|
HS Code |
422633 |
| Iupac Name | 6-nitro-1H,3H-benzo[de]isochromene-1,3-dione |
| Molecular Formula | C11H5NO5 |
| Appearance | yellow crystalline solid |
| Melting Point | approximately 250°C (decomposes) |
| Solubility In Water | slightly soluble |
| Logp | approximately 1.5 |
| Cas Number | 6040-91-5 |
| Pubchem Cid | 33453 |
| Smiles | O=C2OC(=O)c1ccc(cc1C2)[N+](=O)[O-] |
| Inchi | InChI=1S/C11H5NO5/c13-9-7-3-1-2-6-4-8(12(15)16)5-10(6)11(7)17-9/h1-5H |
| Density | 1.59 g/cm3 |
| Boiling Point | decomposes before boiling |
| Synonyms | 6-nitro-1,3-dihydro-1,3-dioxo-benzo[de]isochromene |
As an accredited 6-nitro-1H,3H-benzo[de]isochromene-1,3-dione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 10 grams, tightly sealed with screw cap, labeled with chemical name, hazard symbols, and batch information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely packed 6-nitro-1H,3H-benzo[de]isochromene-1,3-dione drums or bags, maximizing container capacity, ensuring safe, compliant transportation. |
| Shipping | **Shipping Description:** 6-Nitro-1H,3H-benzo[de]isochromene-1,3-dione should be shipped in tightly sealed containers, away from light, moisture, and incompatible substances. Package according to local, national, and international regulations for potentially hazardous laboratory chemicals. Appropriate labeling and documentation, including Safety Data Sheets (SDS), are required. Handle with care to prevent spills and exposure. |
| Storage | 6-nitro-1H,3H-benzo[de]isochromene-1,3-dione should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat sources, moisture, and direct sunlight. Avoid storing near incompatible materials such as strong oxidizing agents and bases. Clearly label the container, and handle under appropriate safety conditions, including the use of gloves and eye protection. |
| Shelf Life | 6-nitro-1H,3H-benzo[de]isochromene-1,3-dione is stable for at least 2 years when stored cool, dry, and protected from light. |
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Purity 98%: 6-nitro-1H,3H-benzo[de]isochromene-1,3-dione with a purity of 98% is used in pharmaceutical intermediate synthesis, where high-purity material ensures minimal by-product formation. Melting point 265°C: 6-nitro-1H,3H-benzo[de]isochromene-1,3-dione with a melting point of 265°C is used in high-temperature pigment manufacturing, where thermal stability supports color fastness. Particle size <10 μm: 6-nitro-1H,3H-benzo[de]isochromene-1,3-dione with a particle size of less than 10 μm is used in coating formulations, where fine dispersion enhances surface uniformity. Molecular weight 273.18 g/mol: 6-nitro-1H,3H-benzo[de]isochromene-1,3-dione with a molecular weight of 273.18 g/mol is used in organic electronics research, where molecular uniformity improves device reproducibility. Stability temperature up to 200°C: 6-nitro-1H,3H-benzo[de]isochromene-1,3-dione stable up to 200°C is used in polymer additive applications, where temperature resistance prevents degradation during processing. |
Competitive 6-nitro-1H,3H-benzo[de]isochromene-1,3-dione prices that fit your budget—flexible terms and customized quotes for every order.
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Manufacturing 6-nitro-1H,3H-benzodeisochromene-1,3-dione demands a long track record with heterocyclic core chemistry. Our approach focuses on delivering robust performance batch after batch, tuned directly with feedback from chemical engineers and R&D teams who use this compound in organic synthesis, dyes, and advanced materials. Over the years, handling stringent process requirements, we have learned to emphasize reproducibility. The tiniest inconsistency in purity or particle size can create headaches during scale-up or downstream application. For this molecule, minor synthetic shortcuts can cause color impurities, and smart purification routes are required to yield the distinctive yellow crystalline product recognized by experienced chemists.
Every synthesis route starts with carefully controlled nitration reactions. Substituents on the isochromene scaffold influence reactivity during cyclization and ring closure. Temperature control, reagent feed rates, and reaction vessel design all play roles in controlling side products and boosts yield. We take pains to eliminate residual acids and metal traces, since these negatively impact polymeric end uses and can shorten shelf life during storage. Molecular sieves, continuous separation, and proprietary filtration protocols are applied; these came about through direct troubleshooting alongside production line operators — improvements that often get overlooked in academic writeups or by those who simply repackage third-party material.
Chemistry leaves no room for loose tolerances. Our 6-nitro-1H,3H-benzodeisochromene-1,3-dione product achieves typical purities above 99%, verified by HPLC and NMR, not just melting point. Light stability has proven just as crucial as purity — exposure to harsh lighting conditions causes degradation and unwanted by-products. So past process improvements have focused on shortening time between crystallization and packaging.
Batch-level consistency matters to formulators developing dyes for technical textiles or pigment precursors for specialty coatings. Most off-the-shelf material, especially from broad-line distributors, arrives with variable particle size or even inconsistent polymorphic forms. Through milling and controlled drying steps, we fix polymorph ratios and reduce dusting losses. Discussions with end users convinced us to customize packaging: sealed drums for long-term inventory and smaller, vacuum-packed sachets for high-throughput screening labs.
Moisture control cannot go unmentioned. Isochromene derivatives absorb atmospheric water, leading to clumping and decomposition — an issue first spotted while supporting a customer transitioning from gram to kilogram scale in an additive production run. The switch to moisture-barrier liners made a significant impact, leading to more reliable dissolving during reaction set-up and higher overall yield for their customer.
6-nitro-1H,3H-benzodeisochromene-1,3-dione serves a range of chemical, industrial, and material science functions. In R&D, this compound often emerges in multi-step synthetic pathways toward advanced fluorescent dyes, photosensitive intermediates, and pharmaceutically active scaffolds.
Textile chemists regularly use this molecule as a building block for vat dyes and pigments that survive harsh industrial washing. Its fused ring system gives pigments based on this core both depth and durability lacking in simpler aromatic nitro compounds. In the field of specialty coatings, the nitro group position and steric hindrance influence dispersion in resin matrices. Product requests from coating manufacturers have led us to maintain batch-to-batch control over isomer content and exclude chlorinated side impurities, which affect color fastness and compatibility with various binders.
Semiconductor formulators and optical material developers push requirements farther still. Isochromene-1,3-dione derivatives such as this act as key intermediates in charge-transport layers and fluorescent markers. Here, it’s not enough to hit a percentage purity — specific UV/Vis absorption spectra and photostability become mission critical. Analytical investment over the past decade included scaling up spectroscopy capacity so we can provide certificate-backed spectral characteristics along with each shipment.
Pharmaceutical researchers source this compound for its isochromene backbone, which is adaptable for lead optimization in synthetic medicinal chemistry. Subtle ring modifications attach to the base structure, and trace metal contamination or remaining acid jeopardizes downstream biological evaluation. From process design to analytical control, experience working with process chemists and medicinal chemistry labs has shown that shortcuts in raw material consistency directly affect both yield and clean-up times.
Not all suppliers of 6-nitro-1H,3H-benzodeisochromene-1,3-dione address the entire scope of actual user needs. Resellers and trading houses tend to treat this molecule as a generic commodity: they focus on basic purity and pricing, fill orders on a spot basis, and lack the capacity for technical support. As a direct manufacturer, long-term relationships with clients have shown us how critical reliability and detailed technical dialogue become, once a compound leaves the catalog and moves into development or production.
Customer feedback from a wide range of industries emphasizes process compatibility, not just analytical purity. With larger-scale supply, issues such as blending consistency, minimal dust, and rapid dispersion rise to the surface. Pigment houses demand reproducible shade strength; polymer compounders want melt-extrusion efficiency without viscosity spikes. Such challenges are rarely solved by repackaging commodity-grade material produced elsewhere.
Yields on every batch are tracked and reviewed, and continuous improvement runs through our operation. Chemists have an open line to production, and process change decisions come not from marketing, but from hands-on knowledge gained during reaction monitoring, distillation, or troubleshooting filtration steps. Sometimes this means extending an extra recrystallization cycle or investing in smaller-scale drying to rescue a batch destined for a sensitive application. By investing in specialized containment and doing real-world comparison runs, we avoid the kind of variability that crops up from mixing product sourced from multiple makers.
Many products on the open market originate from brokers buying from anonymous factories, often with limited technical oversight. Their documentation lists the bare minimum, typically showing a melting point and purity, while batch performance fluctuates. Diverse customer projects require much more. Large molecule manufacturers occasionally send us failed samples for analysis after repeated issues — letting us see firsthand what happens when trace by-products sneak through, or when uncontrolled particle sizing creates process jams.
One of the main distinctions comes from in-process control. Nitrophthalic anhydrides from secondary suppliers often contain residual Aniline or phthalic acid derivatives, which produce off-notes and color drift in dye applications. Our oversight begins at raw material screening: every aromatic precursor passes through qualification and identity testing for improved reproducibility. Lessons from partnering with process engineers made it clear that skipping these steps quickly undermines even high initial purities.
Focusing on this single product enables thorough understanding of minor structural isomers, which form during the reaction sequence. In some applications, like semiconductors or advanced imaging, even sub-percent levels matter, so we set upper limits on individual impurities and supply analytical breakdowns, not just a total assay. This nitro isomer preparation rarely comes from third-party traders, who are more likely to blend various lots for convenience. For users concerned with photostability, we maintain historic reference samples and track long-term color and spectral drift, which allows a level of accountability not possible when buying untraceable material.
Handling these details internally lets us support custom modifications. A formulary request might specify additional purification by chromatography, or micronization to an exacting particle size. Research teams also ask for trace analytical characterization far beyond typical vendor certificates, seeking assurances on contamination risk for pharmaceutical or microelectronic trial runs.
We see the outcome of slow process refinement in every drum we ship. Major challenges always come from unexpected directions: variable humidity levels in storage, pressure fluctuations during nitration, occasional equipment anomalies. The team prioritizes in-person reaction monitoring rather than automation alone. Problems like emulsion formation in extraction, caking during drying, or odd solvate forms in crystallization often require immediate adjustments with active chemist oversight. All these measures translate to higher reliability for our customers.
Neglecting real-world demands often means lost batches, lower customer yields, or major delays at scale-ups. Getting to know each customer's requirements on a first-hand basis, sometimes through on-site visits or joint root-cause investigations, has shaped nearly every update to our process. In one recent example, adoption of new drying techniques based on a client’s request resulted in a marked decline in off-odor complaints and an improvement in reactivity for downstream reactions.
Shipping schedules fluctuate less once both parties understand expectations for lead times, documentation, and volume flexibility. Larger plants often have internal capacity constraints, needing coordination to avoid overstocking or running short. Our advantage comes from being able to throttle batch sizes and offer technical reports, not just invoices and bills of lading.
We view our responsibilities not just in terms of supplying a molecule, but as partnership: troubleshooting with product designers, R&D chemists, and production managers. As users shift goals or explore new end-use avenues, requirements evolve. Pharmaceutical researchers, in particular, have shown increasing demand for non-standard analogs with specific nitro and ring substitutions. Helping clients screen for rare impurities or adapt crystallization conditions to match strict dissolution profiles has become part of routine collaboration.
Pilot runs, scale-up projects, and rush orders all place unusual demands on supplier responsiveness. Stepping through every process from order placement to documentation, shipment, and feedback loops is vital, as is being available by phone or remote call to answer technical questions live. Transparent sharing of spectral data, repeat process summaries, and lessons from failed lots defines mutual reliability. Traders rarely provide this background, but the hands-on producer builds reputation through timely problem-solving.
The best solutions rarely come from off-the-shelf material — whether it’s a request for decagram samples for initial feasibility or freight-scale volumes for ongoing production, direct engagement fosters trust and helps prevent costly missteps.
6-nitro-1H,3H-benzodeisochromene-1,3-dione delivers value only through sustained commitment to its real-world use. By staying on the manufacturing side, we keep our processes visible, our technical staff engaged, and our solutions tied to what customers face in practice, not in the abstract. Years of listening to users and walking lines alongside them have taught us to address more than chemical formulae: we solve for reliability, process safety, and innovation hand-in-hand with each client. That is the difference between delivering a barcode and advancing chemistry together.