Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

4-Ethoxybenzene-1,2-Diamine

    • Product Name 4-Ethoxybenzene-1,2-Diamine
    • Alias 4-Ethoxy-1,2-phenylenediamine
    • Einecs 224-519-9
    • 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
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    230512

    Chemical Name 4-Ethoxybenzene-1,2-diamine
    Cas Number 16727-85-6
    Molecular Formula C8H12N2O
    Molecular Weight 152.19 g/mol
    Appearance Off-white to light brown solid
    Melting Point 97-99°C
    Boiling Point No data available
    Solubility Soluble in organic solvents such as ethanol and methanol
    Smiles CCOC1=CC=C(C(=C1)N)N
    Pubchem Cid 3443117
    Density No data available
    Synonyms 2,3-Diamino-4-ethoxyaniline
    Inchi InChI=1S/C8H12N2O/c1-2-11-8-4-3-6(9)5-7(8)10/h3-5H,2,9-10H2,1H3

    As an accredited 4-Ethoxybenzene-1,2-Diamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "4-Ethoxybenzene-1,2-Diamine, 25g" with hazard symbols, lot number, and manufacturer's details prominently displayed.
    Shipping 4-Ethoxybenzene-1,2-diamine is shipped in tightly sealed containers to prevent moisture and air exposure. It should be handled with care, avoiding extreme temperatures and direct sunlight. The package is clearly labeled, and shipping complies with relevant regulations for chemical substances, ensuring safe transport and storage throughout the shipping process.
    Storage 4-Ethoxybenzene-1,2-diamine 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 from light and moisture. Store at room temperature and ensure the area is free from ignition sources. Properly label the container and keep it away from direct sunlight and heat.
    Application of 4-Ethoxybenzene-1,2-Diamine

    Applications of 4-Ethoxybenzene-1,2-Diamine in Industrial Manufacturing

    4-Ethoxybenzene-1,2-diamine delivers precise performance in selected industrial sectors with proven compatibility and reliable results, enabling manufacturers to meet rigorous product and regulatory requirements. Below we detail several of its most significant downstream application scenarios, covering critical parameters and process conditions relevant for consistent industrial-scale operation.

    1. High-Purity Dye Intermediates for Textile and Leather Coloring

    Industrial dye manufacturers incorporate 4-ethoxybenzene-1,2-diamine into synthetic routes to produce azo and anthraquinone dye intermediates with strong color fastness and high purity. This raw material supports the formation of specific chromophoric systems, minimizing impurities and enhancing brightness or depth for demanding textile and leather coloration lines. Producers favor precise dosing to maintain batch reproducibility and regulatory color index compliance.

    Industry compliance standards

    • OEKO-TEX® Standard 100
    • REACH Annex XVII for restricted amines
    • ZDHC MRSL (Manufacturing Restricted Substances List)
    • ISO 105 family (color fastness test methods)

    Typical usage ratio

    • 3.0%–7.0% by weight in dye synthesis formulations; adjusted according to target color shade concentration and desired chromophore structure

    Downstream process integration

    • Condensation or diazotization steps in azo dye manufacturing sequence
    • Reductive coupling reactions in anthraquinone dye intermediate production

    Final product types

    • Reactive dyes for cellulose fibers
    • Direct dyes for cotton and viscose
    • Acid dyes for wool, nylon, and silk
    • Leather colorants requiring superior light and wet fastness

    2. Pharmaceutical API and Intermediate Synthesis

    The pharmaceutical sector utilizes 4-ethoxybenzene-1,2-diamine as a selective amine reagent for constructing active pharmaceutical ingredient (API) scaffolds or specialized intermediates where positional aminobenzene groups are essential for pharmacological function. In strictly controlled synthesis environments, well-defined addition levels ensure yield predictability and impurity control while satisfying global GMP expectations.

    Industry compliance standards

    • ICH Q7 GMP Guide for Active Pharmaceutical Ingredients
    • USP–NF (United States Pharmacopeia–National Formulary)
    • Ph. Eur. (European Pharmacopoeia) for process chemicals
    • 21 CFR Part 211 (US FDA GMP for finished pharmaceuticals)

    Typical usage ratio

    • 0.5%–4% molar ratio relative to targeted aromatic building block; actual dosage determined by synthetic pathway and substrate reactivity

    Downstream process integration

    • Palladium-catalyzed coupling for diarylamine moieties
    • Reductive amination in heterocycle assembly
    • Selective protection–deprotection sequences

    Final product types

    • Oncology agent intermediates
    • Antimicrobial drug precursors
    • Non-steroidal anti-inflammatory intermediate compounds
    • Specialty amine-containing APIs

    3. High-Performance Polymer Additive Preparation

    Producers of performance polymers depend on 4-ethoxybenzene-1,2-diamine as an integral additive or monomer precursor to develop polymers requiring enhanced thermal resistance or tailored mechanical behavior. Its reactive diamine structure enables users to control crosslink density and modulate polymer chain flexibility, especially in specialty engineering plastics and coatings for automotive, electronics, and aerospace.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management System for specialty chemicals)
    • UL 94 (Flammability of polymeric materials)
    • RoHS 2 Directive (Restriction of Hazardous Substances in Electrical and Electronic Equipment)
    • ASTM D256 (Polymer impact testing methods)

    Typical usage ratio

    • 0.2%–2.5% by weight in polymer resin blend; modulated based on target mechanical performance and processability

    Downstream process integration

    • Co-polymerization with anhydride or isocyanate partners in high-temperature extruders
    • Reactive blending during pre-polymer synthesis batches
    • Additive incorporation in melt blending or compounding lines

    Final product types

    • High-heat-resistant polyamides
    • Crosslinked polyurethane components
    • Functionalized polyimides for flex circuits
    • Automotive thermoplastic parts with enhanced stability

    4. Organic Pigment Intermediate Manufacturing

    Manufacturers of organic pigments apply 4-ethoxybenzene-1,2-diamine in the synthesis of monoazo and disazo pigment intermediates characterized by elevated tint strength and narrow particle size distribution. Its function is pivotal in ring-closure and coupling reactions where electron-donating substituents influence final pigment crystal formation and hue adjustment, leading to colorants suitable for high-quality inks and plastics coloration.

    Industry compliance standards

    • EN 71-3 (Safety of toys — migration of certain elements)
    • AP(89)1 (Resolution on colorants in plastic materials coming into contact with food)
    • ISO 18451-1 (Pigments and extenders—terms and definitions)
    • GMP Regulation (EC) 2023/2006 for food-contact pigments

    Typical usage ratio

    • Depending on pigment class, typically 2.5%–6% by weight relative to the base aromatic structure; higher ratios considered for high-opacity formulations

    Downstream process integration

    • Key coupling stage in monoazo pigment synthesis
    • Ring closure in disazo pigment intermediate formation
    • Purification via controlled crystallization prior to finishing steps

    Final product types

    • Yellow and orange organic pigments for printing inks
    • Special tone pigment dispersions for plastics and coatings
    • Food-contact colorants for packaging applications
    • Inkjet and laser printer grade pigments

    5. Hair Dye Precursor Production

    Certified producers of oxidative hair dye precursors rely on this material to introduce reliable para-aminodiphenyl and related moieties, necessary for color-developing systems operating under ammonia or peroxide developer conditions. Strictly regulated formulation input is essential to achieve reproducible in-use color results and meet all consumer safety and labeling standards in regulated regions.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No. 1223/2009, Annex III
    • Japan MHLW Standards for Quasi-drug Ingredients
    • CTFA/PCPC International Cosmetic Ingredient Dictionary
    • ISO 21148 (Microbiology of cosmetics—general guidance)

    Typical usage ratio

    • 0.1%–1.0% by weight in base cream or emulsion; adjusted per shade intensity and compatibility with target oxidizers

    Downstream process integration

    • Precursor blending step in the colorant formulation line
    • Stabilizer addition during emulsion or gel formation process
    • QC-batch adjusted for regulatory ammonia or peroxide limits

    Final product types

    • Permanent hair color cream kits
    • Professional salon dye developer blends
    • At-home oxidative hair colorants
    • Ammonia-free and low-residue permanent hair coloring systems
    Free Quote

    Competitive 4-Ethoxybenzene-1,2-Diamine prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Introducing 4-Ethoxybenzene-1,2-Diamine: Practical Insights from Our Production Floor

    Why We Make 4-Ethoxybenzene-1,2-Diamine

    Every year, we see changes ripple across specialty chemical manufacturing. One constant remains: the need for reliable, high-purity aromatic diamines capable of withstanding not just demanding customer quality audits, but the rigorous synthesis processes in both research and commercial plants. 4-Ethoxybenzene-1,2-diamine sits among the aromatic intermediates that we put a lot of thought and energy into. From the early days refining our process design, to months spent checking reaction selectivity under variable conditions, we recognize demands for both quality and supply assurance. This molecule, also called 2,3-diamino-4-ethoxyanisole in some chemical catalogues, stands out for its utility in current organic synthesis, dye intermediates, and applications that stretch into pharmaceutical intermediates and performance chemicals.

    A Hands-On Look at Structure and Physical Properties

    Chemists and formulators expect more than a chemical identifier or a stock description. We focus on the real substance: 4-Ethoxybenzene-1,2-diamine brings together a benzene ring with diamino groups at the ortho position (1,2), and an ethoxy functional group at the para-4 site. The structure offers balanced electron-donating properties and influences downstream reactivity, often dictating which coupling or derivatization strategies work best. The crystalline, off-white to tan appearance results from our refined purification steps. Over the years, strict attention to temperature control and solvent selection reduced byproduct retention and, in turn, minimized color changes—an indicator of purity that our experienced eyes have come to recognize almost before the HPLC results are back.

    What Sets This Compound Apart in Manufacturing

    People sometimes overlook the practical difficulties of isolating aromatic o-diamines, especially those with alkoxy substituents. Early processes gave variable yields and impure fractions because the amino groups can oxidize or dimerize before reaching the filtration step. We encountered persistent challenges with impurity control, especially at scale, as unintended by-products form during both nitration and reduction. Refining our reduction cycles, enhancing atmosphere controls, and customizing filtration media made all the difference. Along the way, we noticed that generic methods published for handling other aromatic diamines did not transfer smoothly when working with the ethoxy-substituted variant due to subtle solubility differences.

    Instead of a simple colorimetric endpoint or melting point test, we rely on a combination of HPLC area normalization, GC for trace solvent detection, and NMR for structural confirmation batch after batch. These checks might add hours to the workday, but they eliminate uncertainty for our users in pharmaceutical screening labs and process development teams.

    Model, Specifications, and Real-World Batch Data

    4-Ethoxybenzene-1,2-diamine as we manufacture it carries a model code officially documented as "EBD-210" within our plant. This code links each batch to synthesis route, operator log, in-process control documents, and final COA. On a practical level, most orders ship at a purity of not less than 98% as determined by HPLC using a gradient method developed with input from our QC team and external research labs. Moisture, one of the most frequent early complaints we received, often threatens stability and handling for both us and our end-users. Through consistently drying under reduced pressure and freshly purging storage drums with nitrogen, we keep water content below 0.2% for virtually all outgoing freight, even in humid months when atmospheric moisture is high.

    Particle size does not tend to be a central issue for EBD-210 since end-uses rarely depend on a defined mesh. Still, for those who dissolve it directly in organic solvents, a slightly smaller crystalline cut eases dissolution and speeds up batch turnover. We keep this in mind and source sieves and mills that allow us to hold size distribution to a tight range, visible right out of the drum without the telltale lumps that signal long-range transport under the wrong conditions.

    Sourcing and Sustainability—An Inside Perspective

    Careful sourcing of raw materials makes an impact. For this diamine, we use aniline and ethoxybenzene derivatives, bought only from audited partners who share analytical data and seasonally updated COAs. We focus on trace metal, aldehyde, and amine residuals—not just for purity, but because every failed reduction or runaway side-reaction costs time, solvents, and operator trust. Reduced process waste and solvent emissions come both from newer catalyst systems—we reviewed several and settled on a high-selectivity hydrogenation route made possible by robust in-line temperature sensors—and old-fashioned operational discipline.

    Each year, we revisit waste stream management: we improved our aqueous wash recycle and solvent reclamation ratios, which now recover more than 70% of used materials across quarterly audits. We track total organic emissions and adjust scrubber efficiency, not simply for compliance reasons, but because local communities and our own workforce share the same environment. Time and again, we’ve found downstream users in dyes and API intermediates line up with our goal to minimize residual load and to document it transparently in each COA.

    What Real-World Applications Teach Us

    In dye manufacturing, 4-ethoxybenzene-1,2-diamine serves as a key intermediate for azo and anthraquinone derivatives. What we see is that this diamine offers improved coupling yields, especially in acid and direct dye synthesis, compared to unsubstituted or methoxy-substituted cousins. The ethoxy group plays a role in solubility and dye intensity. Years back, a major textile customer reported challenges with dye bath consistency. Field troubleshooting pointed back to variable purity and trace oxidized amines. Since shifting to our EBD-210 batches, they report sharper color development and less after-wash bleeding. No technical paper replaces the day-to-day impact shared by operators or fabric testers.

    Some pharmaceutical labs use our diamine in the synthesis of core aromatic scaffolds involved in kinase inhibitor or antifungal candidates. Here, every trace impurity, every unknown chromatograph peak, can muddy downstream route selection. Reliable purity—backed with real batch data, not just theoretical specs—becomes a tool for researchers as much as the molecule itself. We get requests to lighten up on certain tests to speed up lead time. In every case, experience shows that skipping a step on in-process TLC or off-hours NMR slows everything down later in the chain.

    Others find value in smaller-scale modifications: students and small labs use the material for developing sensors, working with conjugated polymers, or optimizing arylamine-catalyzed transformations. Our technical support team frequently fields questions about solubility in unconventional solvents or methods to prevent discoloration in preparative runs. We share our own lessons from batch-scale storage and encourage moisture-proof canisters, rapid use after opening, and careful handling to avoid color shift before synthesis is complete.

    Comparing to Other Aromatic Diamines: Field Notes

    Each substituent on an aromatic diamine influences performance in both expected and subtle ways. For example, compared to the widely-used unsubstituted o-phenylenediamine, 4-ethoxybenzene-1,2-diamine holds improved solubility in alcohols and certain polar organics. Years of delivering both products revealed that downstream coupling reactions yield cleaner, more easily purified intermediates when using the ethoxy derivative. Shifts in pKa, steric fit, and electron density impact each step, from colorfastness in dyes to selectivity in pharma applications.

    Methoxy substituents, while chemically related, tend to change melting point and oxidative stability. Our own storage records show fewer complaints regarding gradual darkening for EBD-210 over six-month warehouse periods compared to the methoxy variant. Customers pushing the limits in photostability, especially those scaling pigment or specialty dye classes, find the ethoxy substitution more forgiving in open-vat syntheses where every humidity spike or heating fluctuation matters.

    Some users have compared our EBD-210 directly with entries from alternative sources, and they mention easier batch handling—less caking and lower odor intensity. Our on-site staff, accustomed to the distinctive amine odor of most substituted o-diamines, confirms a slighter, less pungent aroma from the ethoxy derivative following upgraded drying procedures. This means greater comfort for lab workers and factory staff over long hours.

    What’s Behind the Batch Tag: Trust, Traceability, and Personal Investment

    Traceability isn’t a marketing slogan. Every drum of EBD-210 carries a batch number that links it to reactor logs, shift reports, and archived analytical files. Over time, even with some high staff turnover that comes with the industry, we keep a core team who know the quirks of specific process units by heart—the way certain stirrers respond to particle load, the subtle changes in final wash color that signal a need for another rinse. Whenever customers relay field feedback, we check our logs for contributing factors. Once, a shipment flagged for higher-than-expected particle size matched a day with a minor compressed air irregularity in our main mill line, leading to an immediate QC check and process pivot on the next cycle.

    Investing in reliability means we send out fewer emergency replacements, spend less on returns, and get more candid communication from partners trusting our product in high-stakes chemistry. Unlike third-party brokers, we know the smells, sounds, and hands-on details that shape every lot of EBD-210. Even minor process tweaks—a slightly slower addition, a revised filtration sequence—can elevate a batch from acceptable to outstanding. The person who signed the final QC sheet knows that their name matches a shipment, a customer, and real people down the supply chain.

    On the Ground: Process Safety, Handling, and Continuous Improvement

    It’s one thing to talk about technical specs, but another to handle the sheer pungency and chemical reactivity of aromatic diamines day-to-day. We never treat process safety as a box to tick. Our operators wear chemical-specific gloves, face protection, and respirators for transfer and packaging. Over time, these habits have prevented injuries and reduced long-term exposure. With EBD-210, rapid response to spills, temperature excursions, or trace contamination wins more than regulatory compliance; it protects workers and preserves batch value.

    On a practical level, small changes to plant hygiene made outsized impacts. Instituting clean-drum protocols and separate transfer pumps for each amine line slashed cross-contamination risks. We encourage regular refresher training and run scenario drills—experience shows nothing prevents incidents like practice run in the real environment. EBD-210 may not be the largest product line in terms of volume, but it receives the same meticulous oversight as the flagship intermediates.

    Listening to the Market: Customer Needs Drive Innovation

    Some manufacturers chase high throughput or relentless cost reduction. We prioritize clean reactions and robust documentation over a minor boost in output. The most respected feedback we receive comes not as formal complaints, but as quiet requests for slightly better particle flow, reduced odor profile, or tighter QC documentation for new patent filings. We adjust our SOPs accordingly, qualifying new filtration cartridges or running side-by-side batch tests after a user reported solubility inconsistencies.

    In research partnerships, early transparency on supply limits and potential for scale-up allows formulation teams to plan more effectively. No one benefits from optimistic promises unsupported by production capacity. We base our reliability ratings on years of delivery records—and adjust our forecast models as new customers push R&D programs forward.

    The Value of Data: Every Batch Tells a Story

    Data authenticity traces back years for every product. Modern regulatory and customer audits ask for more than a basic COA; they want access to archived raw data, chromatographs, and even operator notes. We provide direct scan access of original test results, linking compound identity and performance data straight to the batch level whenever possible. This transparency reassures buyers when regulatory deadlines loom, and lets both sides track product changes over time. Software upgrades, tighter ring-fencing of analytical results, and continual training sharpen the accuracy of the records we keep.

    Our QC analysts know the pressures researchers face: repeating a failed experiment, altering one variable at a time, and trusting that the issue is not the starting material. Fully disclosing out-of-spec findings, explanation of trends, and notes on underlying raw material variability forms part of our service. Repeat orders build up a performance record and a chain of confidence that can withstand a process investigation or a product recall without panic.

    Anticipating What’s Next: Challenges and Roadmap

    4-Ethoxybenzene-1,2-diamine manufacture is never static. Feedstock fluctuations, environmental regulations, and shifting downstream specs challenge us to rethink protocols. Recently, increased scrutiny around amine content in wastewater urged a new cycle of equipment upgrades and batch run modifications. Our technical managers set up pilot trials, navigating both yield and eco-toxicity requirements without shielding bad results. Improvement sometimes runs into setbacks, but each learning cycle reduces future risk.

    Small molecule workflow rarely makes headlines, yet steady progress in safety, documentation, and waste management reflects in the confidence of our customers using EBD-210 where the unknowns are high and margins slim. This context, rooted in hands-on knowledge and continuous communication, shapes how we build a manufacturing reputation—not just for today, but with an eye on the evolving expectations of researchers, regulators, and the communities who share our chemical landscape.

    Summary: What Our Bench Means for Yours

    Working day-to-day with 4-ethoxybenzene-1,2-diamine, we hold each production step to standards born from both policy and personal pride. Skilled hands track each batch, solve hiccups, and hand off a chain of data as robust as any product we buy ourselves as chemists. Our process choices serve not just regulatory checklists, but the real satisfaction of seeing cleaner reactions, better color development, and smoother handling on the user’s end. The benchmarks we set for EBD-210 come not just from statistics, but from the real consequences of quality and care in action—passed along each time a researcher or manufacturer opens a drum and gets to work.