Chloroxylenol

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Chloroxylenol
Kekulé, skeletal formula of chloroxylenol
Identifiers
CAS number88-04-0 YesY
PubChem2723
ChemSpider21106017 YesY
UNII0F32U78V2Q YesY
EC number201-793-8
KEGGD03473 YesY
MeSHchloroxylenol
ChEBICHEBI:34393
ChEMBLCHEMBL398440 N
RTECS numberZE6850000
ATC codeD08AE05
Beilstein Reference1862539
Jmol-3D imagesImage 1
Image 2
Properties
Molecular formulaC8H9ClO
Molar mass156.61 g mol−1
Melting point114 to 116 °C (237 to 241 °F; 387 to 389 K)
log P3.377
Acidity (pKa)9.76
Basicity (pKb)4.24
Hazards
GHS pictogramsThe exclamation-mark pictogram in the Globally Harmonized System of Classification and Labelling of Chemicals (GHS)
GHS signal wordWARNING
GHS hazard statementsH302, H315, H317, H319
GHS precautionary statementsP280, P305+351+338
EU Index604-038-00-4
EU classificationHarmful Xn
R-phrasesR22, R36/38, R43
S-phrases(S2), S24, S37
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references
 
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Chloroxylenol
Kekulé, skeletal formula of chloroxylenol
Identifiers
CAS number88-04-0 YesY
PubChem2723
ChemSpider21106017 YesY
UNII0F32U78V2Q YesY
EC number201-793-8
KEGGD03473 YesY
MeSHchloroxylenol
ChEBICHEBI:34393
ChEMBLCHEMBL398440 N
RTECS numberZE6850000
ATC codeD08AE05
Beilstein Reference1862539
Jmol-3D imagesImage 1
Image 2
Properties
Molecular formulaC8H9ClO
Molar mass156.61 g mol−1
Melting point114 to 116 °C (237 to 241 °F; 387 to 389 K)
log P3.377
Acidity (pKa)9.76
Basicity (pKb)4.24
Hazards
GHS pictogramsThe exclamation-mark pictogram in the Globally Harmonized System of Classification and Labelling of Chemicals (GHS)
GHS signal wordWARNING
GHS hazard statementsH302, H315, H317, H319
GHS precautionary statementsP280, P305+351+338
EU Index604-038-00-4
EU classificationHarmful Xn
R-phrasesR22, R36/38, R43
S-phrases(S2), S24, S37
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

Chloroxylenol (4-chloro-3,5-dimethylphenol) is an antimicrobial chemical compound used to control bacteria, algae, and fungi in adhesives, emulsions, paints, and wash tanks.[2] It is also commonly used in antibacterial soaps and household antiseptics such as Dettol liquid and cream, and ointments, such as the now discontinued Medicated Vaseline.[3] Studies have shown a low anti microbial activity which is enhanced by additives. Its antibacterial action is due to disruption of cell membrane potentials.[4]

Chloroxylenol is not significantly toxic to humans and other mammals, is practically non-toxic to birds, moderately toxic to freshwater invertebrates and highly toxic to fish.[2] It is a mild skin irritant and may trigger allergic reactions in some individuals. Cross sensitivity with chlorocresol is common.[3]

References[edit]

  1. ^ "chloroxylenol – Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 25 March 2005. Identification and Related Records. Retrieved 7 October 2011. 
  2. ^ a b http://www.epa.gov/oppsrrd1/REDs/factsheets/3045fact.pdf
  3. ^ a b Ascenzi, Joseph M. (1996). "Chloroxylenol: an old-new antimicrobial". Handbook of disinfectants and antiseptics. New York: M. Dekker. ISBN 978-0-8247-9524-5. 
  4. ^ Aly, R; Malbach, H (1988). "Comparative antibacterial efficacy of a 2-minute surgical scrub with chlorhexidine gluconate, povidone-iodine, and chloroxylenol sponge-brushes". American Journal of Infection Control 16 (4): 173–7. doi:10.1016/0196-6553(88)90029-6. PMID 3189943. 

External links[edit]