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HS Code |
351547 |
| Chemical Name | O-Methylanisole |
| Cas Number | 578-58-5 |
| Molecular Formula | C8H10O |
| Molecular Weight | 122.16 g/mol |
| Appearance | Colorless liquid |
| Boiling Point | 172-174 °C |
| Melting Point | -34 °C |
| Density | 0.97 g/cm³ |
| Refractive Index | 1.513 |
| Flash Point | 58 °C |
| Solubility In Water | Insoluble |
| Smell | Pleasant, aromatic odor |
As an accredited O-Methylanisole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 500 mL amber glass bottle labeled "O-Methylanisole, 99%." Features hazard symbols, lot number, and manufacturer’s contact details. |
| Shipping | O-Methylanisole should be shipped in tightly sealed containers, protected from light, heat, and incompatible substances. Handle as a flammable liquid, following all relevant regulations (such as UN 1993 for flammable liquids). Ensure containers are properly labeled, packed in accordance with local and international shipping guidelines, and accompanied by necessary safety documentation. |
| Storage | O-Methylanisole should be stored in a tightly closed container in a cool, dry, well-ventilated area away from heat, sparks, and open flames. Ensure storage away from strong oxidizing agents and incompatible materials. Protect from direct sunlight and moisture. Properly label containers and keep them in a designated chemical storage area to prevent accidental exposure or spills. |
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Purity 99%: O-Methylanisole with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Molecular Weight 122.16 g/mol: O-Methylanisole with a molecular weight of 122.16 g/mol is used in organic laboratory syntheses, where accurate dosages enable precise reaction controls. Boiling Point 172°C: O-Methylanisole with a boiling point of 172°C is used in solvent extraction processes, where its volatility allows for efficient recovery and reuse. Viscosity Low: O-Methylanisole of low viscosity is used in coating formulations, where easy application and uniform spreading are achieved. Stability Temperature up to 120°C: O-Methylanisole stable up to 120°C is used in fragrance manufacturing, where it maintains aromatic integrity under processing conditions. Melting Point -33°C: O-Methylanisole with a melting point of -33°C is used in chemical process industries, where liquid phase is maintained across various operating environments. Flash Point 54°C: O-Methylanisole with a flash point of 54°C is used in controlled laboratory environments, where safe handling and minimized fire risk are required. Water Solubility <0.1 g/100 mL: O-Methylanisole with low water solubility is used in hydrophobic formulations, where separation from aqueous phases is critical. |
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O-Methylanisole, known in chemical circles as 2-methylanisole, draws attention for its mix of reliability and versatility. While it isn’t a household term, folks across chemical and pharmaceutical industries recognize its place and value. Based on my own years spent around labs and process lines, O-Methylanisole never gets lumped in as a “generic” solvent or additive. Its profile—a clear, colorless liquid with a mild aromatic scent—marks it for specialized tasks. As with many products in the anisole family, the arrangement of its atoms means that small shifts in its molecular structure bring out big changes in how it performs.
In routine work, I’ve seen O-Methylanisole deliver performance where some alternatives fall short. With a boiling point higher than plain anisole and a more specific reactivity profile due to that methyl group on the ortho position, it settles comfortably into roles where subtle chemistry matters. Its CAS number often comes up in sourcing conversations, yet true value shows up only when the requirements call for a mix of stability and targeted reactivity. I remember receiving separate requests from fragrance labs and drug research teams, each searching for the right intermediate or a reaction solvent less likely to introduce impurities. Consistent supply and well-documented testing reinforce its reputation among those who prioritize batch consistency and traceability.
The O-Methylanisole model most in use generally sits at a high purity level, usually above 99 percent, important for anybody who cares about managing trace contaminants during multi-step syntheses. Its molecular formula—C8H10O—tells part of the story, but purity numbers and low water content are what researchers and plant managers examine first. From my experience, teams aim for the version with as little mixed isomer contamination as possible. This gives peace of mind when scaling lab work to the pilot stage, or when an ingredient grade has implications for downstream applications.
Hydrophobicity and solvent power often end up guiding choices. In real-world settings, somebody running a reaction isn’t just consulting a textbook—they’re checking to see how a solvent behaves in their exact process, whether it degrades under mild acid or base, or if it holds up under heat. O-Methylanisole carries that methyl group next to the methoxy group, shifting its electronic properties in a way that matters during electrophilic aromatic substitution or Grignard reactions. This isn’t merely academic. When one batch goes slightly off-profile, the difference often comes down to subtle interplays like this, especially if you work with organometallics or want predictability in yield and quality.
In daily practice, O-Methylanisole enters the mix as an intermediate, a solvent, or even as a starting material for more complex molecules. Medicinal chemistry teams tend to reach for it as a building block when designing molecules for both investigational and scaled therapeutic projects. In the fragrance and flavor world, that pleasant aroma isn’t just for show; it provides a core note for custom blends. From what I’ve seen, those who know their way around fine chemicals appreciate the way it blends with other aromatic compounds, with less propensity for unwanted side-products compared to some of its para- or meta-counterparts.
Sometimes, I’ve had small R&D shops ask about using O-Methylanisole in dye synthesis or in pesticide intermediates. Its relatively low toxicity, especially compared with heavier duty reagents, doesn’t make it benign, but most safety teams find it easier to manage when strong-smelling, more reactive solvents aren’t needed. Experienced operators like having a toolkit of solvents and intermediates where trade-offs are understood. In practice, the methyl group on the ortho position doesn’t just change reactivity—it can allow or prevent specific functionalizations during multi-step reactions, giving researchers a handle on selectivity that standard anisole might not allow.
The anisole family covers several members, each with a methyl group in a slightly different spot. That may sound trivial, yet anybody who’s tried using meta- or para-methylanisole in the same reaction learns quickly about how those small structural tweaks affect reactivity and end-product profile. O-Methylanisole stands out because of how it guides reactions—not just by speeding them up, but by nudging product distribution or altering side-product risk.
I can recall a project where the swap from para- to ortho-methylanisole immediately changed purification outcomes. This isn’t because of some mystery property, but because orientation of substituents shifts the electron density over the aromatic ring. For a synthetic chemist, that means getting more of what you want, and less of what you don’t. Compared to regular anisole, which puts the methoxy group without additional methyl, O-Methylanisole’s extra group adds both steric bulk and electronic push, shaping interactions with incoming reactants or catalysts. The result: fewer byproducts, and often easier isolation. For many, this spells cost savings and greater safety, especially when reactions scale into multi-kilogram runs.
Over the years, anyone who spends enough time with solvents and aromatics learns to weigh both the risks and upsides. With O-Methylanisole, the main handling challenges relate to its aromatic nature—not so much due to acute toxicity, but because its vapors and residues linger longer than some aliphatic choices. In well-ventilated labs, these risks become manageable. My own training always emphasized storing it away from oxidizers, and paying attention to fire hazard signage. People often underestimate how a single spilled bottle can perfume an entire lab space. Secondary containment and dedicated storage remain non-negotiable for good practice.
Spills and scrapes do happen. Every time someone gets lax, thinking “it’s just another solvent,” minor accidents can turn into headaches. Wearing the right gloves, keeping splash shields in place, and labeling containers clearly definitely make a difference. You appreciate these habits the first time you handle an unexpected pressure buildup, or when clean-up takes three times longer than expected. In larger operations, teams often combine engineering controls—like explosion-proof fridges or fume hoods—with daily walk-throughs to catch problems early. This isn’t just box-checking, it reflects a respect for both safety and the value of uncontaminated stock.
Any conversation about chemical intermediates touches on supply chain and purity issues. In my own work, reliability nearly always overshadows cost savings. A batch of O-Methylanisole that doesn’t match past performance can set back multi-week projects, especially in scale-up environments. QC labs usually run GC or NMR checks on every lot, flagging even minor deviations. That’s partly because the chemical’s specification—purity over 99 percent, controlled moisture content, trace-level contamination documentation—links directly to batch reproducibility. For pharmaceuticals, nobody wants to introduce unknowns at the intermediate stage. The same counts for regulatory tracking, especially if the end use ever comes under detailed audit.
In my opinion, the best suppliers have earned trust not just through certificates, but by supporting documentation and a willingness to run re-tests if something comes up. Those working with O-Methylanisole for years often prioritize transparency—requesting detailed impurity profiles, asking for actual spectra, and sometimes even conducting joint audit visits to production sites. While any chemical producer can claim quality, only the responsive ones stay at the top of preferred supplier lists. This direct relationship between the technical community and suppliers matters: it closes the loop when new quality issues, application developments, or supply disruptions appear.
Many chemical engineers and lab managers approach O-Methylanisole use cautiously at first, especially if replacing an older solvent or intermediate. Typical sticking points include solubility mismatches, unexpected migration during chromatographic purification, or subtle reaction speed shifts. In pilot line work, I’ve sometimes seen teams double-check reaction times and yields after even minor tweaks to supplier or storage conditions. These aren’t just academic concerns. A sudden impurity spike or storage issue can throw off everything downstream, especially in pharmaceutical syntheses or high-purity fragrance compounds.
One memorable episode in my own career involved a shift in the baseline during HPLC analysis. The culprit? Micro-traces of an isomer, not present at problematic levels according to the spec sheet, but just high enough to affect separation. We circled back to both supplier and method validation until the issue was solved, demonstrating that even small specification shifts can have big technical impacts. These practical details often steer purchasing and application choices as much as bulk price or delivery speed.
Sustainability and regulatory compliance keep growing in importance each year. Though O-Methylanisole generally avoids the red flags of some older solvents—persistent toxicity, heavy metal residue, ozone depletion—it contains an aromatic ring. This drives periodic scrutiny around emissions, disposal, and environmental impact. Companies who handle it at large scale typically invest in closed-loop recovery or incineration set-ups, rather than venting or simple wastewater disposal. From my own observations, those ahead of looming regulations stay proactive: investing in abatement technology, keeping documentation airtight, and switching suppliers if documentation falls short.
On the ground, that can mean working with local agencies to ensure every step aligns with both permitting and best practice. Over the last decade, documentation standards have tightened, pressing both manufacturers and end users to track batch data, effluent logs, and waste records more closely. For many, this amounts to both a technical challenge and a reputational one—no one wants to risk a regulatory delay over poor solvent handling, especially with high-profile pharmaceuticals or specialty chemicals in play.
Not every project budget stretches far enough for boutique reagents, so cost and logistical reliability weigh heavily in procurement decisions. From what I’ve experienced, O-Methylanisole isn’t always the cheapest option—standard anisole or simpler aromatics sometimes edge it out on price. But in the critical tasks where performance and selectivity top the list, spending a bit more delivers measurable returns through easier separation steps, higher yields, or reduced risk of off-spec batches.
Supply reliability makes a difference, especially for companies working across borders. Shipping aromatic compounds involves documentation, restrictions, and a need to understand local import regulations. The most reliable suppliers help smooth this process by providing complete paperwork and clear hazard communication. This isn’t just bureaucracy in action. For sensitive markets or high-volume customers, slow paperwork or missing SDS documents can hold up entire projects—or, worst case, run afoul of customs or environmental standards. Those hard-earned lessons push many teams to develop direct lines to both their own compliance staff and their go-to chemical sources.
In practice, chemists and process engineers offer the strongest voices on what works and what doesn’t. Whether in small labs or production plants, nobody wants to introduce a new solvent or building block without a clear case for its benefits. For many who work in medicinal chemistry, the selective reactivity of O-Methylanisole trumps concerns about price or supply volume. For others in the fragrance arena, its clean scent and stable behavior under mixing and storage become its main strengths.
One thing I’ve heard repeatedly from end users: communication matters most when switching intermediates or solvents. Labs developing new routes or refining yield and selectivity often count on candid feedback loops between bench teams, QC labs, and purchasing. Sometimes, just the act of sharing an application note or a detailed reaction history can solve months of troubleshooting. O-Methylanisole, for all its technical interest, shines brightest in settings where interdisciplinary teams weigh both short-term project needs and long-term operational fit.
Teams looking to make the most of O-Methylanisole usually focus on three areas: technical fit, supply management, and transparent safety planning. On the technical front, trialing small batches remains the surest way to confirm compatibility in both new and established syntheses. Detailed comparison studies, mixing documentation from suppliers with in-house trial data, build stronger cases for wider adoption or permanent switchovers.
On the supply side, locking in qualified suppliers through regular audit, sampling, and batch validation closes much of the risk. Colleagues across pharma, flavors, and chemical manufacturing often pool resources, enrolling multiple sources or developing multi-year relationships with proven performers. This decentralized approach means fewer surprises when a core supplier faces interruption or regulatory pressure. It keeps projects moving even when hiccups hit global logistics networks.
Finally, on the safety and compliance front, embedding regular refresher training and audit cycles into operations transforms what could be a rote, box-checking exercise into a practical asset. Risk doesn’t disappear, but it becomes manageable. I’ve seen firsthand how well-drilled safety teams shut down small incidents fast, protect both people and product, and keep regulatory teams satisfied during unannounced checks. At the end of the day, confidence in a product like O-Methylanisole springs not from simple familiarity, but from accumulated experience and a willingness to stay focused on details that evolve with both markets and regulations.
O-Methylanisole makes its mark by serving as more than just another aromatic compound. It steps confidently into reactions and processes demanding precision, reliability, and well-understood trade-offs. Users from specialty labs to full-scale production recognize its unique blend of properties and the role it plays in projects at the cutting edge of chemistry. Those who get the most out of it draw from a mix of hands-on experience, ongoing learning, and proactive change management. In my own career, that’s the recipe for building lasting solutions and avoiding the painful setbacks that too often haunt poorly-chosen shortcuts. By striking a balance between innovation and grounded decision-making, teams can ensure O-Methylanisole supports both present results and future growth in demanding fields.