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Ald-52 Information

ALD-52, also known as N-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.

Contents

Effects

In TiHKAL, Shulgin touches briefly on ALD-52 in entry 26, LSD. His writings are vague, second hand accounts, saying doses in the 50-175 µg range have resulted in various conclusions. One found that there was less visual distortion than with LSD and it seems to produce less anxiety and was somewhat less potent than LSD. Another report claimed it was more effective in increasing blood pressure. Yet another could not tell them apart.

It has the same characteristics as LSD, but supposedly "without the anxiety, tenseness, and other problems inherent to it".

Dangers

In The Hallucinogens by Hofmann and Osmond (1967), ALD-52 (D,L-acetyllysergic acid diethylamide) 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.

History

It is possible ALD-52 was the active chemical in the "Orange Sunshine" LSD that was widely available in California through 1968 and 1969. The Sonoma County underground chemistry lab of Tim Scully and Nicholas Sand was the source for "Orange Sunshine." It was shut down by the police, and Scully was arrested and prosecuted. This resulted in the first drug analogue trial, where Scully claimed that he and his partners did nothing illegal, because they were producing ALD-52 which was not an illicit drug. However, as the prosecution claimed, there were problems with such a rationale: first, ALD-52 readily undergoes hydrolysis to LSD, and second, the synthesis of ALD-52 required LSD (this was based on the methods available in the scientific literature at the time). Scully was convicted and served time in prison.

See also

References

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External links

Hallucinogens
Psychedelics 5-HT2AR agonists
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Ergolines
Lysergic acid derivatives 2-Bromo-LSD (BOL-148)BromocriptineCabergolineDihydroergocornineDihydroergocristineDihydroergocryptine • Dihydroergometrine (Dihydroergonovine, Dihydroergobasine) • DihydroergotamineErgine (LSA; LA-111; Lysergamide) • ErgocornineErgocristineErgocryptineErgoloid (Dihydroergotoxine) • Ergometrine (Ergonovine, Ergobasine) • Ergometrinine • ErgotamineErgotoxineErgovalineLisurideLSDLSHLysergic Acid • Lysergic acid cyclobutylamide • Lysergic acid cyclopentylamide • Lysergic Acid Methyl EsterLysergolMesulergineMetergolineMethergine (Methylergometrine, Methylergonovine, Methylergobasine) • MethysergidePergolideSyntometrine
Psychedelic lysergamides AL-LADALD-52BU-LADCYP-LADDALDAM-57ErgonovineETH-LAD • IP-LAD • LAE-32LSDLPD-824LSM-775LSHLSD-PipLysergic Acid 2-ButylamideLysergic Acid 2,4-DimethylazetidideLysergic Acid 3-PentylamideMethylergonovineMethylisopropyllysergamideMLD-41PARGY-LADPRO-LAD
Other ergolines Ergoline
Natural sources Achnatherum robustum (Sleepy Grass) Argyreia nervosa (Hawaiian Baby Woodrose) • Claviceps spp. (Ergot) • Ipomoea spp. (Morning Glory, Tlitliltzin, Badoh Negro) • Rivea corymbosa (Coaxihuitl, Ololiúqui)

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