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#1
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There is a vast difference in the chemistry of acetoxy - CH3COO-R - and a phosphorous atom. Acetoxyl groups are inherintly more stable and could pass through the blood/brain barrier intact and take up residence. That I do not dispute. But the P group has been shown to revert to the hydroxyl. It would be interesting, though, to try this hypothesis out with something unique. Say: O-Phosphoryl -4-hydroxy-n.n-dipropyltryptamine. See what that one does based on radio-tagging and dose/response.
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#2
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the structure of the compound might remain unaltered in these exchanges but doesnt the weight change? doesnt molecular weight have something to do with potency in regard to chemical structure? the acetoxys were in theory metabolites of the hydroxy compounds right?are their chemicalpropertiesextremely similar? could you say...smoke a 4acetoxy(their being more stable and whatnot)? qualatatively I find miprocin more akin to its 5methoxy analogue than to mushrooms. which is to say, more powerful. different.... psylocybin is more of an organic experience (no pun intended) while miprocin seems almost mechanical....it is a very clean trip as you said. virtually no unwelcomed effects even at doses ranging to 45 milligrams.Edited by: allyourbase |
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#3
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Quote:
Yes but probably not enough to matter; check Shulgin's comments in TiHKAL under psilocin. Quote:
vice-versa. but they may be active on their own. Quote:
Depends on which properties.... as psychedelics they seem similar though in certain cases (4-HO/AcO-MIPT) the acetoxy may be somewhat less potent, moreso than the molecular weight difference would have suggested. Quote:
There are reports of 4-AcO-DET freebase being smoked and being mucho effective. Quote:
ya, miprocin's amazing. happy trails! <!-- var SymRealOnLoad; var SymReal; Sym() { window.open = SymWinOpen; if(SymReal != null) SymReal(); } SymOnLoad() { if(SymRealOnLoad != null) SymRealOnLoad(); window.open = SymRealWinOpen; SymReal = window.; window. = Sym; } SymRealOnLoad = window.onload; window.onload = SymOnLoad; //--> |
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#4
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<!--
var SymRealOnLoad; var SymReal; Sym() { window.open = SymWinOpen; if(SymReal != null) SymReal(); } SymOnLoad() { if(SymRealOnLoad != null) SymRealOnLoad(); window.open = SymRealWinOpen; SymReal = window.; window. = Sym; } SymRealOnLoad = window.onload; window.onload = SymOnLoad; //-->I meant to add something about smoking 4-acetoxy tryp's vs. 4-HO-tryps. There's a good chemical reason why the former would be easier to smoke. It's because the 4-HO's exist as something called "internal salts". The proton moves from the 4-HO group to the N on the terminal amino group, leaving a negative charge on the former and a positive charge on the latter. Salts generally have higher vaporization points than non-salts. 4-acetoxy's ought to vaporize more readily, as long as they exist in freebase form and not as a salt (i.e., a protonated nitogren and a negative counterion like chloride or something like that). Most 4-acetoxy's on the market are in fact salts, so you'd have to make the freebase. You can check the search engine on that. |
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