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HS Code |
995791 |
| Productname | (R)-(-)-2,2,2-Trifluoro-1-(9-Anthryl)Ethanol |
| Casnumber | 87413-09-0 |
| Molecularformula | C15H9F3O |
| Molecularweight | 262.23 |
| Appearance | White to off-white solid |
| Opticalrotation | [α]D20 = -46° (c=1, CHCl3) |
| Meltingpoint | 86-88°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in common organic solvents such as chloroform, dichloromethane, and ethanol |
| Smiles | C1=CC=C2C(=C1)C=CC3=CC=CC=C3C2C(C(F)(F)F)O |
| Inchi | InChI=1S/C15H9F3O/c16-15(17,18)14(19)13-9-6-8-4-2-1-3-7-11(8)12(13)10-5-9/h1-7,10,14,19H/t14-/m1/s1 |
| Absoluteconfiguration | R |
| Storagecondition | Store at 2-8°C, under dry conditions |
| Application | Chiral alcohol used as a building block in asymmetric synthesis |
As an accredited (R)-(-)-2,2,2-Trifluoro-1-(9-Anthryl)Ethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 1 gram of (R)-(-)-2,2,2-Trifluoro-1-(9-Anthryl)Ethanol, labeled with hazard information and barcode. |
| Shipping | (R)-(-)-2,2,2-Trifluoro-1-(9-Anthryl)Ethanol is shipped in tightly sealed containers, protected from moisture and light. It should be transported as a chemical substance with care, conforming to relevant regulations for organic compounds. Temperature should be controlled to avoid decomposition, and all safety protocols must be strictly followed during transit. |
| Storage | (R)-(-)-2,2,2-Trifluoro-1-(9-Anthryl)ethanol should be stored in a tightly sealed container, protected from light, moisture, and air. Keep it in a cool, dry, and well-ventilated area, ideally at 2–8°C (refrigerator). Avoid sources of ignition and strong oxidizers. Label clearly and store separately from incompatible substances to ensure safety and maintain compound stability. |
Applications of (R)-(-)-2,2,2-Trifluoro-1-(9-Anthryl)Ethanol in Industrial ManufacturingAs a manufacturer of (R)-(-)-2,2,2-Trifluoro-1-(9-Anthryl)Ethanol, we supply key chemical raw material for a range of specialized industrial downstream applications. Our production quality supports demanding synthesis and formulation requirements across advanced pharmaceutical intermediates, chiral catalyst development, luminescent material engineering, and high-sensitivity analytical standards. Below we detail typical use-cases, compliance guidelines, dosing parameters, integration methods, and final product types adopted by industrial partners. 1. Chiral Building Blocks for Pharmaceutical API SynthesisMany pharmaceutical producers use this compound in the synthesis of complex APIs where chirality and fluorinated motifs are essential. It enters synthetic routes that require high enantiomeric excess and robust reactivity, especially for advanced oncology and CNS drug candidates. QC teams monitor the purity and enantiomeric enrichment at each step, incorporating full documentation for regulatory and client batch release. Industry compliance standards
Typical usage ratio
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2. Chiral Auxiliary in Asymmetric CatalysisSpecialty chemical manufacturers leverage the compound as a chiral auxiliary or ligand in asymmetric catalysis R&D, focusing on enantioselective hydrogenation and alkylation processes. Accurate dosing and integration directly affect stereochemical outcome, making full traceability and analytical support essential during scale-up. Industry compliance standards
Typical usage ratio
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3. Luminescent Marker Development for OLED and Sensor MaterialsAdvanced materials producers apply the aroma ring–fluorinated core of the compound in R&D of luminescent markers for OLED displays and photonic sensors. Its structure enables tunable emission with high photo-stability, critical in the design of blue-emitting and near-UV components. During integration, the purity specification directly impacts emission efficiency and lifetime. Industry compliance standards
Typical usage ratio
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4. Analytical Reference Standard in Stereochemistry QCLaboratories and QC centers depend on this molecule as a reference standard for enantioselective chromatography calibration and method validation. Its well-defined stereochemistry, UV absorbance, and chemical stability support routine system suitability testing in regulated environments. Industry compliance standards
Typical usage ratio
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There is a certain rhythm to producing (R)-(-)-2,2,2-Trifluoro-1-(9-Anthryl)Ethanol, and it’s a name that demands respect in the lab. Over the years, our team has learned that running a production line for this molecule means grappling with the quirks of both fluoro-organic chemistry and polycyclic aromatic systems. As a manufacturer, we rarely talk about broad applications or imagined utility. Daily experience tells a different story. Working with fluorinated alcohols and anthracene derivatives, we know purity drives both costs and customer confidence. (R)-(-)-2,2,2-Trifluoro-1-(9-Anthryl)Ethanol brings together a trifluoromethyl group, an anthryl backbone, and a chiral center. Every nuance along the production path—from ambient filtration to careful temperature control—can tip the batch from a reliable staple to a problematic outlier.
Customers often ask about the enantiomeric excess, although fewer ask what it actually means for their chemistry. Synthetic chemists, pharmaceutical researchers, and material scientists rely on absolute configuration to control downstream activity. This particular molecule only matters because it’s the pure (R)-(-) enantiomer. Any drift in configuration ruins the batch for chiral resolution studies or asymmetric catalysis. We use specific resolution agents and a careful optical rotation check with every lot. The difference is clear in applications: when a researcher builds a library or screens an enzyme, the wrong isomer wastes days and stops grant deadlines dead in their tracks. Our control charts don’t just exist for regulatory checkboxing; they’re the best insurance against wasted researcher time.
At a glance, some might lump (R)-(-)-2,2,2-Trifluoro-1-(9-Anthryl)Ethanol with other chiral alcohols or trifluoromethyl analogues. We track differences where it counts. The electron-withdrawing trifluoromethyl group shifts polarity, affecting both reactivity and solubility. Customers often report sharper selectivities in organocatalytic systems, compared to non-fluorinated analogues. The anthryl group, with its robust pi-system, nudges the molecule into photophysical territory. Researchers focusing on fluorescent probes and molecular recognition are drawn in by its unique spectral footprint. In contrast, standard chiral benzylic alcohols lack the bite and brightness this combination brings. Lower volatility than simple aryl alcohols cuts solvent losses and improves safety in scale-up work. Handling differences extend to stability: while aliphatic alcohols may oxidize or degrade, our experience shows the anthryl framework stands up to challenging storage and shipping conditions.
Our manufacturing model reflects the reality that research and early process development leave no leeway for ambiguity. Consistency begins with each batch. Methods get refined over years, not months—solvents, temperatures, and even glassware type have shifted as we chase the optimal mother liquor. Each time a customer calls about spectral data or trace impurities, we pull samples from cold storage and run the same checks we do at release. The baseline target is always over 99% chemical purity and over 99% enantiomeric excess. These aren’t just numbers—they reflect countless hours spent troubleshooting columns, maintaining dry environments, and training new chemists to respect the quirks of anthracene derivatives.
We supply several package sizes because we know a gram for analytical method development serves a different world than a 50-gram bottle going to a pilot plant. Every increment has faced different stressors during filling and transit. From glass ampoules for small quantities to amber bottles for larger deliveries, the packaging reflects lessons learned from feedback. Bottles that survived air-freight drops five years ago now have improved seals, driven by the few complaints that landed on our desk.
Most chiral alcohols sit in catalogs collecting dust. (R)-(-)-2,2,2-Trifluoro-1-(9-Anthryl)Ethanol demands attention throughout its journey. Anyone who’s run an anthracene coupling understands the double edge: strong UV absorption brings both opportunity and headache. Too much light, and batch quality suffers from photobleaching or unwanted side reactions. We built our production suite to block unnecessary UV. It became clear that not all silica columns deliver the same chromatographic performance with this molecule. The fingerprint of fluorinated aromatics requires selective eluents, careful solvent choice, and patience through each TLC run. Over the years, we’ve moved beyond routine TLC monitoring and built more robust HPLC protocols: chiral columns, refrigerated autosamplers, fresh standards every time. Every batch cue and every odd baseline shift becomes a troubleshooting session that drives future improvements.
For some, (R)-(-)-2,2,2-Trifluoro-1-(9-Anthryl)Ethanol is just another line item. On the shop floor and in the lab, niche matters. With its rigid anthryl ring system, the molecule offers advantages in conformationally constrained ligand design. Several teams have shared stories of using it in projects targeting new molecular machines. Others put its chirality to work in benchmarking asymmetric hydrogenations. The bright fluorescence of the anthracene core earns repeat orders from material scientists hoping to build new sensor arrays or supramolecular assemblies. Unlike generic fluorinated alcohols, the defined configuration brings downstream process savings—less purification, higher recoveries in chiral pool syntheses, and less time arguing about stereochemistry on review calls.
Every time an order goes wrong, whether by contamination or shipping damage, we know it’s a blow to trust. Customer calls about crystallization failures, evaporation losses, or odd byproduct peaks go straight to our process team. The unique combination of fluorine and aromaticity means the molecule sometimes surprises even seasoned chemists; polymeric deposits can appear if solvent quality drops, and one poorly sealed bottle can shift the humidity content enough to affect solubility profiles. Our solution isn’t a new marketing spin—it’s ongoing process monitoring, with changes tested at pilot scale before they reach the main floor. We’ve faced real losses from old desiccant packs or static build-up during bottling, so every packaging tweak comes from event review. Regular staff retraining deals with complacency before it creeps in.
We invest heavily in layered analytical checks. Some companies list an HPLC purity threshold and move on. Our reality differs. Each batch undergoes not just HPLC or GC, but FTIR and NMR too. The complex aromatic region means baseline integration is key, and automated software rarely catches low-level contaminants. Shifts in NMR peaks, due to trace amounts of hydrolysis or unwanted fluorination, call for a chemist’s eye. We retest stored samples months after production, matching spectra against customer feedback. Some large buyers care deeply about trace heavy metals, knowing their downstream catalysts can get poisoned by ppb levels. We developed ICP-MS methods specifically for these concerns, even though they slow throughput. None of these steps came by accident. Each check built on real-world mistakes—a batch with a subpar melting point, a solvent peak that wouldn’t go away, feedback from a partner whose product failed an external audit. These are not details to gloss over for the look of a certificate; they’re the cornerstones of keeping trust alive.
Those who’ve spent time amid drums and fume hoods recognize safety as more than paperwork. While (R)-(-)-2,2,2-Trifluoro-1-(9-Anthryl)Ethanol lacks the volatility of many solvents, its anthryl component nudges it toward stricter handling. Gloves, goggles, and careful weighing sound routine, but lessons from spilled batches and splashed wrists keep vigilance high. The compound’s slight bitterness serves as an early warning for spills. Our procedures call for rapid cleanup, full logs, and waste handling that outpaces regulatory requirements. Even with air-conditioned storage, bottles live with silica packs, upright to keep seals tight.
Every transfer between departments—shipping, production, quality assurance—triggers double checks. We’ve learned this diligence from lost batches en route, broken bottles in the warehouse, and customer stories of material that arrived unsalvageable. Anyone who says safety can be templated hasn’t watched the aftermath of an anthryl compound spill on epoxy flooring or heard the hours spent scrubbing residual fluorescence from glassware. This is a reality we live daily, not an abstract risk assessment line item.
Rarely does a week pass without requests for regulatory documentation or compliance queries. Production records, batch-by-batch analytical sheets, and chain-of-custody logs stack up, but this paper trail reflects the trust earned one batch at a time. Regulators and customers now expect more: robust environmental audits, batch-specific hazard sheets integrating the latest toxicology, and traceability down to the solvent lot. Some jurisdictions have started tracking shipment volumes of fluoroaromatics, a nod to both legitimate research interests and misuse concerns. This is not bureaucracy for its own sake; as a manufacturer, we feel these pressures in our process documentation, storage protocols, and disposal practices. Regulators aren’t just looking for box-ticking—they trace every raw material back to approved sources. No off-brand solvents, no skipped purity checks. Each round of regulatory scrutiny has forced us to upgrade tracking, aligning with international data standards and customer transparency demands.
Manufacturing this molecule means living with variability. Temperature fluxes, small changes in water content, or even a fresh silica column can nudge yields and purity. Over the last decade, we’ve learned that batch consistency comes less from fancy automation than from sharp-eyed technicians, detailed batch logs, and close feedback loops with researchers downstream. Subtle trends in yield drop-offs, shifts in color, or onset of faint odors trigger preemptive reviews—the type that folder-driven audits might miss. People on our team develop a feel for shifts in process, sometimes sensing a would-be issue before the instrumentation catches it. Peer review for every major batch deviation matters here. By involving the full team—chemical engineers, QC analysts, shipping—problems often get solved at their source rather than after customer complaints.
Requests come in for new analogues, higher purity levels, or shipments with different solvents—demands shaped by real research needs, not just catalog updates. The chance to scale up production, tweak a resolution step, or reduce process waste keeps our team leaning forward. Recent advances in green chemistry have nudged us toward more sustainable solvents and more energy-efficient routes. The long-term partnerships formed with academic groups push us. Researchers often bring problems to us before they become routine supply headaches. Their feedback steers us toward smarter purification protocols, alternative crystallization solvents, and tightened restrictions on residual metals.
Every successful release owes something to past failures. A batch that failed melting point based on slow ambient humidity creep taught us about desiccant use. A year where yields dropped along with the temperature outside drove a complete overhaul of environmental controls. An out-of-spec chiral column led to new supplier qualification checks for analytical consumables. When one batch shipped with slightly elevated aldehyde impurities, we didn’t just swap to fresh glassware; we changed our raw material source entirely. Each mistake recalibrates future practice, closing off risk avenues with every iteration. Factory records and lessons shared at weekly meetings capture improvements made, preventing both personal and institutional forgetfulness.
Not all value of (R)-(-)-2,2,2-Trifluoro-1-(9-Anthryl)Ethanol shows up in spreadsheets. Our team’s work—their hands, eyes, and instincts—turns rough intermediates into bottles ready for global research. The complicated name represents work that starts early and ends late, shaped by unexpected snowstorms, broken pumps, or the simple fact that a glass column sometimes drips where it shouldn’t. The trust customers show, ordering batch after batch, owes much to consistent relationships. Repeat feedback—both positive and negative—lands on real desks and shelves. Real lives build the reliability attached to every gram we send out.
The demand for (R)-(-)-2,2,2-Trifluoro-1-(9-Anthryl)Ethanol hasn’t followed fads or short-lived hype. Advanced chemistry keeps evolving, and so does the need for precise, reliable starting materials and intermediates. Anyone building chiral libraries, working on photophysical sensors, or designing new ligands knows the headaches caused by unreliable supply chains. We don’t manufacture by spreadsheet margins alone. Conversations with research partners, late-night troubleshooting over phone calls, and the challenge of solving one more batch deviation—all these things matter just as much as today’s yield percentage.
Quality control, exhaustive documentation, and staying stubborn about standards matter because the people counting on this molecule—pharmaceutical teams, academics, materials innovators—set their own reputations by what we deliver. Respecting that responsibility, every shift, every new hire, and every process review comes back to the simple fact: chemistry is about more than molecules. Every bottle represents the lived experience of hundreds of hands in our plant, meeting the evolving challenges of modern synthesis head-on.