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2-(4-Aminophenyl)Ethylamine

    • Product Name 2-(4-Aminophenyl)Ethylamine
    • Alias Phenylethylamine
    • Einecs 218-739-4
    • 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

    427208

    Name 2-(4-Aminophenyl)Ethylamine
    Cas Number 563-41-7
    Molecular Formula C8H12N2
    Molecular Weight 136.20 g/mol
    Appearance White to off-white solid
    Melting Point 62-65°C
    Boiling Point 280°C
    Solubility In Water Soluble
    Density 1.081 g/cm³
    Pka 9.39 (amine group)
    Smiles C1=CC(=CC=C1CCN)N
    Inchi InChI=1S/C8H12N2/c9-8-3-1-7(2-4-8)5-6-10/h1-4H,5-6,9-10H2
    Pubchem Cid 12393

    As an accredited 2-(4-Aminophenyl)Ethylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g of 2-(4-Aminophenyl)ethylamine comes sealed in an amber glass bottle with a tamper-evident cap and hazard labeling.
    Shipping **Shipping Description:** 2-(4-Aminophenyl)ethylamine is shipped in tightly sealed, chemical-resistant containers, protected from moisture and light. It is classified as a laboratory chemical and handled as potentially hazardous. Appropriate labeling and documentation are ensured to comply with local and international regulations. Transport is typically via ground or air, following safety protocols.
    Storage 2-(4-Aminophenyl)ethylamine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Protect the compound from light and moisture. Store at room temperature and minimize exposure to air to prevent degradation. Use proper labeling and ensure access to safety data sheets and emergency procedures.
    Application of 2-(4-Aminophenyl)Ethylamine

    Applications of 2-(4-Aminophenyl)Ethylamine in Industrial Manufacturing

    2-(4-Aminophenyl)ethylamine is a specialty aromatic diamine widely adopted in advanced chemical synthesis. As the direct producer, we supply this intermediate to formulators and manufacturers serving core sectors. Distinct chemical attributes support its participation in targeted downstream applications. Below, we detail several industrial segments employing 2-(4-Aminophenyl)ethylamine as a raw material, with a focus on actual regulations, technical parameters, and practical manufacturing relevance.

    1. Polyimide Resin Synthesis for High-Performance Films

    Polyimide films require high heat resistance and mechanical strength for use in electronics, aerospace, and insulation. 2-(4-Aminophenyl)ethylamine acts as a diamine monomer, reacting with dianhydrides under controlled polycondensation processes. It introduces flexibility and tailored chain structure into the polymer backbone, enhancing performance at elevated temperatures. Manufacturers adjust amine-to-anhydride ratios for target molecular weights and handling viscosity during film casting.

    Industry compliance standards

    • IEC 60216 (Thermal endurance of electrical insulating materials)
    • UL 94 (Flammability standards for plastic materials)
    • RoHS Directive (Restriction of Hazardous Substances, EU)
    • ISO 9001 (Quality management system)

    Typical usage ratio

    • Monomer content: 0.95–1.05 molar equivalent relative to dianhydride
    • Adjustment based on final polymer chain flexibility and end-use specifications

    Downstream process integration

    • Charged to polymerization kettle after other diamines
    • Prepolymer solution casting onto carrier film, followed by thermal imidization

    Final product types

    • Flexible printed circuit boards (FPCBs)
    • High-temperature wire and cable tapes
    • Microelectronic insulation films
    • Flexible display substrates

    2. Epoxy Curing Agent Manufacturing

    Specialty aromatic amines such as 2-(4-Aminophenyl)ethylamine function as key curatives in epoxy formulations, imparting higher glass transition temperatures and modified reactivity profiles. Downstream compounding requires precise control of amine hydrogen equivalents to balance pot life, cure speed, and resultant mechanical properties. This diameter-rich structure is suited for high-solids, low volatility coatings, and adhesives necessitating elevated chemical resistance.

    Industry compliance standards

    • REACH Regulation (EU chemicals safety)
    • ASTM D1763 (Epoxy resin systems for flooring and adhesives)
    • ISO 1043-4 (Plastics – Abbreviations and terminology)
    • ISO 14001 (Environmental management system)

    Typical usage ratio

    • Epoxy-to-amine ratio: 0.8–1.2 stoichiometric equivalents
    • Adjusted for viscosity and cure profile, based on system requirements

    Downstream process integration

    • Dispersed into formulated resin during batch mixing
    • Introduced just prior to application for two-component systems

    Final product types

    • Solvent-free structural adhesives
    • Anti-corrosion protective coatings
    • Elektrical potting compounds
    • Chemical-resistant flooring systems

    3. API Intermediate for Antihypertensive Drug Synthesis

    2-(4-Aminophenyl)ethylamine represents a core intermediate for the synthesis of certain active pharmaceutical ingredients in the antihypertensive drug class. It enters selective reductive aminations and cyclization reactions to construct high-purity drug molecules under cGMP conditions. Upstream, tight control of residual solvent content and heavy metal impurity limits is critical to safeguarding regulatory compliance at each production stage.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • United States Pharmacopeia (USP) monographs
    • European Pharmacopoeia (Ph. Eur.) requirements
    • FDA 21 CFR Part 210/211 (GMP for finished pharmaceuticals)

    Typical usage ratio

    • Reactant input: 1.0–1.1 molar equivalent per target compound, may vary by route optimization
    • Dosed based on purity analysis and yield balancing

    Downstream process integration

    • Loaded to hydrogenation or alkylation reactors after pre-filtration
    • Purity checked prior to final API crystallization or salt formation

    Final product types

    • Benzazepine-class antihypertensive APIs
    • Pharmaceutical grade bulk drugs
    • Tablet and capsule formulations (post-site compounding)

    4. Synthesis of Fluorescent Dye Intermediates

    Due to its electron-donating amine groups and aromatic structure, 2-(4-Aminophenyl)ethylamine provides a reactive site for coupling reactions in the production of specialty dyes, particularly those used in biochemical analysis and imaging. Downstream processes often involve diazotization and azo coupling, where the raw amine must exhibit low metallic contamination to preserve fluorescence efficiency and spectral properties.

    Industry compliance standards

    • EN 71-3 (Migration of certain elements in toy safety dyes and colorants)
    • OECD Guidelines for the Testing of Chemicals
    • ISO 18314-1 (Analytical color measurement standards)
    • REACH Annex XVII (Restrictions on certain hazardous substances in colorants)

    Typical usage ratio

    • Used at 1.0–1.2 molar equivalents during coupling reactions
    • Process optimization based on quantum yield and lightfastness targets

    Downstream process integration

    • Fed directly to diazotization tank under cold aqueous conditions
    • Product isolation by pH-controlled precipitation and filtration

    Final product types

    • High-purity fluorescent dyes for protein labeling
    • Calorimetric assay reagents
    • Fluorescent tracer solutions
    • Specialty inkjet printer colorants

    5. Chain Extender for Modified Polyurethane Elastomers

    Aromatic diamines, including 2-(4-Aminophenyl)ethylamine, serve as chain extenders in rigid and microcellular polyurethane elastomer systems, granting improved resistance to degradation and dynamic load. Formulators utilize controlled addition during prepolymer extension, regulating part hardness and flexibility according to project requirements. Continuous monitoring ensures reaction completion to avoid residual monomers in final elastomer blocks.

    Industry compliance standards

    • ISO 11357 (Differential scanning calorimetry in plastics)
    • ISO 9001 (Quality assurance for elastomer manufacturing)
    • CFR 21 Part 174 (Indirect food additives, polymers for food contact applications)
    • RoHS Directive (Restriction of hazardous substances)

    Typical usage ratio

    • Added at 2–6% by weight relative to prepolymer, fine-tuned for mechanical property targets

    Downstream process integration

    • Metered into prepolymer mixing zone after initial polyol and isocyanate blending
    • Short pot-life cures require precise time and temperature alignment during casting or molding

    Final product types

    • Automotive bumper and fascia elastomers
    • High-resilience industrial rollers
    • Sporting goods protective equipment
    • Custom polyurethane sheets and blocks
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    More Introduction

    2-(4-Aminophenyl)Ethylamine: A Closer Look from the Manufacturer’s Perspective

    Introduction to a Versatile Building Block

    In the world of fine chemicals, some molecules stand apart because they solve real processing challenges. 2-(4-Aminophenyl)ethylamine, also known as p-phenylethylamine, has earned a solid reputation among chemical engineers and industrial chemists for its performance and consistent behavior in complex syntheses. We have spent years refining our process to deliver a compound that’s more than just a raw material — it’s a reliable tool that lets our customers innovate with confidence.

    Model and Manufacturing Consistency

    We manufacture this amine with particular attention to purity and batch-to-batch consistency. Our team insists on starting with high-grade raw benzene derivatives and applies a strict multi-step synthesis pathway that consistently reduces unwanted isomers and contaminants. Purity drives both safety and reaction yield in downstream use, so every lot undergoes GC and HPLC analysis. Typical assay levels for the main compound remain above 99.5% by HPLC, making this a fit for both regulated pharmaceutical research and advanced specialty applications.

    Some industrial buyers ask about the value of a model or reference number, but our experience suggests that reliable traceability flows better from lot-specific documentation rather than abstract codes. Each shipment includes a Certificate of Analysis linking back to the raw materials. This transparency matters most to customers managing regulated formulations.

    Physical Specifications and Handling Experience

    Most customers encounter 2-(4-Aminophenyl)ethylamine as a white to off-white crystalline powder, though temperature and moisture can create subtle shifts in appearance during handling. Molecular weight sits at 136.19 g/mol. Free-flowing texture results from our final drying stage, which takes place under low humidity and vacuum to eliminate any residual water.

    Over many production cycles, we’ve learned that container choice and storage humidity can affect clumping or slight discoloration. Using high-density polyethylene drums with double-lined bags, we keep exposure to air and light to a minimum. We also recommend users store unopened material at room temperature in a dry spot to lengthen its viable shelf life well past a year without noticeable loss of quality.

    Solubility in ethanol and chloroform remains high, and the compound dissolves quickly in most polar organic solvents. Customers in formulation work often tell us that the clean dissolution profile speeds up their process: less concern over undissolved residue leads to better efficiency and cleaner scale-ups. Handling the crystalline material produces only mild odor, mainly due to the aromatic amine function, which can become more pronounced during weighing or in a poorly ventilated area.

    How Customers Use It: Practical Applications from R&D to Production

    Most synthetic chemists value this compound for the reactive amino group on the para position of the phenylethyl chain, offering a direct route for the formation of a wide range of pharmaceutical intermediates, specialty polymers, and electronic materials. Over the years, we’ve seen the largest consumption in pharmaceutical exploration, where researchers connect the core to a variety of pharmacophores by reductive amination or acylation.

    Our conversations with research labs suggest that the material’s clean amine group minimizes side-reactions, even when working under high-temperature or catalytic conditions. We routinely answer inquiries about downstream compatibility, especially for manufacture of substituted benzamides, sulfonamides, and as a coupling partner in peptide and small-molecule synthesis. Because we continually test our output against customer application feedback, we have lowered the limits on critical impurities such as residual aniline or aldehyde byproducts — both of which can interfere with those sensitive reaction pathways.

    Over the last decade, growing demand has come from electronic and polymer chemistry sectors. The ethylamine structure allows chemists to introduce flexibility and hydrophilicity into conjugated polymers and polyamides. Our testing partners report improved polymer chain mobility, which changes melting behavior and physical properties in ways that non-functionalized precursors cannot achieve.

    We also hear from diagnostic reagent makers and dye producers. Here, the compound's clean aromatic ring system and controlled amine function provide a consistent starting point for azo and diazo dye molecules, which find use in colorants and fluorescent labels.

    What Sets 2-(4-Aminophenyl)Ethylamine Apart?

    Some prospective buyers ask us why not simply buy ordinary phenylethylamine, or if there’s a benefit to paying for higher purity grades. Years of manufacturing experience have shown us that alternative raw materials, like lower-purity grades or ortho/meta substituted isomers, bring headaches downstream. Even trace amounts of unwanted isomers change reactivity and can wreck a carefully optimized protocol.

    Other aromatic amines often show unpredictable behavior in either nucleophilic substitution or cyclization reactions, especially if storage has led to oxidation or hydrolysis. We have seen cases where poorly controlled raw materials resulted in color changes, tarry residues, or outright loss of synthetic yield — all of which come back to bite process engineers with higher cleaning or purification costs.

    Customers value our product for its controlled particle size and proven solubility profile, which makes scaling up from flask to kilo-lab or full pilot plant smoother. Some other products on the global market come as sticky oils or agglomerated masses that resist flow through modern formulation or dosing equipment, costing customers time and money in re-processing. Over the years, our technical team has invested in optimizing the crystallization stage and final particle separation, so users spend less time fixing basic raw material issues and more time refining their processes.

    Safety and Environmental Responsibility

    As a chemical manufacturer, we recognize our responsibility not only to deliver a consistent product, but also to minimize risk for our workers and the wider community. Amine compounds like this one require thoughtful handling, both in the factory and at customer sites. We restrict exposure and automate blending, using enclosed transfer systems to prevent airborne dust and unwanted contact.

    Routine training for our operators emphasizes the importance of controlling skin and eye exposure, plus immediate cleanup protocols for spills. Monitoring air in the production hall helps us ensure that off-gassing stays below established occupational exposure limits, based on published guidance from major chemical safety authorities. Because amines can react with acids or oxidizers, we keep tight separation between production lines and maintain active logging of raw material movement.

    Waste minimization and environmental compliance anchor our operations. Synthesis is designed to run with high atom economy and uses solvent recycling at every feasible stage. Most process wastes undergo active neutralization and are safely routed for external incineration or conversion under supervision. Our site participates in ongoing audits and makes results available for major clients, especially those in the pharmaceutical supply chain who share our priority for safe, responsible sourcing.

    For customers, we freely share detailed handling advice, not just generic statements seen on many safety data sheets. Whether it’s designing a feedstock dosing system or adapting an older formulation plant, we draw on decades working at plant scale to offer realistic, field-tested guidance. These efforts pay off in fewer lost-time incidents both at our site and across our customer base.

    Regulatory and Quality Assurance

    Quality management remains a non-negotiable. Our production crews follow validated, reviewed procedures and run every batch through a defined sampling and test protocol. Regular audits by third-party inspectors confirm our alignment with GMP principles for fine chemical manufacture. Each batch receives full lot traceability, and original test data are kept for many years as part of retained sample policy.

    Increasingly, downstream buyers face growing pressure to account for the origin and quality of every input, especially for pharmaceutical research or regulated materials. We assist with documentation, audit support, and technical queries to satisfy these growing due diligence demands. Where possible, we have switched to using raw materials with clear supply-chain provenance, and share full impurity profiles and origin certifications when requested.

    We subject every outgoing drum to additional checks, not just for specification compliance, but for signs of container damage, moisture ingress, or incorrect sealing. Too many competitors overlook this, yet it’s often the difference between a seamless production run and a week lost to investigation and troubleshooting. We also work closely with major shipping partners to prevent transport-related contamination or temperature deviations, so users get material that matches their specification expectations every time.

    Customer Feedback and Continuous Improvement

    We have always valued customer feedback as a path for continuous improvement. Initial requests in the early years focused mainly on purity or packaging size, but experience has taught us that real-world concerns require more than just supplying good product. We listen to users who test small research quantities and those running hundred-kilo campaigns. Recent upgrades to our drying system, for example, came after several partners highlighted trace moisture issues when scaling up polymerizations in the rainy season. Subsequent analytical improvements delivered drier, more stable product even under challenging transport conditions.

    Another theme among our larger buyers has been the need for sharper customer support. Our technical liaisons are often on call to help troubleshoot reactivity concerns or answer detailed application questions. Instead of generic, off-the-shelf responses, we find real value in collecting customer data, running parallel process experiments on our pilot line, and jointly developing better methods. This partnership helps both sides push the limits of what the base chemical can achieve.

    We regularly review packaging formats and dispatch practices to keep up with customer operations, whether that means changing drum sizes, offering tamper-evident seals, or refining labeling conventions to speed up their incoming QA processes.

    Future Directions and Sustainable Sourcing

    Supply chain stability matters more than ever. Disruptions in upstream benzene and nitration intermediates during recent years highlighted how quickly volatility cascades down the line. To address this, we’ve invested in more robust relationships with upstream suppliers and adopted flexible contract models that let us buffer inventory risk. We look ahead by working with new precursor suppliers focused on renewable benzene derivatives, a promising step as more of our customers look to lower the life-cycle carbon impact of their raw materials.

    Energy efficiency is another axis of improvement. We have optimized solvent recovery and heat integration as core parts of every new capacity expansion. Teams routinely revisit synthesis recipes in light of new catalysts or greener alternatives for reduction and purification steps. Where possible, we lean on closed-recycle loops, not just for environmental compliance, but for clear cost savings that strengthen long-term viability.

    Forward-thinking partners now ask about cradle-to-gate footprints, and we supply life-cycle impact data so they can align their own reporting. Sourcing certified renewable energy for much of our production site has already reduced our calculated emissions by a measurable percentage, and we expect further gains as neighboring companies join similar programs.

    Why 2-(4-Aminophenyl)Ethylamine Delivers Real Value

    Chemistry keeps evolving, and not every tried-and-true molecule holds up across new processes and regulatory frameworks. Yet time and again, 2-(4-Aminophenyl)ethylamine proves its staying power because it offers more than a static raw material. Our work puts us close to the scale-up and troubleshooting that real innovation demands. Customers keep coming back because they trust that every drum shipped has gone through checks and hands-on engineering well beyond the basics.

    Experience, reliability, and a dedication to smarter processes set our product apart. Beyond the test results and data files, what really matters is the day-to-day support, technical know-how, and commitment to improvement that only a manufacturer deeply involved in its own process can provide.