Why not try a vomit inducing mixture?

This guide provides the instructions for two throw up mixtures.

You will be provided with all essential information including apparatus, materials and the procedure.

This article will have you the throw up king in no time.

In our project directed toward the total syntheses of tetrodotoxin and its natural and unnatural analogues, we have recently completed the syntheses of 5,11–dideoxytetrodotoxin,13 11–deoxytetrodotoxin,14 and 8,11–dideoxytetrodotoxin15 in enantiomerically pure form on the basis of a Diels–Alder strategy from levoglucosenone.

Among them, 11–deoxytetrodotoxin was the first total synthesis of a naturally occurring tetrodotoxin analogue.

The full details of the total synthesis of tetrodotoxin (1) are described here on a different basic strategy aiming at a higher oxidation stage in earlier stages of the synthesis.

The "relative lethality" was determined as follows.

Reported LD50 figures for the following combinations of experimental animal and route of administration were assembled from the cited literature: iv/mouse, ip/mouse, sc/mouse, iv/rat, sc/rat, iv/guinea–pig, iv/cat, iv/rabbit.

Within each animal/administration–route set, each agent LD50 was converted into a lethality–index relative to sarin, assigning a reference value of 1000 to the sarin LD50 concerned. For example, the sc/mouse index for batrachotoxin is taken as 10 because its sc/mouse LD50 and that of sarin were around 0.002 and 0.2 mg/kg respectively.

In this table, the agents are ranked according to their lowest lethality–index. Only in the case of the italicized synthetic poisons were animal parenteral LD50s unavailable. In these cases, respiratory LCt50s were used instead, except for white arsenic, where an oral LD50 was used.

The respiratory LD50 of sarin in man is estimated to be about 1000 micrograms.

This bean has always been of great interest to the chemist and the immunologist (l–4), partly because it, may readily be obtained in considerable quantities.

Earlier methods of preparation were carried out before the development of modern physicochemical and immunochemical methods for characterizing proteins, and data are therefore lacking on the purity and homogeneity of the products obtained.

In the present report a summary is given of a portion of a study carried out during 1943–45 in consultation and collaboration with other laboratories engaged in parallel investigations, which it is hoped, will soon be published.

Since results and materials were freely exchanged, some of the data included here were obtained on material from other laboratories, as indicated in the text.

Tetanus toxin is produced by Clostridium tetani and is one of the most powerful toxins known. It has a molecular weight of approximately 150,000 and is produced within organisms and discharged into the medium as they autolyze.

Previously the toxin was prepared from culture filtrates after autolysis of the organisms. However, since Raynaud developed a method for extracting the toxin from organisms before they autolyzed (9), several groups have used bacterial extracts as starting material for purifying the toxin (1, 10). This method has the advantage that the toxin is obtained in a more concentrated and purer form than that from culture filtrates (9, 10).

In this study we used bacterial extracts as starting material and developed a simple, rapid method for purification of the toxin which included high–pressure liquid chromatography (HPLC). We first determined the optimal time for harvesting the organisms to extract the toxin reproducibly in maximal yield. For determining the optimal conditions for extraction, we studied the kinetics of release of the toxin from cells in hypertonic solution. Then we purified the toxin by techniques which included gel permeation chromatography by HPLC, a method which has recently become available and has the advantages of being rapid and giving high resolution.

A dose as small as 50 milligrams (ingested) can kill an adult man.

Easily made from common chemicals, cyanide is used as is for poisoning bullets and food, and is used in the making of Hydrogen Cyanide, Cyanogen Chloride, Tabun, and numerous other poison gases.

Ricin is just about the easiest, and at the same time, most toxic poison that a criminal can make. Less than a milligram (1/1,000 of a gram) injected or inhaled will kill a person several times over. For individual killings, it has the advantage of being undetectable in toxicology scans since the poison is a catalyst the starts a chain reaction in the body, and is destroyed  before the symptoms begin to show.

With properly sized and dispersed dry particles, ricin is at least 10x more toxic than the most potent nerve gas. A 1% water solution atomized with a small explosive burster has the same effectiveness as sarin nerve gas. The only disadvantage ricin has is the time it takes for the victims to die is about 1 – 2 weeks. So you won't have the quick tactical effect of nerve gas. But this can also be good in that, using a covert dissemination, the criminal has time to escape before the attack is detected.

This book comprehensively details how to produce both of these deadly poisons out of commonly available materials and ingredients.

This method of making itching powder is extremely easy, highly effective and made out of one very easy to acquire material.

Get started now.

Nicotine is one of the world’s deadliest poisons. Fortunately, it is also incredibly simple to make and employ. This poison can be made out of commonly available tobacco. These instructions detail how to produce this poison enmass.

Mother Nature has some deadly weapons.

Review of human cases and analytical determination of main toxins by high–performance liquid chromatography.

Makes for an informative read.