Benzisothiazolinone

Benzisothiazolinone
Skeletal formula of benzisothiazolinone
Space-filling model of the benzisothiazolinone molecule
Names
IUPAC name
1,2-benzisothiazol-3(2H)-one
Other names
Benzisothiazolinone, Benzisothiazolin-3-one, Benzisothiazolone
Identifiers
2634-33-5 YesY
Abbreviations BIT
ChEBI CHEBI:167099 YesY
ChEMBL ChEMBL297304 YesY
ChemSpider 16567 YesY
Jmol interactive 3D Image
MeSH 1,2-benzisothiazoline-3-one
PubChem 17520
Properties
C7H5NOS
Molar mass 151.18 g·mol−1
Appearance white powder
Melting point 158 °C (316 °F; 431 K)[1]
1 g/l
Hazards
Main hazards Xn, N [1]
R-phrases R22, R38, R41, R43, R50 [1]
S-phrases (S2), S24, S26, S37/39, S61 [1]
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

Benzisothiazolinone (BIT) is a widely used biocide and belongs to the group of isothiazolinones.

Usage

Benzisothiazolinone has a microbicide and a fungicide mode of action. It is widely used as a preservative, for example in:

In paints, it is commonly used as a mixture with methylisothiazolinone. Typical concentrations in products are 200–400 ppm depending on the application area and the combination with other biocides. According to a study in Switzerland, 19% of the paints, varnishes and coatings contained BIT in 2000. The fraction in adhesives, sealants, plasters and fillers was 25%. [3]

Health hazards

It is known as toxicant material for human immune system, and also is classified as irritant for skin, eyes and lungs.[4] It is widely used as active ingredient of many home cleaning products.

References

  1. 1 2 3 4 Record of 1,2-Benzisothiazol-3(2H)-one in the GESTIS Substance Database of the IFA, accessed on 22 October 2007
  2. US EPA. September 29, 2005 EPA Reregistration Decision
  3. Reinhard et al.: "Preservation of products with MCI/MI in Switzerland". Contact Dermatitis. 2001 Nov;45(5):257-64. PMID 11722483
  4. EWG's Skin Deep Cosmetics Database

Literature

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