1P-LSD is a semisynthetic compound of the lysergamide family. It is similar to LSD and is named for the propionyl group bound to the nitrogen of the polycyclic indole group of LSD. Propionyl consists of the carbonyl chain CH 3 CH 2 CO- bound to an amino group.

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1-propionyl-lysergic acid diethylamide, also known as 1P-LSD or Pink Sunshine Acid, is a new LSD-analogue non-regulated by law.

As it is a homologue to ALD-52 it is much comparable to LSD-25. With the introduction of 1P-LSD onto the fine chemical market researchers can intensify their research about lysergamides.

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ALD-52, also known as 1-acetyl-LSD, is a chemical analogue of lysergic acid diethylamide (LSD). It was originally discovered by Albert Hofmann but was not widely studied until the rise in popularity of psychedelics in the 1960s.

ALD-52 is listed as having a lower (approximately 1/5) intravenous toxicity (in rabbits), a lower (approximately 1/8) pyretogenic effect, an equal psychological effect in humans, and double the “antiserotonin” effect as compared with LSD. Human experiments have not been well documented

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AL-LAD, also known as 6-allyl-6-nor-LSD, is a psychedelic drug and an analog of lysergic acid diethylamide (LSD). It is described by Alexander Shulgin in the book TiHKA. It is synthesized starting from nor-LSD as a precursor, using allyl bromide as a reactant.

AL-LAD does not cause a color change with the Marquis, Mecke or Mandelin reagents, but does cause the Ehrlich’s reagent to turn purple because of the presence of the indole moiety in its structure.

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ETH-LAD, 6-ethyl-6-nor-lysergic acid diethylamide is an analogue of LSD. Its human psychopharmacology was first described by Alexander Shulgin in the book TiHKAL. It is a psychedelic drug similar to LSD, and is slightly more potent than LSD itself, with an active dose reported at between 20 and 150 micrograms. This analogue of LSD has subtly different effects to LSD, described as less demanding.

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Lysergic acid 2,4-dimethylazetidide (LA-SS-Az, LSZ) is an analog of LSD developed by the team led by David E. Nichols at Purdue University. It was developed as a rigid analog of LSD with the diethylamide group constrained into an azetidine ring in order to map the binding site at the 5-HT2A receptor. There are three possible stereoisomers around the azetidine ring, with the (S,S)-(+) isomer being the most active, slightly more potent than LSD itself in drug discrimination tests using trained rats. Buy LSZ online. LSZ buy. LSZ vendor. LSZ for sale. LSZ supplier. LSZ reddit vendor

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As it is a homologue to ALD-52 it is much comparable to LSD-25. With the introduction of LSD onto the fine chemical market researchers can intensify their research about lysergamides.

Contrary to popular opinion, it cannot undergo hydrolysis into LSD from contact with moisture in the atmosphere, it is quite stable under atmospheric conditions.

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