3-(Dibutylamino)-1-(1,3-dichlor-6-(trifluoromethyl)-9-phenanthryl)propanol belongs to the class of organic compounds containing a phenanthrene core with halogen and trifluoromethyl substituents, further modified by a propanol group bearing a dibutylamino moiety. In laboratory shelves, this substance grabs attention because of its structural complexity, marked by aromatic ring systems, multiple halogen atoms, and a polar functional group shaped for chemical versatility. In a research context, it carries weight as an intermediate or specialist raw material, largely because phenanthrene derivatives pop up in pharmaceuticals, dyes, and advanced organic materials. With halogen (chlorine, fluorine) and trifluoromethyl groups, this compound behaves differently compared to ordinary phenanthrenes—its electron density, reactivity, and potential for forming interactions step far outside the normal boundaries for simple aromatic alcohols.
The structure of 3-(Dibutylamino)-1-(1,3-dichlor-6-(trifluoromethyl)-9-phenanthryl)propanol combines segments that each bring their own qualities. Its molecular formula runs as C26H30Cl2F3NO, giving it a relatively high molecular weight, which influences solubility and handling. With a phenanthrene backbone, the compound boasts rigidity and stacking potential in crystal lattices; dichloro and trifluoromethyl substitutions crank up its lipophilicity and chemical stability, but these same groups also strike at toxicity and persistence concerns. The dibutylamino tail brings flexibility, a distinctly amine-based odor, and raises the boiling point. Properties like density depend on both the packing of the phenanthryl core and the bulk brought by butyl chains. Usually, this kind of molecule emerges as a solid at room temperature, with appearances ranging from off-white powder to crystalline flakes or pearl-like granules, shaped by manufacturer and purification process; it leans more towards being a fine powder or flakes because of its aromatic-rich skeleton. In solution, its solubility leans on organic solvents—toluene, chloroform, and sometimes ethanol will host compounds like this, while water struggles unless the amine sites get protonated.
Purity treads near the top for applications in synthesis and pharma research; typical batches specify purity above 97%, tested by HPLC or NMR. The material often gets supplied in 10 g, 100 g, or custom bulk packaging, stored tightly capped to avoid exposure to air, light, or moisture. The density of the compound ranges in the ballpark of 1.2 to 1.4 g/cm³, shifting depending on the batch’s exact crystalline form. Storage conditions emphasize keeping the compound cool and dry, since exposure to heat can set off decomposition or trigger harmful vapors. Handling this material demands solid lab practice: safety glasses, gloves, and a fume hood stand out as basics, as organochlorine compounds often pack more risk than plain hydrocarbons. Inhalation or skin contact should not be taken lightly; phenanthrene derivatives, especially ones stacked with halogen and trifluoromethyl groups, can irritate or pose chronic health hazards. Safety data sheets flag warnings such as potential skin and respiratory system irritation, risk of harm if swallowed, and guidance to seek immediate medical attention after exposure.
Finding an HS code for research chemicals like 3-(Dibutylamino)-1-(1,3-dichlor-6-(trifluoromethyl)-9-phenanthryl)propanol often challenges importers, as the compound straddles categories. The closest fit sits under organic chemicals, compounds with nitrogen functional groups, usually classified in the tariff code 2921 (amines and derivatives). Local regulations might demand additional documentation, especially where halogenated aromatics raise red flags; certain jurisdictions require record-keeping for sales and disposal as part of chemical safety initiatives. Cross-border movement relies on compliant labeling, complete chemical registration, and conformance with hazardous material shipping rules. Laboratories and companies treating this as a raw material need to stay abreast of regional regulatory changes, because an oversight could halt shipment or spark compliance fines.
As someone who has handled halogenated aromatic compounds in academic and industrial settings, a couple of realities stand out. Materials like 3-(Dibutylamino)-1-(1,3-dichlor-6-(trifluoromethyl)-9-phenanthryl)propanol show up in specialized roles, from advanced material synthesis to pharmaceutical intermediates, precisely because their properties exceed those of plain hydrocarbons. Each attachment to the core—dibutylamino, dichloro, trifluoromethyl—wasn’t added by accident. They’re there to influence solubility, bioavailability, or chemical resilience in testing reaction conditions. These same modifications, though, introduce risk. Trifluoromethyl groups, for instance, persist in the environment and resist breakdown, so disposal isn’t as simple as pouring leftovers down the drain. Industries introduce solvent recovery and solid waste incineration, reducing impact, but the society-wide impact lands when regulations lag or accidents happen in small, less-watched labs. Education plus stronger oversight sways the balance towards safety; transparency in sourcing, clear handling procedures, and culture of personal accountability inside the lab all lower the odds of accidental exposure or release. Safer labs care about exposure tracking, rapid reporting of spills, and routine training far more than the bare minimum of labeling and glove use.
In every bottle of 3-(Dibutylamino)-1-(1,3-dichlor-6-(trifluoromethyl)-9-phenanthryl)propanol, there’s a mix of possibility and responsibility. The properties that draw in researchers and developers also demand respect for safety, regulatory compliance, and environmental stewardship. It helps to remember that every specification isn’t just a number on a datasheet—it ties to a risk, a rule, or a best practice that someone before learned the hard way. For teams working in advanced synthesis, choosing this material means also buying into rigorous protocols and a willingness to adapt as the chemical landscape moves forward. In the end, the compound’s value grows in hands that treat it with technical skill and a commitment to safety for both people and planet.
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