|
HS Code |
170749 |
| Chemical Name | 3-(Dibutylamino)phenol |
| Cas Number | 10204-56-7 |
| Molecular Formula | C14H23NO |
| Molecular Weight | 221.34 g/mol |
| Appearance | Colorless to light yellow liquid |
| Boiling Point | 360.3 °C at 760 mmHg |
| Density | 0.956 g/cm³ |
| Solubility In Water | Slightly soluble |
| Flash Point | 169.4 °C |
| Pubchem Cid | 2721503 |
| Iupac Name | 3-(dibutylamino)phenol |
As an accredited 3-(Dibutylamino)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 3-(Dibutylamino)Phenol is sealed in an amber glass bottle with a tamper-evident cap, labeled for laboratory use. |
| Shipping | **Shipping Description for 3-(Dibutylamino)phenol:** Ships in tightly sealed containers, protected from moisture, heat, and direct sunlight. Handle as a potentially hazardous chemical; ensure proper labelling and documentation. Store upright, and transport according to local chemical regulations and UN guidelines. Avoid exposure and inhalation during handling and transit. Suitable for ground and air shipments with hazard precautions. |
| Storage | **3-(Dibutylamino)phenol** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers and acids. Keep it protected from light and moisture. Use appropriate secondary containment and label the container clearly. Access should be restricted to trained personnel only. |
Competitive 3-(Dibutylamino)Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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Manufacturing chemicals with functional groups like 3-(Dibutylamino)Phenol requires precision and a deep understanding of both market needs and process chemistry. Each batch crosses numerous checkpoints, not just to meet a narrow set of purity goals, but to streamline functionality for its intended downstream applications. With deep roots in chemical synthesis, we see 3-(Dibutylamino)Phenol as more than a product code: it’s a specialized tool for formulations demanding stable aromatic amines with unique solubility and reactivity balances.
Our daily laboratory work reveals a diverse range of phenolic compounds, but the inclusion of the dibutylamino group brings new possibilities. This molecule’s structure sets it apart from simpler aminophenols or analogs with shorter or branched alkyl chains. The butyl chains attached to the amino group change both the physical properties and the behavior in formulation work. The result manifests in higher compatibility with organic phases, smoother processing in non-aqueous systems, and increased resistance to common forms of oxidation.
Specialists in chemical manufacturing will recognize that even small changes at the molecular level can have a big impact. With 3-(Dibutylamino)Phenol, the longer butyl groups increase hydrophobicity, which often translates into better performance in coatings, organic electronic development, and select pharmaceutical intermediates relying on amphiphilic balance. Colleagues handling N-alkylated compounds have noticed less volatility, improved shelf-life, and smoother solubilization across diverse solvents when compared against shorter-chain analogs.
Producing this compound on a commercial scale stretches far beyond simple reproducibility. While lab-scale syntheses might dip below trace impurity levels, scale-up brings practical hurdles. Diazotization and selective amination require not just careful temperature profiles, but thorough control over side-products like unreacted phenol or secondary amines. Each kilogram we ship reflects months of regular process tuning, hands-on adjustments, and live analytics.
Seasoned chemists in our team constantly cycle between analytical feedback, process engineering, and targeted troubleshooting. Purity and stability of 3-(Dibutylamino)Phenol arise from more than just distillation. Fine-tuning extraction, purification, and storage methods make sure the product resists yellowing or unwanted reactivity, which end-users in the lubricant, dye, and pharmaceutical sectors tend to reference as a “hidden difference” compared to mass-market phenolic intermediates. Each evaluation was born out of years of real-world product testing, frequent customer trials, and constant feedback after application hurdles emerged.
Several industries lean on this intermediate for its durable aromatic core and the adaptable dibutylamine side chain. In our experience, most buyers use it in synthesis of specialty dyes and pigments, leveraging its improved thermal stability and solubility in non-polar matrices. Colorants built on this backbone tend to resist fading and chemical degradation under harsh processing conditions.
Another critical domain comes from organic synthesis where the phenolic group acts as a reactive handle, often protected in situ or coupled using modern catalysis. Our partners developing active pharmaceutical ingredients select this intermediate for cases where its unique reactivity profile allows for selective alkylation, acylation, or carbamate synthesis. The challenge in many modern drug syntheses is to balance reactivity with selective blocking, and this compound often ticks those boxes—helped along by our tight specification development and product consistency over repeated batches.
Within the lubricants industry, certain advanced additive manufacturers have adopted 3-(Dibutylamino)Phenol for formulations targeting enhanced anti-wear properties. The butyl groups provide a balance between oil solubility and boundary film formation, offering an angle not found with more commonly used mono- or di-alkylated aminophenols. Our technical services division actively collaborates with blend engineers to optimize performance, often through custom-tailored purity or solvent-free lots.
Those accustomed to standard aminophenols, such as 3-aminophenol or even dimethylaminophenol, will find the dibutyl version comes with a heavier, more hydrophobic profile. Durability in organic blends and the ease of integration with certain polymers improve with increased bulk. Formulators in coating and polymer resin development note the positive shift in both compatibility and mechanical properties, especially where lower volatility and slower migration matter.
From our bench-scale trials, we’ve seen that replacing shorter-chain aminophenols with 3-(Dibutylamino)Phenol can lower vapor pressure and reduce unwanted side reactions leading to color shifts or stability issues. For development chemists, this means fewer reformulation cycles and a cleaner approval track in performance testing.
The difference also carries over into handling and storage requirements. Bulk lots of dimethylaminophenols, for example, often require more stringent packaging and atmospheric protection. In comparison, 3-(Dibutylamino)Phenol batches ship with more predictable long-term stability, cutting back on waste due to premature yellowing or off-odors. Our bulk storage tanks now see fewer complaints about contamination or storage-driven loss of quality, a win noted both by plant managers and the QC team.
Customers in sensitive applications, particularly pharmaceutical and electronic-grade users, push hard for strict contamination and trace impurity thresholds. Years of working with partners in these fields led us to focus on trace-level analysis using HPLC, GC-MS, and other real-time in-process monitoring techniques. We draw on user feedback to set tighter nitrosamine and metal impurity specs, exceeding many published norms in generic chemical markets.
Our analytical chemists bridge routine production with high-stakes R&D projects, making sure every delivery builds confidence, not just meets a minimum bar. We keep track of color, water content, and residual solvents using validated methods, not just because clients ask for it but because a single batch inconsistency can throw off production for weeks. We consider this a core responsibility—not a sales point—especially knowing how downstream synthetic steps can be so sensitive to the tiniest upstream change.
For us, manufacturing never stops at the point of sale. Many long-term customers look for more than a one-off purchase—they depend on frequent scheduling, reliable inventory management, and rapid technical assistance. We keep active backups on all plant recipes, run quarterly assessments of solvent recycling loops, and maintain redundant instrumentation. These steps cut risk, protect both us and our clients from unexpected supplier hiccups, and reduce lead-time gaps.
In one year alone, shifting demand for this intermediate, especially in high-end dye manufacturing, forced a quick revision of our planning routines. We had to shift reactor time, revise supply forecasts for precursors, and support sudden increases in customer certifications. The lesson that stuck: so-called commodity intermediates quickly become high-criticality materials for niche markets.
End-users emphasize two main priorities: consistent availability and consistent quality. We keep extra scrutiny on every transfer point, record every storage tank washdown, and routinely swap out old packaging materials to keep risks of leaching, foreign matter, or product degradation as low as possible. Our partners in the formulation and blending sector often tell us that small inconsistencies can become big headaches during scale-up. With this in mind, every debate over process change comes down not to cutting costs but to reducing variability.
New users of 3-(Dibutylamino)Phenol regularly reach out to translate lab observations into scalable practices. Some find initial compatibility hurdles, others long for faster dissolution rates or need to know which solvents avoid discoloration risks. Our technical support team, drawn from the same group who built up the production line, becomes a real-world knowledge base. Practical advice rarely makes it to data sheets, but it’s what saves time and plant resources for every new adopter.
One illustrative case: a pigment formulator sought our help because initial pilot lots of 3-(Dibutylamino)Phenol arrived too dark. Side-by-side, we walked through application conditions, pH exposures, and raw material storage with their team. Adjusting stabilization protocols, we updated our isolation steps to reduce exposure to trace oxidants during work-up. The improvement showed up in higher initial brightness and better fade resistance—outcomes none of us expected without this kind of hands-on troubleshooting.
Building on this, we foster regular feedback sessions—direct factory-to-laboratory communication channels that keep both sides informed on new technical hurdles, regulations, or changes in synthetic targets. Our experience shows that successful partnerships grow when both sides commit to openness and routine updates, not just one-off responses.
Over the last several years, international regulations have tightened for both raw chemical handling and end-product contaminants. As a high-functionality intermediate, 3-(Dibutylamino)Phenol can be scrutinized under REACH, TSCA, and increasing regional standards covering amine-based compounds. We dedicated substantial resources to pre-registration, documentation, and tracking so that our exports bypass administrative gridlock.
Health and environmental safety became a top focus area. Our EH&S specialists monitor all new downstream applications, scan for emerging data on toxicity or environmental persistence, and propose process changes or product labeling updates where evidence suggests increased concern. For new customers, we provide both product stewardship guidance and implementation advice—from closed-system transfer setups to best practices for on-site storage.
Over the production cycle, we prioritize worker safety and site hygiene. Every equipment update draws from real incident reports, and every training session reflects actual plant workflow. If an incident in another facility leads to improved containment or new PPE recommendations, we apply those lessons without waiting for external pressure. Results turn up in fewer lost-time injuries and productive operator engagement, both reflected in stable output and a strong retention rate among skilled plant personnel.
Echoing global priorities, our organization actively looks for ways to limit waste, energy use, and emissions. For a compound like 3-(Dibutylamino)Phenol, which draws on several organic solvents and generates non-trivial byproducts, this challenge is neither small nor abstract. We designed process steps that reclaim butylamine from vent streams, reuse solvents across compatible syntheses, and implement in-line monitoring to spot leaks before product or energy is lost.
Completed sustainability projects, like switching to closed-loop nitrogen inerting and updating scrubber systems, have led to measurable reductions in VOC emissions and process water use. These upgrades didn’t just reduce our ecological footprint—they paid real dividends when environmental inspections became stricter or when energy costs surged. Downstream partners benefit from lower environmental impact certifications and greater confidence in long-term supply stability.
Teams working on product stewardship have rolled out regular waste audits and lifecycle analyses, identifying stages where slight improvements in process yield translate to big drops in batch-to-batch emissions. Each step emerged from plant-floor observations, scientific review, and workplace-led innovation sessions. The outcome? Higher reliability for both our buyers and the environment, showing that fine-tuning chemical process lines can serve both pocketbook and planet.
Development chemists and plant process experts know that no intermediate stands still. Over time, we’ve used our feedback loop with R&D teams to propose new derivatives, both as custom orders and as speculative research projects. Some of our most successful product upgrades have come from simple requests: tighter color cutoffs, alternative solvent carriers, or modified purity windows tailored for a customer’s new filing.
We watch trends in pharmaceuticals, electronics, and specialty coatings, ready to switch or expand synthesis routes as demands evolve. Discovery-driven research, fueled by our direct experience, contributed to offshoots like branched dibutylamino derivatives for higher polarity solvents or tailored phenol substitutions for fast-curing resins. Clients gain value through lower total costs, fewer material rejections, and new possible formulations that would have been off-limits even a decade ago.
Years of hands-on production, direct troubleshooting, and collaborative feedback shaped our approach to making and delivering 3-(Dibutylamino)Phenol. This work goes beyond technical bullet points, carrying lessons about quality, adaptability, and partnership. Real value for customers never settles at minimum compliance—it grows from transparency, thoughtful process stewardship, and readiness to tackle new challenges head-on.
As a specialist manufacturer, we welcome insights from users—whether process chemists, formulators, or regulatory managers. Open lines support not just business, but shared long-term success. Every kilogram of 3-(Dibutylamino)Phenol we send out reflects this deeper foundation of trust—built day by day on the shop floor, tested in the lab, and validated by real-world results. For those looking to push application boundaries, these are the elements that truly define the difference.