Description
Buy 4-fluoroisobutyrfentanyl Powder Online
Purchase Powdered 4-fluoroisobutyrfentanyl Online
Purchase 4-fluoroisobutyrfentanyl powder online from a reliable US supplier with guaranteed shipping to any country in the world.
Purchase 4-fluoroisobutyrfentanyl powder, also referred to as 4-FIBF and p-FIBF. This opioid is a structural isomer of 4-fluoroisobutyrfentanyl and an analog of butyrfentanyl. It has been offered for sale online as a designer drug. 4-fluorofentanyl, which has an EC50 value of 4.2 nM for the human?-opioid receptor, is closely related to it.
DESCRIPTION Names: N-(4-fluorophenyl), 4-fluoroisobutyrfentanyl, and para-fluoroisobutyrfentanylpFIBF, 4-FIBF, N-(1-phenethylpiperidin 4-yl)isobutyramide
N-(4-fluorophenyl)-N-(1-phenethylpiperidin-4-yl)isobutyramide is its IUPAC name.
Group of compounds: Other substances
Schedule I of the 1961 Single Convention on Narcotic Drugs contains this chemical.
The formula for InChI is 1S/C23H29FN2O/c1-18(2).23 (27).26(21-10-8-20(24))9-11-2117-14-22 (22-13-16-25)6-4-3-5-7-19/15-12-19/h3-11,18,22H,12-17H2,1-2H3
OZDOSQNUJIXEOR-UHFFFAOYSA-N is the InChI key. O=C(C(C)C)N(C1=CC=C(F)C=C1)C2CCN(CCC3=CC=CC=C3)CC2 are the SMILES.
C23H29FN2O is the formula.
Mass of a molecule: 368.50 g·mol?1
Adverse consequences
Itching, nausea, and possibly fatal respiratory depression are among the side effects of fentanyl analogs that are comparable to those of fentanyl itself. Since the most recent boom in use started in Estonia in the early 2000s, fentanyl analogs have killed hundreds of individuals across Europe and the former Soviet countries, and new variants are still being discovered. 4. Powdered fluoroisobutyrfentanyl for sale
Legality 4-In the US, fluoroisobutyrylfentanyl is classified as a Schedule I controlled drug. It is classified as a Class A drug in the UK. It is classified as a Schedule I substance in Canada.
Additionally, see 3-Methylbutyrfentanyl
4-Fluorofentanyl?-Methylfentanyl 3-Methylfentanyl
Acetylfentanyl
Acrylfentanyl
Fentanylfuranyl
List of analogues for fentanyl
The following are examples of fentanyl analogues where the N-[1-(2-phenethyl)-4-piperidyl]aniline nucleus has extra radicals linked to it, either separately or in combination:
(a) a radical that is affixed to the aniline nitrogen atom and is acetyl, propionyl, butenoyl, or butanoyl:
(b) One or more alkyl radicals joined to the ethyl moiety, each containing a maximum of ten carbon atoms:
(c) Any combination of up to five halogen radicals, alkyl radicals, and/or alkoxy radicals (each containing up to six carbon atoms, including cyclic radicals) joined to each benzene ring
Any chemical not already listed in any schedule that shares structural similarities with fentanyl due to one or more of the following alterations is considered a fentanyl-related substance:
substitution of any monocycle, whether or not it is further substituted within or on top of the monocycle, for the phenyl part of the phenethyl group;
substitution of alkyl, alkenyl, alkoxyl, hydroxyl, halo, haloalkyl, amino, or nitro groups in or on top of the phenethyl group;
replacement of the aniline ring with any aromatic monocycle, whether or not it is further substituted in or on the aromatic monocycle; substitution of the N-propionyl group by another acyl group; and substitution of alkyl, alkenyl, alkoxyl, ester, ether, hydroxyl, halo, haloalkyl, amino, or nitro groups in or on the piperidine ring.
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