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Chlorbisan

From Wikipedia, the free encyclopedia
Chlorbisan
Names
Preferred IUPAC name
2,2′-Sulfanediylbis(5-chloro-3-methylphenol)
Other names
2,2′-Thiobis(5-chloro-3-methylphenol)
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.022.349 Edit this at Wikidata
UNII
  • InChI=1S/C14H12Cl2O2S/c1-7-3-9(15)5-11(17)13(7)19-14-8(2)4-10(16)6-12(14)18/h3-6,17-18H,1-2H3
    Key: HQRDNJVKXWYKAR-UHFFFAOYSA-N
  • InChI=1/C14H12Cl2O2S/c1-7-3-9(15)5-11(17)13(7)19-14-8(2)4-10(16)6-12(14)18/h3-6,17-18H,1-2H3
    Key: HQRDNJVKXWYKAR-UHFFFAOYAD
  • Clc2cc(c(Sc1c(cc(Cl)cc1O)C)c(O)c2)C
Properties
C14H12Cl2O2S
Molar mass 315.21 g·mol−1
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 4: Very short exposure could cause death or major residual injury. E.g. VX gasFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
4
1
0
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Chlorbisan is a toxic halogenated organosulfide.[1] It is used as a microbicide.

References

[edit]
  1. ^ Phenol, 2,2'-thiobis(4-chloro-6-methyl)- at cameochemicals.noaa.gov.