|
HS Code |
130511 |
| Product Name | 2-Fluoro-5-Methylbenzonitrile |
| Cas Number | 70724-05-3 |
| Molecular Formula | C8H6FN |
| Molecular Weight | 135.14 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 209-211°C |
| Density | 1.09 g/cm³ |
| Purity | Typically ≥98% |
| Flash Point | 91°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Synonyms | 2-Fluoro-5-methylbenzenecarbonitrile |
| Smiles | Cc1ccc(F)cc1C#N |
| Refractive Index | 1.527-1.531 |
As an accredited 2-Fluoro-5-Methylbenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100 grams, tightly sealed with tamper-evident cap, labeled with chemical name, CAS number, hazard symbols, and supplier. |
| Shipping | 2-Fluoro-5-Methylbenzonitrile is shipped in tightly sealed containers, protected from light and moisture. It should be packaged according to relevant hazardous material regulations, labeled appropriately, and transported by certified carriers. Handling requires proper protective equipment to avoid inhalation and contact, as the chemical can be harmful. Store in a cool, ventilated area. |
| Storage | 2-Fluoro-5-Methylbenzonitrile should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep it separate from strong oxidizing agents and acids. Ensure proper labeling and store at room temperature. Avoid moisture exposure and use appropriate personal protective equipment when handling the chemical. |
Applications of 2-Fluoro-5-Methylbenzonitrile in Industrial ManufacturingAs a core manufacturer specializing in high-purity aromatic nitriles, we supply 2-Fluoro-5-Methylbenzonitrile to downstream clients focused on advanced material and specialized chemical synthesis. Our quality control, continuous process validation, and collaborative technical support enable customers in targeted sectors to optimize their production efficiency and meet evolving regulatory standards. 1. Pharmaceutical Active Ingredient SynthesisOur clients in pharmaceutical production apply this intermediate in the synthesis of APIs, particularly for anti-inflammatory and central nervous system (CNS) drugs where selectivity and purity profiles are critical. The nitrile group and fluorine substitution pattern support precision coupling and downstream transformations during multi-step synthesis routes, enabling robust process consistency for patented molecule development and generics registration. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Crop Protection and Agrochemical SynthesisCommercial agrochemical formulators utilize this raw material as a selective building block in the synthesis of modern herbicides and insecticides. Its substituted nitrile structure facilitates stepwise construction of active ingredients with desirable environmental and toxicological profiles, in compliance with global agri-regulations. Analytical traceability and batch reproducibility are paramount for downstream synthesis validation and field application scale-up. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Fine Chemical and Specialty Intermediate ProductionManufacturers of advanced organic intermediates rely on this compound when producing custom fine chemicals for electronics, photographic, and specialty resin applications. The nitrile and fluoro functionalities offer programmable reactivity for further derivatization, ring-extension, or insertion chemistry. Custom purity and consistent particle morphology are specified for integration into multi-ton and pilot-scale operations, frequently supporting bespoke R&D and niche market demands. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Advanced Dye and Pigment ManufactureProducers of specialty dyes deploy this aromatic nitrile as a core intermediate in colorant molecule synthesis where exceptional thermal and chemical stability are crucial. Its electronic properties allow for targeted diazotization, coupling, or ring-modification reactions suited for pigments in plastics, coatings, and fiber coloring. Consistent reactivity and minimized metal impurities are mandated for quality grading in high-performance dye sectors. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2-Fluoro-5-Methylbenzonitrile 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
Flexible payment, competitive price, premium service - Inquire now!
Among the building blocks we work with in our chemical plant, 2-Fluoro-5-Methylbenzonitrile stands out for the way it blends fluorinated and aromatic chemistry. Every day, technicians in our main synthesis hall move, measure, and process material by hand and instrument, not just exporting a code on a label, but controlling real flow and monitoring reaction paths. Where some see a catalog entry or a “Benzo derivative,” we see the output of batch hours, temperature controls, and purification that take skilled eyes and patience to truly master.
We're talking about a molecule that carries a benzene ring, a nitrogen triple-bonded to a carbon (nitrile), a fluorine atom, and a methyl group, all held together in a configuration that makes life easier for anyone working with halogenated aromatics. CAS number 448-52-4 might be the international reference, but for us, this is a familiar friend on the production line.
Typical runs of our 2-Fluoro-5-Methylbenzonitrile deliver material at purities exceeding 99%, thanks to carefully staged distillation and crystallization. Residual solvents, moisture, or isomeric cross-contaminants demand constant attention. Each drum or container shares the same analytical signature, confirmed by both our onsite GC and NMR. Compared to analogs with chlorine or bromine substitutions, this compound’s volatility falls in an intermediate zone; it’s neither so hard to handle as pentafluorobenzenes, nor so stubborn as the heavier halides or biphenyls.
To build a fluorinated benzonitrile, our technicians run multi-stage reactions, watching carefully for over-fluorination or competitive methylation—troubles every bench chemist knows. The presence of the fluorine atom at position 2 (ortho to the nitrile) shapes both the reactivity and stability of the compound. We see this during synthesis: yields rise higher, purification smooths out, and color impurities tend to wash out more easily than with other halobenzonitriles.
In the lab, the methyl group at position 5 doesn’t just make it easier to spot on a GC trace, it subtly affects both polarity and boiling point—critical for solvents and process engineers. The comparable 2-chloro-5-methylbenzonitrile or 2-bromo-5-methylbenzonitrile bring heavier atom effects; they sit heavier on a balance, carry higher boiling points, and create more issues with byproduct elimination. Our fluorinated compound, by contrast, gives a cleaner mass spectrum. Yields in follow-on reactions consistently prove easier to optimize, especially where downstream aminations or Grignard reactions become necessary.
In day-to-day operations, process engineers report that this molecule’s moderate boiling point (around 175–180°C at standard pressure) simplifies distillation. Handling precautions still matter—fluorinated aromatics demand closed systems and smooth seals to avoid vapor losses or operator exposure—but as manufacturers, we appreciate that the compound resists hydrolysis and photodecomposition. Warehousing and shipment don’t turn into headaches, unlike with some nitrated or peroxide-sensitive benzene derivatives. We keep stock in fluoropolymer-lined drums, and train staff on material transfer: no amateur shortcuts.
Our main downstream customers come from pharmaceutical and agrochemical development. Synthetic chemists rely on the ortho-fluorine/methyl profile for cross-coupling reactions, nucleophilic aromatic substitutions, and as synthetic handles for custom scaffolds. Where benzonitrile itself proves too reactive or unselective, or when 2,5-disubstituted rings tune solubility or lipophilicity for bioactive compounds, our 2-Fluoro-5-Methylbenzonitrile fills that gap. For active pharmaceutical ingredient (API) discovery and registration, having high, consistent purity makes regulatory filings easier, avoiding requalification or costly retesting.
Competing companies sometimes cut corners with lower-purity lots, poorly managed batch records, or off-grade solvent residues. From experience, such shortcuts complicate everything downstream: catalyst poisoning, unexpected exotherms, or batch failures under process scale. Our own standard operating procedures enforce lot testing not just for assay, but for byproduct fingerprinting—a necessity confirmed by years of customer returns and support calls.
Another lesson from the reactor bay: trace residue control must start at raw material sourcing. We caught a spike in hydrolysis byproducts once, traced it back to a contaminated toluidine source, and had to rework the cleaning protocols on every joint. Every bottle representing 2-Fluoro-5-Methylbenzonitrile carries that level of traceability, because there’s nothing abstract about a stuck reactor or a failed campaign.
Colleagues sometimes talk about “just another benzonitrile.” That disregards how vital substitution pattern and purity are for successful end-product development. For example, even minor isomeric impurities can ruin selectivity in Suzuki couplings or Buchwald-Hartwig aminations, leading to wasted time and resources. We target isomer content below 0.1%, a figure backed by hundreds of QC runs and validated procedures, not marketing copy. Each lot release comes after both NMR integration and mass spec confirmation, so we do not ship trouble to a partner’s lab.
Late-stage pharmaceutical synthesis often pushes small variations in ring substitution to exploit subtle differences in metabolic stability, solubility, or protein interaction. That’s where the 2-fluoro/5-methyl pattern helps medicinal chemists adjust compound properties, searching for better pharmacokinetics or cleaner toxicology. In our experience, every milligram counts, so in-process controls monitor both the main product and possible side products, including unreacted anilines or methylated isomers.
Real-world production also means compliance with regulations. While the compound itself isn’t as tightly regulated as some more exotic halides or nitriles, cross-border transport still demands up-to-date SDS documents, clear purity reports, and safe containment. We never delegate regulatory paperwork to outside vendors; instead, trained compliance officers check each outgoing drum or container. Our batch paperwork lives onsite, not just scanned to a server on another continent. This minimizes border hold-ups and avoids any “open storage” snafus at customs warehouses or client warehouses.
Global supply uncertainty hit the fine chemicals trade in 2022 and 2023. We saw delays caused by feedstock disruptions, particularly with fluoroaromatic intermediates sourced from outside Asia. Our solution grew from direct relationships with raw material producers and a policy of in-plant inventory for both key feedstocks and specialty reagents. When a competing plant suffered a half-year outage due to an upstream fluorination incident, our facility absorbed the demand thanks to flexible batch scheduling and consistent environmental controls.
The manufacturing process for 2-Fluoro-5-Methylbenzonitrile doesn’t just yield a drum of clear, off-white solid. It represents years of accumulated knowledge on safe handling, purification, and environmental protection. Waste streams see in-line treatment and neutralization, and every reactor wash goes through chemical oxygen demand monitoring before discharge. Young chemists in our company learn from senior operators how to handle both the main product and byproducts, collecting and packaging even small “non-conforming” lots for specialized disposal—not just vented or buried as might happen in undocumented operations.
Years in the industry taught us the importance of operator safety training—fluorinated aromatics require special respect. Splash exposure to the skin or inhalation can carry risks not always captured in basic safety manuals. Our PPE protocols, from gloves to vented hoods, stem from real incidents tracked and learned from, not just textbook recommendations. We review near-misses on a quarterly basis, making incremental improvements in hazard control: goggles for every pour, chemical suits for drum transfer, gas monitoring in storage areas.
As a manufacturer, watching a client build a new molecular scaffold off our 2-Fluoro-5-Methylbenzonitrile gives real satisfaction. Whether the end-use lands in a clinical candidate, a crop protection agent, or a photochemical innovation, the starting building block sets the ceiling for product success. Customers rely on technical openness: batch records are not just provided for inspection, but form the backbone of their own regulatory filings and patent submissions.
From time to time, research partners come in with requests for custom packaging, sub-batches, or process modifications. We welcome this level of engagement, but always anchor technical adjustments in what our plant can reliably provide, not a wish list divorced from production reality. If an end-user brings up solubility tweaks or precipitation management, we share our own experience with solvent swapping and filtration—advice rooted in experimental runs, not just literature projections. Whenever a synthetic procedure throws an unforeseen side product, our technical team is available for joint troubleshooting; we’ve seen most of the common process wrinkles over a decade.
Handling benzonitriles lacking a fluorine often changes process economics. We finish more time cleaning up after unfluorinated or polyfluorinated aromatics, which generate larger waste volumes and greater energy input for distillation. The electron-withdrawing effect of the fluorine stabilizes the nitrile moiety, knocking down unwanted side reactions and promoting better throughput on scale-up. In our experience, fluorination at the ortho position compared to para or meta also affects solubility in typical reaction solvents such as DMSO, DMF, or toluene, giving formulators added flexibility.
Other benzonitriles in our product line—like 4-methylbenzonitrile or 3-fluorobenzonitrile—find uses in more limited contexts where their regioisomeric profile suits specialized applications. Versatility makes 2-Fluoro-5-Methylbenzonitrile a central node for cross-couplings and protecting group strategies. Its performance as a synthon outpaces less substituted analogs, especially in cases involving heterocycle formation or selective reduction.
Scaling up production above 100-kilogram batches pushed us to rethink purification—chromatography for small lots, but better crystallization and filtration on the industrial reactor. Each approach takes careful temperature and stoichiometry adjustments: too fast and purity slips; too slow and energy waste follows. Yields can dip when operators lose discipline. Our own plant data showed how even five-degree temperature drift triggers impurity upticks. Quality assurance audits focus on both laboratory results and the workflow habits of our plant teams. Training reoccurs constantly, and lessons learned from pilot campaigns roll back into the next production run, keeping standards from sliding.
Customers building APIs or regulatory submissions count on that consistency. For every kilo delivered, no matter the size of the batch, each specification—moisture content, appearance, melting point, GC purity—receives sign-off by at least two analysts. Repeated seasonal audits and anonymous spot tests throughout the year (especially during cold months when process solvent residues can linger) keep our technicians sharp.
The post-pandemic world reinforced a lesson: single-point supply chains bring outsized risk. We diversified our precursor supply, keeping direct lines to at least two sources for each raw material. Storage protocols now account for potential transit interruptions, with buffer stock rotated proactively, not just filled on demand. The logistical complexity that comes with offshore sourcing—especially for fluorinated or methylated aromatics—means we stay in conversation with shipping partners and logistics planners at every step. By keeping shipment sizes manageable, with redundancy in routing, our plant maintains reliable output even when global freight faces disruption.
Onsite production grants real-time feedback. Process runs that throw off unusual color, odor, or byproduct signals trigger immediate review before a drum leaves the plant. We update both production staff and end-users with process changes, adapting QC methods and shelf-life recommendations from empirical storage trials—real-world data, not theoretical shelf lives.
Trends point toward greater demand for custom-tailored fluorinated building blocks as biologically active molecules test new spaces in both pharmaceuticals and advanced materials. Our team watches patent filings and regulatory updates, adjusting product offerings and documentation in step with new legal and technological standards. As reaction methodologies evolve—shifting towards milder cross-couplings, C-H activation, or photoredox chemistry—the robustness and versatility of the 2-fluoro/5-methyl framework stays relevant.
We anticipate tomorrow’s requests may look different from yesterday’s, requiring even tighter specs, specialized particle size, or new packaging to meet global transportation and environmental requirements. The plant’s modular production lines stand ready to accommodate such evolution, supported by trained technicians and chemists invested in seeing every process step done right.
Working with 2-Fluoro-5-Methylbenzonitrile daily reveals both the potential and challenges of handling specialty chemicals wisely. The lessons come from hands-on operations: late-night distillations, process troubleshooting, and face-to-face client feedback. Raw material quality, operator expertise, batch documentation, traceability, and technical support—these make up the core of what we deliver, not just a chemical formula. Underneath each delivered drum sits a chain of knowledge—our promise that every gram started in a plant that values reliability, safety, and collaboration.