alongside classic wet chemistry, tracing even the low ppm level side-products. Our in-house training repeatedly comes back to one lesson: you feel the impact of a single contaminant far more when you’re running a hundred kilos than in a five-gram method development.

    We’ve shipped to dozens of custom synthesis houses and multinational pharma firms, each with their own strict audit demands. Some are hyper-focused on nitroaromatic stability. Others care more about trace metallic catalysts or unwanted fluorinated side-products—issues that don’t show up at the pilot scale. Our response always comes back to learning from real plant mishaps, not textbook chemistry. Drain valve leaks, supposed “inert” lines that caught atmospheric O2, crystal cakes that collapsed during transfer — we’ve dealt with all of it.

    Applications: More than a Niche Intermediate

    Over the years, we watched our 4-Fluoro-3-Nitrobenzaldehyde make its way into drug discovery labs, agricultural R&D, and materials science teams looking for reactive handles on aromatic rings. Much of the market remains in pharmaceuticals. Its core aldehyde allows for further elaboration — for instance, via reduction, condensation, or coupling reactions — while that para-fluorine directs incoming functional groups and the nitro enhances electrophilicity. Some partners build in new heterocycles; others functionalize further for active ingredients or dye intermediates. Demand varies, but feedback comes back to the same points: most chemicals on paper could do the job, but real-world manufacturers get picked for reproducibility more than theoretical routes.

    Customers told us outright that similar compounds — like 3-Nitro-4-chlorobenzaldehyde — don’t behave the same way in process development. Chlorine can struggle in follow-up substitution, or the ortho/para difference alters yield and purification profiles. Our synthetic chemists routinely test alternatives, but found in several pilot campaigns that the fluorine version offered improved regioselectivity, a cleaner transformation profile, and easier workup. Even trace impurities from “name-brand” vendors gave them more trouble than a less technically perfect but more consistently handled lot. Over time we focused more on documentation, batch records, and repeat training, not just technical specs.

    Process Considerations: No One-Size-Fits-All Chemistry

    Plant-side, we don’t run every batch the same way. Temperature ramp, solvent swaps, and workup pH get adapted for run size as well as impurity trends. Some downstream users expect zero traces of organic base or transition metals, pushing us towards cleaner workups even if the theoretical conversion looks perfect. We used to think single-stage crystallization would clean up the mother liquors nicely. After running that for a few quarters, we saw rare impurities accumulate — slow to show up, but obvious in coupled product analysis. The team shifted to multi-stage workup, sacrificing some throughput for trace purity gains.

    Several clients in pharma told us ordinary solvent drying isn’t enough — batch-to-batch frisks of residual moisture and anhydrous conditions mean the difference between pass and fail in scale-up chemistry. Early on, a customer flagged unknown polymers that would fog up during distillation. It traced back to too-warm warehouse storage and pressure cycling on sealed containers. Now, storage and dispatch routines matter as much as reactor control. Having staff with real materials handling experience changed our approach from “production” to “collaboration.” Chemists now get live QC reports with every lot because, as the downstream experts, they spot patterns in product reactivity that don’t show up on an FTIR printout.

    Safety, Sustainability, and Workforce Training

    Nitroaromatic compounds can be touchy. Anyone who’s handled 4-Fluoro-3-Nitrobenzaldehyde quickly gets familiar with safe storage and spill management. Over the past decade, we shifted procedural focus toward exposure control. Our operators suit up in air-filtered environments, work under local exhaust, and operate with detailed exposure monitoring. It’s hardly glamorous, but investing in continuous training means less absenteeism and fewer safety incidents. We found early on that even a good milligram-scale protocol needs tweaks at the tank scale — filtering, transferring, or even sampling can kick up dust or vapors that undermine a clean record.

    Modern plants also can’t ignore environmental scrutiny. The nitro group offers synthetic flexibility but brings a challenge for waste handling. Our solvent recovery units and effluent monitoring have, over many years, reshaped daily routines — we track and document all streams, with near-daily feedback loops with local city and regional regulators. Switching to lower-toxicity carriers and better filtration cut compliance incidents by two-thirds over five years. Taking that approach isn’t about ticking boxes, but preventing production halts and lengthy investigations, both of which cost far more than preventive upgrades.

    Why Our Manufacturing History Matters More Than Labels

    New clients sometimes ask for global certificates or badges, hoping these assure consistent product. From years of running campaigns through final audit, we know paperwork only tells part of the story. What matters for 4-Fluoro-3-Nitrobenzaldehyde? It’s the batch logs, actual process controls, and technician involvement. We came to understand early that every step — from first pre-cursor procurement to last packing check — creates or risks micro-contaminations. The differences between us and unnamed resellers or traders become clear when a synthetic bottleneck crops up under a tight timeline.

    We’ve stood with customers through scale-up disasters, from blocked pipelines due to crystal morphology changes to delayed shipments from overlooked handling quirks. That sense of partnership, built on real problem-solving, is what shapes our approach to 4-Fluoro-3-Nitrobenzaldehyde. Chemists in our shop floor deal with every process surprise themselves rather than pass problems downstream. We encourage direct dialogue between our plant leads and end-users — the knowledge flows both ways, transforming simple feedback into process tweaks that last over the long term.

    Why 4-Fluoro-3-Nitrobenzaldehyde Stands Out from Other Functionalized Benzaldehydes

    The fluoro and nitro combination on the aromatic ring gives unique reactivity that sets it apart. Fluorine tilts the electronic landscape, pulling electron density, while the nitro amplifies electrophilic substitution potential. We’ve seen that subtle difference in functional group placement throws off parallel reactions — for example, using a chloro or methyl equivalent regularly delivers lower conversions or new, unexpected side products. Over years, customers’ own runs and our internal benchmarking keep circling back: for certain fine chemical and pharmaceutical syntheses, the 4-fluoro, 3-nitro blend hits a performance and quality sweet spot.

    Batch reproducibility marks the real distinction. Anyone can drum up a sample batch of substituted benzaldehyde, but keeping impurity trends low over dozens of runs — and at scale — signals process mastery. Handling also diverges: small tweaks in drying and packaging mean some crystalline aromatic aldehydes clump, degrade, or show scent changes over months in the warehouse. We monitor these details because our buyers do. Comparing 4-Fluoro-3-Nitrobenzaldehyde against similar intermediates shows our production methods deliver better purity, lower residual solvent, and more stable shipping — all learned from actual run failures and customer feedback, not just textbook protocols.

    Issues and Solutions in Production and Logistics

    We run into issues far outside the chemistry. Changing regulatory frameworks keep us on our toes. Some years ago, changes in permitted effluent levels forced a major update of our in-house recovery systems. Instead of slow-walking through compliance, we took the moment to invest in broader solvent recycling, energy use tracking, and more operator cross-training. Long-term, it curbed fines and sped up product release. Waste streams from nitro aldehyde runs now track lower than industry norms — hard-won, but necessary, lessons.

    Supply chain interruptions — whether solvent, glassware, or specialty packing liners — show up, too. Our planner team doubled up sourcing for raw fluorobenzaldehydes, then later built up on-site inventory to buffer against shipment delays. As a crew of chemical manufacturers, we deal head-on with the pain of volatile raw material markets. Pre-negotiating contracts and adding local vendor relationships mean we can keep commitments, even during spikes. Keeping customer lines running requires more than just full shelves — it takes daily communication and, sometimes, creative substitutions negotiated with both buyers and our in-house development team.

    Logistics partners also matter. Years of working with third-party couriers taught us the cost of temperature spikes, improper loading, or simple inattention to batch documentation. For heat and moisture sensitive shipments — like this benzaldehyde intermediate — we directly manage packing checks, route audits, and condition monitoring all the way to the customer’s door. Our experience says strict paper trails and a relationship-based approach make more difference than software-based inventory tools. Over time, these efforts prevented loss, reduced complaints, and encouraged repeat partnerships.

    Continuous Improvement: Listening to Feedback

    Real improvements come from close communication. Sometimes users notice slight color shifts, altered melting point, or trouble in filtration. We treat these as chances to re-examine process design. Our teams run deviation reports any time an out-of-spec sample or customer observation comes in, sharing findings between production and QA without blame or delay. Over a decade, this culture built up a set of internal best practices — not written by consultants, but drawn from operators, QC chemists, and end-users themselves. We don’t pretend every batch comes out perfect, but sharing those small lessons keeps us honest and helps build trust.

    Testing new drying methods, scaling plant capacity, or updating process controls doesn’t happen in a vacuum. Our routine pilot batches for 4-Fluoro-3-Nitrobenzaldehyde feed new data to both our teams and our partners. Direct plant visits by clients have drawn attention to, for instance, overlooked valve wear, transfer line blind spots, and even documentation steps that could speed up handoff. These grounded changes — guided by real-world demands, not marketing — ultimately create tighter processes and better customer experience.

    Partnership in Practice

    Chemical intermediates like 4-Fluoro-3-Nitrobenzaldehyde rarely grab headlines or marketing buzz. They stay behind the scenes in pharma research, fine chemical development, and specialty applications. Yet for those working with these compounds, what matters is trust in routine sourcing, batch reliability, and real partnership during trouble. Our recipe for quality isn’t a secret; it’s about tenacious process control, open communication, and sharing in real risks faced by end-users. That’s what brings buyers back over the years, whether for kilogram samples or multi-ton contract manufacturing.

    This approach sets our team apart from traders or brokers unable to tie production and support together. From on-site technical advice to urgent re-certification, every part of the 4-Fluoro-3-Nitrobenzaldehyde value chain reflects our hands-on experience, technical learning, and willingness to adapt. We take pride in sharing this compound with our partners, confident that each lot represents more than a chemical — it captures a shared investment in high standards, everyday diligence, and a reputation built on doing the right thing, not just the easy thing.