Bwiti
(PVC-Analog Taste-Tester) 03-05-03 10:28 No 413998 |
MPTP Solubility.. | Bookmark | ||||||
Alright, lets say one has a solution of freebase 1,3-dimethyl-4-phenyl-4-propionoxypiperi Love my country, fear my government. |
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Bwiti (PVC-Analog Taste-Tester) 03-05-03 10:49 No 414002 |
what the merck says.. | Bookmark | ||||||
Just looked it up in the 13th edition Merck.. Monograph Number: 6319 Title: MPTP CAS Registry Number: 28289-54-5 CAS Name: 1,2,3,6-Tetrahydro-1-methyl-4-phenylpyri Additional Names: 1-methyl-4-phenyl-1,2,3,6-tetrahydropyri Molecular Formula: C12H15N Molecular Weight: 173.25. Percent Composition: C 83.19%, H 8.73%, N 8.08% Literature References: Piperidine derivative which causes irreversible symptoms of parkinsonism in humans, monkeys. Prepn as hydrochloride by Grignard reaction: A. Ziering et al., J. Org. Chem. 12, 894 (1947). Alternative prepn: C. J. Schmidle, R. C. Mansfield, J. Am. Chem. Soc. 78, 425 (1956). Identification as impurity in "synthetic heroin" and effect on drug users: J. W. Langston et al., Science 219, 979 (1983). Selective destruction of dopaminergic neurons in primates: R. S. Burns et al., Proc. Nat. Acad. Sci. USA 80, 4546 (1983). In vitro metabolism by rat brain monoamine oxidase to 1-methyl-4-phenylpyridinium ion (MPP+): K. Chiba et al., Biochem. Biophys. Res. Commun. 120, 574 (1984). Studies on mechanism of neurotoxicity: J. W. Langston et al., Science 225, 1480 (1984); S. P. Markey et al., Nature 311, 464 (1984). Binding studies in rat brain: C. M. Wieczorek et al., Eur. J. Pharmacol. 98, 453 (1984); B. Parsons, T. C. Rainbow, ibid. 102, 375 (1984); in rat, human brain: J. A. Javitch et al., Proc. Nat. Acad. Sci. USA 81, 4591 (1984). Comparison of idiopathic and MPTP-induced parkinsonism in humans: R. S. Burns et al., N. Engl. J. Med. 312, 1418 (1985). Review: T. P. Singer et al., Trends Biochem. Sci. 12, 266-270 (1987); L. M. Sayre, Toxicol. Lett. 48, 121-149 (1989). Properties: Crystals from heptane, mp 40-42°. bp0.8 85-90°. Melting point: mp 40-42° Boiling point: bp0.8 85-90° ---------------------------------------- Freebase MPTP isn't soluble in heptane? Or, are they talking about recrystallization? Love my country, fear my government. |
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Sunlight (Pioneer Researcher) 03-05-03 13:00 No 414029 |
Recrystallization | Bookmark | ||||||
Yes, they say that the crystals formed in heptane as solvent had that mp. |
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M3Psych 03-06-03 03:42 |
MPTP isn't neurotoxic, MPP+ is.
(Rated as: misinforming) |
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Rhodium (Chief Bee) 03-06-03 04:01 No 414168 |
That is NOT enough! | Bookmark | ||||||
Taking deprenyl will inhibit a large number of MAO-B enzymes, and therefore lower the MAO-B activity throughout the body, but you will never ever completely shut it down, and as long as it is still the least functional, MPTP will be toxic. |
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Megatherium (Hive Bee) 03-06-03 15:44 No 414298 |
The main question is: which procedure do you... | Bookmark | ||||||
The main question is: which procedure do you intend to use to make MPPP? According to me, MPTP formation isn't going to be a problem if you use the procedure from US patent 2765315 since I think the MPTP producing side reaction is mechanistically impossible (see Post 410862 (Megatherium: "Very interesting. Then, in US patent 2765315 a", Methods Discourse) and the other posts in this thread). I wouldn't recommend acylation of the piperidinol (after reaction of PhLi with the piperidone). For safety reasons, I think it would be wise to do a flash chromatography of the product & check it out with TLC (whichever procedure you use). So the best advice is probably not to fuck around with meperidine synths without the proper knowledge, chemicals, equipment and GCMS. Yeah right, do you know how much a GC-MS apparatus costs? Furthermore, the meperidine synth isn't a problem ... the reversed meperidine ester synthesis is ! |
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M3Psych (Newbee) 03-06-03 17:42 No 414324 |
Re: Taking deprenyl will inhibit a large ... | Bookmark | ||||||
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Bwiti (PVC-Analog Taste-Tester) 03-06-03 21:51 No 414384 |
Shit.. | Bookmark | ||||||
Guess I better learn flash chromatography quick. Or, would I rather risk neurotoxicity, because I'm too lazy to take a class on it? Fuck! Yes, US2765315 is what I had my eye on.....Would flash chromotography really remove the neurotoxin? Love my country, fear my government. |
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Megatherium (Hive Bee) 03-06-03 23:25 No 414407 |
To learn about flash chromatography, read: *... (Rated as: excellent) |
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To learn about flash chromatography, read: * Vogel, Textbook of practical organic synthesis, 5 th ed., p. 217 - 220 * J. Org. Chem. (1982) vol. 47 p. 1351 * J. Org. Chem. (1978) vol. 43 p. 2923 The last article happens to be on Rhodium's site, how convenient . ../rhodium/pdf /flash.chromat Yes, flash chromatography will seperate MPPP & MPTP efficiently if you find a good solvent (one which generates Rf values on TLC that are far apart). Flash chromatography is a rather good technique to purify your product, but as I said, I don't think MPTP formation is going to be a problem with this procedure. But, I wouldn't put my substantia nigra on risk - if I were you. So, learn about flash chromatography & be patient (it is rather tedious). |
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Bwiti (PVC-Analog Taste-Tester) 03-08-03 09:43 No 414789 |
Thanks.. | Bookmark | ||||||
Thanks for the advise! Sounds cheaper than buying vacuum distillation equipment. Peace! Love my country, fear my government. |
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Rhodium (Chief Bee) 03-08-03 21:30 No 414863 |
I have uploaded the other article too: TLC... | Bookmark | ||||||
I have uploaded the other article too: TLC Mesh Column Chromatography (../rhodium/pdf /tlc.mesh.col |
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