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HS Code |
188120 |
| Productname | 2-(Benzylthio)-5-Nitrobenzaldehyde |
| Casnumber | 873009-51-1 |
| Molecularformula | C14H11NO3S |
| Molecularweight | 273.31 |
| Appearance | Yellow crystalline solid |
| Meltingpoint | 92-95°C |
| Solubility | Slightly soluble in organic solvents |
| Purity | Typically >98% |
| Storagecondition | Store at room temperature, away from light |
As an accredited 2-(Benzylthio)-5-Nitrobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25g, tightly sealed with a screw cap; labeled with chemical name, CAS, hazard pictograms, and handling instructions. |
| Shipping | **Shipping Description:** 2-(Benzylthio)-5-Nitrobenzaldehyde is shipped in tightly sealed, chemically resistant containers to prevent moisture and light exposure. Packaging complies with all relevant chemical safety and transport regulations. It is labeled with hazard warnings and handled as a laboratory reagent, suitable for shipment via ground or air, depending on destination and regulations. |
| Storage | 2-(Benzylthio)-5-Nitrobenzaldehyde should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light and moisture. Store at room temperature, and avoid prolonged exposure to air. Clearly label the container and follow all relevant safety and handling guidelines. |
Applications of 2-(Benzylthio)-5-Nitrobenzaldehyde in Industrial Manufacturing2-(Benzylthio)-5-Nitrobenzaldehyde plays a significant role as an intermediate in several specialized chemical manufacturing sectors. The following sections detail its use across targeted downstream applications, including key compliance aspects, formula guidelines, workflow stage, and the final goods produced by customers in each market. 1. Advanced Pharmaceutical Intermediate SynthesisPharmaceutical API producers utilize this compound as a key fragment in multi-step synthesis of rare medical agents, particularly within heterocyclic drug classes such as thiazoles and benzothiazoles. The compound’s nitro and benzylthio functionalities allow for regioselective functional group transformations, critical for core ring construction in targeted active drugs. Quality control departs from standard commodity benchmarks—batch traceability, impurity profiling, and residual solvent levels must all meet strict pharmaceutical regulatory requirements. Industry compliance standards
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2. Agrochemical Active Ingredient ManufacturingProducers within the crop protection market employ this raw material in the multi-step synthesis of certain nitroaryl thioether class herbicides and fungicides. Its structure enables selective oxidative cyclizations, which lead to potent bioactive compounds. Stringent documentation of synthetic route, contaminant levels, and batch homogeneity are essential under both REACH and local agricultural guidelines relevant to the region of intended use. Industry compliance standards
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3. Specialty Dye and Pigment IntermediateThis compound acts as a foundational intermediate for manufacturing high-performance organic pigments and specialty dyes. Aromatic nitro functionalities permit subsequent reduction or diazotization, forming reactive species for pigmentation of plastics, coatings, and advanced electronic components. Adherence to purity and heavy metal content limits is necessary for products destined for both industrial and consumer applications. Industry compliance standards
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4. Fine Chemical Building Block in Material Science R&DR&D laboratories and industrial pilot plants leverage this substance for constructing advanced materials, including new functionalized polymers and OLED precursors. The compound’s dual electron-withdrawing and donating substituents allow for the controlled creation of modifiable frameworks under high-yielding condensation and lithiation processes. Material science laboratories require demonstration of repeatable batch reproducibility, well-defined impurity thresholds, and alignment with prior-art research disclosures during project validation. Industry compliance standards
Typical usage ratio
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Our plant has been focusing on the synthesis and supply of advanced aromatic intermediates like 2-(Benzylthio)-5-Nitrobenzaldehyde for years. In the chemistry world, few intermediates offer the reliable performance and versatility seen in this aldehyde derivative. Colleagues and industry partners often ask what sets this product apart from more common benzaldehydes, nitrobenzene derivatives, or the generic building blocks used in pharma, colorant, or material science labs. Drawing on our experience scaling from pilot runs to full batches, this is our view from the production line.
With a nitro group at the 5-position, an aldehyde at the 1-position, and a benzylthio side chain, this molecule pulls together electron-rich and electron-withdrawing features that affect both reactivity and selectivity in downstream chemistry. Chemists face limited options when seeking aromatic aldehydes that handle condensation, cyclization, or nucleophilic addition as cleanly as this one. The modulating effect of the nitro and thioether groups influences how reactions proceed, which matters in both small-scale synthesis and multistep industrial processes. After extensive process development, we control side-product formation, minimize byproducts of over-oxidation, and deliver a product that saves customers hours in purification.
The solid state purity, as we have been able to measure with HPLC and NMR, consistently lands above 99%. The off-yellow, fine crystal form enables smooth discharge, handling, and integration into automated solid-feed systems. Particle size distribution is tight; we’ve noticed that powders trending coarser don’t dissolve as well in customer solvents—something that slows down reaction time and can lead to batch inconsistencies. Stabilizer inclusion is minimal, since a well-controlled process avoids instability at room temperature. Our regular analytical checks review melting point (range 90-95°C), residue on ignition well under 0.05%, and moisture below 0.2% on every lot, not just for our certificates but to head off variability that disrupts synthesis or causes caking. Too many times, overlooked micro-impurities like trace benzyl chloride or toluene stick around if the separation step isn’t carefully engineered; we catch these through a mix of classic distillation and modern column purification, followed by GC-MS for trace organics.
Running large reactors instead of small flasks changes every variable—temperature gradients, mixing, byproduct carryover, and the work-up steps can go from trivial to stubborn problems. Our team spent more than a year working with different oxidizing agents and sulfur sources until residue levels and odor issues dropped to new lows. Customers in the pharmaceutical segment were among the first to comment on the improvement: less post-reaction work-up, clearer mother liquor, fewer column purification cycles needed. We now operate a fully closed system during synthesis and prevent benzyl chloride formation, which many labs complain about in outsourced products.
In many cases, our partners use this molecule for building heterocycles, dyes, and intermediates for bioactive compounds. Having produced and shipped batches for both high-volume needs and exacting milligram-scale research, our process now routinely delivers on the high selectivity for the meta-nitro isomer over its ortho or para cousins. Any cross-contamination with alternative isomers cuts yield and often triggers reprocessing—an issue we have largely eliminated by refinements at the crystallization stage. The manufacturing floor feedback loop now plays a big part in the purity benchmarks our customers expect. There’s simply not a shortcut: missed details at early synthesis multiply downstream, driving up cost and reducing product confidence.
Our years working side by side with downstream chemists inform all our process changes. Many generic aromatic aldehydes don’t combine nitro and thioether modifications. Take regular 5-nitrobenzaldehyde as a comparison; lacking the benzylthio group, its performance lags behind for certain nucleophilic addition steps or as a synthon for complex ring systems. The presence of the benzylthio function doesn’t just change reactivity; it opens up selective alkylation and cross-coupling reactions that are much more challenging with plain or alkoxy derivatives. Feedback from end users—pharma, electronics, and polymer researchers—reflects the value of this flexibility. In hydrogenation reactions and substitution protocols where reaction control makes all the difference, this molecule delivers cleaner conversion and fewer over-reduction products.
Another contrast to commonly used nitrobenzene or benzaldehyde variants lies in handling and shelf life. 2-(Benzylthio)-5-Nitrobenzaldehyde resists oxidation and hydrolysis better than unsubstituted analogues. We’ve logged storage data for more than four years, including trials at 40°C and 75% humidity, and found that the product maintains its structural integrity and color stability far beyond industry mean time-to-failure. This makes logistics simpler and gives our supply partners confidence that what’s dispensed in the lab turns up unchanged at production scale on the other side of the world.
From the manufacturing side, it’s key to appreciate where 2-(Benzylthio)-5-Nitrobenzaldehyde fits within synthesis sequences. Teams working in medicinal chemistry often use it as a precursor to sulfonamide-based bioactive scaffolds. Its functional group setup simplifies downstream sulfoxidation or coupling steps without triggering off-pathway degradation. This efficiency has sped up route scouting for several pharma projects—data we confirm upon request with chromatograms drawn directly from in-process QC samples, not just batch summaries.
Other customers, focused on specialty dyes or electronic materials, value the molecule’s ability to introduce the right balance of rigidity and electronic modulation into complex organic structures. In dye synthesis, coupling this compound with amines or hydrazines gives high-yielding access to azo dyes known for colorfastness and UV stability. Colleagues in the OLED and organic electronics field have had consistent feedback: compared to alternatives like 2-nitrobenzaldehyde, the benzylthio group opens up routes to thioether-bridged molecules that display more stable charge mobility, crucial for thin-film device fabrication.
Another practical insight—the aldehyde’s solubility profile, which blends in most aromatic solvents, makes it a superior choice for multi-step syntheses that require intermediate isolation. Chemists no longer lose product during layer separation or face awkward cleanups once this crystalline powder goes into the mixing tank. Purification steps benefit from its distinct cleavage signals on NMR and tight melting range, shaving hours off of analytical method development—experience we hear echoed in customer batch records.
Quality in this context doesn’t mean ticking boxes—our approach reflects a robust combination of plant know-how, batch records, and real-world issues like transit times and storage conditions. Staff rotate every month through both the analytical and synthesis sections, and not once have we seen a shortcut that paid off in the long run. Every element from raw material QC—like verifying nitrobenzene source beyond lot traceability—to pilot scale batch documentation, builds trust both for our own staff and external auditors. Shipping samples undergo extra GC-MS checks on transit loss and byproduct formation, an onsite practice that began after one key customer flagged oxidative breakdown in a shipment delayed on the docks for forty-eight hours.
Batch reproducibility measures go beyond standard ISO documentation. We changed the quenching agitation protocol based on direct feedback: a batch that started clotting during cooling now stirs down to true crystals. This tuning means less dust, less mess, and a product that weighs out cleanly for our partners—facts borne out in regular crystal habit assessments and ease-of-handling scores shared with receiving labs. Temperature programming and pH adjustment in the final filtration step have cut isolated yield losses by a significant margin since these improvements. Instead of relying on outside testing, our process analysts work in real time to detect any shift in particle size or color, so fielded batches are always consistent.
We’ve experienced that deploying a fully integrated digital system for sample tracking, data collection, and batch release cuts both human error and response time. Having an in-house archive of micro-impurity profiles helps address any customer question directly and quickly. This transparency guarantees traceability and has helped several pharmaceutical and electronics clients gain faster regulatory approval, since the chain of custody from raw material to finished product remains airtight throughout the run.
Why does reactivity and supply reliability matter so much for this advanced aromatic intermediate? Routine conversations with chemists come down to avoided headaches: less time spent battling off-flavors, unexpected tars, or troublesome filtration after unwanted side-products build up. This intermediate eliminates many of those issues. Our grip on side reaction suppression lets customers scale confidently rather than abandon half-worked synthetic routes. We focused on oxygen transfer efficiency, phase separation, and managing batch pH after reviewing hundreds of customer feedback records. Every tweak to the process was born out of a fix to a real pain point, not an abstract “enhancement.”
The aldehyde’s shelf and solution stability mean our logistics partners worry less about shipping times, seasonal temperature spikes, or accidental exposure to humidity. Tracking customer complaints and successes leads us to believe that a lot of what separates one supplier from another boils down to raw, repeatable reliability. Every industry batch that comes back with the same crystal size and color fractions as the test sample in our warehouse builds trust at a level product sheets or registrations never could.
In chemical manufacturing, environmental stewardship sits alongside yield as a measure of a successful process. Our reaction scheme recycles mother liquor and minimizes chlorinated byproducts, which makes the difference for customers concerned about downstream waste processing and costs. We maintain solvent tank reclamation and have cut hazardous residues reported at outflow to below industry reporting thresholds. By using an in-line nitrogen sweep and closed-loop filtrate handling, exposure risk and environmental loading drop significantly during both synthesis and purification—a concern voiced by more and more regulatory groups and safety teams auditing our operations.
Feedback from production-floor staff, not just management, informs our approach: we encourage every technician and shift manager to report spills, process bottlenecks, and minor deviations before they build into larger risks. Modernizing floor and vent protocols grew out of these workday insights, as much as any outside regulation. This keeps our safety record strong, in a manufacturing field where even minor process lapses create hazardous conditions or product downgrading.
Our engagement with research labs, custom synthesis groups, and commercial plants has always started from the genuine technical hurdles experienced with complex molecules—unlike commoditized chemicals, specialty intermediates reveal their value in the day-to-day grind of tricky syntheses or scale-up optimization. The workflow for this nitrobenzaldehyde derivative supports rapid method testing, robust upscaling, and high-throughput library creation in both pharma and materials settings. As synthetic chemistry pushes boundaries in green processing and complexity, reliable supply and stable quality form a foundation no process can take for granted.
We approach partnerships not as transaction points but as shared problem-solving ventures. Chemists exploring unique substitution patterns or advanced solid-phase strategies see real-world difference in switching to an intermediate with higher process selectivity, minimal side reactions, and straightforward downstream purification. Bringing the experience and insights of our plant floor into product development—something few outside pure manufacturing circles can offer—has built ongoing relationships and collaborative troubleshooting platforms that smooth the path from idea to industrial solution. Technical data exchanges are anchored in production realities, not abstract possibilities.
No production process stands still. A significant share of improvements in our 2-(Benzylthio)-5-Nitrobenzaldehyde output trace back to direct user feedback: from optimizing recovery yields to fine-tuning cooling rates and solvent systems for higher product isolation. We run post-delivery surveys, share in-process analytical snapshots, and invite feedback that challenges the status quo. Just last quarter, a partner’s new formulation protocol led us to rethink our moisture controls for certain target particle ranges, reshaping a drying sequence that now benefits multiple segments.
Direct communication with end-users remains our surest gauge of what works. Long after formal batch release, we continue to check in about performance, handling ease, and any unexpected outcomes—an approach that leads to continuous technical dialogue and practical refinements. Building trust and knowledge in this way supports both our development pipeline and our customers' innovation cycles. Chemical manufacturing, at its best, reflects this ongoing, grounded partnership between production and application, ensuring that advanced intermediates like 2-(Benzylthio)-5-Nitrobenzaldehyde deliver more than just a line item on a supply sheet: they enable and accelerate tomorrow’s chemistry solutions.