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HS Code |
652255 |
| Productname | 6,7-Dimethoxy-3,4-Dihydroquinazoline-4-One |
| Casnumber | 14374-45-7 |
| Molecularformula | C10H12N2O3 |
| Molecularweight | 208.22 |
| Appearance | White to off-white solid |
| Meltingpoint | 207-211°C |
| Solubility | Soluble in DMSO, slightly soluble in water |
| Purity | Typically ≥98% |
| Storagecondition | Store at 2-8°C, protected from light |
| Smiles | COc1cc2NC(=O)CNc2cc1OC |
| Inchi | InChI=1S/C10H12N2O3/c1-14-7-3-6-4-8(12-10(13)5-11-6)9(15-2)7/h3-4,11H,5H2,1-2H3,(H,12,13) |
| Synonyms | 6,7-Dimethoxy-3,4-dihydroquinazolin-4-one |
As an accredited 6,7-Dimethoxy-3,4-Dihydroquinazoline-4-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 6,7-Dimethoxy-3,4-Dihydroquinazoline-4-One, sealed with a tamper-evident cap, labeled with hazard warnings. |
| Shipping | 6,7-Dimethoxy-3,4-Dihydroquinazoline-4-One is shipped securely in sealed, chemical-resistant containers to prevent contamination or spillage. Packaging complies with international safety regulations for chemical transport. Shipment includes Safety Data Sheets (SDS) and labeling for proper identification and handling. Temperature and moisture controls are maintained as required to ensure chemical stability during transit. |
| Storage | 6,7-Dimethoxy-3,4-Dihydroquinazoline-4-One should be stored in a tightly closed container, in a cool, dry, well-ventilated area, away from direct sunlight and incompatible materials such as strong oxidizers. Keep at room temperature and protect from moisture. Properly label the storage container, and ensure access is restricted to trained personnel. Always follow safety regulations and laboratory guidelines for chemical storage. |
Applications of 6,7-Dimethoxy-3,4-Dihydroquinazoline-4-One in Industrial ManufacturingAs a dedicated manufacturer of 6,7-Dimethoxy-3,4-Dihydroquinazoline-4-One, we prioritize traceable, efficient, and compliant supply to global industries with advanced downstream formulation needs. Below we outline targeted, real-world application scenarios where this specialty heterocycle sees established demand, each with distinct production and compliance details. 1. Pharmaceutical Intermediate for Antihypertensive API SynthesisMultinational pharmaceutical companies select this compound as a key building block for synthesizing dihydroquinazolinone-based antihypertensive drug substances. Incorporating the material provides scaffold specificity for medicinal chemists addressing cardiovascular formulation demands during API process development. Control of input quality and analytical traceability remain essential throughout active ingredient manufacture to ensure batch-to-batch consistency and regulatory clearance for downstream medicinal products across regulated markets. Industry compliance standards
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2. Key Raw Material for Crop Protection AgentsAgrochemical formulators leverage this material’s specific ring structure in the production of active molecules found in novel herbicides targeting resistant weed populations. Sophisticated process controls ensure removal of residuals and contaminants before final formulation, while strict monitoring of pesticide registration requirements and local residue limits guide all production stages from synthesis through product registration and technical equivalence validation. Industry compliance standards
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3. Synthesis Intermediate for Specialty Dye ManufactureLeading colorant manufacturers incorporate this heterocyclic compound to develop high-purity intermediate structures for technical dyes used in electronics and plastics. Its chemical stability ensures compatibility with advanced dye synthesis while allowing precise chromophore modification. In tightly controlled facilities, production teams track every synthetic batch against both local and international regulatory benchmarks for purity and safety. Industry compliance standards
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4. Chemical Intermediate in Advanced Material Science R&DMaterial science innovation centers and specialty resin producers employ this compound during new monomer and pre-polymer design workflows, especially for projects requiring tailored electron-donating or accepting groups within polymer matrices. Its precise reactivity parameters assist in achieving desired physical properties, with R&D teams documenting all laboratory-scale and upscaled syntheses for compliance with internal protocols and the broader research regulatory landscape. Industry compliance standards
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Deep in our production halls, we spend more hours with 6,7-Dimethoxy-3,4-Dihydroquinazoline-4-One than most will with their morning coffee. This compound doesn’t just represent another line in a product catalog—it reflects ongoing conversations with research chemists, stringent process optimization, and plenty of trial and error. We carry the evidence on our hands from glassware cleaning to final pack-out. It’s a specialty molecule, and every batch reminds us: each gram represents several years of refinement and feedback.
Chemically, 6,7-Dimethoxy-3,4-Dihydroquinazoline-4-One has a place in the broader family of quinazolinones, but some defining traits stand out. The dimethoxy groups on positions 6 and 7 don’t just enhance solubility in research solvents—they also create distinct reaction profiles. For users handling related compounds lacking these substitutions, the differences appear immediately in product isolation and spectral analysis. We know it because every time a chemist wants to switch out to a subtler methoxy pattern, the whole purification pathway changes right along with it.
In our facility, this model means we constantly monitor for the right crystalline habit, color, and odor in quality checks. We see plenty of lookalikes with backbone variants, but our protocols ensure you won’t find this material contaminated by tri- or monomethoxy analogs, or any “shortcut” syntheses where others might cut corners to boost yield. That consistency in isomer content and low-level impurity is also why our long-term collaborators come back for this exact model—it works the way their work demands. Many times, we’ve supplied parallel batches for side-by-side comparison and our analysts can spot the variances between authentic 6,7-dimethoxy and related offshoots with a single glance.
Heat sensitivity ranks high on the list of concerns chemists and process engineers mention to us, second only to moisture control. This dihydroquinazoline derivative doesn’t respond well to careless exposure during scaling, which rings true both on the bench and in process drums. What we ship out holds a fine, moderately hygroscopic powder—if stored poorly after opening, clumping and hydrolysis sneak in within days. Old samples from other vendors sometimes show visible yellowing, but our batches stay visually bright and sharp white under tight packaging. It’s an open secret among manufacturing labs that generics with looser controls lose quality fast.
Solubility doesn’t challenge just research chemists. Formulators have asked us—again and again—about compatibility in DMSO, ethanol, or buffered aqueous solutions. Our internal data show robust dissolution in DMSO at moderate temperatures at stock concentrations used for pharmacological screening. Comparisons against the unsubstituted 3,4-dihydroquinazoline-4-one reveal our dimethoxy variant dissolves better in nonaqueous settings and doesn’t precipitate as abruptly when solvents mix. In chromatographic work, the product’s UV absorbance profile proves especially sharp and reliable, thanks to the position and nature of those methoxy groups. This makes tracking it during complex workflow analysis that much more straightforward. Purity on HPLC, while often advertised at glitzy numbers, holds up at or above 98%—and we back every batchline with data, not just marketing lines.
Working with this molecule takes stubborn patience and discipline. We’ve adjusted reactor temp ramps countless times to keep the final cyclization step from seeding byproducts. Solvent recovery teams push for greener, more closed-loop approaches, yet every process improvement only gets signed off once yield and purity hit demanding targets. Our teams still weigh the merits of batch versus continuous synthesis; what stays clear to us is that regular process review beats inflexible routines. On our worst days, the process throws as many surprises as it does product.
Controlling trace contaminants—mainly mono-methoxyquinazoline analogs and starting material residues—motivates plenty of midnight light-inspections and “one more TLC run just to be sure” habits. Rigorous drying steps, filtering, and constant monitoring of atmosphere matter because any slip shows up in customer applications almost instantly. Running higher purity means more than relying on old SOPs—our team constantly adapts, logs, and retraces steps whenever feedback from researchers, especially in pharma discovery, suggests even a slight hiccup in reactivity or impurity profiles.
A few years ago, we faced yield losses after a seemingly minor switch to a more generic base for the condensation stage. Data showed only a small spike in side products, but the shifts in yield wrecked batch-to-batch reproducibility. After several weeks of diagnostics and process mapping, our crew pinpointed the culprit—and improved final product by sourcing back to the earlier, higher spec reagent. This learning process translates to our ongoing commitment to spend more on reagents and less time working up off-spec product. It’s easy to speak of quality; it’s something else to stubbornly pursue it at every cycle.
We understand why so many chemists select 6,7-dimethoxy-3,4-dihydroquinazoline-4-one as a key building block. Its experienced hands in the lab will tell you that this core carries forward into all sorts of developmental drugs, from anticancer experimentals to agents targeting the CNS. Lead optimization campaigns in med chem almost always bank on quinazoline scaffolds, and it’s no exaggeration—a reliable, functionally pure intermediate like ours cuts down on re-checks, re-orders, and lost time.
Some buyers ask about agricultural applications or whether it can serve as a platform for specialty dyes. It’s not the first tool in those kits but the base quinazoline structure’s bioactivity means parallel explorations keep springing up. We routinely supply to both pharma and non-pharma groups, and those collaborations often return with unexpected application notes: anti-fungal screens, molecular probe building, and plenty in the academic world’s methodology arms race. No two years bring the same suite of end uses, but the thread remains: chemists need reliability and clarity, not unpredictability.
We’ve fielded plenty of requests for custom lot sizes. Institutes sometimes want only a few grams for early-stage SAR studies, while industry partners request multi-kilo campaigns matching tight impurity profiles and batch traceability. We don’t keep secrets about scale-up: isolation and drying behave differently at larger scales, and chasing 100-gram perfection in a single run usually means tweaking solvent volumes, mixing speeds, and temperature programs in ways that only years of hands-on work can fine-tune.
In the crowded landscape of small molecule intermediates, even minor differences lead to wildly altered research results. The addition of two methoxy groups to the quinazoline ring system changes both chemical properties and practical lab behaviors. Our experience shows that isomeric or “unprotected” quinazolinones, which many labs test in parallel, introduce unpredictability at several downstream synthetic steps. The 6,7-methoxy variants, by contrast, deliver more consistent nucleophilic aromatic substitution performance—something that keeps medicinal chemists from reworking their schemes at the analytical validation stage.
We’ve run controlled side-by-side syntheses with closely related compounds, and downstream impurity carryover ranks far lower with our dimethoxy variant than with plain 3,4-dihydroquinazoline-4-one. Liquid chromatography traces back up these findings. Many experienced chemists echo a familiar refrain: after switching to this material, less time goes into masking, scavenging, or trouble-shooting downstream protocols. Setting up a scale-up run for a partner in crop protection chemistry, they noticed early on that trace impurities—showing up as ghost peaks in intermediates—tracked back to insufficiently pure starting material from a third-party source. Using our 6,7-dimethoxy-3,4-dihydroquinazoline-4-one closed the case. Feedback like this informs our relentless pursuit of further improvements.
Every bottle of this compound that leaves our facility ties us to the recipient’s project, whether it’s a single vial in a university basement or a pallet bound for a contract manufacturing site. We know customers have questions: how best to store, how to avoid degradation, what analytical tools serve best for purity confirmation. We always give the same straightforward advice we use ourselves: reseal the container immediately after each use, store at recommended low humidity, and check with independent spectroscopy before critical experiments. LC-MS and NMR have unearthed the rare outlier, and we welcome those data sets—it’s the only way to improve further.
Most clients who’ve reached out about unexpected behavior in a reaction find that root causes stem from a misunderstood work-up or a supplier switch further upstream, not a problem with our product. But these conversations always sharpen our safety, traceability, and feedback systems. Several years ago, an international collaborator flagged what looked like an off-spec batch; shared spectra revealed that the change stemmed not from our material, but from sample mishandling during an intercontinental flight’s temperature fluctuations. Even with that, those details get rolled into our own training and storage improvement routines.
Even routine molecules throw curveballs thanks to volatility in reagents, supply chain breakdowns, and global shipping headaches. We’ve watched certain critical raw materials double in price with no warning, or dry up altogether, thanks to shifts in global regulation or weather events half a world away. During lean years, getting fresh, high-purity starting materials means juggling purchase orders, shipment routes, and customs bottlenecks, all while holding to delivery dates researchers base months of work around.
Fake or adulterated chemical products don’t just exist in rumor. We’ve seen plenty of them thrown into the market, often indistinguishable at first glance from authentic material. Our incoming control program now checks for fingerprint spectrum matches and, after earlier headaches, we digitally watermark every lot’s documentation to ensure traceability. Nailing down authenticity for buyers who’ve been burned by third-party traders helps both our reputation and the broader reliability of the research supply chain. If another manufacturer’s product causes headaches for an end-user, it reflects on the whole sector. So we work double-time to build in those safeguards.
Operating a chemical manufacturing site will force anyone to come to terms with waste, energy use, and safe labor practices. 6,7-Dimethoxy-3,4-Dihydroquinazoline-4-One preparation, handled at both small and large scale, generates solvent emissions and chemical byproducts we have to neutralize or recycle. Even now, process engineers tinker with distillation columns to cut down on solvent losses and adapt multi-use catalyst systems for better environmental performance. Adopting these upgrades isn’t about regulatory compliance alone; most long-stayers in this field recognize that waste reduction means saved costs and better working conditions.
On health and safety, we’ve seen fellow manufacturers trip up from underestimating the handling risks. Skin and eye irritation reports remind us that routine can breed complacency, so we never skip PPE and containment basics on the shop floor. Our staff’s experience serves as proof: regular refresher training and cultural accountability protect both employees and customers. Newer members of the team, seasoned after a year or two, become advocates for strict labeling, careful cleaning, and batch testing that old hands might otherwise overlook. That vigilance builds to safer outcomes and keeps us motivated to do better each production campaign.
Every feedback email, every troubleshooting call, and every late night result shapes the next run of 6,7-Dimethoxy-3,4-Dihydroquinazoline-4-One. What seems like a minor tweak to a reaction time or a stirring protocol sometimes reveals measurable boosts in purity or reduction in processing time. We cherish robust, repeatable processes, but our best material often emerges only after pushing through the discomfort of changing what “worked” before. Suppliers switch, equipment ages, regulatory standards go up—a commitment to ongoing learning bridges the gap from a manufacturing plant to cutting-edge scientific research.
Sometimes, new process analytics—using in-line FTIR or better temperature mapping—spot trouble before it becomes expensive waste. And after all these years, we make space for younger chemists’ ideas just as much as for senior engineers’ gut instincts. In this business, better practice isn’t taught, it’s lived every production shift. The same goes for cleaner workrooms, smarter use of automation, and more efficient energy management.
Some buyers expect all intermediates to come with the same headaches—batch variation, ambiguous paperwork, slow response times to technical questions. They often admit surprise at our dedication to technical transparency. Every run gets tied back to full batch records; every customer receives detailed analytical reports, not just numbers on a label. If a question arises, we connect end users directly with technical staff who’ve worked with this very molecule and handled reaction troubleshooting in real time. This practice has won more long-term trust than any sales pitch.
Having deep relationships with downstream scientists allows us to keep synchronizing process priorities. Analytical spec tweaks, storage condition modification, or even reworking our approach to breaking down bulk material—these improvements are driven by outside feedback as much as internal audits. We’ve found, through years of open discussion, that chemists aren’t looking for perfection so much as predictability and honesty about limitations. They recognize shortcuts and respect the effort invested in doing things right, even as timelines shrink.
6,7-Dimethoxy-3,4-Dihydroquinazoline-4-One isn’t ordinary—nor do we treat its manufacture as a one-size-fits-all routine. Each year, applications multiply as new research uncovers yet another use for this scaffold, whether as a drug candidate, research intermediate, or molecular tool. Our own approach evolves alongside: never standing still, always taking cues from those who trust us enough to test their most innovative ideas with our material. We see ourselves less as stationary producers and more as active participants in a constantly shifting scientific landscape.
All the investments in process control, analytic rigor, and customer relationships stem from one simple truth: the materials we make drive discovery, and every shortfall impacts projects that extend well beyond our walls. We take pride in every kilogram packed, every analytical report issued, and every shared lesson from partners and staff. As fresh challenges arise, we stay committed—to safer, cleaner, and more reliable production, and to serving a global scientific community that builds on our work every day.