Methylisothiazolinone

Methylisothiazolinone
Skeletal formula of methylisothiazolinone
Space-filling model of the methylisothiazolinone molecule
Names
Preferred IUPAC name
2-Methyl-1,2-thiazol-3(2H)-one
Other names
2-Methylisothiazol-3(2H)-one
2-Methyl-4-isothiazolin-3-one
Identifiers
3D model (JSmol)
Abbreviations MIT, MI
606203
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.018.399 Edit this at Wikidata
EC Number
  • 220-239-6
UNII
  • InChI=1S/C4H5NOS/c1-5-4(6)2-3-7-5/h2-3H,1H3 checkY
    Key: BEGLCMHJXHIJLR-UHFFFAOYSA-N checkY
  • InChI=1/C4H5NOS/c1-5-4(6)2-3-7-5/h2-3H,1H3
  • O=C1/C=C\SN1C
Properties
C4H5NOS
Molar mass 115.1 g/mol
Appearance white solid
Hazards
GHS labelling:
GHS05: CorrosiveGHS06: ToxicGHS07: Exclamation markGHS09: Environmental hazard
Danger
H301, H311, H314, H317, H330, H410
P260, P261, P264, P270, P271, P272, P273, P280, P284, P301+P310, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P320, P321, P322, P330, P333+P313, P361, P363, P391, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Methylisothiazolinone (/ˌmɛθəlˌsˌθ.əˈzlɪnn/), MIT, or MI, is the organic compound with the formula S(CH)2C(O)NCH3. It is a white solid. Isothiazolinones, a class of heterocycles, are used as biocides in numerous personal care products and other industrial applications. MIT and related compounds have attracted much attention for their allergenic properties, e.g. contact dermatitis.[1]

  1. ^ Silva, Vânia; Silva, Cátia; Soares, Pedro; Garrido, E. Manuela; Borges, Fernanda; Garrido, Jorge (2020). "Isothiazolinone Biocides: Chemistry, Biological, and Toxicity Profiles". Molecules. 25 (4): 991. doi:10.3390/molecules25040991. PMC 7070760. PMID 32102175.