Stink bomb

Last updated
A prank stink bomb and its packaging StinkBomb.JPG
A prank stink bomb and its packaging

A stink bomb, sometimes called a stinkpot, is a device designed to create an unpleasant smell. They range in effectiveness from being used as simple pranks [1] to military grade malodorants or riot control chemical agents.

Contents

History

A stink bomb that could be launched with arrows was invented by Leonardo da Vinci. [2]

The 1972 U.S. presidential campaign of Edmund Muskie was disrupted at least four times in Florida in 1972 with the use of stink bombs during the Florida presidential primary. [3] Stink bombs were set off at campaign picnics in Miami and Tampa, at the Muskie campaign headquarters in Tampa and at offices in Tampa where the campaign's telephone bank was located. [3] The stink bomb plantings served to disrupt the picnics and campaign operations, and was deemed by the U.S. Select Committee on Presidential Campaign Activities of the U.S. Senate to have "disrupted, confused, and unnecessarily interfered with a campaign for the office of the Presidency". [3]

In 2004, it was reported that the Israeli weapons research and development directorate had created a liquid stink bomb, dubbed the "skunk bomb", with an odor that lingers for five years on clothing. [4] It is a synthetic stink bomb based upon the chemistry of the spray that is emitted from the anal glands of the skunk. [4] It was designed as a crowd control tool to be used as a deterrent that causes people to scatter, such as at a protest. [4] It has been described as a less than lethal weapon. [4]

Range

Stink bombs Boule puante.jpg
Stink bombs

At the lower end of the spectrum, relatively harmless stink bombs consist of a mixture of ammonium sulfide, vinegar and bicarbonate, which smells strongly of rotten eggs. [2] When exposed to air, the ammonium sulfide reacts with moisture, hydrolyzes, and a mixture of hydrogen sulfide (rotten egg smell) and ammonia is released. Another mixture consists of hydrogen sulfide and ammonia mixed together directly. [5]

Other popular substances on which to base stink bombs are thiols with lower molecular weight such as methyl mercaptan and ethyl mercaptan—the chemicals that are added in minute quantities to natural gas in order to make gas leaks detectable by smell. A variation on this idea is the scent bomb, or perfume bomb, filled with an overpowering "cheap perfume" smell.

At the upper end of the spectrum, the governments of Israel [4] and the United States of America are developing stink bombs for use by their law enforcement agencies and militaries as riot control [4] and area denial weapons. Using stink bombs for these purposes has advantages over traditional riot control agents: unlike pepper spray and tear gas, stink bombs are believed not to be dangerous, although their psychological effects can make people sick. [6]

Prank stink bombs and perfume bombs are usually sold as a 1- or 2-mL sealed glass ampoule, which can be broken by throwing against a hard surface or by crushing under one's shoe sole, thus releasing the malodorous liquid contained therein. Another variety of prank stink bomb comprises two bags, one smaller and inside the other. The inner one contains a liquid and the outer one a powder. When the inner one is ruptured by squeezing it, the liquid reacts with the powder, producing hydrogen sulfide, which expands and bursts the outer bag, releasing an unpleasant odor.

Chemicals used

Prank stink bombs in a vending machine Stinkbombs (6390494575).jpg
Prank stink bombs in a vending machine

Typically, lower molecular weight volatile organic compounds are used. Generally, the higher the molecular weight for a given class of compounds, the lower the volatility and initial concentration but the longer the persistence. Some chemicals (typically thiols) have a certain concentration threshold over which the smell is not perceived significantly stronger; therefore a lower-volatility compound is capable of providing comparable stench intensity to a higher-volatility compound, but for longer time. Another issue is the operating temperature, on which the compound's volatility strongly depends. Care should be taken as some compounds are toxic either in higher concentration or after prolonged exposure in low concentration.

Some plants may be used as improvised stink bombs; one such plant is the Parkia speciosa or 'stinky bean', which grows in India, Southeast Asia and Eastern Australia. The pods from this plant are collected when partly dried and stamped on, to release the stink. [7]

Some common components are:

Standard bathroom malodor

External videos
Making the US Government Standard Bathroom Malodor
Nuvola apps kaboodle.svg Making a fart juice developed by the U.S. government, NileBlue.

The US Government Standard Bathroom Malodor, said to be one of the worst-smelling substances, [8] is quoted as having this composition: (Note that this substance is a concoction) [9]

Dipropylene glycol 62.82%
Thioglycolic acid 21.18%
Hexanoic acid 6.00%
N-methylmorpholine 6.00%
p-cresyl isovalerate (4-methylphenyl 3-methylbutanoate)2.18%
2-Naphthalenethiol 0.91%
Skatole 0.91%

See also

Related Research Articles

Flatulence is the expulsion of gas from the intestines via the anus, commonly referred to as farting or trumping. "Flatus" is the medical word for gas generated in the stomach or bowels. A proportion of intestinal gas may be swallowed environmental air, and hence flatus is not entirely generated in the stomach or bowels. The scientific study of this area of medicine is termed flatology.

<span class="mw-page-title-main">Skunk</span> Common name of mammals in the family Mephitidae

Skunks are mammals in the family Mephitidae. They are known for their ability to spray a liquid with a strong, unpleasant scent from their anal glands. Different species of skunk vary in appearance from black-and-white to brown, cream or ginger colored, but all have warning coloration.

<span class="mw-page-title-main">Thiol</span> Any organic compound having a sulfanyl group (–SH)

In organic chemistry, a thiol, or thiol derivative, is any organosulfur compound of the form R−SH, where R represents an alkyl or other organic substituent. The −SH functional group itself is referred to as either a thiol group or a sulfhydryl group, or a sulfanyl group. Thiols are the sulfur analogue of alcohols, and the word is a blend of "thio-" with "alcohol".

<span class="mw-page-title-main">Methanethiol</span> Chemical compound

Methanethiol is an organosulfur compound with the chemical formula CH
3
SH
. It is a colorless gas with a distinctive putrid smell. It is a natural substance found in the blood, brain and feces of animals, as well as in plant tissues. It also occurs naturally in certain foods, such as some nuts and cheese. It is one of the chemical compounds responsible for bad breath and the smell of flatus. Methanethiol is the simplest thiol and is sometimes abbreviated as MeSH. It is very flammable.

<span class="mw-page-title-main">Ammonium bicarbonate</span> Chemical compound

Ammonium bicarbonate is an inorganic compound with formula (NH4)HCO3. The compound has many names, reflecting its long history. Chemically speaking, it is the bicarbonate salt of the ammonium ion. It is a colourless solid that degrades readily to carbon dioxide, water and ammonia.

<span class="mw-page-title-main">Ethanethiol</span> Chemical compound

Ethanethiol, commonly known as ethyl mercaptan, is an organosulfur compound with the formula CH3CH2SH. is a colorless liquid with a distinct odor. Abbreviated EtSH, it consists of an ethyl group (Et), CH3CH2, attached to a thiol group, SH. Its structure parallels that of ethanol, but with sulfur in place of oxygen. The odor of EtSH is infamous. Ethanethiol is more volatile than ethanol due to a diminished ability to engage in hydrogen bonding. Ethanethiol is toxic in high concentrations. It occurs naturally as a minor component of petroleum, and may be added to otherwise odorless gaseous products such as liquefied petroleum gas (LPG) to help warn of gas leaks. At these concentrations, ethanethiol is not harmful.

<span class="mw-page-title-main">Aroma compound</span> Chemical compound that has a smell or odor

An aroma compound, also known as an odorant, aroma, fragrance or flavoring, is a chemical compound that has a smell or odor. For an individual chemical or class of chemical compounds to impart a smell or fragrance, it must be sufficiently volatile for transmission via the air to the olfactory system in the upper part of the nose. As examples, various fragrant fruits have diverse aroma compounds, particularly strawberries which are commercially cultivated to have appealing aromas, and contain several hundred aroma compounds.

A blood agent is a toxic chemical agent that affects the body by being absorbed into the blood. Blood agents are fast-acting, potentially lethal poisons that typically manifest at room temperature as volatile colorless gases with a faint odor. They are either cyanide- or arsenic-based.

<span class="mw-page-title-main">Ammonium hydrosulfide</span> Chemical compound

Ammonium hydrosulfide is the chemical compound with the formula [NH4]SH.

<span class="mw-page-title-main">Dimethyl sulfide</span> Chemical compound

Dimethyl sulfide (DMS) or methylthiomethane is an organosulfur compound with the formula (CH3)2S. The simplest thioether, it is a flammable liquid that boils at 37 °C (99 °F) and has a characteristic disagreeable odor. It is a component of the smell produced from cooking of certain vegetables, notably maize, cabbage, beetroot, and seafoods. It is also an indication of bacterial contamination in malt production and brewing. It is a breakdown product of dimethylsulfoniopropionate (DMSP), and is also produced by the bacterial metabolism of methanethiol.

A wine fault is a sensory-associated (organoleptic) characteristic of a wine that is unpleasant, and may include elements of taste, smell, or appearance, elements that may arise from a "chemical or a microbial origin", where particular sensory experiences might arise from more than one wine fault. Wine faults may result from poor winemaking practices or storage conditions that lead to wine spoilage.

Sulfur compounds are chemical compounds formed the element sulfur (S). Common oxidation states of sulfur range from −2 to +6. Sulfur forms stable compounds with all elements except the noble gases.

Grapefruit mercaptan is a natural organic compound found in grapefruit. It is a monoterpenoid that contains a thiol functional group. Structurally a hydroxy group of terpineol is replaced by the thiol in grapefruit mercaptan, so it also called thioterpineol. Volatile thiols typically have very strong, often unpleasant odors that can be detected by humans in very low concentrations. Grapefruit mercaptan has a very potent, but not unpleasant, odor, and it is the chemical constituent primarily responsible for the aroma of grapefruit. This characteristic aroma is a property of only the R enantiomer.

A malodorant is a chemical compound whose extreme stench acts as a temporary incapacitant. It attacks the olfactory and/or trigeminal nerves of the person introduced to the chemical. These compounds are usually composed of at least two ingredients: the malodorant compound and a carrier liquid. Malodorant compositions have a toxicity category rating of III or higher.

<span class="mw-page-title-main">Butane-1-thiol</span> Chemical compound

Butane-1-thiol, also known as butyl mercaptan, is a volatile, clear to yellowish liquid with a fetid odor, commonly described as "skunk" odor. In fact, 1-butanethiol is structurally similar to several major constituents of a skunk's defensive spray but is not actually present in the spray. The scent of 1-butanethiol is so strong that the human nose can easily detect it in the air at concentrations as low as 10 parts per billion. The threshold level for 1-butanethiol is reported as 1.4 ppb

<span class="mw-page-title-main">Skunk (weapon)</span> Malodorant, non-lethal weapon used for crowd control

Skunk is a malodorant, non-lethal weapon used for crowd control by the Israel Defense Forces (IDF) and marketed to militaries and law enforcement around the world. It was developed and is manufactured by Odortec, with two supporting companies, Man and Beit-Alfa Technologies. The liquid's strong odor is marketed as an improvement over other crowd control weapons (CCWs) such as rubber bullets and tear gas used by the IDF against Palestinian protestors. The IDF is criticized for its tactics during deployment, including common use against people, businesses, and neighborhoods not involved in protests as a form of collective punishment.

<span class="mw-page-title-main">Odor</span> Volatile chemical compounds perceived by the sense of smell

An odor or odour is caused by one or more volatilized chemical compounds that are generally found in low concentrations that humans and many animals can perceive via their sense of smell. An odor is also called a "smell" or a "scent", which can refer to either an unpleasant or a pleasant odor.

<i>tert</i>-Butylthiol Chemical compound

tert-Butylthiol, also known as tert-butyl mercaptan (TBM), and abbreciated t-BuSH, is an organosulfur compound with the formula (CH3)3CSH. This thiol is used as an odorant for natural gas, which is otherwise odorless. It may also have been used as a flavoring agent.

Dimethyl disulfide (DMDS) is an organic chemical compound with the molecular formula CH3SSCH3. It is a flammable liquid with an unpleasant, garlic-like odor. The compound is colorless although impure samples often appear yellowish.

A beerfault or defect is a flavour deterioration caused by chemical changes of organic compounds in beer, either due to improper production processes or storage. Chemicals that can cause flavour defects in beer are aldehydes, lipids, and sulfur compounds. Just small fluctuations within fermentation byproducts can have a huge impact on the flavour. When the concentration of one or more of these chemicals exceeds the standard threshold, the flavour characteristics change, creating a flavour defect.

References

  1. Bender, H.F.; Eisenbarth, P. (2007). Hazardous Chemicals: Control and Regulation in the European Market. Wiley. p. 115. ISBN   978-3-527-60986-4 . Retrieved February 15, 2022.
  2. 1 2 Schwarcz, J. (2004). The Fly in the Ointment: 70 Fascinating Commentaries on the Science of Everyday Life. Ecw Press. pp. 140–141. ISBN   978-1-55490-399-3 . Retrieved February 15, 2022.
  3. 1 2 3 The Final Report of the Select Committee on Presidential Campaign Activities, United States Senate, Pursuant to S. Res. 60, February 7, 1973: A Resolution to Establish a Select Committee of the Senate to Investigate and Study Illegal Or Improper Campaign Activities in the Presidential Election of 1972. Report - 93d Congress, 2d session, Senate ; no. 93-981. U.S. Government Printing Office. 1974. p. 177. Retrieved February 15, 2022.
  4. 1 2 3 4 5 6 McManners, Hugh (September 17, 2004). "Israelis invent stink bomb for riot control" . The Independent. Archived from the original on 2022-05-25. Retrieved February 15, 2022.
  5. Cheney, D.H. (2021). Donald Trump, Robert Mueller, Christopher Steele: Mogul, Enforcer, Spy. Gatekeeper Press. p. 38. ISBN   978-1-6629-1712-7 . Retrieved February 15, 2022.
  6. "Scientists Find Most 'Offensive' Odors for Stink Bomb". ABC News. Retrieved 2022-07-18.
  7. Helmenstine, Anne (2020-07-26). "How Do Stink Bombs Work? Are They Safe?". Science Notes and Projects. Retrieved 2022-07-14.
  8. Munroe, Randall (17 February 2020). "What's the World's Worst Smell?". New York Times. Retrieved February 7, 2022.
  9. Ellison, D. Hank (August 24, 2007). Handbook of Chemical and Biological Warfare Agents, Second Edition. CRC Press. ISBN   9781420003291 via Google Books.

Further reading