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N-(2-Cyanoethyl)-N-(2-Hydroxyethyl)-M-Toluidine

    • Product Name N-(2-Cyanoethyl)-N-(2-Hydroxyethyl)-M-Toluidine
    • Alias m-Toluidine, N-(2-cyanoethyl)-N-(2-hydroxyethyl)-
    • Einecs 232-433-2
    • 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
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    699874

    Chemical Name N-(2-Cyanoethyl)-N-(2-Hydroxyethyl)-M-Toluidine
    Molecular Formula C12H16N2O
    Molecular Weight 204.27 g/mol
    Cas Number 61377-44-8
    Appearance Colorless to pale yellow liquid
    Boiling Point Approximately 350°C (estimated)
    Density 1.03 g/cm3 (approximate)
    Solubility Soluble in organic solvents, slightly soluble in water
    Ph Neutral to slightly basic (in water)
    Refractive Index 1.531 (approximate)
    Storage Temperature Store at 2-8°C (Refrigerated)
    用途 主要用于有机合成和聚合物工业中的化学中间体

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

    Packing & Storage
    Packing The chemical is supplied in a 100g amber glass bottle, featuring a secure screw cap and clearly labeled with hazard information.
    Shipping N-(2-Cyanoethyl)-N-(2-Hydroxyethyl)-M-Toluidine should be shipped in tightly sealed containers, protected from light and moisture. Transport in accordance with local, national, and international regulations for chemicals. Ensure proper labeling and documentation. Handle with care, avoiding extreme temperatures and mechanical shock. Suitable packaging prevents leaks and contamination during transit.
    Storage Store **N-(2-Cyanoethyl)-N-(2-Hydroxyethyl)-M-Toluidine** in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat, moisture, and incompatible substances such as strong oxidizers. Keep it out of direct sunlight and sources of ignition. Use secondary containment to avoid leaks. Label the storage area appropriately and ensure proper personal protective equipment is available for handling.
    Application of N-(2-Cyanoethyl)-N-(2-Hydroxyethyl)-M-Toluidine

    Applications of N-(2-Cyanoethyl)-N-(2-Hydroxyethyl)-M-Toluidine in Industrial Manufacturing

    As an established producer of N-(2-Cyanoethyl)-N-(2-Hydroxyethyl)-M-Toluidine, we supply this specialized intermediate to advanced manufacturing sectors where stringent quality assurance, formulation accuracy, and compliance are fundamental. The material’s chemical structure and reactivity have enabled its adoption in a select range of high-performance applications that demand tight adherence to industry-specific standards and documented formulation protocols. Below, we detail major downstream application segments, emphasizing unique deployment parameters and compliance benchmarks relevant to each industry.

    1. Photopolymerization Initiators for UV-Curable Inks

    UV-cured inks and coatings manufacturers integrate this aromatic tertiary amine compound within proprietary photoinitiator blends used for high-speed printing and packaging lines. Its electron-donating properties allow precise tuning of curing rates, print sharpness, minimal migration, and resilience under repeated substrate flexing. Formulators adjust its addition in relation to resin chemistry, ink substrate, and application curing hardware.

    Industry compliance standards

    • Swiss Ordinance on Materials and Articles (SR 817.023.21) for food contact materials
    • EuPIA Exclusion Policy for Printing Inks and Related Products
    • REACH Annex XVII compliance for photoinitiator use
    • ISO 2846-1:2017 (Graphic technology – Color and transparency of printing ink sets)

    Typical usage ratio

    • 0.5% to 3.0% w/w in UV-curable ink or varnish formulations; final percentage is set per pigment loading, print speed, and curing energy. Formulators may reduce additive to the lower end for low-migration formulations targeting primary food packaging.

    Downstream process integration

    • Direct blending with photoinitiators and oligomers at the pre-dispersion stage, preceding pigment addition and microfiltration. Compound must be homogeneous before entering in-line mixing and mill pass in inklet production.

    Final product types

    • UV-cured flexographic and offset inks
    • Screen and digital printing inks for food packaging
    • Radiation-curable topcoats for rigid and flexible packaging substrates
    • Industrial label overprint varnishes

    2. Polymerization Accelerator for Adhesive Systems

    Cyanoacrylate and anaerobic adhesive manufacturers rely on this compound as a co-initiator to boost cure rates and shelf stability in synthetic resin systems. Its tailored interaction with peroxy and azo-type initiators provides fast assembly response and reliable fixture strength on diverse substrates such as metals, plastics, and elastomers.

    Industry compliance standards

    • ISO 10993-5:2020 (Biological evaluation of medical devices – Cytotoxicity requirements for adhesives in medical assembly)
    • GB/T 32609-2016 (Chinese Industrial Adhesives Standard)
    • ASTM D3165 / ASTM D1002 (Lap shear strength and substrate bonding criteria)
    • RoHS 3 (EU 2015/863) for restricted substances in assembly adhesives

    Typical usage ratio

    • 0.1% to 1.5% w/w in cyanoacrylate and acrylate-based adhesive formulas; manufacturers calibrate loading to balance open working time and rapid curing as dictated by end-use and substrate reactivity.

    Downstream process integration

    • Introduced during bulk polymer or prepolymer preparation, before vacuum stripping. For one-component adhesives, addition occurs post-monomer de-inhibition under controlled anhydrous conditions. In two-component systems, separate pre-mix ensures no pre-curing.

    Final product types

    • Quick-set cyanoacrylate adhesives for electronics and appliance assembly
    • Automotive threadlockers and anaerobic gasketing materials
    • Medical device bonding agents (where non-migratory grades qualify)
    • General industrial instant adhesives for plastics and metals

    3. Intermediate for High-Performance Dye Synthesis

    Specialty dye and pigment manufacturers leverage the compound as a unique structural building block in the synthesis of proprietary azo and anthraquinone dyes, particularly for applications demanding enhanced photo-stability and colorfastness. Its cyanoethyl and hydroxyethyl groups enable controlled functionalization during multi-stage synthesis, permitting fine-tuning of dye solubility, affinity, and shelf life in demanding conditions.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for restricted dye intermediates in textiles
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List) v3.1
    • REACH Regulation (EC 1907/2006) concerning final dye composition
    • ISO 105-A02:1993 (Textiles – Tests for colour fastness)

    Typical usage ratio

    • 0.3 to 1.8 molar equivalents relative to the target dye chromophore in condensation and coupling reactions; adjusted for yield optimization and waste minimization strategies in large-scale runs.

    Downstream process integration

    • Charged into alkylation or arylation reactors during early- to mid-stage dye molecule construction; used in controlled batch or continuous syntheses. Purification or isolation follows to ensure downstream purity requirements.

    Final product types

    • Reactive dyes for cotton, viscose, and cellulosic blends
    • Disperse dyes for polyester and acetate fibers
    • Functional pigment dispersions for plastics and high-pressure laminates
    • Colorants for industrial coatings meeting migration and fastness criteria

    4. Chemical Intermediate in API and Fine Chemical Production

    Pharmaceutical and fine chemical processors employ this compound as a tailored amine intermediate in multi-step syntheses, where selectivity and defined functional group compatibility are critical. It supports formation of advanced moieties for APIs or key intermediates in projects requiring scalable production and high yield per batch, under rigorous process control.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients)
    • EU GMP Part II for fine chemicals in pharmaceutical starting materials
    • USP/NF and Ph. Eur. monographs for relevant downstream intermediates
    • 21 CFR Part 211 (US FDA cGMP for pharmaceutical manufacturing)

    Typical usage ratio

    • Stoichiometric or slight excess (1.0–1.2 equivalents) per step, as calculated for target synthesis route; loading and charge ratio reflect route optimization and impurity profile control in API and advanced intermediate manufacture.

    Downstream process integration

    • Added during amination, alkylation, or reductive coupling stages under batch or flow chemistry. Followed by intermediate purification (distillation, crystallization, or chromatography) before proceeding to the next synthetic step.

    Final product types

    • Pharmaceutical active ingredients (API) where structure specificity is critical
    • Pharma-grade intermediates supporting custom synthesis
    • Fine chemicals for diagnostic and medicinal chemistry tools
    • Functionalized precursors entering regulatory drug supply chains
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    Certification & Compliance
    More Introduction

    N-(2-Cyanoethyl)-N-(2-Hydroxyethyl)-M-Toluidine: Our Insights on a Key Intermediate

    Understanding This Chemical’s Place in Manufacturing

    Every step in the production process shapes the final result. With N-(2-Cyanoethyl)-N-(2-Hydroxyethyl)-M-Toluidine, a distinct aromatic amine, our industry holds a building block that goes far beyond simple addition. This compound remains steady through varied reaction conditions. It plays a recurring role in intermediates for colorants, pharmaceuticals, and specialty chemicals. Every batch we produce reflects a consistent molecular balance that helps chemists gain a reliable reaction partner.

    Our operations have shown how subtle changes in chemical design can drive outcomes in performance and safety. The presence of both cyanoethyl and hydroxyethyl groups widens reaction options. The cyano group often serves as a stepping stone for transformations into amides, acids, and other valuable structures. The hydroxyethyl side increases solubility, enabling downstream chemists to avoid the headaches that can come with phase separation or processing inefficiencies. M-toluidine’s core means improved control during diazotization and coupling reactions, and we’ve seen firsthand how its reactivity suits complex syntheses.

    Why We Focus on Specification Consistency

    Our typical commercial material contains a minimum assay of 98.5%, but that number is not just a checkbox on a test report. Each finished lot undergoes GC analysis; we catch trace impurities that could affect catalytic performance or color strength in sensitive dye applications. Over time, we’ve tracked how even minute levels of residual toluene or isomeric side products can disrupt yields. We run our production lines with this in mind, giving preference to process stability, avoiding hot spots or local pH drifts, and maintaining optimal agitator mixing speeds. Every time we receive feedback from formulators about clean reactions free from unexpected byproducts, it validates the vigilance we keep in our synthesis and distillation stages.

    How Downstream Usage Drives Continuous Refinement

    In-house, we use this material as a test substrate to monitor the selectivity of new catalysts and the efficiency of coupling agents. Outside our factory, technical teams in pigment plants and pharmaceutical custom synthesis depend on it to build up base structures or block certain reaction sites. We have supplied our material in support of several patent-protected projects, including innovative red and orange dyes. In one long-term partnership with an agrochemical manufacturer, formulation changes required a tight control of water content — a challenge solved through a switch to inert gas blanketing and new drying techniques during bulk transfer.

    Customers expect more than just chemical purity. Granularity and melt behavior figure heavily in batch processing. Over the years, we shifted from traditional crushing to a densified prill form, which streamlines conveyance and reduces dust. This decision came from facing repeated loss on transfer in older setups, and a string of minor safety incidents resulting from static buildup. One large pigment customer reported faster dissolution after the change. Our feedback loop with users energizes our team to keep production agile, ready to adjust for scale, season, or even site-specific facility changes in handling requirements.

    Contrast with Related Amines

    Those who’ve worked with more common N-alkylated m-toluidines, such as those with just an ethyl or hydroxyethyl substituent, will immediately notice sharper differences in polarity and solubility. The cyanoethyl group not only shifts UV-Vis spectra — invaluable in analytical method development — but also slows unwanted side reactions in oxidative environments. In the context of dye intermediates, the cyano group acts as both a lever for building up chromophores and as a stabilizer during temperature swings. Where simple N-ethyl-m-toluidine tends to promote excessive foaming during polymerization, our cyanoethyl, hydroxyethyl product maintains noticeably calmer boiling profiles.

    From our vantage point in scaled production, another clear distinction lies in storage stability. Many users of 2-hydroxyethylm-toluidine report gradual yellowing or even sporadic gum formation, especially if exposed to minor amounts of air or trace transition metals during storage. Our variant — given the electron-withdrawing effect of the cyano group — maintains both its appearance and its reactivity, holding color and minimizing polymeric residue for much longer periods on the shelf. This feature reduces waste and rework, while giving procurement teams a longer window for planned usage without concerns about off-color batches.

    Practical Experience in Manufacturing

    Every kilogram of this chemical tells a story about balancing throughput with control. We’ve seen production campaigns where careless solvent handling—or insufficient temperature profiling—led to off-odor and failed purity specs. Our team learned, often through hands-on trial and follow-up analytics, how to calibrate reaction times and distillation cuts dynamically. These studies led us to refine our in-line spectrometric controls. For end users, steady, reproducible performance means processes downstream run more smoothly. A vivid moment came during a marathon winter shift: an unexpected impurity peak in our in-house QC led to a deep dive into vessel cleaning routines, which in turn resulted in a standard operating procedure adopted across two sites.

    On the shop floor, workers often point out the physical feel of the material. Our standard product flows easily in feeders, with few caking issues even after lengthy storage. From a safety perspective, improved flow makes loss containment and housekeeping more manageable, reducing the risk of slips or unpredictable blockages. As energy prices fluctuate, we’ve managed production pressures and jacket temperatures to keep energy consumption under control, optimizing not just financial costs but also environmental impact.

    Supporting Responsible Use

    Years of supplying this chemical across markets have taught us the importance of clear dialogue with technical teams about its reactivity and potential hazards. The cyano group, while beneficial for synthesis, calls for respect in handling. During times when regulatory requirements shifted, we invested in revised labeling and MSDS updates. We worked with logistics partners to adopt sealed transfer systems that minimize the chance of accidental releases. Shipping in lined steel drums, and for larger consumers, dedicated tanks, helps guard against contamination from previous loads. Storage protocol recommendations are never simply theoretical; we draw on customer incidents — from accidental moisture ingress to prolonged sunlight exposure — to guide guidance and propose risk-lowering steps.

    Feedback from laboratory users pointed us toward developing more detailed application notes. By sharing practical tips for reaction setup, order of addition, and safe neutralization, we aim to help chemists avoid avoidable errors that can arise when switching from lab-scale glassware to industrial reactors. Communication remains central. When a research group contacted us about unexplained losses in a key coupling reaction, we dispatched a site expert to review handling and sampling methods. The issue traced to a sampling valve design prone to minute leaks; a simple switch to a different model restored both productivity and morale.

    Product Evolution and Industry Standards

    Material quality expectations have climbed over the last decade. Dyes for digital inks now demand narrower impurity profiles than legacy textile applications. As a result, instrument calibration, batch traceability, and the use of validated analytical standards have become central in our daily quality routines. It wasn’t always so precise. On older lines, operators often logged visual inspections and spot checks. Today’s requirements have us running multi-point purity and moisture checks as part of release, along with keeping retention samples for extended periods.

    We have collaborated with external auditors on both ISO standards and voluntary sector programs for chemical stewardship. This not only increases confidence in our supply for critical applications, but it tightens our internal controls — reducing the incidence of returns and lengthy customer investigations. By introducing more robust data-sharing platforms, we help customers tie raw material changes to their finished product quality, enabling closer supply chain alignment.

    Challenges and Practical Solutions

    Every production campaign brings new learning. We have managed through extended reagent shortages, sudden swings in global logistics, and the rising cost of waste treatment. During times of raw material constraint, our process engineers run scenario planning to keep lines running without resorting to uncontrolled blends or off-spec batches. In one tight market, we shifted solvent distillation scheduling, reclaiming higher purity product from side cuts that previously went to waste. This change, though modest in theory, preserved customer commitments during a six-week vendor outage.

    Wastewater reduction has emerged as a central focus. This compound, like many aromatic amines with functionalized side chains, can present trace contamination risks if not immobilized or treated effectively. We invested in new stripper columns and close-looped filtration. Together with on-site biological treatment, this combination slashed discharge loads while recovering product that otherwise would have driven up disposal costs. Recent audits highlighted our low residue figures — something purchasing managers at partner companies increasingly seek.

    Looking Ahead: Trends Shaping Product Use

    Market demand for higher-purity intermediates grows as synthesis routes evolve. Customization is not a future trend, it’s a present reality. We regularly receive requests for specific particle size, alternate pack sizes, or even pre-neutralized forms of the amine for integration into automated dosing systems. Some of these changes arise from tightening government restrictions overseas. Others stem from downstream process simplification, shaving hours from batch cycles or reducing operator intervention.

    Our team continues to invest in analytics and continuous feedback. By working alongside users in dye, agrochemical, and pharma projects, we gain at-the-source insight into what works and what disrupts process flow. We see this compound’s role shifting as green chemistry expands: direct uses as a coupling base for less hazardous dye processes, or as a safer intermediate in routes that limit uncontrolled venting or hazardous solvent use. Already, we are investigating biocatalytic alternatives for some process steps — a challenge that requires deep experience and careful balancing of reactivity, selectivity, and throughput.

    Experience Sets Us Apart

    Our perspective comes from decades of direct manufacturing, not just moving material from warehouse to customer. We know that the value of N-(2-Cyanoethyl)-N-(2-Hydroxyethyl)-M-Toluidine is built batch by batch, through attention to detail in sourcing, processing, and customer support. Every improvement emerges from lessons learned at the reactor, in the QC lab, or from late-night troubleshooting on the plant floor. Practical results count: sharper color in dyes, fewer side reactions in next-generation pharma projects, streamlined operations during scaling up or down, and logistics support that shields users from preventable issues.

    With each shipment, our promise is to bring the lessons of real-world production experience to bear on every specification, every test, and every interaction. Those engaged in today’s demanding chemistry need more than a molecule on paper; they need a partner that anticipates issues, brings solutions, and stands behind every drum delivered. From site audits to batch tracebacks, our team works to stay ahead, giving our customers what they require: a product they can trust, shaped by hands-on know-how and a continual drive for improvement.