fbpx
Wikipedia

Hexachlorophene

Hexachlorophene, also known as Nabac, is an organochlorine compound that was once widely used as a disinfectant. The compound occurs as a white odorless solid, although commercial samples can be off-white and possess a slightly phenolic odor. It is insoluble in water but dissolves in acetone, ethanol, diethyl ether, and chloroform. In medicine, hexachlorophene is useful as a topical anti-infective and anti-bacterial agent. It is also used in agriculture as a soil fungicide, plant bactericide, and acaricide.[1]

Hexachlorophene
Clinical data
Trade namespHisoHex, Gamophen, Septisol, Turgex, Germa-Medica, Hexachlorophane, Almederm
ATC code
Legal status
Legal status
  • US: ℞-only for human use
  • Rx-only for human use
Identifiers
  • 2,2'-methylenebis(3,4,6-trichlorophenol)-3,4,6-trichloro-2-[(2,3,5-trichloro-6-hydroxyphenyl)methyl]phenol
CAS Number
  • 70-30-4
PubChem CID
  • 3598
DrugBank
  • DB00756
ChemSpider
  • 3472
UNII
  • IWW5FV6NK2
KEGG
  • D00859
ChEBI
  • CHEBI:5693
ChEMBL
  • ChEMBL496
CompTox Dashboard (EPA)
  • DTXSID6020690
ECHA InfoCard100.000.667
Chemical and physical data
FormulaC13H6Cl6O2
Molar mass406.89 g·mol−1
3D model (JSmol)
  • Interactive image
Density1.71 g/cm3
Melting point163 to 165 °C (325 to 329 °F)
Boiling point471 °C (880 °F)
  • C1=C(C(=C(C(=C1Cl)Cl)CC2=C(C(=CC(=C2Cl)Cl)Cl)O)O)Cl
  • InChI=1S/C13H6Cl6O2/c14-6-2-8(16)12(20)4(10(6)18)1-5-11(19)7(15)3-9(17)13(5)21/h2-3,20-21H,1H2
  • Key:ACGUYXCXAPNIKK-UHFFFAOYSA-N

Production edit

Hexacholorophene is produced by alkylation of 2,4,5-trichlorophenol with formaldehyde. Related antiseptics are prepared similarly, e.g., bromochlorophene and dichlorophene.[1]

Safety edit

The LD50 (oral, rat) is 59 mg/kg, indicating that the compound is relatively toxic. It is not mutagenic nor teratogenic according to Ullmann's Encyclopedia,[1] but "embryotoxic and produces some teratogenic effects" according to the International Agency for Research on Cancer.[2] 2,3,7,8-Tetrachlorodibenzodioxin (TCDD) is always a contaminant in this compound's production. Several accidents releasing many kilograms of TCDD have been reported. The reaction between 2,4,5-trichlorophenol and formaldehyde is exothermic. If the reaction occurs without adequate cooling, TCDD is produced in significant quantities as a byproduct and contaminant. The Seveso disaster and the Times Beach, Missouri, contamination incident exemplify the industrial hazards of hexachlorophene production.

Selective removal from market edit

France edit

In 1972, the "Bébé" brand of baby powder in France killed 39 babies. It also did great damage to the central nervous systems of several hundred other babies. The batch of toxic "Bébé" brand of powder was mistakenly manufactured with 6% hexachlorophene. This industrial accident directly led to the removal of hexachlorophene from consumer products worldwide.[3][4]

United States edit

In 1972, the U.S. Food and Drug Administration (FDA) halted production and distribution of products containing more than 1% of hexachlorophene.[5] After that change, most products containing hexachlorophene were available only with a doctor's prescription.[6] The restrictions were enacted after 15 deaths in the United States, and the 39 deaths in France mentioned above, were reported following brain damage caused by hexachlorophene.[7]

Several companies manufactured over-the-counter preparations which utilised hexachlorophene in their formulations. One product, Baby Magic Bath by The Mennen Company, was recalled in 1971, and removed from retail distribution.

Two commercial preparations using hexachlorophene, pHisoDerm and pHisoHex, were widely used as antibacterial skin cleansers in the treatment of acne, (with pHisoDerm developed for those allergic to the active ingredients in pHisoHex). During the 1960s, both were available over the counter in the US. After the ban, pHisoDerm was reformulated without hexachlorophene, and continued to be sold over-the-counter, while pHisoHex, (which contained 3% hexachlorophene - 3 times the legal limit imposed in 1972),[7] became available as a prescription body wash. In the European Community countries during the 1970s and 1980s, pHisoHex remained available over the counter. A related product, pHisoAc, was used as a skin mask to dry and peel away acne lesions whilst pHiso-Scrub, a hexachlorophene-impregnated sponge for scrubbing, has since been discontinued. Several substitute products (including triclosan) were developed, but none had the germ-killing capability of hexachlorophene. (Sanofi-Aventis became the sole European manufacturer of pHisoHex, while The Mentholatum Company owns the pHisoDerm brand today. Sanofi-Aventis discontinued production of several forms of pHisoHex in August 2009 and discontinued all production of pHisoHex in September 2013).[8]

The formula for Dial soap was modified to remove hexachlorophene after the FDA ended over-the-counter availability in 1972.[6]

Bristol-Myers' discontinued Ipana toothpaste brand at one time contained hexachlorophene. [9]

Germany edit

In Germany, cosmetics containing hexachlorophene have been banned since 1985.

Austria edit

In Austria, the sale of drugs containing the substance has been banned since 1990.[10]

Trade names edit

Trade names for hexachlorophene include: Acigena, Almederm, AT7 (dial soap), AT17, Bilevon, Exofene, Fostril, Gamophen, G-11, Germa-Medica, Hexosan, K-34, Septisol, Surofene, M3.[11][12]

References edit

  1. ^ a b c Fiege H, Voges HM, Hamamoto T, Umemura S, Iwata T, Miki H, et al. (2000). "Phenol Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a19_313. ISBN 3-527-30673-0.
  2. ^ "Hexachlorophene". International Agency for Research on Cancer (IARC) - Summaries & Evaluations. IPCS Inchem. 20: 241. 1998 [1979].
  3. ^ "Talcum Suspected in Deaths of 21 French Babies". No. 29 August 1972. New York Times. p. 10. Retrieved 18 March 2020.
  4. ^ "FDA CURBS USE OF GERMICIDE TIED TO INFANT DESTHS". No. 23 September 1972. New York Times. p. 1. Retrieved 18 March 2020.
  5. ^ Germicide Limit Stirs Confusion, New York Times, September 24, 1972, pg. 53.
  6. ^ a b . Archived from the original on April 2, 2016. Retrieved June 16, 2015.
  7. ^ a b Ocala Star Banner, "15 Deaths Cited In Use of Germ Killer, Hexachlorophene" (AP), March 21, 1973. From Google News.
  8. ^ . American Society of Health-System Pharmacists. Archived from the original on 10 September 2014.
  9. ^ "1959 Ipana Toothpaste Ad". YouTube.
  10. ^ Rechtsinformationssystem des österreichischen Bundeskanzleramtes (in German)
  11. ^ "Hexachlorophene". PharmGKB. Retrieved 2012-12-28.
  12. ^ Dept. of Health, Education, and Welfare (1972). "Consumer news". Office of Consumer Affairs. 2 (21): 10.{{cite journal}}: CS1 maint: multiple names: authors list (link)

hexachlorophene, also, known, nabac, organochlorine, compound, that, once, widely, used, disinfectant, compound, occurs, white, odorless, solid, although, commercial, samples, white, possess, slightly, phenolic, odor, insoluble, water, dissolves, acetone, etha. Hexachlorophene also known as Nabac is an organochlorine compound that was once widely used as a disinfectant The compound occurs as a white odorless solid although commercial samples can be off white and possess a slightly phenolic odor It is insoluble in water but dissolves in acetone ethanol diethyl ether and chloroform In medicine hexachlorophene is useful as a topical anti infective and anti bacterial agent It is also used in agriculture as a soil fungicide plant bactericide and acaricide 1 HexachloropheneClinical dataTrade namespHisoHex Gamophen Septisol Turgex Germa Medica Hexachlorophane AlmedermATC codeD08AE01 WHO QP52AG02 WHO Legal statusLegal statusUS only for human use Rx only for human useIdentifiersIUPAC name 2 2 methylenebis 3 4 6 trichlorophenol 3 4 6 trichloro 2 2 3 5 trichloro 6 hydroxyphenyl methyl phenolCAS Number70 30 4PubChem CID3598DrugBankDB00756ChemSpider3472UNIIIWW5FV6NK2KEGGD00859ChEBICHEBI 5693ChEMBLChEMBL496CompTox Dashboard EPA DTXSID6020690ECHA InfoCard100 000 667Chemical and physical dataFormulaC 13H 6Cl 6O 2Molar mass406 89 g mol 13D model JSmol Interactive imageDensity1 71 g cm3Melting point163 to 165 C 325 to 329 F Boiling point471 C 880 F SMILES C1 C C C C C1Cl Cl CC2 C C CC C2Cl Cl Cl O O ClInChI InChI 1S C13H6Cl6O2 c14 6 2 8 16 12 20 4 10 6 18 1 5 11 19 7 15 3 9 17 13 5 21 h2 3 20 21H 1H2Key ACGUYXCXAPNIKK UHFFFAOYSA N Contents 1 Production 2 Safety 3 Selective removal from market 3 1 France 3 2 United States 3 3 Germany 3 4 Austria 4 Trade names 5 ReferencesProduction editHexacholorophene is produced by alkylation of 2 4 5 trichlorophenol with formaldehyde Related antiseptics are prepared similarly e g bromochlorophene and dichlorophene 1 Safety editThe LD50 oral rat is 59 mg kg indicating that the compound is relatively toxic It is not mutagenic nor teratogenic according to Ullmann s Encyclopedia 1 but embryotoxic and produces some teratogenic effects according to the International Agency for Research on Cancer 2 2 3 7 8 Tetrachlorodibenzodioxin TCDD is always a contaminant in this compound s production Several accidents releasing many kilograms of TCDD have been reported The reaction between 2 4 5 trichlorophenol and formaldehyde is exothermic If the reaction occurs without adequate cooling TCDD is produced in significant quantities as a byproduct and contaminant The Seveso disaster and the Times Beach Missouri contamination incident exemplify the industrial hazards of hexachlorophene production Selective removal from market editFrance edit In 1972 the Bebe brand of baby powder in France killed 39 babies It also did great damage to the central nervous systems of several hundred other babies The batch of toxic Bebe brand of powder was mistakenly manufactured with 6 hexachlorophene This industrial accident directly led to the removal of hexachlorophene from consumer products worldwide 3 4 United States edit In 1972 the U S Food and Drug Administration FDA halted production and distribution of products containing more than 1 of hexachlorophene 5 After that change most products containing hexachlorophene were available only with a doctor s prescription 6 The restrictions were enacted after 15 deaths in the United States and the 39 deaths in France mentioned above were reported following brain damage caused by hexachlorophene 7 Several companies manufactured over the counter preparations which utilised hexachlorophene in their formulations One product Baby Magic Bath by The Mennen Company was recalled in 1971 and removed from retail distribution Two commercial preparations using hexachlorophene pHisoDerm and pHisoHex were widely used as antibacterial skin cleansers in the treatment of acne with pHisoDerm developed for those allergic to the active ingredients in pHisoHex During the 1960s both were available over the counter in the US After the ban pHisoDerm was reformulated without hexachlorophene and continued to be sold over the counter while pHisoHex which contained 3 hexachlorophene 3 times the legal limit imposed in 1972 7 became available as a prescription body wash In the European Community countries during the 1970s and 1980s pHisoHex remained available over the counter A related product pHisoAc was used as a skin mask to dry and peel away acne lesions whilst pHiso Scrub a hexachlorophene impregnated sponge for scrubbing has since been discontinued Several substitute products including triclosan were developed but none had the germ killing capability of hexachlorophene Sanofi Aventis became the sole European manufacturer of pHisoHex while The Mentholatum Company owns the pHisoDerm brand today Sanofi Aventis discontinued production of several forms of pHisoHex in August 2009 and discontinued all production of pHisoHex in September 2013 8 The formula for Dial soap was modified to remove hexachlorophene after the FDA ended over the counter availability in 1972 6 Bristol Myers discontinued Ipana toothpaste brand at one time contained hexachlorophene 9 Germany edit In Germany cosmetics containing hexachlorophene have been banned since 1985 Austria edit In Austria the sale of drugs containing the substance has been banned since 1990 10 Trade names editTrade names for hexachlorophene include Acigena Almederm AT7 dial soap AT17 Bilevon Exofene Fostril Gamophen G 11 Germa Medica Hexosan K 34 Septisol Surofene M3 11 12 References edit a b c Fiege H Voges HM Hamamoto T Umemura S Iwata T Miki H et al 2000 Phenol Derivatives Ullmann s Encyclopedia of Industrial Chemistry Weinheim Wiley VCH doi 10 1002 14356007 a19 313 ISBN 3 527 30673 0 Hexachlorophene International Agency for Research on Cancer IARC Summaries amp Evaluations IPCS Inchem 20 241 1998 1979 Talcum Suspected in Deaths of 21 French Babies No 29 August 1972 New York Times p 10 Retrieved 18 March 2020 FDA CURBS USE OF GERMICIDE TIED TO INFANT DESTHS No 23 September 1972 New York Times p 1 Retrieved 18 March 2020 Germicide Limit Stirs Confusion New York Times September 24 1972 pg 53 a b The Milwaukee Sentinel US Order Curbs Hexachlorophene UPI September 23 1972 From Google News Archived from the original on April 2 2016 Retrieved June 16 2015 a b Ocala Star Banner 15 Deaths Cited In Use of Germ Killer Hexachlorophene AP March 21 1973 From Google News Drug Shortages American Society of Health System Pharmacists Archived from the original on 10 September 2014 1959 Ipana Toothpaste Ad YouTube Rechtsinformationssystem des osterreichischen Bundeskanzleramtes in German Hexachlorophene PharmGKB Retrieved 2012 12 28 Dept of Health Education and Welfare 1972 Consumer news Office of Consumer Affairs 2 21 10 a href Template Cite journal html title Template Cite journal cite journal a CS1 maint multiple names authors list link Retrieved from https en wikipedia org w index php title Hexachlorophene amp oldid 1174048317, wikipedia, wiki, book, books, library,

article

, read, download, free, free download, mp3, video, mp4, 3gp, jpg, jpeg, gif, png, picture, music, song, movie, book, game, games.