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'''Dettol''' is the [[trade name]] for a line of [[hygiene]] products manufactured by [[Reckitt Benckiser]]. It has been in use since before 1936, when it was used after surgery as an antiseptic.<ref>{{cite book|last1=Rolleston, H.|title=British Encyclopaedia of Medical Practice, Volume 1, Anus Diseases|date=1936|publisher=Butterworth & Co.|location=London|page=671}}</ref>
'''Dettol''' is the [[trade name]] for a line of [[hygiene]] products manufactured by [[Reckitt Benckiser]]. It has been in use since before 1936, when it was used after [[surgery]] as an [[antiseptic]].<ref>{{cite book|last1=Rolleston, H.|title=British Encyclopaedia of Medical Practice, Volume 1, Anus Diseases|date=1936|publisher=Butterworth & Co.|location=London|page=671}}</ref>


==Composition and chemistry==
==Composition and chemistry==
The original Dettol liquid antiseptic and disinfectant is light yellow in colour in the concentrated form but, as several of the ingredients are insoluble in water, it produces a milky [[emulsion]] of oil droplets when diluted with water, exhibiting the [[ouzo effect]].
The original Dettol liquid antiseptic and disinfectant is light yellow in colour in the [[Concentration|concentrated]] form but, as several of the ingredients are [[Solubility|insoluble]] in water, it produces a milky [[emulsion]] of oil droplets when diluted with water, exhibiting the [[ouzo effect]].


The active ingredient in Dettol that confers its antiseptic property is [[chloroxylenol]] (C<sub>8</sub>H<sub>9</sub>ClO), an [[aromatic chemical compound]]. Chloroxylenol comprises 4.8% of Dettol's total admixture,<ref>{{cite web |url=http://www.mhra.gov.uk/home/groups/spcpil/documents/spcpil/con1412920124477.pdf |title=Summary of Product Characteristics / Dettol Liquid |date=22 November 2010 | publisher=MHRA |accessdate=9 November 2014 }}</ref> with the rest made up by [[pine oil]], [[isopropanol]], [[castor oil]], soap and [[water]].
The active ingredient in Dettol that confers its antiseptic property is [[chloroxylenol]] (C<sub>8</sub>H<sub>9</sub>ClO), an [[aromatic chemical compound]]. Chloroxylenol comprises 4.8% of Dettol's total [[Mixture|admixture]],<ref>{{cite web |url=http://www.mhra.gov.uk/home/groups/spcpil/documents/spcpil/con1412920124477.pdf |title=Summary of Product Characteristics / Dettol Liquid |date=22 November 2010 | publisher=MHRA |accessdate=9 November 2014 }}</ref> with the rest made up by [[pine oil]], [[isopropanol]], [[castor oil]], soap and [[water]].


==Usage==
==Usage==

Revision as of 21:01, 29 March 2016

Dettol
File:Dettol Logo.jpg
Product typeHygiene product
OwnerReckitt Benckiser
CountryUnited Kingdom
Introduced1936
MarketsAustralia, India, Pakistan, South Africa, and the United Kingdom
Previous ownersSSL International
Websitewww.dettol.co.uk
www.dettol.com.au
www.dettol.pk
www.dettol.co.za
www.dettol.co.in

Dettol is the trade name for a line of hygiene products manufactured by Reckitt Benckiser. It has been in use since before 1936, when it was used after surgery as an antiseptic.[1]

Composition and chemistry

The original Dettol liquid antiseptic and disinfectant is light yellow in colour in the concentrated form but, as several of the ingredients are insoluble in water, it produces a milky emulsion of oil droplets when diluted with water, exhibiting the ouzo effect.

The active ingredient in Dettol that confers its antiseptic property is chloroxylenol (C8H9ClO), an aromatic chemical compound. Chloroxylenol comprises 4.8% of Dettol's total admixture,[2] with the rest made up by pine oil, isopropanol, castor oil, soap and water.

Usage

Diluted, Dettol may be used to clean cuts, wounds, etc. and to disinfect environmental surfaces such as household floors and the walls of slaughterhouses etc.

Toxicity

Humans

As with other manufactured household cleaners, Dettol has the potential for causing lethal toxicity. It is poisonous when ingested and even when it is unintentionally inhaled.

In a case report, a 42-year-old British man died from Dettol overexposure in May 2007. The autopsy was not able to conclude whether the lethal exposure to Dettol was via ingestion or inhalation.[3] A medical study which analyzed 177 cases of Dettol intoxications via ingestion in Hong Kong concluded that ″Dettol poisoning resulted in serious complications in 7% of patients, including death".[4]

Animals

Dettol is toxic to many animals, especially cats.[5] Dettol contains the phenol chloroxylenol. Phenols are of particular concern because cats are unable to eliminate the toxins following ingestion. A cat may swallow the product by licking its paws after they have come into contact with it.

In Australia, Dettol spray has been shown to be lethal to cane toads, an invasive species that was introduced from Hawaii, as a result of bad judgment, in 1935. It had been hoped that the amphibian would control the cane beetle but it became highly destructive within the ecosystem. Spraying the disinfectant at close range has been shown to cause rapid death to toads. It is not known whether the toxins are persistent or whether they harm other Australian flora and fauna.

Owing to concerns over potential harm to other Australian wildlife species, the use of Dettol as an agent for pest control was banned in Western Australia by the Department of Environment and Conservation in 2011.[6]

See also

References

  1. ^ Rolleston, H. (1936). British Encyclopaedia of Medical Practice, Volume 1, Anus Diseases. London: Butterworth & Co. p. 671.
  2. ^ "Summary of Product Characteristics / Dettol Liquid" (PDF). MHRA. 22 November 2010. Retrieved 9 November 2014.
  3. ^ Lester Haines (29 May 2007). "'Dettol Man' cleans himself to death". The Register. Retrieved 2 February 2013.
  4. ^ PK Lam, CK Chan, ML Tse, FL Lau (August 2012). "Dettol poisoning and the need for airway intervention" (PDF). Hong Kong Medical Journal. 18 (4): 270–275. PMID 22865169. Retrieved 29 March 2015.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  5. ^ "Cats and poisons". icatcare.org.
  6. ^ Narelle Towie (23 May 2009). "Cane toad poison banned". Perth Now. Retrieved 2 February 2013.
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