Formula: C₁₅H₂₂N₂O

Molar Mass: 246.35 g·mol⁻¹

IUPAC: N-[2-(5-Methoxy-1H-indol-3-yl)ethyl]-N-methylpropan-2-amine

Form: Freebase

5-MeO-MiPT, or 5-methoxy-N-methyl-N-isopropyltryptamine, is a synthetic tryptamine that belongs to the 5-methoxy-substituted indole family, structurally related to 5-MeO-DMT, 5-MeO-DiPT, and MiPT. First synthesized in the 1980s, this compound has been of interest in forensic and analytical research due to its distinct chemical profile and relationship to naturally occurring tryptamines.

⚠️ Safety Precaution:
This product is intended strictly for research and forensic applications. It is not for human or veterinary use. Handle with appropriate safety protocols.

Formula: C₂₃H₂₉N₃O₂

Molar Mass: 379.504 g·mol⁻¹

IUPAC: (6aR,9R)-N,N-Diethyl-7-methyl-4-propanoyl-6,6a,8,9-tetrahydroindolo[4,3-fg]quinoline-9-carboxamide

Form: Blotter

1P-LSD, or 1-propionyl-lysergic acid diethylamide, is a lysergamide derivative first synthesized in 2015. It is a structural analog of LSD, distinguished by the presence of a propionyl group attached to the indole nitrogen. Due to its close structural relationship with LSD, ALD-52, and 1B-LSD, 1P-LSD is frequently examined in chemical research involving lysergic acid derivatives. Researchers have studied its stability, potential degradation pathways, and interactions with chromatography-based detection methods.

⚠️ Safety Precaution:
This product is strictly intended for research and forensic applications. It is not for human or veterinary use. Proper safety protocols should be followed when handling.

Formula: C₁₄H₁₈N₂O₂

Molar Mass: 246.310 g·mol⁻¹

IUPAC: 3-[2-(Dimethylamino)ethyl]-1H-indol-4-yl acetate

Form: Fumarate

First synthesized by Albert Hofmann in 1963, 4-AcO-DMT, or O-Acetylpsilocin, is a semi-synthetic derivative of psilocin. It is structurally similar to the naturally occurring alkaloid found in psilocybin mushrooms, differing only by the presence of an acetoxy group. Due to its close relationship with other tryptamines, it has been studied in the field of forensic and analytical chemistry for its chemical behavior and stability.

⚠️ Safety Precaution:
This product is for research and forensic applications only. Not for human or veterinary use. Handle according to appropriate safety protocols.

Formula: C₁₃H₁₈N₂O

Molar Mass: 218.300 g·mol⁻¹

IUPAC: 3-{2-[Ethyl(methyl)amino]ethyl}-1H-indol-4-ol

Form: Fumarate

4-HO-MET, or 4-hydroxy-N-methyl-N-ethyltryptamine, belongs to the tryptamine family and is structurally related to psilocin, the active metabolite of psilocybin mushrooms. It is an ethyl-substituted homolog of 4-AcO-DMT and shares a similar core structure to naturally occurring tryptamines. First documented by Alexander Shulgin in “TiHKAL,” this compound has been of interest in analytical chemistry for its role in the study of synthetic and naturally derived tryptamines.

⚠️ Safety Precaution:
This product is for research and forensic applications only. Not for human or veterinary use. Handle with appropriate safety measures.