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6,7-Dimethoxyquinazoline-2,4-Dione

    • Product Name 6,7-Dimethoxyquinazoline-2,4-Dione
    • Alias Dacarbazine
    • Einecs 628-31-1
    • 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
    VTB
    Specifications

    HS Code

    189478

    Chemical Name 6,7-Dimethoxyquinazoline-2,4-dione
    Molecular Formula C10H10N2O4
    Molecular Weight 222.20 g/mol
    Cas Number 30181-04-9
    Appearance White to off-white solid
    Melting Point 265-270 °C
    Solubility Slightly soluble in water; soluble in DMSO and methanol
    Inchi InChI=1S/C10H10N2O4/c1-15-7-4-6-5-12-10(14)11-8(6)9(13)3-2-7/h2-5H,1H3,(H2,11,12,13,14)
    Smiles COc1cc2c(cc1OC)C(=O)NC(=O)N2

    As an accredited 6,7-Dimethoxyquinazoline-2,4-Dione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White plastic bottle with screw cap, labeled "6,7-Dimethoxyquinazoline-2,4-dione, 25g, For Laboratory Use Only," with safety information.
    Shipping 6,7-Dimethoxyquinazoline-2,4-dione is typically shipped in sealed, chemical-resistant containers to ensure stability and prevent contamination. It must be labeled for laboratory use, accompanied by a safety data sheet (SDS), and handled in compliance with relevant hazardous material transportation regulations. Store and transport it at room temperature, away from incompatible substances.
    Storage 6,7-Dimethoxyquinazoline-2,4-dione should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, ventilated area, ideally at 2–8°C (refrigerator conditions). Ensure storage away from incompatible substances such as strong oxidizers. Properly label the container and follow all relevant chemical safety guidelines to minimize potential hazards.
    Application of 6,7-Dimethoxyquinazoline-2,4-Dione

    Applications of 6,7-Dimethoxyquinazoline-2,4-Dione in Industrial Manufacturing

    As a direct manufacturer with established technical and quality expertise, we supply 6,7-Dimethoxyquinazoline-2,4-Dione to a focused portfolio of advanced industrial customers. The following application scenarios demonstrate our material’s practical role in key downstream sectors, reflecting the real use cases and requirements of chemical, pharmaceutical, and specialty R&D markets.

    1. Pharmaceutical Intermediates for Anticancer Compound Synthesis

    Pharmaceutical industry researchers utilize this molecule extensively in multi-step organic syntheses as a protected quinazoline core for key oncology drug candidates, including selective kinase inhibitors and tailored DNA-interacting agents. The material enters regulated pilot and commercial flows beginning in medicinal chemistry labs, where its high purity and controlled impurity profile directly impact downstream yields and active pharmaceutical ingredient (API) quality. Batch-to-batch consistency ensures predictable reactivity in subsequent derivatizations critical for preclinical and clinical material supply.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Annex 1 (for sterile production where required)
    • FDA 21 CFR Part 211 cGMP (when integrated into U.S.-bound finished APIs)
    • ICH Q3A/B for impurity profiling where specified by clients

    Typical usage ratio

    • 0.5–2.0 molar equivalents, depending on the synthetic route and scale of target intermediate
    • Adjustment based on reaction stoichiometry and required excess to drive critical steps

    Downstream process integration

    • Added early as a heterocyclic precursor in the amidation/alkylation stage of API synthesis
    • Participates in N-alkylation or C-derivatization followed by deprotection steps
    • QC sample typically drawn post-reaction but pre-purification for IPC assay

    Final product types

    • Intermediate structures for kinase inhibitors
    • Developmental oncology and anti-viral APIs
    • Patent-stage reference compounds for pharmaceutical R&D

    2. High-Purity Reagent for Custom Heterocycle Development

    Custom synthesis labs and specialty fine chemical companies rely on this dione as a core building block for the design of advanced quinazoline-based heterocycles, necessary for the synthesis of lead compounds, fluorescent dyes for biolabelling, and proprietary screening libraries. Robust impurity control and single-batch traceability enable efficient hit-to-lead and analog synthesis projects, especially for exploratory pharmaceutical and agrochemical programs where analytical reproducibility is paramount.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • Responsible Care Management System (as adopted by most global chemical producers)
    • REACH Registration (when supplied to EU customers)
    • Certificate of Analysis (COA) with HPLC, NMR, and ICP-MS analytics as per client SOP

    Typical usage ratio

    • 0.2–1.5 equivalents, batch-specific, as dictated by library size and functional group compatibility

    Downstream process integration

    • Introduced as a primary scaffold in solid-phase synthesis or solution-phase combinatorial chemistry
    • Acts as the substrate for regioselective substitution or derivatization workflows
    • Purified in-line via flash chromatography or prep-HPLC following scaffold modification

    Final product types

    • Specialty heterocyclic intermediates for drug discovery
    • Functionalized biolabeling agents
    • Building blocks for commercial CRO and CDMO screening libraries

    3. Reference Standard and Analytical Reagent in Method Validation

    Analytical chemistry and quality control laboratories utilize this compound as a primary reference and system suitability standard for LC/MS, HPLC, and NMR method development, especially during validation of new pharmaceutical and synthetic routes. High assay value, control over isomeric impurities, and process contamination documentation fulfill the criteria demanded by regulatory authorities and global pharma clients for method qualification and cross-lab reproducibility studies.

    Industry compliance standards

    • Ph. Eur. monograph requirements (where applicable)
    • U.S. Pharmacopeia (USP) Reference Standard guidelines
    • FDA & EMA Method Validation Guidelines
    • ISO/IEC 17025:2017 for calibration and test laboratories

    Typical usage ratio

    • Prepared at 0.01–0.1 mg/mL for reference standard solutions
    • Exact amount defined by analytical method sensitivity, instrument calibration, and sample matrix

    Downstream process integration

    • Prepared as a reference solution for chromatographic injection or as a calibration point
    • Used for specificity, accuracy, and linearity validation of assay or impurity methods
    • Deployed in forced degradation/stability studies as a control

    Final product types

    • Reference standard vials for commercial method kits
    • Quality control samples in regulated pharma production
    • Stability study controls and proficiency test samples

    4. Research Raw Material for Advanced Material Science Projects

    University labs, R&D centers, and specialty material manufacturers use this compound as a foundational aromatic scaffold in the synthesis of functionalized polymers, advanced coatings, and electronic organic materials. The structural rigidity, electron-rich moiety, and compatibility with further modification steps make it a preferred building block for exploring new organic semiconductors, crosslinked film-formers, and experimental resins, especially in prototype device research and specialty materials.

    Industry compliance standards

    • ISO 17034 Reference Material Producer standard
    • University and research institute procurement and record-keeping policies
    • National Laboratory Accreditation Board (NABL) GLP (where pilot studies enter regulated flows)
    • Material Safety Data Sheet (MSDS) provision and risk assessment under GHS/OSHA

    Typical usage ratio

    • 0.1–5.0% by weight in experimental polymerization, adjusted by functional group conversion rate

    Downstream process integration

    • Integrated at the monomer blending or pre-polymer stage of advanced polymer synthesis
    • Used in solution or melt for further condensation, cross-linking, or surface modification
    • Batch and run tracked for reproducibility and experimental records

    Final product types

    • Model organic semiconductors
    • Functional coatings for R&D devices
    • Crosslinked specialty polymers for laboratory testing
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    Certification & Compliance
    More Introduction

    Introducing 6,7-Dimethoxyquinazoline-2,4-Dione: Real-world Perspective from a Chemical Manufacturer

    Innovation Originates on the Factory Floor

    Every day in our plant, shifts start early and finish late, with teams in white coats and steel-toed boots splitting focus between yield and purity. Tucked inside our specialty production line sits a crystalline compound known as 6,7-Dimethoxyquinazoline-2,4-Dione. Through years of trial, pilot-scale refinement, and process feedback from our R&D chemists, this molecule has carved out a niche, reflecting the intersection of engineering persistence, regulatory scrutiny, and end-user collaboration. From our hands-on perspective, the story isn’t just one of molecules or machinery. It’s the result of persistent efforts to improve, control, and standardize at every step, driven by real feedback from customers in pharmaceuticals, discovery labs, and advanced chemistry.

    Practical Details: What Sets 6,7-Dimethoxyquinazoline-2,4-Dione Apart

    We manufacture 6,7-Dimethoxyquinazoline-2,4-Dione to precise standards, consistently achieving high purity grades that exceed 98%, confirmed by HPLC and NMR. Most of what leaves our production line comes in the form of a free-flowing off-white to light yellow powder, delivering both batch consistency and reliability under variable transport and storage conditions.

    Our standard lot size runs from pilot quantities to multi-kilo orders, handled with a focus on transparency. Our in-house quality team tracks every gram, matching batch data with physical samples to catch inconsistencies before product release. We keep solvents and process byproducts to a minimum, knowing that residual contaminants can disrupt downstream reactions or invalidate research data. Our process engineers still recall initial struggles with solvent selection; some methods gave decent yields but triggered downstream instability. Only by cycling through different solvent systems, guided by chromatographic and crystallization data, did we settle on the current methodology, which consistently produces tight melting point windows and stable shelf life under standard storage.

    Product Usage: Real Applications Meet Daily Challenges

    6,7-Dimethoxyquinazoline-2,4-Dione has made an impact in medicinal chemistry, particularly as a scaffold for the synthesis of heterocyclic drug candidates. Several academic partners rely on its rigid backbone for modifying selectivity and reactivity in kinase inhibitor research. Our customers report that the double ketone arrangement invites nucleophilic substitution, helping medicinal chemists build libraries of molecules for bioactivity screening.

    In our manufacturing experience, researchers order this compound not because it’s a catalog staple, but because its methoxy groups at the 6 and 7 positions help block undesired side reactions, channeling chemistry towards defined products. This is not true for every quinazoline derivative, especially those lacking these protective groups. Our technical service team routinely supports synthetic chemists looking to couple or alkylate specific positions on the quinazoline ring. Time and again, feedback shows two things: reactivity is predictable, and the compound’s shelf-life makes it possible to push experiments on a longer timeline.

    Lab Performance—and Where Other Compounds Fall Short

    We routinely manufacture and test related quinazoline diones, comparing head-to-head their ease of handling, stability, and adaptability under varied conditions. One big advantage with 6,7-Dimethoxyquinazoline-2,4-Dione: minimal clumping in humid environments. Several alternative compounds, especially those without methoxy protection, show greater sensitivity to water and oxygen, requiring inert gas curtains and protective packaging. In contrast, our product withstands normal atmospheric conditions during lab handling and aliquoting, streamlining both storage and workflow.

    In terms of solubility, our internal testing confirms that this compound shows good solubility in standard organic solvents like DMSO and acetonitrile, but limited solubility in aqueous buffers or alcohols. We've seen customers attempt direct dissolution in water, leading to partial precipitation or cloudiness; our own trials point to the benefits of dissolving in DMSO, followed by dilution, when working in assays or high-throughput formats.

    We’ve compared this product extensively with 6,7-dichloro and 6,7-dihydroxy variants. The methoxy substitution not only tunes electronic properties of the aromatic ring—making nucleophilic attack more selective—it also means lower handling risk, since methoxy groups lack the reactivity of free hydroxy or halide substituents. One research partner noted that switching from a chloro to a methoxy variant cut back on side product formation and made QC analysis simpler.

    Process Know-how: Compliance, Documentation, and Reliability

    Production of 6,7-Dimethoxyquinazoline-2,4-Dione runs under tight controls, shaped by both regulatory frameworks and decades of operator experience. Each batch receives full analytical documentation: NMR confirms the structure, HPLC measures purity, and GC looks for volatile residues. Every shipment leaves our plant with these traceable details. Our documentation isn’t designed just to satisfy audits; it comes from repeated lessons on what can go wrong when batch records and supply chain traceability lag behind. Early on, one data gap caused a foreign shipment to be held up for weeks because customs couldn’t match product identity to origin.

    We stay in close contact with leading pharma and chemical safety experts, adjusting internal procedures as guidelines evolve. From day-to-day, this means our workers receive regular training not just in chemical handling and waste minimization, but also in batch data recording—details that matter to both regulatory compliance and customer trust. Our compliance lead holds every record to a double standard, combining regulatory requirements with feedback from returning clients who have flagged inconsistencies in the past.

    Supporting Innovation—Direct Manufacturing Brings More Than Price Advantage

    As a direct manufacturer, we manage the details that often get lost in distributor supply chains. This has proven critical for research teams that need custom batch sizes or direct access to technical support. On several occasions, customers came to us after resellers supplied similar-sounding quinazoline diones, only to discover that subtle modifications—different protecting groups or impurities—derailed their project timelines. In response, our production team committed to both backward and forward traceability, maintaining archived samples for each batch so customers can request additional analytics or repeat orders with confidence.

    Our relationship with research chemists goes beyond supplying catalog chemicals. Real research demands dialogue, especially since complex projects often push compounds into non-standard applications. We regularly field questions about solvent compatibility, reactivity with specific electrophiles, or even reaction scale-up; in each case, we draw on our in-house pilot production batch files and notes from previous syntheses.

    One tangible impact: several clients now send us their proposed reaction schemes, seeking feedback on where the chemical might perform differently depending on batch history, storage conditions, or even small shifts in spectral purity. As manufacturers, we see firsthand how even minor process changes—different pressure conditions, fresh solvent lots, slight alterations in crystallization protocols—ripple down to finished product consistency. With our scale and experience, we work to flag possible pitfalls and suggest actionable changes, saving development teams time and budget.

    Responsible Manufacturing: From Waste Streams to Worker Safety

    Making 6,7-Dimethoxyquinazoline-2,4-Dione means dealing with multiple upstream feeds and downstream byproducts. Our plant recycles recovered solvents and uses closed-loop transfer systems to cut down atmospheric VOC emissions. Where older methods sent chlorinated wash streams into energy-intensive disposal, our current process team built a regeneration loop that reuses the majority of these materials. Waste tracking passes through digital systems with regular third-party spot checks, part of a broader push to limit ecological impact.

    Worker safety drives every decision on the line. Switches in process chemistry—sometimes minor, sometimes transformative—arise from routine operator safety reviews. Several years ago, a batch deviation prompted our health and safety team to re-engineer our glovebox handling standards for certain intermediate steps. Equipment upgrades followed, with operators actively involved in risk mapping. We learned quickly that even low-toxicity compounds present respiratory or vesicant risks if containment fails. This hands-on feedback has pushed new protocols that now govern all handling of this product from raw feed to final packaging.

    Beyond regulatory compliance, our team culture supports transparent reporting and inter-department communication, with continuous feedback from ground-level operators pointing out where product improvement opportunities exist. Routine “stop-the-line” authority means no team member stays silent when they spot contamination or packaging flaws; this ethos has prevented costly product recalls and kept our client satisfaction high over the long term.

    Real Differences: 6,7-Dimethoxyquinazoline-2,4-Dione vs. Other Quinazoline-2,4-Diones

    Manufacturing a series of quinazoline-2,4-diones, we have now seen how tweaks at the 6 and 7 positions transform user experience. The dimethoxy variant is less volatile and exhibits greater oxidative stability than free hydroxy- or chloro-substituted analogues. We no longer see the batch-to-batch color shift or odor profile changes that plagued early runs with other derivatives. This stability difference might not appear in catalog listings, but it eliminates experimental noise and enables longer shelf lives without protective atmospheres.

    Our analytical lab regularly benchmarks finished lots of all quinazoline derivatives on the same HPLC and GC methods. Methoxy-substituted material produces sharp chromatographic peaks, less tailing, and shows higher combined purity. Researchers working at microgram or milligram scale report more predictable yields and repeatable NMR integrations—critical for patent submissions or regulatory filings.

    Storage and transport introduce fewer surprises. Ambient shipments sometimes expose materials to air and light; with competing compounds, we have recorded degradation, brown discoloration, or foul odors upon delivery. The dimethoxy variant arrives intact, meeting product release specs even after weeks en route to overseas destinations.

    One challenge came from clients scaling up syntheses in flow reactors. Compared with hydroxy derivatives, the 6,7-dimethoxy compound resisted polymerization and stuck less to tubing and fritted glassware, allowing smoother flow and easier equipment cleaning. This small operational detail returns value in uptime and lower resource requirements for maintenance.

    Understanding the End User: Listening Directly to Lab Chemists

    Most customers buying 6,7-Dimethoxyquinazoline-2,4-Dione want more than a raw material; they want product reliability backed by real-world know-how. We consult with both academic research labs and pharmaceutical companies, tracking which physical or chemical details matter most to day-to-day workflow. Early feedback shaped our drying protocols: our initial production method, borrowed from bulk chemical handling, left trace moisture that caused inconsistent dissolution. Now, all outgoing batches undergo rigorous moisture reduction and batch-specific Karl Fischer analysis. The result is consistent solubility and fewer failed assay runs.

    Some chemists reached out after observing unexpected NMR peaks, suspecting minor byproducts or incomplete purification. Our in-house analytics team welcomes these queries, running additional 2D NMR or mass spectral scans to rule out or document micro-impurities. Open communication has built trust and led us to tweak crystallization and washing steps for greater selectivity, directly impacting purity and performance.

    We find that real support means sharing both data and lived experience. Our support team often helps labs troubleshoot reactions, such as whether to pre-warm the material for better dissolving, or how to handle low-yielding coupling steps. In this way, every batch—a product of both hard science and hand-driven care—carries with it lessons internal to our team and driven by partners in the field.

    Sustaining Value: Ongoing Product Development and Quality Feedback

    Continuous improvement defines how we maintain product quality and relevance in competitive research markets. Biannual reviews bring together analytics, production, and client services staff to review both complaint logs and customer success stories. On several occasions, this feedback loop flagged subtle but persistent issues, such as particle size drift that complicated fine weighing by analytical teams. As a result, we installed new milling and sieving stages, maintaining tight control on powder morphology and preventing unwanted agglomerates.

    Technical discussions with clients lead us to trial new derivative syntheses or to develop custom packaging for sensitive applications. We recall one project where a biotech partner needed sealed vials for robotic pick-and-place workflows. Our packaging staff worked directly with the client’s automation engineers, prototyping different formats until we hit the mark.

    These collaborative tweaks ripple back into our internal standard operating procedures, shaping how we train new staff and document finished goods. Every change passes through QA, ensuring the next batch meets lessons learned from real lab use—not just from manual but also from scaled robotic operations in modern discovery setups.

    Integrating into the Larger Supply Ecosystem

    Global supply networks have seen disruptions in recent years, affecting everything from raw material access to shipping timelines. Our role as primary manufacturer provides some buffer—direct relationships with precursor suppliers, ability to shift upstream sources, in-house quality validation. Still, external volatility remains. Our response includes holding higher on-site inventories of key precursors, working with multiple validated vendors, and supporting customers with upfront insight into lead times.

    Transparent, detailed batch documentation and process flexibility help us weather raw material specification changes or transportation delays. We communicate openly with research buyers and procurement staff, giving them early warnings and alternatives, while providing the in-depth technical support needed to modify research designs if supply shifts impact project timelines.

    Looking Forward: New Challenges and Shared Progress

    Future development will continue to reflect feedback from customers, regulatory bodies, and industry partners. As new areas of research demand ever-higher standards for purity, consistency, and process traceability, our manufacturing process will evolve. Long-term relationships with our laboratory partners show that success results from open dialogue, detailed documentation, and a willingness to adjust in response to real use.

    Our experience manufacturing 6,7-Dimethoxyquinazoline-2,4-Dione reinforces the value of both technical rigor and hands-on engagement across all process stages. Direct oversight of production, quality, and delivery continues to deliver value, minimize risks, and strengthen innovation.