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: Hemi-L-Tartrate

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: C₂₅H₃₃N₃O₂
Molar Mass: 407.55 g·mol⁻¹
IUPAC: (8β)-1-pentanoyl-N,N-diethyl-6-methyl-9,10-didehydroergoline-8-carboxamide hemi-L-tartrate
Form: Hemi-L-Tartrate

1V-LSD, or 1-valeroyl-lysergic acid diethylamide, is a lysergamide first introduced in 2022. It is structurally similar to LSD and 1P-LSD, with a valeroyl group at the indole nitrogen. This chemical modification has made it a subject of study in forensic and analytical chemistry, particularly in research related to lysergamide degradation pathways and detection techniques. The compound is often examined in relation to other alkylated lysergamides, offering insight into how molecular alterations impact stability and solubility in laboratory settings.

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

Formula: C₁₅H₂₀N₂O
Molar Mass: 244.33 g·mol⁻¹
IUPAC: N-[2-(5-Methoxy-1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine
Form: Fumarate

5-MeO-MALT, or 5-methoxy-N-methyl-N-allyltryptamine, is a synthetic compound within the tryptamine class, structurally related to other methoxy-substituted tryptamines such as 5-MeO-DALT and 5-MeO-DMT. This compound features a methoxy group at the 5-position of the indole ring and an N-methyl-N-allyl substitution on the ethylamine side chain.

Researchers focus on its chemical properties, synthesis pathways, and analytical characterization, contributing to the broader understanding of substituted tryptamines.

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

Formula: C₂₃H₂₉N₃O₂
Molar Mass: 379.504 g·mol⁻¹
IUPAC: (6aR,9R)-4-cyclopropionyl-N,N-diethyl-7-methyl-4,6,6a,7,8,9-hexahydroindolo[4,3-fg]quinoline-9-carboxamide
Form: Hemi-L-Tartrate

In the intricate world of lysergamides, 1cP-LSD makes its mark as a novel addition. Christened as “Curie” by the pioneers who first unearthed its potential. 1cP-LSD, a derivative of LSD, was first introduced in 2019. It features a cyclopropionyl group at the nitrogen position, differentiating it from other lysergamides. Chemically, it shares a similar backbone with 1P-LSD and ALD-52, making it a relevant subject in forensic analysis of lysergamide compounds.

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

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.

Formula: C₁₅H₂₂N₂O·HCl
Molar Mass: 282.81 g·mol⁻¹
IUPAC: N-[2-(5-Methoxy-1H-indol-3-yl)ethyl]-N-methylpropan-2-amine hydrochloride
Form: Hydrochloride Salt

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.

The hydrochloride salt (HCl) form of 5-MeO-MiPT improves its stability and solubility, making it well-suited for laboratory handling and reference standard development.

⚠️ 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: C₁₅H₂₀N₂O₂
Molar Mass: 260.337 g·mol⁻¹
IUPAC: [3-[2-(dimethylamino)ethyl]-1H-indol-4-yl] propanoate
Form: Fumarate

4-PrO-DMT, or 4-propionoxy-N,N-dimethyltryptamine, is a synthetic tryptamine that shares structural similarities with 4-AcO-DMT and psilocin. First synthesized in 2019, it features a propionoxy ester substitution at the 4-position of the indole ring, distinguishing it from other tryptamines commonly studied in forensic and analytical chemistry.

This compound has gained interest in research due to its chemical relationship to natural and semi-synthetic tryptamines, making it a key reference point in comparative tryptamine studies.

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

Formula: C₁₄H₂₁NO₃
Molar Mass: 251.326 g·mol⁻¹
IUPAC: 2-{3,5-dimethoxy-4-[(2-methylprop-2-en-1-yl)oxy]phenyl}ethanamine
Form: Fumarate

Methallylescaline, commonly known as MAL, is a synthetic phenethylamine and an analog of mescaline. It was first synthesized and documented by Alexander Shulgin in “PiHKAL,” where its chemical properties were explored in relation to other mescaline derivatives. MAL is characterized by the presence of a methallyloxy group, distinguishing it from traditional mescaline. It is used in analytical chemistry for comparative structural analysis with other substituted phenethylamines.

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

Formula: C₁₄H₂₀N₂O
Molar Mass: 232.327 g·mol⁻¹
IUPAC: 3-{2-[Methyl(propan-2-yl)amino]ethyl}-1H-indol-4-ol
Form: Fumarate

4-HO-MiPT, or 4-hydroxy-N-methyl-N-isopropyltryptamine, is a synthetic tryptamine that belongs to the same chemical class as psilocin, 4-HO-MET, and 4-AcO-DMT. First synthesized in the late 1970s by Alexander Shulgin, this compound is part of a group of substituted 4-hydroxytryptamines, which are closely related to naturally occurring alkaloids found in various fungi.

Structurally, 4-HO-MiPT is the isopropyl homolog of psilocin, differing by the presence of an N-methyl-N-isopropyl group in place of the dimethyl group in psilocin. Due to its distinct molecular properties, it has been studied in forensic and analytical chemistry as part of research into synthetic tryptamines.

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

Formula: C₂₁H₂₇N₃O
Molar Mass: 337.467 g·mol⁻¹
IUPAC: (6aR,9R)-N,N-diethyl-7-ethyl-4,6,6a,7,8,9-hexahydroindolo-[4,3-fg]quinoline-9-carboxamide
Form: Hemi-L-Tartrate

A Rare Gem in the Lysergamides World:

ETH-LAD, or 7-ethyl-lysergic acid diethylamide, is a rare lysergamide that has been studied for its unique structural features. It belongs to the same chemical family as LSD, AL-LAD, and PRO-LAD, differing by the ethyl substitution at the 7-position of the indole ring. Originally synthesized in the 1950s, ETH-LAD has remained a lesser-known compound, though it has been periodically examined for its relationship to other ergoline derivatives. Due to limited production, this compound is becoming increasingly scarce in research circles.

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

Formula: C₂₆H₃₁N₃O₂
Molar Mass: 417.55 g·mol⁻¹
IUPAC: 1‐cyclopropanecarbonyl‐(8ß)-N,N-diethyl-6-(prop-2-enyl)-9,10-didehydroergoline-8-carboxamide hemi-L-tartrate
Form: Hemi-L-Tartrate

1cP-AL-LAD, or 1-cyclopropionyl-6-allyl-lysergic acid diethylamide, is a structural analog of AL-LAD, featuring a cyclopropionyl substitution at the nitrogen position. First synthesized in 2021, this lysergamide is studied for its unique chemical properties in relation to its parent compound, AL-LAD, as well as its broader relationship with LSD derivatives.

The addition of the cyclopropionyl group is a key point of interest in forensic chemistry, as it alters the compound’s molecular profile, influencing analytical techniques used in research.

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

Formula: C₂₇H₃₅N₃O₂
Molar Mass: 433.596 g·mol⁻¹
IUPAC: (8β)-1-(1,2-Dimethylcyclobutane-1-carbonyl)-N,N-diethyl-6-methyl-9,10-didehydroergoline-8-carboxamide
Form: Hemi-L-Tartrate

1D-LSD, or 1-dimethylcyclobutane-lysergic acid diethylamide, is a structural analog of 1V-LSD, introduced as a next-generation lysergamide. It features a dimethylcyclobutane-carbonyl group at the nitrogen position, differentiating it from earlier lysergamide derivatives.

This compound is used in comparative forensic analysis to examine molecular modifications within the lysergamide class. Its recent introduction has made it an important reference in lysergamide-related studies.

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

Formula: C₁₃H₁₈N₂O
Molar Mass: 218.300 g·mol⁻¹
IUPAC: 2-(5-Methoxy-1H-indol-3-yl)-N,N-dimethylethanamine
Form: Freebase

5-MeO-DMT, or 5-methoxy-N,N-dimethyltryptamine, is a naturally occurring tryptamine found in various plant species and the secretions of the Colorado River toad (Incilius alvarius). First synthesized in 1936, it is structurally related to DMT and bufotenine, differing by the presence of a 5-methoxy substitution on the indole ring.

The compound has been a subject of interest in forensic chemistry due to its occurrence in both natural and synthetic sources, making it valuable for analytical research on tryptamine derivatives.

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

Form: 4-HO-MET & 5-MeO-MALT (Fumarate)

Form: 5-MeO-MiPT (HCI salt)

The variety pack includes a carefully curated selection of our most popular tryptamines, all meeting our stringent quality control standards.

5-MeO-MALT, 4-HO-MET, & 5-MeO-MiPT are analytical reference standards categorized as tryptamines. This product is intended for research and forensic applications.

WARNING This product is not for human or veterinary use.

The variety pack includes a carefully curated selection of our most popular lysergamides, all meeting our stringent quality control standards.

1P-LSD blotters contain 100mcg each.

1V-LSD blotters contain 150mcg each.

1D-LSD blotters contain 150mcg each.

This pack includes a selection of lysergamides with distinct structural modifications, providing a comparative reference for forensic and analytical studies. Lysergamides, derived from lysergic acid, have been a subject of extensive research due to their unique molecular frameworks.

WARNING This product is not for human or veterinary use.