making bomb speed

[ancient powers]

Now speed sucks when you have to deal with crap people and crap dope. But if you could cut out all the bullshit and supply yourself with pure meth. You could get alot of shit done.

I don't eat
and I don't sleep
But I have the cleanest
house on the street
METH!

[ancient powers]

Extraction Technique: Straight to E
A Novel Pill Extraction Technique
by Videoeditor, HTML by Rhodium
The following is for educational and informational purposes only. It is not the posters intent that this information be used for anything that would be considered illegal or in violation of any international laws. The poster accepts no responsibility for any and all activities that may be carried out as a result of the information contained herein. Check your local, state and federal laws. The poster shall not be held liable and indemnified from impeachment for the use, misuse, injury, death, imprisonment or fellation due to the application of this information.
- Summary -
SWIVE is back with a new twist for producing clean pseudo HCl in high yields from an ever changing array of pills. It's not only water less like Straight to B, its simpler with no A/B at all. Its Straight to E or straight to the extraction. It is a simple extraction method that will bypass most of today’s modern adulterants and will return a very high yield of clean pseudo HCl. This can then be recrystallized or turned into free base to produce a pristine product. This method was written to be easily scalable and is very over the counter. Average yields have been 80% to 90% of clean pseudo HCl.
- Definitions -
In this write up SWIVE will use the phrase "for every box of pills used" This stands for every box of 48 x 60mg, or 96 x 30mg, or 20 x 120mg or 10 x 240mg.
Text appearing in red denotes actions that should bee followed exactly for best results.
Text appearing in green denotes FAQ's (frequently asked questions).
- Materials -
• Three beakers or other heat proof glassware containers
• (approximately 200ml for every box of pills used)
• One elemeyer flask or other heat proof glassware container
• (approximately 200ml for every box of pills used)
• One graduated cylinder 100ml -200ml or other liquid measuring device in mls
• Two 5" glass funnels or plastic fuel funnels
• Filter Paper or coffee filters
• Glass stirring rod or bamboo skewers
• Hot plate
• Small fan
• Small scale weighing in grams
• Safety glasses, latex gloves
• Thermometer that is scaled to at least 120°C
- Solvents -
• 91% - 99% Isopropyl Alcohol (drug store)
• MEK Methyl Ethyl Ketone (paint / hardware store)
• VM&P Naptha - no substitutions (paint / hardware store)
• (Do Not use Colemans, pet ether, lighter fluid, etc.)
• Xylene (paint / hardware store)
- Drying Aids -
• Oven dried Epsom Salts or Washing Soda (drug / food store)
• Salt (food store)
- Abstract of Procedure -
• Make extraction fluid.
• Place whole pills into beaker.
• Add extraction fluid.
• Heat to boiling, stirring until pills dissolve.
• Filter while hot into elemeyer flask.
• Repeat two times.
• Return combined extractions to clean beaker.
• Add Xylene
• Heat to 105°C to boil off alcohol.
• Filter out pseudo HCl.
• Wash pseudo HCl with MEK and let dry.
- Standard Procedure -
01) For every box of pills used: combine the following solvents and drying materials in a clean beaker and in the following order:
• 70ml Isopropyl Alcohol
• 70ml VM&P Naptha
• 2 grams of salt
• 4 grams of dried epsom salts or dried washing soda
02) Stir with a glass rod for a few minutes, then let settle for 10 minutes. Depending on how much water was in the isopropyl alcohol to start with the mixture will settle into 2 layers or 1 layer with damp solids at the bottom.
Why not use pre dried solvents to begin with? - that is perfectly ok if you have them, but I have noticed that adding the isopropyl and naptha together almost always releases some water no matter how dry they were ahead of time so I would not skip this step.
03) Filter this into the elemeyer flask leaving any solids or bottom liquid layer behind and then transfer this solution into the second clean beaker.
04) Place whole pills in to the third clean beaker.
Why whole pills? Don’t I need to grind them up first? - no we are trying to keep loss to a minimum and grinding is not necessary as the isopropyl / naptha mixture will dissolve them very well.
05) Pour 1/3 solvent mixture over pills.
06) Place the beaker on the hotplate and bring to a boil using medium hi heat. Use the small fan to keep vapors from accumulating. Stir occasionally with a glass rod until pills have dissolved into powder. Let boil for 1-2 minutes.
07) Place a funnel with filter paper in to the elemeyer flask. Filter the solvent mixture while hot leaving as much of the solids in the beaker as possible.
08) Return any solids to the beaker and repeat steps 5 through 7 two times combining the extractions in to the elemeyer flask.
09) For every box of pills used add to the combined extractions:
- 50ml Xylene
10) Transfer the extraction mixture back to the empty solvent beaker and place the beaker on the hotplate. Bring to a boil using the small fan to keep vapors from accumulating. Boil until the solution reaches 105°C.
11) Using a clean funnel and filter paper filter off the pseudo HCl while the solution is hot.
12) Rinse the pseudo HCl with a generous amount of MEK while in the funnel.
13) Remove filter and filter cake from funnel and allow to dry completely. (no more MEK smell)
14) Weight and enjoy, yield should be between 80% to 90%

How to Perform the "Straight to E" Extraction
Commentary by Geezmeister
There is a way to do this technique. Do it Exactly The Way It Is Written.
Do this one time just like it is written.
This technique, done by the book ONE TIME will answer every question you have about it. If you don't have a thermometer go buy one. Do it just like DA MAN says.
Geezmeister went out and bought four boxes of white sixties. He obediently followed the procedure, since VE would not answer any of his silly little questions, being smartassed enough to know the procedure would answer them for him.
First time, less than two hours start to finish...well, less the absolute drying time for all the MEK to evaporate off.
Yield: 98.3% Go figure. Total of 9.6 grams of fine white pseudo HCl crystals just like the ones Geez has been harvesting from the xylene clean pseudo precipitation technique. Mind you, I haven't reacted these yet. I have not recrystalized these yet. I am as dubious as I can be because frankly, this is too good to be true, and you probably know my attitude about things that are too good to be true. Most of them are.
I poured the greenish-yellowish rinse MEK into the jar with the naptha/xylene and it looks just like the solvents look after I do xylene, naptha, MEK and acetone boils before extracting. And I already have that pseudo HCl in the filter drying. It Looks Fine.
My mind tells me that VideoEditor has done it again. He has combined the weaknesses of a couple of solvents with the strength of another, anticipated the timing and use, and combined several different concepts in ways they have not been combined before. The use of naptha as a gakk solvent during the extraction of the pseudo HCl by the IPA alcohol is a stroke of genius I would never have struck upon. The added benefit of using the naptha to drive out the remnants of moisture from the IPA is brilliant. The yield leaves me with only one thought, and that is why the hell I let him figure this out. Man, I wish I could have claimed I thought this one up.
VideoEditor deserves the Nobel Prize in foilant foiling and is hereby nominated for the position of Professor Emeritus and Department Chairman, College of Extractomania, Hive University.

[ancient powers]

Producing White Phosphorus at Home
Back a couple decades ago there was a book on magic that had a method for
producing white phosphorus "at home" - which works, I've tried it. You
use a variation on the alchemists method of reducing bone meal with
carbon compounds in an iron retort. The retort is made from a pipe
nipple, and end cap, and a bell reducer, coupled to an iron pipe to use
as a condenser. It's easy to make, but -CAUTION-, as it bears a lot of
resemblance to a pipe bomb, and my guess is that the local authorities
would never believe the difference.
Anyway, you mix bone meal with charcoal and syrupy evaporated urine, then
wet the stuff with sulfuric acid and roll it into little balls. You put
the balls into the retort, build a roaring fire around it - it needs to
get to bright orange heat - and condense the white phosphorus in a bucket
of water. You have to be careful to 1) not get poisoned, WP is extremely
dangerous, 2) not suck back water and cause a steam explosion, 3) not
plug up the condenser and make a real pipe bomb out of the thing, and
finally, 4) not immolate yourself in the fire.
Once you have white phosphorus, you can make red phosphorus by adding
just a -trace- of iodine to the water under which the white phosphorus
must be kept, and putting the jar out in the sunlight. Of course, it
will take a long time to convert.

[ancient powers]

there are many ways to obtain Iodine crystals.
it will depend of the purity you will need and if you
want to prepare the Iodine first and then proceed to
crystalize it. The Iodine is a substance that sublimes easily,that means
that once the crystals are formed
they will pass even at room temperature to gaseous
state quickly and directly without going into a liquid
state instead.So in order to keep your crystals you
will need an extra special care.
Ok, lets see an easy experiment supposing you want
to prepare the Iodine first:
You will need:
Bunsen burner and asbestos square (or a hot plate)
Tripod and tin lid
Beaker, 250 ml
Separating funnel 100ml
Evaporating dish
Hydrogen peroxide 20 volume
Tetrachloromethane or dichloromethane
Distilled water
1M solution of Sulphuric acid
Supply of ribbon seaweed(Laminaria) - that you can
obtain a a biological supply store or from the
sea shore
Procedure
(You must work at a fume cupboard)
1-Collect and dry about a dozen 50cm lenghts of the
seaweed and heat them strongly on a tin recipient
until they are reduced to ash; probably it will
reduce a quite small quantity, about a spoonful.
2- Add to the ash 20 ml of distilled water
in a beaker, and heat the suspension until it boils.
3 - Filter the suspension
4 - Acidify the filtered with Sulphuric acid solution
5 - Add then the hydrogen peroxide solution
You will observe the formation of a brown color due
the iodine liberation from the iodine ions present
6- Transfer the mixture to a separating funnel
7 -Extract the Iodine with tetrachloro methane or other
solvent. The result is an organic solution of iodine.
8 - In order to obtain crystals , the solvent may be
allowed to evaporate at room temperature, by
placing it in an evaporating dish in a fume cupboard.
It will result crystals of iodine or rather gray-
black brilliant flakes.

[ancient powers]

How To Manufacture Meth -- True Iodine Recipe
by MethodMan
________________________________________
NOTICE: TO ALL CONCERNED Certain text files and messages contained on this site deal with activities and devices which would be in violation of various Federal, State, and local laws if actually carried out or constructed. The webmasters of this site do not advocate the breaking of any law. Our text files and message bases are for informational purposes only. We recommend that you contact your local law enforcement officials before undertaking any project based upon any information obtained from this or any other web site. We do not guarantee that any of the information contained on this system is correct, workable, or factual. We are not responsible for, nor do we assume any liability for, damages resulting from the use of any information on this site.
________________________________________
No lies here folks this recipe will manufacture methamphetamine this will get you into trouble if you do this BE CAREFUL!
First of all let's talk about supplies:
• 1 Case Regular Pint size Mason Jars ( Used for canning)
• 2 Boxes Contact 12 hour time released tablets.
• 3 Bottles of Heet.
• 4 feet of surgical tubing.
• 1 Bottle of Rubbing Alchohol.
• 1 Gallon Muriatic Acid ( Used for cleaning concrete)
• 1 Gallon of Coleman's Fuel
• 1 Gallon of Aceton
• 1 Pack of Coffee Filters
• 1 Electric Skillet ( If you don't know what iam talking about i will have pics later)
• 4 Bottles Iodine Tincture 2% (don't get the declorized it won't work)
• 2 Bottles of Hydrogen peroxide
• 3 20 0z Coke Bottles (Plastic type)(with Lids/caps)
• 1 Can Red Devils Lye
• 1 Pair of sharp scissors
• 4 Boxes Book Matches (try to get the ones with brown/red striker pads)
• 1 pyrodex baking dish
• 1 Box execto razor blades single sided
• 1 digital scale that reads grams
• 2 gallons distilled water \
• 1 Roll Aluminum foil tape
That's what you would have to go buy if you wanted to make meth.
First things first -- the Iodine Crystals. Take one 20 oz, plastic Coke Bottle and pour 4 Bottles 2% tincture into it.
Add Hydrogen Peroxide to this. Use only 1/2 a bottle of Hydrogen peroxide. After this you know, the gallon jug that the Muriatic acid comes in take the cap off and fill this cap level with the acid. Add the acid to the coke bottle (Place in a freezer for at least 30 mins).
While the Iodine crystals are being made we are going to extract the Phsuedo from the Contacts. You are going to need a towel for this so go get one. Take the pills out of one box, add it to one of the mason jars fill with rubbing alchohol just enough to cover the pills let set for 3 minutes. Remove pills and take the towel and wipe the top coating off the pills this will remove the wax. Do the same with the other box of Contacts as well, after this add those wiped off pills only 10 to a clean mason jar. On top of this add 1 bottle of Heat do the same for the other box of Contact. Let theese two mason jars with pills, heat stand for 30 minutes. Then shake the jars till pills are completly broke down then let the jars sit again for 4 hours or until the Heats is completly clear . Once clear cyphon the heat off (Not the powder stuff at the Bottom you don't want this it will fuck your dope up).
Well anyway syphon the heat off with a piece of the sergical tubing syphon this into a pyrodex baking dish place in microwave on high till the heat is almost evaporated. Take out of microwave. Now plug up your electric plate set the pyrodex dish on this on about 180 deg continue evaporating till you get a white powder on the pyrodex (Carefull not the burn the phsudo if it turns yellow it's burned) after you get it dried take a razor blade and scrape this powder up. (put this asside for later use)
Now we are going to get the red phosphorus from the book matches take a pair of scissors and cut along the edge of the phosphorus do the whole four boxes of match book matches then take 1 small coffee cup will work to this coffee cup add about 1/4 the way with Acetone dip the match book strike pads into the acetone for 10 seconds this will loosen the phosphorus so it will be easier to scrape with the razor blades. ( put the phosphorus in an empty match book box to let dry. Now it's time to get the iodine crystals get a clean mason jar on top of this place 1 coffee filter and pour the contents of the iodine +muriatic+Hydrogen Peroxide into the filter ( do it slowly don't over pour) well once you get though with the filtering on top of the coffee filter will be a black substance ( This is iodine crystals) dry them by wraping in more coffee filters till you get a pretty good thick pile around the original filter place on ground and step on it to get the rest of the liquids off save this for the cook.
next take your digital scales wiegh your pills first say you had 2 grams of pill powder then weigh out an equal amount of iodine crystals then for the phosphorus devide the total weight of pills by 3 3 will go into 2 1 time so if you had 2 grams pill powder you should have 2 grams iodine crystal 1 gram phosphorus Now its time to make the cook jars you will need 2 clean mason jars with lids 1 foot surgical tubing poke a hole in both jar lids place one end of the tubing into each jar lid and seal with foil tape (buy this at walmart for about $ 1.60 well anyway seal off the tubes as well as you can so you should have 2 mason jars with lids that have surgical tubing foiled taped and sealed. ok this is the cook in one mason jar add distilled water in it fill it half way close the lid on it. now get you hotplate hot first at 180 degreese F when the plate get hot then its time to add the Iodine+pill powder to the other mason jar not the one with water in it once you get both Iodine and pill powder to the jar add 6-10 drops of distilled water to this place it on the hotplate now add the phosphorus once you put this in the jar there is going to be a imediatereaction place the other lid with hose onto the jar screw on tightly then turn your hotplate up to 400 degrees f let this cook for 1 hour to an hour and a half the best way to tell when it is done is when the contents of the cook jar doesn't boil anymore once this has happened turn the hotplate off and let the jar cool so you can touch it now its time to see if we have dope once it has cooled open the lid and you should smell rotten egg like smell if it has this smell congrads you have dope now we have to remove the dope from the black goey substance to this jar add about 1/4 cup of distilled water and seal the jar with a lid that has no holes in it and shake the jar till all the substance on the botom of the jar has come off into the water
next take another clean mason jar and place a coffee filter and filter the cook jars contents though the filter now on the filter is your phosphorus save this for another cook later on just putt it in a dry coffee filter and put it somewhere dry and safe now you have a jar filled with a yellow honey looking substance if its this color you have done good at cooking the dope now to this add colemans fuel fill the jar about full just leave anough room for shaking now add 1-2 table spoons red devil lye let the jar sit for about 5 mins then place lid on the jar and shake the hell out of it then sit the jar somewhere to rest for about 30 mins Now we are going to pull the dope out of the coleman fuel and the product is going to be 90% methamphetamine to do this fallow what i say exactly syphon the coleman fuel into an empty 20 oz coke bottle syphon off much as you can trying not to get the substance off the bottom of the jar once you have the coleman fuel in the coke bottle add about 4-6 coke bottle caps of water to this now add one drop of muriatic acid to the coke bottle place lid on bottle and shake the hell out of it place upside down so it want fall and get your hotplate hot 400 degrees f on top of the hotplate place a clean pyrodex bowl on it now take the coke bottle still upside down and loosen up on the cap let the water drain into the pan don't get any coleman fuel into the pyrodex bowl now the water will evaporate while it is doing this take a coffee cup add acetone to it fill it 1/4 the way up now once the water has dried on the plate take plate off with gloves and add a small amount of acetone to the pyrodex bowl it will sizzle swirl it arouund and if all works out good ther will be circle crystals all over the pyrodex bowl scrape up with a razor and enjoy Methamphetamine :-) This with 2 boxes of Contacts will make anywhere from 2-3 grams meth....

[StonerBill]

meth aint bad bro

so many things are required in chemistry!!!

[digital 3.0]

Lets talk about the Iodine, first off. Now in the instructions printed there are 2 variations of iodine preperation, the one included with the full overview of the reaction says that after filtering not to wash the crystals. But ive read from several sources that not washing the chlorines from the iodine with the muriatic is bad, but I also hear that that acid ensures a good reaction to form hydriodic acid with the red.


Any thoughts on this? Wouldn't want anyone blowing themself up now would we?

[LSDMIKE]

Lets talk about the Iodine, first off. Now in the instructions printed there are 2 variations of iodine preperation, the one included with the full overview of the reaction says that after filtering not to wash the crystals. But ive read from several sources that not washing the chlorines from the iodine with the muriatic is bad, but I also hear that that acid ensures a good reaction to form hydriodic acid with the red.


Any thoughts on this? Wouldn't want anyone blowing themself up now
would we?

nevermind I missundaztood :o

[ancient powers]

THIS PROCEDURE WILL SHOW YOU HOW TO EXTRACT IODINE CRYSTALS FROM DRUGSTORE IODINE TINCTURE.


WARNINGS: THIS PROCEDURE CAN PRODUCE TOXIC FUMES. ALWAYS PERFORM THIS OUTSIDE. STRONG ACIDS ARE INVOLVED THAT CAN CAUSE BURNS OR OTHER INJURIES. ALWAYS WEAR SAFETY GOGGLES. LAST BUT NOT LEAST, IODINE STAINS LIKE NOTHING ELSE. I DROPPED SOME CRYSTALS ON MY CARPET AND 4 YEARS LATER THE STAINS KEEP COMING BACK. DO NOT MESS UP.
DESCRIPTION
IODINE TINCTURE IS AN ALCOHOL BASED SOLUTION OF IODINE SALTS. IT IS COMMONLY SOLD IN DRUGSTORES AS A OLD TOPICAL ANTISEPTIC. AT TIMES, IT IS USEFUL TO HAVE CRYSTALLIZED IODINE, OR I2. I2 CAN BE FOUND IN NUMEROUS PRODUCTS, HOWEVER EXTRACTION IS USUALLY DIFFICULT OR EXPENSIVE. PURE I2 CAN BE USED TO DISINFECT SUSPICIOUS DRINKING WATER. IT ALSO HAS USES IN EXPLOSIVES.
THIS SIMPLE PROCEDURE WILL CONVERT THE SALTS IN TINCTURE TO I2 WHICH WILL FALL OUT OF SOLUTION AS FINE PURPLE CRYSTALS.


MATERIALS
-30% HYDROCHLORIC ACID - "MURIATIC ACID" IN HARDWARE STORES
-BLEACH
-TINCTURE OF IODINE
-COFFEE FILTERS
EQUIPMENT
-MISC. GLASSWARE
PROCEDURE
WHY?

1. FIND SOME TINCTURE OF IODINE. IT COMES IN SMALL BOTTLES AND IS SOMEWHAT EXPENSIVE. YOU MAY HAVE TO SEARCH HARD BECAUSE ITS SOMEWHAT OBSOLETE NOW. DO NOT USE POVIDONE IODINE.
POVIDONE IODINE HAS A CHEMICAL ADDED TO PREVENT STINGING WHEN USED AS AN ANTISEPTIC. FOR WHATEVER REASON, POVIDONE IODINE IS CHEAPER AND AVAILABLE IN LARGER QUANTITIES, BUT I'M TOLD IT WILL NOT WORK.
2. POUR A FEW BOTTLES INTO A FLASK. USE MORE THAN ONE BOTTLE AT A TIME. THE REASON IS THAT YOU'LL LOSE A FRACTION OF THE IODINE IN VARIOUS WAYS, AND IF YOU USE A SINGLE BOTTLE THERE WILL BE TOO LITTLE IODINE LEFT TO RETRIEVE SUCCESSFULLY.
3. ADD AN EQUAL VOLUME OF WATER TO THE IODINE. THEN ADD ABOUT ~5ML OF HYDROCHLORIC ACID PER BOTTLE OF IODINE. STIR. THEN ADD ~10ML OF BLEACH PER BOTTLE OF IODINE. STIR. BEWARE FUMES. YOU SHOULD SEE THIS: THE ACID HELPS CONVERT THE IODINE SALTS (KI, NaI) TO THE DESIRED FORM. NOTE, EXCESS REAGENTS IS USUALLY NOT A PROBLEM.
4. PREPARE TO FILTER BY PUTTING TWO COFFEE FILTERS OVER THE MOUTH OF A BEAKER. BE SURE TO USE TWO OR MORE FILTERS. THE ACIDS WILL ATTACK THE PAPER, AND ALONG WITH MOISTURE, CAN BREAK THE FILTER.
5. DILUTE AND FILTER THE SOLUTION. YOU NOW HAVE I2.
TIPS
DON'T TRY TO STORE I2 IN A PLASTIC BAG, AS THE CRYSTALS SLOWLY TURN TO GAS AND WILL LEAK THROUGH THE PLASTIC.
DON'T LET THE CRYSTALS SIT OUT TOO LONG; THEY SUBLIMATE RAPIDLY AND YOU'LL LOSE MUCH OF THEM.
DON'T DROP ANY ON YOUR CARPET BECAUSE THE STAINS WILL COME BACK FOR YEARS NO MATTER HOW GOOD YOU CLEAN THEM AND YOUR MOM WILL KILL YOU.

[ancient powers]

woops I missed one of the recipes for the thread

[digital 3.0]

How about the red phosphorous from match book strikers?

I know the plates contain red, but removing the glue from the red so that it won't be coated and can actually react how in the hell do you get the glue off that?

Even scraping or even soaking plates in Acetone wouldn't remove the glue fully. Thoughts?

[digital 3.0]

Im pretty sure this whole procedure yields a whole lot of bullshit junk...its not sophisticated and will just catch felonies. Not the crystal you're looking for.

[ancient powers]

THE MATCHBOOK RED PHOSPHORUS BIBLE
________________________________________
Materials:
• 5 Gallon Bucket
• Drill (1/2" chuck)
• Mud/Paint/Concrete Mixer
• Coffee Filters
• Strainer (big enough to fit over pot and bucket opening)
• 2 gallon Cooking Pot
• Tin Snips or Scissors
• 200 Matchbook Boxes
• 2 Gallons Acetone
• Sulfuric Acid
• Hydrochloric Acid
• Water
• Iodine
Extracting Red Phosphorus from Matchbooks:
1. Rip off matchbook covers. Line up as many matchbook covers as you can cut through with tin snips or good, sharp scissors. Cut out and save all the striking strips.
2. Drill 3/4" hole in the lid of the 5 gallon bucket. Put the mud mixer through 3/4" hole in lid and into the drill.
3. Dump the 200 matchbook boxes worth of striking strips (10,000 striking strips) into the 5 gallon bucket. Pour 1.5 gallons of acetone into the bucket. Cover bucket by inserting mud mixer then snapping on the lid.
4. Mix Contents for about 5 minutes. Check to see if strips are mostly white on account of the phosphorous/glue being washed off. If not then continue mixing.
5. Take off the lid and pull out mixer. Put the strainer on the cooking pot and pour all the acetone in. Pull out all strips from strainer and bucket and place on clean table or in a bowl. The strips will be covered in residual red phosphorus, so rinse them by placing the strainer on bucket and throwing a handful of strips in it. Then slowly pour some of the acetone in the cooking pot, through the strainer until strips are clean. Empty strainer into garbage. Continue until all strips are rinsed.
6. Pour all the acetone/RP into the cooking pot. Let the RP settle for about 15 minutes. Slowly pour off the acetone. Keep pouring as long as the acetone is pretty clear. The last bit of acetone will be reddish colored. Filter this through a coffee filter in the strainer. Scrape the mushy RP back into the pot or dry the filters, roll and ball them up well, then unfold. All the RP will fall right out in a dust.
Cleaning Matchbook Red Phosphorus:
Sulfuric/hydrochloric acid wash: (This can be done as 2 different washes) With mushy RP in cooking pot, pour enough 1:1 water/sulfuric to cover the glob. (It's optional now to add heat or not. If so then add no more than enough for a light boil) Mix contents for 5 to 10 minutes. Add an equal amount of hydrochloric acid and continue mixing for 5 to 10 minutes. If heat was applied take off now. Add an equal amount of cold water. Filter through a coffee filter in the strainer. Scrape the chunky RP off the filters back into the cooking pot. (This will eat up a lot of small paper fibers, hair, cotton, lint or whatever.)
Acetone wash: Add enough acetone to cover the globs and chunks of RP. (Again you can add heat if you like. Bring it to a controlled boil.) Mix for 5 to 10 minutes. Let cool or add a little cold water. Filter RP same way and return it to pot. (This will remove any glues or other acetone solvent junk.)
Water wash: Add enough distilled water to cover the RP globs. Bring this to a boil for 5 to 10 minutes. Filter out the RP and leave in filters to dry out. When dry roll and ball up filters then brush out dust. Collect dust in a baggie and store. (This is a general cleaning to remove any chemical residue.)
Other washes: Any of the following solvents have been safely used to wash RP... Methanol, Ethanol, Denatured alcohol, Isopropanol, Toluene, Xylene. These would be done the same as written above.
Screening: Put the RP in a stainless steel screen or plastic/steel mesh style coffee filter and run acetone through it. The RP is washed through the screen with the acetone, and any particles larger than the screen apertures are filtered out.
Washing order:The order does not matter as long as the RP is finished off with an acetone wash then a distilled water wash.
Prefiring Red Phosphorus
React RP/I2:Weigh out your RP and put it into a bottle. Add half as much I2 to it and shake it up. Add (dropwise) H2O2 when not reacting. Continue shaking and adding drops of H2O2 until it's done reacting.
Filter out RP: After prefiring add water and shake. If it won't loosen up then put the bottle in boiling water for 5 minutes. Filter the water/RP/I mix. Wash the RP with acetone then water. Dry it out, baggie and save for a rainy day.
Note: Make sure drill has a 1/2" chuck.
This was compiled from many sources and through trial and error was refined to what you see. It was written to be printed up and used as a reference for anyone like swim that hasn't been able to get lab grade RP. Swim's current run was scaled down using a 2 gallon bucket with 114 boxes! It took over 3/4 gallon of acetone to extract the RP. Clean up will be H2SO4/HCl, acetone, H2O, prefire, acetone, H2O, done!
Swim is expecting to yield about 250mg per box. They're hoping to end up with an even ounce.
________________________________________

[ancient powers]

Now that I think about it. Since I've been off dope now for a few years. I dont know If I could go back. I just wanted the best recipes that I have found online gathered to one place. So If something ever happens to me. The world has got the goods. Meth is good when your fat and or lazy. Or even crazy. I have been transformed by the sheer terror that meth brings. I will never be the same in a good way. There are some people out there who can benefit from this drug as well if used properly. Ya right!

[pedaltopedal]

There are some people out there who can benefit from this drug as well if used properly. Ya right!

It's a very thin line that one is walking when trying to use this drug responsibly. I have yet to meet anyone (in person) who can honestly say that they've succeeded in doing so. I wasn't able to.

[notparanoid]

Some little birdie told me that "shocking" the rp with lye in it's last cleaning stage that would make it react better and would bring back more goodies.:mad:

I believe that it just may be a pH shift from the alkalinity of the lye but different people say different things.:confused:

Also, how are you titrating the stuff properly on the boil method mentioned here without having a pH meter <question>

Where i'm from the method of I2 generation using tincture, h202, and a cap of muriatic is the way preferred. Does the i2 generation mentioned in this thread -- using sodium hypochlorate
(NaClO) leave much Chlorine salts, does cleaning normally get all out, and does that effect processes <question>:toetap05:

[notparanoid]

Also mentioned here is a formulary involving 1:2:2 ratio where a:b:c == RP:Base:I2 and I've always been told that a 1:2:2.5 or even a 1:2:3 produces higher yields

I'm not claiming to be any guru or anything. I just have my curiosities. I have been out of the circle for a little while. Just needed a little bit of time to regroup, if you will...

[notparanoid]

Referring to Ancient Powers last post in this thread: 250mg per box seems a little low per box; when you refer to box you are referring to like 48 60's , 96 30's, or 20 120's right

[digital 3.0]

Okay so you clean the red, the white, and the I. You have all your stuff ready to go...how about a homemade consenser? I hear not losing pressure makes it go a lot faster, like ductaping a ballon on the top acts to keep pressure in. And what to look for during the reaction? This post is the shit its what you said, gathering everything into one place.

[aushy]

The method i've read which looked most credible requires you to reflux the (pseudo)ephedrine, iodine, red phosporus for 12 hours. I'll see if I can digg up the instructions

[ancient powers]

Yeah I didnt write any of those recipes. They were the best ones I found for stuff. If I ever get around to workin with the stuff. Shit isnt free. But the recipes seem the closest thing to the truth. If I were to have a lab and supples I could write some better instructions. But you guys are more than welcome to make the neccesary corrections needed to produce the truth about cookin meth in your kitchen.

[ancient powers]

Yeah I didnt write any of those recipes. They were the best ones I found for stuff. If I ever get around to workin with the stuff. Shit isnt free. But the recipes seem the closest thing to the truth. If I were to have a lab and supples I could write some better instructions. But you guys are more than welcome to make the neccesary corrections needed to produce the truth about cookin meth in your kitchen.

[LSDMIKE]

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