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2-(Cyclohexylthio)-5-Nitrobenzaldehyde

    • Product Name 2-(Cyclohexylthio)-5-Nitrobenzaldehyde
    • Alias ALD00653
    • Einecs 424-640-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    168924

    Product Name 2-(Cyclohexylthio)-5-Nitrobenzaldehyde
    Chemical Formula C13H15NO3S
    Molecular Weight 265.33 g/mol
    Cas Number 63069-38-9
    Appearance Yellow solid
    Melting Point 99-101 °C
    Solubility Slightly soluble in organic solvents
    Purity Typically ≥ 98%
    Storage Conditions Store at 2-8°C, protected from light
    Smiles C1CCC(CC1)SC2=C(C=C(C=C2)[N+](=O)[O-])C=O
    Inchi Key VPDZAYIUPQZSQQ-UHFFFAOYSA-N

    As an accredited 2-(Cyclohexylthio)-5-Nitrobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams, tightly sealed, labeled "2-(Cyclohexylthio)-5-Nitrobenzaldehyde," with hazard and handling precautions displayed.
    Shipping 2-(Cyclohexylthio)-5-Nitrobenzaldehyde is shipped in tightly sealed containers to prevent moisture and air exposure. It is packaged according to standard chemical safety protocols, typically under inert atmosphere if needed. Transport follows regulations for hazardous materials, ensuring protection from extreme temperatures, sunlight, and mechanical impact during transit.
    Storage Store 2-(Cyclohexylthio)-5-Nitrobenzaldehyde in a tightly sealed container, away from light and moisture, in a cool, dry, and well-ventilated area. Avoid sources of ignition and incompatible materials such as strong oxidizers. Ensure appropriate labeling and store in a dedicated area for hazardous chemicals, following all relevant safety protocols and local regulations for storage of organic compounds.
    Application of 2-(Cyclohexylthio)-5-Nitrobenzaldehyde

    Applications of 2-(Cyclohexylthio)-5-Nitrobenzaldehyde in Industrial Manufacturing

    2-(Cyclohexylthio)-5-Nitrobenzaldehyde serves as a specialized intermediate in advanced synthesis routes across several production sectors. As the direct manufacturer, we deliver this intermediate to downstream facilities requiring strict quality parameters for regulated and high-value transformation. The outlined application scenarios detail practical use, compliance needs, recommended loading, and integration sequence for real manufacturing streams.

    1. Pharmaceutical Intermediate for Thioether-Substituted Drug Compounds

    Process chemists in pharmaceutical plants incorporate this compound in multi-step synthesis of active pharmaceutical ingredients (APIs) where thioether and aromatic nitro groups are essential pharmacophores. Its use as an advanced intermediate supports construction of benzaldehyde-derived scaffolds for anti-infective or CNS-targeted drugs. Restrictions on process impurity and carried-over residuals demand in-line monitoring during scale-up.

    Industry compliance standards

    • Good Manufacturing Practices (GMP) ICH Q7
    • EU Regulation (EC) No 1907/2006 (REACH) for intermediates
    • 21 CFR Part 211 (US cGMP for finished pharmaceuticals, intermediate controls)
    • USP/EP acceptance specifications for process intermediates

    Typical usage ratio

    • Typically 0.4–0.8 molar equivalents per target API batch, adjusted for synthesis yield optimization and impurity control limits

    Downstream process integration

    • Introduced in Stage 2 or Stage 3 of API synthesis as a key coupling or modification point; often combined with secondary amine or hydrazine reactants for downstream ring-closure or reduction

    Final product types

    • Finished bulk API (anti-tubercular agents, CNS-active intermediates)
    • Crude or purified intermediates supplied for final purification at partner sites
    • Reference standards for pharmaceutical analytical labs
    • Precursor building blocks for regulatory submission batches

    2. Agrochemical Intermediate for Selective Fungicide Synthesis

    Manufacturers of protective agrochemical actives employ this thioether benzaldehyde in the design of target-selective fungicides, where sulfur and nitro groups impact spectrum and environmental stability. The raw material passes through nitro reduction, cyclization, or alkyne functionalization depending on the desired fungicidal backbone. Stringent tracking applies for trace and solvent impurities, with traceability required to guarantee downstream field safety profiles.

    Industry compliance standards

    • FIFRA Registration & EPA Pesticide Registration Manual (USA)
    • ISO 9001:2015 (Raw material traceability)
    • FAO Specifications for Plant Protection Products
    • REACH Annex VII for intermediates—environmental data

    Typical usage ratio

    • Commonly 5–15% weight/weight proportion relative to total intermediate charge, frequently varied by target yield and fungicide selectivity design

    Downstream process integration

    • Feeds into mid-stream heterogeneous reduction or condensation stages prior to ring assembly and formulation with carrier agents

    Final product types

    • Technical-grade fungicide actives for field crops
    • Spray adjuvants for systemic fungicide penetration
    • Protected agrochemical intermediates for on-site formulation
    • Registered active ingredient formulation concentrates

    3. Electronic Chemicals: Photoresist and Dye Precursor Synthesis

    In electronic and semiconductor material supply, downstream facilities utilize our aromatic nitrothioether compound for photoresist building blocks and deep-color dye precursors. The material’s structural features allow modification steps critical for wavelength-specific absorption and electron mobility, both in display device production and printed circuit photolithography. High purity with controlled metal and particulate levels are closely monitored on batch release.

    Industry compliance standards

    • SEMATECH Quality Protocols for Advanced Materials
    • IEC 62474 for restricted substances in electronics
    • RoHS Directive 2011/65/EU (applicable for precursors of regulated substances)
    • UL 746A (Materials for electrical and electronic applications)

    Typical usage ratio

    • Applied at 1.5–3.5% by mass in prepolymer or dye synthesis batches, modulated by end-use absorption targeting and substrate compatibility

    Downstream process integration

    • Introduced in initial monomer or prepolymer step, frequently followed by reduction, substitution, or coupling to form dye-bearing functional groups or light-sensitive sites

    Final product types

    • Photoresist formulations for semiconductor wafer processing
    • High-performance color dye solutions for OLED/LED displays
    • Immersion lithography materials
    • Advanced imaging and PCB etchant compounds

    4. Specialty Polymer Production for Functional Materials

    Producers of thioether-functionalized specialty polymers deploy this compound as a comonomer or functional modifier in high-value polymeric chains. The material supports flexible design in advanced engineering plastics, including membrane materials and sensor matrices. Substantial attention focuses on dispersibility, reaction efficiency, and control of unreacted aldehyde/nitro content in the final resin.

    Industry compliance standards

    • ISO 9001:2015 for specialty polymer manufacture and QA
    • ASTM D638 for mechanical property validation
    • REACH status for monomer use in EU-sold polymers
    • ISO 14001 environmental management for waste stream control

    Typical usage ratio

    • Loaded at 2–6 mol% of total monomer content, adjustable for target cross-linking density, film permeability, or functional group display

    Downstream process integration

    • Reacted during prepolymerization or co-polymerization stages, followed by thermal or photoinitiated curing; aldehyde and thioether content monitored by NMR or titration

    Final product types

    • Ion-selective polymer membranes
    • Functional coatings for chemical sensors
    • Self-healing advanced engineering plastics
    • Smart packaging films with controlled permeability
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    Certification & Compliance
    More Introduction

    2-(Cyclohexylthio)-5-Nitrobenzaldehyde: Harnessing Experience for Reliable Synthesis

    Understanding 2-(Cyclohexylthio)-5-Nitrobenzaldehyde

    Every day in our laboratory, clarity comes from experience—years of careful benchwork and supply deliveries that made one thing clear: quality inputs lead to dependable results. For anyone exploring nitroaromatic chemistry, 2-(Cyclohexylthio)-5-Nitrobenzaldehyde stands out for its performance in complex syntheses. Its unique structure, where a cyclohexylthio group couples with the nitrobenzaldehyde backbone, provides distinct reactivity and functional possibilities. Our team noticed that in reactions requiring robust electron-withdrawing functionality along with sulfur reactivity, this compound offered smoother progression than standard nitrobenzaldehydes or simpler alkylthio analogues.

    Our production experience shows that demand often comes from those seeking intermediates for more specialized downstream products—pharmaceutical leads, agricultural research agents, or new materials with targeted properties. During multi-step synthesis, side reactions and instability threaten yields. Introducing cyclohexylthio modification brings resilience to the molecule, preserving the integrity of the aldehyde function. The extra bulk in the cyclohexyl ring delays unwanted side reactivity compared to less sterically hindered analogues like methylthio or ethylthio nitrobenzaldehydes.

    Model and Specifications

    Chemists ask about consistency every time, whether for developing a new process or scaling up. Over the years, we established tight controls on moisture and purity, using HPLC and NMR validation at each batch. Our standard offering comes as a pale yellow to ochre crystalline solid, melting above 80°C and demonstrating sharp, well-defined signals in the aromatic and aliphatic regions of NMR. Residual solvents never exceed 0.5%, with assay values above 98%. Tailoring these benchmarks involved trial, error, and dialogue with several research clients. Their feedback informed our protocol for crystallization and final handling, preventing clumping and minimizing degradation during storage. We never rely on theoretical data alone; instead, we watch for baseline purity in practice, with each shipment released only after hands-on chemist approval.

    Packaging makes a difference, especially for light- and air-sensitive chemicals. We avoided clear glass and thin polymer sachets after early batches showed surface oxidation around exposed edges. Amber glass and inert atmospheres now define our packaging, based on lessons from repeated shipments overseas and months-long shelf tests in variable climates. Each vessel gets sealed at low humidity; all outgoing shipments ship in secondary protective containers. We learned that this care isn’t overengineered—our guarantee depends on it.

    Applications in Research and Industry

    The most frequent conversation we hold about 2-(Cyclohexylthio)-5-Nitrobenzaldehyde happens in the context of custom synthesis. Academic and pharmaceutical clients use it to forge complicated frameworks, merging the aldehyde group in condensation reactions or as a precursor for nitro reduction and sulfur-based transformations. The cyclohexylthio group, compared to lighter alkylthio groups, gives higher yields by resisting base- or acid-mediated elimination. It takes the heat of prolonged reactions with less by-product formation—a detail noticed in our partners’ scale-up trials and mirrored during internal kinetic studies.

    Every production run brings stories from the field. Once, a medicinal chemist described frustration with competing side products using 2-(methylthio)-5-nitrobenzaldehyde. Swapping to the cyclohexylthio analogue deemed a turning point, with final target yields improving by over 15%. Others in materials discovery found the molecule’s robust structure helpful in post-synthetic modifications, especially when assembling heterocyclic libraries. Across the board, when rigorous stability matters—be it a week-long multistep route or a single high-temperature condensation—it’s always this molecule that survives the process and upholds yield.

    What Sets 2-(Cyclohexylthio)-5-Nitrobenzaldehyde Apart

    Experience on the ground separates advertising from real-world utility. A comparison with direct cousins, such as 2-(Methylthio)-5-nitrobenzaldehyde or unsubstituted 5-nitrobenzaldehyde, illustrates real performance gains. The methylthio variant slips easily into unwanted demethylation side reactions, especially under basic conditions. We saw brown tars instead of white to yellow solids when tests extended past the routine two hours. Ethylthio options improve on this, though not enough to justify their consistently lower yields under high-temperature requirements.

    Cyclohexylthio delivers something tangible: resistance to strong bases, lower volatility, and less odor in the lab. Its aromatic aldehyde core handles traditional nucleophilic addition, while the larger thioether blocks the chaos that more labile groups introduce during workup. Bench tests in our facility routinely confirm improved overall material recovery, even in reactions that punish the molecule with extremes of temperature or pH.

    Much of the ingenuity arises from sulfur’s position. Direct alkylthio substitutions sometimes lead to rapid oxidation or cleavage. Cyclohexylthio bridges that challenge, weathering oxidizing conditions in a way that leaves the core structure unharmed. In shelf-life studies stretching more than a year, product stored under anhydrous conditions showed near-complete structural integrity, with less than 2% decomposition. The technical advantage moves out of textbooks and into day-to-day synthesis: result stability, better yields, and simpler purification. This feedback flowed directly from our partners, who run frequent analytical checks on received shipments.

    User Experience and Evolving Expectations

    Ramifications of poor intermediate stability ripple quickly. Skipping over time-consuming purification saves resources in both small and large production. Reliable intermediates like 2-(Cyclohexylthio)-5-Nitrobenzaldehyde shorten these cycles. A senior chemist once walked us through their switch to this compound for assembling candidate drugs with sensitive aromatic cores. Their team marked the reduction in batch-to-batch variability; purification columns yielded predictable, repeatable fractions after months of frustrating unpredictability with other thioether versions.

    This isn't luck, but managed, intentional improvement. It comes from iterative process development, matching the end user's needs. Dozens of historical production runs showed that even small variations in raw cyclohexylthiol purity or nitrobenzaldehyde precursor lead to major shifts in final product color and odor. Our experience taught us that only the cleanest starting materials result in customer satisfaction and repeat business. Quality control systems, rooted in those insights, now monitor every step, not only the endpoint.

    Today’s researchers show sophistication, pressing for not just chemical but process transparency. Full analytical data, independent chromatograms, and open communication back up our products. It’s standard now to ship materials with digital batch certificates and side-by-side chromatograms for client review. We value these checks, knowing they catch trends before problems surface. Improvements in analytical transparency enhance trust, and—crucially—directly influence the outcomes in our clients’ workflows.

    Supply Chain, Availability, and Environmental Commitment

    Recent years brought global disruptions, raw material bottlenecks, and logistical delays. Silver linings appeared with long relationships with trusted upstream suppliers—those who commit to both consistent quality and responsible sourcing. There’s little tolerance for bypassing established safety or quality protocols. We work hands-on with vetted partners; sporadic or grey-market sources never earned a place at our table. Auditing suppliers helps us keep heavy metal content low and avoid cut corners on critical steps like thioetherification.

    Solvent recovery systems, waste minimization in the mother liquors, and energy-efficient condenser setups form part of our routine. Not every chemical producer commits to this—resource-saving adds hours and cost. But fielding customer questions and regulatory reviews proved this approach builds more than goodwill. It leads to cleaner product and fewer trace contaminants. Colleagues returning for repeat batches remind us that these habits matter more than a glossy data sheet.

    Shipping remains a challenge for sensitive chemicals in fluctuating global conditions. Years ago, customs hassles and regulatory surprises taught us to pre-clear shipments and keep compliance documentation assembled. Every shipment passes through hazmat review and export paperwork checks, smoothing delivery and keeping customers focused on their projects, not red tape or unexpected delays.

    Supporting Modern Synthetic Needs

    The toolkit of contemporary chemistry grows each year. New ligands, diverse catalysts, and automation in reaction monitoring change what’s possible at the bench. Through it all, the building blocks either support the innovation—or slow it down. 2-(Cyclohexylthio)-5-Nitrobenzaldehyde earned its place in the toolbox, side by side with classic nitrobenzaldehydes and newer, more specialized aldehydes. We keep pace with demand by monitoring usage trends, scaling production not by prediction alone but by direct requests and ongoing feedback from regular users.

    Several research groups working on azole derivatives or redox-active intermediates pointed to the cyclohexylthio compound’s performance as a game changer. They appreciated not only its durability but the breadth of chemistry it enabled—fewer breakdowns, reliable sulfur insertion, and clean conversion in late-stage transformations. Innovation happens at the interface of reliability and possibility; our ongoing goal is to ensure customers reach that intersection every time.

    Fast-changing regulatory landscapes call for adaptation. Over time, we updated handling, labeling, and shipment to meet safety requirements not only domestically but in international research environments. No compromise gets taken when new guidance appears concerning chemical exposure or environmental standards. Periodic risk reviews and team trainings keep standards current, with documentation provided to support compliance wherever shipments land.

    Transforming Chemical Manufacturing One Molecule at a Time

    In the end, the field rewards those who value hands-on know-how and proven approaches over shortcuts. Our collective experience in manufacturing 2-(Cyclohexylthio)-5-Nitrobenzaldehyde reflects that commitment. Every kilogram produced tells a story—of challenging timelines, client requests at all hours, and the ongoing chase for both performance and trust. We don’t promise what’s not sustainable. Instead, we commit to maintaining the standards that brought our product to the forefront for this class of aldehyde.

    Professional chemists and industry partners drive our continuous improvement. We listen: batch notes, raw material feedback, and even failure reports guide our process development and quality checks. No product stands still, and our own capacity is built on learning by doing, by adapting to real synthesis challenges that emerge in the laboratory. Offering analytical support upgrades, process suggestions, and after-sales troubleshooting, we remain closely engaged—not as a distant manufacturer, but as partners invested in tangible research outcomes.

    Reviewing the journey of 2-(Cyclohexylthio)-5-Nitrobenzaldehyde from conceptual intermediate to trusted research mainstay gives context to every gram dispensed, every report shared, and every success story returned to us by our customers. Experience taught us what details matter: careful raw materials, advanced analytics, climate-aware packaging, and responsive technical support. The result has been a steady track record, counted on by those who demand both chemical innovation and manufacturing know-how.

    The Road Ahead

    As research standards rise and the march of technology transforms chemistry, only manufacturers grounded by accountability and skill will keep pace. Our ongoing commitment combines pragmatic experience with a dedication to meeting today’s synthetic needs—plainspoken quality, transparent process, and partnership every step of the way. From the earliest days of bench production to the tightly controlled, commercial-scale deliveries of today, 2-(Cyclohexylthio)-5-Nitrobenzaldehyde has become not just a product but a benchmark for what attentive, experienced manufacturing can achieve.

    Here, every molecule originates in proven methodologies, tested under conditions that real chemists and end users set. Each step, from synthesis to shipment, benefits from open communication and hard-earned expertise. That continues to make the difference. Keeping our standards steady means delivering more than intermediate chemicals—it means supporting possibility itself, for every new research direction and challenge on the horizon.