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HS Code |
497201 |
| Product Name | 9-Anthracenemethanol |
| Purity | 99.5% |
| Chemical Formula | C15H12O |
| Molecular Weight | 208.26 g/mol |
| Appearance | White to yellowish powder |
| Melting Point | 178-182°C |
| Boiling Point | 440.2°C at 760 mmHg |
| Density | 1.25 g/cm3 |
| Cas Number | 1468-95-7 |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Synonyms | 9-Anthracenylmethanol |
| Storage Temperature | Store at 2-8°C |
| Smiles | OCc1c2ccccc2ccc2ccccc12 |
| Flash Point | 210.3°C |
| Ec Number | 215-984-8 |
As an accredited 9-Anthracenemethanol (99.5%) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 9-Anthracenemethanol (99.5%) is packaged in a 25g amber glass bottle, securely sealed, with hazard labeling and product information. |
| Shipping | 9-Anthracenemethanol (99.5%) is shipped in tightly sealed, chemically compatible containers to prevent contamination and spillage. Packages are clearly labeled according to hazardous material regulations and protected with cushioning material. Shipping is typically via ground or air, following all relevant safety and documentation guidelines for laboratory chemicals. |
| Storage | **9-Anthracenemethanol (99.5%)** 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. Store at room temperature or as indicated on the supplier’s datasheet. Ensure effective labeling and keep away from sources of ignition. Follow all standard chemical storage protocols. |
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Purity 99.5%: 9-Anthracenemethanol (99.5%) with high purity is used in organic synthesis for photochemical studies, where it ensures reproducible reaction outcomes and minimal side reactions. Molecular Weight 210.25 g/mol: 9-Anthracenemethanol (99.5%) of molecular weight 210.25 g/mol is used in fluorescence probe development, where it provides precise spectral emission profiles. Melting Point 162–164°C: 9-Anthracenemethanol (99.5%) with a melting point of 162–164°C is used in the preparation of crystalline host matrices, where it yields uniform crystal growth for optoelectronic applications. Photostability: 9-Anthracenemethanol (99.5%) exhibiting high photostability is used in the creation of photonic devices, where it maintains long-term fluorescence intensity. Low Moisture Content: 9-Anthracenemethanol (99.5%) with low moisture content is used in organometallic catalysis, where it prevents hydrolytic degradation and preserves catalyst performance. Solubility in Organic Solvents: 9-Anthracenemethanol (99.5%) with high solubility in organic solvents is used in thin-film fabrication, where it ensures homogenous film formation for electronic device applications. Thermal Stability up to 150°C: 9-Anthracenemethanol (99.5%) with thermal stability up to 150°C is used in thermal curing processes, where it supports processing without decomposition. UV Absorption Peak at 254 nm: 9-Anthracenemethanol (99.5%) with a UV absorption peak at 254 nm is used in spectrophotometric assays, where it offers sensitive detection and quantification of analytes. |
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In the world of specialty chemicals, 9-Anthracenemethanol with its impressive purity of 99.5% stands out for scientists and innovators hungry for reliability and performance. The chemical, often known simply as 9-AM, carries the formula C15H12O and shows up in labs as a pale yellow powder or crystalline solid. Its structure speaks to its lineage—anchored by an anthracene core, with a single methanol group at the 9-position, giving it a set of chemical properties nothing else quite copies. From my perspective working with research teams, that purity matters. Anything less invites inconsistent results or wasted effort, making 99.5% a practical standard rather than only a technical bragging point.
High-purity chemicals such as this aren’t just trophies for a shelf. Tiny impurities muddle reactions, skew spectroscopy, or derail synthesis plans. In organic photochemistry, where 9-Anthracenemethanol finds a frequent home, trace contaminants can quench excited states or create dark byproducts. For researchers chasing subtle signals or evaluating new reaction mechanisms, this kind of reliability lets the experiment, not the chemical, take the stage. The difference may seem small from the outside, but after digging through the noise in test data or seeing strange spots appear in chromatography, you grow to respect a product that delivers consistency run after run.
With 99.5% purity, any leftover material sits at minuscule amounts—less than five parts in a thousand. Contaminants such as residual hydrocarbons or oxidized traces become rare enough not to matter in most setups. The molecular weight lands at 208.26 g/mol. Melting occurs between 120 and 125 degrees Celsius, making it pretty easy to handle in a basic lab, and it holds up under modest heating without quick decomposition. Dissolving well in solvents such as ethanol, dichloromethane, or acetonitrile makes it flexible for practical reactions or preparative methods. These aren’t just trivia points: In my own experience, rapid solubility means time saved preparing solutions and more reproducible product yields week after week.
So, what draws chemists and engineers to 9-Anthracenemethanol? The answer circles back to its anthracene backbone. This structure gives it unique photophysical properties. In organic photochemistry, 9-AM gets tapped as a fluorescent probe or as a photoactive substrate. For instance, researchers studying energy transfer or singlet oxygen generation appreciate its responsive emission. Its strong absorption in the UV region makes it a reference material for quantum yield calibrations. Often, I’ve seen it used as a standard in fluorescence spectroscopy, letting analysts calibrate their instruments with confidence.
Beyond photochemistry, this compound steps into organic synthesis. The hydroxymethyl group opens doors, letting chemists build more complex molecules or tether anthracene units together. Researchers synthesizing new molecular sensors, functional dyes, or even pharmaceutical intermediates use this functional branching point to introduce fluorescence alongside reactivity. I’ve watched as folks explore sensor arrays for environmental testing, attaching 9-AM and tracking changes in its fluorescence to detect heavy metals or toxins.
Practically, 9-Anthracenemethanol plays a role in fine-tuning polymers. For polymer chemists aiming to blend fluorescence or photoactivity into plastic films, this compound acts as a functional monomer. By incorporating it, engineers can build optical marking systems or anti-counterfeiting labels. Anyone who has investigated smart packaging knows how valuable an easily workable, stable, and photochemically active molecule can be in new materials.
And for students, small research labs, and advanced teaching courses, 9-AM supplies an accessible way to demonstrate photophysics, molecular engineering, or fluorescence microscopy without venturing into high-cost exotic materials. It offers big lessons about molecular behavior using a solid that stores easily and resists the headache of rapid degradation.
At first glance, someone might ask why not pick plain anthracene, 9-anthraldehyde, or one of the many anthracene derivatives available on the market. The answer comes down to practical chemistry. Plain anthracene has none of the easy functionalization offered by the methanol group. It also dissolves less readily in protic solvents, which can force extra steps in reaction setup. Again, that simple -CH2OH group attached to the 9-position turns up the versatility.
Compared to 9-anthraldehyde or 9-anthracenecarboxylic acid, 9-AM brings extra flexibility. The aldehyde groups of 9-anthraldehyde make it prone to oxidation and instability in air. 9-AM proves more robust in most storage conditions, and less sensitive to trace water in solvents, which is a quiet but frequent frustration in humid climates. The carboxylic acid version tends to aggregate and can complicate purification or analysis with strong hydrogen bonding, leading to less reliable outcomes.
In direct experience, switching between anthracene derivatives drives home how differences in functional groups affect both process and product, especially in organic synthesis or advanced material design. 9-AM allows chemists to build out diverse side chains through mild reactions, from etherification to Suzuki coupling, whereas either simpler or more reactive compounds box researchers in with limited routes or tough purification challenges.
Many outside the lab don’t always appreciate what “99.5%” really means. In practical terms, it isn’t just about hitting a regulatory threshold or lining up numbers in a catalog. Researchers invest weeks, even months, building projects that depend on that final decimal point. Instruments set up for trace fluorescence analysis won’t forgive hidden stabilizers or strange byproducts. Suppliers offering lower grades sometimes tempt buyers with price, but the hidden cost in unreliable or irreproducible data more than erases any savings.
From personal experience, nothing saps morale in a research group so quickly as a failed experiment traced back to something as mundane as a sub-standard reagent. Having a pure, reliably sourced anthracene derivative changes the pace and confidence in tackling challenging synthetic problems or setting up new teaching labs. Experienced technicians and new graduate students alike notice the difference—solubility, color, and even odor can reveal issues before instruments confirm them, but a top-tier material so often saves that headache.
Getting hold of 9-Anthracenemethanol isn’t especially difficult through reputable chemical suppliers, but storage and handling always need attention. The compound has good shelf stability under dry, dark conditions. Glass containers with tight-fitting lids keep it safe from moisture and light, prolonging its usefulness. In my lab days, storing near strong oxidants or in humid spaces could shorten its shelf life and degrade its fluorescent response. For users without access to professional storage, simple steps—using desiccators or amber glass bottles—make a real difference.
Though not classed as a high-hazard chemical, any work involving aromatic hydrocarbons brings exposure concerns. Nitrile gloves and standard goggles handle most risks during weighing and solution preparation. The compound has a mild, sometimes sweet odor, but working in a fume hood eliminates any chance of inhalation exposure. Safe chemical handling habits, drilled into everyone from interns to group leaders, keep the focus on science, not accidents.
Waste management comes into play for larger operations. While small quantities can be deactivated by standard organic waste procedures, bigger users should work with established collection and disposal services. This point doesn’t always get enough attention in academic labs, but thoughtful waste protocols keep operations smooth and regulators happy.
Beyond traditional quenching studies and synthesis, interest grows every year in new areas where anthracene derivatives leave a mark. Organic electronics, for instance, draw on the strong luminescence and electron mobility of anthracene cores. 9-AM holds promise as a precursor for blue-emitting organic LEDs, and researchers are investigating new blends with polymers for advanced displays or lighting systems. Its accessible price and open functional group give start-ups and university groups entry to a competitive field once dominated by expensive rare-earth compounds.
Green chemistry applications look especially promising. 9-Anthracenemethanol provides a handle for attaching to biodegradable polymers, perhaps opening the door for tracking, anti-counterfeit, or smart labeling that doesn’t leave behind microplastics or heavy-metal residues. Initiatives focusing on sustainable materials often choose known, manageable aromatics as stepping stones, and 9-AM fits well into this ethos. A few years back, I worked on a project exploring detectable packaging where safety, reproducibility, and minimal environmental after-effects all mattered equally. Here, a well-behaved, functional starting chemical made innovation possible.
No chemical comes without a few trade-offs. Despite its handy functional group, 9-Anthracenemethanol remains an aromatic hydrocarbon, meaning all the usual care with organic solvents and decomposition byproducts holds true. UV reactivity—so useful in experiments—brings limits to applications in outdoor or high-light environments. While some researchers use this to advantage, as in photodegradable materials, others searching for stability in sunlit spaces seek more robust alternatives.
In academic environments, cost per gram can stretch tight budgets, particularly at the higher purity levels. Bulk users negotiate directly with suppliers for price breaks, but small teams sometimes stick with less pure or alternate products, trading some reliability for savings. Long term, this suggests a role for tiered supply, with crystal-clear documentation describing exact impurity profiles, so buyers can make informed decisions rather than gamble with unknowns.
Opportunities exist for suppliers and users to engage on chemical quality and transparency. Clear, batch-specific analysis sheets and open channels for user feedback raise the standard, especially in an era where publications and patents depend on replicable, traceable work. Purchasers of 9-Anthracenemethanol deserve consistency so their time and labor don’t get sunk by guesswork around reagent purity.
For users stepping up from entry-level or mixed-anthracene products, collaborative partnerships can make a difference. Seasoned chemists often run side-by-side test reactions with both high- and low-purity versions, applying thin-layer chromatography or HPLC analysis to document differences in outcomes. This shared experience, passed on to students and techs, builds a knowledge base that moves teams ahead faster. I’ve seen the value of even simple crowd-sourced databases that list observed side effects, batch discrepancies, or purification tips—a kind of open-source troubleshooting that supports everyone facing similar challenges.
As photonics, sensors, and electronic devices grow more central to society, demand for versatile, high-purity aromatic compounds will only rise. 9-Anthracenemethanol sits at an intersection of accessible price, practical chemistry, and reliable performance. Emerging research aims to expand its uses into fields like molecular machines, DNA intercalators, and real-time environmental sensing. Collaboration between producers and end-users, focused on transparent, trustworthy chemical specifications, will help shape new breakthroughs that depend on repeatable, solid results.
At heart, good chemistry relies on trust—trust in your knowledge, trust in your team, and trust in your materials. High-purity 9-Anthracenemethanol supports all three by giving scientists and engineers a solid benchmark, free from the distractions or confusion of unknown contaminants. In classes and professional practice alike, having access to well-documented, reliable reagents lets energy flow into creativity, not firefighting.
Looking out over years of lab work, I recognize the small frustrations that add up—strange colors, suspect melting points, experiments that just won’t repeat. Over time, vigilance about chemical choice pays off in fewer wasted hours and higher confidence in reported results. 9-Anthracenemethanol (99.5%) is more than a line in a catalog. It winds up as a trusted ally for anyone who cares about making every experiment count, making new things work, and building the next wave of chemical innovation.