Chloroxylenol
Chloroxylenol | |
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Systematic name 4-Chloro-3,5-dimethylphenol[1] | |
Identifiers | |
CAS number | 88-04-0 |
PubChem | 2723 |
ChemSpider | 21106017 |
UNII | 0F32U78V2Q |
EC number | 201-793-8 |
KEGG | D03473 |
MeSH | chloroxylenol |
ChEBI | CHEBI:34393 |
ChEMBL | CHEMBL398440 |
RTECS number | ZE6850000 |
ATC code | D08 |
Beilstein Reference | 1862539 |
Jmol-3D images | Image 1 Image 2 |
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Properties | |
Molecular formula | C8H9ClO |
Molar mass | 156.61 g mol−1 |
Melting point | 114 to 116 °C; 237 to 241 °F; 387 to 389 K |
log P | 3.377 |
Acidity (pKa) | 9.76 |
Basicity (pKb) | 4.24 |
Hazards | |
GHS pictograms | |
GHS signal word | WARNING |
GHS hazard statements | H302, H315, H317, H319 |
GHS precautionary statements | P280, P305+351+338 |
EU Index | 604-038-00-4 |
EU classification | Xn |
R-phrases | R22, 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
- ↑ "chloroxylenol – Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 25 March 2005. Identification and Related Records. Retrieved 7 October 2011.
- ↑ 2.0 2.1 http://www.epa.gov/oppsrrd1/REDs/factsheets/3045fact.pdf
- ↑ 3.0 3.1 Ascenzi, Joseph M. (1996). "Chloroxylenol: an old-new antimicrobial". Handbook of disinfectants and antiseptics. New York: M. Dekker. ISBN 978-0-8247-9524-5.
- ↑ 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
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