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2-Chloro-4-Fluorobenzaldehyde

    • Product Name 2-Chloro-4-Fluorobenzaldehyde
    • Alias 2-Chloro-4-fluorobenzalhyde
    • Einecs 700-931-0
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    820279

    Cas Number 446-37-7
    Molecular Formula C7H4ClFO
    Molecular Weight 158.56 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 79-81 °C at 4 mmHg
    Density 1.38 g/cm³
    Refractive Index 1.579
    Solubility In Water Slightly soluble
    Smiles C1=CC(=C(C=C1Cl)F)C=O
    Inchi InChI=1S/C7H4ClFO/c8-6-2-1-5(4-10)3-7(6)9
    Synonyms 2-Chloro-4-fluorobenzaldehyde; Benzaldehyde, 2-chloro-4-fluoro-
    Purity Typically >98%
    Storage Temperature Store at 2-8°C

    As an accredited 2-Chloro-4-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 "2-Chloro-4-Fluorobenzaldehyde, 25g," with hazard symbols, lot number, and safety information on white label.
    Shipping 2-Chloro-4-Fluorobenzaldehyde is shipped in secure, tightly sealed containers, compliant with chemical safety standards. It is protected from moisture, direct sunlight, and incompatible substances. Proper labeling, including hazard warnings, ensures safe handling during transit. Shipping follows all relevant regulations for hazardous materials to guarantee safe and efficient delivery.
    Storage 2-Chloro-4-Fluorobenzaldehyde should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from direct sunlight. Keep it away from incompatible materials such as strong oxidizing agents and bases. Store at room temperature and avoid moisture exposure. Properly label the container and ensure access is restricted to trained personnel following appropriate chemical hygiene practices.
    Application of 2-Chloro-4-Fluorobenzaldehyde

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

    2-Chloro-4-Fluorobenzaldehyde serves as a critical intermediate in specialized industrial sectors. Its precise reactivity and controlled purity enable manufacturers to achieve reliable synthesis outcomes in complex organic production lines. Below, we detail core downstream application scenarios, including mandatory compliance, recommended dosing levels, integration points, and tangible end products.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    Pharmaceutical producers utilize 2-Chloro-4-Fluorobenzaldehyde as a building block in stepwise organic syntheses, especially for the preparation of pharmacologically active compounds containing substituted benzene rings. The material supports structural modifications required in developing antihypertensive agents and select central nervous system drugs. Producers determine the aldehyde’s charge ratio based on route specificity, balancing reagent conversion rates with impurity controls. Its controlled introduction within multi-step API syntheses ensures consistent batch yields.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidelines for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapters <823> and <857>
    • European Pharmacopoeia (Ph. Eur.) standards on intermediates
    • FDA 21 CFR Part 211 – Current Good Manufacturing Practice for Finished Pharmaceuticals

    Typical usage ratio

    • Generally 0.9–1.2 molar equivalents per target synthesis step, adjusted according to downstream molecular design and reaction yield requirements

    Downstream process integration

    • Introduced during the condensation or formylation reaction to build intermediate scaffolds in the API synthesis route
    • Charged as a neat liquid or pre-dissolved batch-wise into solvent under inert atmosphere for sensitive transformations
    • QC sampling verifies aldehyde conversion in follow-up steps

    Final product types

    • Antihypertensive agent intermediates
    • Selective serotonin reuptake inhibitor (SSRI) cores
    • Benzamide and benzylamine derivatives
    • Experimental oncology investigational APIs

    2. Agrochemical Synthesis Component

    Major crop protection manufacturers use the material to form functionalized benzene derivatives in the synthesis of specific herbicides and fungicides. Its electron-withdrawing substituents facilitate targeted halogenation patterns critical for producing stable, high-activity crop chemicals. Accurate dosing supports tight downstream impurity profiles and minimization of byproducts, with integration typically handled at the early synthesis stage.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • FAO/WHO Code of Conduct on Pesticide Management
    • REACH Regulation (EC) No 1907/2006 for chemical safety
    • OECD guidelines for chemical testing, Series on Pesticides No. 1–21

    Typical usage ratio

    • Between 0.7–1.1 mole per mole of downstream active herbicide or fungicide synthesis, with adjustments for crop protection molecule stoichiometry

    Downstream process integration

    • Used at initial synthetic step for generating aryl halide intermediates
    • Integrated by controlled batch feed, in solvent system specific to crop protection chemistry
    • Subsequent purification to separate product from unreacted ingredient

    Final product types

    • Pre-emergent herbicide intermediates
    • Benzaldehyde-based systemic fungicides
    • Wheat and maize selective weed-control actives
    • Cereal rust preventative co-formulants

    3. Specialty Dye and Pigment Manufacture

    2-Chloro-4-Fluorobenzaldehyde is a core aromatic precursor in the synthesis of fine chemical intermediates for dyes and pigments with high lightfastness and chemical resistance. It allows synthetic colorant manufacturers to achieve sharp spectral properties necessary in automotive, textile, and industrial pigment lines. Usage varies with the chromophore complexity, ensuring process adaptability for color purity specifications.

    Industry compliance standards

    • ISO 13320:2009 (Particle size analysis – Laser diffraction methods)
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) guidelines
    • REACH Safety Data Sheet (SDS) requirements
    • OEKO-TEX® Standard 100, Annex 6 for dye safety

    Typical usage ratio

    • Ranges from 1.0–1.5 mol per mol of colorant backbone precursor, optimized in lab for brightness and stability

    Downstream process integration

    • Added to initial aromatic substitution or condensation stage to introduce halogenated aldehyde group
    • Included in batch reactor charge prior to chromophore ring closure step
    • Process monitored to minimize polycondensate side products

    Final product types

    • High temperature resistant organic pigments
    • Fluorescent textile dyes
    • Automotive paint dispersions
    • Fade-resistant coloring agents for plastics

    4. Liquid Crystal Material Synthesis

    Manufacturers specializing in advanced display materials deploy this benzaldehyde derivative to introduce key electronic and steric effects into mesogenic core structures. These cores are fundamental in tuning thermal, optical, and phase change performance of liquid crystal mixtures supplied for LCD and OLED backplane fabrication. Process engineers adjust charge ratios to control molecular length and fluidity transitions across broad temperature ranges.

    Industry compliance standards

    • IEC 61249-2-21:2015 (Halogen-free materials for printed boards and other interconnecting structures)
    • RoHS Directive 2011/65/EU compliance for halogenated components
    • JIS C6242 standards for electronic chemicals
    • REACH restrictions on aromatic aldehydes in electronic applications

    Typical usage ratio

    • Normally 0.95–1.05 molar equivalents relative to mesogen precursor, fine-tuned for electro-optic property targets

    Downstream process integration

    • Dispensed into condensation reaction vessel for aryl aldehyde addition to core LC precursor
    • QC-confirmed purity to avoid phase separation in liquid crystal blends
    • Batch documentation for full lot traceability from raw feed to final mixture

    Final product types

    • Liquid crystal display (LCD) mixture intermediates
    • OLED precursor compounds
    • Polymer-dispersed liquid crystals for smart glass
    • Electro-optical switching materials

    5. Fine Chemical Synthesis for Fragrance and Aroma Compounds

    Selective specialty fragrance manufacturers use 2-Chloro-4-Fluorobenzaldehyde as a tailor-made intermediate to synthesize aromatic compounds featuring unique halogenated notes. This raw material imparts customized olfactory properties in high-value perfume ingredients and aroma raw chemicals, with reaction design focused on minimizing off-odors or unwanted byproducts from aldehyde handling in esterification or reductive amination routes.

    Industry compliance standards

    • International Fragrance Association (IFRA) Code of Practice
    • FEMA GRAS (Flavor and Extract Manufacturers Association – Generally Recognized As Safe) status for synthetics
    • EU Regulation (EC) No 1223/2009 on cosmetic products
    • ISO 9001:2015 for fine chemical production

    Typical usage ratio

    • Established between 0.8–1.2 mol per mol of aroma precursor, adjusted for product profile intensity and processing route

    Downstream process integration

    • Batch-fed into reductive amination step to produce halogenated benzyl alcohol derivatives
    • Used in esterification for specialized aroma molecule synthesis
    • Monitored for residual aldehyde to meet finished product safety limits

    Final product types

    • Complex synthetic perfume bases
    • Specialty aroma chemicals for food flavorings
    • High-purity fragrance intermediates
    • Cosmetic scenting agents
    Free Quote

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    Certification & Compliance
    More Introduction

    2-Chloro-4-Fluorobenzaldehyde: Our Approach to Precision Chemistry

    Setting the Stage for Reliable Advanced Intermediates

    Decades of hands-on production tell us that success in fine chemicals comes from a persistent pursuit of control. Every batch teaches something new. Our workflow with 2-Chloro-4-Fluorobenzaldehyde shows this spirit of constant improvement, harnessing both deep process knowledge and the unvarnished feedback of actual plant operations. Markets often ask for new modifications, tighter specs, fresher insight into reaction byproducts. Yet, the practical side means holding the line on consistency and keeping eyes peeled for even the slightest sign of impurity drift.

    Our Take on the Value of 2-Chloro-4-Fluorobenzaldehyde

    As a manufacturer, we look beyond catalog numbers and purity claims. Each molecule of 2-Chloro-4-Fluorobenzaldehyde carries both the rigor and unpredictability that come with handling aromatic halogenated benzaldehydes in scale. This compound, C7H4ClFO, often stands at a pivotal stage for agrochemical intermediates, pharmaceuticals, and a variety of specialty resins. Chemists come to us for the specific substitution pattern of the chlorine in the ortho position and the fluorine in the para. Such an arrangement allows for precise downstream functionalization, something more challenging or outright impossible with mono-halogenated or non-fluorinated analogues.

    In the field, bench results sometimes mislead. Scaling up from grams to hundreds of kilograms, issues crop up around residue, unconverted starting material, and limits of solvent recycling. We found that attention to temperature ramp rates and aggressive gas scrubbing makes the difference between a product fit for registration samples and one that cannot pass internal benchmarks. Many years in the aromatic halide and aldehyde space taught us to expect surprises and design processes to recover from them quickly. Teams at our plants chase not just yield, but the sort of ‘problem-free’ shipment customers remember us for.

    What Sets This Benzaldehyde Apart in Synthesis

    Other aldehydes may have a similar skeleton, but for structure-activity relationships in pharma and pesticide R&D, no substitute covers all bases. Subtle changes in halogen position on the ring result in dramatic performance differences. We’ve assisted clients who attempted to swap in 3-chloro or 3-fluoro analogues, only to find that activity disappears or unwanted isomers corners the process with costly byproducts. It is not just an academic nice-to-have: the combined electron-withdrawing effects from both chlorine and fluorine push downstream reactivity into windows where cleaner couplings or additions are possible. Over time, scale-up partners learn to value the reliability this brings to complex syntheses.

    Bulk traders shy away from offering this product with extensive analytical backup. Our standards evolved directly from customer feedback. Routine checks now include not only HPLC purity but also GCMS to catch trace side-reactions that can play an outsized role in active ingredient formation later on. This level of scrutiny comes from years spent troubleshooting puzzles caused by stray impurities. We maintain rigorous documentation at every stage, from the handling of o-chlorobenzaldehyde precursors to the distillation steps that lock in the true isomer content.

    Working with Industry Trends: Compliance, Safety, and Sustainability

    There is pressure in the marketplace to align materials supply with regulatory priorities. Our team tracks any update to REACH, TSCA, and downstream chemical legislation. With halogenated aromatics, regulators often require more than the average material disclosure. We engage auditors not as a box-ticking exercise, but to keep production defensible for the long haul. Sampling, testing, and shipping logs don’t just exist for inspectors—they feed directly into process improvement and batch traceability for partners running clinical or pilot-scale trials.

    Worker protection during manufacture matters. Many aldehydes release strong odors or cause dermal sensitivity. Every shift, our plant operators draw on process ventilation design, PPE use, and ongoing hygiene checks developed from lived experience. Training never stops. Incidents involving exposure or improper venting shape each revision of our job SOPs.

    Disposal of aromatic halides brings its own environmental question marks. We’ve invested in liquid waste treatment units and thermal vents to limit halogenated emissions. These are not after-the-fact measures but central features. Clients appreciate this commitment, especially those under pressure to reduce environmental footprints across entire value chains.

    The Nuts and Bolts: Specifications Grounded in Experience

    Labs and production partners want their material to arrive with numbers matching the COA, not just within vague allowable margins. For 2-Chloro-4-Fluorobenzaldehyde, standard deliveries come with HPLC purity above 99%. Moisture picks up quickly due to the aldehyde group’s reactivity, so we use nitrogen-inerted packaging and low-humidity storage. In years past, too casual an approach led to batches that showed yellowing or degraded on long transport routes. Odd odors or abnormal color tints always involve root-cause review, not just a quick rework and reship.

    Physical appearance is usually white to light yellow crystalline powder, melting in the range of 47-50°C by capillary method. Density and solubility get tracked because isolated product often lands in solvent systems for formulation work almost immediately after it hits a customer’s dock. Those reactions rely on predictable dissolving times and capacity. Any odd adducts or residues from mother liquor get flagged upfront.

    We must point out: 2-Chloro-4-Fluorobenzaldehyde resists the general trend toward lower-toxicity intermediates. Its particular combination of halogens can add challenges for waste handling and downstream functionalization work. Customer R&D and compliance teams sometimes shift away from polyhalogenated intermediates, but the unmatched versatility for certain target molecules brings them back. Our job has been to make its handling, transport, and use transparent enough that users avoid surprises, especially as chemical registrations in big markets force more thorough disclosure with each passing year.

    Users and Common Applications: Beyond the Brochure

    Shortcuts seldom pay off in scale-up chemistry. That’s one hard lesson from our time running hundreds of metric tons through multiple reactors. Chemists and formulators come calling when their process routes stall with simpler derivatives. 2-Chloro-4-Fluorobenzaldehyde shows up in situations where finished products—herbicides, fungicides, or small-molecule APIs—demand a tightly controlled ring substitution. Sometimes a research partner chases a novel lead structure; other times, a formulary upgrade calls for improvements in product shelf life or activity.

    Compared to mono-halogenated benzaldehydes, this product delivers higher selectivity in subsequent nucleophilic aromatic substitutions. For bioconjugation, the electron-shifting impact from fluorine often opens up specific reaction fields unavailable to mere chlorinated variants. Custom syntheses for emerging actives—especially where patent families rest on unique halide patterns—use this material to simplify downstream protection-deprotection cycles, limit isomeric drift, or control metabolic stability.

    We have worked with both global companies and small custom synthesis labs. The former appreciate the solid, reproducible batch footprints. The latter come back because our direct experience and willingness to troubleshoot on the technical side saves time, money, and wasted labor. This isn’t a product where cut-and-paste technical support or faceless bulk shipping does the job. Each inquiry, every sample request, gets routed through staff with long memories of which customers encountered which quirks over the years.

    How We Navigate Day-to-Day Production

    Manufacturing this benzaldehyde presents a balancing act between speed and selectivity. Chlorination and fluorination reactions offer little room for error: go too fast, and you risk forming side products; go too slow, the economics shift against you. Staff monitor temperature, agitation, and gas flows at all hours, using control charts built from real, sometimes messy, historical data rather than idealized batch logs.

    Our reactors work overtime certain periods during the year, especially when downstream users kick off campaign runs. Batch planning juggles demands for smaller experimental lots and full-container-loads shipping to multinational buyers. Associates learned to pre-empt shipping delays or customs holdups by anticipating export documentation needs early. Regular feedback from logistics partners feeds right back into our planning window—every missed shipment or delayed customs clearance puts pressure on the consistency our customers depend on.

    Old hands in our production teams sometimes catch issues that instrument alarms miss. We welcome this ‘street-level’ knowledge, updating work instructions not only with results from analytical gear but also with tips from operators who spot off-odors, crystal clumping, or odd solubility quirks before lab results even catch up.

    Lessons Learned from Decades of Fine Chemical Supply

    We have had to walk back process changes more than once. On occasion, raw material shifts or new solvent systems led to unanticipated trace impurities that challenged our purification steps. Each time, we gathered data, rechecked incoming goods, and made sure no low-level missteps rolled forward into downstream supply. These lessons remind us that manufacturing specialty chemicals never follows a static recipe. Each iteration in the process needs real-world validation, not just a box-tick on a protocol sheet.

    Our relationships with customers grow over time not just from volume but from frank conversation when performance or compliance issues come up. A pharma user struggling with regulatory submission on a new intermediate batch will often return to us for side-by-side troubleshooting. This trust comes from our willingness to run extra analytics, share candid findings, and adjust shipping or documentation on the fly to support urgent needs.

    Several times clients have asked for tailored packaging or alternate transport protocols, especially when moving into regulated markets or pilot-scale manufacturing. We respond rapidly, using lessons learned from earlier projects to sidestep the pitfalls unique to aromatic aldehydes. The practical takeaway: chemical supply in this category rewards flexibility rooted in experience. Formula adaptation, changes in lot size, even custom impurity specs—our technical support staff know that no two users navigate precisely the same application landscape.

    Key Distinctions from Other Benzaldehydes

    Chemical suppliers sometimes lump all substituted benzaldehydes into a single category. In practice, single-halogen or non-fluorinated versions lack the dual reactivity and selectivity delivered here. The ortho-chloro and para-fluoro pattern enables synthetic strategies that would fail or stall with 4-chlorobenzaldehyde, 2-fluorobenzaldehyde, or benzaldehyde itself. We’ve coordinated dozens of method trials alongside customer labs documenting higher final yields, reduced side reactions, and smoother isolations from this material versus substitution with structurally similar aromatic aldehydes.

    Another persistent question involves handling: certain isomers or unsubstituted analogues generate more byproduct or change pH in downstream formulations. Detailed feedback helped us fine-tune purification, drying, and packaging routines. Many procurement teams ask why certain vendors quote at drastically different price points. Production experience shows that what looks like a comparable chemical actually diverges in cost, yield, and practicality at full scale, especially with halogenated aromatics.

    Navigating Supply Chain Volatility and Planning Ahead

    It’s never enough to run a tight operation inside our own gates. Supply chain jitters ripple through the specialty chemicals world. Unexpected events—port lockouts, raw material shortages, new import regulations—can throw off months of planning. We cultivate backup vendors, maintain lean inventory practices, and track global logistics in real time. The flexibility we build into our own purchasing decisions turns out critical when downstream users confront unplanned project surges or compliance audits. Our clients get an honest timeline and detailed update, not wishful thinking or finger-pointing, if disruptions threaten delivery windows.

    Risk management often sits unseen, but the dividends show up clearly during disruptions. Detailed digital recordkeeping, batch-level tracebacks, and supplier qualification aren’t just regulatory cover. They amount to an insurance policy for our partners who need both material traceability and clear documentation for every shipment. The same rigor protects against recalls or regulatory snags down the line, especially in closely monitored industries like pharmaceuticals and agrochemicals.

    Supporting Continuous Innovation: Not Just Supply, But Partnership

    Innovation builds on a back-and-forth between chemists, engineers, and production. Over the years, we noticed a simple trend: the best project outcomes grow from steady dialogue about bottlenecks, required specs, and unplanned process deviations. Technical staff work directly with R&D and QC teams at user sites, not hiding behind call centers. Questions about stability, impurity carryover, process adaptation with new equipment, or scale-up parameters receive attention at the plant level and from our lab—all based on actual runs, not recycled sales scripts.

    Requests sometimes arrive mid-campaign when clients discover a need for expedited analysis or documentation. Our teams jump into action, analyzing retained samples, checking raw material lots, or researching batch records. Sometimes we rerun spectral analysis after new impurity signals appear in customer applications. Coordinating third-party retesting, updating supporting documents, and making hands-on suggestions all reflect a genuine investment in partnership. When manufacturing partners show this type of dedication, more reliable product development and market success follow.

    A Culture Rooted in Process, Learning, and Transparency

    Our team’s strongest asset lies in combining tradition and improvement. Site visits and audits prompt new questions every year. There is always another layer of compliance regimen or customer-specific query to address. Each challenge brings new solutions, from modifying reaction work-ups to adjusting purification procedures based on fresh analytical insights. Behind this adaptability sits a reservoir of plant history, technical logs, and accumulated know-how that helps customers navigate evolving demands for documentation, registration, and overall product stewardship.

    We’ve seen the industry shift toward demands for data transparency and broader environmental stewardship. Modern buyers look for actual evidence behind every claim—analytical spectra, process origin, impurity breakdown, and sustainability features follow every drum. Older habits of opaque data release or generic COA sheets give way to granular information based on every batch’s unique fingerprint.

    Today, no customer works in isolation. The journey of 2-Chloro-4-Fluorobenzaldehyde from feedstock to advanced intermediate relies as much on responsiveness and institutional memory as on technical infrastructure. Every year, smarter regulation, tighter specs, and more complex applications challenge us to move from simple commodity supply to genuinely collaborative production. By focusing on actionable feedback and direct problem-solving, our teams help ensure that each batch serves as a building block for the next generation of chemical innovation.