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HS Code |
704689 |
| Cas Number | 578-00-5 |
| Iupac Name | 1-(2-methoxyphenyl)ethan-1-one |
| Molecular Formula | C9H10O2 |
| Molar Mass | 150.18 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Melting Point | 6-8 °C |
| Boiling Point | 246-248 °C |
| Density | 1.079 g/cm³ |
| Flash Point | 104 °C |
| Refractive Index | 1.535 |
As an accredited 2'-Methoxyacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2'-Methoxyacetophenone, tightly sealed, labeled with chemical name, formula, hazard symbols, and batch information. |
| Shipping | 2'-Methoxyacetophenone is shipped in tightly sealed containers, away from heat, sparks, or open flames. It should be stored in a cool, dry, and well-ventilated area, following standard chemical handling protocols. Proper labeling and safety data sheets accompany the shipment to ensure compliance with transportation and safety regulations. |
| Storage | 2'-Methoxyacetophenone should be stored in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances. Keep the container tightly closed and protected from direct sunlight and moisture. Store at room temperature, and avoid exposure to strong oxidizing agents. Ensure the storage area is equipped with appropriate spill containment and that only trained personnel handle the chemical. |
Applications of 2'-Methoxyacetophenone in Industrial Manufacturing2'-Methoxyacetophenone serves as a critical building block in several industrial sectors, particularly within fine chemical, pharmaceutical, and fragrance synthesis. Its favorable reactivity and functional group profile allow manufacturers to incorporate it efficiently into downstream processes where precision and compliance requirements are essential. Below are key application segments detailing industry-specific practices and integration. 1. Pharmaceutical Intermediate for Active Compound SynthesisPharmaceutical manufacturers employ 2'-Methoxyacetophenone as a key intermediate during the synthesis of multiple active pharmaceutical ingredients (APIs), especially in the preparation of compounds containing aryl ketone substructures such as antipyretic, analgesic, and anti-inflammatory drugs. Chemists select this raw material for its reliable reactivity in Friedel-Crafts acylation, condensation, and reduction reactions, enabling multi-step synthesis pathways under controlled batch or continuous processes. Close monitoring of trace impurities and residual solvents remains essential, with all production aligned to stringent cGMP and validation standards for global pharmaceutical ingredient supply. Industry compliance standards
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2. Fragrance Ingredient Synthesis for Fine PerfumesFlavour and fragrance manufacturers utilize 2'-Methoxyacetophenone in the synthesis of aromatic ketone derivatives that impart sophisticated anisic and woody notes in premium fragrance formulations. The material enters precision-controlled acylation and methylation reactions to yield core intermediates, often under batch or semi-batch conditions with continuous quality assessment using GC-MS. Traceability throughout the process and compliance with IFRA and REACH registration demands strict adherence to allowable impurity and residual solvent thresholds, supporting downstream blending into luxury perfumes. Industry compliance standards
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3. Agrochemical Intermediate for Herbicide SynthesisAgrochemical formulators select 2'-Methoxyacetophenone during the synthesis of advanced herbicidal active ingredients where the methoxyacetyl motif increases biological selectivity and persistence. The substance feeds into multi-step alkylation and condensation reactions under temperature- and humidity-controlled manufacturing environments, with compliance enforced by local and global pesticide regulations. Systematic process documentation and traceability ensure safe downstream integration in high-volume herbicide lines. Industry compliance standards
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4. Photoinitiator Precursor for UV-Curable ResinsIn advanced materials manufacturing, 2'-Methoxyacetophenone provides the key aryl ketone structure for photoinitiator chemistry needed in UV-curable coatings, inks, and adhesives. Downstream producers rely on controllable purity and functional group integrity, especially when preparing benzoin-type or α-hydroxyketone photoinitiator families. The compound’s integration requires tailored batch timing and solvent compatibility to ensure downstream crosslinking performance under UV exposure, with all raw material tracking to global regulatory frameworks covering consumer and industrial finished goods. Industry compliance standards
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5. Synthesis of Fine Chemical Intermediates for Dye ManufactureManufacturers in the dye sector incorporate 2'-Methoxyacetophenone to construct azo and anthraquinone dye intermediates, taking advantage of its selective reactivity for introducing functionalized aryl groups. Producers run acylation and methylation reactions under optimized temperature and pH, closely monitoring for color development markers via TLC and UV–vis spectroscopy. Compliance with regional chemical safety directives and quality protocols ensures output meets specification for further coupling or reduction in synthesis routes for textile, leather, and specialty dye applications. Industry compliance standards
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Years on the production floor have shown how seemingly small variations in a chemical can lead to major headaches for users. 2'-Methoxyacetophenone holds its own in a crowded field of aromatic ketones because it delivers rare predictability. Our team produces this material from phenol and acetic anhydride using a methylation protocol that we tweaked many times, always chasing cleaner yields and tighter control of byproducts. The final product comes in colorless to pale yellow clear crystals, free from problematic tars and resins that usually show up in hastier syntheses. This extra bottle-washing and filtration seem excessive to some, but customers tell us every season that the lot consistency matters far more than abstract claims about “high purity.”
The maintained GC area percentage for the main component typically surpasses 99%. Each kilo is tracked with batch records, showing every parameter from start to finish. Moisture content remains below 0.3%, and our monitors keep an eye on trace phenolic impurities, which tend to cause off-odors if left unchecked. With a melting point reliably above 37 degrees Celsius and trace water content held back during storage, what leaves our filling unit mirrors the reference samples kept in our retained inventory vault.
Facial cream formulators, fragrance designers, and pharmaceutical teams all approach acetophenones with their own priorities. The way 2'-Methoxyacetophenone spreads its faintly sweet, balsamic scent at room temperature drives its popularity among fragrance and flavor compounders. Compared with the more common 4'-methoxyacetophenone or even unsubstituted acetophenone, this ortho-methoxy version softens sharp notes and seems to linger longer on substrates. Perfumers picking between these options almost always notice the way 2'-Methoxyacetophenone rounds out spicy or woody accords, letting them tune the overall scent without drifting toward harshness.
Chemical synthesis teams value its higher electron density at the para position, a property we often explain to visiting interns. That methoxy group doesn’t just affect aroma—it directly shapes reactivity in Friedel-Crafts acylation and Mannich reaction work. The way it activates neighboring ring sites means production chemists can achieve selective derivatization, whether building out larger APIs or designing new polymerizable units. The difference sounds subtle in theory, but in the lab results it’s clearer: reduced byproduct burden, easier purification, smoother scale-up. These small differences turn hours of troubleshooting into painless downstream processing.
Customers sometimes ask if there’s really much difference between acetophenones from company to company. For a while in the early 2010s, we wondered ourselves. Then a few years back, a major European fragrance customer called to say his usual batch—picked up from a generalist supplier—set off weird notes halfway through his annual production cycle. He'd never noticed this in our material. That episode set us off delving into factors that rarely show up in data sheets: what residual solvents lurk in trace amounts, which sealing methods block in atmospheric oxygen, and how long samples can rest before off-color formation becomes noticeable even to the human eye.
Our experience led us to abandon an older copper-catalyzed approach and settle on a selective process that reduced residual benzaldehyde and non-volatile tars. The impact jumped out in accelerated ageing tests. Nine months in, color stability and scent held firm while comparison batches from other sources discolored or grew faintly musty. That’s not marketing spin—these were dozens of side-by-side samples, scrutinized by the noses and eyes of people who live and breathe aromatic chemicals every day.
Many acetophenone derivatives look comparable on paper, yet actual handling exposes sharp contrasts. Production of 2'-Methoxyacetophenone in our setup leaves very little residual acidity, which matters for applications requiring acid-sensitive formulation—typically those using natural waxes or fats. During batch transfer, we insist on glass or stainless steel lines, as lower-grade equipment tends to give up trace metals when handling the product at elevated temperatures. Over the years, replacing plastic transfer hoses and switching to nitrogen blanketing cut visible surface corrosion to zero and stretched shelf life beyond twelve months in most storage settings.
We often field questions about solvent residuals. With 2'-Methoxyacetophenone, our short-path condensation and careful vacuum stripping keep common offenders below detection limits. Many industries, especially those feeding the pharma pipeline, demand strict compliance with recent ICH Q3C solvent guidelines. Keeping showing customers third-party GC and NMR scans backs up what our internal QCs demonstrate: that even lots held in stock for a full production season compare to freshly synthesized batches when it comes to smell and visual clarity.
We see requests for para-methoxyacetophenone almost as often as the ortho isomer. Scientists who’ve worked with both will recall that the ortho-methoxy substitution pattern, as in 2'-Methoxyacetophenone, donates electron density differently, influencing regioselectivity in follow-up synthetic routes. The complexity this brings lets research teams experiment with otherwise hard-to-achieve molecular architectures and create products holding new intellectual property value. Put simply, our ability to tune the synthesis controls lets chemists skip laborious column purifications or repeated crystallizations.
Outdoor storage in hot climates proved a problem in the past. After a heat wave led to the observation of subtle yellowing in open drums, we moved to improved thermal insulation and white reflective packaging. These steps preserved the melting range as tested at regular intervals, and stopped trace oxidative color changes, especially after six months of shipment. As these small details add up, so does user trust. Customers send us finished formulations and intermediate samples to double check for off-notes or unexpected trace side products—a mark of trust built up over repeated problem-solving, not just public specs.
Automated reactors and process control software achieve many things, but in our experience, operator skill still makes the crucial difference. Our batch records show that temperature excursions during methylation or imprecise addition rates of acetic anhydride can spike byproducts and lower selectivity. Team members rotate through cross-training and review near-miss events, and every instance sharpens technique—meaning batches produced by our shift teams look and perform the same regardless of season or staff changes. No glossy brochure can replicate years of hands-on learning about agitation rates or de-colorization tweaks. We recognize the people who spot early warnings and intervene before stubborn impurities build up in the reactor floor drains or vacuum lines.
Customers frequently ask, “Why can’t all sources deliver on similar specs?” Years of practice answers that. Larger, commodity-style factories focus on sheer output, sometimes using shortcut batch times or broader temperature windows. We learned that a few extra hours of slow ramp-up, careful monitoring for color at the end of distillation, and redundant filtering lines give us tighter consistency, even as competitors boast about lower costs per kilo. Downtime from blocked filters or mystery residues has taught us to stick with these details, since solving customer complaints costs more—in goodwill as well as expense—than getting it right at origin.
Direct comparisons with 4'-methoxyacetophenone or plain acetophenone shape our internal QA meetings. The ortho isomer exhibits subtle but important differences; it dissolves into most esters and alcohols with greater ease, shows higher refractive index readings, and fades more gradually under UV exposure. These aren’t lab curiosities. One polymer customer told us switching to our product cut discoloration rates in cast sheets by 40%. Another fragrance user measured a 22% longer scent retention time for finished soaps versus the para isomer. These real-world performance shifts drive repeat purchases because our shipments keep meeting those same high benchmarks.
Choosing between methoxyacetophenone isomers means weighing not just odor or melting point, but how each intermediate plays with other actives or excipients. Some API projects fail when impurities from closely related but less pure grades compromise downstream hydrogenation or methylation steps. Solubility in polar and non-polar solvents remains crucial for paint and resin chemists, who report easier blending and fewer rejection batches with our grade than with those targeting broader spec windows. Several brands make claims about universal performance, but in hands-on use, those minor variabilities steer big purchasing decisions.
Many who purchase chemicals assume finished goods are always pure, yet invisible traces dictate success or failure, especially in skin-contact materials and sensitive pharmaceuticals. Downstream users report that trace aniline or cresol byproducts—trivial to spot at first—can sour aged beauty formulations. We screen for these using sensitive LCMS routines and keep records open to long-term partners for third-party audits. The drive to limit potential allergens, even in those batches destined for indirect contact applications, dominates our R&D cycles year after year.
Storage and repacking represent another frequent challenge. Material that is mishandled in repackaging—left in unlined drums or transferred in a humid warehouse—soon shows measurable differences in both lab data and sensory evaluation. Our drums double as bulk and shipping containers, ground and inerted on filling. Our own team pulls reserve samples from each batch, logging visual, chromatographic, and scent checks at 1, 3, 6, and 12 months. Rather than relying on customer feedback to catch storage faults, we catch slipping batches before they ever leave the dock.
In recent years, downstream partners have brought sharper focus on responsible chemistry and greener sourcing. Making 2'-Methoxyacetophenone still requires classic aromatic acylation pathways, but we conduct regular reviews of solvent and vent scrubbing setups. Onsite wastewater recycling, halogen scrubbers, and energy consumption audits shape much of our annual improvements. Each solvent run goes to closed-loop disposal; by 2023, we cut over 95% of halogen vent releases compared to mid-2010s practices.
Large-scale chemical synthesis doesn’t lend itself easily to sweeping green transformations, but experience has made us realists and planners. We voluntarily publish annual environmental disclosures detailing recovery rates, emissions, and waste—data reviewed by partners and local authorities alike. Certifications earned from these efforts open doors to new buyers, but the real benefit comes in reduced regulatory downtime and easier permit renewals. 100% of process water now goes through onsite biological treatment before plant exit. These changes started as compliance needs, but soon became key quality drivers: cleaner process lines, less downtime from blockages, and less risk of product taint from carryover residues.
Producing a specialty ketone like 2'-Methoxyacetophenone creates a web of relationships. Whether it’s a perfumer chasing a signature note or a polymer chemist trying to simplify cleaning between runs, long-term connections make all the difference. We take pride in hosting customer audits, sharing our batch logs, and opening up the lab for hands-on discussions. The best innovations—like the year we shifted to an anti-static, oxygen-excluding drum liner—came from joint problem-solving after hearing persistent user feedback about trace color shift and airborne contamination.
Batches ship out with traceability numbers that tie back not just to a production date but to the operator, QC sign-off, and analytical suite summary. This transparency builds confidence and allows partners to trace back root causes if any issue ever arises. Most customers now request split samples for co-analysis, and some even ask for extra analytical runs on custom packing lines or different atmospheric conditions to simulate their own incoming raw material checks.
The world of chemical manufacturing rarely stands still. Each year brings regulatory updates, shifting market needs, and technical requests from end-users. We track trends closely—whether it’s new safety limits in personal care law, tighter restrictions on trace aldehydes for FDA registration, or demands for closed-system delivery for fire safety insurance concerns. Our in-house team stays in touch with those forecasting these changes, and anticipates modifications to synthesis routes or purification steps to get ahead of compliance headaches.
Pharmaceutical partners now request full impurity profiling and matching against evolving ICH requirements, not just certificates referencing outdated standards. Our response has been to routinely update analytical protocols, tighten secondary purification after main distillation, and train new staff on the details of allergen minimization, even for materials not yet flagged on major regulatory watchlists. The result: more batches pass quality assurance on the first attempt, and customers avoid costly rework or timing disruptions in critical launches.
Every kilogram of 2'-Methoxyacetophenone coming off our lines reflects real-world lessons forged through trial, error, and a willingness to listen to feedback from those who blend, refine, or formulate with this unique material. While data sheets and batch cards summarize technical specs, true value rests in observed consistency, openness to verification, and ongoing attention to details others may overlook. Downstream partners depend on us not just for a product, but for a relationship founded on openness, steady delivery, and the shared goal of zero surprises in the field. Actual use cases—whether in luxury perfumery or cutting-edge pharmaceutical synthesis—continue to shape how we refine, analyze, and support every container shipped. The result: a standard built on trust, shaped by the people who turn chemistry into something more.