Pseudoephedrine AcetateJust a reprint. What do I think? Well, I would  dịch - Pseudoephedrine AcetateJust a reprint. What do I think? Well, I would  Việt làm thế nào để nói

Pseudoephedrine AcetateJust a repri

Pseudoephedrine Acetate

Just a reprint. What do I think? Well, I would like the titled material to be analogous to chloroephedrine, but this is just a salt of the amine using acetic as the acid, a result of the isolation process from pills. Much of it is in traffic in Mexico; apparently the superlabs also purchase material which at one time was in pills. The second article is about a seizure.

Meth Synthesis W/ephedrine, HI, Red Phosphorus
by Cousin Singe
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All you people who want an easy meth systhesis – They don’t exist! You have to know some chemistry. Learn some (yes it takes some discipline) or be doomed to fail.

So, again, this information is posted for information purposes only. I accept no responsibility for anyone actually using this. If you do you will be subject to state and federal laws and will be subject to fines and/or imprisonment. If you are stupid enough to actually manufacture meth you WILL probably go to prison. This is the 90's.

So to make meth from ephedrine- Using l- or pseudo ephedrine place 1000 gms of ephedrine, 250gms of red phosphorus, and 1000ml of hydriotic acid in a suitable round bottom flask. Fit the flask with a reflux condenser and reflux the mixture for 48hrs at 120 degrees C. Add a 10% solution of sodium hydroxide until the Ph is 14. You should get an oil layer and a water layer. Separate the oil layer in a separatory funnel and put it a flask with 3 volumes of water. Rig the flask for distillation and distill the oil water mixture until the oil is mostly gone (except for highly colored globs of oil.) In the reciever flask there should be two layers, an upper oil layer and a lower water layer. Separate the oil layer and mix it with 10% hydrochloric acid until the Ph is 7.6. evaporate the water and it will crystallize into methamphetamine hcl.

——

“We have observed that mixtures containing red phosphorus, iodine and either concentrated HCl or glacial acetic acid do convert ephedrine to methamphetamine; however, when the phosphorus is omitted, methamphetamine is not formed. Ephedrine was reacted with red phosphorus and iodine in refluxing water, varying the ratios of red phosphorus and iodine; when red phosphorus and iodine are in excess of ephedrine in a 1:3.8:7.2 molar ratio (ephedrine:red phosphorus:iodine) methamphetamine is formed and the ephedrine is consumed in 8 hours.”

Anyone have any thoughts, experience with the typical E-RP-HA when the usually separate step of creating the hydriotic acid is omitted and the three chemicals are just reacted in refluxing water. It seems like that is what is being described (along with acid substitution).

——

Materials:

1. 30ml bottle tincture iodine containing 2% iodine, sodium iodide 2.4%, alcohol 47%, rest H20

2. 5 Sinustop Herbal Decongestant tablets containing 60mg crystaline pseudoephedrine HCl each mixed with some herbal ingrediants. Or 300mg of ephedrine obtained thru some other method.

3. 5 road flares.

4. Bottle of drain cleaner containg conc. H2SO4

5. Bottle white distilled vinegar

6. Red devil Lye containing sodium hydroxide

7. Spray can of brake cleaner containing 1,1,1 trichloroethylene or 1,1,1 trichloroethane

Procedure:

A. Purifying pseudoephedrine:

1. Take the 5 decongestant capsules, empty their contents into a small funnel with a coffee filter. Pour 50ml of cold water through the filter, and collect the liquid in a small jar.

2. Add a 1/4tsp of lye to the collected liquid. You should immediately smell the odor of ephedrine.

3. Put the resultant solution in another small jar, and add 50ml of brake cleaner, then close the lid and shake vigorously. Let stand so that the layers seperate.

4. Using a turkey baster, suck up the bottom brake cleaner layer out of the jar and put it into a small bowl.

5. Add 50ml of vinegar and heat the resultant mixure over low heat in a frying pan with 1/2 inch of water. Thus a water bath. Do not use a gas stove, since the brake cleaner vapors will produce toxic phosgene if there is contact with a flame. Instead use a hot plate or electric stove at low heat only.

6. Heat the bowl in the water bath until no more liquid is left. At the bottom will be a solid layer of a pseudoephedrine acetate.

B. Preparing the red phosphorus:

1. Scrape the red phosphorus off of the caps of the 5 flares and store for later use. You should get about 0.1g per flare.

C. Preparing the iodine/HI solution:

1. Pour the entire bottle of the iodine tincture into a small ceramic bowl. Heat on the above type water bath until no more alcohol is left. Let cool, put in a small polyethylene jar, and add 0.1ml of the H2SO4 drain cleaner. Thats about 1/4inch of liquid in the end of an eye dropper. This converts the sodium iodide to HI. You now have a solution of iodine and HI. 2. Add the red phosphorus, and heat bottle in a water bath until the purple iodine color goes away.

D. The reaction:

1. Add the pseudoephedrine acetate to the solution of HI/I and phosphorus, and heat on a water bath for 24 hours.

E: Extraction:

1. Cool the reaction solution and add 1/2tsp of lye. Take the solution and perform steps A3-A6. 2. You will end up with methamphetamine acetate that you can scrape from the bowl.

Congradulations! You have circumvented all of law enforcement and have greatly contributed to the end of the “drug war”. (or contributed to the outlaw of all flares, iodine tincture, vignegar, drain cleaners, and auto store chemicals and coffee filters as will happen in the next year)

Best regards, Cousin Singe

————

FAQ fodder…

If methamphetamine looks waxy or oily, it is probably contaminated with the HI salt of meth, an oily by-product of the red-phosphorous/HI reduction of ephedrine–the most prevalent method of clandestine manufacture.

The HI salt is soluble in acetone, while the HCL salt is only very slightly soluble. The HI salt could be washed out, basified, and then precipitated with HCl gas to give methamphetmine HCL.

When completely dry, methamphetamine HCL is soluble in chloroform, while ephedrine HCL is not. This would provide a convenient method of separation.

[Reference: Skinner, Harry F., "Methamphetamine Synthesis Via Hydriotic Acid/Red Phosphorous Reduction Of Ephedrine," Forensic Science International, Vol 48, 1990, pp. 123-134]
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Pseudoephedrine axetatChỉ là một in lại. Những gì tôi nghĩ? Vâng, tôi muốn các tài liệu có tiêu đề là tương tự như chloroephedrine, nhưng điều này là chỉ một muối của Amin sử dụng axetic như axit, một kết quả của quá trình cô lập từ thuốc. Phần lớn của nó là lưu lượng truy cập ở Mexico; dường như các superlabs cũng mua vật liệu mà một lúc vào thuốc. Bài viết thứ hai là về thu giữ.Meth tổng hợp W/ephedrin, HI, phốt pho đỏbởi người Anh em họ SingeThông báo: Để tất cả có liên quan nhất định tập tin văn bản và tin nhắn trên thỏa thuận này trang web với hoạt động và các thiết bị mà sẽ là vi phạm các liên bang, bang và địa phương pháp luật nếu thực sự thực hiện hoặc xây dựng. Quản trị web của trang web này không biện hộ cho các vi phạm của bất cứ pháp luật. Tập tin văn bản và tin nhắn căn cứ của chúng tôi là dành cho mục đích thông tin. Chúng tôi đề nghị bạn liên hệ với cán bộ thực thi pháp luật địa phương của bạn trước khi cam kết bất kỳ dự án dựa trên bất kỳ thông tin thu được từ này hoặc bất kỳ trang web nào khác. Chúng tôi không đảm bảo rằng bất kỳ thông tin trên hệ thống này là chính xác, hoàn toàn khả thi hoặc thực tế. Chúng tôi là không chịu trách nhiệm, và cũng không làm chúng tôi chịu bất kỳ trách nhiệm pháp lý, thiệt hại do việc sử dụng bất kỳ thông tin trên trang web này.Tất cả các bạn những người muốn một systhesis dễ dàng meth-họ không tồn tại! Bạn cần phải biết một số hóa học. Tìm hiểu một số (có phải mất một số kỷ luật) hoặc được doomed đến thất bại.Vì vậy, một lần nữa, thông tin này được đăng cho mục đích thông tin. Tôi chấp nhận không chịu trách nhiệm cho bất cứ ai thực sự sử dụng này. Nếu bạn làm bạn sẽ tùy thuộc vào nhà nước và pháp luật liên bang và sẽ phải chịu tiền phạt và/hoặc bị cầm tù. Nếu bạn là stupid, đủ để thực sự sản xuất meth bạn sẽ có thể đi đến nhà tù. Đây là những năm 90.Vì vậy, để làm cho meth từ ephedrin-sử dụng l - hoặc giả ephedrin nơi 1000 g của ephedrin, 250gms của phốt pho đỏ, và 1000ml hydriotic axit trong một flask phù hợp vòng dưới. Phù hợp với flask này với một bình ngưng trào ngược và trào ngược hỗn hợp cho 48hrs tại 120 độ C. thêm một 10% giải pháp của natri hyđroxit cho đến khi độ Ph là 14. Bạn sẽ nhận được một lớp dầu và tầng chứa nước. Tách các lớp dầu trong một kênh separatory và đặt nó một flask với 3 khối lượng nước. Giàn khoan bình cho chưng cất và chưng cất dầu hỗn hợp nước cho đến khi dầu là chủ yếu là đi (ngoại trừ những đống cao màu dầu.) Trong reciever flask nên là hai lớp, một lớp dầu trên và tầng chứa nước thấp. Tách lớp dầu và trộn nó với 10% axít clohiđric cho đến khi độ Ph là 7.6. bốc hơi nước và nó sẽ tinh vào methamphetamine hcl.——“We have observed that mixtures containing red phosphorus, iodine and either concentrated HCl or glacial acetic acid do convert ephedrine to methamphetamine; however, when the phosphorus is omitted, methamphetamine is not formed. Ephedrine was reacted with red phosphorus and iodine in refluxing water, varying the ratios of red phosphorus and iodine; when red phosphorus and iodine are in excess of ephedrine in a 1:3.8:7.2 molar ratio (ephedrine:red phosphorus:iodine) methamphetamine is formed and the ephedrine is consumed in 8 hours.”Anyone have any thoughts, experience with the typical E-RP-HA when the usually separate step of creating the hydriotic acid is omitted and the three chemicals are just reacted in refluxing water. It seems like that is what is being described (along with acid substitution).——Materials:1. 30ml bottle tincture iodine containing 2% iodine, sodium iodide 2.4%, alcohol 47%, rest H202. 5 Sinustop Herbal Decongestant tablets containing 60mg crystaline pseudoephedrine HCl each mixed with some herbal ingrediants. Or 300mg of ephedrine obtained thru some other method.3. 5 road flares.4. Bottle of drain cleaner containg conc. H2SO45. Bottle white distilled vinegar6. Red devil Lye containing sodium hydroxide7. Spray can of brake cleaner containing 1,1,1 trichloroethylene or 1,1,1 trichloroethaneProcedure:A. Purifying pseudoephedrine:1. Take the 5 decongestant capsules, empty their contents into a small funnel with a coffee filter. Pour 50ml of cold water through the filter, and collect the liquid in a small jar.2. Add a 1/4tsp of lye to the collected liquid. You should immediately smell the odor of ephedrine.3. Put the resultant solution in another small jar, and add 50ml of brake cleaner, then close the lid and shake vigorously. Let stand so that the layers seperate.4. Using a turkey baster, suck up the bottom brake cleaner layer out of the jar and put it into a small bowl.5. Add 50ml of vinegar and heat the resultant mixure over low heat in a frying pan with 1/2 inch of water. Thus a water bath. Do not use a gas stove, since the brake cleaner vapors will produce toxic phosgene if there is contact with a flame. Instead use a hot plate or electric stove at low heat only.6. Heat the bowl in the water bath until no more liquid is left. At the bottom will be a solid layer of a pseudoephedrine acetate.B. Preparing the red phosphorus:1. Scrape the red phosphorus off of the caps of the 5 flares and store for later use. You should get about 0.1g per flare.C. Preparing the iodine/HI solution:1. Pour the entire bottle of the iodine tincture into a small ceramic bowl. Heat on the above type water bath until no more alcohol is left. Let cool, put in a small polyethylene jar, and add 0.1ml of the H2SO4 drain cleaner. Thats about 1/4inch of liquid in the end of an eye dropper. This converts the sodium iodide to HI. You now have a solution of iodine and HI. 2. Add the red phosphorus, and heat bottle in a water bath until the purple iodine color goes away.D. The reaction:1. Add the pseudoephedrine acetate to the solution of HI/I and phosphorus, and heat on a water bath for 24 hours.E: Extraction:1. Cool the reaction solution and add 1/2tsp of lye. Take the solution and perform steps A3-A6. 2. You will end up with methamphetamine acetate that you can scrape from the bowl.Congradulations! You have circumvented all of law enforcement and have greatly contributed to the end of the “drug war”. (or contributed to the outlaw of all flares, iodine tincture, vignegar, drain cleaners, and auto store chemicals and coffee filters as will happen in the next year)Best regards, Cousin Singe————FAQ fodder…If methamphetamine looks waxy or oily, it is probably contaminated with the HI salt of meth, an oily by-product of the red-phosphorous/HI reduction of ephedrine–the most prevalent method of clandestine manufacture.The HI salt is soluble in acetone, while the HCL salt is only very slightly soluble. The HI salt could be washed out, basified, and then precipitated with HCl gas to give methamphetmine HCL.When completely dry, methamphetamine HCL is soluble in chloroform, while ephedrine HCL is not. This would provide a convenient method of separation.[Reference: Skinner, Harry F., "Methamphetamine Synthesis Via Hydriotic Acid/Red Phosphorous Reduction Of Ephedrine," Forensic Science International, Vol 48, 1990, pp. 123-134]
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