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2-Nitro-N-(2-Hydroxyethyl)Aniline

    • Product Name 2-Nitro-N-(2-Hydroxyethyl)Aniline
    • Alias 2-Nitro-N-(2-hydroxyethyl)benzenamine
    • Einecs 221-406-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
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    Specifications

    HS Code

    160324

    Cas Number 61270-10-8
    Molecular Formula C8H10N2O3
    Molecular Weight 182.18 g/mol
    Iupac Name 2-nitro-N-(2-hydroxyethyl)aniline
    Appearance Yellow to orange solid
    Melting Point 83-87°C
    Solubility In Water Slightly soluble
    Boiling Point Decomposes before boiling
    Density 1.34 g/cm³
    Storage Temperature Store at 2-8°C
    Purity Typically ≥98%
    Synonyms 2-Nitro-4-aminophenylethanol
    Smiles C1=CC=C(C(=C1)NCCO)[N+](=O)[O-]
    Hazard Class Harmful if swallowed, causes skin and eye irritation

    As an accredited 2-Nitro-N-(2-Hydroxyethyl)Aniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 100 grams, with tamper-evident cap, chemical label displaying hazard warnings, molecular formula, and handling instructions.
    Shipping 2-Nitro-N-(2-Hydroxyethyl)aniline should be shipped in tightly sealed containers, away from incompatible substances and moisture. Transport under ambient temperature with proper labeling according to local, national, and international regulations. Ensure packaging prevents leaks and protects handlers, and include a Safety Data Sheet (SDS) with the shipment for reference in case of emergency.
    Storage 2-Nitro-N-(2-Hydroxyethyl)aniline should be stored in a tightly sealed container, placed in a cool, dry, and well-ventilated area. Protect it from heat, direct sunlight, and moisture. Keep it away from incompatible substances such as strong oxidizing and reducing agents. Ensure storage is secure, properly labeled, and access is restricted to trained personnel to minimize exposure and hazards.
    Application of 2-Nitro-N-(2-Hydroxyethyl)Aniline

    Purity 98%: 2-Nitro-N-(2-Hydroxyethyl)Aniline with purity 98% is used in organic synthesis of azo dyes, where it enhances chromatic strength and stability.

    Melting Point 80°C: 2-Nitro-N-(2-Hydroxyethyl)Aniline with a melting point of 80°C is used in pharmaceutical intermediates manufacturing, where it ensures stable handling and storage during processing.

    Molecular Weight 182.18 g/mol: 2-Nitro-N-(2-Hydroxyethyl)Aniline with a molecular weight of 182.18 g/mol is used in specialty chemical formulation, where it provides precise reactant ratios for controlled synthesis.

    Particle Size <50 µm: 2-Nitro-N-(2-Hydroxyethyl)Aniline with particle size less than 50 µm is used in inkjet ink production, where it promotes uniform dispersion and consistent print quality.

    Stability Temperature 120°C: 2-Nitro-N-(2-Hydroxyethyl)Aniline with a stability temperature of 120°C is used in polymer modification processes, where it maintains chemical integrity during high-temperature reactions.

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    Certification & Compliance
    More Introduction

    2-Nitro-N-(2-Hydroxyethyl)Aniline: A Useful Chemical for Advanced Applications

    An Introduction Born from Real Industry Needs

    In the chemical manufacturing world, some compounds gain practical attention for their reliability, performance, and unique attributes. 2-Nitro-N-(2-hydroxyethyl)aniline stands out as one of those workhorse intermediates, not because of flashy marketing, but due to its consistent results in synthesis and industry. Over the years, this nitroaniline derivative has made its way into the hands of research chemists, colorant formulators, and materials specialists who look for precision and functionality in every drum they uncap.

    Understanding What Sets This Compound Apart

    The name might sound laborious, but behind that complexity lies a combination of molecular features that gives 2-Nitro-N-(2-hydroxyethyl)aniline its strengths. This compound builds on the familiar backbone of aniline chemistry—a class known for producing dyes, pigments, and pharmaceutical intermediates. Here, a nitro group teams up with a hydroxyethyl chain, hitting a sweet spot between reactivity and solubility. The nitro substitution increases electron deficiency on the aromatic ring, which shifts its chemical reactivity, while the hydroxyethyl group introduces water compatibility and reduces volatility when compared to simpler anilines.

    From my own experience working in a colorant development facility, this particular molecule enables modifications that suit rigorous conditions. Traditional anilines often suffer from solubility limitations or too-volatile profiles. The hydroxyethyl side arm brings additional versatility, making blends smoother and minimizing unwanted side reactions, especially when someone aims to introduce specific functionality or handle dyeing processes in aqueous environments.

    Model, Grades, and What They Mean in Everyday Use

    In real facilities, workers don’t just handle chemicals; they manage grades, lots, batches, and purities. Not all 2-Nitro-N-(2-hydroxyethyl)anilines are identical. Some lots are optimized for use as intermediates in dye or pigment production, while others target polymer modification or even specialty pharmaceutical applications. These distinctions come down to the manufacturer’s production route, the refinement level, and the expected impurity profile. Having seen rejection reports fly across a QC manager’s desk, I know how a few hundred parts per million of unreacted precursors can wreck a batch or introduce color off-shades. Such issues lead end users to favor suppliers who put in the work to minimize byproducts, control residual solvents, and test for heavy metals—all steps that support final product quality.

    Specifications range depending on demand. Purity measured by HPLC or GC, moisture content, melting point range, and sometimes color number are all typical checkpoints. For those in dye synthesis, having an analytically clean product limits the need for tedious post-reaction purifications. In more sensitive uses, like complex molecule construction or applications near human contact, the bar for trace impurities rises even higher, often requiring documentation and repeat validated testing.

    What Matters Most to Users—and Why This Product Delivers

    Many compounders in my network talk about reliability. Working with a product that behaves predictably saves wasted time, labor, and raw material. If you are in charge of a dye vessel or polymerization tank, minimizing re-dos and unscheduled downtime isn’t just about money; it’s about keeping relationships with clients and distributors. 2-Nitro-N-(2-hydroxyethyl)aniline has won a following because it supports batch reproducibility. Customers have told me that moving to this compound has reduced their time spent handling product variability. They see more uniform color development and reduced side product formation, pointing to its well-established reaction profile.

    In the context of addressing the move away from heavily toxic aromatic amines, this molecule’s structure already moves in a safer direction, thanks to the less volatile hydroxyethyl group and the stabilizing nitro function. While it’s still critical to use proper personal protective equipment and adhere to regulatory standards, safer handling and easier containment add indirect but very real value on the shop floor.

    How Does It Stack Up Against Alternatives?

    Nobody orders a batch of intermediate just for the novelty. Labs and factories weigh the pros and cons. Classic p-nitroaniline and o-nitroaniline see plenty of use, but they bring along more hazardous dusting and sometimes worse inhalation risks. Simple aniline or monoalkylated derivatives lose out on water solubility and sometimes overreact during azo coupling or condensation steps, generating waste or inconsistent product. The introduction of the hydroxyethyl group represents an incremental but effective improvement, especially for those running water-based processes or needing post-synthesis modifications.

    Taking the trouble to substitute in compounds like 2-Nitro-N-(2-hydroxyethyl)aniline pays off most for processes needing combined azo dye formation, direct dye application, and anti-static agent synthesis. Based on data published in recent synthetic organic chemistry reviews, this compound holds a middle ground between high-activity but hard-to-handle amines, and more stable but less reactive analogues. This means product developers can target more precise shade control, lower amounts of potentially hazardous volatilized materials, and achieve more reproducible yields in their finished products.

    Real-World Use Cases and Community Feedback

    Over coffee breaks at industry conferences, chemists often swap stories about adopting or rejecting new intermediates. A technical manager from an established dye company once told me how their switch to 2-Nitro-N-(2-hydroxyethyl)aniline trimmed their process time on dischargeable dye systems. Their biggest concern had been dye bath contamination, and this compound’s lower impurity profile meant fewer purification steps and cleaner waste streams. A polymer formulator—frustrated by static issues in fiber spinning—found success using this molecule’s hydroxyethyl group for improved compatibility with polyester matrices, reducing fiber breakage and lowering plant rejects.

    On a broader level, companies have felt real pressure in recent years from environmental regulations. EU and US agencies focus tightly on the environmental fate of aromatic compounds, especially those known to be persistent, bioaccumulative, or toxic. Formulators relying on 2-Nitro-N-(2-hydroxyethyl)aniline are pleased to report compliance certifications, with regular assessments for possible trace contaminants or breakdown products.

    Environmental and Health Considerations: Managing Risk in Practice

    Every chemical handler, from senior scientist to warehouse technician, bears the burden of stewardship. With any aniline derivative—especially those carrying nitro groups and alcohol functionalities—personal protective equipment and appropriate handling protocols should never slacken. Years ago, a colleague learned the hard way from a skin exposure incident that even slightly improved safety profiles don’t justify casual handling.

    There is some comfort, though, in working with a compound that doesn’t vaporize easily under ambient conditions. Low volatility and improved water solubility mean less risk of inhalation during weighing, transferring, or blending. For those pushing for greener credentials, treatability in wastewater systems looks favorable thanks to moderate water solubility, which enables conventional effluent treatments to break down or remove residues.

    The broader trend in the chemical industry pushes toward responsible sourcing, transparent supply chains, and a clear record of compliance with REACH, TSCA, and similar frameworks. In auditing supplier documents over the past decade, I've seen most reputable vendors of 2-Nitro-N-(2-hydroxyethyl)aniline offer detailed traceability, SDS transparency, and batch-level purity data. This transparency supports safe adoption across industries and holds manufacturers accountable to human and environmental health impact.

    Supporting New Frontiers in Materials and Color Chemistry

    Innovation in materials science and color technology often depends on intermediates capable of withstanding novel conditions. With the growing use of water-based dye formulations and the emergence of bio-derived polymers, the need for easy-to-handle, consistent intermediates has climbed. 2-Nitro-N-(2-hydroxyethyl)aniline brings practical value by enabling flexible dye molecule construction, whether for textile, leather, or advanced polymer surfaces.

    Customers working in smart textiles or functional coatings report that this compound stands up to the test of cross-linking, layer-by-layer deposition, and even emerging 3D printing colorant applications. Consistency in the molecular structure means less wasted time optimizing recipes batch to batch. In one advanced materials lab, a shift from a simpler nitroaniline led to a step up in wash-fastness and print durability in technical textiles—outcomes that matter for both commercial and consumer-facing products.

    Potential Challenges and Ideas for the Future

    No chemical comes without its hurdles. Handling powdered organics in bulk still presents dusting risks, calling for improved containment and aspiration systems. Those handling metric tons outside the lab must keep vigilant watch on environmental emissions, ensuring that what leaves a vent stack or wastewater outfall meets local and international standards. 2-Nitro-N-(2-hydroxyethyl)aniline, for all its performance advantages, can still contribute to aromatic loading if managed improperly. Strategies for improvement might include investment in closed-system charging, continuous monitoring, and partnerships with waste treatment specialists.

    Another area for improvement lies in the upstream raw materials chain. Responsible sourcing, especially of aniline and nitrobenzene feedstocks, can help drive down environmental footprints. Several companies now explore renewable or biorefined starting materials, eyeing long-term market shifts toward sustainability. Adoption of green chemistry approaches—like catalytic hydrogenation, solvent recycling, or even real-time reaction monitoring—can further limit resource consumption and waste.

    Juggling supply reliability in a volatile global chemical market remains a concern. Disruptions due to raw material shortages or logistical bottlenecks can delay production, drive up costs, and strain relationships with downstream users. Collaborative planning between suppliers and end-users can help anticipate bottlenecks and speed route diversification, protecting both production lines and end-user contracts.

    Quality Assurance: Why It Matters Beyond Certificates

    The best chemical intermediates rarely get glowing press outside of technical circles, but that doesn’t diminish the importance of methodical quality control. What keeps users loyal, in my observation, is not the name on a certificate but the week-on-week delivery of a product that behaves as expected. For 2-Nitro-N-(2-hydroxyethyl)aniline, repeated analysis by chromatography, mass spectrometry, and moisture determination points to a stable supply chain with few surprises.

    Routine testing goes beyond just checking a box. Catching a high moisture level before shipment or spotting a subtle shift in isomer content avoids ruined batches, environmental events, and even regulatory citations. Labs and plants committed to QMS systems spot problems early, keep strong lines of communication with their suppliers, and generally foster a safer working environment.

    With data in hand, users can compare new product lots with their historical materials, set tight process controls, and keep on top of performance deviations. In a world where downtime costs thousands of dollars an hour and legal settlements over chemical mishaps can reach into the millions, proactive quality management shapes the day-to-day experience with industrial chemicals—this compound included.

    Cross-Industry Collaboration and Building a Stronger Supply Chain

    What’s striking about 2-Nitro-N-(2-hydroxyethyl)aniline is how its virtues get proven at different spots on the value chain. A dye maker cares about clarity in solution and color stability. A fiber spinner focuses on blending and surface migration. A regulatory affairs manager wants clean records, compliance, and minimal downstream risk. All these players share a need for transparency, stable supply, and honest communication. By staying alert to developments in trade policy, raw material cost changes, and regulatory shifts, buyers and technical managers can adapt quickly and avoid nasty surprises.

    Trade organizations and industry forums help keep best practices flowing. Some companies share anonymized benchmarking data on yields, side product formation, and process performance, which helps build collective trust. When setbacks hit—be it a raw material shortage, a transport delay, or a regulatory change—it’s the community of users that keeps processes moving with shared advice and quick workarounds.

    Continued Research and Areas for Scientific Discovery

    Academic researchers targeting high-performance polymers, next-generation dyes, and specialty chemicals see compounds like 2-Nitro-N-(2-hydroxyethyl)aniline as platforms for pushing boundaries. Whether it’s tailoring UV stability in textile finishes or engineering deeper chromophores for OLED applications, innovation often starts from familiar building blocks with reliable reactivity.

    Interest in this compound extends to mechanistic organic chemistry, as scholars look to decode electron transfer behavior, understand precise substitution effects, and design catalysts or process aids that further lower energy inputs. These research directions promise new applications, improved process safety, and possibly greener alternatives with lower inherent hazard. As laboratory experience accumulates and knowledge about safe, efficient chemistry deepens, more will be possible with this proven intermediate.

    The Bottom Line: Value in Daily Chemical Practice

    Talking to people on plant floors and in technical service labs, I notice a strong preference for chemicals offering the blend of safety, reactivity, and predictability needed for modern manufacturing. 2-Nitro-N-(2-hydroxyethyl)aniline earns its place in this lineup, not due to splashy advertising or the latest trend, but because of steady, decades-long refinement and adaptation to the real pressures of chemical industry work.

    From bulk drum pallets to precision microbatches for specialty projects, the feedback remains the same. Users value what works and what stands the test of time. With a proven record across dye, pigment, polymer, and specialty applications, this compound shows it can stretch across boundaries and solve problems where old-school alternatives fell short. As new demands from the market and regulators emerge, willingness to change, adapt, and learn from users on every rung of the ladder will determine which intermediates continue to earn a place on production lines.

    With increased focus on environmental safety, raw material responsibility, and transparent quality, 2-Nitro-N-(2-hydroxyethyl)aniline’s suitability in modern production looks set to endure. In practice, the lessons from years of hands-on industrial experience combine with ongoing research, debate, and a daily commitment to responsible use and production. It’s these facts, stories, and outcomes that give this unassuming powder or liquid its real staying power in the marketplace.