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HS Code |
333323 |
| Cas Number | 829-43-6 |
| Molecular Formula | C9H11NO2 |
| Molecular Weight | 165.19 |
| Appearance | Off-white to light yellow solid |
| Melting Point | 62-65°C |
| Boiling Point | 319.6°C at 760 mmHg |
| Density | 1.17 g/cm3 |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥98% |
| Synonyms | 2-Amino-1-(4-methoxyphenyl)ethanone |
| Smiles | COC1=CC=C(C=C1)C(=O)CC2=CC=CC=C2N |
| Storage Temperature | 2-8°C |
| Flash Point | 147.9°C |
| Ec Number | 212-560-5 |
As an accredited 2-Amino-4'-Methoxyacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 2-Amino-4'-Methoxyacetophenone supplied in a tightly sealed amber glass bottle, labeled with product details and safety information. |
| Shipping | 2-Amino-4'-Methoxyacetophenone is shipped in tightly sealed containers, protected from moisture and light. The package is labeled according to hazardous material regulations, and includes a safety data sheet. Transport is conducted under ambient conditions, meeting all chemical safety and regulatory requirements to ensure safe and compliant delivery. |
| Storage | 2-Amino-4'-Methoxyacetophenone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances like strong oxidizers. Protect from direct sunlight and moisture. Clearly label the container, and store at room temperature unless otherwise specified. Always follow proper chemical hygiene practices and refer to the material safety data sheet (MSDS) for additional safety instructions. |
Applications of 2-Amino-4'-Methoxyacetophenone in Industrial ManufacturingAs an established manufacturer of 2-Amino-4'-Methoxyacetophenone, we supply this specialty intermediate for selective industrial applications where its chemical structure enables essential functionalities. The following segments highlight real-world integrations in commercial downstream processes, focusing on the practical aspects of formulation, compliance, production, and finished product outcomes. 1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) Synthesis2-Amino-4'-Methoxyacetophenone serves as a core building block in manufacturing specific APIs, particularly in the synthesis of cephalosporin antibiotics and certain kinase inhibitors. In multi-step pharmaceutical synthesis, this compound delivers targeted functional groups that facilitate downstream reactions with high selectivity. Manufacturers rely on its consistent purity and reactivity profiles to maintain batch reproducibility and meet stringent regulatory expectations during scale-up from kilo-lab to commercial production. Its integration into route development allows for safer and cost-effective access to advanced intermediates that cannot be substituted by other compounds without process redesign. Industry compliance standards
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2. Advanced Dye and Pigment ManufacturingIn the dye sector, 2-Amino-4'-Methoxyacetophenone acts as a key precursor for high-purity azo and anthraquinone compounds used in specialty textiles, digital printing, and security inks. Its electron-donating methoxy group and ortho-amino configuration permit the synthesis of colorants with tuned absorption bands, fastness, and chromatic performance required for fashion or anti-counterfeit applications. Downstream formulators select this intermediate for its ability to yield highly stable colorants, especially in environments where light and chemical resistance are needed over long-term use. Industry compliance standards
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3. Fragrance and Aroma Ingredient SynthesisIn the aroma chemicals industry, 2-Amino-4'-Methoxyacetophenone provides the basis for functionalizing benzene rings with methoxy- and amino-substituted acyl groups, critical for producing musky, vanilla, and powdery olfactory notes used in perfumery and fine fragrance formulations. Its highly selective acylation potential enables process chemists to control the introduction of odor-active compounds without side products that could affect olfactory purity. Rigid QC and regulatory requirements for trace levels and residuals have led to controlled deployment of this intermediate in aroma compound synthesis lines. Industry compliance standards
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4. Agrochemical Intermediate DevelopmentIn the agrochemical sector, 2-Amino-4'-Methoxyacetophenone features in the synthesis of several selective herbicide intermediates and insecticidal scaffolds. Its particular substitution pattern enables the development of active compounds with programmable biocidal selectivity and lower non-target toxicity. Manufacturers engaged in crop protection R&D benefit from the stability and high assay of this raw material, allowing efficient process scale-up and compliance with escalating regulatory thresholds on precursor residues and final product purity. Industry compliance standards
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5. Specialty Chemical Synthesis for Photographic ChemicalsPhotoresist and photographic processing solution producers leverage 2-Amino-4'-Methoxyacetophenone in the preparation of organic compounds essential for stabilizing image-forming layers and managing optical properties of light-sensitive films. Its functional groups help achieve the necessary reactivity in coupling or blocking steps during the production of imaging formulations where precise photochemical performance is demanded. Stability in both high-pH and high-shear environments supports superior control over process yield and consistency across batch productions. Industry compliance standards
Typical usage ratio
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Speaking as a long-time manufacturer of aromatic intermediates, the production of 2-Amino-4'-Methoxyacetophenone reflects quite a bit about how chemical development tracks with actual real-world needs. In the laboratory and on the shop floor, this compound—often recognized for its sharp acetanilide backbone and methoxy-substituted structure—comes up more often than you’d expect. Its chemical model aligns under the formula C9H11NO2, with a typical purity surpassing 99% after proper recrystallization and distillation. The solid itself appears as pale yellow to off-white crystals, displaying good stability under ambient storage, though we always keep humidity and light exposure in check to avoid any unwanted alteration over time.
In my experience, each batch is judged by much more than a GC number or a melting range. Users in fine chemicals, pharmaceutical intermediates, and even scent creation have specific, sometimes unpredictable demands. A batch of 2-Amino-4'-Methoxyacetophenone should deliver not just high assay but also straightforward handling, clean conversion, and minimal side reactions during downstream processing. In our line, the subtle difference between a reliable lot and a problematic one often comes down to purity control and moisture levels—issues that barely register in a catalog listing but matter a lot to a hands-on chemist. We achieve these through continuous refinement of our acetylation and methylation stages, always guided by on-the-ground feedback from our own technical teams and end users.
2-Amino-4'-Methoxyacetophenone competes against several related acetophenone derivatives. Each version offers something a little different in reactivity, workability, or safety profile. Not all acetophenone-based products incorporate both the amino and methoxy group at the exact positions found here. The para-methoxy and ortho-amino configuration of our product makes it particularly valuable in building complex molecules, frequently appearing as an essential step in heterocyclic chemistry and as a precursor in synthesizing quinoline and indole derivatives.
We’ve seen heavy demand from crop science groups and pharmaceutical developers looking for selective synthons that speed up reaction sequences and minimize byproducts. In the lab, our partners have found that the 2-amino group confers unique nucleophilicity, facilitating key condensations and substitutions that would otherwise stall or require tougher conditions. The para-methoxy adds electron density, improving both solubility and reactivity, while also affecting how the molecule engages with various reagents.
I can recall a time when a customer shifting from a basic acetophenone discovered significant yield improvements after moving to the 2-amino-4'-methoxy derivative. Their original process generated lots of tar and intractable side products. With this compound, we saw the reaction profile sharpen, giving them cleaner separations and, from my plant’s point of view, fewer headaches tied to effluent treatment and residue disposal. This scenario plays out repeatedly wherever our product gets adopted for new chemistry.
Compared to meta- or ortho-methoxy analogs, the para substitution offers more predictable outcomes. The molecular symmetry at play doesn’t just look good on paper; it pushes homogeneous mixing and brings down unwanted complications in catalyst performance. Day to day, this means better throughput and fewer surprises during scale-up. And while several aminoacetophenone variants exist, none have matched the sales or satisfaction we’ve encountered with this specific configuration—not just according to our marketing teams but based on headaches reported (and avoided) in plant production logs.
Working with this compound, our teams encountered the most interest coming from pharmaceutical intermediates—especially those constructed with complex ring systems. Research groups use it as a direct building block for synthesizing 4-quinolones and benzoxazines, where the electron-donating effect of the methoxy group helps in driving cyclizations under relatively mild conditions. In dye and pigment manufacture, the high purity of our batches means fewer off-colors and clean endpoint determination. Specific wishes from fragrance formulators also pushed us to enhance our purification steps, leading to an extra-clear product that avoids imparting off-notes in finished blends.
We’ve also watched agrochemical innovators take advantage of the compound’s dual functional groups to achieve selectivity that basic acetophenone can’t deliver. In some customer cases, after switching to our material, overall synthesis times dropped by up to 20%, thanks to improved intermediate yields and more control at each stage. Our technical hotline often fields questions about what impurities to look out for—an especially critical concern in regulated industries and clinical research. Based on our QC data, the two most important specs we guarantee are minimal residual solvents and a significant reduction in para-methoxyacetophenone contamination. Our continuous batch improvements stem from exactly this kind of direct technical interaction, not from catalog copywriting.
As makers, we’ve learned the importance of strict quality management. Production doesn’t stop at hitting an assay spec—they want batches to behave identically every time. Over the years, we’ve fought stubborn variability in crystal habit, flowability, and odor, which comes from tiny shifts in reaction temperature or mixing efficiency. Resolving these required tighter control of starting materials, better reactor cleaning protocols, and frequent inline monitoring.
Several years ago, we invested in expanded filtration and drying tools, which cut down on batch cross-contamination and ensured less carryover from previous productions. We fine-tuned not only the main reaction but the entire packaging process so each drum or bag arrives as expected. Our warehouse logistics aren’t just an afterthought—improper sealing or excess vibration during transit can promote clumping, leading to problems at the formulation stage. We pack in moisture-barrier bags and box with foam inserts for bulk shipments, always adjusting based on the season and the length of travel. We’ve also logged feedback directly from customers when batches encounter temperature extremes in freight. This dialogue has prompted us to add temporary cold packs during summer months for sensitive deliveries, raising the bar for what customers expect from their chemical partners.
Some clients compare this product to other aminophenones, particularly for performance in multi-step syntheses. The arrangement of its functional groups offers less steric hindrance, and downstream reactions feature higher conversion rates. The addition of the methoxy moiety tends to raise the melting point modestly, giving better control with temperature-sensitive protocols. In fragrance development, the methoxy group's subtle sweet note shows up in certain aldehyde blends—another reason perfume chemists specify this product over plain acetophenone. In pigment production, we’ve seen that its impurities do not easily transfer color or induce turbidity, which cannot be said for less refined alternatives.
I’ve witnessed some chemists try to substitute this compound using more common aminoacetophenones to save costs, but these attempts frequently backfire. The reactivity misaligns, and yields drop as side reactions mount. They often revert to our product, motivated by saved time and lower total residuals in the end product. Through application testing, quarter after quarter, our results consistently show that key reactions—like Schiff base formation or catalytic hydrogenation—run smoother with the para-methoxy group in place. Our data shows a drop in required reagent excess, translating to measurable savings for those in high-throughput environments.
From the outset, we target strict lot traceability. Regular in-process sampling helps us identify impurity trends, with rapid adjustment to reagent feeds or reaction temperatures based on actual yield data, not theoretical values. Issues rarely spring from the textbook points; the surprises are in residual solvents, crystalline byproducts, or minor odorous contaminants, which only turn up in real-world handling and pilot-scale trials.
We’ve faced practical hurdles in the drying process, since over-drying leads to static charges that complicate subsequent blending, while under-drying introduces moisture risk that can cause caking or impair downstream reactivity. Through refining our vacuum-drying methods and adapting cooling routines, we built up a robust, repeatable operation. These hard-earned lessons inform every production run—direct experience far outweighs any PDF protocol or external audit in shaping what actually lands in a customer’s lab or plant.
Safety isn’t taken for granted, either. Our experience shows that 2-Amino-4'-Methoxyacetophenone lacks some of the volatility problems of lighter acetophenones, minimizing airborne exposure and VOC management issues. Storage protocols tailored to this profile allow for longer shelf lives and cleaner inventory management. Whereas some related compounds generate storage headaches due to reactivity with ambient oxygen or acids, our product stores comfortably under ambient nitrogen, with little need for specialized containers except in high-humidity environments.
Our business thrives on long-term relationships, not one-off transactions. Operators and R&D partners share their frustrations and requests, and we channel these into how we shape each batch. Once, a large-scale pigment manufacturer reported inconsistent melting points in their in-house checks. Our technical team dug deep, traced the issue back to a subtle contamination in one grade of methoxy precursor, and revamped our supplier audits and in-house filtration schedules as a result. This hands-on troubleshooting not only solved their bottleneck but elevated our entire operation’s performance.
Customers from regulated sectors often ask about batch documentation and traceability. Responding directly, we log every step from raw material reception to final QC release. Full chromatograms, residual solvent analyses, and even historical reaction logs help our partners meet tough audit demands—from pharma startups all the way to large multinational fragrance houses.
Feedback from small-scale research groups also shapes our practice. Some request tighter control over particle size or additional analytical data, which led us to extend our testing beyond standard assays and add NMR or LC-MS confirmation on request. Our plant teams regularly receive requests for project-specific modifications—small tweaks in order to boost downstream performance. These collaborative approaches close the loop between product and user, building trust and ensuring that the delivered compound adds value—not just to a process, but to the final commercial outcome.
Innovation in our sector isn’t just about launching new molecules; it grows from refining production, listening to users, and adapting to fast-changing industry demands. We track emerging trends, like green synthesis or demand for safer, lower-waste processes. As regulatory landscapes evolve, particularly for substances listed as SVHC or flagged under REACH or TSCA monitoring, we stay a step ahead, minimizing undesirable byproducts and expanding our analytical reach.
Digital tracking now streamlines our process management, enabling real-time adjustments from the floor and unlocking deeper process insight. In the age of AI-guided manufacturing, those who ignore front-line knowledge tend to fall behind. We rely on direct analog data—batch logs, operator feedback—and integrate these with automated quality checks that flag even minor deviations, often before they trouble the next department.
By improving each production stage and focusing on real user needs, our team ensures that working with 2-Amino-4'-Methoxyacetophenone goes beyond just buying a chemical. It becomes a partnership, shaped by years of trial, direct technical feedback, and those unglamorous—but essential—routine adjustments that guarantee stable supply, consistent quality, and real-world results.
Supply chains for specialty aromatics flex dramatically with global market swings. Raw material access and logistical disruptions forced us to diversify sourcing without sacrificing material quality. During COVID-19, we doubled efforts to validate new suppliers, built up buffer stocks, and even engineered minor synthesis route adjustments to compensate for interrupted shipments. Through open discussion with R&D partners, we kept projects moving, even as freight prices and lead times soared.
New regulations require not just cosmetic quality changes, but meaningful reductions in solvent use, emissions, and hazardous residuals. We responded by investing in solvent recovery and switching to greener alternatives where efficacy held. Alongside this, continuous staff training and open channels for reporting operational concerns elevate our workforce to a key driver in compliance and performance improvements. This loop of feedback and correction keeps us sharp, vigilant, and ready for the next turn in regulatory expectations.
Making 2-Amino-4'-Methoxyacetophenone isn’t just an exercise in scale and chemistry—it’s a living record of adaptation, a blend of traditional skills and modern process control. Our plant operators know the quirks of this reaction and funnel their observations straight into our process improvement cycles. Many in our team started at the bench or with hands-on experience running reactors; their knowledge feeds the customer as directly as any business plan or sales call.
I’ve watched our engineers and chemists troubleshoot odd color bursts, temperature anomalies, and material flows—always tuned to the signals a well-run batch sends. Sometimes, pattern recognition born of decades beats high-end sensors in catching early signs of trouble. Sharing this expertise means our product doesn’t just serve today’s needs but creates a base for tomorrow’s discoveries, whether in fine chemicals, modern APIs, or high-performance pigments.
Reflecting on what sets our 2-Amino-4'-Methoxyacetophenone apart, the answer lies in the spirit of manufacturing: Every kilogram reflects choices to chase after purity, stability, and customer support, shaped by dynamic industry standards and evolving practical know-how. Close collaboration with users and disciplined attention to incremental process upgrades give our partners the confidence to move fast, minimize rework, and scale up with as few surprises as possible.
The journey doesn’t finish after a container leaves our warehouse. Long-term product excellence means staying available for customer questions, sharing new insights from the field, and being open to tough feedback. Through this constant dialogue, both sides—manufacturer and user—elevate chemical standards, reducing waste, sidestepping regulatory pitfalls, and keeping the wheels of innovation moving. In the end, real value flows not from buzzwords or boastful specs, but from the quiet, day-in and day-out effort of people who care about keeping chemistry practical, clean, and relentlessly forward-looking.