|
HS Code |
934530 |
| Iupac Name | 4-(2-methylaminoethyl)phenol |
| Molecular Formula | C9H13NO |
| Molar Mass | 151.21 g/mol |
| Cas Number | 59-21-6 |
| Appearance | White to off-white crystalline solid |
| Melting Point | 112-115°C |
| Boiling Point | 272°C |
| Solubility In Water | Soluble |
| Density | 1.13 g/cm³ |
| Pka | 9.6 (phenolic OH) |
As an accredited 4-(2-Methylamino-Ethyl)-Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled "4-(2-Methylamino-Ethyl)-Phenol, 100g." Label includes CAS number, hazard symbols, and handling instructions. |
| Shipping | **Shipping Description:** 4-(2-Methylamino-Ethyl)-Phenol should be shipped in tightly sealed, chemical-resistant containers, clearly labeled and appropriately packaged to prevent leaks or spills. It must comply with local and international hazardous materials regulations, using appropriate cushioning and secondary containment, and accompanied by a Safety Data Sheet and customs documentation where required. |
| Storage | Store 4-(2-Methylamino-Ethyl)-Phenol in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and acids. Protect from direct sunlight and moisture. Clearly label the storage area, and ensure it is accessible only to trained personnel. Wear appropriate personal protective equipment when handling. |
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On the production floor, 4-(2-Methylamino-Ethyl)-Phenol stands out for its blend of reliability and versatility. Over years of manufacturing various specialty intermediates, this compound keeps earning a place on our critical paths, mainly thanks to its performance in reductive amination, polymer stoppers, and several resin chemistries.
With a molecular formula of C9H13NO and a purity specification defined by GC greater than 99%, our experience tells us that this quality consistently meets the requirements for fine chemical synthesis. The practical handling value of a melting range around 83–85°C and good aqueous solubility make it a favorite among operators who are looking for solid reliability without extra complication in downstream processing.
Every season brings its own challenges in production. We have worked with plenty of compounds that promise reactivity or selectivity on paper only to fall short once the batch volume scales or reactions get fussier. 4-(2-Methylamino-Ethyl)-Phenol isn’t one of those. It behaves with predictability in strongly nucleophilic substitution and Mannich reactions, and the methylamino group resists side-reactions even if pH swings or minor impurities crop up. Most of our client feedback still emphasizes ease of workup and high final yields in active pharmaceutical ingredients where this building block sees use.
Several small-molecule API teams prefer 4-(2-Methylamino-Ethyl)-Phenol as a starter because it lets them avoid harsh reagents or elaborate protection-deprotection strategies. I can name a number of times where batch-to-batch performance stayed within 1.5% for reaction conversion, whether we were using it in 20 kg or 1.5 ton syntheses—a real test of line stability.
Production teams gravitate to this molecule for how it cuts through fuss in purification. The hydroxyl group on the aromatic ring keeps the molecule anchored in aqueous environments and helps separation steps, unlike fully substituted aniline derivatives which can linger in organic phases. Process chemists who manage chromatography columns comment that it breaks cleanly from most byproducts, so there’s less downtime and loading pressure.
From hands-on experience, we avoid overemphasizing claims about overall “efficacy,” since the real question is always about usable yield, crystallization time, and impurity carryover. When filtered and dried under vacuum, 4-(2-Methylamino-Ethyl)-Phenol compresses to a pale crystalline solid that stores easily at room temperature with low sensitivity to air or humidity. These properties have helped many clients cut costs by shortening drying times and simplifying their environmental controls.
Each production lot goes through a direct alkylation route with inline analytical monitoring—something my team insisted on after running into variability from older batchwise methods. This continuous process enables tighter control over reaction exotherm and lowers formation of benzylic impurities. Over the last three years, statistical trending reports have shown less than 0.11% total related substances by area in finished lots.
Switching from iron-catalyzed reductions to catalytic hydrogenation (which we completed in 2017) eliminated trace metal residues. It also improved color and shortens the finishing step. This adjustment was not just about hitting industry marks—it translated to fewer cGMP deviations and made life easier for our colleagues downstream who validate outgoing materials.
Fine chemical synthesis accounts for the largest share of our consumption, especially among clients in drug discovery, polymer formulation, and advanced material labs. In one real-world project, we supplied this compound for synthesis of intermediate bisphenol reagents for high-performance adhesives. The feedback centered on reproducible amination and better adhesion profiles compared to their earlier phenethylamine-based process.
We also see strong demand from dye and pigment manufacturers seeking specific chromophore substitutions. The molecule’s lone pair activation makes it well-suited as a coupling partner for azo or Schiff base chemistry. Our technical support team has worked side-by-side with R&D groups, providing not only typical COA but full DSC profiles and impurity mapping, so bench scientists don’t run blind.
It’s tempting to lump all methylamino-phenols together, but practical applications bring differences into focus. For example, 4-(2-Methylamino-Ethyl)-Phenol contains a beta-amino side chain, unlike pure para-aminophenol, which rarely enables N-alkylation without extra steps. The two-carbon spacer in our product allows for more flexible coupling, which process developers appreciate during scale-up to bulk volumes.
When compared with 4-hydroxyphenethylamine (tyramine), the presence of the secondary methyl group means greater resistance to oxidation and less risk of off-color development—a point anyone in dye, pigment, or ink chemistry notices almost immediately. Amine reactivity favors this molecule for certain resin crosslinking processes, which take advantage of the activated methylamino group for efficient conjugation. These practical differences drive formulators to specify this compound over more common analogs, especially when strict reproducibility is required.
When you have moved hundreds of metric tons through a plant, handling quirks become second nature. 4-(2-Methylamino-Ethyl)-Phenol has a powder habit, non-hygroscopic granularity, and moderate dustiness on open transfer. We use localized LEV setups, but in a benchtop bottle, users rarely face bridging, caking, or rapid oxidation. Operators in our plant rely on standard PPE and avoid open flames, because amine-phenol blends display low flash points, but we haven’t recorded incidents from short exposure or spillage, which is rare for phenolic intermediates.
Our long-term samples show that the crystalline form resists polymorphic shifts over ambient storage. We recommend closed, dry containers only for operational neatness and to hold maximum shelf-life. Over the last ten years, we’ve seen no measurable loss of potency or color change in sealed drums. Shipping under standard UN carton or drum protocols suits this product well—no need for refrigerated carriers or special lining.
Direct feedback from client labs often shapes our QC focus. One industrial adhesives client reported a 20% jump in final adhesive strength after switching from N-methyl-p-aminophenol to this compound. The increased chain length let their reactants build more robust networks. In another case, an API manufacturer dropped a distillation step and cut monthly solvent spend by roughly $80,000 after switching to this phenol derivative. That’s a bottom-line change that makes an R&D director pay attention.
Feedback channels give us early warning if a shipment underperforms. In 2020, we detected traces of a new low-level impurity from a supplier’s reagent switch. Pulling customer and in-house test records side by side, we traced reactions that had slightly slower kinetics and adjusted purchase specs to ensure it won’t happen again. Closed-loop learning with end users continues to make our process more robust—and keeps us out of the apology business.
No product reaches commercial scale without a few rough patches. We learned early on that improper reactor cleaning between batches could drag metallic traces into the product, setting off headaches down the line. This challenge forced an overhaul of our steam-cleanout and nitrogen purge protocols, a decision that cut impurities and led to more consistent purity levels than we had managed before.
During high-humidity months, blending too fast created static cling and powder float, risking uneven filling. By adopting slower auger speeds and anti-static lining, our team solved both the waste and ergonomic complaints that came from operating the filling line. We keep notes on every production weirdness, so future scale-ups move smoother.
Some challenges also come from the global supply chain. Securing high-grade precursor amines remains a moving target, especially when global commodity pricing or shipping disruptions throw off delivery schedules. To counter this, we’ve kept secondary sourcing and longer-term contracts. Clients who value on-time delivery and backup logistics started noticing improvements in both reliability and transparency.
There’s a reason long-term buyers stick with our production. Over years of manufacturing 4-(2-Methylamino-Ethyl)-Phenol, we’ve learned that facts do the talking. Real production records show a recurring yield range around 98%, with out-of-spec batches dropping below 0.2%—most flagged in-process, not after bottling. We built out our QC lines with a focus on NMR, HPLC, and UV-Vis tracking, not just post-reaction TLCs, so both small and bulk buyers see the same data-driven approach behind every lot sold.
Process validation involves triple-blind sampling, side-by-side reference runs, and a choke-point check where any batch drift triggers a line hold. This reality comes from years of watching what happens when shortcuts breed costly callbacks or delayed releases. Marketing buzzwords don’t prevent problems, but well-documented process control can satisfy records compliance from smaller clients up to multinational partners.
Our technical team keeps hearing about new target molecules, custom syntheses, and ever-changing regulatory requirements. In high-throughput screening for new drug candidates, chemists seek building blocks that are both reactive and safe to manipulate. This molecule fits that balance. It lets formulation scientists side-step more toxic aromatic amines and provides pathways to streamlined synthesis of beta-hydroxyamines, antimicrobials, and custom dyed resins.
Expanding into battery binder and electronic coating markets, our pilot trials show that 4-(2-Methylamino-Ethyl)-Phenol delivers strong crosslinking in phenolic resin matrices. The secondary amine configuration allows for better electron transfer in thin film applications. Test partners notice smoother mixing, finer grain dispersal, and less phase separation, especially during rapid curing. These kinds of advances help everyone from startup formulators to established multinationals meet tomorrow’s targets with one less variable in their raw material chain.
Quality doesn’t happen just by the numbers—it comes from seeing how attention to detail affects every drum loaded and every kilogram shipped. We back up what we manufacture with real-world examples, ongoing batch data, and open-door site visits. This approach continues to anchor trust and repeat business, as buyers recognize that the difference between a passable intermediate and a go-to staple lies in the everyday follow-through.
From formulation to bulk shipment, our team’s experience handling 4-(2-Methylamino-Ethyl)-Phenol shapes how we solve problems, anticipate needs, and set the bar for what a reliable intermediate can do. Decades of batch tracking, direct feedback loops with process engineers, and a refusal to tolerate “good enough” have given this chemical a lasting place in our product line—and our partners’ manufacturing plans.
In the world of chemical manufacturing, changes never stop—a new application, a revised standard, or a stricter regulatory update keeps everyone on their toes. 4-(2-Methylamino-Ethyl)-Phenol has proven its value, not through lab talk, but through thousands of test results and years of real use. As markets push for cleaner, more reliable intermediates, feedback and lessons from every completed batch go back into sharpening what we deliver.
Trust in a product, especially one that plays a recurring role in countless syntheses, comes from seeing it work, batch after batch. From our perspective as a hands-on manufacturer, every shipment carries not just a few numbers on a certificate but the stamp of experience, craftsmanship, and years of focused practice. This remains the way we do things—and what we plan to keep delivering in every lot of 4-(2-Methylamino-Ethyl)-Phenol leaving our plant.