Benzylfentanyl

Benzylfentanyl
Names
	Preferred IUPAC name N-(1-Benzylpiperidin-4-yl)-N-phenylpropanamide
Identifiers
CAS Number	1474-02-8 ;
3D model (JSmol)	Interactive image;
ChemSpider	220920;
ECHA InfoCard	100.014.559
EC Number	216-014-7;
PubChem CID	252141;
UNII	9BV2D1A57H ;
CompTox Dashboard (EPA)	DTXSID00163705 ;
	InChI InChI=1S/C21H26N2O/c1-2-21(24)23(19-11-7-4-8-12-19)20-13-15-22(16-14-20)17-18-9-5-3-6-10-18/h3-12,20H,2,13-17H2,1H3 Key: POQDXIFVWVZVML-UHFFFAOYSA-N;
	SMILES CCC(=O)N(C1CCN(CC1)CC2=CC=CC=C2)C3=CC=CC=C3;
Properties
Chemical formula	C21H26N2O
Molar mass	322.452 g·mol−1
Density	1.113 g/cm3
Boiling point	502.2 °C (936.0 °F; 775.3 K)
Vapor pressure	3.36×10−8 mmHg
Legal status	DE: Anlage I (Authorized scientific use only); US: List I (a precursor);
Hazards
	GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H301, H412
Precautionary statements	P264, P270, P273, P301+P316, P321, P330, P405, P501
NFPA 704 (fire diamond)	3 0 0
Flash point	257.5 °C (495.5 °F; 530.6 K)
	Lethal dose or concentration (LD, LC):
LD50 (median dose)	500 mg/kg (oral, as HCl salt, est.)
Safety data sheet (SDS)	CATO Research Chemicals
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Benzylfentanyl (R-4129) is a fentanyl analog. It was temporarily placed in the US Schedule I by emergency scheduling in 1985 due to concerns about its potential for abuse as a designer drug, but this placement was allowed to expire and benzylfentanyl was formally removed from controlled substance listing in 2010, after the DEA's testing determined it to be "essentially inactive" as an opioid. It was added as a List I precursor instead in 2020 after it was determined that it was being used in fentanyl manufacture, which was previously thought to be beyond the technical capability of illicit labs. Benzylfentanyl has a K_i of 213 nM at the mu opioid receptor, binding around ⁠1/200⁠ as strong as fentanyl itself, though it is still slightly more potent than codeine.