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HS Code |
166323 |
| Iupac Name | 1',3',3'-trimethyl-6-nitro-1',3'-dihydrospiro[chromene-2,2'-indole] |
| Molecular Formula | C20H19N3O3 |
| Molar Mass | 349.39 g/mol |
| Appearance | Yellow to orange solid |
| Melting Point | 176-178°C |
| Boiling Point | Decomposes before boiling |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in ethanol, DMSO, chloroform |
| Cas Number | 36840-86-1 |
| Smiles | CC1(C2=CC3=C(C=C2[N+](=O)[O-])OC4=C1N(C)C=C4)C(C)(C)C3 |
| Chemical Class | Spirooxazine |
| Functional Groups | Nitro, methyl, spirocyclic, indoline, chromene |
| Color Change Property | Photochromic (colorless to colored under UV) |
| Storage Conditions | Store in a cool, dry place, protected from light |
As an accredited 1',3',3'-trimethyl-6-nitro-1',3'-dihydrospiro[chromene-2,2'-indole] 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 5-gram amber glass bottle with a screw cap, labeled with compound name, purity, and hazard information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 1',3',3'-trimethyl-6-nitro-1',3'-dihydrospiro[chromene-2,2'-indole]: Securely packed, moisture-proof, labeled drums or bags for safe chemical transport in a 20-foot container. |
| Shipping | **Shipping Description:** 1',3',3'-Trimethyl-6-nitro-1',3'-dihydrospiro[chromene-2,2'-indole] is shipped in a tightly sealed container, protected from light and moisture. Handle as a laboratory chemical; ensure packaging prevents breakage and leakage. Accompany with appropriate safety documentation. Transport in compliance with local regulations, using appropriate labeling for organic compounds and any hazardous attributes. |
| Storage | Store **1',3',3'-trimethyl-6-nitro-1',3'-dihydrospiro[chromene-2,2'-indole]** in a tightly sealed container in a cool, dry, well-ventilated area, away from direct sunlight and sources of ignition. Keep separate from strong oxidizers and acids. Use only in a chemical fume hood and avoid prolonged exposure to air and moisture. Ensure proper labeling and access only to trained personnel. |
| Shelf Life | Shelf life of 1',3',3'-trimethyl-6-nitro-1',3'-dihydrospiro[chromene-2,2'-indole]: Stable for 2 years if stored cool, dry, protected from light. |
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Purity 98%: 1',3',3'-trimethyl-6-nitro-1',3'-dihydrospiro[chromene-2,2'-indole] with 98% purity is used in photochromic dye formulations, where it ensures consistent and reversible color change under UV exposure. Melting Point 186°C: 1',3',3'-trimethyl-6-nitro-1',3'-dihydrospiro[chromene-2,2'-indole] with a melting point of 186°C is used in thermal imaging sensor manufacturing, where it provides high thermal stability during device operation. Particle Size <10 μm: 1',3',3'-trimethyl-6-nitro-1',3'-dihydrospiro[chromene-2,2'-indole] with particle size below 10 μm is used in precision inkjet printing, where it delivers fine resolution and uniform color distribution. Stability Temperature up to 120°C: 1',3',3'-trimethyl-6-nitro-1',3'-dihydrospiro[chromene-2,2'-indole] stable up to 120°C is used in light-sensitive polymers, where it maintains optical performance in elevated temperature environments. Molecular Weight 366.40 g/mol: 1',3',3'-trimethyl-6-nitro-1',3'-dihydrospiro[chromene-2,2'-indole] with molecular weight 366.40 g/mol is used in organic electronics research, where its defined structure enables reproducible charge-transfer studies. |
Competitive 1',3',3'-trimethyl-6-nitro-1',3'-dihydrospiro[chromene-2,2'-indole] prices that fit your budget—flexible terms and customized quotes for every order.
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Manufacturing unique fine chemicals involves precision, effort, and a clear understanding of how even the smallest difference in a molecule’s structure can give rise to specific properties that our customers depend on. One compound that stands out in our lineup is 1',3',3'-trimethyl-6-nitro-1',3'-dihydrospiro[chromene-2,2'-indole]. Through years of hands-on production and quality testing, we have come to appreciate what makes this molecule noteworthy and where it finds its place among competing dyes and indicators.
In the world of chemical manufacturing, certain structures carry special traits. The spiro linkage connecting chromene and indole rings delivers a unique blend of stability and reactivity, a combination necessary when aiming for sensitivity in environmental or analytical applications. Our direct experience confirms that the three methyl groups not only enhance solubility in a variety of organic solvents, but they also subtly affect both color and switching behavior. Integrating the nitro group at the 6-position shifts absorption characteristics, making this molecule useful for specialized photochromic and solvatochromic projects, as well as trace-level colorimetric detection.
Our chemists have spent countless batches tuning reaction conditions to consistently yield pure, crystalline material, which matters in lab and industry workloads alike. By steady optimization of solvents, reaction temperature, and purification methods, we keep product quality consistent run after run. In contrast to heavily substituted analogues, the specific pattern of methyl and nitro substituents here strikes a balance: easy dissolution avoids clumping in typical carriers or matrices, and well-defined reactivity makes it preferable to non-nitro analogues for applications that demand photochemical response without sacrificing shelf life.
From customer feedback and our own R&D group, we know demand for stable, switchable dyes is not limited to a single sector. One of the primary uses grows out of the distinctive color-changing property that develops upon exposure to acid, base, or polarized light—making this compound valuable as a pH indicator and sometimes in security printing. The underlying reason lies in the way the spiro carbon serves as a pivot point for electron shifting. Subtle differences in ring electronic environments translate to clear visual transitions, appreciated by both research chemists and industry manufacturers.
Our experience with this product demonstrates good compatibility in organic polymer matrices, which expands the range of end uses. Scientists seeking a reversible, visible signal incorporate this dye into plastic films and coatings for reversible labels or anti-counterfeiting marks. Compared to more traditional dyes, the fuller spiro[chromene-indole] structure grants better resistance to unwanted side reactions during polymer processing, a fact we can confirm after subjecting both trial batches and scaled-up productions to heat and UV stress tests.
Each batch comes off our reactors having met rigorous internal QA thresholds; we focus on purity and crystal habit because these tunables affect not only reactivity, but downstream processing in customer setups. Staff pour decades of synthetic know-how into selecting the right crystal seeding and filtration steps, and tweaks in washing solvents often improve outcomes more than increasing scale. This level of craftsmanship gives our clients confidence when running batch after batch of sensitive diagnostic kits or photochromic plastics—testimonials have confirmed a noticeable performance difference compared to lower-quality imports, especially in lab bench settings that must operate without downtime.
It helps that our lab remains hands-on. Our technical team—consisting mainly of chemists—stays alert to shifting patterns of demand. As regulations tighten on certain classes of dyes, the precise matching of substituents in 1',3',3'-trimethyl-6-nitro-1',3'-dihydrospiro[chromene-2,2'-indole] ensures compliance with the latest standards. Years ago, reports of unwanted migration of free nitroaromatics in pigment films highlighted the need for stable linkages, and our process purposely limits potential for byproduct formation. As a result, not only do we achieve greater repeatability in downstream application, but handling characteristics meet the needs of both bulk blenders and high-precision formulators.
In competitive chemical supply, substituent choices separate true specialty materials from generic ones. Our product carries three methyl groups and a nitro group in specific locations for targeted effect. Running stability and lightfastness tests side-by-side, we observe that analogues lacking the nitro group usually begin to fade faster under UV exposure. Nitro-free versions suit applications calling for pure photo-stability, but in use cases focusing on responsiveness—either as a switching dye or trace indicator—our 6-nitro compound simply outperforms.
Several customers once considered basic spiro[chromene-indole] variants before moving to this upgraded version. The reason: reliability in routine high-throughput testing. Consistency in color shift (rather than muted or “off” tones), better powder flow, and the lack of detectable off-odors all factored into their switch. Detailed reports sent from downstream quality control labs often contain side-by-side photographs of reactions—images that unmistakably reveal why small modifications in ring structure matter. This level of feedback helps us refine further, and confirms the impact of thoughtful engineering at the molecule level.
Not every compound can claim a role in both research and scaled production, but our experience suggests that this chemical serves both. University labs often order it for teaching photochemistry and as an exemplar of spiro compound reactivity in advanced synthesis courses. The clear, strong color change—even visible from across a classroom—lets students understand in real time what their theoretical lessons promise. At volume, coating manufacturers and diagnostic assay designers specify our product for its consistency: the same transitions, batch after batch, across different polymer hosts or solvent blends.
Production feedback drives ongoing adjustments. Our facility’s logbooks track peaks in demand by application type. Certain seasons bring more requests from synthetic chemists using the compound as an intermediate for advanced molecules. At other times, colorant manufacturers come calling, looking for convincing color shifts in consumer goods. By refusing to cut corners on key inputs and strict oversight during multi-step synthesis, we touch off fewer headaches for downstream users who otherwise waste hours fixing preventable issues—clumping, degradation, or incompatibility with plasticisers—which bedevil suppliers who take a cheaper, less controlled production route.
It’s tempting to push capacity without tightening controls, but across decades, we’ve learned that reliable quality wins customer trust. Every kilogram exhibits the same color strength, solubility, and crystalline form—verified by spectra, melting range, and physical assays in our quality control lab. Many of our long-term partners, who came to us after struggling with uneven batches elsewhere, stay loyal because replacements for off-batch material cost far more in lost time than any upfront savings from bargain suppliers. In technical dye spaces, one bad lot can sink an entire week’s worth of production or, worse, compromise regulatory filings.
People on our production floor take pride in seeing that signature deep yellow or red crystalline form at every inspection. They know sweat and expertise go into every reactor charge, and they take personal interest in every customer’s project. This approach feeds back into continuous improvement: real-world loading levels, temperature tolerances, and solvent compatibility factors all shape tweaks to our protocols.
Creating 1',3',3'-trimethyl-6-nitro-1',3'-dihydrospiro[chromene-2,2'-indole] in bulk involves more than mixing ingredients. The nitro group’s presence adds risk in both forming and handling intermediates, demanding rigorous attention to reaction conditions and safety practices. Mistakes in temperature, pressure, or reagent quality, even at trace levels, spiral into lost yield or out-of-spec batches. Years ago, we lost several lots early in scale-up, before refining our temperature profiling step and source monitoring for amine and aldehyde inputs. Each hard-won lesson became standard operating procedure, now saving headaches for new staff.
Disposal and environmental controls play as big a role as bench chemistry. Treatment of nitro-aromatic byproducts follows waste minimization best practices. Our internal review committee oversees each process revision to keep emissions low and workplace safety high. We share regular updates with local environmental oversight groups, staying ahead of changing rules so our chemists keep working without interruption.
Research partnerships fuel progress. Our site welcomes academic and industrial visitors interested in joint development or scale-up. Countless conversations have sharpened our approach—sometimes a minor procedural change led jointly with a customer has cut production time without denting purity. We once worked side by side with a large-coating firm’s chemists to pre-test solubility in a novel plasticizer, extracting data that ended routine quality-control failures. Such collaborative efforts let us bridge the gap between benchtop discovery and factory scale, a trait not all chemical makers can claim.
Industry gatherings and conferences deepen insight into the technical needs facing end users. Photonics lab researchers have shown us laboratory notebook pages detailing the precise kinetic profiles they seek, helping us tweak batch conditions for higher responsiveness. Diagnostic firms under tight regulatory scrutinies pass along technical bulletins that we build into our standard specification checks. Whether in conference halls or onsite visits, dialogue beats guesswork every time.
Making fine chemicals at scale brings another set of realities—raw materials rise and fall in price or may suddenly become scarce. Our procurement division learned to diversify sourcing after early disruptions, and we strengthen relationships with raw material producers who offer steady, high-quality feedstocks. Fluctuating prices for substituted indoles or aromatic aldehydes matter less when we forecast and secure back-up suppliers. Our forward contracts and contingency planning mean customers rarely face delays, even when global events slow logistics elsewhere.
We also invest in keeping up-to-date on changing regulations regarding nitro aromatics, chromene derivatives, and solvent use. Internal compliance experts guide our product teams, ensuring continued confidence for large customers who cannot risk surprises from discontinued reagents or last-minute formula tweaks due to overlooked restrictions. We log and address every batch issue as a learning opportunity, translating those lessons into tighter process controls and stronger relationships with customers downstream.
Advances in synthetic chemistry continue to shape our methods. Automation in reactor control, data-driven process analysis, and the adoption of safer, more efficient solvents form the backbone of ongoing upgrades. Each new advance grew from deep in-plant experience—knowing which controls deliver the best batch-to-batch reproducibility and how minor phase changes during crystallization impact both usability and shelf life.
New research developments keep pushing the envelope. Custom derivatives and application-specific modifications remain a future growth area we watch closely. Whether customers seek faster switching, enhanced stability, or compatibility with new composite materials, we keep laboratory and production staff connected so feedback travels rapidly. Upcoming development cycles will focus especially on formulations for smart sensors and next-generation diagnostic kits, areas demanding the reliability and performance characteristics we have honed.
Working with partners through cycles of R&D and volume production means chasing more than transient profits. We invest in robust documentation, transparent communication, and steady supply because our customer’s work depends on it. Loyalty goes both ways: supporting customers as they scale up secures both market stability and shared technical progress. Feedback taken seriously, from field-application scientists and technical directors alike, goes back into the lab and shapes how technicians approach every reaction run.
Many of the world’s most promising research projects or consumer innovations still begin with molecules produced by hand and watched over by people who care deeply about purity, reliability, and long-term supply. Our focus on 1',3',3'-trimethyl-6-nitro-1',3'-dihydrospiro[chromene-2,2'-indole] delivers exactly those values, with every step of manufacturing shaped by decades in the industry—not just standard specifications copied from textbooks, but the precise adjustments, technical conversation, and pride that underline a real manufacturer’s work.