DMT-Nexus member
Posts: 26 Joined: 18-Aug-2012 Last visit: 26-Jan-2013 Location: USA
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Hello I was just wondering if anyone had any experiences with LSH I cant seem to find much on it any input would be appreciated.
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 DMT-Nexus member
Posts: 134 Joined: 30-Oct-2011 Last visit: 01-Jan-2023
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I guess what may be forming is LST (Lysergic Acid Tetraethylamide) rather than LSH* but I'm no chem whiz. Doing CWE then adding acetaldehyde in a cold environment with plenty of agitation has yielded some exeptional experiences. Really amped up the euhoria and about cancelled the sedation. Slight increase in visual effect and an electric body feel. These changes seem commonplace in those whom successfully experiment with the combination. A better source of acetaldehyde might be White or Sherry wine (they should smell like apples; as acetaldehyde does). These could be great choices to use for overnight hydro-alcoholic extractions. Cold-brewed coffee is also an acetaldehyde source; vasodialating and adding good energy to boot! The Cinnemaldehyde combo is even more of an obvious change. The peaks is at 15 minutes; but it lasts as long. Much stonger vids; true OEV are possible at what would otherwise be a normal dose. It is about twice as potent. Be safe. *http://herbs.maxforum.org/2012/10/17/we-were-wrong-about-lsh/#post7 All readable matter in the above post is ficticious.
Any similarities to real life are purely coincidental.
Without prejudice.
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DMT-Nexus member
Posts: 26 Joined: 18-Aug-2012 Last visit: 26-Jan-2013 Location: USA
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That's interesting I will have to try this sometime thanks for your input  anyone else have any info?
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 analytical chemist
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Posts: 7463 Joined: 21-May-2008 Last visit: 14-Jan-2025 Location: the lab
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a tetraethylamine definitely doesn't exist (Nitrogen doesn't have 5 valence electrons), and there's no evidence to suggest other adducts form with the addition of various essential oils given the typical reaction conditions posted. this isn't some neat redox reaction with a simple small molecule, people are talking about an addition reaction to a chiral molecule with a stereocenter that readily isomerizes. "Nothing is true, everything is permitted." ~ hassan i sabbah "Experiments are the only means of attaining knowledge at our disposal. The rest is poetry, imagination." -Max Planck
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 DMT-Nexus member
Posts: 1999 Joined: 13-Jun-2011 Last visit: 24-Jun-2018
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benzyme wrote:this isn't some neat redox reaction with a simple small molecule, people are talking about an addition reaction to a chiral molecule with a stereocenter that readily isomerizes. Lose Control, Free My Soul, Break Me Open, Make Me Whole."DMT kicked my balls off" - od3
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DMT-Nexus member
Posts: 26 Joined: 18-Aug-2012 Last visit: 26-Jan-2013 Location: USA
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benzyme Do you think it is possible that the acetaldehyde may be reacting with the other ergot alkaloids present in the seeds.
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 analytical chemist
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Posts: 7463 Joined: 21-May-2008 Last visit: 14-Jan-2025 Location: the lab
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it's not probable that the acetaldehyde present, if any, is reacting with anything because the reaction equilibrium favors LSA formation. I've mentioned this several times (pardon me if this is the first time you've read it), but for some reason, people who don't comprehend the concept seem to think faith makes the reaction occur, and they are convinced that they really make LSH rather than a minty LSA cocktail. *edit* on a side note, I've also mentioned that it's plausible that another pharmacological effect is occurring with these essential oils being consumed. "Nothing is true, everything is permitted." ~ hassan i sabbah "Experiments are the only means of attaining knowledge at our disposal. The rest is poetry, imagination." -Max Planck
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DMT-Nexus member
Posts: 26 Joined: 18-Aug-2012 Last visit: 26-Jan-2013 Location: USA
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That may be true but that doesn't explain why people are describing better experiences with this so called "LSH" You seem to be experienced with with chemistry what do you think is causing this. It may be placebo but I haven't tried this so I wouldn't know. flickedbic do you think it is possible that what you experienced was placebo.
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 analytical chemist
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Posts: 7463 Joined: 21-May-2008 Last visit: 14-Jan-2025 Location: the lab
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I just told you, in the edit. people report synergistic effects all the time, consuming various foods/drugs that alter the quality of mushroom and mescaline experiences. I see no reason the same could not apply to LSA. "Nothing is true, everything is permitted." ~ hassan i sabbah "Experiments are the only means of attaining knowledge at our disposal. The rest is poetry, imagination." -Max Planck
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DMT-Nexus member
Posts: 26 Joined: 18-Aug-2012 Last visit: 26-Jan-2013 Location: USA
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That's a good point thanks benzyme. Well whatever it is, it seems to work from what i hear so I will try this for myself and get back to you. I think that this may be a good alternative to LSD It may not be the same thing but hey Its natural.
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 analytical chemist
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it's definitely intriguing, methinks, and you get peace of mind because you pretty much know what you are consuming. keep experimenting. "Nothing is true, everything is permitted." ~ hassan i sabbah "Experiments are the only means of attaining knowledge at our disposal. The rest is poetry, imagination." -Max Planck
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DMT-Nexus member
Posts: 26 Joined: 18-Aug-2012 Last visit: 26-Jan-2013 Location: USA
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I definitely will, I will get back you when I get some results. Let me know if you find any info on the subject.
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DMT-Nexus member
Posts: 26 Joined: 18-Aug-2012 Last visit: 26-Jan-2013 Location: USA
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Ok so i came up with some interesting results. I first tryed the LSH extraction with white whine like flickedbic described and I had a overall better experience more euphoria ect. And it defiantly wasn't placebo. Then I tryed drinking the white whine and taking the LSA at different times and It worked with that method which means that benzyme was most likely right about the acetaldehyde having a synergistic effect with the LSA.
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DMT-Nexus member
Posts: 1 Joined: 24-Jun-2013 Last visit: 24-Jun-2013 Location: spain
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benzyme wrote:a tetraethylamine definitely doesn't exist (Nitrogen doesn't have 5 valence electrons), and there's no evidence to suggest other adducts form with the addition of various essential oils given the typical reaction conditions posted.
this isn't some neat redox reaction with a simple small molecule, people are talking about an addition reaction to a chiral molecule with a stereocenter that readily isomerizes. You couldn't be more wrong! After experimenting with aldehydes, I have determined that aldehydes are able to bind to nitrogen atoms with only a single bond available. This means that LSH does not form from the reaction of LSA and acetaldehyde. A molecule much closer to LSD is formed. We thought LSC looked something like this: http://imageshack.us/scaled/landing/708/lscone.jpgIn reality what will form is something like this: http://imageshack.us/scaled/landing/827/lsctwo.jpgTherefore, the reaction between LSA and acetaldehyde would not produce LSH: http://imageshack.us/scaled/landing/22/lsht.jpgIt would produce LST [Lysergic Acid Tetraethylamide]: http://imageshack.us/scaled/landing/708/lstr.jpgWhich has just three more carbon atoms than LSD: http://blogs.bu.edu/ombs...cture-of-LSD-300x246.jpgThe nitrogen with the single methyl group can be replaced by aldehydes. Mesembrine, mitragynine, and rhynchophylline have only single bonds available for their nitrogens, and mesembrine has a methyl group covering up its only nitrogen. All three of those molecules can be reacted with aldehydes to produce molecules with modified pharacokinetics. Therefore LST would result from the reaction of acetaldehyde and LSA; not LSH. im sorry but your'e wrong
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 Not I
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Posts: 2007 Joined: 30-Aug-2010 Last visit: 23-Sep-2019
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Bilbo92 wrote:benzyme wrote:a tetraethylamine definitely doesn't exist (Nitrogen doesn't have 5 valence electrons), and there's no evidence to suggest other adducts form with the addition of various essential oils given the typical reaction conditions posted.
this isn't some neat redox reaction with a simple small molecule, people are talking about an addition reaction to a chiral molecule with a stereocenter that readily isomerizes. You couldn't be more wrong! After experimenting with aldehydes, I have determined that aldehydes are able to bind to nitrogen atoms with only a single bond available. This means that LSH does not form from the reaction of LSA and acetaldehyde. A molecule much closer to LSD is formed. We thought LSC looked something like this: http://imageshack.us/scaled/landing/708/lscone.jpgIn reality what will form is something like this: http://imageshack.us/scaled/landing/827/lsctwo.jpgTherefore, the reaction between LSA and acetaldehyde would not produce LSH: http://imageshack.us/scaled/landing/22/lsht.jpgIt would produce LST [Lysergic Acid Tetraethylamide]: http://imageshack.us/scaled/landing/708/lstr.jpgWhich has just three more carbon atoms than LSD: http://blogs.bu.edu/ombs...cture-of-LSD-300x246.jpgThe nitrogen with the single methyl group can be replaced by aldehydes. Mesembrine, mitragynine, and rhynchophylline have only single bonds available for their nitrogens, and mesembrine has a methyl group covering up its only nitrogen. All three of those molecules can be reacted with aldehydes to produce molecules with modified pharacokinetics. Therefore LST would result from the reaction of acetaldehyde and LSA; not LSH. im sorry but your'e wrong So first off your nomenclature is wrong. Tetraethylamide does indeed imply 5 bonds to a tetravalent nitrogen like benzyme imagines. What you have shown is diethylamide..... The other two nitrogens which you have ethyl groups on are tertiary amines and are thus not amides... So it's not tetraethyl amide. Secondly, can you show any sort of NMR evidence for the second LSC adduct you propose above? The reason I ask is the first cinnaminaldehyde addition you show in structure one is quite unstable and in the presence of water would easily undergo amide hydrolysis thus making it very unlikely that the second adduct would form. Believe me, I want this to be true as much as everyone else, but unless someone can show the presence of these species via NMR then I'm inclined to agree with Benzyme... and I'm usually the guy saying everything doesn't require a publication.. BTW I also agree with Benzyme that it could be a favorable drug-drug interaction going on.. If your religion, faith, devotion, or self proclaimed spirituality is not directly leading to an increase in kindness, empathy, compassion and tolerance for others then you have been misled.
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 Not I
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Posts: 2007 Joined: 30-Aug-2010 Last visit: 23-Sep-2019
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One more quick thought. If someone would just show the existence of some new spots via TLC it would go a long way towards supporting these adduct theories... If your religion, faith, devotion, or self proclaimed spirituality is not directly leading to an increase in kindness, empathy, compassion and tolerance for others then you have been misled.
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