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Names | |
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IUPAC name
2-(4-tert-butylphenoxy)cyclohexyl prop-2-yne-1-sulfonate
| |
Other names
Omite, Comite, Uniroyal D014
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Identifiers | |
3D model (
JSmol)
|
|
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.017.279 |
KEGG | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C19H26O4S | |
Molar mass | 350.47 g·mol−1 |
Appearance | dark amber viscous liquid |
Density | 1.10 g/cm3 |
0.5 ppm | |
Solubility | miscible in organic solvents |
Hazards | |
Safety data sheet (SDS) | Cornell University |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Propargite ( IUPAC name 2-(4-tert-butylphenoxy)cyclohexyl prop-2-yne-1-sulfonate, trade names Mitex, Omite and Comite) is a pesticide used to kill mites (an acaricide). [2] Symptoms of excessive exposure are eye and skin irritation, and possibly sensitization. It is highly toxic to amphibians, fish, and zooplankton, as well as having potential carcinogenity. [3]
http://onlinelibrary.wiley.com/doi/10.2903/j.efsa.2011.2087/epdf
![]() | |
![]() | |
Names | |
---|---|
IUPAC name
2-(4-tert-butylphenoxy)cyclohexyl prop-2-yne-1-sulfonate
| |
Other names
Omite, Comite, Uniroyal D014
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.017.279 |
KEGG | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C19H26O4S | |
Molar mass | 350.47 g·mol−1 |
Appearance | dark amber viscous liquid |
Density | 1.10 g/cm3 |
0.5 ppm | |
Solubility | miscible in organic solvents |
Hazards | |
Safety data sheet (SDS) | Cornell University |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Propargite ( IUPAC name 2-(4-tert-butylphenoxy)cyclohexyl prop-2-yne-1-sulfonate, trade names Mitex, Omite and Comite) is a pesticide used to kill mites (an acaricide). [2] Symptoms of excessive exposure are eye and skin irritation, and possibly sensitization. It is highly toxic to amphibians, fish, and zooplankton, as well as having potential carcinogenity. [3]
http://onlinelibrary.wiley.com/doi/10.2903/j.efsa.2011.2087/epdf