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ALD-52

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Summary sheet: ALD-52
ALD-52
Chemical Nomenclature
Common names ALD-52, 1-Acetyl-LSD, 1A-LSD, 1A-LAD, Orange Sunshine
Substitutive name 1-Acetyl-N,N-diethyllysergamide
Systematic name (6aR,9R)-4-Acetyl-N,N-diethyl-7-methyl-4,6,6a,7,8,9-hexahydroindolo-[4,3-fg]-quinoline-9-carboxamide
Class Membership
Psychoactive class Psychedelic
Chemical class Lysergamide
Routes of Administration

WARNING: Always start with lower doses due to differences between individual body weight, tolerance, metabolism, and personal sensitivity. See responsible use section.



Oral
Dosage
Threshold 30 µg
Light 30 - 100 µg
Common 100 - 175 µg
Strong 175 - 325 µg
Heavy 325 µg +
Duration
Total 8 - 14 hours
Onset 20 - 40 minutes
Come up 1 - 2 hours
Peak 3 - 5 hours
Offset 3 - 5 hours
After effects 4 - 24 hours









DISCLAIMER: PW's dosage information is gathered from users and resources for educational purposes only. It is not a recommendation and should be verified with other sources for accuracy.

Interactions


1-Acetyl-N,N-diethyllysergamide (also known as ALD-52, 1-Acetyl-LSD, 1A-LSD, 1A-LAD, and mistakenly as Orange Sunshine) is a novel synthetic psychedelic of the lysergamide chemical class that produces "classical psychedelic" effects reported to be virtually indistinguishable from those of LSD when administered. It is a closely related structural analog and a suspected prodrug of LSD, meaning it is inactive until it enters the body and is converted into LSD.[citation needed]

ALD-52 was originally discovered by Albert Hofmann in his study of LSD analogs[citation needed], but it did not enter mainstream awareness until psychedelics came to occupy a central role in the 1960s Western youth counterculture. ALD-52 gained public notoriety when it supposedly distributed in the 1960s as LSD under the now-famous name "Orange Sunshine." This was later disproven (see section below).

Alexander Shulgin touches briefly on the subject of ALD-52 in the commentary section of LSD-25 in the book TiHKAL ("Tryptamines I have Known and Loved").[1] His writings are based on second-hand accounts which state that doses in the 50-175 µg range result in various effects that are not particularly distinct from LSD. His reports indicate that it produces less visual distortion than with LSD as well as less anxiety and tenseness, while also being somewhat less potent than LSD. Another report found the two substances to be indistinguishable.[1]

These reports are generally consistent with anecdotal reports of its effects that have followed since it was made accessible for the first time as a research chemical.

Today, ALD-52 is available on the research chemicals online gray market as part of a series of designer drug lysergamides which include compounds like AL-LAD, ETH-LAD, 1P-LSD and PRO-LAD. While it only has a short history of human use, reports almost unanimously agree that it is nearly identical if not slightly preferable to LSD due to its relatively mellow nature at common doses and the low likelihood of it possessing any unexpected toxicity due to its likely prodrug status. Nevertheless, it is still strongly advised to approach this potent psychedelic with the proper amount of precaution and harm reduction techniques if choosing to use it.

History and culture

This History and culture section is a stub.

As a result, it may contain incomplete or wrong information. You can help by expanding it.

In 2017, it came to light that the infamous "Orange Sunshine" variety of LSD that was widely available in California through 1968 and 1969 was not ALD-52 as it was long held by the hippie generation and that "Orange Sunshine" was just a very well made batch of 250 microgram per unit batch of LSD. The notorious psychedelic chemist it was attributed to, Nick Sands, confirmed that the claim of synthesizing the unscheduled drug ALD-52 and selling it as LSD was completely fabricated for his and Tim Scully's court case to argue that they were not guilty of selling LSD.[2]

Chemistry

ALD-52, or 1-Acetyl-N,N-diethyllysergamide, is a semisynthethic molecule of the lysergamide chemical class. ALD-52 is a substituted derivative of lysergic acid. ALD-52's structure contains four rings, a bicyclic hexahydroindole fused to a bicyclic quinoline group. This core structure of ALD-52 is an ergoline derivative, and has tryptamine and phenethylamine structures embedded within it. ALD-52 contains a N,N-diethylcarboxamide functional group bound to R8 of the chemical structure. It is additionally substituted at carbon 6 with a methyl group.

ALD-52 is homologous to 1P-LSD, which contains a propionyl group bound to CH3CO- instead of the acetyl group bound to the same location. It is unknown how these differences account for differences in the two compound's activity.

Pharmacology

Further information: Serotonergic psychedelic

ALD-52 likely acts as a 5-HT2A partial agonist. The psychedelic effects are believed to come from ALD-52's efficacy at the 5-HT2A receptors. However, the role of these interactions and how they result in the psychedelic experience continues to remain elusive.

ALD-52, alongside with 1P-LSD, is believed to act as a prodrug to LSD, though it is unclear as to whether it is capable of exerting its own effects.[citation needed]

Subjective effects

Anecdotal reports from many users suggest that the effects of ALD-52 are essentially the same to that of its close structural relative LSD with whatever differences being so small so as to be considered virtually indistinguishable from one another. In comparison to other psychedelics such as psilocin, LSA and ayahuasca, ALD-52 is significantly more stimulating and fast-paced regarding the specific style of its physical and cognitive effects, in line with other lysergamides.

While it is unclear to what extent these have any pharmacological basis, anecdotal reports from the community tend to report ALD-52 as being slightly less potent and visual, with a mellower, less anxiety-provoking headspace that comes at the expense of less depth, giving it the reputation for being a more recreational variant of LSD. It has been speculated that this is due to a slightly extended, less jarring come up period that allows the user to become more acclimated to the changes in head space. As one increases the dose however, it is reported to lose this character and subjectively converge with the effects of a high-dose LSD experience.

Disclaimer: The effects listed below cite the Subjective Effect Index (SEI), an open research literature based on anecdotal user reports and the personal analyses of PsychonautWiki contributors. As a result, they should be viewed with a healthy degree of skepticism.

It is also worth noting that these effects will not necessarily occur in a predictable or reliable manner, although higher doses are more liable to induce the full spectrum of effects. Likewise, adverse effects become increasingly likely with higher doses and may include addiction, severe injury, or death ☠.

Physical effects

Visual effects

Cognitive effects

Multi-sensory effects

Experience reports

Anecdotal reports which describe the effects of this compound within our experience index include:

Additional experience reports can be found here:

Combinations

  • Cannabis - When used in conjunction with cannabis, both the visual and cognitive effects of ALD-52 can be intensified and extended with extreme efficiency. This should be used with extreme caution, especially if one is not experienced with psychedelics. Many users sometimes report a dramatically more intense visual trip when combining it with THC concentrates such as hashish as opposed to cannabis flower; however, this can also amplify the anxiety, paranoia, confusion and psychosis producing aspects of cannabis to a dangerous degree, which can often act as a catalyst for suddenly turning an enjoyable experience into an overwhelming "bad trip".
  • Dissociatives - When used in combination with dissociatives, the geometry, euphoria, dissociation and hallucinatory effects are often greatly enhanced. Dissociative-induced holes, spaces, and voids while under the influence of ALD-52 can result in significantly more vivid visuals than dissociatives alone present, along with more intense internal hallucinations, confusion, delusions and chances of a psychotic reaction. Additionally, users should be aware that there are reasons to believe that this combination may result in unforeseen neurotoxic effects, so a strong sense of caution and independent research are highly advised if one decides to experiment with this combination.
  • MDMA - When used in conjunction with MDMA, the physical and cognitive effects of MDMA become amplified. The visual, physical and cognitive effects of ALD-52 are also intensified with an overwhelming euphoric pleasure manifested through uniquely pleasurable body highs and headspaces, and uniquely colorful and awe-inspiring visuals. The synergy between these substances is unpredictable, and it is best to start with markedly lower dosages than one would take for both substances individually. Additionally, users should be aware that there are reasons to believe that this combination may result in unforeseen neurotoxic effects,[citation needed] so a strong sense of caution and independent research are highly advised if one decides to experiment with this combination.
  • Alcohol - This interaction is not typically recommended due to alcohol’s ability to cause dehydration, depression and thought disorganization which can negatively affect a trip if taken in high dosages. This combination is however reasonably safe in low doses and when used responsibly, this can often take the edge off a trip as well as dull its psychedelic effects in a fashion somewhat similar to benzodiazepines, albeit more stressful on the body.
  • Benzodiazepines - When used in combination with benzodiazepines, benzodiazepines can, depending on the dosage, slightly to completely reduce the intensity of the cognitive, physical and visual effects of an ALD-52 trip. They are very efficient at stopping "bad trips" at the cost of amnesia and reduced trip intensity. Caution is advised when acquiring them for this purpose, however, due to the very high addiction potential that benzodiazepines possess.
  • Psychedelics - When used in combination with other psychedelics, each drug's physical, cognitive and visual effects intensify and synergize strongly. The synergy between those substances is unpredictable, and for this reason generally not advised. If choosing to combine psychedelics, it is recommended to start with lower dosages than one would take for either substance individually.

Toxicity and harm potential

The toxicity and long-term health effects of recreational ALD-52 use do not seem to have been studied in any scientific context and the exact toxic dose is unknown. This is because ALD-52 is a research chemical with very little history of human usage. Anecdotal evidence from people within the psychonaut community who have tried ALD-52 suggests that there are no negative health effects attributed to simply trying the drug by itself at low to moderate doses and using it very sparingly (but nothing can be completely guaranteed). With respect to toxicity, its close molecular similarity and the likely prodrug relationship to LSD suggests it is highly unlikely to be any more toxic than LSD itself, though this has yet to be scientifically validated. However, it has been postulated that it can act as a potential trigger for those with underlying psychiatric conditions, so those with either a personal or family history of mental illness are generally advised not to use this substance. Independent research should always be done to ensure that a combination of two or more substances is safe before consumption.

Tolerance and addiction potential

ALD-52 is not habit-forming and the desire to use it can actually decrease with repeated administration. Like with most psychedelics, it is thought to be most often self-regulating rather than self-reinforcing.

Tolerance to the effects of ALD-52 build almost immediately after ingestion. After that, it takes about 5-7 days for the tolerance to be reduced to half and 14 days to be back at baseline (in the absence of further consumption). ALD-52 presents cross-tolerance with [[Cross-tolerance::all psychedelics]], meaning that after the consumption of ALD-52 all psychedelics will have a reduced effect.

Dangerous interactions

Although many substances are safe on their own, they can become dangerous and even life-threatening when combined with other substances. The list below contains some common potentially dangerous combinations, but may not include all of them. Certain combinations may be relatively harmless in low doses of each but can still increase the risk of unpredictable injury or death. Independent research should always be done to ensure that a combination of two or more substances is safe before consumption.

Legality

This legality section is a stub.

As such, it may contain incomplete or wrong information. You can help by expanding it.

  • United Kingdom: As of January 7th, 2015, ALD-52 is specifically named in the U.K. Misuse of Drugs Act as a Class A drug.[4]
  • Latvia: ALD-52 is illegal in Latvia. Although it isn't officially scheduled, it is controlled as an LSD structural analog due to an amendment made on June 1, 2015.[5]

See also

Literature

  • Nichols, D. E. (2016). Psychedelics. Pharmacological Reviews, 68(2), 264-355. https://doi.org/10.1124/pr.115.011478
  • Passie, T., Halpern, J. H., Stichtenoth, D. O., Emrich, H. M., & Hintzen, A. (2008). The Pharmacology of Lysergic Acid Diethylamide: A Review, 14, 295–314. https://doi.org/10.1111/j.1755-5949.2008.00059.x
  • Nichols, D. E. (2016). Psychedelics, (April), 264–355. https://doi.org/10.1124/pr.115.011478.
  • Carhart-Harris, R. L., Muthukumaraswamy, S., Roseman, L., Kaelen, M., Droog, W., Murphy, K., … Nutt, D. J. (2016). Neural correlates of the LSD experience revealed by multimodal neuroimaging. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.1518377113
  • Vollenweider, F. X., & Kometer, M. (2010). The neurobiology of psychedelic drugs: implications for the treatment of mood disorders. Nature Publishing Group, 11(9), 642–651. https://doi.org/10.1038/nrn2884
  • Halberstadt, A. L. (2015). Recent advances in the neuropsychopharmacology of serotonergic hallucinogens. Behavioral Brain Research, 277, 99–120. https://doi.org/10.1016/j.bbr.2014.07.016
  • Thisted, D. M. R. A., & Nichols, D. E. (2005). Distinct temporal phases in the behavioral pharmacology of LSD: dopamine D2 receptor-mediated effects in the rat and implications for psychosis, 427–435. https://doi.org/10.1007/s00213-005-2183-9
  • Nichols, C. D., Garcia, E. E., & Sanders-bush, E. (2003). Dynamic changes in prefrontal cortex gene expression following lysergic acid diethylamide administration, 111, 182–188. PMID: 12654518

References

  1. 1.0 1.1 Shulgin, A., & Shulgin, A. (1991). Erowid Online Books: "TIHKAL" - #26 LSD-25. Retrieved April 14, 2017.
  2. Ask Erowid: ID 3189 : Was Orange Sunshine actually ALD-52? | https://erowid.org/ask/ask.php?ID=3189
  3. Talaie, H., Panahandeh, R., Fayaznouri, M. R., Asadi, Z., & Abdollahi, M. (2009). Dose-independent occurrence of seizure with tramadol. Journal of medical toxicology, 5(2), 63-67. doi:10.1007/BF03161089
  4. ACMD (10 June 2014). "Update of the Generic Definition for Tryptamines" (PDF). UK Home Office. p. 12. Retrieved 10 June 2014. 
  5. Noteikumi par Latvijā kontrolējamajām narkotiskajām vielām, psihotropajām vielām un prekursoriem (2.4.punkts) | http://likumi.lv/doc.php?id=121086