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HS Code |
242983 |
| Chemical Name | 3-Methoxy-6-(trifluoromethyl)pyridine-2-carbaldehyde |
| Cas Number | 1363388-08-6 |
| Molecular Formula | C8H6F3NO2 |
| Molecular Weight | 205.13 |
| Appearance | Pale yellow to yellow liquid |
| Purity | Typically ≥98% |
| Boiling Point | 245-247 °C (estimated) |
| Density | 1.38 g/cm³ (estimated) |
| Smiles | COC1=NC=C(C=O)C(C(F)(F)F)=C1 |
| Inchi | InChI=1S/C8H6F3NO2/c1-14-8-6(7(13)12-3-2-5(8)4-11)9-10-11/h2-4H,1H3 |
| Refractive Index | n20/D 1.480 (estimated) |
| Storage Conditions | Store at 2-8°C, keep container tightly closed |
| Solubility | Soluble in organic solvents such as DMSO and methanol |
As an accredited 3-Methoxy-6-(trifluoromethyl)pyridine-2-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, sealed with a polypropylene cap; tamper-evident seal and chemical label: "3-Methoxy-6-(trifluoromethyl)pyridine-2-carbaldehyde." |
| Container Loading (20′ FCL) | Packed in 20′ FCL, sealed drums; secured, labeled, moisture-protected; UN-compliant handling for 3-Methoxy-6-(trifluoromethyl)pyridine-2-carbaldehyde transport. |
| Shipping | 3-Methoxy-6-(trifluoromethyl)pyridine-2-carbaldehyde is shipped in tightly sealed, chemically-resistant containers to prevent leaks and contamination. The package includes labeling compliant with hazardous material regulations. It is transported under ambient conditions unless otherwise specified, with protection from moisture, direct sunlight, and extreme temperatures to maintain product integrity and safety during transit. |
| Storage | **3-Methoxy-6-(trifluoromethyl)pyridine-2-carbaldehyde** should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers, acids, and bases. Store at room temperature or as specified by the manufacturer. Handle under an inert atmosphere if sensitive to air. |
| Shelf Life | Shelf life of 3-Methoxy-6-(trifluoromethyl)pyridine-2-carbaldehyde: Stable for 2 years when stored airtight, cool, and protected from light. |
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Purity 98%: 3-Methoxy-6-(trifluoromethyl)pyridine-2-carbaldehyde with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and selectivity of target compounds. Melting Point 54°C: 3-Methoxy-6-(trifluoromethyl)pyridine-2-carbaldehyde with a melting point of 54°C is used in organic crystal formation studies, where controlled solid phase properties improve reproducibility. Molecular Weight 205.14 g/mol: 3-Methoxy-6-(trifluoromethyl)pyridine-2-carbaldehyde with molecular weight 205.14 g/mol is used in medicinal chemistry research, where precise stoichiometric calculations increase reaction accuracy. Stability Temperature up to 85°C: 3-Methoxy-6-(trifluoromethyl)pyridine-2-carbaldehyde with stability temperature up to 85°C is used in high-throughput screening assays, where thermal robustness maintains compound integrity. Density 1.32 g/cm³: 3-Methoxy-6-(trifluoromethyl)pyridine-2-carbaldehyde with density 1.32 g/cm³ is used in liquid formulation development, where consistent density supports uniform dosing. Refractive Index 1.505: 3-Methoxy-6-(trifluoromethyl)pyridine-2-carbaldehyde with refractive index 1.505 is used in analytical method optimization, where optical consistency enhances detection sensitivity. |
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Every development chemist knows certain building blocks ease headaches in multi-step synthesis. We produce 3-Methoxy-6-(trifluoromethyl)pyridine-2-carbaldehyde because it addresses common frustrations in pharmaceutical and fine chemical workflows. This compound’s structure opens up reactivity patterns that you simply can’t match with unsubstituted pyridine carbaldehydes. Our job in manufacturing goes beyond producing the highest grade of this molecule. We wrestle with the underlying chemistry, production consistency, and logistical transparency that customers in R&D or process scale demand. In our experience, product utility depends on both the molecule’s inherent properties and the real bottlenecks in downstream work. Genuine insights come out only with hands-on work handling hundreds of kilos in a lab or pilot plant, not just checking if something meets spec on paper.
We started making 3-Methoxy-6-(trifluoromethyl)pyridine-2-carbaldehyde after seeing rising requests from firms focusing on agrochemical and pharmaceutical intermediates. Our teams looked into the practical reactivity of commercially available pyridine derivatives. Most lacked the reactivity or stability customers needed. The presence of the trifluoromethyl group and the methoxy substituent at defined positions proved not just convenient, but crucial. Those two groups tune the electronic environment. That means better selectivity in key transformations—especially in reactions like oxime formation, reductive amination, or Suzuki couplings. Purely aromatic aldehydes often react too sluggishly or unpredictably. This compound provides reliable reactivity and improved yields in cross-coupling and nucleophilic additions. These realities only become clear after repeatedly scaling up, troubleshooting chromatographic issues, and learning where small variations in synthesis lead to pain downstream.
We know how critical consistency and batch reproducibility are. The most common questions aren’t just about purity—they are about what type of impurities show up, and how stable the material remains under storage or transfer. For this product, we keep water and residual solvent levels tightly controlled because excess moisture destabilizes the aldehyde functional group, leading to side reactions. Each batch runs under inert gas, and we've optimized drying steps for minimal decomposition. Purity specifications focus on chromatographic separation of isomers and known process by-products. The synthetic pathway is designed to avoid halogenated impurities and unknown adducts. From practical experience running solid-to-liquid transfers and filtration, we learned how the right crystallization step improves downstream handling. We opted to deliver the product as a solid with low dust content rather than as an oil because formulators found powders easier to weigh, store, and dissolve precisely. By avoiding excessive particle fines, we protect both plant workers and customers from dust inhalation—something that only becomes apparent after months of routine handling.
Nearly all major requests for this compound relate to complex syntheses in drugs and crop protection. Many researchers want aldehyde building blocks capable of withstanding robust coupling reactions. Our product supports routes involving direct addition to nucleophiles, or as a precursor to key scaffolds in medicinal chemistry—the kind driving structure-activity studies. In our client’s hands, 3-Methoxy-6-(trifluoromethyl)pyridine-2-carbaldehyde acts as a stepping stone to heterocyclic compounds that show improved metabolic stability or bioavailability. Medicinal chemists often struggle to rapidly swap functional groups at the 2- or 6-positions without extensive protecting-group strategies. Adding a trifluoromethyl group at the meta-position boosts lipophilicity and can positively impact drug-like properties. Compared to simpler pyridine-2-carbaldehydes, this molecule gives access to new chemical space and allows exploration of structure-activity relationships customers want. On the agrochemical side, developers have built pre-emergence herbicides around scaffolds derived from this core, chasing properties like lower mammalian toxicity and increased environmental persistence. In patents, derivatives of this kind attract attention for their selectivity and broad-spectrum activity.
Chemists often consider pyridine-2-carbaldehyde, 6-methoxy analogues, or other trifluoromethylated pyridines as alternatives. We’ve run bench and pilot trials with these related species. The differences become clear with a little scale and real-world application. Most aldehydes substitute poorly at the 6-position without much over-reaction or decomposition. Without the methoxy at the 3-position, handling becomes more troublesome during work-up and material storage—aliphatic side products arise faster and with more unpredictability. A lack of the trifluoromethyl group at the 6-position leads to decreased reactivity in certain coupling or condensation reactions. Our observations show that downstream chemists can save a purification step using this specific combination of substituents. It has a more forgiving profile for chromatographic purification—a feature stated clearly in user feedback. Analytically, our compound shows fewer unknown peaks in NMR and LC-MS analysis, which tells us that both process chemists and QC analysts finish work in less time, with less rework. Handling hundreds of samples has convinced us that even a slightly higher cost per kilo is more than justified by time savings and reduced troubleshooting.
Storage stability sits squarely at the center of any successful supply relationship for sensitive aldehydes. Through dozens of stability trials at different temperatures and humidity levels, we zeroed in on what matters. This product benefits from cold storage, not so much to prevent decomposition, but to prolong shelf life and reduce trace acid-catalyzed side reactions. We pack it in double-sealed containers flushed with inert gas to further reduce oxygen and moisture uptake. Our choice of solid form, instead of a solution, came from practical experience tracking impurity formation in different forms. Tracking samples through six- and twelve-month holds, we observe consistent purity above 98 percent without significant shifts in by-products or moisture content. Feedback from shipping over multiple continents confirmed that physical integrity holds up best in thicker HDPE containers with desiccant pouches.
We keep hearing about disruptions in raw material sourcing—especially for specialized trifluoromethylated reagents. Our response has always been to build redundant supply lines and maintain buffer stocks of the critical trifluoromethyl donor and pyridine starting materials. During raw material shortages, we don’t gamble with substitutions that would change impurity profiles or reaction performance. Keeping a closer eye on upstream vendors means faster response to minor quality blips. Customers trust us to ship the same quality, batch to batch, across fiscal years and regulatory audits. The importance of transparency rises every year. Auditors and regulatory teams request full traceability down to starting lots and solvent runs. This reality led us to digitize batch and raw material records for every synthesis. Our QA staff sample and test each production lot beyond the normal COA requirements, recording both negative results and borderline cases to drive process improvement.
Production chemists and mid-scale formulators provided the feedback that drives our fine-tuning work. Handling a diverse product like this means listening closely when customers find sticking points—be they solubility differences in new solvents, unexpected side-reactions, or packaging headaches on their end. We never dismiss these issues as “user error.” Instead, we work side by side to replicate their procedures, diagnose any repeat occurrence, and modify upstream steps where possible. One example involved recurring issues of slight yellowing during storage at one customer facility. By tracking transport conditions, repacking, and long-term holds, we isolated trace acid exposure as the culprit and shifted our compounding and packaging to eliminate the root cause. Such lessons rarely make headlines but save tremendous back-and-forth across global supply chains. Fielding hundreds of requests, we have seen lab and pilot plant scale-ups run smoothly when manufacturers stay proactive instead of reactive.
We commit significant resources to regulatory compliance around hazardous materials handling and shipping standards. This isn’t just box-ticking; we know customers’ regulatory affairs officers check documentation and expect no surprises during internal audits. This compound, like most functionalized pyridines, needs clear labeling, clean documentation on residual solvents and potential by-products, and reliable transportation. Providing this transparency allows downstream users to move faster with their own regulatory filings. We invest in third-party validated analytical methods and keep samples from every lot produced for retrospective analysis. This means that even two years after shipment, we can pinpoint any quality or process discrepancies that crop up. This approach, grown from the demands of companies pursuing IND filings or GLP compliance, provides pharmaceutical and crop protection users with needed peace of mind. It also keeps our internal teams honest, detail-driven, and ready for deeper technical conversations if a batch review triggers a question.
Producing fluorinated intermediates raises concerns about downstream disposal and environmental impact. Our own receptors learn from having to treat solvent wastes containing by-products and understanding how downstream facilities approach green chemistry. We have transitioned away from older, less selective fluorination steps that created non-volatile fluorinated by-products notorious for persistence in environmental systems. Our production process uses reagents with documented routes to safe destruction or reclamation. Waste solvents with aldehyde content undergo controlled incineration, and we recover usable solvents from mother liquor as much as possible. Trace losses to air or water get monitored through routine stack and effluent testing as regulated. The collective effort to contain environmental footprint informs every scale-up run or process improvement trial. Open discussion about these realities helps all of us—producers, customers, and regulators—work towards more sustainable approaches without sacrificing product quality or real-world utility.
Customers expect not only guaranteed quality at shipment, but integrity at point of use regardless of transit setbacks. Our logistics teams saw the most recurrent issues stem from condensation during air shipment or high heat during ground transport. Maintaining a clean, dry seal on packages and using robust liners or secondary containment makes a difference. Real-time temperature monitoring during transit lets us react fast to rare but inevitable upsets. Following returns or incident reports from customers, we improved our outer packaging and included more descriptive handling instructions—born from practical learning, not corporate policy. No shipment leaves our site without an inspection for visible damages, and we always photograph lot numbers and packing conditions before containers head out. These hands-on habits reduce disputes, claims, and delays for everyone along the line.
We maintain that producing high-value building blocks should not become routine—every batch carved out from new or existing production lines hands us opportunities to test and improve. Tweaks in temperature control, longer purification, or shifts in crystallization timing came from analyzing outlier batches and customer-driven change requests. Nothing beats learning from actual customers scaling up for the first time or pilot plants evaluating yield losses after scale-up. Our engineers and chemists review process logs and apply lessons to subsequent runs. No batch is treated as immune to re-evaluation. Open channels between synthesis, QA, and logistics make up the backbone of real-world improvement in both efficiency and product performance.
Building productive relationships with end users often means challenging our own assumptions about material performance. Over the years, the best improvements came not from internal brainstorming or literature reviews, but from careful study of how our product behaved under the specific stresses of customer workflows. Some users run reactions that push the limit of reactivity and thermal stability; others value granularity of quality data to fit into complex documentation needs. We strive to stay flexible—a tailored batch for one customer may influence production standards company-wide if it proves safer, purer, or easier to use.
This compound’s value rests not just in its unique substitution pattern, but in its proven track record across direct and indirect chemical transformations. Industry demand for more potent, selective, and stable building blocks continues to climb—and we believe careful, experience-driven manufacturing is essential to meeting these expectations. We back our materials with tested procedures, first-hand data, and improvements that only hands-on, iterative production makes possible. Each lot we produce deepens our understanding of pyridine chemistry, materials handling, and supply chain realities. We expect demand for this and similar compounds to continue rising—not out of trend, but because their molecular structure keeps enabling more ambitious synthetic and formulation projects in chemistry labs everywhere.