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mfk last won the day on April 7

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  1. Video tutorials on how to make cannabis are listed below. // Good luck.
  2. mfk

    mfk - LSD

    If you have a degree in organic chemistry, this tutorial will explain you how to make LSD (for in game purposes, of course.) Always use red or yellow photographic dark room light bulbs during any step of LSD manufacture. Direct sunlight, electric filament, or fluorescent light bulbs (etc.) will hurt the above compounds. Dark room bulbs are cheap and are a must. Keep all forms of H2O out of the reaction. Thoroughly dry all the glass ware to be used. Use a drying tube filled with anhydrous MgSO4 (calcium chloride reacts with amines in an unfavorable way and should not be used). I can't be there to hold your hand and guide you through every step, so unless the formula says to add water, the drying tube should be in use, and after the water addition is over, the drying tube goes back on. This way the reaction is always protected even if it does not need to be. Better safe than sorry. Also, if you're not sure if you should use dry reagents, use dry reagents anyway. Also dry the lysergic acid (as described above) and any other precursors in whatever drying process required for that compound before use. Dry the finished LSD or even any intermediate along the way after you have completed the product. Likewise, dry an intermediate that you may have purchased from a chemical supplier. Keep oxidizing agents from these items. Even the oxygen in the air can oxidize some of these compounds. The formula states that during some of the reactions above, an inert gas (nitrogen) must be used for an atmosphere inside the reaction vessel. Nitrogen can be obtained in small bottles (tanks) at a very reasonable fee, without any questions asked. Make sure you use a regulator and introduce a slow stream into the vessel by way of a gas inlet tube or an equivalent. Always flush the vessel before putting any reagents into it (flush the air out with nitrogen). I would use a nitrogen atmosphere from the very beginning of the formula to the very end, even if the formula did not specify its use. Very few of the above formulas call for a nitrogen atmosphere during evaporation, but I feel this may be bad for yield and or potency. LSD has many doses per gram, and if you lose 1/2 g because you were too cheap to use three dollars worth of nitrogen, you have lost about 2,000 doses at $5 a dose = $10,000 of LSD wasted. Better safe than sorry? Also, any precursors you make or buy should be stored in a nitrogen atmosphere, as should LSD. This can be done by poking a gas inlet tube into the vessel trust above or a little below the substance) flushing the air out with a moderate stream of nitrogen then quickly reinstall the cap or stopper. Never subject these compounds to excessive heat, or any type of temperature warmer than the inside of your refrigerator. Even LSD maleate will decompose in excess heat, so store in a refrigerator. Keep evaporation procedures cooled. This will slow the evaporation process down, but that is better than losing the product. Some of the above formulas require heat for a reaction. This is Ok, but do not exceed the temp stated at any time and never heat longer than needed. Also, nitrogen atmospheres are used during heating operation. // 3-Indolepropionic acid, 94.5 g (0.5 mole) is dissolved in 600 ml of water containing 20 g of NaOH. The solution is mixed with 100 g of Raney Nickle catalyst and hydrogenated at room temp in a steel bomb at about 3,500 psi until the uptake of hydrogen stops (about 20-30 hours). Filter off the catalyst and wash it with a little water to remove the product that is clinging to it. Add 85 ml of concd HCl acid to the filtrate, and cool. If your reduction is incomplete, you will now have unreacted starting material separate, and this must be removed by filtration. Benzoylate the filtrate (the Schotten and Baumann method is preferable), using 210 ml of 12 N NaOH 180 ml of benzoyl chloride. Keep the solution alkaline throughout the benzoylation, and keep the temp below 40°C by cooling. When the benzoyl chloride is fully reacted, the reaction mixture is cooled and acidified with 300 ml of HCl acid. Filter the crude product by filtration, wash with water, and extract with four 1 liter portions of hot water. Separate, and crystallize the resulting syrupy product from a few volumes of methanol. Filter and wash with a little cold methanol to get a little over 100 g that melts at 151-153°. This is l-Benzoyl-3-beta-carboxyethyl-2,3-dihydroindole. This can be purchased to eliminate this step. 1-Benzoyl-5-keto-1,2,2a,3,4,5,-hexahydrobenzindole. 118 g of the above product (1-benzoyl-3-B-carboxyethyl-2,3-dihydroindole) is mixed with 200 ml of pure thionyl chloride. This solution is allowed to stand for 30 min, then it is warmed gently for 15-21 min on a steam bath. Excess thionyl chloride is completely evaporated with the temp maintained between 22-26°C in vacuo. The crude acid chloride is dissolved in dry carbon disulfate. This solution is added, in a thin stream, to a well stirred suspension of 240 g of aluminum chloride in 1750 ml of carbon disulfate in a 5,000 cc flask. Note: this must be done under a fume hood. A complex will separate and bog down the stirring device. Heat this mixture under reflux with stirring for 1 hour. Decompose this mixture by adding 500 g of ice, 250 ml of concd HCl acid, and 500 ml of water, all while good stirring is continued. Cooling of this operation is affected by periodic distillation of the carbon disulfate in vacuo. After the decomposition is complete, any remaining carbon disulfate is removed completely in vacuo, and the product is extracted with 2 liters of benzene. The extract is washed well with 500 ml of 2 N NaOH in three portions, and then with water. Dry (with the usual magnesium sulfate), and evaporate to a small volume in vacuo. Add this small volume to several portions of ether to get the ketone to crystallize (add slowly), and filter, then wash with ether to get 85 g of pure title product, mp: 146-147°C. 1-Benzoyl-4-bromo-5-keto-1,2,2a,3,4,5-hexahydrobenzindole. A solution of the above indole (305 g) in 2,200 ml of glacial acetic acid is warmed to 40°C. While the reaction is illuminated with a 250 watt bulb, 352 g of pyridine hydrobromide perbromide is added in portions, over 5 min with shaking. The solution is then heated to 60° and is held between there and 55°C for 30 min. Treat the mixture with carbon, and evaporate to a small volume in vacuo. The residue is taken up with 2,200 ml of chloroform, and wash this solution with several portions of water, dry as above, and concentrate in vacuo. Crystallize the residue from 2,200 ml of 50% acetic acid and 50% ether to get 270 g of title product that melts at 180.5-181.5°C. Another crop can be obtained from concentrating the fltrates. Yield: 30 g of less pure product. 1-Benzoyl-2,2a,3,4-tetrahydro-4-methyl-2-methyl-1,3-dioxolan-2-yl-methyl-aminobenzindol-5-(1H)one. A solution of the last indole product above (270 g) and 307 g of methylaminoacetone ethylene ketol in 4,500 ml of dry benzene is refluxed for 21 hours under a slow stream of nitrogen. The mixture is cooled and 151 g of methylaminoacetone ethylene ketol hydrobromide is filtered off. The filtrate is washed with ice water, then extracted with 2.5 liters of cold dilute HCl acid containing 150 ml of the concd acid. The acid extracts are immediately added to an excess of ice cold dilute NaOH. Extract with 1 1iter of chloroform, dry over magnesium sulfate, treat with carbon and concentrate by evaporation in vacuo. The residual ketol-ketone is crystallized from acetone to yield 220 g, mp: 135-136°C. 5-Keto-4-N-methyl-N-acetonylamino-1,2,2a,3,4,5-hexahydrobenzindole. 20 g of the above product is dissolved in a mixture of 250 ml of concd HCl acid and 250 ml of water, and the solution is kept under nitrogen for 5 days at 37°. Cool the mixture, treat with carbon, filter, and concentrate the filtrate in vacuo to a small volume. Treat the residue with an excess of sodium bicarbonate, extract with cold chloroform, and remove the chloroform by evaporation in vacuo at room temp. The crude diketone is powdered, slurried with 75 ml of benzene-ether, and filtered. Yield: 9.8 g, mp: 105-107°C. 9-keto-7-methyl-4,5,5a,6,6a,7,8,9-octahydroindolo-(4,3)isoquinoline. 25 g of the above product is mixed with 550 ml of absolute ethanol. Stir this mixture under nitrogen and cool to -15° with an external freezing mixture. Sodium methoxide is added (17 g) and the mixture is stirred for 10 min at -10 to -12°. Cool to -25°, and the product is filtered and washed (while still in the funnel) with cold ethanol and ether. Without exposure to air the crude ketone is immediately slurried with a little ice water and filtered. Wash with ice water, ethanol, then ether (all cold) to yield 16 g of product melting at 145-147°. 4-Acetyl-9-keto-7-methyl-4,5,5a,6,6a,7,8,9-octahydroindolo-4,3-quinoline. 24 g of the last product is added to 80 ml of cold acetic anhydride. The mixture is held at 25° for about 5 min, then thoroughly cooled, filtered, and the product (a solid) washed with ether to yield 20.5 g, mp: 169-170°. A second crop is obtained by concentrating the mother liquor by evaporation. A mixture of the last product (1.0 g) and 10 g of palladium carbon (5%), in 35 ml of xylene, is heated under reflux for 4 hours. The catalyst is filtered and extracted with hot methanol and chloroform. The combined extract filtrates and the initial filtrate are combined and evaporated in vacuo. The residue is recrystallized from water to give 0.6 g of a monohydrate product that melts at 255-256°. This product is called 4-acetyl-4,5,5a,6-tetrahydro-9-hydroxy-7-methylindolo-(4,3fg)-quinolinium hydroxide betaine. 4-Acetyl-9-hydroxy-7-methyl-4,5,5a,6,7,8,9,10-octahydroindolo-(4,3fg)-quinoline. 1 g of the above betaine in a mixture of 20 ml of ethanol and 5 ml of water, is treated with 0.08 g of sodium borohydride, and this solution is refluxed for 10 min and kept at 25° for 1 hour after the reflux is finished. The solvent is distilled off, and the residue is taken up in a mixture of chloroform and water. The chloroform solution is separated, dried as above, and then the solvent is distilled off. The residue is recrystallized from a nitromethane-ethyl acetate mixture to yield 0.2 g (21%), mp 193-196°. Not only is this a small scale, but it is a poor yield, requiring you to perform it several times to get enough product to perform the next step. When you have more than enough, convert the product into its hydrochloride form by dissolving in dry methanol and precipitating with dry hydrogen chloride. 4-acetyl-9-chloro-7-methyl-4,5,5a,6,6a,7,8,9-octahydroindolo-(4,3fg)-quinoline hydrochloride. 3.1 g of the above product in its hydrochloride form is dissolved in 75 ml of liquid sulfur dioxide contained in a glass lined, high pressure bomb, or autoclave. Thionyl chloride (1.2 ml) is added and the vessel is sealed and kept at 25° for 6 hours. Vent the vessel carefully and remove the mixture. Evaporate the sulfur dioxide while keeping the volume of the solution constant by the slow addition of dry ether. The amorphous chloro hydrochloride is filtered, washed with ether (dry) and dried by evaporating in vacuo to give 3.5 g of product, mp:130-135°. 4-Acetyl-9-cyano-7-methyl-4,5,5a,6,6a,7,8,9-octahydroindolo-(4,3fg)-quinoline. 40 g of dry, powdered sodium cyanide, is added to ice cold liquid hydrogen cyanide and stirred gently with ice bath cooling. Speed up the stirring, continue the cooling, and add 7.5 g of the amorphous product directly above. Continue stirring for 30 min, then the hydrogen cyanide is distilled under enough reduced pressure to keep it coming over the condenser at a temp below 10-12°. The residue is mixed with chloroform and ice water, and the resulting mixture is filtered. The organic layer of the filtrate is separated and the aqueous layer is extracted with two separate portions of chloroform. The combined extracts (this would include the separated chloroform, as usual) are dried over magnesium sulfate, decolorized, and the solvent removed by distillation in vacuo. Crystallize the product in ethyl acetate. Yield: 3.3 g, mp: 173-174°. Recrystallize again for extra purity. 9-Carbomethoxy-7-methyl-4,5,5a,6,6a,7,8,9-octahydroindolo-(4,3fg)-quinoline. 1 g of the last product is mixed with 15 ml of methanol and 0.25 ml of water. With external (ice bath) cooling add 2 ml of concd sulfuric acid slowly. Seal this solution in a high pressure bomb with a glass liner (or in a glass tube taking safety precautions in case of explosion) with a nitrogen atmosphere, and heat at 100° for 23-24 hours. Note: I have seen a big pressure cooker (like gramma cans peas with) work for some of these bomb procedures. I do not recommend it, but here is how to do it right, if you feel you must. Use only the great big heavy duty models, in excellent condition, set the pop off (relief valve) for near maximum position; never, ever tamper or modify this valve to get more pressure. Put the product in a glass beaker, put it in the cooker, flush with nitrogen, heat and stay in a different house during the reaction. Carefully turn off heat, notice or record pressure gauge after time has elapsed. Wait until pressure drops noticeably, bleed off remaining pressure and get product. Treat the mixture with decolorizing carbon and then evaporate to 10 ml. Pour onto a mixture of 30 ml of chloroform, ice, and 10 g of sodium bicarbonate. Separate the chloroform layer, and extract the aqueous phase with three 10 ml portions of chloroform. The combined chloroforms are dried, evaporated to dryness in vacuo, and the product is crystallized from benzene to give 1/2 g of product that melts at 159-160°. You may purify more by recrystallizing from ethyl acetate. This is not very much product. As with the procedure 4 steps back, you will have to perform this step over and over. If you try to double or triple the amounts given, you may get more product, but you will hurt the yield. dl-Lysergic acid. 3.9 g of the last product is mixed with 78 ml of 1.5% potassium hydroxide solution. Reflux for 30 min under nitrogen. 8.5 g of hydrogen sodium arsonate, and Raney Nickle (16 g wet), that has previously been deactivated by boiling in xylene suspension is added and the mixture is refluxed and stirred under a nitrogen atmosphere for 20 hours. The solution is treated with carbon, and the crude lysergic acid is precipitated by neutralization to pH 5.6, and then filter it off and wash with water. Yield: 1.04 g. A second crop is obtained in the usual manner (0.15 g). Purify by dissolving in dilute ammonium hydroxide, treat with decolorizing carbon, and reprecipitate with carbon dioxide to get a mp of 242-243°. Lysergic acid can be made from many ergot derivatives by hydrolysis of these compounds. These compounds include ergonovine, ergotamine, ergokryptine, ergosine, methysergide, ergine, and a few others. Total synthesis of these compounds is impractical, as lysergic acid is made before the alkaloid. You could stop the operation as soon as you reach lysergic acid, otherwise you will have to hydrolyze as described below. There are many analogs of these alkaloids that end with the ine suffix. These are not as suspicious as the former because they lead to an inactive iso-LSD. They will look like this: the ergotamine isomer = ergotaminine, the ergonovine isomer = ergonovinine, etc. These analogs are easily converted to the active forms or they may be used exactly as the non-iso versions to give the iso-LSD, which is converted very easily to LSD as also described below. https://erowid.org/archive/rhodium/chemistry/psychedelicchemistry/chapter7.html Good luck.
  3. mfk

    mfk - MDMA

    Alternative with sassafross oil - https://www.scribd.com/doc/33865652/Complete-MDMA-Synthese // Consumers prefer tablets over gel caps. You should use pharmaceutical grade ingredients. Dosage must be carefully controlled. To compete against the myriad of products on the market, the tablet must be strong and have a good appearance, therefore for example typical Amsterdam tablets are well-made with creative logos; however, there is no reason a smaller producer cannot achieve similar results, for example. You will need; Active hydrochloride (your favorite honey) screened through a fine stainless steel screen, you can find such as in the kitchen section of most department stores. then screen it into a fine powder. 1 kg will make about 10,000 tablets. Microcrystalline cellulose (MCC). This is the best binder. It compresses into a hard tablet. It is insoluble, thus acting as a disintegrant and a binder. Buy 2 kg for every 1 kg of active you plan to press. Lactose Powder. (USP grade--any other grade will be off-white, almost yellowish, which only matters for esthetics) This is a binder also known as milk sugar. It has less compressibility than MCC, but provides a sweet taste and imparts a sheen to the tablet. Buy 1 kg of lactose for every 1 kg of active you plan to press. Magnesium Stearate (NF grade). This is a lubricant. It is a fine white powder that looks and feels like corn starch. One kg will be enough for 250,000 tablets. Stearic Acid powder. (NF vegetable origin). This is another lubricant. If you cannot get stearic acid in powder, screen it, just as you screened the active. 1 kg will be enough for 125,000 tablets. MCC can be realistically obtained from the larger supply houses, the kind that supply pharmaceutical manufacturers. Lactose powder, alternative for MCC, can be bought in a pharmacy without a prescription. Mag stearate and vegetable stearic acid (aka stearin) can be found by calling around in the Yellow Pages to pharmacy supply houses and chemical companies. You can also find manufacturers and distributors on the web/deep web. In a nutshell: 25% active. 50% MCC. 22% Lactose. 1% magnesium stearate. 2% stearic acid. Your goal is to make a 400mg pill that contains 100mg of the active ingredient. Per 1000 g of active (for 10,000 pills = 100 mg active each) use the following quantities of excipients: 2000 g MCC 880 g Lactose powder 40 g Magnesium stearate 80 g Stearic acid Weigh the excipients into a large bowl with an airtight cover. Do not add the active ingredient, yet. Mix the excipients for 15 minutes. Add the active ingredient (you must screen it first) to a bowl containing the excipients and shake for 15 minutes again. Real pharmaceutical companies use a cone mixer to prepare tablet ingredients. A cone mixer works on the same principle as you shake a bowl. Buy/make your own punch and dye set. Use 20 grams of this mixture to adjust your tablet press, until you have a 400 mg pill that is hard. Adjust the fill depth until you have a 400mg tablet and adjust the top punch for hardness. Wear disposable plastic gloves during the entire process of weighing, mixing etc. Wear a dust mask over your mouth and nose (this protects you as much as it protects the quality of the tablets). Wash your hands. Once opened, store excipients in airtight containers to avoid contamination. ALWAYS wear gloves when you put the tablets into plastic bags. Good luck.
  4. for anyone interested in really developing their IC characters as a drug manufacturer, JWH is a great way to kick start off your criminal activities. // For the first time the synthesis of jwh was carried out in 1995. Later, substances of this kind were widely popularized in the mass media and on the Internet, as a result of which they became widely popular, since, being widely available and completely legal, they gave an effect comparable to that of traditional narcotic drugs. The reason this post is named JWH-”xxx” is because you can manufacture it with various chemicals (for example 1-nafindol, which is synonymous with JWH-018 and 2-chlorphenindole, are nothing more than ordinary blanks for the synthesis of JWH-018 and the synthesis of JWH-203). JWH is in the form of oil (it varies from the powder merely in the fact that the powder is more suitable for transporting and storage, but otherwise they are identical), and from 100g, 500g of oil is obtained. The proportion is 1:5. Here are the necessary related chemical substances: - DMSO (dimethyl sulfoxide) is a chemical substance with the formula - (CH3) 2SO. colorless liquid) - Sodium hydride in mineral oil. - Amil Methyl (Synonyms: 1-Bromopentane; n-Amil Methyl; 1-Bromopentane for synthesis; n-Amyl bromide) - (cannot be subject to low temperatures) Also; - Flat-bottomed flask (3-6 liters). - Reflux condenser (used to condense vapors and return condensate to the reaction mass. These are usually installed vertically. Buy a chemistry set and roleplay taking this from it). - Measuring glass (heat-resistant). In a dry flask, equipped with a reflux condenser, pour 20ml of sodium hydride, then 100ml of dry DMSO (mixed, added in small portions, 5-10g, heat the mixture, also good cooling is necessary). Stir it at room temperature for 30 minutes. Then add 77g of n-pentyl bromide (amyl bromide). Maintain the reaction mixture at 65 g. celsius for 3 hours on a hotplate with occasional mixing. Rinse the reaction mixture 3 times with water in a 5-fold volume. In order to rinse, pour 200 ml of oil into beaker and pour water. Mix thoroughly and allow the oil to settle, then drain the water. The recipe for the synthesis of JWH 018 is not complicated, follow the instructions and follow the proportions (per 1g of nafindol, 0.2 sodium hydride, 0.76 amyl) and you will get a quality product. From here on out roleplay extracting the JWH on a hot-plate with a closed spiral. The top layer is collected and the bottom layer is discarded. There is a fair choice of suitable solvents for this purpose (availability, ease of use, quality of extraction etc). Here is a brief description of the most convenient and common solvents: Ethyl alcohol (drinking, medical, etc.) - is available (in pharmacies, 96%). Non-toxic, the main prejudice is that the alcohol solvent is polar, so, it captures dirt, thus; the product is more fetid. Acetone - too easy to get. Passive RP buying nail polish with acetone from Verona Mall and you're set. It evaporates much faster than alcohol, but polar - so it pulls dirt. You should carry work out in a well-ventilated room, because sniffing this is lethal. Petroleum ether (gasoline ‘Zippo’ etc) - Differs in weak volatility, stinks like gasoline, but non-polar. Anesthetic ether (diethyl, sulfuric, medical) - dangerous. Very unstable, very fetid and explosive, but provides the best results. If you have any knowledge in organic chemistry, you will realize why using this is more cost efficient than the rest. Others - regular gasoline etc. I don’t recommend solvents such as toluene. Herbs - passive roleplay buying them from a store or order them through a courier. Here, the solvent is acetone. Then roleplay packing the herb mixture up in tea packets. You now have a kilo of spice you can easily VM. Good luck.
  5. (( lsia as a faction is dead, maybe you can even take it over as CEO ))
  6. fuck u

    1. eoozy

      eoozy

      wheres ,mine

    2. mfk
  7. mfk

    fuck u

    1. Serx

      Serx

      suck my dick

    2. mfk
  8. fuck you

    1. magnolia

      magnolia

      do i know you?

    2. mfk

      mfk

      i dont give a fuck go suck a dick

  9. fuck you

    1. Ambidextrous

      Ambidextrous

      awe the junkie reject is angry

    2. mfk

      mfk

      awe the alcopop sipper with occasional hesburger craving speaks

  10. boys jack my style like copy & paste

  11. jason bureell is a drug pin from small town in Africa where he do illegal with chandan and form a gang. then they go to us via container ship and smuggle 1300kg cocaine but got caught by los santos police department and was just jailed for 1 month. once free, jason became afiliated legal with rs haul and steal some from it. then jason came across chandan in los santos and remember the africa gang. now jason has apartment in east los santos, where he try to make methapetamine. he sometimes help chandan run cowboys gay pimp ring. to be update.
  12. never forget who switch on u

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