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Candy Flipping (LSD & MDMA)

Hippy Flipping (Shrooms & MDMA)

Love Flipping (Mescaline & MDMA)

Kitty Flipping (Ketamine & MDMA)

Elephant Flipping (PCP & MDMA)

Robo Flipping (DXM & MDMA)

Nexus Flipping (2-CB & MDMA)

Adam & Eve in the garden of Eden (MDMA, MDEA, & MBDB)

Candy Flipping...

The combination of LSD and ecstacy. The correct way to do this is

to take the LSD 3 hours before the e so that you start peaking on the

LSD at the same time you start rolling on the ecstacy. Some people feel

that the ecstacy takes away all the negative aspects of LSD and makes

all the visuals more beautiful. There is also a uniquw synergistic effect

that occours as well. The LSD takes the body feeling of the ecstacy and

gives it a roller coaster effect. It can be described as peaking various times

on the ecstacy and every next peak becomes more intense than the last one.

Hippy Flipping...

The combination of Magic Mushrooms and ecstacy. The correct way to do this

is to take the ecstacy and on the 4th hour of the ecstacy you eat the mushrooms.

The mushrooms bring the e back on in full force. The body tingle turns into a deep

buzzing and it can be a very liquifying experience. Also, the ecstacy gives one the

ability to dance more than one would have if one had just taken the mushrooms.

Love Flipping...

The combination of Mescaline and ecstacy. Very similar to Candy Flipping yet you take

the Mescaline at the same time as the e. They both enhance each other. The Mescaline

and e both are very empathic substances. The empathy is doubled imensley to the

point where one can feel another person's emotions who is accross the room.

Kitty Flipping...

The combination of Ketamine and ecstacy. The e is taken 10 minutes before the K.

While one is in the K hole one can communicate with another person who is Kitty Flipping

through physical contact. Although, communication passed between each other only

consists of single words, the single words seem to represent an entire sentance.

The e gives the K more insight into ones self as well and the K hole is generally

brighter and more positive.

Elephant Flipping...

The combination of PCP and ecstacy. Taken at the same time. The body high is

incredibly intense in the sense that the PCP gives one the feeling that one is floating

and almost weightless. The PCP numbs the body so that one only feels the E. A

description would be of one soaking in a pool of ecstacy.

Robo Flipping...

The combination of DXM & ecstacy. The e is taken 20 minutes before the DXM.

The feeling is similar to that of Elephant Flipping & Kitty Flipping. One feels the

sensation that one is floating and movement of the body causes euphoria. The body high

is an incredibly buzzing and one feels as though the e is worming underneath the skin

and trying to push out from inside. Although it sounds scary it is very intense and

plesant.

Nexus Flipping...

The combination of 2-CB and ecstacy. The e is taken first and the 2-CB is taken

towards the end of the e trip. The 2-CB brings out the erotic feeling that the

e masks and it changes the mental state to a more intellectual leval.

Adam & Eve in the garden of Eden...

The combination of MDMA, MDEA, & MBDB. All taken simultaneously. Said to be

the most complete ecstacy experience. Thoughts flow like water. The experience is

directed outward as well as inward. Empathy is felt for every person one comes in

contact with.

Just like all our novel research chemicals, when you buy 4-MeO-PCP from us you can guarantee that you are getting the finest quality 4-MeO-PCP synth sourced directly from our Asian lab. We know that our prices are extremely competitive but realise that there may be cheaper websites selling 4-MeO-PCP which has been cut down or even worse mixed with unidentified substances. This can be particularly hazardous to unscrupulous chemists who will at best suffer from inaccurate testing conditions and at worst could be putting their health & safety at risk. We are happy to answer any questions you may have about our chemicals and always aim to respond to emails with 3 hours (during business hours 9.00 - 5.30). Please note any questions which pertain to illegal usage of our materials will be deleted without answer. - See more at: http://www.plantfoodpalace.com/4-meo-pcp.html#sthash.g7wppCAc.dpuf

4-MeO-PCP (1 - [1 - (4-methoxyphenyl) cyclohexyl]-piperidin) ist ein Piperidin-Verbindung auf engem Zusammenhang mit der Verbindung 3-MeO-PCP verwandt. Methoxydine wie es häufiger wird in der Forschung Chemische Industrie bezeichnet wird angenommen, dass ein guter Ersatz im Labor für die kürzlich verboten Methoxetamine sein. Dieses aufregende neue Arylcyclohexylamin vergleichbar mit Ketamin hat aber etwas andere Auswirkungen aufgrund seiner veränderten Bindungseigenschaften Profil an verschiedenen Ziele, insbesondere als signifikant wirksamer als NMDA-Antagonist, während mit um die gleiche Potenz als Dopamin-Wiederaufnahme inhibitor.As mit all unseren Chemikalien 4 -MeO-PCP ist ausschließlich als Referenzprobe zur Verwendung in Laboratorien und ist nicht für jeden in-vivo Forschung erlaubt. - Sehen Sie mehr an: http://www.plantfoodpalace.com/4-meo-pcp.html # sthash.g7wppCAc.dpuf

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Hipersalivasyon veya Pityalismus salya üretimin artması anlamında kullanılan Latince kökenli bir terimdir. Ağız boşluğundaki tükürük ve salgı bezlerinin, herhangi bir nedenle aşırı salgı yapması halini anlatır. Bu durumda salgıların ağız dışına taştığı görülebilir. Sürekli olarak ağız dışına çıkan salgılar bir süre sonra ilgili bölgede tahrişe neden olur.

ReactionScheme II. Synthesis of PCP via enamines:

This method is used less frequently in underground synthesis, but has the advantage of not involving toxic cyanide compounds. The first step of the reaction is the dehydration of piperidine and cyclohexanone to form an enamine. The addition of anhydrous p-toluenesulfonic acid or dry HBr produces an intermediate imminium salt. Reaction of this salt with phenylmagnesium bromide yields PCP. This method is most applicable to cyclic secondary amine analogs such as piperidine, pyrrolidine, or morpholine, rather than an acyclic N-substituent such as ethyl or dimethyl (ref. 8, 12 ).

This route has an overall yield of ~70%, with a difficulty rating of 3 out of 10, and a hazard rating of 2 out of 10 (ref. 64).

Procedure:

Step 1. Preparation of cyclohexenyl piperidine: A solution of 98 g (1.0 mole) of cyclohexanone, 100 g (1.17 mole) of piperidine, and 2 g (0.0105 mole) of p-toluenesulfonic acid in 300 ml of toluene is refluxed under azeotropic distillation conditions until the evolution of water stops (about 13 hours). The best method for this is to use a Dean Stark or Barrett water trap, but if one is not available, it may be improvised with a distillation head as described in Vogel's Textbook of Practical Organic Chemistry.

Either p-toluenesulfonic acid or dry HBr gas can be used in the next step. The intermediate cyclohexenyl-piperidine (enamine) from the previous step is best used crude, but it can be distilled with adequate vacuum.

Step 2, method A. Use of p-toluenesulfonic acid: 190 g of p-toluenesulfonic acid monohydrate in 250 ml of toluene is heated under a Dean Stark trap until all the water is removed. This is then added to 165 g of cyclohexenyl-piperidine in 500 ml of ether with ice cooling to keep temp at 0 deg C. A solution of 1 mole of phenylmagnesium bromide is prepared as in Scheme I from 157 g of bromobenzene and 24 g of Mg turnings in 750 ml of ether. This is added to the cyclohexenyl piperidine while holding the temp at 0 to 5 deg C. The mixture is stirred for an additional 30 min after the dropwise addition is complete.

A mixture of saturated aqueous ammonium chloride and ammonium hydroxide is added to neutralize the excess phenylmagnesium bromide (approx. 100 gm of NH4Cl and 20 ml of strong NH40H in enough water to make a saturated solution). The ether layer is then removed in a separatory funnel, dried by the addition of potassium carbonate, filtered, and evaporated to give PCP. This can be converted to the hydrochloride salt by dissolving it in an excess of isopropanol saturated with HCl gas and precipitating with ether, followed by crystallization from a mixture of ether and isopropanol.

Step 2, method B. Use of HBr gas: The reaction mixture from step one is diluted to 2 L with dry toluene and dry HBr gas was bubbled through until the solution is acidic. The resulting slurry is added at once to a cold (5 deg. C) stirrred solution of phenylmagnesium bromide prepared from 236 g (1.51 moles) of bromobenzene and 38 g of Mg (1.56 moles) in 1 L of dry ether. The temperature will rise to 45 C and the mixture should be stirred for an additional 30 minutes.

300 ml of 48% aqueous HBr is then added, producing the HBr salt of PCP, which is filtered from the reaction mixture. The crude HBr salt is then basified with NaOH, extracted with hexanes, toluene, etc., and either evaporated to yield PCP freebase or treated with isopopanol saturated with HCL, followed by dilution with ether to give PCP hydrochloride.

The combination of PCP and ecstacy. Taken at the same time. The body high is incredibly intense in the sense that the PCP gives one the feeling that one is floating and almost weightless. The PCP numbs the body so that one only feels the E. A description would be of one soaking in a pool of ecstacy.

THE TRIED AND TRUE HOME PRODUCTION METHOD FOR "METHAMPHETAMINE" By: The Leftist Also known as:"CRYSTAL","METH","CRANK","SPEED" etc..........List of chemicals and materials:Dilute Hydrochloric acid--> This may be purchased at the hardware store.Its sold as a brick and driveway cleaner. They call it muriatic acid.Sodium Hydroxide--> This, you probably already have. Its called "lye" at mostplaces, its drain cleaner.Ethyl Ether--> You'll probably have to make this. Don't worry, its a breeze.Just go to your local K-mart or Auto parts store, and get a can of that"STARTING FLUID" it comes in a spray can. Its used for cold weather startingof gasoline engines."VICKS" Nasal Inhalers--> USE ONLY VICKS!! No other kind will work that Iknow of. These are at any drug store or grocery, etc. You need 12 of 'em, butdon't buy 'em by the dozen. Unless its wintertime, then you can just sayyou're from some nursing home, and your stockin' up for the patients. Otherwisebuy 'em 2 at a time,if possible. Get a friend to help you. The druggists at thedrug store usually will know whats goin on if you buy quantity.+++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++ LIST OF EQUIPMENTTwo large eyedroppersTen small glass bottlesOne large glass or porcelin bowlCoffee filtersOne small jar with a topOne pyrex baking dishOne glass test tube------------------------------------------------------------------------------- -==*(> N O T I C E <)*==- PLEASE! DONT SMOKE IN THE SAME ROOM WHEN YOU DO THIS. OPEN A WINDOW IN THE ROOMIF POSSIBLE FOLLOW THESE INSTRUCTIONS EXACTLY. THIS RECIPE HAS BEEN TESTED ANDTHIS IS THE BEST WAY TO DO IT. DON'T TAKE SHORTCUTS, AND DON'T EVEN START TO DOTHIS UNLESS YOU HAVE ABOUT 3 HOURS SPARE.-------------------------------------------------------------------------------%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% PREPARING ETHER!(DO THIS FIRST)Take one of the small bottles,and spray starter fluid in it till it lookshalf-full. then fill the rest of the way with water, cap the bottle and shakefor 5 minutes. Then, draw off the top layer with the eyedropper, and throw awaythe water layer. repeat this until you have about 3 oz. of ether. put the capon it, and put it in the refrigerator if you can.(if you cant, dont worry aboutit) youll use this in the procedure below. %%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%% THE TRIED AND TRUE HOME PRODUCTION METHOD(1) Break open the inhalers, a pair of real sharp scissors does this good.Place the cottens that were inside in a jar and close the lid.(remember you useall 12 cottens.)(2) In the bowl, combine 1- 1/3 oz. water and 2/3 oz. muriatic acid.Shredcottens in this solution, and knead for 5 minutes with hands.(ALWAYS BE SURETHERES CLEAN RUBBER GLOVES on your hands.) you can do it barehanded if youvegot tough skin.Squeeze all juice out of filters after you knead,and throw emaway.(3) Filter the remaining liquid into the quart jar. It will be neccasary to dothis several times to get that awful smelling oil out. The chemicals in theinhalers have been bonded to the Hcl, and the oils have been filtered off.throw the filters away.(4) Pour enough of the solution into a small bottle to fill it 1/3 full. saveany leftover juice for the second batch.(5) Pour 1/4 teaspoon of the lyle crystal into the bottle and agitate.Do thisstep until the mixture remains cloudy. (6) Fill the bottle from step (5) up the rest of the way with Ether.Cap thebottle, and agitate for about 8 minutes. It is very important to expose everymolecule of the free-base to the Ether for as long as possible.(7) Let the mixture settle. There will be a middle layer that is very thick.tap the side of the bottle to get this layer as thin as possible.(8) Remove the top layer with the eyedropper, being careful not to get any ofthe middle layer in it. Save the ether and throw the rest away.(9) Fill a bottle half-way with water and about 10 drops of Hcl. pour the toplayer that you saved, and shake for about 2 minutes.when it settles, remove thetop layer, and throw the top layer away. The free base has now been bonded withthe Hcl in the water.(10) if theres any juice left from step (3), repeat the process with that.(11) Evaporate the solution in the pyrex dish, using low heat. The slower youevaporate the solution, the better. Ive found, that placing it on top of a hotwater heater works best.The crystals that remain are pure meth-amphetamine hydrochloride. (synonymouswith desoxyephidrine hydrochloride)^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^*^NOTES: It's a good idea to do this when your not fucked up. desoxyephedrine isthe same thing as meth-amphetamine, just different names. Wash your handsthoroughly, and use rubber gloves. Don't wash your hands with soap, then gostickin' your fingers in this stuff. Soap will have a neutralizing effect onthis process.This stuff is real good. Don't do too much you can overdose if you take toomuch. The best way to do this stuff if you don't mainline is to take a ball alittle bit smaller than a pea, and put it in a asprin capsule and swallow that.Or else snort the crystal, you may want to cut it with vitamin b-12 or mannitolbefore you do this. When buying the inhalers, look for the exp. date. Dont buyreal old inhalers, or try to improve this recipe unless you know how to do it.12 inhalers is all you need dont use more than 12. Its best to throw all thewastes into the same bag and dispose of it properly. this shit is so smellyyoull get busted by mom if ya dont. Be safe, and dont get busted with the shit.they WILL put you in jail for possesion, in case you didn't know.x,,