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2,4-Dichloro-3-Ethyl-6-Aminophenol Hydrochloride

    • Product Name 2,4-Dichloro-3-Ethyl-6-Aminophenol Hydrochloride
    • Alias BCECF
    • Einecs 273-299-2
    • 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
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    Specifications

    HS Code

    998692

    Chemical Name 2,4-Dichloro-3-Ethyl-6-Aminophenol Hydrochloride
    Cas Number 61315-15-1
    Molecular Formula C8H10Cl2NO · HCl
    Molecular Weight 242.54 g/mol
    Appearance Off-white to pale yellow crystalline powder
    Melting Point 200-210°C (decomposes)
    Solubility In Water Soluble
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Synonyms 2,4-Dichloro-3-ethyl-6-aminophenol hydrochloride; DCEAP·HCl
    Ph Of 1 Solution 4.0 - 6.0
    Boiling Point Decomposes before boiling
    Safety Precautions Handle with gloves and eye protection; avoid inhalation

    As an accredited 2,4-Dichloro-3-Ethyl-6-Aminophenol Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A tightly sealed amber glass bottle containing 25 grams of 2,4-Dichloro-3-Ethyl-6-Aminophenol Hydrochloride, labeled with safety and handling information.
    Shipping 2,4-Dichloro-3-Ethyl-6-Aminophenol Hydrochloride is shipped in tightly sealed containers, protected from moisture and light. It is packaged according to hazardous material regulations, ensuring safety and compliance during transit. Proper labeling and documentation accompany the shipment, and temperature control is maintained if required to preserve chemical stability and integrity.
    Storage 2,4-Dichloro-3-Ethyl-6-Aminophenol Hydrochloride should be stored in a tightly sealed container, away from light, moisture, and incompatible substances. Store at room temperature in a cool, dry, well-ventilated area. Avoid exposure to heat and humidity. Clearly label the container and keep it in a secure chemical storage cabinet, away from acids and oxidizing agents.
    Application of 2,4-Dichloro-3-Ethyl-6-Aminophenol Hydrochloride

    Applications of 2,4-Dichloro-3-Ethyl-6-Aminophenol Hydrochloride in Industrial Manufacturing

    2,4-Dichloro-3-Ethyl-6-Aminophenol Hydrochloride is a key intermediate incorporated into multiple advanced chemical synthesis tracks. As a raw material manufacturer, we supply this compound strictly for downstream industries with proven demand based on regulated formulation requirements, established processing steps, and mature product validation. The following application scenarios represent the core industrial use paths where this ingredient integrates within global manufacturing operations.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    This compound functions as a critical building block in the multi-step synthesis of certain API molecules, especially in the development of second- and third-generation antihistamine and anti-inflammatory drugs manufactured under regulated conditions. Its halogenated aminophenol structure allows chemists to incorporate it during targeted amide, ether, or heterocycle coupling steps required in modern pharmaceutical pipelines, particularly where specific chlorine or ethyl substitutions are prerequisites for biological activity.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF and European Pharmacopoeia (Ph. Eur.) monograph compliance for intermediates
    • FDA 21 CFR Part 211 – Current Good Manufacturing Practice for Finished Pharmaceuticals
    • EudraLex Volume 4 – GMP for APIs and intermediates

    Typical usage ratio

    • Ranges from 0.5% to 4% weight basis in synthesis batches, with actual concentration depending on target molecule and yield optimization studies; process development labs confirm the feedstock ratio by HPLC consumption analysis.

    Downstream process integration

    • Added during early or central stages of multi-step organic synthesis as a coupling or condensation participant, using solvent-phase or catalytic conditions depending on desired chemical transformations; purity is verified before incorporation to minimize side reactions.

    Final product types

    • Anti-allergic drug APIs (e.g., chlorphenamine derivatives)
    • Non-steroidal anti-inflammatory drugs (NSAIDs) precursors
    • Specialty amide-containing pharmaceutical agents
    • Intermediates for downstream GMP synthesis use

    2. Dyes and Pigments Intermediate for Specialty Colorants

    Colorant producers utilize this material as an intermediate for synthesizing certain azo and anthraquinone dyes where amino and chlorinated substitution patterns dictate hue stability, fastness, and chemical resistance. By precisely incorporating this intermediate during diazotization, coupling, or closed ring formation, downstream operators achieve enhanced batch reproducibility for textile, inkjet, and plastic coloration applications.

    Industry compliance standards

    • REACH Annex XVII (EU) – Restricted Substances in Dyes
    • OEKO-TEX® Standard 100 (class for dye intermediates)
    • ISO 9001:2015 – Quality Management in Specialty Chemicals
    • ZDHC Chemical Management Protocols for Textiles

    Typical usage ratio

    • Applied in 1.2% to 3.5% weight range per dye batch, the exact percentage adjusted based on target chromophore density and color saturation requirements; formulations optimized via pilot production runs.

    Downstream process integration

    • Charged into colorant synthesis reactors after initial sulfonation or coupling steps; used as a coupling component with diazonium salts to produce structured pigment molecules with specified fastness and shade characteristics.

    Final product types

    • High performance textile dyes
    • Inkjet and digital printing colorant bases
    • Plastic masterbatch pigments
    • Paper and packaging colorants

    3. Agrochemical Intermediate for Herbicide Synthesis

    Within the agrochemical sector, this chlorinated aminophenol serves a distinct role as a molecular precursor for selected herbicide actives, especially those requiring functionalized aromatic rings with specific halogen and amino group placements. Process engineers introduce this intermediate to core synthesis reactions—such as nucleophilic substitution or condensation—under strictly regulated technical conditions, ensuring consistent quality that meets registration requirements for crop protection product registrations.

    Industry compliance standards

    • FAO/WHO Specification Guidelines for Plant Protection Products
    • ISO 9001:2015 and ISO 14001:2015 (Quality & Environmental Management)
    • Regulation (EC) No 1107/2009 – EU Plant Protection Product Approval
    • China GB 4839/2014 – General Rules for Pesticide Formulation

    Typical usage ratio

    • Formulators apply within 2% to 5% molar equivalents relative to the key cyclization or substitution agents; usage tailored during scale-up depending on reaction yield and active loading requirements.

    Downstream process integration

    • Incorporated into synthesis reactors following intermediate halogenation or nitration steps, enabling direct condensation or further functionalization to yield herbicidal compounds before final purification and formulation.

    Final product types

    • Selective herbicide technical concentrates
    • Active ingredient (AI) bulk material for formulation
    • Granular and suspension herbicide formulations
    • Emulsifiable concentrate (EC) crop protection products

    4. Fine Chemicals Building Block for Advanced Polymer Additives

    Specialty polymer producers leverage this dichloroethylaminophenol as a reactive precursor for customized stabilizer, cross-linker, and antioxidant additive synthesis. Its electron-donating and halogenated functional groups enable precise tailoring when introduced into advanced polymerization or grafting reactions, especially for high-spec plastics, coatings, or elastomer compounds where tailored reactivity and UV resistance are critical.

    Industry compliance standards

    • ISO 14001:2015 – Environmental Management for Polymer Production
    • REACH registered substance compliance (EU)
    • ASTM D256 – Standard Test Methods for Plastics Additives
    • FDA 21 CFR (where applicable for indirect food contact)

    Typical usage ratio

    • Integrated at 0.3% to 2.5% mass per total additive charge, adjusted according to polymer base, cross-link density, and target service performance profiles; QA sampling confirms additive interface uptake during scale-up.

    Downstream process integration

    • Added during masterbatch blending or in-situ copolymerization—often following primary monomer addition and prior to full polymerization; used in both melt-phase and solution-phase polymer processing lines.

    Final product types

    • Antioxidant masterbatches for engineering plastics
    • UV-stabilized polymer composites
    • High-durability elastomeric sealing compounds
    • Performance coating resins
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    Certification & Compliance
    More Introduction

    Discover 2,4-Dichloro-3-Ethyl-6-Aminophenol Hydrochloride from a Manufacturer’s Perspective

    Our Experience with 2,4-Dichloro-3-Ethyl-6-Aminophenol Hydrochloride

    Over the years, our team has developed and refined the synthesis of 2,4-Dichloro-3-Ethyl-6-Aminophenol Hydrochloride, often abbreviated as DCEAP-HCl. Each batch tells a story of chemistry in practice—precision, consistency, and unyielding commitment to both quality and safety. Unlike simple intermediates, this compound consistently attracts attention from pharmaceutical R&D and specialty chemical sectors, largely due to its versatility and strong reactivity profile. Chemists look for performance and reliability in every application, and based on feedback from our direct buyers, DCEAP-HCl delivers on both these counts. As the manufacturer, we see the molecular journey up close: starting with stringent raw material selection, carrying through reaction control, followed by separation and purification where minor shifts in temperature, solvent ratios, or stirring speed can dramatically alter yields or impurity levels. That hands-on expertise surfaces in each shipped drum or pallet.

    Key Model and Specifications: How We Define Quality

    Whenever we discuss 2,4-Dichloro-3-Ethyl-6-Aminophenol Hydrochloride with our clients, questions quickly turn to grade, assay, and impurities-permissible. Clients run critical syntheses, so the confidence in quality—verified at our in-house lab with HPLC, NMR, and titration—is not an abstract promise, but an everyday reality. Typically, we supply it in crystalline powder form, white to light beige in color, with a purity of 98% minimum by HPLC. Moisture content stays tightly controlled—usually below 0.5% by Karl Fischer titration. The hydrochloride salt form offers improved solubility over the base material and minimizes batch-to-batch performance variances noticed in free bases. We set an iron content limit below 10 ppm, which is crucial in sensitive applications where trace metals trigger side-reactions.

    Our technicians have learned through trial and error how even seemingly minor process changes—shifting a quench timing by ten minutes, or tweaking the acid-base adjustment—can make the difference between a good day and a production loss. It’s this diligence and refusal to cut corners that have earned customers’ long-term trust. They want the same chemical, at the same high level, every time. Real-world consistency comes from practical know-how, laboratory discipline, and sometimes old-fashioned stubbornness not to accept less.

    What Sets DCEAP-HCl Apart from Related Compounds

    We regularly see buyers weighing DCEAP-HCl against other chlorinated aminophenols or related intermediates like 2,4-dichloro-6-aminophenol or ethylated o-dichlorophenols. Each molecule carries subtle differences—the placement of the ethyl group at the 3-position in DCEAP-HCl, for example, has a noticeable effect in subsequent derivatization reactions, making it a preferred intermediate for those aiming for certain pharmacophores. In my time overseeing custom synthesis projects, requests for isomeric purity or specific positional substitutions often come in from only the most careful researchers—those who have seen side-products from off-the-shelf materials wreck a pilot-scale run.

    Older approaches sometimes used the non-ethylated versions thinking similar reactivity would suffice, but actual lab data (and some costly post-mortems on stalled projects) reveal otherwise. The ethyl group’s electronic and steric effects fundamentally alter downstream chemistry, influencing final product yields and impurity profiles. We've received direct feedback from a handful of global generic pharma companies that only DCEAP-HCl met their requirements for a sought-after intermediate—no amount of purification from other aminophenol derivatives could match its performance reliability.

    Where DCEAP-HCl Finds Its Place in R&D and Commercial Synthesis

    Pharmaceutical labs and specialty chemical manufacturers frequently request DCEAP-HCl when developing new APIs. It often plays a pivotal role in forming pharmacophoric cores or complex heterocycles—a precise fit where both the dichloro and ethyl substitutions are not optional but essential. Agrochemical R&D teams, too, have adopted this compound, especially for assembling advanced pesticide candidates where selective substitution and moderate electron-donating capacity fine-tune bioactivity. Some have shared that substituting with more common aminophenols alters activity or is flagged in stability studies.

    From our vantage point, the workflows involving DCEAP-HCl are rarely simple one-step reactions. Most chemists deploy it as a building block for Suzuki couplings, amide formations, or heterocycle closures, leveraging its controlled reactivity. Supply chain teams, on the other hand, value predictable lead times, shelf-stability, and robust packaging—areas we have built up knowledge by tackling real hurdles. For example, minor moisture ingress during storage can catalyze unwanted side-reactions, so we developed new packaging protocols and found that even desiccant selection plays a role in maintaining batch stability.

    Lessons Learned in Manufacturing DCEAP-HCl

    Over the years, we have come to realize that seemingly routine operations—vacuum drying, in-process filtration, or crystal re-slurrying—shape both purity and performance. Early attempts at scale-up magnified issues not evident in beaker chemistry, such as filter clogging or color formation. We went back to troubleshoot, adjusted solvent systems, and introduced controlled crystallization windows to sharpen purity specifications. Realistically, what looks simple on paper can require dozens of pilot runs, tank cleanings, and team huddles. Many improvements have come from direct conversations with the chemists using our product, especially after joint troubleshooting over batch failures or unexpected side reactions.

    After implementing a closed-loop solvent recovery system, we saw batch consistency jump and environmental metrics improve. Every minor increment in process control, from accurate pH monitoring to gentle neutralizations, contributes to the reputation DCEAP-HCl has with our buyers. Auditors now come looking for batch histories and deviation logs, and our team maintains tight traceability protocols—every kilogram can be traced by lot through synthesis, quality control, and shipment.

    Quality Commitments: What Trusted Sourcing Means in Practice

    Our core belief is that consistency matters more than the latest brochure language or thumbnail samples. For DCEAP-HCl, this means meticulous cleaning between campaigns, validated cleaning protocols, and pre-emptive equipment maintenance. Each batch systematically undergoes both wet chemical assays and advanced instrumental analysis. Failures are documented and dissected in weekly meetings, and corrective actions documented. Problems do arise—ceiling leaks, pump failures, or supply chain slowdowns—but our culture rewards transparency and prompt fixes. Regular clients know we don’t mask problems; we call, discuss, and deliver fresh material if needed to prevent their own supply interruptions.

    The reality of compliant chemical manufacturing is that we work under the scrutiny of regular inspections—not just by government or international bodies, but sometimes by our most demanding customers whose own compliance teams probe every detail. This has driven us to keep clear, updated safety data, manage compliant MSDS sheets, and train every staff member on handling both routine and non-routine deviations or crises. When a shipment is delayed by customs or transit damage, our logistics and compliance teams step in, coordinate remanufacture if required, and keep customers continuously updated. Years of experience have taught us that trust grows or fades in the moments when something does go wrong.

    Potential Issues and How Manufacturers Address Them

    Our field isn’t without its challenges. Sourcing high-quality raw materials can force last-minute supplier audits or necessitate contract changes, particularly if we spot a trend in impurity profiles. Supply shortages—sometimes caused by international trade disruptions or upstream force majeure—have at times triggered emergency meetings with our procurement staff. When prices of key starting materials spike, larger holding stocks and alternative sourcing become strategies to maintain rolling production. For DCEAP-HCl, raw material stability impacts everything: poor chlorination or amination feeds can sabotage even the best in-house process. That’s not just theory; we have received contaminated shipments in the past, leading to immediate batch holds and round-the-clock root cause analysis. Lessons learned from those experiences now guide supplier evaluation and contract formulation.

    Solvent recycling and waste handling remain perennial operational concerns. We have invested extensively in effluent treatment systems and closed-loop recycling of chlorinated solvents partly to keep our production floors compliant, but also because we know chemical manufacturing’s footprint must shrink. This isn’t marketing speak—it’s a visible change on the shop floor, reducing odor complaints, regulatory headaches, and environmental risks. Such practices have been recognized during regulatory audits, but more importantly, we see immediate reductions in input waste and cleaner working environments for our teams.

    By working alongside hazard analysis and risk management consultants, we’ve mapped critical control points across the DCEAP-HCl value chain: from tank farm integrity to on-site emissions monitoring. During process revisions, we run multiple hazard and operability studies and maintain strict containment protocols for handling hydrochloride dust. Staff wear appropriate PPE and undergo routine health monitoring. Our approach to occupational safety isn’t paternalistic—it grows out of seeing the risks firsthand and acting before small issues escalate.

    Innovation Through Direct Application Feedback

    Direct dialogue with customers distinguishes our innovation process from what one finds at third-party traders or generic suppliers. Pharmaceutical scientists sometimes invite us to sit in on scale-up trials or process troubleshooting meetings, fostering a spirit of partnership we appreciate. We've adapted granulation size, improved filtration protocols, and even suggested modifications in client quenching steps based on observations at their sites and ours. Each process tweak is documented, reviewed, and sometimes forms the nucleus for continuous improvement—whether that’s a modification to our reactors, or simply a change to packaging size based on end-user feedback. In a sense, every kilogram shipped carries the imprint not just of our technical know-how, but also the shared expertise of end-users worldwide. For us, chemical manufacturing is not a solitary pursuit but a collaborative cycle of production, feedback, and innovation.

    This approach has led to special grades of DCEAP-HCl—pharma, tech, or custom performance specs—produced in close cooperation with select buyers. Custom requests often catalyze improvements across our standard product lines: filtration media changes, alternate drying techniques, or even in-line analytics. Some of our highest-purity batches were initially developed for research consortia working on breakthrough therapies, then later adopted by agrochemical clients needing greater confidence in reaction consistency. Diverse applications, whether in lab-scale peptide synthesis or multi-ton pharmaceutical campaigns, reinforce and refine our core competencies.

    Why Reliable Manufacturing Matters Beyond Specification Sheets

    End-users often ask if DCEAP-HCl can be simply procured from any supplier, but our experience suggests the difference between batches—sometimes from different regions or unregulated channels—can mean the difference between a launch and a recall, between process success and repeated troubleshooting. Batch consistency, impurity threshold adherence, and rigorous documentation underpin the trust that translates into repeat orders from established pharmaceutical and agrochemical customers. Each issue resolved, be it a minor deviation in melting point or a question about solubility, has made the manufacturing practice more robust—and makes us less likely to overlook those same pitfalls again.

    A recent example involved one client identifying a new chromatographic impurity trace, only detectable at the parts-per-million level but correlated with an increase in side-products downstream. Their notification led us to review every step—from solvent grade to analytical calibration standards—ultimately making a change that closed the impurity gap. That story captures our philosophy: no product, not even a well-trodden one like DCEAP-HCl, is ever “finished”—each batch offers new lessons, new challenges, and new opportunities to surpass previous efforts.

    Continuous Improvement and Looking Forward

    Looking ahead, ongoing investments in both people and plant will remain essential to keeping up with the evolving expectations around DCEAP-HCl. We hire trained chemists for the lab bench and support longtime operators with ongoing technical education, ensuring every hand in the process recognizes quality not as an abstract metric but as something lived on the factory floor. Experience teaches that no automated system, no matter how clever, can fully replace the practiced eye and intuition of a seasoned process engineer spotting something ‘off’ during a reactor charge or filtration step. Our commitment extends into sustainability, with ongoing focus on reducing solvent emissions, energy input, and process waste at every stage.

    With each campaign, our factory becomes a living library of real-world feedback, process tweaks, and practical solutions—none of which would exist without the everyday, hands-on engagement of the manufacturing crew, the R&D partners, and the clients who share our standards for excellence. For buyers, the track record and experience behind each kilogram of DCEAP-HCl offers more than a chemical. It brings the assurance that comes only from consistency earned through years of dedicated work in synthesis, process safety, compliance, and innovation.