|
HS Code |
252901 |
| Cas Number | 5315-79-7 |
| Molecular Formula | C16H10O |
| Molecular Weight | 218.25 g/mol |
| Iupac Name | 1-Hydroxypyrene |
| Appearance | Pale yellow to greenish yellow powder |
| Melting Point | 170-172 °C |
| Solubility In Water | Slightly soluble |
| Density | 1.292 g/cm³ |
| Pubchem Cid | 10211 |
| Synonyms | Pyren-1-ol |
| Unii | 3687DU6N67 |
| Flash Point | Approximately 246 °C |
| Smiles | C1=CC2=C3C(=C1)C=CC4=CC=CC=C4C3=CC=C2O |
As an accredited 1-Hydroxypyrene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1-Hydroxypyrene, 5 grams, is supplied in a tightly sealed amber glass bottle with warning labels and clear chemical identification. |
| Shipping | 1-Hydroxypyrene is typically shipped in tightly sealed containers made of suitable, chemical-resistant materials to prevent contamination and exposure. The substance should be transported under controlled conditions, away from heat and direct sunlight, in compliance with relevant regulations and guidelines. Appropriate hazard labeling and documentation must accompany the shipment to ensure safe handling. |
| Storage | 1-Hydroxypyrene should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible materials such as strong oxidizers. Protect from light and moisture. Use appropriate personal protective equipment (PPE) when handling. Clearly label the storage container and keep it in a designated chemical storage area with restricted access. |
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Purity 98%: 1-Hydroxypyrene with purity 98% is used in fluorescence spectroscopy calibration, where enhanced signal clarity is achieved. Melting point 207°C: 1-Hydroxypyrene with a melting point of 207°C is used in thermal stability studies, where precise phase transition analysis is possible. Molecular weight 218.23 g/mol: 1-Hydroxypyrene with molecular weight 218.23 g/mol is used in environmental tracer research, where accurate quantification in water samples is ensured. Particle size <10 µm: 1-Hydroxypyrene with particle size <10 µm is used in solid-state sensor fabrication, where improved sensor surface uniformity is obtained. Stability temperature up to 140°C: 1-Hydroxypyrene with stability temperature up to 140°C is used in chromatographic analysis, where reliable compound integrity during analysis is maintained. UV absorption λmax 345 nm: 1-Hydroxypyrene with UV absorption λmax 345 nm is used in analytical standards preparation, where reproducible optical measurements are facilitated. Solubility in methanol 15 mg/mL: 1-Hydroxypyrene with solubility in methanol 15 mg/mL is used in solution-phase fluorescence experiments, where consistent sample preparation is achieved. Fluorescence quantum yield 0.75: 1-Hydroxypyrene with fluorescence quantum yield 0.75 is used in biochemical probe development, where high sensitivity detection is enabled. |
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Walk into any research lab focused on environmental monitoring or health research, and you’ll notice how often 1-Hydroxypyrene comes up. Behind the technical name lies a compound that quietly shapes how scientists track and evaluate pollution exposure. 1-Hydroxypyrene, with its formula C16H10O or often referenced by its CAS number 5315-79-7, serves as a key biomarker for understanding human exposure to harmful polycyclic aromatic hydrocarbons (PAHs). This particular molecule forms when our bodies metabolize pyrene—one of the more common PAHs released from incomplete burning of coal, oil, tobacco, or even grilled foods.
What sets 1-Hydroxypyrene apart among the crowd of similar compounds isn’t only its molecular formula or purity grade. Scientists choose it because it provides reliable evidence directly tied to real-world exposure, not just theoretical risks straight from test tubes. Researchers frequently measure 1-Hydroxypyrene in human urine to gauge actual contact with environmental PAHs. In the world of chemical analysis, dependable markers hold real value, since environmental decision-making eventually affects public health, regulatory standards, and even economic planning.
Behind the scenes, a lot depends on the purity and stability of this compound. Most research-scale access involves finely powdered, light yellow 1-Hydroxypyrene, typically available in purity levels above 98%. That level of quality matters if you want to draw trustworthy conclusions—in my lab days, a single impure batch could wreck months of careful sampling and cost much more than the price difference between higher and lower grades.
The compound has carved out a central role in environmental science. Testing agencies rely on it as a marker to spot increased cancer risk linked to burning activities or urban pollution hotspots. Universities set up long-term studies on how breathing city air over decades can raise PAH metabolite levels in blood or urine. Factory occupational health studies keep tabs on employees who handle coal tar or asphalt. Even food safety authorities track shifts in biomarker concentrations after dietary interventions, urging safer cooking techniques or limiting exposure to certain charred foods. So for many—students, researchers, and medical staff—access to the right chemical isn’t just another checkbox. It enables the work that powers real change.
We all hear about air pollution, but it becomes personal when you measure actual absorption by the body. That’s where 1-Hydroxypyrene’s importance shines. Its role as an internal exposure marker means that scientists and policymakers can finally bridge the gap between what floats in the air and the effects inside people. Air monitors might flash warning levels, but those numbers sometimes carry an air of uncertainty. By regularly tracking 1-Hydroxypyrene in a population’s urine, public health teams finally get a down-to-earth snapshot of genuine exposure and risk. After all, abstract numbers on a monitor don't replace the hard facts that emerge when you look at what’s actually accumulated in the body.
Where this compound really stands apart from the sea of other potential markers is its human relevance. Less direct markers might signal background levels or theoretical presence in an environment. 1-Hydroxypyrene directly reflects PAH uptake, even integrating exposure across many routes—soot in city air, residues on food, or cigarette smoke. Over the years, studies spanning urban Beijing to rural South America have found heightened 1-Hydroxypyrene among groups breathing polluted air or eating heavily charred meat. When I first learned about this, it changed the way I thought about that occasional barbecue and the invisible risks carried home by people working in road repair.
Some people ask why not just use pyrene itself, or a similar PAH metabolite? Specificity matters. Only some biomarkers reliably link back to certain PAH sources, and some linger far longer in the body than others. 1-Hydroxypyrene’s chemical properties, like its solubility and metabolic profile, help it serve as a tighter indicator. Advanced purification techniques yield powder that dissolves in organic solvents like DMSO or ethanol, features essential during fine-scale analytical work in mass spectrometers or chromatographs.
In the early 2000s, a handful of attempts used fluoranthene or benzo[a]pyrene metabolites for environmental assessment, but results stayed too noisy or broad to serve as regulatory tools. In contrast, 1-Hydroxypyrene bridges that gap and now sees wide adoption by organizations like the World Health Organization or European environmental agencies. It shows up in standardized protocols for evaluating worker exposure at production plants and in population health surveys across continents.
Suppliers often provide lots of technical jargon: melting point near 244–246°C, clear spectral fingerprints by NMR and HPLC, and purity above 98% as measured by GC or LC-MS. Those features aren’t there just for show. Lab techs use thin-layer chromatography and other basic tests right out of grad school to confirm identity and check for impurities. All it takes is a single contaminant to send a false alarm during an expensive study.
Occasionally a sample comes in as a slightly greying yellow powder, suggesting oxidation or moisture contamination—those batches often fail critical controls. Enough burnt samples have crossed my lab bench to remind me how batch consistency cuts down on wasted time and frustration. End-users in routine environmental surveillance or clinical studies rely on fresh, well-packaged material. Most high-quality product arrives in amber glass bottles sealed from light and air, giving the best shot at long-term stability.
Alternative markers exist, but each carries trade-offs. For example, benzo[a]pyrene diol epoxide could, in theory, measure similar processes, but its instability and toxicity add unnecessary lab hazards. In contrast, 1-Hydroxypyrene’s stability and clearer metabolic route simplify analysis. Sometimes a new paper proposes alternative metabolites or molecular proxies, yet they rarely offer the depth of validation seen in decades of 1-Hydroxypyrene research. For global studies or longitudinal data collection, only markers with well-documented properties can hold up across changing teams and geographies.
In clinics, cheap and accessible measurement counts nearly as much as accuracy. Analyzing 1-Hydroxypyrene levels can be automated using common instruments—high-performance liquid chromatography and tandem mass spectrometry—ensuring the data can be trusted and rapidly compared between different labs or cities. Regulatory authorities trust the results as both sensitive and specific, reinforcing its status as a gold standard.
Labs in lower-income settings sometimes struggle to access high-purity chemicals at reasonable prices. Here, large global suppliers and even campus-based chemical sharing programs can make a real difference. My own experience working on a student-run sampling initiative showed me how crowd-sourcing supplies between universities kept our river water research afloat—sometimes the difference between progress and being stuck on backorder for a crucial standard felt enormous.
Researchers often discuss open data, but the sharing of reference standards rarely gets the same attention. Setting up regional repositories or public–private partnerships to ensure quality control and timely access could put 1-Hydroxypyrene-based monitoring in the hands of more health centers, especially those tracking urban-rural disparities or vulnerable groups at risk for exposure.
Some regions rely on in-country synthesis to dodge import taxes and streamline delivery, but variations in quality sometimes pop up. International scientific networks have a role to play—not only to spot potential problems with off-spec batches, but to coordinate cross-border training in batch verification, sampling protocols, and result interpretation, so every data point counts for public health.
Many people outside specialty labs rarely see the direct impact chemistry makes on public life. Yet, in the long-term campaign for cleaner air and water, precise chemical markers like 1-Hydroxypyrene deliver the hard facts needed to push for safer policies and better awareness. In cities choking under smog alerts or rural communities downwind of industrial sites, this compound becomes a piece of the puzzle that powers newspaper headlines, fuels government debates, and shapes strategic interventions.
Policymakers looking to address air and water quality increasingly recognize the value of tracking biomarkers. If epidemiologists notice a spike in 1-Hydroxypyrene across a city after new power plants or relaxed environmental regulations, the data can serve as a warning flag, sometimes prompting action long before cancer cases skyrocketing or costly hospitalizations mount up. The numbers also help counter misinformation that often clouds public discussion around pollution.
The broader community gains a voice when equipped with reliable environmental health data. School groups can run ‘citizen science’ urine surveys, local clinics gather baseline levels after a refinery moves in, or advocacy groups use evidence to lobby for safer regulations. In every case, access to a trusted compound makes the difference between speculation and credible reporting.
No system works flawlessly. Problems with counterfeit or low-purity chemicals, especially in regions with patchier regulation, can skew findings and erode trust. Academic journals and technical conferences increasingly publish watchlists on problematic suppliers or batches. Encouraging more transparency in sourcing and certification can help rebuild trust. In parallel, ongoing training for field teams—sometimes just students working overtime to finish a master’s thesis—keeps techniques sharp and results robust.
Some critics ask if 1-Hydroxypyrene can truly represent all forms of PAH exposure, since other PAHs sometimes take different metabolic paths. Research groups now combine this marker with supplementary measurements, such as genetic susceptibility or cross-reference with additional PAH metabolites, to build a full picture. The field keeps evolving: what served as the gold standard a decade ago won’t always stay best forever. Yet, as of now, few rivals match it for real-world relevance and practicality.
A product with widespread use in population health and the environment can’t depend on vague standards or casual production. I’ve seen the difference careful documentation and rigorous batch testing bring—one poor supplier nearly derailed a major local health survey when their inconsistent product led to erratic readings. Now, most respected labs rely only on suppliers who provide detailed analysis reports, third-party certifications, and clear production traceability.
Future developments may bring more advanced markers or multiplex panels, but today, most projects hinge on the continued availability of trustworthy 1-Hydroxypyrene. Responsible supply chains and open communication between buyers, sellers, and scientific users build the foundation for meaningful research and real world impact.
Advances come quickly, with automated sample handling or AI-driven data analysis promising to streamline future studies. Still, every leap forward leans on high-quality core materials—starting with dry, uncontaminated, accurately labeled 1-Hydroxypyrene. The drive for ever-lower detection limits and broader surveillance ties right back to that first step: having a substance whose properties match printed specifications and whose effects on results have been painstakingly validated.
Change takes cooperation—between governments that set health policies, labs that do the testing, and communities eager to back cleaner living. Making sure people understand why such a nuanced product matters can spark more support for robust funding, stronger regulatory oversight, and fairer access for all researchers, not just those in the world’s best-funded institutions.
Looking ahead, the world’s relationship with chemical monitoring tools like 1-Hydroxypyrene won’t stay static. As regulators update guidelines in response to heavier urbanization, new sources of pollution, or unexpected challenges like wildfires, the role of reliable exposure markers grows. Supplies must keep pace, held to uncompromising standards that ensure every measurement still means what it should. The researchers and technicians who keep an eye on quality, training, and public transparency will make all the difference.
Strong environmental health policies start far from the negotiation table. They take root in careful lab work, evidence backed by compounds like 1-Hydroxypyrene. Wherever the next challenge appears—bustling megacities, isolated towns downwind of industry, remote mountain villages grappling with power station fallout—having the right reference standard until better markers emerge keeps us moving toward safer air and a cleaner future.