Metamfetamīna un amfetamīna sintēzes metožu salīdzinājums

Jordan Belfort

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kāpēc Al/Hg ir norādīts tikai maksimāli 100 g ? jūs varat veikt šo reakciju līdz 200 l laikā..... un iznākums ir tikai 80 procenti ar pareizām attiecībām, jo īpaši, ja jūs izmantojat nitro kā šķīdinātāju un metilamīna avotu, protams, tas sajauksies daudz labāk, jo tas neizvārīs metilamīnu no jūsu reakcijas, jo tas GENERĒS.
 

Jordan Belfort

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Sajauc labāk, jo tas veido aezotropu ar eļļu un metanolu
 
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Fernandohatescorn

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Sveiki, Leckart meth reakcijai p2p ar N-formu ir teikts, ka 30-38% yeild vai ir iespējams lielāks yeilds un kāds procents?
 

Osmosis Vanderwaal

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Vai nav bērza reakcijas? Interesanti, kā sinhronizācija efedrīna prekursoru sākšanai būtu salīdzināma? 🤔
 

GhostChemist

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Bērza reakcija būs vēlāk
 

Osmosis Vanderwaal

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18 months ago, I wrote that. I've learned a lot. There's still along way to go, but a birch reaction in the strict sense is our of the range of most drug cooks, and what you see people doing to make meth is more of a "birch-like reaction" or I like to call it the solvated electron, although that's about as big a mis-monoker as saying it's a birch. The lithium/ammoniated nonpolar solvent shouldn't even work, but I've seen it with my own eyes. You guys ever get to this method?
 

jasper

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Vai jūs varat izveidot video par NaBH4 procesu nav labas ķīmijas priekšzināšanas, bet ļoti vēlaties apgūt šo metodi
 

Methodman

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Man ir daži papildjautājumi. Kādas metodes padara labākus rīkus. Es nedomāju, ka gala molekula ir tāda pati. Šie p2p. I dont. Zinu, ar ko viņi dooing. Bet tas vienkārši nav tas. Hollow. Pseido. Es nekad nepavadītu dienu guļot un. ēst. Pat bērzs bija atšķirīgs tad tas hipo atšķirīgs tad orto. Bet tur bija. sava veida standarts. Tas diezgan js labs laiski. Un džerkošanai. Jebkuras domas
 

sumof666

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Ja jūs pērkat "rīkus", kas ir tirgū(un es domāju, ka jūs to darāt), domāju, ka ne vairāk kā tad.
20 % no jūsu "rīka" ir ĪSTAIS RĪCĪBA.
Atkarībā no tā, kā tirgotājs parasti jūs atradīsiet, iespējams, kofeīnu, kreatīnu.
Vēl viens faktors ir tas, kāda skābe tika izmantota, lai radītu amfetamīna sāli. Vislabāk, ja tā sulfiuric 6 tad biopieejamība ir visaugstākā, ja tika izmantota ortofosforic tā mazāk aviable jūsu šūnām. Ja tiktu izmantota citronskābe, jūs varētu izmantot ēdamkaroti, lai sajustu kādu triecienu.
Tā es to redzu.
visas metodes, kas noved pie Afreebase molekulas izveides, kā tā ir apstrādāta un kas ir izmantots, lai atšķaidītu jūsu GEAR atkarīgs, kā tas iedarbojas uz jums.
Man skaidrs amf sulfāts darbojas tāpat bez metodes ietekmes.
 

sumof666

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Ja jūs pērkat "rīkus", kas ir tirgū(un es domāju, ka jūs to darāt), domāju, ka ne vairāk kā tad.
20 % no jūsu "rīka" ir ĪSTAIS RĪCĪBA.
Atkarībā no tā, kā tirgotājs parasti jūs atradīsiet, iespējams, kofeīnu, kreatīnu.
Vēl viens faktors ir tas, kāda skābe tika izmantota, lai radītu amfetamīna sāli. Vislabāk, ja tā sulfiuric 6 tad biopieejamība ir visaugstākā, ja tika izmantota ortofosforic tā mazāk aviable jūsu šūnām. Ja tiktu izmantota citronskābe, jūs varētu izmantot ēdamkaroti, lai sajustu kādu triecienu.
Tā es to redzu.
visas metodes, kas noved pie Afreebase molekulas izveides, kā tā ir apstrādāta un kas ir izmantots, lai atšķaidītu jūsu GEAR atkarīgs, kā tas iedarbojas uz jums.
Man skaidrs amf sulfāts darbojas tāpat bez metodes ietekmes.
 

Berlin777

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Why all the sources tell different yields for amphetamine synthesis via Leuckart?
 

Chemtrail

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Great post !! Your a gentleman and a scholar!!
 

Osmosis Vanderwaal

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I'd like to see how an electroreduction stacks up here, the fact that there's a lot less chemicals suggests it's cheaper to make, and therefor a better value
 

Chemtrail

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If you were to add LiAlH4 to that "Synthesis Comparison Methods" chart

How will LiAlH4 measure up ??

Or Sodium Cyanoborohydride measure up ??
 

GhostChemist

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This synthesis carried out without LiBH4 or NaBH3CN
Because synthesis with these reducing agents are dangerous
 
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Chemtrail

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Dangerous because there cannot be any water H2O none at all?, with these reducing agents
 

GhostChemist

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yes
and for the NaBH3CN, this reagent during long-term storage can generate HCN and subproducts
but this reducing agents very selective in some syntheses
 

Chemtrail

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Thank you

Seems not only dangerous (because of violent reaction with water)

But LiAlH4 and NaBH3CN are expensive too

My labrat thinks NaBH3CN takes a long time 24-48+ hours
and LiAlH4 takes 4-24 hours
For RXN reduction time

Both have really good yeilds
 

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These reducing reagents are apply in different synthesis, as example for the selective reduction of functional groups
 

Chemtrail

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My labrat is jealous of that guy who has "creditentials" within the science community (Sigma-Alrich, Fisher, university and science-related businesses), has permits/licenses and/or identification that allows access to
access to some of these precursors that we (we * as in a bunch of amateur clandestine hobbist druggies that cook drugs in their parents basement, when Momma is not looking lol) dream of ..

My labrat dreams of having a liter of phenylacetone and trying out the various METHods of reducing the ketone

Life is but a dream
 
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