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Ethyl 2-Methylbenzoate

    • Product Name Ethyl 2-Methylbenzoate
    • Alias Ethyl o-toluate
    • Einecs 210-313-5
    • 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
    VTB
    Specifications

    HS Code

    514060

    Chemicalname Ethyl 2-Methylbenzoate
    Molecularformula C10H12O2
    Molecularweight 164.20 g/mol
    Casnumber 614-30-2
    Appearance Colorless liquid
    Boilingpoint 223-225°C
    Meltingpoint -24°C
    Density 1.03 g/cm³
    Refractiveindex 1.515
    Flashpoint 98°C
    Solubilityinwater Insoluble
    Odor Pleasant, fruity
    Smiles CCOC(=O)C1=CC=CC=C1C

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

    Packing & Storage
    Packing Ethyl 2-Methylbenzoate, 100 mL: Clear glass bottle, tightly sealed, labeled with chemical name, CAS number, hazard pictograms, and handling instructions.
    Shipping Ethyl 2-Methylbenzoate is typically shipped in sealed, airtight containers to prevent leakage and contamination. It should be transported in compliance with chemical safety regulations, away from heat sources and incompatible materials. Proper labeling and documentation are required. Use appropriate protective gear when handling to ensure safety during loading and unloading.
    Storage Store ethyl 2-methylbenzoate in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and properly labeled. Protect from direct sunlight and moisture. Use appropriate chemical-resistant containers. Handle with care, using suitable personal protective equipment to minimize exposure. Follow all relevant safety procedures and regulations.
    Application of Ethyl 2-Methylbenzoate

    Applications of Ethyl 2-Methylbenzoate in Industrial Manufacturing

    Ethyl 2-Methylbenzoate serves as an essential specialty ester for multiple industrial segments, particularly where precision formulation and consistent physical properties contribute to finished material quality. The following sections detail the key application domains, each demonstrating distinct downstream integration, compliance requirements, and functional roles in end-use products.

    1. Flavor and Fragrance Compound Synthesis

    Flavor and fragrance houses utilize Ethyl 2-Methylbenzoate as a key aromatic intermediate, valued for its sweet, balsamic profile which enhances a range of fragrance and flavor compositions. Its predictable volatility and stability at typical compounding temperatures make it ideal in creating nuanced notes. Perfumers and compounders integrate this ester in bulk blending tanks, balancing it with other aroma chemicals during accord development, where it supports both top and body notes for fine fragrances, personal care, and specialty flavors.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • EU Regulation (EC) No 1223/2009 for Cosmetics
    • Food Chemicals Codex (FCC), where used in food-grade flavors
    • REACH Regulation (EC) No 1907/2006 – Registration, Evaluation, Authorisation and Restriction of Chemicals

    Typical usage ratio

    • 0.01%–0.1% in finished fragrance concentrate
    • 0.001%–0.02% in finished food flavoring preparations (adjusted for application and regulatory restrictions)

    Downstream process integration

    • Added during bulk blending of aromatic chemicals
    • Used in the top/middle note batch compounding stages
    • Dissolved in alcohol or carrier oil bases for direct olfactory evaluation and adjustment
    • Filtered before final filling and packaging

    Final product types

    • Fine fragrances (perfumes, eaux de toilette, colognes)
    • Personal care fragrances (soaps, lotions, deodorants)
    • Air freshener bases
    • Processed food flavoring agents (bakery, confectionery, beverage compounds)

    2. Pharmaceutical Intermediate for API Synthesis

    Ethyl 2-Methylbenzoate functions as a critical building block in pharmaceutical manufacturing, particularly for active pharmaceutical ingredients (APIs) and key intermediates. Medicinal chemists employ this ester in esterification and subsequent functional group transformations within the synthesis route for analgesic and anti-inflammatory agents. It enters controlled reaction vessels, supporting scalable batch or continuous-flow synthesis in GMP-certified facilities. Process engineers manage precise stoichiometry and reaction monitoring to ensure high-purity isolations suitable for downstream pharmaceutical processing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) standards for pharmaceutical intermediates
    • European Pharmacopoeia (Ph. Eur.) monographs, where applicable
    • 21 CFR Part 210/211 – US FDA cGMP regulations for drug production

    Typical usage ratio

    • Varies from 1–15% molar equivalent with respect to target product, based on multi-step synthesis pathway
    • Excess adjusted for specific conversion efficiency and target yield

    Downstream process integration

    • Introduced at the esterification or acylation step of the synthesis train
    • Reacted in glass-lined or stainless steel reactors under inert atmosphere for precise reaction control
    • Followed by purification (distillation/crystallization) prior to further derivatization or coupling reactions toward API completion
    • Quality control testing per pharmacopeial and GMP standards before release to subsequent production steps

    Final product types

    • Pharmaceutical active ingredients such as non-steroidal anti-inflammatory drugs (NSAIDs)
    • Specialty pharma intermediates for custom synthesis contracts
    • Precursor materials for hospital generics and branded medicines

    3. Plasticizer Co-Monomer for Polymer Modification

    Polymer manufacturers utilize Ethyl 2-Methylbenzoate as a specialty ester plasticizer and co-monomer to tailor the flexibility, solubility, and processing characteristics of selected plastics and resins. Its molecular structure allows controlled miscibility and enhances flow properties in polymers such as cellulose acetate and polyvinyl derivatives. Resin formulators incorporate this additive at the compounding or pre-polymer mixing stage, targeting improved end-use product durability and handling in consumer and technical films, molded ware, and specialty coatings.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for polymer production
    • EU Regulation (EU) No 10/2011 for plastics intended to come into contact with food (if applicable in end-use)
    • ASTM D1894 (Plastic Film and Sheeting: Coefficient of Friction)
    • RoHS Directive 2011/65/EU for restricted substances in electrical/electronic equipment

    Typical usage ratio

    • 2–10 phr (parts per hundred resin) as a plasticizer or co-monomer, adjusted based on polymer matrix and target physical properties

    Downstream process integration

    • Added to resin melt in heated compounding extruders
    • Blended in solvent-based polymer solutions prior to film casting or coating
    • Dosed during emulsion polymerization for specialty adhesives
    • Uniformly dispersed using high-shear mixers or roll mills

    Final product types

    • Flexible plastic films for packaging
    • Electro-insulating coatings
    • Plasticized molding compounds
    • Specialty water-based adhesives

    4. Fine Chemical Intermediate for Agrochemical Synthesis

    Chemical producers engaged in crop protection intermediate synthesis integrate Ethyl 2-Methylbenzoate as a selective reactant in the multi-step preparation of specialized herbicide and fungicide molecules. Its ester function facilitates clean acyl transfer and aromatic substitution reactions, and its physical properties offer manageable handling during scale-up. Production chemists manage addition in jacketed reactors, optimizing temperature and reflux profiles to maximize conversion for technical-grade agrochemical intermediates.

    Industry compliance standards

    • ISO 9001:2015 Certification for agrochemical manufacturing
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) guidelines
    • Regulation (EC) No 1107/2009 for plant protection products in the EU
    • US EPA 40 CFR Part 158 – Data requirements for pesticide registration

    Typical usage ratio

    • Employed as 5–25% stoichiometric equivalent in synthesis, adjusted per route and targeted molecular yield

    Downstream process integration

    • Charged during controlled acylation or ester-exchange reactions in the early or mid-stage synthesis train
    • Reacted under anhydrous conditions to prevent hydrolysis or side reactions
    • Purified through vacuum distillation or solvent extraction prior to final downstream conversion
    • Strict in-process quality control following FAO/WHO and market-specific agrochemical requirements

    Final product types

    • Technical-grade herbicide intermediates
    • Selective fungicide precursor compounds
    • Advanced bulk agrochemical actives
    • Branched benzoate intermediates for plant growth regulators
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    Certification & Compliance
    More Introduction

    Ethyl 2-Methylbenzoate: Practical Insight from the Producer’s Side

    A Closer Look at a Reliable Aromatic Ester

    Some chemicals have a character that fits right into formulas without causing fuss. Ethyl 2-methylbenzoate falls into that camp. At our manufacturing site, this ester earns its reputation for steady performance, clean profile, and easy handling. Its structure — a methyl group tucked on the aromatic ring’s ortho position, joined by an ethyl ester — sounds simple. Yet that touch of methyl, right next to the carboxyl group, makes a genuine difference once it’s in the pipeline or the lab glassware.

    Specifications and Practical Aspects

    We produce ethyl 2-methylbenzoate to meet industrial demands, not just lab-scale curiosity. The standard model has a purity exceeding 99 percent, which we confirm by gas chromatography and rotating batch sample checks. Experience shows lower-purity batches deliver variable performance, especially during downstream synthesis. During multi-step processes, impurities compound trouble — this is as true in fragrance blending as it is in pharma intermediates. Low moisture is essential for reactivity, so we take steps to cap water content under 0.1 percent. Color stays almost water-clear, avoiding yellowing that complicates inspection and signals unwanted oxidation.

    Odor is a curious point. Some materials arrive harsh or smoky; ours leans toward sweet-floral, almost fruity. The subtlety matters when it heads into high-end fragrances. Boiling point — around 237–240 °C — helps dial in distillation recipes. Density clocks in near 1.05 g/cm³ at room temperature. Even plain storage tells a story: containers cleaned of all acidic residue, dry nitrogen used to blanket, since air and sunlight slowly degrade even a tough aromatic compound. Safety protocols account for mild eye and skin irritation, but our regular staff rarely find surprises after so many years handling it.

    Production Process: Reliability over Complexity

    The most common route uses 2-methylbenzoic acid and ethanol, catalyzed by acid, under reflux. In our experience, batch yields climb above ninety-five percent without heroic efforts. Running stainless reactors staves off metal contamination, which would otherwise hang around in the finished material. During neutralization and washing, we collect all aqueous waste separately to avoid cross-contamination. Final distillation brings out the sharpest, cleanest product — and leaves that persistent greenish top note behind in the pot residue. Our QC steps catch off-spec shipments, and we never ship a batch that trails haze, cloudiness, or shows rapid decomposition on accelerated storage tests.

    Applications: Picking the Right Tool for the Job

    Most ethyl 2-methylbenzoate winds up in fragrances and flavors. Manufacturers like the material because it mimics fruity, berry, and rose nuances — that’s hard to substitute. Formulators use it in fine perfumes as a core note enhancer; they covet its ability to bridge sharp and sweet with a long-lasting undertone. Industrial users value uniformity here, not simply the name. Too much aldehyde content or impurity changes scent character, so consistent purity makes or breaks a formula. It’s fair to say, just a few grams mixed in a base alters the balance of an entire kilo batch.

    Pharmaceutical companies draw on this compound as a synthetic intermediate, particularly for antihistamines and certain local anesthetics. Its ortho-methyl arrangement opens up various reaction routes and keeps byproduct formation low. We’ve found that reaction times align predictably when the starting ester passes strict physical and chemical checks. Fine chemicals suppliers tell us substitution with plain ethyl benzoate, or the para-methyl variant, drops conversion rates and often triggers troublesome side reactions. Chemistry at scale punishes half-steps and prefers a well-tested raw material.

    Specialty plasticizers, photoinitiators, and niche agricultural formulations have found space for this ester in their process trees. It disperses well, avoids clashing with more reactive amines or acids, and stands up to storage for over a year without major property shifts. Manufacturers outside fragrance rarely publicize the ingredient, but steady repeat orders over years tell their own story.

    Comparing Ethyl 2-Methylbenzoate with Related Esters

    Producers sometimes field questions from buyers looking to swap out products for price or availability reasons. It’s tempting to view ethyl 2-methylbenzoate as interchangeable with basic ethyl benzoate, as both share an aromatic ester backbone. Differences in odor, reactivity, and downstream compatibility quickly dispel that notion. The methyl substituent at the ortho position changes both sterics and electronics — it’s not just a minor tweak. We have tracked reactivity in model reactions: ortho-methyl esters react more selectively in Friedel–Crafts acylations, leading to cleaner mixtures. In fragrance blending, that methyl group adds a layer of warmth that straight ethyl benzoate never delivers. Flavor creators recognize the berry character missing from the non-methylated parent.

    Para-substituted versions (ethyl 4-methylbenzoate) exist, popular in some regions and a few specific applications. We’ve trialed these in-house for comparison. Para-arrangement often brings higher thermal stability — but it shifts odor further from the mild, rounded profile ours supplies. Downstream, that difference matters in final product character. Other alkyl variations (methyl, isopropyl, butyl benzoates) each have clear property profiles. Based on solvent power, odor, volatilization rate, and downstream reactivity data, ethyl 2-methylbenzoate holds a distinct position. Users chasing a particular effect — either aromatic nuance, selective reactivity, or shelf-life stability — find few drop-in replacements.

    Experience shows that, despite suggestions, using unrelated esters cuts performance over time. One large fragrance customer shifted a portion of production to ethyl benzoate due to pricing pressure, only to face client returns about muted, flat base notes. Their switch back was swift and complete. For fine chemicals, unanticipated impurities from the wrong ester trickled through multi-stage synthesis, creating significant purification headaches. Painful lessons like these reinforce our policy: select the compound that matches your endpoint, not just your supply line.

    Addressing Supply, Handling, and Practical Industry Feedback

    As manufacturers, we hear from customers struggling with logistic issues. Ethyl 2-methylbenzoate ships well under conventional packaging — 200-liter drums of high-density polyethylene or coated steel. Fragile glass never fares well at volume. Drums must remain tightly sealed; we’ve had a handful of reports where improperly sealed packaging led to mild hydrolysis and visible instability after humid shipping legs. Fast turnover and robust packaging now minimize those risks. Larger scale shipments, up to ISO tank level, work well for bulk fragrance houses or pharma companies needing consistent feedstock.

    Shelf life draws out skepticism from new users, but in practice, ethyl 2-methylbenzoate shows robust stability. We regularly retest inventory up to twenty-four months after production, with no meaningful decrease in purity, provided it’s stored in a cool, shaded, dry environment. Chemical drums need to avoid direct sunlight and high heat, as with most aromatic esters. A single poorly ventilated warehouse corner proved the point: trace impurities multiplied after a summer’s exposure. Internal protocols now insist on stricter warehouse management, and we share those recommendations openly with customers setting up their own stock.

    From an environmental perspective, production creates waste streams, especially from washing and neutralization. We recognized the need to control effluent content and installed charcoal and lime filtering, trapping organics before water leaves the plant. Local inspections confirm drops in total aromatic discharge, and we recycle more solvents in-house — partly driven by cost, mostly by experience watching regulations tighten each year. Aromatic esters never fully vanish; responsible handling of both output and waste is now a given, not an afterthought.

    Our technical feedback loop relies on honest conversation with long-term customers. The most valuable lessons come not from uncritical praise, but from complaints and surprises. Over years, we’ve fine-tuned purification steps because two or three upset customers—one in a Brazilian flavor house, another in a German fine chemicals plant—challenged early versions that failed their own tough GC analyses. Those calls may take time to resolve, but batch-by-batch improvement pays off with lasting loyalty and lower rejection rates.

    Continuous Improvement and Quality Control

    Consistency matters more than paper specs. We check daily batches against established lots using internal reference samples and run regular mass spec confirmation. Labs sometimes find anomalies even in apparently flawless product — these early warnings stop quality drift before it spreads through an export shipment. During scale-up, we review each process tweak for knock-on effects; even small catalyst changes can shift impurity profiles out of range.

    End users sometimes bring up solvent trace residues. We switched from conventional cleaning regimes to a new oxygen-free drying method after discovering low-level oxidized byproducts causing off-odors in long storage. Technical staff monitor not just major peaks, but minor signals that point to trace instability. Where odd signals arise in customer labs, our technical team digs in rather than brush it aside. Confidence in quality starts with tight in-house controls, not just meeting the minimum standard.

    Improvement cycles span the whole chain. A packaging redesign five years ago, prompted by a customer’s feedback, improved drum pourability and sealed in aroma for longer. Our filling equipment now receives regular overhauls, and each operator double checks drum counts, minimizing the risk of unmarked product or mislabeled lots. This real-world diligence stems from years of small avoidable errors building up and impacting both relationships and brand confidence.

    Market Outlook and Value Beyond the Lab

    Ethyl 2-methylbenzoate’s place in the market ties closely to quality and reliability. Demand in fragrance and flavor blends follows consumer tastes, which shift but never abandon the need for nuanced berry or rose bases. Pharma-grade intermediates depend on tighter standards, forcing the producer to raise internal benchmarks. Most customers now expect sustainability reports and respect for local regulation. From our vantage point, the business rewards transparency and readiness to invest in facility upgrades, emissions reductions, and continuous training for operators and QC staff alike.

    Global supply patterns influence availability and price, but relationships built on decades of quick communication and open documentation remain essential. During raw material shortages, customers lean on our regular shipment history, knowing we allocate product to long-term partners before opening orders to the spot market. As manufacturing footprints spread to new geographies, we adapt logistics to meet regulations and shipment needs in each region. What works for a Paris fragrance plant may not suit a Mumbai pharmaceutical site — and experience handling customs, storage nuances, and local transport proves key.

    Complaints rarely revolve around the compound’s technical limits. Instead, challenges stem from shifting rules in chemical management, new product safety declarations, or restricted use lists. We support customers navigating these changes with detailed documentation — and amend our own formulations when necessary. End users now care as much about traceability and environmental record as they do about cost or speed. The best chemical manufacturers recognize that value comes in both molecules and steady, trustworthy service.

    Looking Toward Tomorrow: Challenges and Solutions from the Production Floor

    Operational improvements drive better results for both producer and customer. Tracking and minimizing waste, stabilizing yield, and reducing downtime act as persistent goals. Digital logs replace old paper charts for both compliance and convenience. We’ve added redundancy to analytical testing, ensuring no single machine or operator becomes a weak link.

    Sustainable sourcing now counts almost as much as technical achievement. Petrochemical derivatives bring scrutiny; we explore renewable sources for upstream intermediates. Biotech fermentation pathways -- still in early development -- promise future alternatives, though full commercial scale lies ahead. End users regularly ask about carbon footprint, production energy use, and circular economy initiatives. Experience tells us that adopting best-practices early — not scrambling at regulation deadlines — earns respect and long-term business.

    Operators work closely with quality teams, fostering shared ownership of each drum shipped. Small changes to process plumbing or cleaning routines root out recurring bottlenecks, and regular feedback sessions gather problem reports before they grow. Staff turnover remains low, in no small part due to a culture that respects skill-building and internal communication.

    In the broader market, automation increases safety and steadiness, though judgment built on years handling volatile esters remains irreplaceable. Instrument readings can catch most problems, but the practiced eye — or nose — identifies subtle off-notes computers may miss. Training new staff to pick up these cues takes time and patient mentorship.

    Final Thoughts from a Chemical Manufacturer’s Perspective

    Ethyl 2-methylbenzoate delivers a blend of practicality and specificity shaped by many years of industry feedback. Its unique aromatic profile, paired with reliable process performance, places it apart from other benzoate esters. Each step from raw material handling, through synthesis, purification, packaging, and shipment, demands diligence and grounded expertise.

    As producers, our reputation stands on the lived experiences of customers worldwide using this aromatic ester in flavors, fragrances, and intermediate synthesis. Technical detail, steady improvement, and direct conversation form the backbone of our work. It’s a steady path, paved with facts and lessons learned from both triumphs and setbacks, pushing us to set higher standards. Tracing a drum’s journey from reactor line to customer site, we see the finished product as the beginning of another industry story, shaped by chemistry done right.