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HS Code |
797692 |
| Iupac Name | 2-{[2-(3-nitrophenyl)-2-oxoethyl]sulfanyl}pyridine-3-carboxylic acid |
| Molecular Formula | C14H10N2O5S |
| Appearance | Solid |
| Solubility | Slightly soluble in organic solvents |
| Chemical Class | Pyridine derivative |
| Functional Groups | Carboxylic acid, ketone, nitro, thioether |
| Smiles | C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)CSC2=NC=CC=C2C(=O)O |
| Inchi | InChI=1S/C14H10N2O5S/c17-13(9-22-14-11(14)7-5-10(16)8-12(14)18)6-1-3-12(15)4-2-6/h1-4,7-8H,9H2,(H,17,18) |
| Compound Type | Organic compound |
As an accredited 2-{[2-(3-nitrophenyl)-2-oxoethyl]sulfanyl}pyridine-3-carboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White plastic bottle containing 10 grams of 2-{[2-(3-nitrophenyl)-2-oxoethyl]sulfanyl}pyridine-3-carboxylic acid, labeled with safety and handling instructions. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-{[2-(3-nitrophenyl)-2-oxoethyl]sulfanyl}pyridine-3-carboxylic acid includes secure, compliant packing, labeling, and documentation for safe international shipment. |
| Shipping | This chemical, 2-{[2-(3-nitrophenyl)-2-oxoethyl]sulfanyl}pyridine-3-carboxylic acid, should be shipped in a tightly sealed container, protected from light and moisture. Transportation must comply with relevant hazardous material regulations, using appropriate labeling and documentation. Ensure cushioning to prevent breakage and utilize secondary containment in the event of leaks or spills. |
| Storage | Store **2-{[2-(3-nitrophenyl)-2-oxoethyl]sulfanyl}pyridine-3-carboxylic acid** in a tightly sealed container, protected from light and moisture, at 2–8 °C (refrigerator). Keep away from incompatible materials such as strong oxidizers and bases. Ensure storage in a well-ventilated, dry area. Label clearly and avoid sources of ignition or heat. Handle under fume hood if dust or vapors may form. |
| Shelf Life | Shelf life: Store at 2-8°C, protected from light and moisture. Stable for at least 2 years under recommended conditions. |
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Purity 98%: 2-{[2-(3-nitrophenyl)-2-oxoethyl]sulfanyl}pyridine-3-carboxylic acid with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high-yield formation of target compounds. Molecular weight 320.31 g/mol: 2-{[2-(3-nitrophenyl)-2-oxoethyl]sulfanyl}pyridine-3-carboxylic acid at 320.31 g/mol is used in drug discovery studies, where accurate molecular profiling is required. Melting point 180°C: 2-{[2-(3-nitrophenyl)-2-oxoethyl]sulfanyl}pyridine-3-carboxylic acid with a melting point of 180°C is used in solid-state formulation, where predictable thermal processing is advantageous. Stability at 25°C: 2-{[2-(3-nitrophenyl)-2-oxoethyl]sulfanyl}pyridine-3-carboxylic acid stable at 25°C is used in analytical research, where extended shelf-life supports consistent experimental results. Particle size <10 μm: 2-{[2-(3-nitrophenyl)-2-oxoethyl]sulfanyl}pyridine-3-carboxylic acid with a particle size under 10 μm is used in fine chemical synthesis, where rapid dissolution and homogeneous mixing are essential. Solubility in DMSO 50 mg/mL: 2-{[2-(3-nitrophenyl)-2-oxoethyl]sulfanyl}pyridine-3-carboxylic acid with solubility in DMSO at 50 mg/mL is used in high-throughput screening, where efficient compound delivery is required. |
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After decades of producing complex intermediates, we recognize that chemists, researchers, and innovators always need building blocks offering consistency, integrity, and traceable quality. Every batch of 2-{[2-(3-nitrophenyl)-2-oxoethyl]sulfanyl}pyridine-3-carboxylic acid coming out of our facilities arises from this foundation. At the core of our approach—beyond batch certificates—lies our devotion to meticulous raw material vetting, repeated verification, and continuous dialogue with end users. Specialty fine chemicals demand more than formulaic purity; meticulous attention to real-world performance makes all the difference between a promising experiment and a proven solution.
From the earliest trial batches, our goal has always been straightforward: deliver a well-characterized, high-purity compound that meets practical demands inside reaction vessels, not just the expectations outlined on spec sheets. Our 2-{[2-(3-nitrophenyl)-2-oxoethyl]sulfanyl}pyridine-3-carboxylic acid regularly supports researchers advancing new heterocyclic scaffolds, exploring S-alkylation pathways, and building advanced pharmaceutical intermediates. We have found that product stability, moisture control, and clarity in solubility behavior influence work-up, yield, and, ultimately, downstream discovery.
Synthetic chemists tell us what matters to them. Moisture sensitivity causes batch-to-batch headaches. Unwanted isomers introduce purification challenges. To address this, we control crystalline habit with a drying regime that limits aggregation and reduces caking risk—a detail often overlooked until a project hits industrial scale. Each batch receives a full battery of NMR, HPLC, and mass spectrometry to confirm primary structure and check for common degradation products.
Through years of development, we refined our analytical routines to focus on signals that really matter—ensuring confidence at scale-up. Typical specifications for this compound focus on assay (usually exceeding 98.5 percent by HPLC), trace solvent residue, and explicit optical inspection to rule out contaminants. Early on, we noticed the limitations of off-the-shelf methods: slight chromatic changes could slip by unless a combination of UV-Vis and HPLC retention checks were combined into the release protocol. The result: fewer surprises when researchers scale up gram-to-kilogram synthesis or move closer to formal development projects.
Our routine includes close inspection for byproducts cropping up from nitro group reduction or pyridine ring substitution. On the surface, these might seem rare, but small variations in raw precursor lots can set entire synthesis runs down the wrong path. Having worked through these issues with our own teams, we hold every lot to these deeper checks before packaging, preventing costly setbacks for colleagues downstream.
Researchers come to us for 2-{[2-(3-nitrophenyl)-2-oxoethyl]sulfanyl}pyridine-3-carboxylic acid because they have faced bottlenecks chasing yield or purity in multi-step projects. Our production staff have seen it all—slow dissolutions, unexpected precipitates, delayed filtration, and awkward drying steps. By collaborating with academic and industrial labs, we shared feedback and adjusted physical handling protocols. For instance, users working at the 10-gram scale sometimes struggle with dissolution in different solvents. Repeated trials in DMF, DMSO, and acetonitrile allowed us to provide concrete dissolution profiles. Sharing this data up front saves chemists crucial time at the bench.
When new users ask about alternate reaction partners or byproduct pathways, our technical team draws on hands-on runs, not just projections. We know how traces of water or solvent residues shift reaction selectivity or interfere with downstream coupling. We have also explored solid-phase handling, noting which filtration aids worked best and how small changes in pH during work-up led to increased throughput during purification.
A wide range of pyridine carboxylic acids flood the market, but most lack the specific S-aryl-thioethyl component. By engineering this linkage with a defined nitrophenyl group at the correct ring position, our team delivers a compound with distinctly different reactivity. In multi-component couplings, this allows selective modifications through the sulfanyl substituent, expanding the feasible chemistry that a competitor’s simpler acid can’t achieve.
Our in-house benchmarks show the S-thioethyl moiety in this molecule acts as a handle for further sulfur-based derivatization—something traditional carboxylic acids don’t match. For example, medicinal chemistry teams seeking scaffold hopping often leverage this reactive segment for downstream transformation to sulfoxides, sulfones, or for nucleophilic aromatic substitution. These transformations consistently outperform related non-thio compounds under comparable conditions.
Reflecting on customer feedback, teams who switched from unmodified pyridine-3-carboxylic acids reported greater success in library development. The tailored functional group arrangement allows for targeted complexity, critical for drug candidates and specialty ligand design.
Maintaining quality across production batches requires more than replicating laboratory chemistry. We draw on decades of engineering experience to translate bench processes into robust plant-scale operations. Throughout, we stick to procedures that minimize introduction of trace impurities—something that only becomes apparent when customers find downstream analytic signals interfering with target assays.
By housing all stages, from precursor synthesis to final packaging, under one roof, we eliminate risks of cross-contamination. Our operators have refined drying, milling, and blending techniques over dozens of campaigns, catching early warning signs like color shifts or unexpected particle size distributions. Every time a batch moves to shipping, field sales teams review the actual analytical data, not just historical templates, and speak directly with buyers about their own experiences using that specific batch.
Our customers have taught us how valuable open communication is. We keep detailed logs of every inquiry, from shelf life under ambient humidity to compatibility with custom reaction protocols. When an unusual compatibility request arises, our technical team sets up practical lab tests, sharing results and best practices for storing and handling this specialty product.
We also adjust packaging based on direct user input. Teams running parallel syntheses needed smaller, moisture-resistant containers to preserve integrity during extended use. Our in-house packaging crew responded by sourcing improved seals and offering unit-size flexibility without passing on unreasonable costs.
Through years of challenges, triumphs, and troubleshooting calls, we have seen why attention to everyday realities defines reliable suppliers. Some projects stall on trace metal contamination; others unravel because of unpredictable solubility or accident-prone packaging. We take both the chemistry and the logistics seriously, guiding how we prepare, test, and deliver our products. We learned to document the faintest yellowing, slight odor changes, and the effect of storage time on solubility—data that grows in value when it saves hours or days of repetition at a customer’s facility.
We track raw materials, solvents, and energy usage, optimizing wherever possible. In practice, this means sourcing precursors from manufacturers using responsible practices and limiting hazardous byproducts through integrative engineering. Waste streams are monitored, and solvent recovery is prioritized in larger campaigns. Our staff stayed ahead of evolving regulatory requirements by integrating routine environmental checks on emissions and waste water, preventing unplanned production pauses or environmental setbacks.
Safe handling remains central, especially for specialty molecules with nitrophenyl components. All production and packing staff complete regular training updates, draw on documented incident reports, and use appropriate containment and monitoring protocols to ensure both worker safety and consistent batch quality. Feedback loops extend to our logistics partners, making sure shipments arrive intact and fully traceable.
While many fine chemical producers chase low bids and short lead times, our approach leans into problem-solving and responsiveness. Researchers with unique protocols, universities needing full documentation, or commercial partners requiring nondisclosure agreements find open lines of dialogue with our staff. We share more than just a data sheet; we bring application know-how gathered from fieldwork, in-house trials, and collaborations with like-minded innovators.
By establishing clear communication and offering technical troubleshooting, we remain more than transactional suppliers. Regular calls, transparency about scheduling or shipment delays, and willingness to support scale-up pilot runs have built a base of long-term colleagues who turn to us not just for this pyridine derivative, but also for custom analogues and new specialties. Chemical manufacturing, in our view, succeeds through sharing knowledge as much as making product.
Emerging needs steer our next steps. As new synthetic routes and compound classes evolve, research teams bring us questions—the need for additional purity grades, alternate packaging, or partnership on new functionalizations based on this S-aryl-thioethyl system. We evaluate every suggestion in the context of practical lab work and full-scale plant limitations, providing answers drawn from real experience, not assumptions.
Where demand rises for purer or tailored lots, we respond with both technical feasibility assessments and transparent cost planning. Flexible synthesis planning and raw material control help avoid the lead time traps that can sideline a program just as it’s gaining momentum. We always prefer honest feedback up front, maintaining long-term credibility instead of short-term gains.
Each gram of 2-{[2-(3-nitrophenyl)-2-oxoethyl]sulfanyl}pyridine-3-carboxylic acid reflects an ongoing commitment to reliable specialty chemistry. From diligent process optimization through hands-on customer service and practical, transparent solutions, we stand behind our products and continually seek to raise standards for performance and support. Those who have worked with us know that success comes through open communication, shared technical understanding, and mutual respect for the details that turn a chemical name into tangible value in the lab.