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2-Ethoxyphenyl Isothiocyanate

    • Product Name 2-Ethoxyphenyl Isothiocyanate
    • Alias 2-Ethoxyphenylisothiocyanate
    • Einecs 'EINECS 210-319-9'
    • 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

    310695

    Name 2-Ethoxyphenyl Isothiocyanate
    Cas Number 13185-22-9
    Molecular Formula C9H9NOS
    Molecular Weight 179.24 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 148-150 °C (20 mmHg)
    Density 1.14 g/cm3 (at 25 °C)
    Refractive Index 1.609 (at 20 °C)
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles CCOC1=CC=CC=C1N=C=S

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams, sealed with a screw cap, labeled as 2-Ethoxyphenyl Isothiocyanate, with hazard warnings.
    Shipping 2-Ethoxyphenyl Isothiocyanate should be shipped in tightly sealed containers, protected from light and moisture. It must be handled as a hazardous chemical, complying with local, national, and international transport regulations. Appropriate hazard labeling and documentation are required, and the substance should be kept away from incompatible materials during transit.
    Storage 2-Ethoxyphenyl Isothiocyanate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from moisture and sources of ignition. Protect it from direct sunlight and incompatible substances such as strong acids and oxidizing agents. Use secondary containment and clearly label storage spaces to prevent accidental exposure or leakage. Store at recommended temperature, typically at or below room temperature.
    Application of 2-Ethoxyphenyl Isothiocyanate

    Applications of 2-Ethoxyphenyl Isothiocyanate in Industrial Manufacturing

    As a direct manufacturer of 2-Ethoxyphenyl Isothiocyanate, we support established industrial users with consistent and quality-driven product integration. The following sections outline proven application scenarios grounded in authentic downstream industry practice, including regulatory context, necessary formulation guidance, operational processing steps, and specific finished product outputs.

    1. Pharmaceutical Intermediate Synthesis for Oncology APIs

    Pharmaceutical manufacturers use 2-Ethoxyphenyl Isothiocyanate as a critical building block in synthesizing advanced intermediates for oral and injectable oncology drug substances. The compound's reactivity enables the formation of thiourea linkages, facilitating stepwise construction of key heterocyclic scaffolds present in kinase inhibitor drugs. Downstream process engineers typically introduce this intermediate during mid-stage coupling reactions under controlled conditions, with continuous QC to ensure minimal isothiocyanate residue in the API. Analytical validation and batch release require strict compliance with international pharma standards to guarantee both worker safety and end-product purity.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU EudraLex Volume 4 GMP guidelines
    • United States Pharmacopeia (USP) General Chapters for processes using isothiocyanates
    • Related Drug Master File (DMF) procedures

    Typical usage ratio

    • 5–15 mol% relative to primary precursor; adjusted to reaction stoichiometry for batch yield
    • Optimization based on impurity profile, with pilot scale validations before cGMP upscaling

    Downstream process integration

    • Charged into jacketed reactors at intermediate synthesis stage—post-initial condensation, pre crystallization
    • Monitored by in-line HPLC to confirm complete reaction and limit residual isothiocyanate content

    Final product types

    • N-arylthiourea core intermediates for targeted anti-cancer agents
    • Heterocyclic active pharmaceutical ingredients with antineoplastic application
    • API intermediates for FDA-registered oncology formulations

    2. Agricultural Fungicide Active Ingredient Synthesis

    Crop protection formulators utilize this isothiocyanate derivative in constructing select arylthiourea-based fungicides, where its incorporation confers both broad-spectrum efficacy and increased compound stability. The material enters the reaction during process steps involving nucleophilic substitution with aniline derivatives, facilitating the assembly of protective agents for cereal and vegetable crops. Formulation batches must undergo stringent residue analysis, and downstream manufacturers follow regional and global agrochemical guidelines, ensuring traceability throughout the production cycle.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications
    • OECD Principles of Good Laboratory Practice (GLP) for test batches
    • EU Regulation (EC) No 1107/2009 (placing plant protection products on the market)
    • China GB 2763 Maximum Residue Limits for Pesticides in Food

    Typical usage ratio

    • 1.5–4% w/w in crude synthesis phase, dependent on crop and regional regulatory MRL requirements

    Downstream process integration

    • Reacted in agitated vessels as a key reagent during the functionalization of backbone structures
    • Residual monitoring before final encapsulation or formulation blending

    Final product types

    • Arylthiourea fungicide active ingredients
    • Formulated seed treatment concentrates for field application
    • Water-dispersible granule (WG) and suspension concentrate (SC) pesticide products

    3. Fine Chemical Synthesis of Specialty Dye Intermediates

    Specialty dye manufacturers employ 2-Ethoxyphenyl Isothiocyanate in the production of intermediates needed for high-performance azo and sulfur dyes. Its application facilitates the introduction of sulfur-containing moieties, bringing about desired chromophore properties and lightfastness, especially for polyamide and acrylic textile fibers. The compound is typically dosed directly during diazotization or coupling with aromatic diamines, requiring solvent control and monitoring for complete isothiocyanate consumption. Robust batch documentation ensures traceability to international environmental and chemical safety standards throughout the workflow.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for restricted substances
    • REACH Regulation (EC) No 1907/2006—chemical registration and safety assessment for dyes
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 13321:2006 for dye product quality control

    Typical usage ratio

    • 0.7–2.5% w/w relative to chromogenic moiety precursors
    • Adjusted for molar substitution efficiency and desired dye shade depth

    Downstream process integration

    • Dosed in batch dye intermediates synthesis, typically added post-diazotization
    • Solvent-based processing using inert atmosphere for isothiocyanate stability

    Final product types

    • Azo dye intermediates for textile coloration
    • Sulfur dye precursors for high-washfastness applications
    • Reactive dye components used by textile mills and pigment compounders

    4. Development of Chemical Reagents for Analytical Laboratories

    Manufacturers supplying analytical reagent companies select 2-Ethoxyphenyl Isothiocyanate for use in developing derivatizing agents that enhance detection sensitivity in chromatographic and spectrometric assays. Its strong electrophilic character makes it valuable for pre-column derivatization of primary and secondary amines, facilitating separation and quantification of amino acids and peptides by HPLC and LC-MS. Controlled additions and documentation protocols align with certified chemical supply chain standards, ensuring impurity control and reagent traceability for accredited quality laboratories worldwide.

    Industry compliance standards

    • ISO 17034:2016—Competence of Reference Material Producers
    • ISO/IEC 17025—Testing and calibration laboratory accreditation
    • ACS Reagent Grade specifications
    • Applicable GHS/CLP chemical labeling regulations

    Typical usage ratio

    • 0.05–0.2 mmol per analyte sample for reaction scale in derivatization buffer
    • Adjusted based on instrument detection sensitivity and sample concentration

    Downstream process integration

    • Prepared in specialized reagent kits, added during pre-analytical sample prep protocols
    • QC tested for reagent blank integrity and derivatization efficiency

    Final product types

    • Pre-packaged HPLC/GC/LC-MS derivatization reagent kits
    • Certified analytical standards for laboratory research use
    • Sample preparation reagents marketed to food, pharma, and environmental analysis labs
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    Certification & Compliance
    More Introduction

    2-Ethoxyphenyl Isothiocyanate: Purpose-Built for Demanding Synthetic Routes

    Introduction

    Across the landscape of fine chemical production, every compound has a story. 2-Ethoxyphenyl Isothiocyanate earned its place in our portfolio from working side by side with customers in pharmaceuticals, dyes, and specialty intermediates. Years of direct feedback from lab benches and pilot-scale batches shaped how we manufacture, purify, and distribute this compound today. As the actual producer—steps away from the reactors, glassware, and control panels—we know what makes a difference in practice. This is not another standard aromatic isothiocyanate. Instead, this material occupies a spot that technicians and researchers return to, based on its reactivity, versatility, and clean handling.

    Model, Purity, and Real-World Specifications

    Our typical production specification for 2-Ethoxyphenyl Isothiocyanate reflects the batchwork and repeated process runs we have carried out. Most labs and pilot plants request at least 98% purity by GC and HPLC, verified after isolation and before packaging. We keep residual solvents under strict control, since any trace of toluene or DMF can compromise certain downstream transformations—well known among those who actually scale up synthetic methods. We continuously optimize vacuum handling, choice of solvents, and temperature control at the isothiocyanation stage to push the impurity levels lower.

    As soon as we receive an order, material flows straight from our reactor lines under nitrogen. No unnecessary exposure. Every container has been cleaned and tested on-site, avoiding any off-notes or cross-contamination that might interfere with analytical applications. Many years ago, an early batch picked up contamination from a neighboring line, a lesson that steered us toward tighter quality practice and separate reactive areas. Today, our team includes operators who remember that run, shaping a company culture that values clean product above all else.

    Practical Uses in Synthesis and R&D

    Chemists return to 2-Ethoxyphenyl Isothiocyanate for a reason. The compound excels at introducing isothiocyanate moieties onto aromatic backbones, supporting both exploratory research and routine medicinal chemistry campaigns. Its structure—a phenyl isothiocyanate ring linked with an ethoxy group at the ortho position—gives it unique reactivity in nucleophilic aromatic substitution and coupling reactions. Many medicinal chemistry teams use this building block to open new SAR directions, since the ethoxy substituent often improves solubility and bioavailability in lead series, in ways a methyl or unsubstituted core cannot.

    We have worked with process teams scrutinizing downstream steps, watching how reaction rates depend on substituent effects. Many aromatic isothiocyanates stall under certain conditions, but this ethoxy variant pushes through—especially in the formation of thioamides and ureas under gentle warming. Customers often ask if the extra cost is justified over standard phenyl isothiocyanate or methyl variants. What we tell them comes straight from decades in this field: subtle electronics from the ethoxy group help control selectivity and reduce byproducts, especially under scale-up.

    Handling, Packaging, and Stability Insights

    2-Ethoxyphenyl Isothiocyanate emits a sharp, distinctive odor—anyone who’s handled it knows this immediately. In our facility, we package the product in amber glass lined with PTFE seals, not just plastic or metal caps. Our team found out early that the compound reacts even with trace water, creating fouling and strong-smelling side-products. This led us to design a closed system with minimal air ingress, extending shelf-life and keeping the first use as potent as fresh batches out the dryer.

    We learned to monitor not only the bulk purity but also the moisture content. Too much exposure and you notice yellowing, an unmistakable sign that decomposition has started. A lesson straight out of our QA records: any lot showing more than 0.5% increase in color or non-volatile residue gets reprocessed, not shipped. That standard comes from years of testing how the material performs after a month or two in real-world storage climates, not just at the point of manufacture.

    Why Not Just Use the Common Alternatives?

    The question comes up from customers familiar with phenyl isothiocyanate, a mainstay in protein sequencing and labeling. That product is easier to source, often at lower prices. What is often overlooked is how the ethoxy substitution alters both reactivity and work-up profiles, providing improved selectivity. In our experience, research teams trying to swap out the ethoxy version for basic phenyl isothiocyanate report lower yields, cloudier analytical results, or a host of sticky byproducts. The extra electron-donating strength of the ethoxy ring stabilizes transition states in many functionalizations.

    On the scale-up side, we once partnered with a customer on a kilo-process—using both standard phenyl and ethoxy-phenyl isothiocyanates side by side. Good reaction control with the ethoxy version meant less byproduct, reducing the time needed on downstream purification. This outcome made a strong case for sticking to the narrower product, even if it requires a more complex synthetic route on our end.

    Manufacturing Process: Designed for Consistency

    Our production method reflects long periods of process development, trial, and error. Making 2-Ethoxyphenyl Isothiocyanate at scale means finding the sweet spot between throughput and cleanliness. At the heart of our plant, a low-moisture environment supports the isothiocyanation of 2-ethoxyaniline, using phosgene alternatives that deliver a sharper reaction profile and minimize dangerous off-gassing. Over years of running batches, operators have fine-tuned shot addition rates, catalyst choices, and in-process sampling.

    Each time we scale up, we watch for reproducibility—not just in isolated product, but in how easy the material is to handle in downstream glassware or reactors. We know the runtime limitations: push too hard, and you make heavy tars; too gentle, and unreacted starting material sneaks through. Our most skilled operator, who has handled thousands of kgs of aromatic isothiocyanates, routinely trains new hires by showing the subtle color changes and odors that signal a clean endpoint.

    Purity, Impurities, and Real Consequences

    Trace impurities matter in specialty chemicals. Our clients in medicinal chemistry flag unknown peaks right away. For 2-Ethoxyphenyl Isothiocyanate, avoided impurities like unreacted 2-ethoxyaniline, aromatic amine byproducts, or disulfide-linked dimers make the difference between a clean analytical result and a frustrating dead end. Several years ago, we spent months troubleshooting gas chromatograms full of ghost peaks—eventually traced to storage vessel contamination upstream. This led to overhauling storage and cleaning protocols.

    Every batch gets subjected to multi-point QC: visual clarity, odor check, HPLC, GC-MS, moisture determination, and direct NMR. The direct link from our QA lab to the reactor hall lets us spot problems before they leave our plant. One time a peak appeared at m/z +16, traceable to a small oxidized impurity. Years of experience gave us a quick fix—tightening nitrogen blanketing and reducing dwell time at the oxidation-sensitive stages.

    Applications Beyond Pharmaceuticals

    Beyond the world of drug discovery, 2-Ethoxyphenyl Isothiocyanate finds a role in agrochemical research, dye manufacture, and materials science. In dye chemistry, the ethoxy group grants colorfastness and deeper tinctorial strength. We work with customers in pigment development exploring brighter, more robust hues that withstand exposure and processing. In specialty adhesives, isothiocyanates provide strong linking groups for advanced resins or industrial sealants.

    Our experience shows the highest value applications involve sensitive reactions where selectivity matters. Customers appreciate reliable, clean material since slight impurities may turn a pigment batch from a deep blue-violet to a muddy brown. We learned that lesson early, providing analytical support and sample analytics for customers responding to subtle color complaints. In several projects, our isothiocyanate allowed a lower use level in dye formulations than less substituted analogs, offering better efficiency for the end user.

    Customer Experiences and Field Support

    Our day-to-day contacts are with process chemists and research leads, not just procurement departments. This direct line lets us gather real stories: which batch worked best for a critical library, or where product handling tripped up a project. Years ago, one pharmaceutical client requested a custom impurity profile, targeting extreme purity for a lead optimization campaign. We ran dedicated vessels, cleaned reactors with several solvents, and collected feedback across dozens of kilogram-scale batches. Their team reported higher throughput and more reliable bioassay results, a win for both their timeline and ours.

    On the production floor, we host regular plant tours and audits, welcoming technical visitors from partners worldwide. Watching our operators charge reactors, check product color, and inspect seals first-hand builds a type of trust that digital certificates never match. Oftentimes, a visiting chemist picks up a faint difference in odor or hue—quick conversations on the line clarify expectations and avoid downstream surprises. This relationship, preserved through direct collaboration instead of faceless supply chains, shapes every decision about improving product quality or process robustness.

    Regulatory, Safety, and Transport Considerations

    Isothiocyanates demand respect in the chemical plant. Strict PPE protocols, constant air monitoring, and robust fume extraction are standard in our facility. Our long history working with regulatory inspectors taught us which points in the process need double-checking, from batch labeling to secondary containment. Packing all material in sealed, shock-resistant glassware stops leaks in transit and prevents contamination on delivery. As staff, we handle every lot as if it were destined for our own labs—each shipment tracked and traced, with rapid response in case of carriage delays or unexpected conditions.

    The toxicity profile and handling precautions for 2-Ethoxyphenyl Isothiocyanate are similar to other aromatic isothiocyanates, with an added sensitivity to moisture and air. We provide clear instructions for safe opening, use, and disposal, informed by real-world experience inside and outside our plant. If questions arise in the field, our technical team draws on actual incident reports and mitigation protocols from past batches, not just theory. Over time, this collective knowledge reduces both unexpected exposures and batch-to-batch variability in the client’s operation.

    Lessons Learned from Years of Production

    Learning in chemical manufacturing rarely comes from flawless runs. Instead, it comes from surprises: an unexpected impurity, a batch that fails to crystallize, customer feedback on a subtle handling issue. Decades producing 2-Ethoxyphenyl Isothiocyanate taught us the details that make batch production succeed: when to swap a filtration aid, the precise limit for residual moisture, the draft angle best suited for amber bottles in transport. These are not arbitrary standards, but proven steps to keep the product as reliable as possible.

    We found that routine, small checks—like weighing each package by hand—pay big dividends. Digital scales help, but nothing replaces an operator’s sense of what is standard weight and volume. Once, a subtle leak caused a drift; catching it early meant saving a whole customer batch from being written off. Sharing stories and case studies inside the plant helps the team learn faster than from written procedures alone.

    Comparing to Other Isothiocyanate Choices

    Customers often debate whether to opt for straight phenyl or methylphenyl isothiocyanates as more common analogs. While those options perform in basic labeling reactions or as test substrates, our experience highlights the unique fit for the ethoxy variant. The extra chain imparts better solubility and sometimes reduces product volatility, making batch handling easier on both the bench and the factory floor. Years ago, we studied product stability across storage temperatures and found the ethoxy compound suffered less degradation than methyl substitutes in humid environments. For clients in the tropics or settings with basic warehouse conditions, this translates to less off-odor and fewer surprises upon opening.

    Researchers report greater flexibility in derivatization with the ethoxy group—it moderates both electron density and reactivity, making synthesis routes cleaner and more controllable. Applications dependent on crystallization, such as intermediate isolation before pharmaceutical hydrazide production, see noticeable yield and handling benefits. This feeds back to our R&D group, pushing us to keep the batch process tuned for subtle impurity control and consistent output over time.

    Response to Global Supply Chain Challenges

    Recent years tested global chemistry supply chains. Raw material sourcing, freight interruptions, and increased scrutiny on import-clearance protocols challenge every specialty chemical manufacturer. We kept 2-Ethoxyphenyl Isothiocyanate output steady by pre-stocking critical feeds, running parallel process steps, and maintaining direct sourcing relationships for every intermediate. These moves arose not from theory but lived experience reacting to truck delays, customs inspections, and evolving documentation trends.

    We also field requests for rush deliveries or special pack sizes for just-in-time R&D needs. Our team stays flexible, ready to split production batches or reclean small glassware runs as needed. The choice to stay close to every stage of production, from reagent sourcing to filling the last storage vessel, remains our best answer to volatility in the chemical market.

    Continuous Improvement: What’s Next?

    Our approach is not static. Every fresh production run brings lessons and new directions. Whether by adjusting drying protocols, moving to more selective catalysts, or tightening packaging seals, we lean on our operator’s practical expertise and customer suggestions. Recently, we piloted a digital tracking platform to log every step in the batch record—from raw material lot input to final labeling at the filling station. Capturing real-time deviations and operator notes lets our QA team spot problems before they scale.

    We welcome customer audits and encourage open communication about issues and improvement areas. Each season brings opportunities to fine-tune the operation—adding new analytical instrumentation, swapping out filtration media, or testing more robust glassware. Every step aims to deliver better material for critical research and production needs.

    Closing Reflections

    Manufacturing 2-Ethoxyphenyl Isothiocyanate is more than process chemistry—it reflects an ongoing commitment to product reliability, safety, and transparent collaboration. Every bottle placed in the hands of a research chemist or process operator carries the weight of our team’s dedication to quality, practical experience with fine details, and the lessons learned from decades in chemical manufacturing. Working at the origin, not simply in the supply chain, means owning the outcomes and supporting customers as partners in innovation.