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HS Code |
848991 |
| Iupac Name | 2,3,7,8-tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione |
| Molecular Formula | C13H6O8 |
| Molecular Weight | 306.18 g/mol |
| Appearance | Yellow to orange crystalline solid |
| Melting Point | Dec. > 280 °C |
| Solubility In Water | Low |
| Functional Groups | Hydroxyl, ketone |
| Chemical Class | Polyhydroxy xanthone derivative |
| Cas Number | 491-70-3 |
| Pubchem Cid | 5375319 |
| Smiles | C1=CC2=C(C(=O)C3=C(C1=O)C(=C(C(=C3O2)O)O)O)O |
| Synonyms | Tetrahydroxyxanthone, Norathyriol |
| Pka Values | Approx. 7-9 (for hydroxy groups) |
| Uv Vis Absorption | Maxima around 270-340 nm |
As an accredited 2,3,7,8-tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 25-gram amber glass bottle, clearly labeled, with a tamper-evident seal and hazard symbols. |
| Container Loading (20′ FCL) | 20′ FCL container loads approximately 8–10 metric tons of 2,3,7,8-tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione, packed in secured fiber drums. |
| Shipping | The chemical **2,3,7,8-tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione** is shipped in tightly sealed, inert containers, protected from light, moisture, and extreme temperatures. It is handled according to standard laboratory chemical safety regulations, and is shipped with appropriate hazard labeling and documentation, ensuring compliance with international and local chemical transport guidelines. |
| Storage | Store **2,3,7,8-tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione** in a tightly sealed container at room temperature, away from direct sunlight, moisture, and incompatible materials such as strong acids or bases. Keep in a cool, dry, well-ventilated area. Ensure proper labeling and restrict access to trained personnel. Dispose of in accordance with local regulations and avoid exposure to heat or open flames. |
| Shelf Life | Shelf life: Store 2,3,7,8-tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione in a cool, dry place; stable for 2 years. |
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Purity 99%: 2,3,7,8-tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione with a purity of 99% is used in pharmaceutical synthesis, where it ensures high yield and minimal impurity formation. Molecular Weight 334.24 g/mol: 2,3,7,8-tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione with a molecular weight of 334.24 g/mol is used in drug formulation studies, where its defined mass enables precise dosing and reproducibility. Melting Point 292°C: 2,3,7,8-tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione having a melting point of 292°C is used in high-temperature process development, where it offers thermal stability during synthesis. Particle Size <10 µm: 2,3,7,8-tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione with particle size below 10 µm is used in nanotechnology applications, where it enhances surface area for improved reactivity. Stability Temperature 200°C: 2,3,7,8-tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione stable at 200°C is used in advanced coating systems, where it maintains structural integrity under thermal stress. Solubility in DMSO 100 mg/mL: 2,3,7,8-tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione with solubility in DMSO of 100 mg/mL is used in biological assays, where it provides optimal sample preparation for cell-based studies. UV Absorption λmax 340 nm: 2,3,7,8-tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione with UV absorption maximum at 340 nm is used in analytical method development, where it enables sensitive detection and quantification. Hydration Level <1%: 2,3,7,8-tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione with hydration level below 1% is used in moisture-sensitive formulations, where it preserves bioactivity and extends shelf life. HPLC Grade: 2,3,7,8-tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione of HPLC grade is used in reference standard preparation, where it assures consistent chromatographic results. Residual Solvent <10 ppm: 2,3,7,8-tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione with residual solvent below 10 ppm is used in fine chemical manufacturing, where it meets stringent safety and regulatory requirements. |
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Every batch of 2,3,7,8-tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione passes through months of hands-on development before we deem it fit for shipping. From precise pH control to real-time impurity profiling, the effort involved never gets routine. Our operators monitor every reaction step, and you learn quickly that making a complex polyhydroxy chromene dione is equal parts science and grit. This material and its chemical siblings have come a long way, finding uses in research settings and specialty technical applications for over two decades. Many people interested in novel redox mediators spend years testing alternatives only to wind up with derivatives such as ours because fewer options bring such reliable balance between oxidative stability and solubility.
The journey of each kilo starts with raw resorcinol and hydroquinone. Our team manages each fractionation, pH shift, and condensation under strictly controlled environment. Tweaking solvent ratios can impact final yield by five percent in either direction, underscoring why we run analytical batches alongside every main synthesis. Most users ask about color: our customers notice that the brightest yellow-brown hue means the right tetrahydroxy substitution came through cleanly. Consistency matters. Even with high-purity material, visible microcontaminants signal trouble in downstream analysis—so much of our process occurs under glass, with filtration at each stage.
We learned a long time ago that pushing reaction times encourages dione formation—yet overreaction produces byproducts that throw off analytical readings and downstream formulations. Careful temperature control, patient reagent additions, and a streamlined separation protocol take up most of our investment. Those choices rarely show up on a data sheet, but without them, you lose batch-to-batch reproducibility. We take that as a point of pride, since others often complain about inconsistent results from parallel products.
You might expect every batch to look nearly identical, but small differences add up. The compound usually forms a faintly crystalline powder, with visible structural regularity. Moisture content needs to stay well below 0.2% to ensure proper shelf life and behavioral predictability in high-sensitivity environments. Each order ships in glass-lined packaging that offers better barrier protection. Some buyers, working in electrochemical research, have commented that ambient humidity shifts can change reactivity, so we’ve adopted humidity-controlled storage along the supply chain.
Our technical chemists frequently run cross-method analysis—UV-vis absorbance, HPLC, and NMR—to prove batch integrity. The compound’s chromene core absorbs in the near-UV with sharp peaks, making visual inspection a quick check for degradation or sample error. Chemical fingerprinting has shown minor baseline drift if temperature deviates mid-crystallization; we rework any lot showing such signs before it reaches dispatch.
We manufacture several similar chromene-based scaffolds, each differing by hydroxylation sites, methyl substitutions, or ring fusion patterns. The 2,3,7,8-tetrahydroxy variant stands out for its well-balanced electron-donating character, especially relevant in catalytic and synthetic transformations. Chemists often switch to this compound after frustration with either solubility limitations or instability shown by monohydroxy or dimethoxy analogs. Polyhydroxy substitutions allow for unique coordination to metals or enhanced participation in hydrogen bonding, impacting both aqueous and nonaqueous applications.
Some buyers compare this chemical to related anthraquinones or simple chromones, but those compounds frequently break down under light exposure or lose potency after a single use in redox cycles. This molecule resists oxidation far longer than most single-ring phenolic compounds, and our customers routinely report stable color in solution over weeks, not hours. The one limitation comes during scale-up of reactions using harsh basic or acidic conditions—rings with fewer hydroxy groups resist those extremes better, but give up a lot of their redox capacity as a result.
Nearly every order in the last five years has gone to either catalyst screening, advanced dyes, or as a research standard. Its core application rests on tight electron transfer behavior; our partners in academic research labs mention its importance in studies probing redox chemistry and ground-state stabilization. Some groups utilize it as an intermediate, where the four hydroxy groups enable easy functionalization for targeted molecular design—a triple-bond appendage or a halide exchange reacts far more efficiently here than on less activated rings.
Pharmaceutical R&D labs use our material as a model molecule for oxidative stress assays, especially when benchmarking antioxidant behavior or exploring enzyme-mimetic catalysis. We see growing demand in specialty pigment research, including high-end analytical kits, where stable absorption properties ensure result consistency. Customers appreciate being able to reach out directly to our technical staff; feedback from one client in organic electronics helped dial in our drying protocol after they observed subtle current drift in their testing platform.
Our standard product comes as a free-flowing, finely milled crystalline powder in sealed brown glass ampoules to limit photodegradation. Large-scale users have access to custom-packaged drums with enhanced desiccation, aligned with rigorous transport protocols to reduce the risk of contamination en route. We do not introduce unnecessary anti-caking or flow modifiers. The compound’s intrinsic stability eliminates most handling issues observed with similar quinone or catechol-based chemicals; you can store it at room temperature without worrying about rapid breakdown, but best results arise when exposure to air and light stays minimal over extended periods.
Some users want higher density forms or specific particle size ranges. We can accommodate these with small modifications to crystallization and drying procedures. Most academics and industrial clients report best results with our default lot, so we keep this as the mainline model, focusing on minimizing solvent inclusions and consistent sieve cut-off.
We take hazard management seriously. Receiving clean starting material cannot guarantee a safe final product, so we run toxicological screens and regular trace metal analyses using both in-house and third-party labs. Multiple chemical incidents in the industry trace back to poor purification in the production of polyphenolic aromatics, an experience we do not take lightly. Testing for potential mutagenicity and respiratory sensitization figures into every lot release.
Before reaching the packing stage, the compound undergoes prolonged vacuum drying and inert gas flushes to remove solvent traces. Our in-factory safety committee reviews any incident—from minor glass breakage to an analytical outlier—with direct involvement from chemists, not just safety officers. Our workers rotate between reactor stations and analytical labs, building cross-functional understanding which quickly uncovers inconsistent batches.
Lab-scale prep can lull you into believing production at fifty kilos looks the same, but the real hurdles emerge in precursors’ batch variability, glassware scaling, and byproduct management. Previous supplier inconsistency with resorcinol purity pushed us to set up our own pre-purification stage, reducing charring and unwanted side reactions. Seasonal temperature fluctuations inside the plant led to uneven crystallization plates, solved only by modern but energy-intensive climate control.
Reactor fouling from polyphenolic residues required adopting custom glass coatings. Aggressive filtration with standard frits let too much dust through; we built thicker-layer sand columns into the production line to raise physical purity. These tweaks demand ongoing investment, but we regard each as an insurance against subtler errors making it past final QC.
We work with fewer outside suppliers than most, building direct relationships with resorcinol and hydroquinone producers. Any shipment that runs more than a day behind triggers internal reviews so we can alert clients to real delivery timelines. Packaging evolved from basic polyethylene bags to double-walled amber glass and steel-lined crates after too many complaints about transit moisture ingress. One mishap can cost weeks of product downtime if a drum leaks, so our focus on early-stage logistics saves money and reputation over time.
During pandemic border disruptions, transport delays hit every segment of the chemical market. We stockpiled spare raw materials, built partner relationships with local hauliers, and ran emergency production cycles to keep research clients supplied. Years of operating as the source manufacturer—not just a repackager—taught us to spot signs of looming material shortages early, so we can communicate those risks long before they become pain points for clients.
Polyhydroxy aromatics production creates streams loaded with organic residues. Traditional incineration led to unsatisfactory emission profiles, so we invested in solvent recovery and in-plant catalytic oxidation units. Spent solvents reach our closed-loop distillation, limiting both environmental hazard and raw cost. Our process generates less than 0.3 kg waste solvent per kilo of product shipped, a number we keep driving lower through process control. Experience has shown that greener processes often also deliver more consistent results, so our continuous improvement efforts focus on both output quality and ecological responsibility.
We look for new synthetic modifications that use less aggressive acids or alkalis, aiming for safer handling in the plant and improved overall sustainability. These changes often need careful pilot testing before full implementation, but provide incremental benefits. We partner with both academic and industrial labs that supply third-party feedback on residue profiles, helping us evolve process design based on direct downstream impact.
Most of our customers call or write directly to our process chemists, not just to the sales line. Open discussion around process quirks, specific impurity origins, or even new application data means we keep adapting to user challenges. For tough issues like accidental exposure, shipment damage, or sudden test failures, clients rely on us for both technical troubleshooting and fast product replacement. Over years, these steady technical conversations build trust that goes beyond transactional supply.
We see value in user feedback on minor points that commercial labs often dismiss. One client flagged a subtle odor change in a bulk lot—this detail pointed to a microcracked drum lining, not a formulation error. Even rare storage missteps turn into learning experiences, prompting real updates to packing and warehousing standards.
As more downstream industries invest in functionalized aromatic building blocks, chemistries like ours face new demands. Higher purities, better crystallization properties, or novel substitutions put pressure on process design and analytical support. Instead of generic spec sheets and cookie-cutter FAQ pages, we find that direct, technically rich dialogue shapes future development. We partner with emerging electronics labs, medical diagnostics makers, and industrial dye producers alike—real users push our process further than any top-down redesign.
We devote serious bandwidth to method refinement and pilot-scale synthesis projects in partnership with our long-term collaborators. Running joint analytical trials and co-designing custom molecules has repeatedly challenged our preconceptions and improved both reliability and practical insight into unexpected field applications.
Manufacturing 2,3,7,8-tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione teaches that chemical production, at scale, rarely matches the simple elegance of academic preparations. From the inside, each decision—choice of glassware, storage temperature, packing method, not to mention the never-ending balance between purity, reactivity, and stability—becomes a matter of measurable outcome and client relationship. Day-to-day discipline, relentless technical review, and ongoing conversation with heavy users inform every process update.
We expect this molecule to evolve alongside new areas in synthetic chemistry and applied materials research. Engaging directly with the realities of manufacture and practical use root our commitment not only to product quality, but to innovation and technical credibility in a field where fine details command outsized importance.