|
HS Code |
527694 |
| Common Name | P-(Dimethylamino)phenol |
| Iupac Name | 4-(Dimethylamino)phenol |
| Cas Number | 619-60-3 |
| Molecular Formula | C8H11NO |
| Molecular Weight | 137.18 |
| Appearance | Light brown to beige crystals |
| Melting Point | 67-70°C |
| Boiling Point | 285°C |
| Solubility In Water | Slightly soluble |
| Density | 1.110 g/cm³ |
| Pka | 9.8 |
| Smiles | CC1=CC=C(C=C1)N(C)C |
| Pubchem Cid | 12303 |
| Hazard Statements | Harmful if swallowed, causes skin and eye irritation |
| Uses | Intermediate in dye and pharmaceutical synthesis |
As an accredited Phenol, P-(Dimethylamino)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g amber glass bottle with tamper-evident cap; hazard labeling, chemical name "Phenol, P-(Dimethylamino)-" and safety information displayed. |
| Shipping | **Shipping Description for Phenol, P-(Dimethylamino)-:** Phenol, p-(Dimethylamino)- should be shipped in tightly sealed containers, away from light, moisture, and incompatible substances. Use appropriate hazardous material labeling and documentation, and follow local regulations for the transport of chemicals. Handle with care; avoid sources of ignition and ensure ventilation during transfer. |
| Storage | Phenol, p-(Dimethylamino)- should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from heat, light, and moisture. Store at room temperature and ensure proper labeling. Use appropriate corrosion-resistant shelving and keep away from sources of ignition. Follow all chemical hygiene and safety protocols. |
Competitive Phenol, P-(Dimethylamino)- prices that fit your budget—flexible terms and customized quotes for every order.
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On the production line, a material rarely earns the respect of both technical experts and actual end users. Phenol, P-(Dimethylamino)-, known to many of us by its chemical structure featuring the para positioning of the dimethylamino group, stands out from typical substituted phenols due to its reactivity and operational range. We have handled this compound over years of manufacturing, closely supervising synthesis and downstream processing, and the experience always reminds us that chemistry is as much about refining quality as it is about maintaining consistency.
From the outset, Phenol, P-(Dimethylamino)- starts with clean aromatic feedstock. Our team manages the methylation and subsequent amination, carefully controlling reaction temperature to ensure the dimethylamino group attaches precisely at the para site, not drifting to the ortho or meta positions. Excess reagents do no one any favors, so our plant applies rigorous stoichiometric controls. Even during scaling, the color and odor of intermediates give us early clues on the reaction’s progress—a lesson that no sensor or instrument has fully replaced. Quality doesn’t stem from automation alone. Eyes, experience, and a slight whiff near the flask tell seasoned crew members much about what’s happening inside.
Within our facility, batches of Phenol, P-(Dimethylamino)- undergo multiple stages of purification before they reach target performance. Physical form is usually pale crystalline—though batch-to-batch, slight yellowing tells veteran operators if something changed upstream. True to practice, each lot goes through gas chromatography and NMR checks, with keen attention to trace amine or phenolic impurities. The melting point, a classic evaluation, routinely falls within a tight temperature range, and a deviation—no matter how slight—sparks team discussions. Sensitivity to light and oxygen remains on our radar; we’ve learned that properly sealed packaging and dry nitrogen flushing make a noticeable difference over months in storage.
We produce Phenol, P-(Dimethylamino)- to the technical specifications requested by our partners. For most users, purity above 99 percent remains critical. This standard means more than just numbers—it minimizes side reactions, especially for downstream syntheses where a stray methyl group or unreacted phenol throws work off balance. Over time, we have established protocols to remove trace dimethylaniline and other roots from incomplete reactions, ensuring batches leave our plant aligned with the best laboratory benchmarks.
Solubility checks extend to organic solvents and some aqueous mixtures. For processes that demand homogeneity in methanol, ethanol, and acetone, we verify the solubility index before shipping. Filtration setups have improved based on customer feedback; flow tests now match real use. Colorimetric stability also features in routine QC, since commercial users in dyes and analytical chemistry depend on spectral behavior remaining stable, batch after batch. Unlike off-the-shelf distributors, we trace back every minor shift. The chromatogram peaks, the UV spectrum—these become the plant’s daily language.
Phenol, P-(Dimethylamino)- serves different industries, with roots in advanced organic synthesis, specialty dye manufacture, and certain diagnostic reagents. Its unique para-dimethylamino substitution grants strong electron-donating ability, which influences its reactivity profile across disciplines. University groups seeking intermediates for novel heterocycles come to us after running small-scale reactions with commercially available stock, then noticing the difference in reactivity between standard phenols and our tightly controlled version. In analytical labs, the compound’s sharp absorption and colorimetric response support color development in selective assays.
The dye sector especially values our approach. Routine syntheses demand consistent chromophore behavior, with colorfastness and absorption wavelengths staying true. In practice, even small changes in the phenol's purity or positional substitution can shift dye shade dramatically, so our staff works closely with partners to analyze spectral consistency. One case stands out—an R&D team from a textile colorant producer ran dozens of color tests before realizing that contaminants from another supplier caused shifts in hue outside ISO tolerances. After switching to our phenol, color reliability snapped into place.
Pharmaceutical research leverages this compound as a core intermediate. The para-dimethylamino group often features in lead candidates aimed at neuroactive agents. Our process provides the structure with sharp reproducibility, no traces of byproducts that could confound kinetic studies or cell assays. As with other fine chemicals, our customers find that data reliability hinges on the quality of starting materials. Lower-purity phenols purchased as bulk commodity often fail in downstream scale-up, where tighter analytical controls expose inconsistencies invisible during early synthetic work.
Electronics applications also show up—phenol fragments containing electron-donating groups like dimethylamino play roles as stabilizers, UV absorbers, or polymer modification agents. We have observed that their performance in high-value coatings and thin films links back to the uniformity and control over each batch’s microstructure. Intensive titration testing has demonstrated that even ppm-level iron or chlorine contamination causes major headaches in optical finishes, so we built our product lines around aggressive removal and triple-checking of trace elements before drums ever leave the plant.
New production teams often ask what distinguishes our p-dimethylamino phenol from other methylated phenols or amino-substituted versions, such as ortho or meta isomers. Most chemical textbooks list substitution effects, but operational reality tells a subtler story. The para arrangement significantly increases resonance effects, boosting electron density on the ring and thus shaping further reactions, especially in azo coupling and dye intermediate manufacture. Years of comparative analysis have shown that ortho isomers suffer from steric hindrance, while meta placement weakens sought-after resonance stabilization in dyes and intermediates.
We have realized that only strict process discipline produces batches free from positional isomer contamination. Even a small amount of ortho- or meta-dimethylamino byproduct in a shipment will compromise reactivity in diazo coupling reactions, throwing off both the shades of dyes and the yields of downstream steps. As a manufacturer, we bear responsibility for this consistency—not because quality control demands it, but because wrong results cost our customers time and resources. This sense of responsibility never goes away, no matter how familiar the product or the volume moved.
Another aspect that sets this product line apart stems from investment in both process control and feedback. Over years, we have updated reactor control systems to detect intermediate concentrations at subtle thresholds, using both in-line spectroscopy and traditional batch sampling. Maintenance teams learned to anticipate catalyst fouling and byproduct accumulation by smell, sight, and instrument. The generations who have worked alongside us, from senior process chemists to junior operators, each carry forward lessons about troubleshooting that go beyond digital systems.
In early days, unexpected fouling in condenser lines threatened batch integrity, especially in humid weather. By tracing the problem to a drift in feedstock grade during the rainy season, we changed how raw materials were stored and handled, ordering regular pre-drying and implementing improved overheads to filter incoming air. These real-life corrections never show up on datasheets, but every operator in our building knows that small disruptions—caught and fixed quickly—preserve the performance customers expect.
Comparisons with other aromatic amines also reveal important divergences. Some competitors produce broader-cut phenol derivatives through routes that do not tightly regulate substitution. Over time, we have found that minimizing side reactions impacts scalability for custom orders, especially for partner companies scaling pilot projects to full industrial output. Early collaborations revealed that “good enough” purity markers on someone else’s specification sheets did not guarantee matching real-world yields or color metrics on the application floor. We learned that transparent communication, detailed batch reporting, and openness to on-site audits make all the difference over product cycles that span years.
Reactivity optimizations also mark a clear line. Higher-purity p-dimethylamino phenol responds more predictably in coupling reactions, making it easier for downstream users to control reaction times and end-product properties. Trials run in our lab with older, less refined grades always led to inconsistent outputs. Corrective measures—longer purification, higher reagent charge—drive up costs and burn up schedules, so process improvements feed directly back into product reliability.
Safety also enters the discussion, not just as regulatory compliance but as a cultural value. As manufacturers, we encounter solvents and intermediates that require strong respect for risk. Our team spends time on safety reviews not for auditing boxes, but because generations of plant employees have seen how minor lapses cascade into greater hazards. We maintain detailed training for handling and incident response, paying attention to situations unique to our material—like its mild but persistent odor and potential for skin irritation at certain concentrations. Customers sometimes ask us about shipping incidents or minor discrepancies in packaging seals, and our staff explains with practical examples from the production floor—no issue gets brushed aside because a number on a form “meets guideline.”
As partners work with Phenol, P-(Dimethylamino)- in applied research or production, questions often arise about troubleshooting reactions or purifying downstream intermediates. We find that some knowledge only accumulates through repeated hands-on trials. For example, customers scaling up dye intermediates frequently report increased tar formation or unwanted color drift in summer months. We have found that small environmental shifts—ambient humidity, temperature jumps, longer jar-standing times—amplify batch-to-batch variations. Our technical support takes these into account, recommending slight modifications based on our own production history: using closed systems, adjusting reagent ratios, and shortening intermediate hold times for predictable results.
In additional work with analytical users, stability is a recurring concern. Even with high-purity supply, analysts see sensitivity to ultraviolet exposure or trace oxygen. We share technical notes from our own stability testing: storage away from direct sunlight, use of brown glass when possible, and rapid sampling minimize oxidative drift in spectrophotometric readings for months at a time. Our own instrument records track every anomaly—a testament to the value of maintaining tight batch records and comparing them with results from labs in the field.
We have also assisted small-scale pharmaceutical researchers encountering issues with unwanted byproducts in amine-functionalization steps. Sharing details about our own purification strategies—layered solvent washes, vacuum drying, and staged filtration—has helped these groups refine their own separation work. Joint troubleshooting discussions go beyond mere product complaints: we see opportunity to exchange practical experience and boost outcomes for both sides.
A recent pattern in electronics applications shows demands for increased control over elemental impurities. Trace copper or iron in Phenol, P-(Dimethylamino)- causes measurable instabilities in optoelectronic coatings. In response, our process team isolated source contamination back to condenser coil materials and explored more inert alternatives. After switching, regular ICP-MS reports reveal a drop in trouble spots—a clear example where a plant-level change solves a product-level problem, and where open communication with customers drives long-term improvements.
As chemical manufacturers, we feel the weight of responsibility in each drum and bag that leaves the loading dock. Phenol, P-(Dimethylamino)- may appear as just another specialty intermediate on paper, but real-world performance connects directly to the care and transparency with which every batch is made. The fine-grained details—color, trace impurities, IR and UV consistency—articulate the difference between a reliable process and wasted effort down the line. Quality is the result of constant vigilance, shared experience, and a willingness to listen to partners who rely on what we produce.
Over the years, building trust has meant sharing both successes and production setbacks. Broken glassware, unexpected batches falling out of spec, real-life stories of corrosion impacting performance—these experiences, traded between plant floor and application lab, shape every improvement in our product. After all, no real manufacturer hides behind numbers alone. Hands-on experience, a sharp nose, and strong relationships with users enable us to keep Phenol, P-(Dimethylamino)- performing at the level research and industry require.
We welcome every technical dialogue, every request for deeper data or on-site troubleshooting. After decades in the business, we know there are always new lessons waiting. Quality, safety, and transparency—these aren’t slogans pasted on a website, but the lived reality of making a specialty chemical work day in and out, for every batch, every project, every partner.