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3-Methylbenzyl Alcohol

    • Product Name 3-Methylbenzyl Alcohol
    • Alias m-Toluyl alcohol
    • Einecs 202-678-6
    • 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
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    Specifications

    HS Code

    282576

    Chemical Name 3-Methylbenzyl Alcohol
    Synonyms m-Tolylmethanol, m-Methylbenzyl alcohol
    Molecular Formula C8H10O
    Molecular Weight 122.16 g/mol
    Cas Number 580-99-2
    Appearance Colorless liquid
    Boiling Point 220-222 °C
    Melting Point None (liquid at room temperature)
    Density 1.02 g/cm³ (at 20 °C)
    Refractive Index 1.534-1.536
    Flash Point 106 °C
    Solubility In Water Slightly soluble
    Odor Aromatic odor

    As an accredited 3-Methylbenzyl Alcohol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3-Methylbenzyl Alcohol is packaged in a 500 mL amber glass bottle, tightly sealed, and labeled with hazard and chemical identification information.
    Shipping 3-Methylbenzyl Alcohol is shipped in tightly sealed containers made of glass or compatible high-density polyethylene. It should be stored and transported in a cool, well-ventilated area away from sources of ignition or strong oxidizers. Proper labeling, adherence to hazardous material guidelines, and compliance with relevant transport regulations are required.
    Storage 3-Methylbenzyl Alcohol should be stored in a tightly closed, properly labeled container in a cool, dry, well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep it separated from oxidizing agents and acids. Store at room temperature, protecting from moisture, and ensure compliance with relevant safety and chemical storage regulations.
    Application of 3-Methylbenzyl Alcohol

    Purity 99%: 3-Methylbenzyl Alcohol with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency.

    Low Impurity Content: 3-Methylbenzyl Alcohol with low impurity content is used in fragrance formulation, where it provides a clean olfactory profile and minimizes side reactions.

    Molecular Weight 136.19 g/mol: 3-Methylbenzyl Alcohol with molecular weight 136.19 g/mol is used in specialty chemical production, where precise molar calculations optimize reaction efficiency.

    Melting Point 7°C: 3-Methylbenzyl Alcohol with melting point 7°C is used in laboratory reagent preparation, where consistent phase behavior is required for reproducible results.

    Viscosity 14.5 cP: 3-Methylbenzyl Alcohol with viscosity 14.5 cP is used in resin modification, where it controls the flow properties for uniform coating application.

    Stability Temperature 120°C: 3-Methylbenzyl Alcohol with stability temperature 120°C is used in industrial process solvents, where thermal stability prevents decomposition during high-temperature operations.

    Color <10 APHA: 3-Methylbenzyl Alcohol with color <10 APHA is used in cosmetic ingredient production, where low color ensures transparent and visually appealing formulations.

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    Certification & Compliance
    More Introduction

    3-Methylbenzyl Alcohol: A Reliable Choice for Advanced Applications

    Every so often, a chemical compound comes along that shifts the pace in research and industry labs. 3-Methylbenzyl Alcohol has built a quiet reputation for itself, earning a place among chemists who care about purity, reliable performance, and consistent results. It looks like a clear, colorless liquid at room temperature, but its value extends well beyond its first impression. Specialists rely on it as both an intermediate and a building block, especially when they're after specific aromatic alcohol characteristics in the finished product.

    Unpacking the Model and Specifications

    Plenty of lab tools get attention for physical size or design, but with 3-Methylbenzyl Alcohol, it’s the chemical structure that does the heavy lifting. The core—an aromatic ring with a methyl at the third position and a benzylic alcohol group—brings together a unique combination. The compound shows a molecular formula of C8H10O and tips the scale at about 122.16 g/mol. Chemically speaking, it stays stable under normal conditions, which gives a boost to storage and handling in both academic and industrial settings. Its boiling point hovers around 233°C. This isn’t a flashy number, but it often signals the compound’s advantage in processes that call for precise distillation. The melting point remains above typical room temperature, which lines up with its reliable liquid state as delivered by most major suppliers.

    Some folks look for solubility, and here, 3-Methylbenzyl Alcohol finds usefulness in organic solvents like ether, chloroform, and benzene. Its low solubility in water limits its applications a bit, though that’s rarely a problem in labs where water-compatibility isn’t the priority. The product stands out in purity levels. In reputable supply chains, it’s not uncommon to see minimum purities above 98%, cutting down on the guesswork for downstream reactions.

    Everyday Usage in Laboratories and Industry

    People who handle 3-Methylbenzyl Alcohol notice its versatility long before they thumb through spec sheets. In fragrance labs, the compound finds regular use as a starting material for musk-like notes and subtle aromatic undertones. It mixes well with other aromatic compounds, and seasoned perfumers blend it in formulations requiring reliable backbone molecules. I remember watching a fragrance developer layer it with aldehydes to tweak the base of a floral accord, noting that the gentle toluene-like scent laid below sharper notes and helped “round out” the character of the finished blend.

    Industrial chemists have another view. 3-Methylbenzyl Alcohol fits well in the production of certain pesticides and pharmaceutical intermediates. The methyl substitution on the benzene ring doesn’t just add novelty; it leads to products that bring improvements in stability and reactivity in downstream synthesis. In medicinal chemistry, the benzylic alcohol group opens doors for further transformation, sometimes forming esters or ethers that become active pharmaceutical ingredients. People leveraging this compound benefit from its mild reactivity—enough for transformation, not so much that it triggers unwanted side reactions.

    Chemical engineers point out that it also plays a role as a solvent or a co-solvent, especially where a medium-polar aprotic environment gives an edge. In my experience, the ability to dissolve certain resins or specialty dyes allowed streamlined processing, reducing reliance on heavier or more expensive solvents. That brings benefits in waste reduction and streamlines cleanup, which matters in both large-batch industrial production and small-scale research synthesis.

    Key Differences from Similar Products

    At a glance, it’s easy for someone new to the field to confuse 3-Methylbenzyl Alcohol with its close relatives—benzyl alcohol or even m-methylbenzyl alcohols from different positions on the ring. The position of the methyl group matters, sometimes dramatically affecting reactivity, odor profile, or downstream conversion rates. While benzyl alcohol (the parent compound) brings a generalist’s toolkit to the table, 3-Methylbenzyl Alcohol tends to deliver a narrower, but often more predictable, range of transformations. I’ve seen colleagues attempt to swap out one for the other during troubleshooting and quickly find out that yields and selectivity can drop or that the desired intermediate isn’t forming as expected. It’s not just about the structure—processes built for the 3-methyl substituted version can behave quite differently from those built for other isomers, often due to subtle changes in electron density around the ring or steric hindrance at the methylene group.

    In fragrance work, the odor character changes between the regular benzyl alcohol and its methylated analogues. Some methylbenzyl alcohols lend a woody or balsamic tone; 3-Methylbenzyl Alcohol’s scent nuance tends to drift toward a mild, sweet woody note, making it unique for particular types of perfume bases. Perfumers don’t just pick chemicals for their volatility profile, but also for their nuanced “bottom notes,” which set the character once more volatile components evaporate. Over time, you start to recognize that differences in isomer purity can translate to distinctive shifts in finished fragrance. Choosing one version over another comes to matter quite a bit, especially in premium formulations where every detail counts.

    Quality Assurance and Source Considerations

    Whether someone is working on a research project or preparing industrial-scale synthesis, the reputation of their supplier impacts more than just immediate costs. High-purity 3-Methylbenzyl Alcohol usually comes from established brands that can document their processes, offer batch-specific certificates of analysis, and maintain strong logistics. As a chemical researcher, I learned not to cut corners sourcing aromatics—low-grade product means risk of contamination, inconsistent yields, and often, a longer troubleshooting loop than the initial price savings justify.

    Testing protocols for 3-Methylbenzyl Alcohol typically include GC (gas chromatography) or NMR (nuclear magnetic resonance) confirmation. Many R&D chemists check not only the compound itself, but also for possible contaminants such as toluene, xylene, or unreacted starting materials that might be present in traces from incomplete reactions. Reliable testing helps keep scaling-up projects on track and avoids nasty surprises mid-process, which can waste both time and costly reagents further down the line.

    Why the Importance Goes Beyond Formulas

    Some might brush off yet another aromatic alcohol as just one of many benzylic compounds, but working with 3-Methylbenzyl Alcohol brings to light broader insights about chemical sourcing and modern manufacturing. Gradually, the value shifts from price-per-liter alone to include questions of traceability, reproducibility, and health and environmental safety. With regulators scrutinizing all steps in the supply chain, establishing best practices from the beginning means fewer headaches later. In one pharmaceutical project, our team had to backtrack several steps after finding low-level impurities in a final product traced to contaminated starting materials. That experience hammered home the need to prioritize well-documented, consistently sourced materials, especially when those materials might become part of a drug product subject to global regulatory review.

    The need for responsible chemical stewardship gets stronger, too. Handling 3-Methylbenzyl Alcohol in well-ventilated spaces with robust spill and disposal procedures is part of everyday good lab habits. Over time, responsible labs train their people in not just the “what” of using chemicals, but the “how”—limiting exposure, tracking volumes, and ensuring that unused chemicals don’t sit around deteriorating in back cabinets. The safety sheets are more than paperwork; they form a practical guide as teams juggle synthesis tasks with operational safety. Years ago, the consequences of a neglected bottle became crystal clear after a minor spill caused extra clean-up and paperwork that easily could have been prevented with better labeling and periodic safety checks.

    Addressing Common Issues and Solutions

    Every lab and manufacturer wrestles with challenges around chemicals like 3-Methylbenzyl Alcohol. Longer supply chains bring risk of delays or inconsistent product quality, especially during global disruptions. One direct approach is to build long-term relationships with multiple trusted suppliers, not just chasing the lowest price. Having a backup (or two) can keep projects moving if one source stalls or goes offline due to shipping hiccups, regulatory change, or natural disaster.

    An issue that sometimes flies under the radar centers on waste handling and sustainability. Aromatic alcohols like this one don’t always break down easily in local treatment plants. Facilities getting ahead of the curve invest in on-site neutralization, reclamation from spent solvents, and safe third-party waste handling. When looking for improvements, consider traceability not only from the supplier’s warehouse to your loading dock, but also from your lab’s disposal to the final treatment site. One university chem lab adopted a color-coded labeling and centralized collection system. Lost bottles dropped sharply, spills nearly vanished, and inventory tracked at-a-glance—a reminder that big changes sometimes start with small tweaks.

    Beyond that, education and training answer many headaches before they start. I learned early on to never assume that someone new in the lab could distinguish between 3-Methylbenzyl Alcohol and similar-looking chemicals at a glance. Good habits—like double-checking labels, using unique shelf locations for high-use compounds, and maintaining up-to-date chemical logs—go a long way. In an industry context, some companies run periodic competency checks, updating SOPs based on real-world near-miss reports rather than waiting for a regulatory audit to force change. If you’ve seen even one delayed batch from a mix-up involving close relatives of 3-Methylbenzyl Alcohol, you remember to tweak your training program for next time.

    Choices for Researchers and Manufacturers

    Some decisions boil down to balancing price, quality, and delivery reliability. For fragrance formulators, shifting a base note or adjusting a top note sometimes calls for substituting in 3-Methylbenzyl Alcohol, despite a higher price compared to basic benzyl alcohol. An experienced nose can tell the difference, and so can loyal customers when a signature scent subtly changes. In pharma synthesis, the upfront cost pales next to the value of high-purity product reducing batch failures or limiting downstream purification headaches. Even outside those fields, anyone looking to minimize process downtime, optimize yield, or avoid recalls benefits from knowing their starting material meets robust standards.

    Folks just starting out sometimes underestimate how quickly small issues can snowball. I’ve seen workshops where a sole clogged filter, caused by an unexpected precipitation from an impure batch, threw the entire process off schedule. Most teams learn to keep running logs of issues, pinpoint sources of recurring problems, and create checklists for every new shipment. For some shops, setting aside isolated production runs for validation with new sources helps catch trouble before affecting the main line.

    In large-scale industry, batch variability can show up as slight changes in yield, unexpected coloration, or minor differences in scent profile if the compound forms a key note in a product. Regular testing gets built into QC programs, and lean teams appreciate quick GC or HPLC runs that clear lots for production. Here, the cost of analysis folds into the real world price of maintaining brand consistency, protecting downstream equipment, and holding to schedule.

    Future Trends: Regulation, Sustainability, and Innovation

    The chemical industry sits in a moment of rapid regulatory change, especially around aromatic chemicals used in scents, flavors, and pharma. While 3-Methylbenzyl Alcohol isn’t high on the restricted list in most places, producers and users can’t afford to rest easy. As public interest grows in trace amounts of residual aromatics in finished goods and environmental discharge, responsible labs keep up with regulatory signals. That can mean swapping out materials in forward-looking programs, or at least developing contingency plans for tougher scrutiny tomorrow.

    Sustainability turns up in more R&D meetings, too. Sourcing aromatics from renewable feedstocks, cutting solvent waste, and even recycling unused product make a growing difference, not just as a marketing pitch but as a requirement from regulators and large buyers. In my own networks, I’ve seen early-stage pilots on biobased toluene and benzyl derivatives, stretching the limits of fermentation and catalytic conversion technology. It’s not just a pipe dream—lab-scale batches trickle toward commercial feasibility, bringing the day closer when specialty chemicals like 3-Methylbenzyl Alcohol come from waste streams rather than fossil feedstocks. Anyone planning ahead recognizes this transition and factors in sourcing flexibility for the years ahead.

    Innovation still matters. New forms of encapsulation for slower, controlled release of aromatic alcohols, updated analytical techniques for ever-lower impurity limits, and customizable blends tailored to emerging markets keep industry researchers engaged. Those immersed in fragrance, pharma, or specialty chemicals know that no product can stand still indefinitely. They look for compounds like 3-Methylbenzyl Alcohol that offer a high degree of chemical predictability and a base for further transformation—whether for creating rare isolates, boosting synthetic throughput, or supporting safer, greener alternatives.

    Real-World Stories: What the Data Shows

    Many seasoned chemists and engineers keep records of unexpected results tied to sourcing or handling decisions. A multi-year dataset in our own lab tracked product consistency using two different suppliers for 3-Methylbenzyl Alcohol. Variability in trace contaminants showed up in only one supplier’s shipments, and detailed batch-by-batch records let us help the vendor identify an upstream process step that needed tightening. The lesson? Choosing not only the right chemical, but also tracking lots, recording minor differences, and giving feedback upstream makes life easier in the long term. It’s easy to overlook the impact of a minor contaminant until it lands in a final product and triggers rework or downtime.

    Similar lessons apply in fragrance and flavor labs. Some new technicians assume close relatives of 3-Methylbenzyl Alcohol—like 4-methyl or 2-methyl isomers—will suffice. Veteran noses quickly prove otherwise, showing how overlap at a formula level leads to big differences in a finished scent. R&D teams starting new projects learn to run small panel tests and use analytical tools to compare consistency, odor profile, and blending characteristics. Companies that skip these steps often run into repeat customer complaints, traceable once the right investigation shines a light on the ingredients involved.

    Sharpening Practices for the Future

    Best practices with a compound like 3-Methylbenzyl Alcohol rarely boil down to a single formula. Instead, teams refine workflows over time, learning from missteps and sharing process tricks. That might mean updating batch labeling systems, automating log entries with barcode scanners, or even drawing up photo reference sheets to keep high-use aromatics from mixing during busy production stages. It might mean reaching out to suppliers after QC hiccups, setting explicit expectations, or even organizing monthly reviews of handling and waste management procedures.

    Training stays central. Teams that invest in practical, hands-on sessions with real scenarios—spills, mix-ups, instrument malfunctions—build muscle memory that written protocols can’t match. Professionals who regularly walk new staff through proper storage and disposal of chemicals like 3-Methylbenzyl Alcohol notice fewer errors, faster response times, and a culture of safety that eventually takes root in everyday habits. As regulations get tighter and product lines diversify, these habits shift from “nice-to-haves” to essential.

    Technology lends a hand, as well. More labs digitize their chemical inventories, track bottle ages, and spot underutilized stock before expiry. Automated reminders prompt technicians to check labeling, rotate older product to the front, and clean up misplaced bottles. The results? Less waste, fewer process interruptions, and a better relationship with environmental health audits.

    Final Thoughts: The Ongoing Value of 3-Methylbenzyl Alcohol

    People sometimes dismiss “smaller” specialty chemicals as replaceable, but hands-on experience teaches otherwise. For those in fragrance, pharmaceuticals, fine chemicals, or research, the choice to use 3-Methylbenzyl Alcohol can spell the difference between seamless production and a backlog of rework. Its performance stands up under scrutiny, its specificity weeds out many variables, and its traceability roots teams in practices aligned with today’s regulatory and ethical expectations. Staying sharp about sourcing, handling, and waste isn’t just about getting product out the door—it's about future-proofing careers, reputations, and the integrity of every result tied to this distinctive aromatic alcohol.