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2-Fluoro-4-Methylbenzoic Acid

    • Product Name 2-Fluoro-4-Methylbenzoic Acid
    • Alias 2-Fluoro-p-toluic acid
    • Einecs 224-420-1
    • 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
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    Specifications

    HS Code

    125210

    Chemical Name 2-Fluoro-4-Methylbenzoic Acid
    Cas Number 403-29-0
    Molecular Formula C8H7FO2
    Molecular Weight 154.14 g/mol
    Appearance White to off-white solid
    Melting Point 119-122°C
    Boiling Point No data available
    Solubility In Water Slightly soluble
    Density 1.297 g/cm3
    Purity Typically ≥98%
    Smiles CC1=CC(=C(C=C1)C(=O)O)F
    Inchi InChI=1S/C8H7FO2/c1-5-2-3-6(8(10)11)7(9)4-5/h2-4H,1H3,(H,10,11)
    Storage Conditions Store at room temperature, in a tightly closed container

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

    Packing & Storage
    Packing Amber glass bottle, 25 grams, white screw cap, safety seal; labeled with chemical name, formula, hazard symbols, and batch details.
    Shipping **Shipping Description:** 2-Fluoro-4-Methylbenzoic Acid is shipped in tightly sealed containers, protected from moisture and incompatible materials. Packages are handled as hazardous chemicals and labeled according to transport regulations (IATA, IMDG, DOT). It is shipped with a Material Safety Data Sheet (MSDS), typically by ground or air with proper documentation and handling precautions.
    Storage 2-Fluoro-4-Methylbenzoic Acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers or bases. Protect from moisture and direct sunlight. Recommended storage temperature is room temperature, ideally between 2°C and 8°C. Always follow standard chemical storage guidelines and safety protocols.
    Application of 2-Fluoro-4-Methylbenzoic Acid

    Applications of 2-Fluoro-4-Methylbenzoic Acid in Industrial Manufacturing

    2-Fluoro-4-Methylbenzoic Acid is widely adopted as a precision intermediate in the synthesis workflows of fine chemical, pharmaceutical, and specialty materials industries. As an original manufacturer with advanced purification and analytical capabilities, we support global producers in regulated segments with tailored grades, consistent quality, and end-to-end process integration.

    1. Pharmaceutical Intermediate Synthesis

    This acid serves as a structurally important raw material in the multi-step synthesis of active pharmaceutical ingredient (API) intermediates, particularly in the anti-inflammatory and oncology drug segments. Its unique fluorine substitution and methyl group deliver advantages for specific molecular configurations required by target APIs. End users typically introduce it after halogenation or amidation steps, allowing high-purity conversion during condensation reactions. Process engineers adjust input ratio and reaction time to minimize impurities and maximize batch yields within permitted limits, following strict international compliance systems.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) purity and identification
    • US FDA 21 CFR Part 211 for process controls
    • Chinese Pharmacopoeia (CP) for registered products

    Typical usage ratio

    • 0.8–1.2 molar equivalents vs. target substrate, adjusted for Reactivity and impurity profile.

    Downstream process integration

    • Fed into condensation, esterification, or amidation reactors as a chain-building intermediate.
    • Purity (≥99%) screened by HPLC before release to next synthesis stage.

    Final product types

    • Pyridine-based API intermediates
    • Non-steroidal anti-inflammatory therapeutics precursors
    • Cancer drug scaffold components
    • Specialty amide linkage intermediates

    2. Agrochemical Production (Herbicide & Fungicide Intermediates)

    This material is crucial in manufacturing select fluorinated benzoic derivatives, which are essential building blocks for modern crop protection actives. The methyl and fluoro groups provide necessary structural elements for field stability, rainfastness, and bioactivity. Formulation engineers introduce it in controlled ratios in chlorination or carboxylation stages, with close attention to byproduct minimization in line with agrochemical process QC demands. Global regulatory traceability applies at all handling and documentation stages.

    Industry compliance standards

    • FAO/WHO Specifications for plant protection products (manuals, identity, and purity protocols)
    • REACH Regulation (EU) 1907/2006
    • ISO 9001:2015 quality management for raw material traceability
    • China National Standard (GB) for pesticide manufacturing

    Typical usage ratio

    • 5–15% as a core intermediate in the active ingredient, with process chemists adjusting according to reaction pathway and endpoint product purity.

    Downstream process integration

    • Introduced after alkylation or halogenation steps; often serves as ring precursor or branching group source.
    • QC checks for residual acid are performed post-synthesis before formulation blending.

    Final product types

    • New-generation triazole fungicide precursors
    • Fluorinated herbicide active compounds
    • Intermediate stock for pre-emergent weed control chemicals
    • Crop-specific plant growth regulator base materials

    3. Liquid Crystal Materials for Display Technologies

    Leading optical and electronics manufacturers utilize this material as a specialty intermediate in the synthesis of liquid crystal compounds for advanced display panels. The precise structural configuration promotes specific dipole and orientational properties required in thin-film transistor and high-contrast LC applications. The acid is introduced early in the synthesis, then transformed through esterification and coupling protocols under inert atmospheres. Strict clean-room protocols and contamination controls are maintained throughout, in alignment with electronics-grade standards.

    Industry compliance standards

    • IEC 61340-5-1 (Electrostatics for electronic assemblies)
    • RoHS Directive (EU) 2011/65/EU for restricted materials
    • ISO 9001:2015 process quality for electronics manufacturing
    • JEITA display material guidelines (Japan Electronics and Information Technology Industries Association)

    Typical usage ratio

    • 1.5–6% as a ring-building intermediate for target LC monomers; adjusted for target viscosity and alignment property.

    Downstream process integration

    • Added during initial organic synthesis before esterification, then isolated, purified, and polymerized for LC mixture preparation.
    • Handled in sealed, controlled-environment reactors to prevent contamination or moisture ingress.

    Final product types

    • High-birefringence liquid crystals for TFT-LCD panels
    • Mixed LC compounds for OLED and IPS displays
    • Photo-alignment agents for precision pixel control
    • Display-grade specialty monomers and oligomers

    4. Specialty Polymer Synthesis

    This compound acts as a chain modifier and co-monomer in the controlled synthesis of high-performance aromatic polyesters and polyamides. The precise fluorinated aromatic structure enhances thermal stability and chemical resistance, key factors in engineering plastics and advanced coatings for electronics, automotive, and consumer devices. Process setup includes multi-stage polycondensation or transesterification, with feedstock addition closely monitored by gravimetric and chromatographic systems for optimal molecular weight control. Material grades comply with required polymer and electronics standards for specific downstream needs.

    Industry compliance standards

    • ASTM D3418 for thermal property analysis
    • UL 94 plastics flammability standard for electronics
    • IEC 60216-1 for thermal endurance of electrical insulation materials
    • ISO 14001 for environmental management in polymer manufacturing

    Typical usage ratio

    • 2–8 mol% in polycondensation reactions, based on required thermal properties and crystallinity; adjusted for end-use functional requirements.

    Downstream process integration

    • Charged during initial monomer mix in melt or solution polymerization; functions as chain stopper or structural modifier.
    • Integration verified by NMR and GPC profiling before final extrusion or molding.

    Final product types

    • High-temperature resistant polyesters (e.g., specialty PBT blends)
    • Halogenated engineering polymers for automotive connectors
    • Electronic encapsulation materials for microcircuit protection
    • Wear-resistant functional coatings and composite modifiers
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    Certification & Compliance
    More Introduction

    2-Fluoro-4-Methylbenzoic Acid: Practical Insights from the Production Line

    Working Directly With 2-Fluoro-4-Methylbenzoic Acid

    Our experience starts with raw materials. 2-Fluoro-4-Methylbenzoic Acid, with the CAS number 446-17-3, offers a unique character in aromatic acid chemistry. Its formula, C8H7FO2, gives it a straightforward structure—methyl and fluoro groups attached to the benzoic acid backbone. In our plant, that means handling a compound that brings both selectivity and reactivity to organic synthesis.

    During synthesis, the methyl and fluoro substitutions change how the molecule acts. They tweak electron density on the aromatic ring, making the acid useful in different coupling and substitution reactions. When technicians prepare it for shipment, the white to off-white crystalline powder forms easily under controlled crystallization, avoiding agglomeration and ensuring proper particle size. Those qualities help downstream processes, especially for fine-tuning reactivity and solubility.

    Comparing to Other Benzoic Acid Derivatives

    We’ve run many benzoic acid derivatives through our reactors, and each one brings its quirks. With 2-fluoro-4-methylbenzoic acid, adding the fluoro group at the 2-position shifts the acidity just enough to influence reactivity with nucleophiles and electrophiles. The methyl group at the para-position, compared to standard benzoic acid or even its ortho counterpart, gives more steric bulk and influences physical properties like melting point and solubility in polar solvents.

    Take 4-methylbenzoic acid as an example. The simple para-methyl substitution lacks the electronegativity that fluorine provides. Reactions with electrophilic agents show less selectivity, and downstream modifications sometimes require more steps. 2-Fluorobenzoic acid, on the other hand, increases electron withdrawal but lacks the methyl’s solubility and steric effect. In daily operations, balancing these factors shapes a manufacturer’s decision when tailoring intermediates for pharmaceuticals or specialty chemicals.

    Specifications That Shape Production and Use

    Our standard batches of 2-fluoro-4-methylbenzoic acid run at typical purities above 98%. After crystallization, we run HPLC and NMR checks on every lot. Water content remains tightly controlled through vacuum drying, giving a fine, flowing powder that speeds weigh-outs and prevents clumping in automated dispensing systems. This consistency comes from precise temperature and solvent controls in our plant’s crystallization vessels, an approach that considerably reduces off-spec material.

    We’ve learned over the years that controlling trace metal ions early on—at the acid chlorination stage—means less trouble when customers use the acid as a pharmaceutical intermediate. Almost all clients target downstream coupling reactions, where sensitive catalysts react poorly with lingering trace metals or unreacted starting materials. Ensuring reliable assay and low impurity profiles helps production lines run longer without shutdowns for troubleshooting.

    Common Applications and Their Realities

    Most 2-fluoro-4-methylbenzoic acid we ship out heads for pharmaceutical intermediate synthesis. Its unique substitution pattern fits metabolic stability and reactivity requirements in medicinal chemistry. We hear regularly from clients who use it to build fluoroaromatic compounds or introduce the group as a placeholder in complex synthesis. Compared to other benzoic acids, the presence of fluorine resists metabolic degradation. Medicinal chemists value that resilience when designing active ingredients that stay in the bloodstream longer.

    In the crop protection industry, a subset of our product finds use as a building block for fluorinated agrochemicals. Chemists prefer this material over standard benzoic acid derivatives when looking for environmental persistence and selectivity in biological systems. Because of the electron-withdrawing effect, this molecule adjusts biochemical properties without the unpredictability that comes with bulkier or more reactive substitutions. In these applications, our experience proves that high lot-to-lot purity keeps production headaches to a minimum, reducing revalidation requirements.

    Handling, Stability, and Safety Considerations

    Inside the plant, we store 2-fluoro-4-methylbenzoic acid away from moisture and direct sunlight. The molecule shows good stability under ambient conditions, but as always, dry powder handling means dust containment systems and proper PPE. Our operators have never reported reactivity hazards under standard storage conditions, which makes inventory management more straightforward than some of the more active acyl halides or sulfur-based derivatives.

    In the production environment, the acid responds predictably when heated or dissolved in polar organic solvents. Operators find its odor mild compared to many other substituted benzoic acids, making it comfortable to handle during weigh-outs and transfers. In terms of environmental fate, the fluoro group means breakdown in soil and water systems occurs more slowly, so waste streams get routed with care through incineration—avoiding direct release. We monitor effluent to make sure there’s no detectable product loss before final treatment.

    Processing Differences: Practical Notes From the Line

    For chemists stepping into the lab or plant, a few differences in 2-fluoro-4-methylbenzoic acid set the stage for downstream success or headaches. Unlike unsubstituted benzoic acid, this compound’s relatively low solubility in cold water can force changes in crystallization or filtration protocols. In the reactor, the electron-withdrawing fluoro group makes nucleophilic aromatic substitution more feasible under milder conditions. This is a small but valuable advantage, especially for pharmaceutical manufacturing lines aiming for fewer process steps.

    The methyl group bumps up hydrophobicity, making extractions into organic phases easier. Manufacturing teams often optimize for this trait, pulling higher yields in less time compared to other fluorinated benzoic acids lacking a methyl group. We’ve adjusted our purification protocols over time, incorporating less aggressive solvents and reducing solvent consumption—pushing sustainability without sacrificing product quality.

    Troubleshooting Real-Life Manufacturing Challenges

    From charge to charge, minor process adjustments sometimes turn into major changes for the team. Seasonal humidity shifts, for instance, can affect powder flow. To address this, we invested in additional in-line dryers. Switching from rotary to vacuum drying cut down on surface moisture, which keeps clumping at bay during bagging and storage. A while back, one customer flagged inconsistent tablet yields in a pilot plant. After checking their incoming material, it turned out particle size distribution drifted outside our standard window—a result of minor changes in recrystallization temperature. We implemented stricter temperature ramp controls and restored customer process reliability.

    In one batch, trace halide impurities nearly derailed a pharmaceutical campaign, putting a key API at risk during scale-up. By focusing on raw material screening and reagent purity, our technical team locked down the process, delivering a cleaner acid and keeping downstream chemistry on track. Our approach focuses on transparency and feedback: batch histories stay open for review with every kilogram we ship, and those discussions help everybody meet regulatory demands with less stress.

    Supporting Green Chemistry and Safe Manufacturing

    Our operations team keeps sustainability front of mind. Wherever we can, we recover solvents and recycle mother liquors so resource efficiency improves over time. Because fluorinated aromatics challenge waste treatment, every step is designed to keep mother liquor volumes manageable for safe processing. We’ve replaced older solvent systems with greener alternatives, cutting hazardous waste volumes and reducing our plant’s overall environmental footprint.

    On-site, we run regular safety and spill drills for every material, even relatively stable compounds like 2-fluoro-4-methylbenzoic acid. By keeping loads well within warehouse shelf life, we avoid the pitfalls of holding onto ageing product. Every month, random lots undergo confirmatory retesting for purity and trace byproducts. This approach gives end users a reliable product while satisfying regulatory and safety audits.

    Learning From Each Run: Process Improvements

    Over the years, the transition from smaller batch runs to a semi-continuous process allowed our plant to tighten reaction controls and boost product consistency. Inline monitoring by FTIR and continuous slurry sampling pick up shifts in impurity profiles long before visible problems appear. When changing solvent suppliers, we ran a series of split-lot trials and followed products to customers’ synthetic labs, giving us real-world feedback instead of only relying on in-house data.

    Early in production, we saw higher pyrene and polyaromatic byproducts from poorly purified starting materials. Adjusting the heating ramps and improving raw material traceability cut these errors to nearly zero. That translates to smoother downstream chemistry for our customers, especially in cases where strict regulatory filings need supporting analytical records.

    End-Use Feedback and Ongoing Collaboration

    Customers in the pharmaceutical and agrochemical industries share their pressure points freely: process reproducibility, waste reduction, and reactivity control top the list. By handling those conversations with openness rather than sales talk, we see formulations come together more efficiently, raw materials last longer before retests, and pilot plant campaigns avoid late-stage surprises. An end-use chemist once pointed out shifts in melting point they hadn’t anticipated, tracked back to slight isomer impurities. Our plant updated column purification protocols, cleaning up the product and stabilizing downstream synthesis yields.

    By working directly with downstream users, our batches reflect feedback—not just chemical specs. Partnership means both our team and our clients build better chemicals together, learning what works, not just what reads well on a data sheet.

    The Value of Consistency and Direct Experience

    Success in chemical manufacturing, especially with specialty acids like 2-fluoro-4-methylbenzoic acid, rests on years of practical effort. Every tank and tote carries the sum total of manufacturing improvements, customer feedback, and chemical best practices. We’ve learned these lessons batch by batch, not from abstract principles, but from the heated conversations on the production floor and the real outcomes in downstream labs.

    Years of hands-on experience with this compound shows us where corners can’t be cut and where process changes make a big difference. Batch integrity, operational transparency, and willingness to fix small issues before they become large ones—these drive better chemistry, one run at a time.

    Looking Ahead: Innovation and Ongoing Reliability

    Demand for well-defined fluoroaromatics continues to rise as pharmaceutical and advanced material applications grow. Our plant evolves with it. We test new reactor materials and catalyst choices, aiming for more efficient conversion and lower impurity levels. Industry standards tighten every year, pushing us to test more, document more, and tighten every parameter from delivery timelines to traceability.

    Adaptation comes not from chasing every passing trend but from keeping a close eye on what chemists need: reliable reactivity, clarity about impurities, and assurance that every pack of product matches the last. Over a decade of production has built in-house expertise into every shipment. No matter how synthesis routes shift, product quality and direct communication remain the backbone of our manufacturing commitment.

    Building Tomorrow’s Chemistry—One Lot at a Time

    Making 2-fluoro-4-methylbenzoic acid at industrial scale involves more than clean reactors and tight specs. Each day’s output reflects our drive for quality and an honest, straightforward approach to chemical manufacturing. Knowledge, not just certificates, carries our product into research labs, pilot plants, and commercial production lines worldwide.

    Collaborating closely with customers, watching for small shifts in reactivity or product handling, and adjusting quickly to local feedback all keep our process efficient and our output trusted. We keep looking for ways to drive environmental responsibility, safe handling, and process improvements—always aiming to help end users do better chemistry.

    Every shipment delivered builds new understanding, strengthens problem-solving skills, and adds to a story shaped by hands-on experience, daily focus, and pride in the final material. 2-fluoro-4-methylbenzoic acid, with all its quirks and advantages, represents what a manufacturer’s attention to detail and open dialogue can achieve.