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1,2-Diethoxybenzene

    • Product Name 1,2-Diethoxybenzene
    • Alias Veratrole
    • Einecs 202-582-1
    • 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

    622015

    Chemical Name 1,2-Diethoxybenzene
    Molecular Formula C10H14O2
    Molecular Weight 166.22 g/mol
    Cas Number 2032-47-9
    Appearance Colorless to pale yellow liquid
    Boiling Point 243-246 °C
    Melting Point -17 °C
    Density 1.03 g/cm3
    Refractive Index 1.511
    Flash Point 99 °C
    Synonyms O-Diethoxybenzene, 1,2-Bis(ethoxy)benzene
    Solubility In Water Insoluble
    Pubchem Cid 14414

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

    Packing & Storage
    Packing 250 mL amber glass bottle with a screw cap, labeled "1,2-Diethoxybenzene," featuring hazard symbols and manufacturer details.
    Shipping 1,2-Diethoxybenzene is typically shipped in tightly sealed containers made of materials compatible with organic solvents, such as amber glass bottles or HDPE jugs. It should be stored and transported at room temperature, away from direct sunlight, sources of ignition, and incompatible substances. Follow all local, national, and international transport regulations.
    Storage 1,2-Diethoxybenzene should be stored in a tightly sealed container in a cool, dry, well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers. Avoid moisture and keep the storage area free from ignition sources. Clearly label containers and store at room temperature. Use proper chemical storage guidelines to prevent contamination and accidental exposure.
    Application of 1,2-Diethoxybenzene

    Applications of 1,2-Diethoxybenzene in Industrial Manufacturing

    As a committed manufacturer, we supply 1,2-Diethoxybenzene for precise industrial use where technical standards define value across several downstream segments. Below, we detail real application scenarios with clear compliance, process, and formulation considerations for each sector.

    1. Intermediate for High-Performance Antioxidants in Lubricant Additives

    Specialty lubricant producers use 1,2-Diethoxybenzene as a critical intermediate in synthesizing diarylamine-based antioxidants. This application demands careful control over reaction purity and side product minimization to ensure reliable oxidation resistance in severe service oils and greases. Our production delivers low-residual aromatic impurities, supporting strict QC in alkylation or hydroxyalkylation stages, and providing consistent performance in finished additive packages.

    Industry compliance standards

    • REACH Regulation (EU) No 1907/2006
    • ASTM D4951 Standard for Lubricant Additive Content
    • API Lubricant Service Categories
    • ISO 9001:2015 for Quality Management

    Typical usage ratio

    • Formulators employ 1,2-Diethoxybenzene at 3-10% mol ratio in antioxidant synthesis, ratio adjusted based on target molecular weight and substitution profile of final diarylamine derivatives.

    Downstream process integration

    • The raw material enters as a nucleophilic aryl source during the first step of diarylamine or diaryl ether synthesis, often after a deprotection or direct alkylation reaction under controlled base catalysis.

    Final product types

    • Detergent motor oils (PCMO, HDMO)
    • Industrial hydraulic fluids
    • Multipurpose greases
    • Compressor lubricants for severe environments

    2. Precursor in Fine Chemical Synthesis for Pharma Intermediates

    Manufacturers of pharmaceutical intermediates employ 1,2-Diethoxybenzene as a key ring-protected building block. This compound supports protected aromatic substitution to yield catechol derivatives post-deprotection, essential in active pharmaceutical ingredient (API) synthesis pathways, especially for cardiovascular and neuroactive agents. Control over solvent residues and trace metal levels is crucial to meet downstream regulatory requirements during critical path organic transformations.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF General Chapters Chemical Purity Standards
    • European Pharmacopoeia (Ph. Eur) Residual Solvents Guidance
    • 21 CFR Part 211 cGMP Requirements

    Typical usage ratio

    • Chemists typically use 1,2-Diethoxybenzene in a 1:1 stoichiometry in electrophilic aromatic substitution, with excess for yield control depending on the route and desired catechol protection pattern.

    Downstream process integration

    • The material serves as a masked dihydroxybenzene moiety, introduced early to protect reactive phenol positions during stepwise synthesis, and cleaved under acidic or reductive conditions before final API construction.

    Final product types

    • Intermediates for L-DOPA analogues
    • Precursors for entacapone synthesis
    • Api building blocks with catechol substructures
    • Selective cardiovascular drug intermediates

    3. Functional Monomer in High-Temperature Polymer Production

    Engineered plastics manufacturers leverage 1,2-Diethoxybenzene as a functionalized aromatic monomer for specialty polyether or polyester polymers. Thanks to its controlled electron-donating groups and ortho configuration, it influences polymer backbone flexibility and resistance to hydrolytic degradation. Consistent purity and moisture content are critical for reproducible polymerization, particularly in melt processing where discoloration must be minimized for transparent end products.

    Industry compliance standards

    • ISO 9001:2015 for Quality Management Systems
    • FDA 21 CFR 177.1590 (Polysulfone Resins), when polymers are destined for food contact
    • RoHS Directive 2011/65/EU for electronic materials applications
    • ASTM D638 Mechanical Property Measurement for Polymers

    Typical usage ratio

    • Used at 5–20% mol fraction in specialty copolymers, depending on required aromaticity and ether functionality; process engineers adjust feed based on target molecular weight.

    Downstream process integration

    • Operators introduce 1,2-Diethoxybenzene during the batch or continuous polycondensation step, often co-monomerized with halogenated or hydroxy-functional partners to yield custom backbone architectures.

    Final product types

    • High-temperature-resistant films
    • Insulating polymer foams
    • Specialty coatings for electronics
    • Fiber-reinforced thermoplastic composites

    4. Chemical Intermediate in Dye and Pigment Synthesis

    Specialty colorant manufacturers apply 1,2-Diethoxybenzene as an aromatic intermediate to introduce ortho-dialkoxy substitution in azo and quinone dye precursors. The molecule helps modulate electron density in aromatic systems, improving chroma intensity and lightfastness. High batch-to-batch consistency and control of byproducts such as mono-alkoxylates are mandatory for predictable hue and dye purity, particularly in color calibration for textiles and plastics.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile chemicals
    • EN 71-3:2019 Toy Safety for migration of colorants
    • ISO 105-A02:2019 for Color Fastness to Light
    • REACH Annex XVII Chemicals Regulation

    Typical usage ratio

    • Material is dosed at 2–8% by weight in the main condensation batch, with adjustment based on desired color depth and target molecule substitution points.

    Downstream process integration

    • 1,2-Diethoxybenzene is introduced during diazotization or oxidative coupling phases, participating directly in chromophore-forming reactions prior to crystallization and purification of the pigment batch.

    Final product types

    • High-brightness azo dyes for textile printing
    • Anthraquinone pigments for plastics
    • Inkjet ink colorants
    • Specialty color concentrates for automotive coatings
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    Certification & Compliance
    More Introduction

    Introducing 1,2-Diethoxybenzene: More Than Just an Ether Compound

    Every molecule tells its own story. For years, our team has focused on aromatic ethers, and 1,2-Diethoxybenzene has stood out in both its structure and the possibilities it unlocks for industry. Chemists working with this compound recognize its unique pairing of two ethoxy groups directly bonded to the benzene ring in adjacent positions. This structure already makes it quite distinct from other di-alkoxybenzenes, and our direct manufacturing approach lets us deliver consistent quality and controlled batch properties.

    Reliable Composition and Strict Purity Standards

    Every batch we produce follows clear standards. 1,2-Diethoxybenzene, with its CAS number 2050-50-6, forms as a clear, colorless to pale yellow liquid at room temperature—a property retained from careful process controls. Over the years, we’ve established an in-house assay target that consistently keeps actual purity above 99%. Trace moisture and synthesis by-products add risks for sensitive downstream uses, so we maintain water content below 0.05%, and check for residual acids, aldehydes, and other organics each time. This commitment makes a critical difference for labs and plant engineers who count on reliable materials when precise results matter most. Packing and storage follow nitrogen purging and light-resistant drums, preventing any deterioration or contamination through the supply chain.

    Applications Rooted in Experience

    People often ask what sets 1,2-Diethoxybenzene apart compared to alternative ethers. In day-to-day operations, it becomes clear during synthesis or formulation work. As a specialty intermediate in organic synthesis, this compound finds steady demand in the creation of pharmaceuticals, pesticides, and dyes. Its ortho-configuration enables selective substitution and coupling reactions that might prove inefficient or unworkable with its 1,4- or 1,3- counterparts, thanks to the altered electron distribution and steric accessibility. For instance, during aryl ether cleavage, the neighboring ethoxy groups boost reactivity in ways chemists appreciate when optimizing synthetic routes. We’ve seen this compound used to introduce custom side chains or build up more complex functional structures, benefitting from its good solubility in non-polar and moderately polar organic solvents.

    As for selectivity, our clients often favor 1,2-Diethoxybenzene in fine chemical routes when para-isomers risk unintended cross-coupling or when meta-substitution cannot offer the same directed metalation or cyclization outcomes. With each shipment, we work closely with process chemists to discuss reaction conditions, solvent compatibility, and the impact of minor impurities on catalyst life or downstream isolation yields. This hands-on communication has let us refine our purification processes and even adapt production parameters to serve projects in need of ultra-high purity or bespoke isomer ratios.

    Key Differences From Other Diethoxybenzenes

    While there are several diethoxybenzene isomers—and even more alkoxy substitutes—the 1,2-pattern brings benefits not easily swapped for other configurations. Through direct feedback from synthetic chemists and repeat analysis in our process lab, the ortho structure reveals advantages in reactivity, ease of ring functionalization, and unique behaviors during stepwise transformations. Para and meta isomers may offer different solubilities or steric properties, but only the ortho compound enables certain ortho-effects during C-H activation or Friedel-Crafts-based schemes. For those developing novel heterocyclic scaffolds or working on enzymatic studies, the subtle shifts in resonance effects and intramolecular interactions can tilt the outcome of a project. Drawing from these experiences, we do not treat 1,2-Diethoxybenzene as a simple commodity. Its manufacturing also carries tighter control protocols, as ortho isomers often prove trickier to isolate in standard synthetic routes. By controlling secondary reactions and carefully selecting starting phenol grades, we keep batch consistency high—a feature that can distinguish a minor yield boost or a cleaner final product down the line.

    Troubleshooting and Practical Insights

    Like most aromatic ethers, 1,2-Diethoxybenzene offers solid stability under routine lab handling, but it can become prone to gradual oxidative discoloration if stored in open-air environments or exposed to strong UV light. Years of plant experience have driven us to refine our storage protocols. Light-barrier drums and nitrogen blankets stop oxygen ingress, preserving clarity and limiting trace by-product formation. Our customers working in pharmaceuticals—especially in API intermediate manufacturing—have taught us that minor discoloration or unexpected off-odors create costly validation headaches. We’ve adjusted our workflow, from distillation column parameters to tank transfer rates, to provide reassurance at every stage. Product analysis extends beyond what’s listed on the assay sheet. We regularly test for peroxide buildup and quantify acid values, arming procurement and QA teams with the facts for each delivery. On rare occasions, customers have reported issues linked to trace solvent residues after lengthy storage. In response, we cut tail fractions out of the collection window and re-validated drum purging practices, shortening our average lead time for drum rotation to below 60 days.

    Environmental and Regulatory Realities

    Handling organic ethers brings regulatory attention and calls for care. Our operating location subjects production to region-specific environmental controls, with regular wastewater analysis and air handling checks. The compound itself features a moderate vapor pressure and is not classified among the highest-risk substances, but we never downplay the value of good neighbor relations and safe plant practice. Our process engineers have re-tooled venting and solvent recovery steps to shrink waste streams each year. Residual process solvents receive vapor phase recovery or safe incineration, and every operator wears full PPE during filling and transfer. These measures start long before a finished drum leaves our site. In case any material escapes containment, our on-call hazmat team drills quarterly on spill response. Based on customer audits and regulatory reviews, we post full traceability records and batch certifications, ensuring compliance documentation keeps pace with evolving national and global standards. As markets shift toward tighter ESG criteria, we remain prepared for even tougher oversight and invest steadily in cleaner technologies—not just to satisfy rules, but to earn trust from families living near our facility and keep our own teams healthy.

    Supporting Formulation and R&D Teams

    Research teams often rely on suppliers who grasp the realities of daily lab work. We understand that unexpected variance—subtle changes in purity, lingering moisture, or undetected by-products—can derail weeks of research. By running our own pilot applications and maintaining robust QA arms, we troubleshoot issues before they reach the customer. Not every batch heads straight for a large-scale reactor; some mix into resin blends or advanced polymer additives, where predictable evaporation and compatibility scores are essential. Our technical staff collaborate with downstream partners, troubleshooting both synthesis hiccups and scaling challenges. We freely share detailed spectra and impurity profiles, and invite feedback on any observed anomalies or bottlenecks. During technology transfers or trial batches, we arrange live sample tracking and open up our production logs, giving customers every assurance that each drum holds exactly what their experiment needs. This practical, open approach beats rote compliance for most bench chemists and project leads we serve.

    Years of Experience, Continuous Learning

    Our relationship with 1,2-Diethoxybenzene began decades ago, back when market demand followed the tides of large pharma schedules and dye plant turnarounds. Adapting to ever-smaller batch runs for custom projects, and catering to high-throughput screening labs, forced us to rethink what consistency looks like. Old habits from bulk chemical handling gave way to the sharper, more targeted controls that specialty chemicals now demand. For example, switching to multi-stage fractional distillation helped us keep non-volatile impurities from creeping into finished material. Batch-to-batch variance dropped, reassuring end users with demanding trace analysis standards. The move to single-use steel valves and rapid, closed transfers boosted purity, setting a new bar for reliability. Output volumes scaled from tankers to drum and even small-container delivery, accommodating pilot plant requests and university labs.

    Feedback cycles push us to adapt. Chemists adopting greener chemistry have reduced reliance on hazardous reagents, so we run routine tests for unreacted alkylating agents and trace halides. If a customer points out a potential improvement—be it tighter specs for LC/MS analysis, better inert packaging, or printed COAs with more granular impurity cutoffs—we rarely hesitate to modify internal procedures. Our development chemists maintain a research pipeline, testing process improvements under real-world scenarios. This history keeps the material flowing with fewer headaches, building confidence batch after batch.

    Market Access and Global Logistics

    As the chemical marketplace globalized, our distribution network expanded to reach customers on every continent. Each country brings different regulatory hurdles, labeling nuances, and customs quirks. To avoid project delays, we collaborate directly with shipping partners to handle materials safely. All shipments leave our site only after passing rigorous documentation and transit checks, with material safety data and batch reports attached. We reserve buffer stock throughout the year, which lets us manage unpredictable demand spikes and cover disruptions in ocean freight or last-minute air cargo. Proximity to major ports and years of relationship-building with shipping managers lets us pre-clear cargo, minimize hold times, and avert spoilage during transit, particularly for warm climates or destinations with less-developed cold-chain infrastructure. Our flexibility extends to packaging, supporting everything from small glass lab bottles to 200-liter drums with inert liners. In close feedback with global customers, we regularly re-assess shipping configurations, packaging durability, and customs documentation, keeping projects on track for both small biotechs and multinational industrial customers.

    Outlook and Next Steps

    Innovation in specialty chemistry never stops. 1,2-Diethoxybenzene carries niche uses in established sectors—pharmaceuticals and dyestuff above all—but its core chemistry holds untapped potential. In recent years, academic researchers have flagged its value as a model compound for studying ring substitution dynamics, exploring green solvent alternatives, and probing new routes toward bioactive molecules. Our technical group stays connected to conferences, publishes updates in synthesis bulletins, and invites suggestions from research labs working on novel transformations. This culture of sharing challenges and victories creates opportunities for real growth in both industrial and academic domains. Through our ongoing dialogue with users, we see shifts toward more precise, smaller-batch sourcing, with customers asking not just for high-purity product but also custom packaging, dedicated batch runs, and regulatory insight. We plan our production and R&D pipeline around these market realities, balancing scale with flexibility—never cutting corners on quality, safety, or honest communication.

    Commitment to Partnership

    Behind every drum of 1,2-Diethoxybenzene stand real people—process chemists laboring over optimization cycles, QA technicians monitoring dozens of purity metrics, and customer liaisons fielding urgent calls for additional documentation. Our aim is not only to manufacture a molecule, but also to serve as a long-term partner for formulation success. Through every stage, from order placement to material transition in your facility, we stay ready to answer questions and help resolve any issues that might arise. That mindset explains much about our ongoing investments—not just in new equipment, but also in training, documentation, and open lines of communication. This approach wins loyalty over quick sales, especially when researchers and production teams know they have real input into every process that shapes the final product.

    Years of manufacturing 1,2-Diethoxybenzene have taught us that every batch tells a story: about the care put into chemical transformation, about understanding what downstream users actually need, and about the discipline required to keep improving with every feedback loop. Whether your interest centers on bulk manufacturing or specialized R&D projects, you can rely on us not only for the product, but for a hands-on partnership that strengthens your own outcomes. Through ongoing listening, refining, and mutual learning, we keep working to elevate the role of this underappreciated aromatic ether in the modern chemical landscape.