Isothiazolinone

Names

IUPAC name

1,2-Thiazol-3-one

Other names

Isothiazolin-3-one; 3(2H)-Isothiazolone

Identifiers

CAS Number

1003-07-2^Y

3D model (Jmol)

Interactive image
Interactive image

ChemSpider

87509^N

ECHA InfoCard

E57JT172V7^N

InChI=1S/C3H3NOS/c5-3-1-2-6-4-3/h1-2H,(H,4,5)^N
Key: MGIYRDNGCNKGJU-UHFFFAOYSA-N^N
InChI=1/C3H3NOS/c5-3-1-2-6-4-3/h1-2H,(H,4,5)
Key: MGIYRDNGCNKGJU-UHFFFAOYAO

SMILES

O=C1NSC=C1
c1csnc1O

Properties

Chemical formula

C₃H₃NOS

Molar mass

101.127

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

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Infobox references

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

Methylisothiazolinone (MIT, MI)
Chloromethylisothiazolinone (CMIT, CMI, MCI)
Benzisothiazolinone (BIT)
Octylisothiazolinone (OIT, OI)
Dichlorooctylisothiazolinone (DCOIT, DCOI)
Butylbenzisothiazolinone (BBIT)

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 can cause hypersensitivity by direct contact or via the air.

References

This article is issued from Wikipedia - version of the 9/22/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.

Isothiazolinone

Applications

Biological implications

See also

References