|
HS Code |
231913 |
| Iupac Name | 1-fluoro-2-methylbenzene |
| Cas Number | 321-60-8 |
| Molecular Formula | C7H7F |
| Molecular Weight | 110.13 g/mol |
| Appearance | Colorless liquid |
| Boiling Point | 109-111 °C |
| Melting Point | -37 °C |
| Density | 1.012 g/cm³ |
| Refractive Index | 1.497 |
| Flash Point | 24 °C |
| Solubility In Water | Insoluble |
| Odor | Aromatic |
As an accredited O-Fluorotoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | O-Fluorotoluene is packaged in a 500 mL amber glass bottle, securely sealed with a screw cap and appropriately labeled. |
| Shipping | O-Fluorotoluene is shipped as a hazardous liquid, typically in tightly sealed, chemically resistant containers such as glass bottles or metal drums. It should be labeled according to international regulations, protected from heat and ignition sources, and transported with proper documentation and safety measures to prevent leaks, spills, or vapor inhalation. |
| Storage | O-Fluorotoluene should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers and acids. Protect the container from direct sunlight and physical damage. Avoid exposure to heat and moisture. Ensure proper labeling and keep away from food and drink. Handle using appropriate safety precautions. |
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Purity 99.5%: O-Fluorotoluene purity 99.5% is used in pharmaceutical intermediate synthesis, where high-purity ensures minimal by-product formation. Boiling Point 156°C: O-Fluorotoluene with a boiling point of 156°C is used in solvent extraction processes, where precise boiling enables efficient component separation. Molecular Weight 110.12 g/mol: O-Fluorotoluene molecular weight 110.12 g/mol is used in agrochemical manufacturing, where accurate dosing enhances formulation consistency. UV Absorbance <0.01 at 270nm: O-Fluorotoluene UV absorbance <0.01 at 270nm is used in dye precursor production, where low absorbance ensures optimal coloration. Moisture Content <0.05%: O-Fluorotoluene moisture content <0.05% is used in electronic chemical applications, where low moisture prevents unwanted reactions during synthesis. Density 1.08 g/cm³: O-Fluorotoluene density 1.08 g/cm³ is used in specialty polymer synthesis, where uniform density contributes to predictable polymer chain propagation. Stability Temperature up to 80°C: O-Fluorotoluene stability temperature up to 80°C is used in continuous-flow reactors, where thermal stability maintains reaction efficiency. GC Assay >99%: O-Fluorotoluene GC assay >99% is used in fine chemical manufacturing, where high assay guarantees product integrity. |
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O-Fluorotoluene comes up again and again in fine chemical manufacturing, especially in medicinal chemistry. For chemists who need a reliable aryl halide, the difference between cutting corners and getting high-purity O-Fluorotoluene shows up in both yield and purity. To those in the lab, it's more than just another reagent. This compound lays the groundwork for a wide range of pharmaceuticals, agrochemicals, and specialty products, all of which depend heavily on the quality and consistency of their starting materials.
Working with O-Fluorotoluene reminds me of the time I was supporting research on new analgesic agents. Structurally, O-Fluorotoluene carries a methyl group at the ortho position relative to a fluorine atom on the benzene ring. That seems like a subtle shift, but it changes the way the molecule behaves. Flanked by methyl and fluorine, this compound stands apart from its isomers—meta-fluorotoluene and para-fluorotoluene. I’ve noticed that O-Fluorotoluene has particular appeal in cross-coupling reactions, where position and steric effects impact selectivity and reactivity. It's that unique balance of reactivity and stability that makes it attractive for building more complex structures.
Chemists searching for the right O-Fluorotoluene often focus on purity. A model with over 99% GC purity cuts down on the noise in any reaction, meaning fewer byproducts and less time in purification. The right bottle of O-Fluorotoluene brings confidence. The colorless, volatile liquid has a characteristic aromatic odor and clear labeling on density, boiling point, and refractive index. In real-world lab situations, boiling points tend to hover near 130°C, and this matters. If you’ve spent time distilling or evaporating off solvents, you know how small differences in physical data can either support a project or send you back to square one. For those with sensitive analytical equipment, reliable refractive index readings also flag off potential contamination or degradation.
Hazard information deserves attention. O-Fluorotoluene is flammable and demands careful handling. Strict adherence to ventilation and storage protocols isn’t optional; I remember a small solvent spill that became a lesson in the limits of “caution” versus proper fume hood use. Researchers should always check and follow current lab safety standards, not only for O-Fluorotoluene but for any halogenated aromatic compound.
O-Fluorotoluene finds its strength in synthesis. I’ve seen it welcomed as a building block in Suzuki and Heck reactions, with fluoro-substituted aromatics often leading to better drug candidates or more robust agrochemicals. Experience shows that the ortho-fluoro group can influence the electronics of a molecule, offering medicinal chemists a handle on photostability, metabolic resistance, and even the way the compound interacts with biological targets. This advantage becomes clear when comparing candidate molecules for clinical evaluation: a shift in a single atom position can mean the difference between success and a failed trial.
For scale-up, those involved in manufacturing appreciate O-Fluorotoluene for its reliable performance. Its compatibility with a range of catalysts and reaction conditions means less troubleshooting, less downtime, and fewer headaches when repeating batches. In my own experience supporting both R&D and production settings, the value of a compound like this is measured in operational confidence. From gram-scale to multi-kilogram synthesis, O-Fluorotoluene maintains its quality and minimizes variability or unexpected side reactions.
Looking at what makes O-Fluorotoluene different from its cousins comes down to molecular structure. Unlike p-fluorotoluene or m-fluorotoluene, the ortho isomer shows a stronger directing effect in electrophilic substitution. For practitioners in medicinal chemistry, this supports selective functionalization—not just “good enough” chemistry. I’ve worked with many who notice lower yields and more side products when switching away from the ortho isomer. That’s not just anecdotal; research on aromatic substitution patterns and reactivity highlights the impact of fluorine’s electronegativity and the methyl group’s position.
This difference plays out in downstream processing, too. O-Fluorotoluene’s unique properties feed directly into the selectivity of metal-catalyzed couplings. While other toluene derivatives may struggle with sluggish reactions or unwanted rearrangements, the ortho isomer delivers cleaner results, making regulatory filings and quality control less of a paperwork nightmare. Anyone who’s been through a drug approval process knows how small differences at the starting material stage ripple all the way to final approval.
Anyone sourcing O-Fluorotoluene should look for traceability and batch documentation. In my experience, verifying the path of raw materials prevents future problems. Analytical data—like GC, NMR, and MS spectra—backs up purity claims, and helps labs comply with regulatory bodies such as the FDA or EMA. Maintaining full backward traceability, including details about synthetic routes and impurity profiles, means less risk of surprise recalls or lost batches.
This point comes home every time a new regulatory hurdle appears. Drug development doesn’t follow a straight path, and rerunning synthetic lots because of missing documentation sets projects back months. Choosing vendors who offer this transparency spares teams the added cost and frustration that follow poor documentation or undisclosed changes in manufacturing.
In today’s market, global supply chain disruptions have taught labs to pay attention to trusted sources of O-Fluorotoluene. Some may look for the lowest price, but anyone who has managed a research program knows that inconsistent supply can derail even the best strategies. Over the years, we’ve shifted sourcing strategies to emphasize supplier reliability, not just baseline compliance ratings. The supply of key reagents like O-Fluorotoluene may ebb and flow, but strong vendor relationships, communication, and multi-source contracts help maintain stability for long-term projects.
Recent years have brought increasing scrutiny on environmental compliance, especially for halogenated aromatics. Engaging with suppliers who invest in greener synthesis or improved containment systems appeals not only to regulatory agencies but also to teams looking to build a stronger sustainability record. O-Fluorotoluene doesn’t escape these concerns, though its relatively simple synthetic route often means better atom economy compared to more complex molecules.
With O-Fluorotoluene, proactive risk management shapes the difference between an incident-free operation and costly disaster. Having spent time auditing labs and manufacturing sites, I’ve seen first-hand how robust employee training, fire suppression systems, and secondary containment infrastructure make a huge difference. Safety isn’t a checklist; it’s a culture. Regular safety briefings, up-to-date labels, and easy access to SDS documents form the backbone of a safe lab.
Environmental responsibility enters the equation through emissions controls and solvent recycling. Recovery systems for volatile solvents, such as O-Fluorotoluene, cut down waste and emissions. Operators investing in carbon capture, better scrubbers, and efficient distillation decrease both permit headaches and actual pollutants. Policy isn’t keeping up with chemistry in every corner of the world, but major players now recognize that failing to address emissions leads to fines, public backlash, and long-term health impacts. I’ve seen facility-wide programs to capture and treat aromatic vapors not only pay off in compliance but also in employee health and retention.
O-Fluorotoluene isn’t just a legacy reagent from the golden age of organic chemistry. Today’s drug pipelines and specialty chemical programs tap into the peculiar benefits of the ortho-fluorine substitution. Analytical labs continue using the compound to calibrate instrumentation or prepare standards for fluorinated contaminants. The compound’s volatility and well-documented spectral signatures make it a reliable internal reference, especially for GC or NMR methods. For up-and-coming researchers, handling O-Fluorotoluene bridges academic theory and real-world industrial practice; selecting and using such reagents is one of the first steps in moving beyond textbook chemistry.
Colleagues with backgrounds in materials science point out even broader uses—O-Fluorotoluene forms intermediates in the production of liquid crystals and advanced polymers. In these applications, batch uniformity influences not just experimental outcomes, but also material properties such as dielectric constant or thermal stability. Reliable supply and documented consistency maintain product quality over years of iterative development.
Investing in a consistent supply of O-Fluorotoluene stops problems before they start. The cost of subpar batches grows with the complexity of end products. I recall multi-step syntheses where a contaminated lot changed the impurity profile of final drug candidates, forcing full-scale re-analysis at considerable cost. Clear communication between labs, purchasing, and suppliers has proven key to avoiding these mishaps. Using quality agreements, specifying analytical requirements in purchase orders, and conducting random spot checks combine to safeguard projects from preventable interruptions.
Stepwise improvements in upstream chemical management—notifying labs of lot changes, maintaining dual sourcing, and preparing contingency stock—address the unpredictability of global logistics. While it takes time and coordination up front, these steps keep high-impact projects on track. My own teams have built in such redundancies after costly lessons, and the peace of mind pays off every time a global shipment runs late or a regulatory audit gets rescheduled with little warning.
Today’s generation of chemists learns about O-Fluorotoluene not just from textbooks, but through real-time troubleshooting and process improvement. The difference between protocol and practice shows up in how teams react to unexpected results. Senior staff who share knowledge about the quirks of O-Fluorotoluene—its reactivity under certain conditions, impact of slight impurities, and best ways to store—help junior colleagues grow faster. I’ve seen that authentic experience passed down through hands-on demonstrations and case study reviews, not just formal training modules.
Coupling experience with a willingness to adapt means teams are better prepared to adopt new quality or safety guidelines, and anticipate rather than merely react to regulatory change. Many improvements in handling O-Fluorotoluene—from the right glove materials to ideal ventilation setups—originated with those who worked through the details first-hand, not through desk-bound policy.
The story of O-Fluorotoluene demonstrates how foundational reagents support breakthroughs in new drugs, materials, and agricultural solutions. Leaders in R&D know that such basic chemicals represent leverage points; getting them right speeds up ROC curves, shortens development cycles, and reduces time to market for life-changing products. Early investment in knowledge, safety, and supply pays dividends all the way through regulatory filings and scale-up.
Chemists and process engineers who value transparency, sustainable practices, and experience-driven decision-making ensure that O-Fluorotoluene remains both a reliable staple and a source of competitive advantage. Engaging directly with suppliers, staying on top of evolving regulations, and keeping a pulse on industry developments have all shaped my perspective and results in real lab settings.
Reflecting on O-Fluorotoluene’s place in advanced synthesis, I see a compound that rewards thoughtfulness and preparation. Those who look beyond specs and see the connections between fine chemical sourcing, safe operation, and downstream innovation position themselves not just for compliance, but for genuine progress. In every bottle, there’s the opportunity to move science forward—a point that deserves consideration from both newcomers and veterans in the field.