2C-B-FLY

$250.00$1,200.00

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Buy 2C-B-FLY Online; aka: 8-bromo-2,3,6,7-benzo-dihydro-difuran-ethylamine or 2-(8-bromo-2,3,6,7-tetrahydrofuro[2,3-f] [1]benzofuran-4-yl)ethanamine.

A group of phenethylamine derivatives referred to as the FLY compounds, named for their insect-like appearance of two “wing-like” furan or dihydrofuran rings fused on the opposite sides of the central benzene ring, have been identified with allegedly potent hallucinogenic effects. 2C-B-fly is the dihydrodifuran analog of the Schedule I hallucinogen 4-bromo-2,5-dimethoxyphenethylamine (2C-B). It is expected to show similar activity to 2C-B, which acts as a partial agonist at the 5-HT2A serotonin receptor and demonstrates high binding affinity for the 5-HT2B and 5-HT2C serotonin receptors. This product is intended for forensic and research purposes.

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In theory, dihydrodifuran analogues of any of the 2Cx / DOx family of drugs could be made, and would be expected to show similar activity to the parent compound. So in the same way that 2C-B-FLY is the dihydrodifuran analogue of 2C-B, the 8-iodo equivalent 2C-I-FLY would be the dihydrodifuran analogue of 2C-I, and the 8-methyl equivalent 2C-D-FLY would be the dihydrodifuran analogue of 2C-D.

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RESEARCH ONLY! NOT FOR HUMAN CONSUMPTION..

Product Description References

1. Reed, E.C., and Kiddon, G.S. The characterization of three fly compounds (2C-B-FLY, 3C-B-FLY, and Bromo-Dragon FLY). DEA Microgram Journal 5(1-4), 1-8 (2007).

2. Pichini, S., Pujadas, M., Marchei, E., et al. Liquid chromatography-atmospheric pressure ionization electrospray mass spectrometry determination of “hallucinogenic designer drugs” in urine of consumers. Journal of Pharmaceutical & Biomedical Analysis 47(2), 335-342 (2008).

3. Monte, A.P., Marona-Lewicka, D., Parker, M.A., et al. Dihydrobenzofuran analogues of hallucinogens. 3. Models of 4-substituted (2,5-dimethoxyphenyl)alkylamine derivatives with rigidified methoxy groups. Journal of Medicinal Chemistry 39, 2953-2961 (1996).

4. Chambers, J.J., Kurrasch-Orbaugh, D.M., Parker, M.A., et al. Enantiospecific synthesis and pharmacological evaluation of a series of super-potent, conformationally restricted 5-HT2A/2C receptor agonists. Journal of Medicinal Chemistry 44, 1003-1010 (2001).

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10g, 25g, 50g, 100g

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