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== Applications == == Applications ==
Isothiazolinones are ]s used to control ], ], and ] in ], ], ] and ] water systems, ] systems, ] and ] agents. They are frequently used in ] products such as ]s and other ] products, as well as certain ] formulations. There, often combinations of MIT and CMIT (known as ''Kathon CG'') or MIT and BIT are used. Isothiazolinones are ]s used to control ], ], and ] in ], ], ] and ] water systems, ] systems, ] and ] agents. They are frequently used in ] products such as ]s and other ] products, as well as certain ] formulations. Often, combinations of MIT and CMIT (known as ''Kathon CG'') or MIT and BIT are used.


== Biological implications == == Biological implications ==

Revision as of 13:45, 14 January 2011

Isothiazolinone
Names
IUPAC name 1,2-Thiazol-3-one
Other names Isothiazolin-3-one; 3(2H)-Isothiazolone
Identifiers
CAS Number
3D model (JSmol)
ECHA InfoCard 100.225.492 Edit this at Wikidata
PubChem CID
CompTox Dashboard (EPA)
SMILES
  • O=C1NSC=C1
Properties
Chemical formula C3H3NOS
Molar mass 101.12 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Isothiazolinone is a heterocyclic chemical compound. Derivatives of isothiazolinone are used as biocides, including:

The derivative butylbenzisothiazolinone (BBIT) also exists, but does not have the same importance.

Applications

Isothiazolinones are antimicrobials used to control bacteria, fungi, and algae in cooling water systems, fuel storage tanks, pulp and paper mill water systems, oil extraction systems, wood preservation and antifouling agents. They are frequently used in personal care products such as shampoos and other hair care products, as well as certain paint formulations. Often, combinations of MIT and CMIT (known as Kathon CG) or MIT and BIT are used.

Biological implications

Together with their wanted function, controlling or killing microorganisms, isothiazolinones also have undesirable effects: They have a high aquatic toxicity and some derivatives (namely CMIT) can cause hypersensitivity by direct contact or via the air.

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