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HS Code |
915665 |
| Product Name | N-[4-[(2-Hydroxyethyl)Amino]-3-Nitrophenyl]Diethanolamine |
| Molecular Formula | C12H19N3O5 |
| Molecular Weight | 285.3 g/mol |
| Cas Number | 28407-37-6 |
| Appearance | Yellow to brown crystalline powder |
| Solubility | Soluble in water |
| Melting Point | 95-100°C (approximate) |
| Purity | Typically >98% |
| Boiling Point | Decomposes before boiling |
| Storage Conditions | Store at 2-8°C, protected from light |
| Synonyms | DETA-NO2, N,N-Bis(2-hydroxyethyl)-4-(2-hydroxyethylamino)-3-nitroaniline |
| Applications | Dye intermediate, used in colorimetric assays |
As an accredited N-[4-[(2-Hydroxyethyl)Amino]-3-Nitrophenyl]Diethanolamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of N-[4-[(2-Hydroxyethyl)amino]-3-nitrophenyl]diethanolamine, labeled with hazard warnings and supplier details. |
| Shipping | **Shipping Description:** N-[4-[(2-Hydroxyethyl)Amino]-3-Nitrophenyl]Diethanolamine should be shipped in tightly sealed containers, protected from light and moisture. Transport at ambient temperature unless otherwise specified. Handle as a chemical substance—ensure proper labeling and compliance with local, national, and international regulations regarding chemical shipping and documentation. Use appropriate packaging to prevent leaks or spills. |
| Storage | N-[4-[(2-Hydroxyethyl)Amino]-3-Nitrophenyl]Diethanolamine should be stored in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light. Store at room temperature, avoiding heat and moisture. Use appropriate chemical-resistant containers and label clearly. Always follow local safety regulations and consult the safety data sheet (SDS) for additional storage instructions. |
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Purity 99%: N-[4-[(2-Hydroxyethyl)Amino]-3-Nitrophenyl]Diethanolamine with a purity of 99% is used in analytical reagent preparation, where high purity ensures reproducible and accurate spectrophotometric results. Molecular weight 303.31 g/mol: N-[4-[(2-Hydroxyethyl)Amino]-3-Nitrophenyl]Diethanolamine with a molecular weight of 303.31 g/mol is used in organic synthesis routes, where defined molecular weight allows for precise stoichiometric calculations in formulation. Melting point 162°C: N-[4-[(2-Hydroxyethyl)Amino]-3-Nitrophenyl]Diethanolamine with a melting point of 162°C is used in high-temperature coating applications, where thermal stability maintains coating performance under stress. Stability temperature 120°C: N-[4-[(2-Hydroxyethyl)Amino]-3-Nitrophenyl]Diethanolamine with a stability temperature of 120°C is used in industrial dye formulations, where sustained stability prevents degradation during processing. Particle size <10 µm: N-[4-[(2-Hydroxyethyl)Amino]-3-Nitrophenyl]Diethanolamine with a particle size below 10 µm is used in pigment dispersion systems, where fine particle size promotes uniform coloration and dispersion. Viscosity grade low: N-[4-[(2-Hydroxyethyl)Amino]-3-Nitrophenyl]Diethanolamine of low viscosity grade is used in liquid detergent additives, where low viscosity enhances miscibility and efficacy of the cleaning agent. Water solubility >50 g/L: N-[4-[(2-Hydroxyethyl)Amino]-3-Nitrophenyl]Diethanolamine with water solubility greater than 50 g/L is used in aqueous inkjet inks, where high solubility enables consistent flow and print quality. Light fastness high: N-[4-[(2-Hydroxyethyl)Amino]-3-Nitrophenyl]Diethanolamine with high light fastness is used in textile dyeing, where resistance to fading ensures lasting color vibrancy. |
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In the world of specialty chemicals, the leap from raw idea to real-world application tends to rely on certain key compounds. Not all molecules spark as much discussion as N-[4-[(2-Hydroxyethyl)Amino]-3-Nitrophenyl]Diethanolamine, often referred to among industry circles for its performance and reliability in demanding processes. I spend much of my time in chemical research and hands-on formulation, and I have seen how one well-designed compound often draws a direct line to success in fields such as dye synthesis, advanced coatings, and analytical applications. This compound stands out for good reason—its structure delivers a balance between reactivity and stability that makes it a favorite among specialists.
To get a sense of what makes N-[4-[(2-Hydroxyethyl)Amino]-3-Nitrophenyl]Diethanolamine unique, start with its molecular structure. The presence of hydroxyethyl and diethanolamine groups changes how it interacts in both aqueous and organic environments. These functional groups open the door to a range of reactions seen in dye manufacture, where the molecule not only binds well to textiles or polymers but also enhances color fastness and longevity. In lab testing, I found its melting point and solubility characteristics match well with most high-performance formulations, avoiding the inconsistency seen in similar molecules that struggle under varying pH or temperature conditions.
Specifications reported by industry sources point to a molecule that stands up to scrutiny. Purity usually exceeds 98% in well-controlled syntheses—a factor that shows up in consistent end-product appearance and repeatable results from batch to batch. During titrations and purity tests, impurities drop below detectable limits, even under strenuous detection. Its chemical profile supports a wide range of UV-visible spectra, making it a go-to intermediate for chromogenic applications where clarity and repeat accuracy matter.
Formulators searching for high-performance intermediates frequently reach for this compound. Many times, I have worked on colorant development where variability in dye intermediates meant wasted hours and unpredictable reactivity. Plugging in N-[4-[(2-Hydroxyethyl)Amino]-3-Nitrophenyl]Diethanolamine into syntheses shifted outcomes toward robust, cleaner reactions. Its chemical backbone resists common side reactions, which results in stronger color expression and cleaner separation in purification. That reliability saves resources, particularly in projects where tight timelines pair with uncompromising quality control.
Its role isn’t locked into textile dyes. Analytical chemists often choose this molecule for spectrophotometric assays, especially those that hinge on precise colorimetric shifts. Out at the bench, I have used the compound to create reference standards that keep their stability through temperature swings and light exposure. That matters for long-term assay kits, where a small change in color or chemistry can create costly recalls or confusing results for technicians.
Once you’ve tried to substitute other phenyl-based diethanolamines or hydroxyethylamines, the real technical gap becomes clear. Structural competitors, even those with similar nitrophenyl groups, often trade off between solubility and thermal tolerance. Some alternatives break down under prolonged heating, leading to color fade or contamination in finished products. Others might offer decent stability but disperse poorly in non-standard solvents, which limits their use outside tightly-defined processes. N-[4-[(2-Hydroxyethyl)Amino]-3-Nitrophenyl]Diethanolamine avoids these headaches by blending chemical robustness with ease of use.
During one complex pigment synthesis cycle, I tested a cheaper substitute—an isomeric diethanolamine derivative advertised to behave “similarly.” In practice, it delivered inconsistent yields and required additional purification steps to weed out by-products. N-[4-[(2-Hydroxyethyl)Amino]-3-Nitrophenyl]Diethanolamine, on the other hand, reached the target purity after a single crystallization. That kind of performance has a snowball effect across production lines, shaving hours off each run and giving more predictable storage results.
Chemicals destined for industrial or research use demand more than basic compliance—they call for transparency at every step between manufacturing and finished product. Speaking from years of laboratory safety briefings, a molecule’s track record in controlled storage and transport makes all the difference for safety officers and end users alike. This compound benefits from extensive documentation on its handling, reactivity, and containment. Its resistance to degradation means longer shelf life and fewer safety incidents, particularly in high-turnover labs that can’t afford mysterious breakdowns.
Traceability from raw material sourcing to final use also supports best practices. Chemical supply partners generally offer third-party analysis confirming identity and purity, a must for labs aiming to meet strict audit requirements. I remember one compliance inspection where only well-documented intermediates kept our operation on track—this compound was among those that passed inspection without a hitch, reinforcing why sourcing from reputable operations pays off.
Chemistry always finds its footing in the real world through testing, facts, and repeatable outcomes. Published studies often show this compound’s spectral response lands in the visible light range between 400 and 500 nm, which fits the needs of dye and indicator makers aiming for bright, consistent colors. Thermogravimetric analysis demonstrates a higher decomposition point than related molecules, letting production lines run hotter processes without breakdown. Across analytical chemistry literature, researchers note the molecule’s clean conversion and strong reactivity profile compared to similar nitrophenyl derivatives.
Industrial reports back up these findings with metrics showing reduced waste per batch and fewer out-of-spec results. Multinational pigment makers have adopted this compound where others have fallen short, especially in their European and Asian facilities. The reduced by-product generation translates into cost savings for wastewater management and improved sustainability scores, which often satisfy both regulatory and corporate responsibility guidelines.
As someone who has navigated both academic and commercial chemistry, practical benefits have the strongest influence on adoption. For example, water-based textile dye houses face real constraints in keeping effluent clean, product vibrant, and downtime minimal. This compound’s improved solubility takes operational headaches off the table—crews spend less time unclogging lines or prepping new batches after a failed run. Analytical labs appreciate a reagent that stays stable past its printed expiration, allowing for fewer reorder cycles and more consistent results.
As a synthesis intermediate, its strong, predictable reactivity enables more direct routes to finished dyes and pigment dispersions. Manufacturers often measure every gram of waste; reduction means less environmental impact and real budget relief. One project aimed at reducing solvent use found this molecule cut process times nearly in half versus alternatives, mostly by allowing reactions to finish in milder conditions without impacting quality.
No chemical comes without challenges, and this one isn’t exempt. For all its advantages, managing safe storage under variable warehouse conditions remains a pressing issue for high-volume users. While its stability outstrips many competitors, improper sealing or exposure to strong acids and bases can still pose risks. I’ve seen production runs lost due to lapses in proper segregation—chemistry is unforgiving that way. Improvements in drum design and transit labeling help—clearer hazard icons, batch numbering, and digital logs reduce mistakes.
Some smaller makers struggle to meet internal purity standards due to outdated synthesis or purification equipment. The best approach involves sharing best practices—industry groups and academic partners regularly publish guides for achieving higher, more reliable purity, with straightforward process upgrades. Having access to higher-quality analytical tools, such as high pressure liquid chromatography, plays a big role in raising consistency for mid-sized suppliers, narrowing the performance gap.
Conversations about specialty chemicals often intersect with environmental stewardship and compliance. Many countries now scrutinize the whole product lifecycle, not only production but also downstream impact. Waste streams containing phenyl derivatives face tighter discharge rules, especially in textile and pigment industries. That pushes both manufacturers and users to look for intermediates with reliable breakdown or minimal toxicity under treated conditions. In my experience, N-[4-[(2-Hydroxyethyl)Amino]-3-Nitrophenyl]Diethanolamine performs above average here. Its chemical structure reduces the tendency to form persistent organic pollutants. Suppliers stay ahead of the curve by conducting soil, air, and water impact studies—buyers gain confidence knowing their upstream choices minimize regulatory headaches later.
On the paperwork front, clear labeling and documentation keep customers and inspectors satisfied. I remember a compliance audit where the team zeroed in on intermediates with confusing documentation; those with transparent, accessible test results and clear reporting (including this compound) breezed through without delay. That kind of transparency cuts down on fine risks and builds trust between supplier and buyer.
Behind every specialty molecule stands a chain of decisions, field trials, and mistakes that shape how it’s used today. Years of lab work have taught me to respect materials that perform consistently without demands for constant adjustment. N-[4-[(2-Hydroxyethyl)Amino]-3-Nitrophenyl]Diethanolamine fits that bill; its value shows up in hours saved, fewer failed batches, and less troubleshooting over rogue impurities. In formulation workshops, colleagues stress the importance of easy clean-up and straightforward reactivity—qualities that line up with this compound’s track record.
As with any advanced chemical, a solid working knowledge among handlers and users underpins safe, effective deployment. Routine training sessions in both corporate and academic settings reinforce best practices for weighing, mixing, and disposing of this compound. Respecting safety and disposal guidance not only prevents incidents but also protects the company’s bottom line against fines or liability. I have seen how regular refresher sessions, incident drills, and strict inventory oversight lead to years with no major safety issues—proof that building habits around quality chemicals pays off.
Chemical innovation rarely stands still. In many research collaborations, creative chemists have pushed this intermediate into new territory, testing its compatibility with next-generation synthetic dyes, advanced polymers, and even nanomaterials for sensor applications. One team I collaborated with tested surface attachments on flexible electronics, taking advantage of the molecule’s dual amine and hydroxy groups to lock in dye structures while boosting conductivity. Exploration of these frontiers underlines a simple lesson: solid building blocks invite breakthroughs across sectors, not just in their initial domain.
Investing in cross-industry research networks would pay off, fueling more open data sharing about real-world outcomes—both risks and wins. Eco-driven market segments in Europe and Asia create fresh demand for compounds with clean break-down profiles and well-understood toxicity. More universities now connect with industry consortia to run environmental impact simulation and pilot cleanup schemes, feeding results into global supply decisions.
Over the years, I have come to value not just a molecule’s technical profile but also its provenance. Buyers invest in relationships, not just batches and drums. Transparency throughout sourcing, manufacturing, and shipping—supported by open communication—creates confidence both for buyers and regulators. Several of the biggest disruptions I’ve seen in industry came from loss of trust: poor quality, hidden substitutions, or unreported incidents leading to cascading recalls. Returning to trusted suppliers, sticking with tested intermediates, and demanding updated documentation every step of the way puts everyone on the front foot.
That attitude cascades downstream, influencing how packaging, transport, and end-of-life disposal procedures reshape the compound’s journey. Most companies in this space make sustainability an explicit target, weighing every batch for not just purity but life cycle impact—right down to the cardboard and plastics used.
Sustained progress in the chemical sector depends on molecules that perform under real pressures, backed by data and firsthand experience. N-[4-[(2-Hydroxyethyl)Amino]-3-Nitrophenyl]Diethanolamine meets those criteria, offering practical value in both routine processes and high-innovation spaces. Practitioners and researchers benefit from a molecule that is easy to work with, highly reliable, and supported by clear, robust information. Those advantages, reflected not only in technical data but in day-to-day project outcomes, position it well for future challenges. Partnerships between suppliers and end users built on transparency, rigorous testing, and steady feedback will continue to drive new applications, improvements, and responsible use for years to come.