Walking into any modern laboratory, the shelves give you a clear look at chemistry’s influence on today’s industries, and this long-named compound, known for its complex molecular structure and practical properties, stands out. Chemists know its formula: C25H24ClNO2. It lands firmly in the family of synthetic organic molecules rooted in a quinoline core, specifically bearing a 7-chloro substitution. This articulated structure brings both robust stability and unique reactivity under controlled conditions. People working with new specialty materials, drug discovery, or even high-value custom chemicals see this compound not just as a sequence of rings and chains but as a building block opening new research paths.
Solid under standard conditions, 2-(2-(3S)-(3-(2-(7-chloro-2-quinolinyl)-ethenyl)phenyl)-3-hydroxy-propyl)phenyl)-2-propanol may appear as flakes or fine powder, depending on its preparation and purity. Its density tends to stand close to 1.3 g/cm³, giving it a sort of comfortable heft in a weighing dish. The presence of both a secondary alcohol (hydroxy group) and aromatic rings influences its melting and solubility behaviors, making it a versatile intermediate that can move easily between different phases and reactions. Under a microscope or with a scoop in the lab, you’d see a pale, sometimes off-white, crystalline material — not likely to flow, but easy to grind into workable forms when precision weighs in.
People tracking this molecule for industrial or research-scale application should reference its HS Code—often falling under 29334900 for customs purposes, matching its classification as an organo-nitrogen compound. Its specific rotation and stereochemistry (3S configuration) add an important layer for research in chiral synthesis or in applications demanding stereochemical integrity. Chemists checking a printout of specifications note purity levels typically at or above 98%, with residual moisture content kept under strict limits. Analytical results from NMR, mass spectrometry, and IR provide fingerprints so anybody taking custody of the material knows exactly what they have. Crystal size and appearance shift in response to different crystallization solvents—choices that can affect the suitability for downstream applications or solid formulation work.
The 7-chloro-2-quinolinyl backbone flags certain chemical hazards familiar to anyone who works with halogenated aromatics. Safe handling procedures demand gloves, goggles, and good ventilation. Contact with skin or eyes deserves immediate attention, and accidental ingestion or inhalation should prompt rapid medical assessment. This compound is not flammable, but dust generation during handling requires minimizing airborne particulates with fume hoods or dust masks. MSDS documentation flags possible harmful effects on aquatic life and highlights the importance of secure storage, far from incompatible agents like strong oxidizers or bases. Disposal of waste and spillage follows hazardous waste guidelines all over the world—and labs know local compliance teams check this point.
Raw materials for this molecule start in petrochemical streams or base aromatic compounds, including basic quinoline derivatives and chlorinated aromatics. Skilled workers in chemical plants blend, chlorinate, and further react these pieces, work up the resultant mixtures, and purify the target product. Scientists see value in the propanol sidechains for linking to other molecular scaffolds, whether in potential pharmaceutical leads, specialty dyes, or in custom electronic materials where the quinoline nucleus plays a part. Every batch brings an opportunity—and anyone earning a living at the bench knows tracing these raw inputs through the process isn’t just policy; it’s how safe, reliable work gets done.
In practice, manufacturers offer this compound as powder, flakes, or, occasionally, prilled or crystalline pearls, based on customer needs and stability in transit. The choice depends on intended use and bulk scale, with densest packing favored for global shipments. Drums lined for chemical compatibility protect the contents from moisture, light, and temperature extremes. In larger refineries or pilot plants, bulk solutions in compatible solvents help move larger amounts efficiently for downstream processing. Labels must bear hazard information and UN numbers, so everyone from courier to customs agent to the end user knows what sits inside—and all paperwork matches up for smooth transport.
Some of the real-world obstacles with advanced molecules like this surround access to high-purity intermediates, reliable supply chains, and regulatory pressure. Producers balancing demand for innovation and low environmental impact have to consider greener routes, alternative solvents, and tighter emissions controls. As a synthetic chemist, seeing the field move incrementally towards more sustainable processes feels rewarding, but the work is far from finished. Enforcement of safety rules, transparency about potential hazards, and community engagement around chemical manufacturing sites remain high on public agendas.
Meeting science’s demand for new molecules does not always require reinventing the wheel but calls for incremental improvements across synthesis, safety, and education. Encouraging transparent reporting of property data—like melting points, densities, and handling precautions—in public databases gives researchers, manufacturers, and regulators a shared baseline. Industry-wide, many call for updated training in safe handling and proper disposal, with routine audits, not just for compliance but for long-term workplace health. Investment in facilities that minimize exposure risk and environmental harm adds up over time, proving that thoughtful stewardship matters as much as technical progress. Chemical producers who lead here usually gain trust and repeat business from customers who value reliability and responsibility on top of raw technical performance.
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