Buy 3-fpm ( 3-Fluorophenmetrazine ) (also known as 3-FPM, 3-FPH and PAL-593) is a phenylmorpholine-based stimulant and fluorinated analogue of phenmetrazine
Buy 4-fluoroisobutyrfentanyl powder
Buy 4-fluoroisobutyrfentanyl powder (also known as 4-FIBF and p-FIBF) is an opioida is an analog of butyrfentanyl and structural isomer of 4-Fluorobutyrfentanyl and has been sold online as a designer drug. It is closely related to 4-fluorofentanyl, which has an EC50 value of 4.2 nM for the human ?-opioid receptor.
Names: 4-Fluoroisobutyrfentanyl para-fluoroisobutyrfentanyl, N-(4-fluorophenyl)-N-(1-phenethylpiperidin 4-yl)isobutyramide pFIBF, 4-FIBF,
IUPAC name: N-(4-fluorophenyl)-N-(1-phenethylpiperidin-4-yl)isobutyramide
Substance group: Other substances
This substance is included in Schedule I of the 1961 Single Convention on Narcotic Drugs
InChI Key: OZDOSQNUJIXEOR-UHFFFAOYSA-N SMILES: O=C(C(C)C)N(C1=CC=C(F)C=C1)C2CCN(CCC3=CC=CC=C3)CC2
Molar mass: 368.50 g·mol?1
Side effects of 4-fluoroisobutyrfentanyl
Side effects of fentanyl analogs are similar to those of fentanyl itself, which include itching, nausea and potentially serious respiratory depression, which can be life-threatening. Fentanyl analogs have killed hundreds of people throughout Europe and the former Soviet republics since the most recent resurgence in use began in Estonia in the early 2000s, and novel derivatives continue to appear.
4-Fluoroisobutyrylfentanyl is a Schedule I controlled substance in the United States. In the UK, it is a Class A drug. In Canada, it is a Schedule I drug.
List of fentanyl analogues
Fentanyl analogues, in which the N-[1-(2-phenethyl)-4-piperidyl]aniline nucleus has additional radicals, either alone or in combination, attached as follows:
(a) an acetyl, propionyl, butenoyl or butanoyl radical, attached to the aniline nitrogen atom:
(c) any combination of up to 5 alkyl radicals and/or alkoxy radicals (each with up to 6 carbon atoms, including cyclic radicals) and/or halogen radicals, attached to each of the benzene rings
Replacement of the phenyl portion of the phenethyl group by any monocycle, whether or not further substituted in or on the monocycle;
substitution in or on the phenethyl group with alkyl, alkenyl, alkoxyl, hydroxyl, halo, haloalkyl, amino or nitro groups;
substitution in or on the piperidine ring with alkyl, alkenyl, alkoxyl, ester, ether, hydroxyl, halo, haloalkyl, amino or nitro groups;
replacement of the aniline ring with any aromatic monocycle whether or not further substituted in or on the aromatic monocycle; and/or
replacement of the N-propionyl group by another acyl group.