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Freebasing

The cleanup of this oil is exactly like that which was done in Method 1. The oil is dissolved in about SOOmL of 3N HCl and the solution extracted with TOOmL of DCM. The chemist remembers that in this particular case the MDMA or meth is going to stay in the HCl/water but that unreacted, valuable MD-P2P or P2P is going to be in that DCM so it, of course, is saved. The HCl/MDMA solution is then basified with concentrated NaOH so that at around pH 9 the happy little beads of final, freebase product will appear in the solution. As usual, the oil is extracted with DCM, dried through Na2S04 and the DCM removed by distillation. The final product here is usually a little darker in color than the product achieved in Method 1, but it is still remarkably clean and may be crystallized as is with the crystallization process removing most of the color impurities. Of course the chemist may wish to vacuum distill to afford clear product. The average yield with this method is 60-70%. [Pg.103]

Dear readers please take notice Not once has the flask left the stirplate since the formamide and P2P reaction started up to the last point where MDA freebase was liberated. That s pretty damn convenient. Technically, the Leuckart reaction can continue as a one pot synthesis from the last part of P2P cleanup right up to final product. [Pg.115]

Well, that s about as rounded an education on Leuckart reactions as Strike can give. Strike feels that after reading all of those similar, repetitious steps, one can start to get a good feel for where a product is at any given moment. Stuff like what happens to MDA when it s mixed with acid or base, or what happens to ketones (P2P) under the same circumstances. One can see now that it is possible to not only isolate safrole and P2Ps chemically but that the same can be true for the final MDA or meth freebase oil. Repeated washings with acid or base and solvent can effectively clean up a compound to an almost presentable state without the use of vacuum distillation, it can happen, one only needs have confidence in the chemistry. [Pg.116]

They are actually using crystallization to purify the amine from any non-amine contaminants. They later freebased the crystals and fractional distilled to get pure amphetamine with a yield of 50%. [Pg.119]

So now we have a modified method where one has ammonia, methylamine or ethylamine freebase saturated in a small amount of DMF. The author next suggested that a power pulse protocol would not necessarily be needed, but that the power output from the microwave should be between 20-40% of full power. Also, the water in the clay would still be needed for the reaction. [Pg.125]

METHOD 2 [89]--1M MDA or benzedrine and 1M benzaldehyde is dissolved in 95% ethanol (Everclear), stirred, the solvent removed by distillation then the oil vacuum distilled to give 95% yellow oil which is a Schiff base intermediate. 1M of this intermediate, plus 1M iodomethane, is sealed in a pipe bomb that s dumped in boiling water for 5 hours giving an orangy-red heavy oil. The oil is taken up in methanol, 1/8 its volume of dH20 is added and the solution refluxed for 30 minutes. Next, an equal volume of water is added and the whole solution boiled openly until no more odor of benzaldehyde is detected (smells like almond extract). The solution is acidified with acetic acid, washed with ether (discard ether), the MDMA or meth freebase liberated with NaOH and extracted with ether to afford a yield of 90% for meth and 65% for MDMA. That s not a bad conversion but what s with having to use benzaldehyde (a List chemical) Strike wonders if another aldehyde can substitute. [Pg.159]

In a plastic container the chemist dissolves her golden yellow freebase oil into some DCM, ether or ethanol. The chemist then starts a steady dripping of the sulfuric acid into the HCl/salt and white, puffy HCI gas will start to exit the glass rod or pipette which is at the end of the hose. That tip is then plunged into the sol-vent/freebase solution to bubble the gas through the solvent. [Pg.248]

There is a very important point to stress about the above procedure. Strike listed ether, DCM and ethanol as crystallization solvents. But the one chemists should use is DCM. That s right...DCM Strike is telling all of you right now that DCM is an absolutely superior solvent for crystallization. In fact it is so good that one need not purify the freebases acquired from the ends of half of the recipes in this book. [Pg.249]

Most of the final product producing recipes in this book will provide for the chemist to take up the final free base product in DCM. Usually the freebase oil in the DCM is dark. Used to be that Someone-Who-ls-Not-Strike (SWINS) would have to distill the freebase to get clear yellow oil before crystallizing because when SWINS used ether or ethanol as a crystallization solvent, the colored crap would contaminate the final product. But not with DCM. Even with the grungiest (well...not too grungy) freebase, the crystals that come out are pure snow. The DCM so strongly solvates the contaminants that none remain in the mass of crystalled final product. The filter cake is sooooo clean even in the darkest solvent ... [Pg.249]

There are some alternatives to this HCI generator type of crystallization. There are, of course, canisters of HCI gas that can be purchased. Also, one can crystallize with very concentrated (fuming) HCI by pouring the stuff directly into the ether/freebase [26]. Regular 35% HCI can do this too, but the water content may dissolve the MDA.HCl or make the crystals sticky which means that the chemist will have to dry the solution by removing the water. [Pg.249]

She also had experimented with LSD and cocaine freebasing numerous times within the past 2 years. Throughout her history of substance abuse she experienced an increasing frequency of periods of dazed consciousness and blackouts multiple times yearly, while under the influence of alcohol. Further, she reported that other family members had chemical dependency problems, though her parents never abused drugs/a1cohol. [Pg.216]

N,N-DMT DMT (N,N-dimethyltryptamine) is one of the most hallucinogenic compounds known. DMT is not active orally (unless in the form of an ayahuasca brew), but must be smoked in it s freebase form to experience its effects. (DMT can be taken orally when mixed with a MAOIs, but this is not recommended for the first time user.) The body quickly builds a tolerance for the drug. Your DMT dose must be taken within 60 seconds. Any more of the drug after this first minute will not enhance the experience. It is recommended to give at least one hour before attempting another DMT trip. [Pg.5]

The total quantum yield [4>cs(total)] for CS is decreased to 0.17 in dimethyl-formamide (DMF) due to the competition of the CSH from Fc-ZnP-H2F+-C6o (1.63 eV) to Fc-ZnP- -HzP-Cso (1.34 eV) versus the decay of Fc-ZnP-Fl2P -C6o to the triplet states of the freebase porphyrin (1.40 eV) and the Ceo (1.50 eV) [47]. In contrast to the case of most donor-acceptor-linked systems, the decay dynamics of the charge-separated radical pair (Fc -ZnP-H2P-C6o ) does not obey first-order kinetics, but, instead, obeys second-order kinetics [47]. This indicates that the mframolecular electron transfer in Fc -ZnP-H2P-C6o" is too slow to compete with the diffusion-limited inter-molecular electron transfer in solution. [Pg.231]

Crack Cocaine Street Names Freebase. Mexican speedballs (crack w/ methamphetamine), roosten tornado (ovct 40 street slang terms) Use Crack is cocaine that comes in a rock crystal that can be heated and its vapors smoked. The tOTn crack ref s to the crackling sound heard when it is heated Actions CNS stimulant induces euphoria. Highly addictive Effects Acute CV or cerebrovascular emergencies (heart attack or stroke), could result in sudden death. Cocaine-related deaths are often a result of cardiac arrest or seizure followed by resp arrest (see also Cocaine)... [Pg.339]

Freebase cocaine and crack cocaine, each containing cocaine base, are prepared from cocaine hydrochloride by adding ammonia and ether or sodium bicarbonate and heat, respectively. Applying heat to evaporate the ether can cause the ether to ignite, which can cause severe burns. In preparing crack cocaine, the... [Pg.63]


See other pages where Freebasing is mentioned: [Pg.29]    [Pg.99]    [Pg.100]    [Pg.104]    [Pg.110]    [Pg.115]    [Pg.116]    [Pg.119]    [Pg.119]    [Pg.121]    [Pg.122]    [Pg.122]    [Pg.124]    [Pg.138]    [Pg.159]    [Pg.160]    [Pg.195]    [Pg.196]    [Pg.201]    [Pg.241]    [Pg.247]    [Pg.248]    [Pg.248]    [Pg.250]    [Pg.44]    [Pg.68]    [Pg.133]    [Pg.138]    [Pg.96]    [Pg.119]    [Pg.199]    [Pg.199]    [Pg.199]    [Pg.64]   
See also in sourсe #XX -- [ Pg.33 , Pg.45 ]

See also in sourсe #XX -- [ Pg.71 , Pg.123 , Pg.124 ]

See also in sourсe #XX -- [ Pg.40 ]




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