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HS Code |
644666 |
| Chemical Name | 2-(N-Propylthio)Nicotinic Acid |
| Cas Number | 45534-69-6 |
| Molecular Formula | C9H11NO2S |
| Molecular Weight | 197.25 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 128-132 °C |
| Solubility | Soluble in common organic solvents |
| Purity | Typically ≥98% |
| Storage Temperature | 2-8 °C |
| Synonyms | 2-[(Propylthio)]pyridine-3-carboxylic acid |
| Smiles | CCCSC1=NC=CC=C1C(=O)O |
As an accredited 2-(N-Propylthio)Nicotinic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-(N-Propylthio)Nicotinic Acid, 5 grams, supplied in a sealed amber glass bottle with tamper-evident cap and clear labeling. |
| Shipping | 2-(N-Propylthio)Nicotinic Acid is shipped in tightly sealed containers to prevent contamination and moisture exposure. Packages are clearly labeled according to regulatory requirements and handled as a laboratory chemical. Shipping is typically conducted via certified carriers, with all necessary documentation and safety measures to ensure compliance with local and international transport regulations. |
| Storage | 2-(N-Propylthio)Nicotinic Acid should be stored in a tightly sealed container, away from moisture and incompatible substances. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature (15–25°C). Protect from direct sunlight and sources of ignition. Ensure easy access to safety data sheets and use appropriate personal protective equipment when handling. |
Applications of 2-(N-Propylthio)Nicotinic Acid in Industrial Manufacturing2-(N-Propylthio)Nicotinic Acid supports specialized downstream industries, where its molecular reactivity and physicochemical profile offer distinct performance advantages in targeted pharmaceutical intermediates, advanced agrochemical synthesis, and specialty pigment manufacturing. Below, we present detailed application scenarios, reflecting both production realities and the strictest industrial quality frameworks. 1. Pharmaceutical API Intermediate SynthesisIn small-molecule drug development, this compound functions primarily as a thioether-bearing nicotinic acid intermediate, enabling the stepwise construction of pyridine ring-containing APIs, including modified nicotinamide derivatives with enhanced pharmacokinetics or metabolic stability. Manufacturers typically select this raw material at the advanced intermediate stage, ensuring precise sulfur incorporation and controlled side-chain reactivity during multi-step synthesis workflows for antihypertensive or central nervous system agents. Industry compliance standards
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2. Agrochemical Synthesis for Fungicidal ActivesDownstream agrochemical producers utilize this compound as a key building block to construct heterocyclic thioether motifs in new-generation fungicides targeted at cereal and fruit protection. By integrating the propylthio functional group, manufacturers achieve increased molecular hydrophobicity and controlled field persistence, directly influencing the spectrum of activity and environmental behavior required by regulatory agencies. Industry compliance standards
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3. Dye and Pigment Intermediate ManufacturingIn the colorants industry, especially for specialty dyes and pigments based on pyridine motifs, 2-(N-Propylthio)Nicotinic Acid acts as an intermediate to introduce electron-donating thioether groups, which enhance chromatic intensity and persistence under industrial dyeing conditions. Colorant producers use the compound in high-temperature and high-pressure synthesis sequences to develop tailor-made pigment dispersions with increased lightfastness and resistance to aggressive textile processing chemicals. Industry compliance standards
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4. Fine Chemical R&D and Reference Material SynthesisR&D laboratories and custom synthesis plants use 2-(N-Propylthio)Nicotinic Acid to create defined analytical standards and supply reference intermediates in high-precision traceability workflows, particularly for pharmaceutical and analytical reagent industries where high-purity derivatives confirm synthetic pathway validity or offer distinctive spectral markers in method validation. Industry compliance standards
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From the perspective of a manufacturer deeply rooted in fine chemical synthesis, 2-(N-Propylthio)Nicotinic Acid has taken a central role in our product catalog. The journey to scale up this compound from bench-scale reactions to multi-kilogram batches taught us much about the unique requirements of processing sulfur-containing heteroaromatics and the handling of pyridine derivatives in real-world conditions. The chemical structure, a nicotinic acid scaffold bearing a propylthio group at the 2-position, offers properties that set it apart from standard nicotinic acid derivatives often seen in research and early pharma development.
2-(N-Propylthio)Nicotinic Acid isn’t just a result of combining reagents by the book. Our eldest chemical engineer likes to say that handling sulfur and pyridine together demands both vigilance and respect for the volatile realities of live chemistry. We have seen the compound produce stable, reliable yields only in reactors where temperature management, purity of inputs, and air exclusion get uncompromising attention. The finished product typically crystallizes as an off-white powder, odor hinting at its thioether identity, and solubility that meets the needs of further transformation or formulation. Typical specifications meet a minimum purity of 98% by HPLC, with strict control over propyl chain isomers, pyridine by-products, and inorganic impurities.
We manufacture using a multi-stage process that begins with the sulfidation of halonicotinic acid, protecting the pyridine ring from over-reaction, and controlling the alkylation to selectively introduce the n-propylthio side chain. Each batch undergoes assessments for residual solvents, water content, heavy metals, and batch-to-batch consistency. Every parameter matters, especially as research users and pilot plant operators depend on predictable behavior from gram to kilogram scale.
Over the years, we've seen customers request tighter specifications as their projects move from early screening to intermediate-scale synthesis. At first, only a handful of research groups worried about minor thiol residues or isomeric contaminants. Now, as this compound finds its way into more regulated or process-sensitive applications, we’ve updated our purification steps. Recrystallization, multiple solvent washes, and periodic review of chromatography method development have made a difference.
Instead of working to a theoretical purity, our laboratory takes each batch analysis seriously, comparing new runs against rigorous reference standards. Retained samples from each batch help us resolve any client queries about performance anomalies. Our shift supervisors routinely check not only the HPLC traces but also color, melting range, and IR spectra—real markers of stability over weeks and months. Clients have told us that reproducible impurity profiles reduce validation runs and avoid surprises in subsequent synthetic steps.
Consistency, in our view, has come less from written protocols and more from the daily vigilance of skilled producers. Any operator here would say small deviations in solvent ratios or heating rates show up clearly during later stages. Overreliance on automation sometimes hides these factors. We believe the right balance links machinery with direct human oversight, especially when producing heteroaromatics or thioethers like 2-(N-Propylthio)Nicotinic Acid.
Much of the demand we see for this compound comes from pharmaceutical researchers and process chemists in agrochemical pipeline development. Medicinal chemistry teams often choose 2-(N-Propylthio)Nicotinic Acid as a scaffold for novel bioactive molecules, especially when sulfur linkage gives the desired metabolic stability or electronic effects. The presence of the nicotinic acid framework hooks into established synthetic sequences while the propylthio group modulates solubility and reactivity for targeted functionalization.
In our experience, we’ve noticed that as screening libraries shift towards more S-containing heteroaromatics, our sales of this acid trend upward in parallel. Feedback from one client project suggested that introducing the n-propylthio group led to a new class of kinase inhibitors with improved pharmacokinetics in animal models. The same structural features have caught the attention of agrochemical discovery teams, where they relate the thioether’s stability to environmental breakdown profiles. We sometimes assist with alternate salt forms or co-crystallization efforts for clients who need improved formulation or handling properties.
We have shipped this product to destinations as varied as pilot plants in Europe and specialized start-up synthesis labs in the US. Each context brings nuances—high-throughput screening groups focus on milligram samples, while process development chemists regularly order multi-kilo lots and expect precise technical documentation. Over the past decade, the growing recognition of sulfur heterocycles as bioisostere partners has spurred steady increases in bulk requests.
Our technical team also runs in-house reactivity tests, exploring chlorination, oxidation, or amide coupling possibilities for customers needing proof-of-concept before investing in scale-up. Direct feedback loops from users influence the way we approach packaging, labeling, and technical bulletins. When a batch once showed unexpected sensitivity to light, we switched to amber glass packaging—a simple adaptation that comes from listening to those on the receiving end.
From inside the plant, it’s clear this compound carves out a strong middle ground between parent nicotinic acid and more conventional thioether derivatives. Unlike methyl- or ethylthio analogs, the n-propylthio modification produces a notable shift in both side-chain lipophilicity and chemical reactivity. Scientists tuning molecular properties—looking for fine control over plasma clearance or membrane permeability—notice this. Compared with methylthio versions, the propylthio acid often delivers higher retention times in LC analyses, offering a direct handle for purification and tracking.
We have run side-by-side stability studies. The n-propylthio group shows greater resistance to oxidation under storage than more branched or shorter-chain thioethers. This impacts shipment: batches shipped to monsoon-affected regions arrived unchanged after weeks in transit, while an earlier shipment of ethylthio analog fared less well, giving mild odor and color changes by the time it reached the client. These subtleties might not appear on a raw specification sheet but influence real costs and laboratory hassle.
In the lab, 2-(N-Propylthio)Nicotinic Acid often tolerates a broader range of reaction conditions. Nucleophilic substitutions on the ring progress smoothly without the decomposition seen in structurally similar acids. During scale-up work with clients, we observed higher isolated yields and fewer side reactions with this propylthio acid. These facts reflect both the chemical resilience of the molecule and the process control we bring to its manufacture.
Some advanced users modify this acid further, for instance, incorporating it into peptidomimetic frameworks or as a precursor for cephalosporin side chains. Here, the longer-chain thioether delivers both synthetic handle and improved organoleptic features, such as reduced pungency and enhanced crystallinity for clean workups. One client switched to the propylthio acid from a more volatile thiomethyl analog after running into repeated inhalation annoyance among staff—a practical, if rarely reported, benefit.
Working with sulfur-functionalized pyridines has taught us how easily batch outcomes can turn on small factors. Early in our production practice, we faced unexpected foaming during neutralization steps, which traced back to trace contaminants in a minor raw material. Thorough line cleaning and improved pre-filtration now keep things under control. Handling fumes in pre-alkylation steps pushed us to invest in better local ventilation and activated carbon trapping for off-gasses.
Operators have become highly skilled in detecting subtle changes—color, viscosity, trace by-product formation. When external temperatures climb, our teams adapt cooling profiles to avoid runaway reactions. These lessons have filtered back into our training manuals and shaped the design of new reactors—extra sampling ports make in-process monitoring faster and safer. No automation eliminates the need for regular human assessment, whether that means sniffing for thioether traces or inspecting crystallization tanks by hand.
Reflections from batch logs reveal how critical the timing of sulfidation and temperature ramps becomes for clean product isolation. We once attempted a process shortcut by raising the concentration of base during alkylation, resulting in double-alkylated impurities hard to remove downstream. Returning to a more controlled regime restored both yield and throughput. Such adjustments, rooted in real operational feedback, support both quality and cost control across our manufacturing site.
The regulatory climate has grown tighter over recent years. We respond by reviewing batch records, maintaining detailed process logs, and investing in analytical upgrades. QA teams now run ICP-MS rather than only colorimetric heavy metal checks on every lot—a shift reflecting sharper scrutiny by industrial health and safety teams. Our approach melds hands-on process understanding with formal QA protocols.
After the reactor work concludes, attention turns to how 2-(N-Propylthio)Nicotinic Acid handles storage, shipment, and end use. Packing the acid in double-lined containers, with desiccant bags included, limits moisture uptake—a risk amplified in coastal and humid regions. Clients in climates with high ambient moisture have commented on how our packaging choices limit caking and preserve free-flowing powder between batches, saving time during weighing and formulation.
We track stability under varied light and temperature exposures. Storing away from direct sun and at moderate temperature keeps the acid stable for twelve months or longer, well within the requirements of research teams and pilot plants. Shorter chain analogues sometimes require more aggressive packaging, as they degrade faster. We have never seen significant change in appearance or purity for the propylthio acid under standard storage.
International shipments require paperwork, but we focus just as much on practicalities—customs regulations, transit times, and winter/summer shipping conditions. Our logistics crew prepares shipments as if they’re sending reagents for their own experiments, with extra insulation for air transport and quick release customs documentation. We keep backup samples from each outgoing lot in controlled storage, so customer support always has traceability records, in case questions arise about lost or damaged consignments.
Our relationship with 2-(N-Propylthio)Nicotinic Acid users stretches well beyond simply selling powder. Chemists at the receiving end want reliable documentation, responsive support, and a sense that the supplier shares their sense of urgency. We have dedicated technical staff who answer questions about reactivity, batch registration, or troubleshooting downstream couplings. Sometimes a phone call clarifies more than a technical sheet, so live communication remains a staple.
Feedback loops run both ways. When a pharma group in Asia encountered batch-to-batch variability with a previous supplier, our technical team reviewed their work-up conditions and offered a slight procedural adjustment that restored their yields. In another case, an academic research team requested alternate particle sizing to fit their automated reactor, so our plant manager redesigned the final milling step to deliver a finer, more consistent granulate.
Process innovation draws on both market signals and hands-on experience. Users ask for improvements—reduced odor, finer particle flow, lower trace metal content—in ways that directly shape our planning. Our production line investments reflect these requests. When clients’ projects scale up from tens of grams to tens of kilograms, we adapt with parallel reactors, additional purification trains, and more rigorous documentation.
Occasionally, clients request modifications—a specific counterion, buffered salt, or altered hydration level. We address these by testing compatibility and offering trial batches for evaluation. The most successful interventions spring from understanding not only the chemistry but also the industrial context. Our teams visit client sites, learn about their downstream processing, and bring those insights back into our own production adjustments. This kind of feedback-driven cooperation keeps both sides nimble and up to date.
We produce a range of heterocyclic building blocks—quinolines, pyridines, benzimidazoles—and each comes with its own challenges. Compared to our basic nicotinic acid or methylthio pyridine lines, 2-(N-Propylthio)Nicotinic Acid requires more attentive material handling due to sulfur volatility concerns. The payoff comes in higher product integrity, better storage behavior, and wider reaction scope. Our handling of this acid now informs CMC filings for several drug projects.
From a plant scheduling angle, thioether products require separate work-up zones to avoid cross-contamination and odors in unrelated lines. Water management and exhaust scrubbers receive greater use, protecting both staff and neighboring production lines. As a result, we rotate operators familiar with the nuances of the propylthio acid’s synthesis and recovery, reducing mistakes and cementing a sense of pride among those who consistently turn out high-grade material.
Compared to more complex sulfur-containing heterocycles, the propylthio nicotinic acid represents a balanced compromise—accessible precursor chemistry, predictable scale-up, and moderate cost structure. Equipment cleaning after each batch still demands more effort than our wholly oxygen- or nitrogen-substituted lines, but the longer-term value for customers keeps production on a firm footing.
As demand and application areas evolve, so too do our approaches to production efficiency and quality assurance. The rise of green chemistry prompts us to seek safer, lower-waste alternatives for sulfidation steps. Trials with improved solvent recovery systems and phase-transfer catalysts have begun to reduce both environmental load and operational costs.
Collaborations with academic labs give us early visibility on mechanistic advances that might improve selectivity or lower risk. Our R&D team pilots such innovations on small batches before committing to plant-wide changes. Continuous improvement means analyzing every failed batch, every unexpected impurity, and every lost lot traceability as a learning event, not just a cost.
Transparency and reliability will always stand as our foundation, not only for regulatory compliance but as the cornerstone of our relationships with end users. Whether a client’s work lies in drug development, agriculture, or catalyst research, we understand the stakes behind each order. From product origination to final packaging, every decision and every intervention traces back to a network of skilled hands and keen eyes committed to real-world quality.
The manufacture and supply of 2-(N-Propylthio)Nicotinic Acid connect chemistry, process engineering, logistics, and customer collaboration. Each batch carries the markers of both precise control and adaptive learning. Our performance reflects confidence in both the compound and the people behind it. With every order met and every challenge faced, we continue refining both product and process for the chemists and engineers who depend on consistent, trustworthy supply.