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Buy 5-Meo-DIBF online

5-Methoxy-N,N-diisopropylbenzofuranethylamine (also known as 5-MeO-DiBF) is a novel psychedelic substance of the benzofuran class that produces psychedelic and stimulating effects when administered. 5-Meo-DIBF For Sale Online

It is related in structure to 5-Methoxy-N,N-diisopropylbenzofuranethylamine.

This compound has little to no history of human usage prior to its September 2015 release on the online research chemical market.

Very little is known about the pharmacological properties, metabolism, and toxicity of 5-MeO-DiBF.

Due to its extreme novelty and unknown toxicity profile, it is highly advised that one use harm reduction practices if using this substance.

5-Meo-DIBF, or 5-methoxy-N,N-diisopropylbenzofuranethylamine, is a synthetic heterocyclic alkaloid molecule of the benzofuran class.

Benzofuran is a bicyclic structure formed by the fusion of a benzene ring and a furan ring, a five member aromatic ring containing an oxygen substituent.

5-Meo-DIBF is composed of a benzofuran group attached at R3 to an amino group via an ethyl side chain.

It is substituted at R5 of the benzofuran heterocycle with a methoxy (MeO) functional group CH3O−; it also contains two isopropyl chains bound to the terminal amine RN of its tryptamine backbone (DiBF).

The benzofuran group of  is closely related in structure to the indole found in tryptamines; benzofuran contains an oxygen group at the same location that indole contains a nitrogen.

As such, 5MeO-DiBF is closely related in structure to the psychedelic tryptamine 5-Methoxy-N,N-diisopropylbenzofuranethylamine. 5MeO-DiBF is the benzofuran analogue of .

5MeO DiBF likely acts as a 5-HT2A partial agonist.

The psychedelic effects are believed to come from its efficacy at the 5-Methoxy-N,N-diisopropylbenzofuranethylamine and 5-HT2 family of serotonin receptors. However, the role of these interactions and how they result in the psychedelic experience continues to remain elusive.

This compound is several times less potent as a serotonin agonist than 5MeO-DiPT.

It has relatively more activity at 5-HT1A, but still shows strongest effects at the 5-HT2 family of receptors

5-MeO-AMT typically is consumed orally in 2.0- to 4.5-milligram dosages, although dosage amounts vary widely. The drug also may be administered via snorting or smoking. Typically, users begin to feel the drug’s effects within 1 hour after administration. The hallucinogenic effects generally last for 12 to 18 hours.

5-MeO-AMT typically is abused by teenagers and young adults. The drug is used at raves, nightclubs, and other venues where the use of club drugs, particularly MDMA (3,4-methylenedioxymethamphetamine, also known as ecstasy), is well-established. 5-MeO-AMT also is used at private parties.

5-MeO-AMT produces various negative physical and psychological effects in users. Physical effects include visual and auditory disturbances and distortions, nausea, vomiting, and diarrhea. Psychological effects associated with the use of  5-MeO-AMT include terrifying hallucinations and emotional distress. The drug also diminishes user inhibitions, which can result in high-risk sexual activity or accidental injury.

Yes, 5-MeO-AMT is illegal for human consumption. It is an analog of 5-MeO-DIPT and AMT, which are Schedule I drugs under the Controlled Substances Act. According to 21 U.S.C. § 813, “a controlled substance analog(ue) shall, to the extent intended for human consumption, be treated, for the purposes of any Federal law as a controlled substance in Schedule I.

” Thus, authorities can prosecute drug offenses involving 5-MeO-AMT in the same manner as offenses involving 5-MeO-DIPT and AMT. (See 21 U.S.C. § 802(32) for the definition of a controlled substance analog(ue).)