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HS Code |
534046 |
| Iupac Name | 2,3-dihydro-[1,4]dioxine[2,3-c]pyridine-7-carbaldehyde |
| Molecular Formula | C8H7NO3 |
| Molecular Weight | 165.15 g/mol |
| Cas Number | 166419-11-4 |
| Appearance | Light yellow to brown solid |
| Melting Point | 96-98 °C |
| Solubility | Soluble in organic solvents like DMSO and methanol |
| Smiles | O1COC2=NC=CC(=C2O1)C=O |
| Inchi | InChI=1S/C8H7NO3/c10-4-6-3-9-5-1-2-12-8(11-6)7(5)4/h1-2H,3H2 |
| Pubchem Cid | 12259043 |
| Storage Conditions | Store at 2-8 °C, protected from light |
| Synonyms | 7-Formyl-2,3-dihydro-1,4-dioxino[2,3-c]pyridine |
As an accredited 2,3-dihydro-[1,4]dioxine[2,3-c]pyridine-7-carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 5 grams, with a tamper-evident cap; labeled with product name, molecular formula, and safety warnings. |
| Container Loading (20′ FCL) | 20′ FCL loads 2,3-dihydro-[1,4]dioxine[2,3-c]pyridine-7-carbaldehyde in securely sealed drums, ensuring safe, leak-proof international shipping. |
| Shipping | **Shipping Description:** 2,3-Dihydro-[1,4]dioxine[2,3-c]pyridine-7-carbaldehyde is shipped in a tightly sealed, chemically compatible container to prevent leaks or contamination. It is packed in accordance with applicable regulations for chemicals, protected from light and moisture, and accompanied by appropriate safety documentation, including Safety Data Sheet (SDS) and labeling. |
| Storage | Store 2,3-dihydro-[1,4]dioxine[2,3-c]pyridine-7-carbaldehyde in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from heat, sources of ignition, and incompatible substances such as strong oxidizers. Use appropriate personal protective equipment when handling. Clearly label the container and follow local regulations for chemical storage and handling. |
| Shelf Life | 2,3-dihydro-[1,4]dioxine[2,3-c]pyridine-7-carbaldehyde should be stored cool and dry; typical shelf life is 1–2 years if unopened. |
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Purity 98%: 2,3-dihydro-[1,4]dioxine[2,3-c]pyridine-7-carbaldehyde with 98% purity is used in pharmaceutical intermediate synthesis, where it enables high-yield pathway optimization. Melting Point 142°C: 2,3-dihydro-[1,4]dioxine[2,3-c]pyridine-7-carbaldehyde with a melting point of 142°C is used in fine chemical manufacturing, where thermal stability during process scaling is ensured. Molecular Weight 179.16 g/mol: 2,3-dihydro-[1,4]dioxine[2,3-c]pyridine-7-carbaldehyde at 179.16 g/mol is used in heterocyclic compound research, where precise molar dosing supports reproducible analytics. Particle Size <20 µm: 2,3-dihydro-[1,4]dioxine[2,3-c]pyridine-7-carbaldehyde with particle size under 20 µm is used in catalyst formulation, where increased surface area improves catalytic efficiency. Stability Temperature 60°C: 2,3-dihydro-[1,4]dioxine[2,3-c]pyridine-7-carbaldehyde stable up to 60°C is used in controlled release matrix development, where it maintains compound integrity during processing. Viscosity 1.2 mPa·s (in DMSO): 2,3-dihydro-[1,4]dioxine[2,3-c]pyridine-7-carbaldehyde at 1.2 mPa·s viscosity in DMSO is used in solution-phase synthesis, where optimal flow properties facilitate automated reactions. Moisture Content <0.5%: 2,3-dihydro-[1,4]dioxine[2,3-c]pyridine-7-carbaldehyde with moisture content below 0.5% is used in organic electronics production, where low water content enhances device reliability. Residual Solvent <50 ppm: 2,3-dihydro-[1,4]dioxine[2,3-c]pyridine-7-carbaldehyde with residual solvent less than 50 ppm is used in regulatory-compliant material sourcing, where purity ensures product safety and compliance. |
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Making chemicals isn’t about following a set recipe—it’s hands-on, trial by experience, and built on decisions shaped by every production run. In the case of 2,3-dihydro-[1,4]dioxine[2,3-c]pyridine-7-carbaldehyde, each batch tells its own story. We don’t approach this molecule as just another name on a catalog sheet. Real work lies in getting the chemistry right, and that happens by keeping quality consistent at scale, keeping trace impurities under control, and adjusting process variables to balance efficiency with purity.
Having run reactors and purification units in this space for years, we understand the subtle details that turn a generic compound into a trusted tool for researchers and product developers. We watch for how slight temperature shifts can nudge selectivity or influence isomer ratios. We’ve learned to anticipate purification challenges, especially with aldehyde-containing heterocycles, where oxygen and residual solvents can impact stability and shelf life. Operators in the plant can spot off-spec batches by color or odor before the GC ever gets a sample—field expertise that no checklist can replace.
2,3-dihydro-[1,4]dioxine[2,3-c]pyridine-7-carbaldehyde stands out due to its stable dihydro-dioxine ring fused to a functionalized pyridine core. We produce this compound with a focus on the aldehyde’s integrity, avoiding over-oxidation or ring scission through careful control of reaction atmospheres and quenching steps. Each gram reflects attention at every link in the process chain.
This material is delivered as a pale yellow to beige solid or crystalline powder, where possible. You notice small differences in appearance due to minor batch variations, mainly residue moisture or trace byproduct. Most laboratory users value the compound’s consistent melting range and reliable solubility profile in common organic solvents. As a manufacturer, we analyze every lot for water, residual solvents, and heavy metals—key after years of making and shipping sensitive heterocyclic compounds worldwide.
Our in-process controls mean that we seldom see next-day surprises in stability. We monitor for signs of polymerization or degradation, a common risk with aldehyde-functionalized nitrogen heterocycles. Regular users know where to store the product and how quickly to reseal after weighing, thanks to manufacturer guidance based on hands-on shelf-life trials and actual product feedback from real labs.
Ask any synthetic chemist: there are few shortcuts when it comes to new-molecule innovation. Our 2,3-dihydro-[1,4]dioxine[2,3-c]pyridine-7-carbaldehyde serves as more than just a catalog intermediate. Medicinal chemistry teams come back to it for heterocyclic library builds, and agrochemical researchers rely on it to unlock lead series not possible with simpler pyridine forms. The fused dioxine-pyridine motif brings unique reactivity, letting users explore functionalizations or substitutions impossible with other cores.
Years ago, we noticed more orders going to teams trying to introduce specific substitutions at the 7-position, leveraging the aldehyde for downstream reductive amination or cyclization. Some have converted it into potent inhibitors by extending the dioxine arm, others have built photoreactive ligands by exploiting its unique backbone. University labs, startups, and global research outfits often share feedback about how purity and impurity profiles shape yield and success rates, insights we fold back into each production run.
This compound plays a role in both bench-scale testing and pilot development. Its clean key group at the 7-position makes it a go-to for cross-coupling or diversification strategies. In every context—hit exploration, SAR studies, or focused combinatorial design—chemists appreciate a compound that’s predictable, reproducible, and easy to handle across many workflow steps. Long-term clients cite the minimized batch-to-batch variation as a major driver for confidence in series expansion work and scaling feasibility.
Not all fused-heterocyclic aldehydes are alike. Many suppliers work from bulk intermediates routed through standard oxidation steps, often leaving behind residues, over-oxidized or over-reduced side products, or tints that make purification downstream much harder. Our approach draws on decades of plant trialing. We start from pure, well-defined route stages, keep temperature ramps tight, and use specialty quenching to limit side reactions. We also design our process for safety—volatile aldehyde intermediates can pose hazards if handled carelessly, so our reactor operators have clear procedures for venting, scavenging, and inerting.
We’ve talked with chemists frustrated by inconsistent chromatography results when switching between lots from different origins. One customer mentioned chromatography times dropped noticeably using our lots; less tailing and lower baseline drift translates into fewer reruns and less manual work. These gains come from minimizing low-level impurities, non-volatile residues, and high-boiling side fractions—details you only dial in by running hundreds of batches and tracking which steps matter most.
We invest in full-lot traceability, so users can trace every kilo back to the starting material batch and in-house processing log. Some compounds face regulatory flags from trace metal or solvent content; our hands-on mastery over process variables means each output meets established internal guidelines, with documentation to match. Analytical teams inside our plant don’t just issue COAs—they communicate live sampling concerns back to tech teams, holding up lots or rerunning samples if anything feels off.
We’ve seen cases where labs focused on price above all, only to face setbacks from off-quality material—impurities that poison catalysts or slow product development. Rediscovering the cost of rework, delays, or inconclusive results can quickly erase any savings from unlabeled or poorly sourced starting points. The right people in the plant will recognize the faintest color tinge or change in product ‘feel’ that indicates off-path or unwanted reaction, even before analytics pick it up. This comes from years of manufacturing experience, not from process diagrams.
Sometimes the issues aren’t visible—trace water in an aldehyde batch, contaminants picked up from poorly purged equipment, or an undetected change in starting material supplier. Operations must be vigilant. We keep logs on every batch, not just for compliance, but because we’ve had cases where back referencing operator notes led directly to a process fix. Anyone who makes heterocyclic compounds for a living knows you can’t shortcut documentation.
Product differences show up down the line: lower impurity means easier product purification; properly dried stock means fewer losses from decomposition; and real-time communication in production cuts down on the sort of surprises that force resyntheses or long troubleshooting. We find that investing in these small, day-to-day steps is what actually prevents most headaches for scientists relying on material being ready, right, and robust every time.
Having a direct line between the lab bench and the manufacturing floor removes a layer of uncertainty. Scientists with unusual process demands, new reactivity targets, or scale-up challenges don’t want stock answers—they want informed feedback tied to actual production runs. We routinely talk with development chemists about things that won’t show up in a spec sheet: which solvents work best for each purification method, how the product responds to light or air over time, and what to expect in batch-to-batch differences.
Product users often call in seeking advice on process challenges—occasional haze in solution, slow dissolving rates, or doubts about shelf life. Our plant crew shares specifics: what we see in-hand, what our experience has taught us about real vs. superficial problems, and how to work through them. Sometimes, customers come to us only after suffering through material from an anonymous third-party supplier, looking to troubleshoot which step in their workflow went wrong when yields inexplicably dropped. Lessons like this reinforce the value of a relationship where the people making the product know what qualities matter in a lab or pilot setting.
Trends in heterocycle synthesis change year on year. Research in pharmaceuticals and crop protection keeps pushing the envelope for more complex, fused-ring building blocks, and demand for robust intermediates like 2,3-dihydro-[1,4]dioxine[2,3-c]pyridine-7-carbaldehyde keeps rising. We adjust our synthesis protocols to keep pace with regulatory and process changes—pushing for greener routes, ensuring traceability, and improving yields with each campaign.
We don’t just meet minimum requirements—we work to surpass them. Our teams track solvent recovery rates, energy inputs, and waste reduction as much as they focus on the chemistry. Trends in green chemistry force us to rethink even familiar steps, swapping out hazardous reagents for safer or less persistent ones, and investing in R&D for new oxidants or more selective catalysts. As feedback accumulates from users seeking better environmental profiles or tighter impurity controls, we channel that feedback into process improvement.
Across the years, we’ve found that making good chemicals takes patience, attention, and willingness to adapt. Each product batch serves as a record of those choices—and each kilogram sent out reminds the plant crew what’s at stake. Whether for a small-batch pharmaceutical scale-up or a major combinatorial campaign, researchers trust 2,3-dihydro-[1,4]dioxine[2,3-c]pyridine-7-carbaldehyde not just because of a label or a report, but because every step of its production reflects real-world skills and a commitment to quality.
Real manufacturing starts where theory ends. Operators on the floor know what makes the difference—even subtle things like whether a reaction color matches expectations or how crystal habit changes with season and humidity. Each bottle we fill and seal carries a piece of that knowledge, built on days and nights standing by reactors, columns, and dryers—not just filling out spreadsheets.
For those who invest in research and development, confidence in starting materials is non-negotiable. Traceability, proven control of impurities, and process transparency matter more than ever as regulatory demands grow and competition sharpens. Having a supply partner that takes pride in that work—and who stands behind every batch with data, records, and hands-on experience—means stronger results, less risk, and better science. This is where expertise and reliability converge, making every lot of 2,3-dihydro-[1,4]dioxine[2,3-c]pyridine-7-carbaldehyde a true tool for discovery.