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5-Amino-1,4-Benzodioxane

    • Product Name 5-Amino-1,4-Benzodioxane
    • Alias 5-Amino-2,3-dihydro-1,4-benzodioxine
    • Einecs 631-099-6
    • 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

    183315

    Chemical Name 5-Amino-1,4-Benzodioxane
    Cas Number 17249-49-4
    Molecular Formula C8H9NO2
    Molecular Weight 151.16 g/mol
    Appearance Solid (typically off-white or beige powder)
    Melting Point 87-89°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles c1cc2c(cc1N)OCCO2
    Inchi Key ZRIGKNJFWOOLGE-UHFFFAOYSA-N
    Purity Typically >98% (depends on supplier)
    Storage Condition Store in a cool, dry place, tightly closed

    As an accredited 5-Amino-1,4-Benzodioxane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 5-Amino-1,4-Benzodioxane, 25g: Supplied in a sealed amber glass bottle, labeled with hazard information and product details for laboratory use.
    Shipping 5-Amino-1,4-Benzodioxane is shipped in tightly sealed containers, protected from light and moisture. It should be packed according to standard chemical safety regulations, including appropriate labeling and documentation. The package should be handled with care, avoiding excessive heat, and shipped by authorized carriers in compliance with local, national, and international transport regulations.
    Storage **Storage of 5-Amino-1,4-Benzodioxane:** Store 5-Amino-1,4-Benzodioxane in a tightly sealed container, away from light, heat, and moisture. Keep at room temperature, in a cool, dry, well-ventilated area, and away from incompatible substances such as strong oxidizers and acids. Use appropriate safety labeling and ensure limited access to authorized personnel. Follow all local safety regulations and guidelines for storage.
    Application of 5-Amino-1,4-Benzodioxane

    Applications of 5-Amino-1,4-Benzodioxane in Industrial Manufacturing

    As a manufacturer dedicated to the production of high-purity 5-Amino-1,4-Benzodioxane, we supply this specialized intermediate to support strict process needs in downstream sectors with established real-world applications. Below, we present four focused industrial application scenarios with process insights, regulatory requirements, formulation details, and examples of finished goods.

    1. Pharmaceutical Intermediate for Central Nervous System (CNS) Active APIs

    5-Amino-1,4-Benzodioxane serves as a key building block in the synthesis of select CNS pharmaceutical active ingredients, including anti-anxiety and antihypertensive compounds. API manufacturers incorporate it at an early stage for ring closure or as an amine source in stepwise organic synthesis routes. Each stage in the process must comply with pharmaceutical quality benchmarks, making traceability and batch consistency essential. Its introduction takes place during the condensation or coupling steps where controlled reaction conditions are monitored in line with EU and US pharmacopoeias.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP/NF (United States Pharmacopeia/National Formulary) monographs for CNS agents
    • European Pharmacopoeia (Ph. Eur.) Chapter 5.10 for impurities
    • Good Distribution Practice (GDP) for transport and storage

    Typical usage ratio

    • 0.12–0.19 molar equivalents per synthetic batch; actual proportion set according to target molecule yield and reaction design, with adjustment for pathway-specific requirements

    Downstream process integration

    • Charged as a raw amine precursor during multi-step organic synthesis prior to ketone or carboxylic acid functionalization; followed by isolation and purification for subsequent transformation into API core structure

    Final product types

    • Escitalopram and derivatives (selective serotonin reuptake inhibitors)
    • Benzodioxane-based antihypertensive agents
    • API intermediates for CNS disorders
    • Research compounds for neuropharmacology studies

    2. Dye and Pigment Synthesis for Specialty Colorants

    Advanced pigment manufacturers utilize 5-Amino-1,4-Benzodioxane as an aromatic amine source in the synthesis of certain high-performance organic dyes. Its molecular structure supports coupling reactions with diazonium salts to introduce colorfast chromophores. The selection and precise metering into the batch impacts the spectral and fastness properties of the end pigment, which must meet applicable environmental and safety restrictions on aromatic amines.

    Industry compliance standards

    • REACH Regulation (EC 1907/2006) Annex XVII (restriction on aromatic amines in dyes)
    • EN 71-3 migration limits for toys and textiles
    • OEKO-TEX® Standard 100 for textile dyes
    • ZDHC MRSL v3.1 compliance for safe chemicals in manufacturing

    Typical usage ratio

    • 3–12% by weight of dye intermediate charge; ratio optimized based on target chromophore and batch scale, taking account of molar reactivity of primary amine substituent

    Downstream process integration

    • Added during the azo-coupling or condensation reaction phase as primary amine donor, leading to formation of dye backbone before subsequent stabilization and milling steps

    Final product types

    • High-purity azo and anthraquinone dyes for technical textiles
    • Specialty colorants for plastics and films
    • Water-based pigment dispersions for coatings
    • Color bases for inkjet printing applications

    3. Polymer Additive for Specialty Engineering Plastics

    Producers of engineering polymers integrate 5-Amino-1,4-Benzodioxane as a co-monomer or chain-modifying agent within select high-performance plastic grades. Its presence enables targeted tuning of melt flow, rigidity, and thermal profile, especially in applications where precise aromatic amine incorporation influences polymer backbone structure. All material selection must reflect downstream compliance requirements for safe handling and performance in demanding conditions, such as electrical insulation or medical device substrates.

    Industry compliance standards

    • UL 94 flammability standards for plastics
    • FDA 21 CFR 177.1595 for allowable substances in polycarbonate resins
    • ISO 9001:2015 for manufacturing process quality
    • RoHS Directive 2011/65/EU for electronic applications

    Typical usage ratio

    • 0.4–1.5% by weight added to polymerization reactor; dosage adjusted per target polymer chain length and desired end-use performance attributes

    Downstream process integration

    • Fed as a reactive monomer or functional additive during melt polymerization stages, resulting in co-polymer or modified backbone structure, followed by extrusion or granulation into pellet form

    Final product types

    • Thermoplastics for electrical insulation (e.g., high-voltage connectors, relay housings)
    • Medical grade plastics for device housings
    • Specialty engineering films
    • Precision-molded parts for automotive or aerospace sectors

    4. Fine Chemical Intermediate for Agrochemical Synthesis

    Leading agrochemical manufacturers employ 5-Amino-1,4-Benzodioxane as an intermediate in the multi-step synthesis of select herbicide or fungicide actives. Its amine functionality enables it to participate in condensation or cyclization steps that construct biologically active rings. Regulatory scrutiny of synthetics for agriculture drives compliance at each batch, particularly in monitoring amine-derived residues and verifying absence of prohibited byproducts.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius pesticide standards
    • ISO 9001 certified quality processes for agrochemical intermediates
    • OECD Test Guidelines for regulatory dossiers
    • European Chemicals Agency (ECHA) registration for intermediates

    Typical usage ratio

    • 0.25–0.62 mol equivalents per stage; defined by target molecule design and reaction yield metrics specific to herbicide or fungicide type

    Downstream process integration

    • Charged during initial amination or subsequent ring closure reactions to build out the central pharmacophore, followed by purification, formulation, and product stabilization

    Final product types

    • Selective herbicide actives for broadleaf weed control
    • Systemic fungicides for cereal and vineyard protection
    • Intermediates for proprietary crop protection agents
    • Research compounds for agricultural R&D
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    Certification & Compliance
    More Introduction

    5-Amino-1,4-Benzodioxane: Shaping a Reliable Foundation for Specialty Synthesis

    At our facility, the production of 5-Amino-1,4-Benzodioxane demonstrates what careful chemical engineering and practical know-how can do for fine chemical applications. The story behind this aromatic amine starts with precision—attention to hydration levels, strict control on impurities, and direct experience in batch reproducibility. It's a process nobody can shortcut. Our capabilities have grown from years of adaptation and relentless troubleshooting, learning where bottlenecks develop and how purity profiles drift. Here, it’s not just another compound on an inventory; it's a result of tailored approach to customer needs from pharmaceutical and agrochemical projects.

    Why 5-Amino-1,4-Benzodioxane Remains Relevant in Synthesis

    The market doesn’t reward complacency, especially with building blocks like 5-Amino-1,4-Benzodioxane. The consistent demand stems from its role in synthesizing bioactive molecules—medicinal chemistry teams rely on its responsive amino group paired with the rigid backbone structure. Medicinal chemists mention it for a reason: it enables rapid library creation when designing small molecules for screening. We’ve worked with research labs that faced hurdles scaling up benzo-fused intermediates, realizing that commercial off-the-shelf materials often carry byproducts that muddy the next reaction step. We strip ambiguity from the process by analyzing for trace-level contaminants, keeping NMR signals sharp and the amine free for modification.

    Academic groups and research-driven companies push us further by tweaking their own protocols. Our team relates to those pressures. People do not want to waste days troubleshooting a batch when a single foreign spot on the TLC can spoil isolation. That level of frustration is familiar to us. It’s why our quality assurance team adjusts purification sequences and revisits drying conditions with every new lot. We see the stress points before they reach the customer and make process decisions from that vantage.

    Specifications That Influence Real-World Outcomes

    For 5-Amino-1,4-Benzodioxane, the demands are straightforward—keep the amine group available, minimize phenolic byproducts, and avoid color impurities that suggest partial oxidation. Our standard output ships as a light-brown to pale yellow crystalline solid; the color window points to subtle differences in precursor routes and the integrity of reducing agents. The melting point stays inside the expected range, a result of strict batch-wise temperature monitoring and slow crystallization. Water content comes tightly controlled, recognizing moisture will impact downstream formylations and amidations. Those working on peptide couplings have mentioned their appreciation for consistently dry stocks—the difference shows up quickly when reagents are sensitive.

    Typical assay values rest above 98%, measured through HPLC and rechecked using limit tests on known impurities. We have engaged third-party labs for cross-validation, especially after process modifications, keeping transparency high and data reliable. In conversations with long-term partners, it’s clear that few batches survive direct chromatographic comparisons unless every step is examined, so walking the line between speed and quality sits at the foreground of our process.

    Model and Scale-Up Practices

    The in-house process model uses a sequential approach: precise benzodioxane ring formation followed by directed amino group introduction. Each step depends on solvent choice and reaction temperature gradient. Years spent refining agitation speeds and choosing the right phase separation strategies allow our team to isolate the product effectively, keeping batch sizes consistent from pilot to ton-scale production.

    Feedback from scale-up is invaluable. Workers on the shop floor notice that cooling rates after the final reaction lead to variable crystallization. In several campaigns, we learned that rushing this step traps mother liquor—so, whenever surface dryness looks perfect too soon, a deeper check confirms whether occlusion happened. This kind of hands-on pattern recognition helps us design training protocols for new operators. We don’t pass on the product until it behaves the same every time, whether it moves by drum or jar.

    How This Compound Differs From Other Benzodioxane Derivatives

    Other benzodioxane-based materials offer functional variety: halide, nitro, or alkoxy groups at various positions. Each substitution pattern influences reactivity. The amino function at the 5-position selected for this compound improves its ability to undergo selective coupling and condensation reactions. Chemists working in the CNS drug space, for example, reach for this building block when developing potent bioisosteres. The unprotected amine tolerates mild acidic or basic conditions, offering flexibility in protection-deprotection schemes, especially relative to its nitro or halide counterparts.

    In the manufacturing setting, we see fewer issues with side reactions compared to more heavily functionalized derivatives. The 1,4-benzodioxane core brings rigidity which serves well for predictable structure-activity relationships. Customers hesitate with overprotected derivatives, as these usually call for additional deprotection, raising costs and lengthening timelines. That experience taught us to maintain the amine’s accessibility, never blocking reactivity for a minor gain in shelf stability. For labs in early-stage drug discovery, that matters more than presenting a cosmetic color improvement or exaggerated impurity profile.

    Usage Characteristics Informed by End-User Feedback

    Our work does not end at shipping. End-users tell us how the material acts—reactivity profiles, solubility issues, odors betraying decomposition. We’ve learned from customer pilot runs that excessive particle size variation impacts dosing accuracy in formulation labs, so a sieve analysis runs hand-in-hand with our final inspection. In kilo-scale alkylation campaigns, crystal habit affects handling losses; we mill carefully to avoid static, knowing that powder clinging translates to waste.

    Pharma teams, especially those synthesizing final-stage actives or focused on analog screening, cite the amine’s powerful versatility. It enters peptide coupling, sulfonamide formation, urea derivatization, and heterocycle synthesis. The freedom to proceed in either water or organic solvent without complicated pre-treatment saves time. In one case, a collaborator highlighted how reliable batch dampness allowed them to bypass pre-drying—an edge that can mean an extra cohort tested in the same working day. These interactions drive deeper improvements in our lot testing procedures.

    Contract development and manufacturing organizations draw on our experience with odd-lot requests. Sometimes an intermediate stage fails to meet solubility targets due to unanticipated polymorph formation; our history handling multiple crystallization schemes often provides the necessary workarounds. Being present for support through sample re-analysis and process troubleshooting builds trust beyond price or contract terms.

    Process Developments and Refinements

    We put stock in continuous improvement. There are points where solvent recovery or catalyst regeneration directs us toward greener routes. Years back, we switched our amination to a milder protocol, which shaved off energy use and lessened trace metal carryover. That change led to repeatable color profiles and improved downstream purification, even if the capital outlay pinched for a quarter. Results in the drum speak for themselves—lower heavy metal content and a sharper, faster melt run.

    Third-party audits pushed us to review cleaning validation data. The outcome: more robust tank washing and tighter limits on cross-batch impurity. Customer inspections exposed small details, like overlooked gasket degradation or valve seating, and re-emphasized the link between nut-and-bolt reliability and chemical quality. We act on these findings because they affect the outcomes our users see in their labs and reactors.

    Lean manufacturing initiatives also surfaced ways to cut waste. Scrutiny of byproduct profiles identified routes where side reactions produce persistent yellow tints or faint odors, so we adjusted reagent addition rates and optimized agitation profiles. Real-world feedback from formulation chemists then confirmed that these improvements delivered cleaner NMR and LC-MS traces. This hands-on iterative approach replaces theory with facts gathered from each release.

    Packaging Choices Informed by Handling Realities

    Shipping hygroscopic and air-reactive materials leads us to invest in sealed, moisture-proof packaging. Over the years, customers in high-humidity regions voiced concerns about caking and clumping. We responded with double-bagged inner liners and tamper-evident closures, minimizing the risk that atmospheric moisture slips through. Engineers tested sample shipments through temperature and pressure cycles, simulating rough handling and storage lags. This cut reports of stickiness, which can gum up feed systems and pilot reactors.

    We’ve also listened when clients needed labeling with batch-specific assay and impurity data. Having fast scan-access to certificates of analysis means fewer phone calls and no lag between incoming goods and in-process testing. We handle stability samples on staggered schedules, gathering data at real storage temperatures to map long-term performance. That investment pays off—with less material held back for retesting, supply chain managers line up their procurement cycles with real confidence.

    Sustainability and the Push for Greener Chemistry

    Pressure toward more sustainable chemistry prompted us to rethink several ingrained habits—energy use, solvent choice, purification techniques. Audits revealed solvents with high regulatory scrutiny, so we prioritized swaps to less volatile carriers and shared outcomes with key partners. Reduced-waste filtration systems now play a role from kilo to ton scale. Feedback loops from pilot sites allowed us to track whether these changes influence downstream yields or introduce new contaminants.

    Hazard management features strongly in every batch review. 5-Amino-1,4-Benzodioxane production previously pushed the limits of amine handling exposure; now, in-line sensors watch for ammonia and related amines, protecting both operators and the finished material. With process intensification, we try to reclaim waste heat and minimize vented off-gas. These steps keep risk at bay in routine work and satisfy customer audits covering everything from effluent to carbon reporting.

    Cost accounting comes together with sustainability when tracking solvent recapture rates or water recycling. Nobody prefers mandates for change, so showing concrete gains—a lower waste disposal bill or smaller storage footprint—brings change forward organically. Our documentation tracks what finishes in the drum and what remains on the floor, so improvements stay anchored in data rather than feel-good stories.

    Regulatory Experience and Customer Collaboration

    Process validation, document control, and change notification form a backbone of our reliability. We keep up with evolving standards out of necessity, not just compliance. Regulatory teams in our clients’ organizations rely on transparent, method-specific impurity profiles. Our analytical records stretch back across campaigns, showing reproducible performance. Audit teams find what they need—method reports, impurity trend lines, and cross-referenced batch histories. Consistent, direct relationships with regulatory bodies smooth new lines of communication as protocols adjust.

    We’ve sat through clarifications with health authorities on compound classification and trace element guidelines. Samples sent to contract labs allow us to demonstrate confidence in our internal measurements. Real stories emerge here—a lot stuck in customs due to labeling discrepancies, batches delayed by missing analytical pages, or incoming questions about stability data from changed packaging. Our solution comes from methodically collecting supporting data and investing in analyst training, so that troubleshooting becomes another step in our normal workflow.

    Facing Research and Commercialization Challenges

    New synthetic schemes in both lab and kilo-scale operations uncover surprises. We are quick to spotlight challenges to partners, such as route-specific impurity carryover or sensitivity to specific solvents. This candor emerges from daily experience—nobody benefits from smooth talk that ignores latent risks.

    Drug development teams juggling parallel studies value the ability to adjust batch sizes up or down. Since we run pilot equipment and large-scale reactors side by side, it’s straightforward to respond to shifting needs. The process doesn’t suffer from scale-dependent variability, as all equipment experiences routine cleaning and verification. That means fewer out-of-spec results and less second guessing when transferred between sites or production lines.

    Sometimes, a customer needs a tweak—a certain salt form, an altered drying time, or a custom grind to fit an automated filling line. We gather the shop floor team, outline constraints, and solve through direct communication. The time investment pays off when we hear about successful downstream process validation or a faster regulatory sign-off.

    Lessons and Looking Ahead

    Experience teaches that producing 5-Amino-1,4-Benzodioxane extends beyond the batch record. Each campaign refines our process, informed by continuous use, evolving regulatory pressures, and problem-solving with researchers from many disciplines. Material that started as a specialty intermediate now supports broad applications—from medicinal screening to advanced material synthesis.

    We measure progress by tangible outcomes: consistency in reactivity, clarity in assay reports, and the rarity of customer complaints. The feedback loop spans every stage, from process chemistry down to logistics. There’s no room for complacency—the stakes for failed intermediates include months of lost work, resources tied up, and diminshed trust built over years.

    As research and development needs accelerate, our role stretches into new territory. We step up with ideas and improvements, open communication, and the resolve to see every batch deliver on its promise. Our experience in producing 5-Amino-1,4-Benzodioxane remains as much about serving dedicated scientists as it is about refining a product. The learning never pauses and neither does our drive to meet, then raise, the standard.