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4F-PHP has an IUPAC name of 1-(4-fluorophenyl)-2-(pyrrolidin-1-yl)hexan-1-one, an exact mass of 263.17, and a molecular weight of 263.35. The chemical formula for the new research chemical is C16H22FNO. The chemical is so new that information is not available so we must look at the analogue of 4F-PHP in order to learn more.

Research on compound was published by ACD/Labs', US Environmental Protection Agency's EPISuite, and ChemAxon. In the reports by ACD/Labs the chemical has 2 hydrogen acceptors, 0 hydrogen donors, 5 freely rotating bonds, an index of refraction of 1.538, with a surface tension of 40.0±3.0 dyne/cm, a flash point of 119.0±12.5 °C and a boiling point of 340.8±25.0 °C at 760 mmHg.

The research published by US Environmental Protection Agency's EPISuite showed the boiling point to be 326.57, a melting point of 96.11, and water solubility at 25 deg C (mg/L): 139.4. Removal in wastewater treatment showed total removal at 26.14%, total biodegradation at .29% total sludge adsorption at 25.84%, and total to air at 0.01%.

ChemAxon published a topology analysis, which revealed an atom count of 38, bond count of 39, cyclomatic number of 2, chain atom count of 6, chain bond count of 7, asymmetric atom count of 1, and rotatable bond count of 5. Under geometry, the report revealed a dreiding energy equal to 52.41 kcal/mol with a volume equal to 238.97 Å3, a minimal projection area equal to 48.46 Å2 and maximum projection area equal to 67.71 Å2.

4F-PHP is research chemicals and intended for research purposes only in a controlled laboratory for scientific and forensic study and are NOT intended for human or animal consumption.

4F-PHP goes by the formal and systematic IUPAC name of 1-(4-fluorophenyl)-2-(pyrrolidin-1-yl)hexan-1-one, it has a relative molar mass of 263.35 grams and an empirical formula of C16H22FNO.

4F-PHP may also go by the name 4-fluro-pyrrolidinohexiophenone. It is an analogue of the compound alpha-pyrrolidinohexiophenone with 4F-PHP distinguished from its parent compound by having the aromatic ring fluorinated in the para position.

Fluorination of drug compounds can sometimes increase bioavailability and lipophilicity and the highly electronegative character of fluorine can change the topographical charge of the molecule interfering with metabolism and giving the compound a longer half life. The electronegative fluorine atom should make the carbonyl less polar and reduce reactivity of the compound.

4F-PHP belongs to the class of chemicals known as substituted cathinones.

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