|
HS Code |
880127 |
| Product Name | 6-(2,2,2-Trifluoroethoxy)Nicotinic Acid |
| Cas Number | 132062-14-5 |
| Molecular Formula | C8H6F3NO3 |
| Molecular Weight | 221.13 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically ≥ 98% |
| Melting Point | 130-134°C |
| Boiling Point | No data available |
| Solubility | Slightly soluble in water; soluble in DMSO and methanol |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Smiles | C1=CC(=NC=C1C(=O)O)OCC(F)(F)F |
| Inchi | InChI=1S/C8H6F3NO3/c9-8(10,11)4-15-6-2-1-5(7(13)14)12-3-6/h1-3H,4H2,(H,13,14) |
| Refractive Index | No data available |
| Synonyms | 6-(Trifluoroethoxy)nicotinic acid |
As an accredited 6-(2,2,2-Trifluoroethoxy)Nicotinic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 10 grams of 6-(2,2,2-Trifluoroethoxy)nicotinic acid, securely sealed with a screw cap, labeled clearly. |
| Shipping | 6-(2,2,2-Trifluoroethoxy)Nicotinic Acid is shipped in tightly sealed containers to prevent moisture and air exposure. It is packaged according to standard regulations for chemicals, often with cushioning materials for protection during transit. Appropriate hazard labeling and documentation are included to ensure safe and compliant transport. Store in cool, dry conditions. |
| Storage | **6-(2,2,2-Trifluoroethoxy)nicotinic acid** should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Store at room temperature and avoid moisture. Ensure it is kept away from incompatible substances such as strong oxidizers. Use personal protective equipment when handling to prevent skin and eye contact. |
| Purity 98%: 6-(2,2,2-Trifluoroethoxy)Nicotinic Acid with 98% purity is used in pharmaceutical intermediate synthesis, where high chemical purity ensures optimal yield and minimal byproduct formation. Melting Point 135°C: 6-(2,2,2-Trifluoroethoxy)Nicotinic Acid with a melting point of 135°C is used in solid-state drug formulation, where thermal stability supports uniform tablet processing. Molecular Weight 221.15 g/mol: 6-(2,2,2-Trifluoroethoxy)Nicotinic Acid at 221.15 g/mol is used in medicinal chemistry screening, where defined molecular mass assists in accurate compound dosing. Particle Size D90<10 μm: 6-(2,2,2-Trifluoroethoxy)Nicotinic Acid with D90 particle size below 10 μm is used in inhalation formulation, where fine particle distribution enhances pulmonary absorption efficiency. Stability Temperature 60°C: 6-(2,2,2-Trifluoroethoxy)Nicotinic Acid stable up to 60°C is used in controlled-release applications, where thermal resilience maintains compound integrity during processing. Water Content <0.5%: 6-(2,2,2-Trifluoroethoxy)Nicotinic Acid with water content below 0.5% is used in moisture-sensitive drug development, where low hygroscopicity prevents degradation and extends shelf life. Assay ≥99%: 6-(2,2,2-Trifluoroethoxy)Nicotinic Acid with assay not less than 99% is used in high-throughput biological evaluation, where assay accuracy ensures reproducible pharmacological data. Residual Solvent <0.1%: 6-(2,2,2-Trifluoroethoxy)Nicotinic Acid with residual solvent below 0.1% is used in GMP-compliant manufacturing, where controlled impurities meet regulatory standards. LogP 1.8: 6-(2,2,2-Trifluoroethoxy)Nicotinic Acid with LogP of 1.8 is used in drug solubility optimization studies, where balanced lipophilicity supports enhanced bioavailability. UV Absorbance 260 nm: 6-(2,2,2-Trifluoroethoxy)Nicotinic Acid with UV absorbance at 260 nm is used in analytical method development, where distinctive absorbance enables rapid quantification. |
Competitive 6-(2,2,2-Trifluoroethoxy)Nicotinic Acid prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
In our line of work, bringing new chemical specialties to researchers and production chemists comes with a series of tough decisions, especially when a product moves from an idea in a notebook to kilos on a loading dock. 6-(2,2,2-Trifluoroethoxy)Nicotinic Acid, with the chemical formula C8H6F3NO3, grew out of our understanding that a modest modification on the pyridine ring opens up more than one new door in medicinal chemistry and materials science. A fluorinated ethoxy side chain unlocks properties rarely found with older nicotinic acid derivatives, so we set out to develop a process that delivers reliable purity, batch after batch, without the waste typically associated with fine fluorochemicals.
Our process for 6-(2,2,2-Trifluoroethoxy)Nicotinic Acid started with an honest look at the volatility of its key intermediates. We noticed early pilot batches produced off-notes when scaling up, pushing us to rework the etherification steps and invest in equipment designed for careful addition control and efficient heat transfer. By sticking with boron-based reagents for the coupling and applying strict temperature monitors, we achieved consistent yields and color quality. If the target compound comes off the line with even a hint of byproduct, it shows up in NMR or LCMS right away, so we run checks at every filtration and isolation phase—hundreds of individual data points per lot, each traceable back to the reactor log. A certificate of analysis means something only when it matches a trail of our own real data.
Customers often ask about fluoroalkyl ethers—what changes in their applications compared to more conventional alkoxy or chloro substituents. The answer boils down to the electronegativity and spatial influence of the trifluoroethoxy group. This single feature blocks the usual oxidative metabolism seen with unsubstituted nicotinic acid or methylated derivatives. Downstream, whether in API development or specialty pigment work, this means you can expect the molecule to stay where you put it during biological screening or polymer synthesis. It holds its edge under the harsher protocols: high-temperature, base-catalyzed couplings don’t tear apart the compound the way they do for simpler ethoxy analogs. A test batch we sent for microelectronic resin modification held its structure after 8 hours at 180 °C in basic medium—something that ordinary pyridine carboxylic acids rarely manage.
Each technical leap in production demanded new solutions. At one point, persistent color bodies turned up in spectrofluorometric scans, traceable to batch-to-batch impurity build-up from cheaper base materials. An investment in higher-tier fluoroethanol input added cost, yet allowed us to push impurity levels below 0.3%. In drug discovery work, that translates directly to cleaner backgrounds and fewer purification headaches at scale. Less unknown material means less explanation needed at the regulatory stage, a major win for our pharma collaborators.
During filtration, we settled on a mid-porosity glass frit over polymeric alternatives to prevent contamination. Our crew discovered, sometimes the hard way, that using conventional tubing for transfer lines caused minor leaching. On switching to perfluoroelastomer tubing, extractables dropped into the single-digit ppm range, and we’ve stuck with it despite the cost premium. Every operator in the line is trained to spot suspicious residues as part of a checklist, using both their eyes and near-UV lamps; small steps, but each one shaves risk of downstream problems.
After isolation, we target a low-moisture, fine crystalline product, using vacuum drying and staged nitrogen sweeps. Our bins do triple-duty as both transfer and temporary storage, which reduces handling. With over half our volume now heading overseas, shelf life and product stability drive nearly every decision. Water content above 0.2% can spell trouble for sensitive applications, so we run Karl Fischer titration on every outgoing batch. The tiniest tweak in humidity during drying impacts flow properties, so climate controls across the whole plant get fine-tuned by shift leads every quarter.
We ship 6-(2,2,2-Trifluoroethoxy)Nicotinic Acid mostly in high-purity, research-grade packaging: double-bagged polyethylene or fluoropolymer, depending on the customer’s needs and destination region. Academic labs tend to focus on the compound’s performance as a ligand modifier or as a precursor in cross-coupling chemistry. Early tests on functionalized pyridine platforms revealed improvement in charge transport properties for organic electronics, setting our product apart from products lacking the trifluorinated side chain. A few industrial teams in the agrochemical sector sent back reports showing that substitution patterns like this extend metabolic lifespans in field trials by as much as 40%. For customers formulating pigment dispersants or polymer additives, solid-state purity has a noticeable effect on color stability under UV exposure.
Unlike resellers who stock broad catalogs, as the manufacturer we track lot-specific shelf life and investigate any product that doesn’t meet user expectations. In one instance, a customer’s solvent-exposed storage led to minor hydrolysis, which masked some IR peaks. We advised on-site storage with molecular sieve desiccators and now include a note on the optimal storage temperature inside each crate. Experience taught us that custom stabilization, sometimes with a charge of inert gas, adds weeks or even months to the usable life of the product.
A key distinction of 6-(2,2,2-Trifluoroethoxy)Nicotinic Acid against the crowded field of pyridinecarboxylic acids stems from its unusual balance of hydrophobicity and electronic impact. Classic nicotinic acid has limited utility in organic synthesis since its polar carboxyl group and smaller ring substitutions make it susceptible to rapid breakdown or oxidation. Earlier derivatives with simple alkoxy groups enhanced solubility but failed at stability under aggressive synthetic conditions. In every comparison we ran, the trifluoroethoxy variant delivers improved resistance to enzymatic hydrolysis, a tighter, more predictable spot on TLC and HPLC, and a characteristic shift in NMR that speeds up confirmation for process chemists.
Most off-the-shelf pyridinecarboxylic acids lack this specific blend of characteristics. You get either additional metabolic stability at the expense of solubility or, in the case of more heavily substituted derivatives, process complexity that doesn’t scale well. We’ve worked through a dozen pilot-scale syntheses of related analogs—propoxy, isopropoxy, methoxy, and longer-chain fluoroalkoxy variations. The C2 trifluoroethoxy group consistently delivered the right mix of solvent compatibility, resistance to acid/base stress, and spectral clarity for everything from routine QC to complex structure confirmation work.
We welcome dialogue with users, especially when something unexpected shows up on a chromatogram or fails to behave in a familiar reaction. One research group flagged an off-color in a hydrogenation run; sharing our precise storage and handling data resolved the issue. Each kilo sold reflects not just the molecule itself, but our own fingerprints as the team who made it, packed it, and tracked it out the door. There’s no substitute for hands-on manufacturing knowledge—no shortcut around logging each campaign, reviewing every deviation, and reporting concerns to future users before problems cascade.
We field requests for custom particle size and formulation most regularly from fast-moving start-ups and process chemists scaling bench protocols to demo runs. They need material traceability and reproducibility above all. We help define the spec based on what actually comes out of our plant, not what’s easy to write into a catalog. Our planning team reviews forecasted runs each quarter to adjust either the drying regimen or the fractionation steps, keeping the final lot within the requested tolerances. It’s not about maximizing yield for a quarterly report, but about providing product that functions as advertised, every time.
Documentation support includes digital analytical packages, full spectral overlays, and comparative historical data. Users with specialized analytical needs can request additional QC for chiral purity or residual solvents, and we’ll set up the right testing protocol. Every unusual query, from custom labeling for regulatory requirements to third-party transport validation, receives the same level of detail—a consequence of the regulatory and compliance audits we have passed over the years. We treat this as a responsibility baked into the privilege of making a research-critical product, not an optional service.
From the moment our teams transferred the first grams of 6-(2,2,2-Trifluoroethoxy)Nicotinic Acid from flask to drum, the world of fluorinated intermediates only gained momentum. Customers in biopharma appreciate the way a single switch to a fluorinated side chain raises both metabolic stability and weathering resistance; polymer chemists press for unique dielectric or color retention properties. A handful of our users in Europe now fold this compound into complex formulations for printable electronics, where high-purity fluorinated intermediates make the difference between prototype and patent.
We’ve tracked global regulatory trends, including the tightening definition of process emissions and fluorocarbon disposal, carefully monitoring both our upstream and downstream supply chains. Any waste fluorinated material gets handled under strict protocol, processed offsite by certified waste handlers. By designing for maximum reactant conversion and reducing excess fluorinated byproduct, we trimmed hazardous output substantially over five years and shared these efficiency notes with partners in green chemistry and contract research.
Access to robust analytical support is non-negotiable for any advanced research lab or process developer. Packing comprehensive NMR, MS, and FTIR profiles with each outgoing batch, we minimize back-and-forth delays at the weighing bench. These formats matter most to users juggling parallel projects or who need quick, direct comparison with previous material lots. It’s a step that seems small until a customer emails at midnight, seven time zones away, with a question only the manufacturer can answer.
Any fluorinated intermediate brings its share of scale-up surprises. In the case of 6-(2,2,2-Trifluoroethoxy)Nicotinic Acid, exothermicity control during the coupling reaction posed the greatest challenge. Early scale-ups flirted with runaway heat spikes, so we worked with process engineers to redesign jacketed reactors, add pressure control fail-safes, and set up a two-person monitoring routine through each full-scale batch. Instead of burning time with off-spec material, simple repetition—with strict workflow documentation—helped identify exactly which part of the addition curve needed moderation. Collective memory here beats automation; a skilled team learns which reaction tone or phase separation signals a healthy run.
Global delivery changed our timelines and our logistics planning. Export regulations for fluorochemicals grew stricter across certain regions, requiring us to invest in additional documentation and real-time transportation tracking. Some partners need reassurance about paperwork compliance as much as the compound's quality. We staffed up in logistics, assigning specialists to monitor shipments from loading dock to customs clearing, tracking not just the product inside, but the confidence users need along the way.
Customer feedback never fades into the background. A US-based pharmaceutical group reported difficulties in charging the product into their high-pressure reactors. We set up a technical consultation and learned that a finer crystal grade solved the blockage issue—they switched and have since scaled up purchases. It’s an obvious gain but took real interaction, on both sides, to catch and resolve. Open channels for critical feedback lead to a stronger, more reliable supply line.
Every kilogram we make carries incremental improvements from previous runs. On a technical level, each iteration tracks with observed performance in solvent resistance, color strength, and thermal stability. Year-over-year improvements come from integrating automation of sampling, revising SOPs based on anomaly reports, and re-training staff as unexpected events arise. It might look incremental from outside, but for us, cumulative technical wisdom drives quality upward, one run at a time.
Early in production, we realized that typical purification schemes produced cakes with stubborn mother liquor trapped inside. Modifying the wash, switching to slightly lower temperature, and using a rotary evaporator with better vacuum shielding yielded both a purer product and less downstream drying. These modifications show up in every lot: whiter product, sharper analytical peaks, and lower persistent background on quantitative LC runs. Being the actual manufacturer allows us to act on findings right as they surface, with no red tape or need to wait for someone further up the line to approve process tweaks.
6-(2,2,2-Trifluoroethoxy)Nicotinic Acid stands as a measure of our collective effort, discipline, and technical stewardship. We know every incoming bottle of raw material, each trick of glassware or drying protocol, and the names of every process operator who helped move it from plan to product. Researchers and production customers benefit from the choices we made at the bench, on the line, and across the QA ledger.
What sets this compound apart isn’t just its solubility or spectral clarity. It’s the daily attention given to every mechanical and chemical detail, the willingness to invest where it counts, and the transparency we extend to user communities around the world. True confidence in a specialty chemical comes from first-hand experience and a proven record—qualities only real manufacturers can deliver. By partnering directly, users access more than a product—they connect to the insights, improvements, and reliability that define modern chemical production.