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| Research Chemicals Piperazines, Phenethylamines, Tryptamines & other Research Chemicals or designer drugs. |
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#1
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2-methylamino-1-</span>(3,4-methylenedioxyphenyl)butan-1-</span>one and what is the DOSAGE (oral...) and DURATION??? i tried to search for info but i couldn't find anything (pikhal, erowid, lycaeum,....) Is it the same as Methylone ? The butane instead of propane... does it makes differences ? Edited by: _jo_ |
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#2
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or is it MDBD ? but the -1-one should make it different ? and i also wondering what are those molecules : 1-(4-fluorophenyl)propane-2-amine 1-(3,4-methylenedioxy-phenyl)-2-pyrrolidin-1-yl-pentan-1-o ne Edited by: _jo_ |
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#3
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methyl jones, or mebylone I think. the -1-one indicates a double bonded oxygen or ketone group.
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#4
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1-(3,4-methylenedioxy-phenyl)-2-pyrrolidin-1-yl-pentan-1-o ne this would presumably be a pyradine-like(structurally related to benzene) ring with a ketonatedamyl hydride bit coming offtrying to mimicthe carbon stringstructure of an amphetamine, all with a classic PEA/amphetamine carrier structure.I would NOT want to be the first to try this substance.Edited by: allyourbase |
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#5
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it's not very helpful to spread these nicknames before the substance hasnt gained any popularity. and since it probably never will one shouldnt start giving misleading nicknames to it. call it the beta-keto analog of mbdb if you want. the last one shouldnt be very potent because of its long sidechain. i think i read in pihkal that they dont seem to have any activity. but i dont know what the pyrrolidin-ring alters, it's located around the nitrogen afaik. |
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#6
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yes pls stay away from nicknames as descriptives.
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#7
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As far as I know, no one on this forum has yet tried any of those
compounds. Here's some info from another forum: Quote:
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#8
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Ok thank every body... I was actually looking for nicknames because i'm
used to read trip-reports before try products, and i couldn't find anything about those. Now i can, thanks. I understand nicknames can be problematic for such unknown RCs... i still have a question for you: 1-(4-fluorophenyl)propane-2-amine is it 4-FMP ?? |
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#9
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no,
1-(4-fluorophenyl)propane-2-amine is 4-FA (4-fluroamphetamine) |
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#11
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Quote:
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#12
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Quote:
I wasn't aware there was a "real" 4-FMP, but rather that the name 4-FMP was just not technically a very good abbreviation (I guess it stands for 4-Fluoro-alpha-Methyl-Phenethylamine). Same chemical, AFAIK. *<!-- 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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#13
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Hmm, strange that it would be given the 'wrong' name. Irrigardless of the topic, I thikn it would be MDPPP as an abreviation because those are the letters that each main part starts with |
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#15
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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; //--> The compound mentioned originally, i.e. the MBDB/Methyl-J homologue of methcathinone</span>, has been referred to as Mebylone</span>, Methyl-Jones</span>, and Butylone</span> in various posts and by various persons. I do agree that it is unwise to tack nicknames onto substances before they are thoroughly researched, and even then giving a substance a nickname can occasionally create a force of suggestion or an aire of implied effects that taints the subjective bioassay, and often leaves the experimenter confused and/or disappointed. Think of all the folks that tried "foxy" (5-MeO-DIPT), and then got pronouced nausea followed by the shits for a few hours. What's the appropriate web-chat abbreviation to be used here? Oh yeah-- Y</span>our M</span>ileage M</span>ay V</span>ary (YMMV). Also-- "MDPPP" is IMO just a bit too reminiscent of MPPP and MPTP, which were the fucked-up merperidine analogues that caused all those sudden outbreaks of instant Parkinson's disease in the mid-1980's, prompting the hysterical knee-jerk media term "designer drugs" and helping to encourage the passing of the Controlled Substance Analogue Act (CSAA) by congress. Either that, or it sounds like another piperazine compound, like TFMPP or PMMBP. Just my opinion though. <!-- 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; //--> Edited by: Eirias |
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#16
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http://www.erowid.org/experiences/exp.php?ID=44549
Quote:
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#17
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is this case, Shulgin would have to be wrong. 'Butylone' makes it sound as if it has a mutylene groupbecause of the similarity to methylong and ethylon. There will obviously be confusion due to that. methylJones is the best so far
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#19
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Regarding 1-(3,4-methylenedioxy-phenyl)-2-pyrrolidin-1-yl-pentan-1-o ne: Quote:
I posted this on another forum and will repost because it exactly applies here: WARNING! The name "MDPPP</font>" has been applied to two different compounds. One of them has been discussed in this thead, and is also known as MDPV, aka 1-(3,4-methylenedioxy-phenyl)-2-pyrrolidin-1-yl-pentan- 1-one, aka 3',4'-methylenedioxy-2-pyrrolidin-1-yl-valerophenone. This is a ketone with a five-carbon chain. However, there is also a similar compound, chemically identical except for the fact that it has a three-carbon chain. Its chemical name is 3',4'-methylenedioxy-alpha-pyrrolidinopropiophenone. Link: http://amphetamines.com/mdppp/ The confusion results from the fact that propane (3 carbons) and pentane (5 carbons) both begin with the letter "p". The name MDPV is pretty umambiguous because the "v" stands for "valerophenone", another name for "pentanophenone". These compounds likely have different dosages. The five-carbon compound, MDPV, is reportedly active at just 5 mg. I have no information as to the activity of the three-carbon compound. Be sure you know which one you're working with!</font> <!-- 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; //--> <!-- 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; //--> Edited by: gn2osis |
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#20
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this would presumably be a pyradine-like(structurally related to benzene) ring with a ketonatedamyl hydride bit coming offtrying to mimicthe carbon stringstructure of an amphetamine, all with a classic PEA/amphetamine carrier structure.I would NOT want to be the first to try this substance.That's a mixture of gobbledegook and plain incorrect. It has nothing to do with pyridine (which is a heterocyclic six membered aromatic compound). It refers to pyrrolidine, which is aheterocyclic fivemembered non-aromatic compound. As to what a ketonated amyl hydride is, god alone knows. The compound is a ketone with a substituted benzene ring (sub with 3,4-methylenedioxy group) on one side of the carbonyl group, and a butyl chain, with a pyrrolidine ring attached via the nitrogen to the carbon adjacent to the carbonyl group. It is vaguely a modified amphetamine structure (very vaguely) that is a specific dopamine reuptake inhibitor, active in humans at around the 5mg mark, orally |
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