Names | |
---|---|
Preferred IUPAC name
O-Ethyl S,S-diphenyl phosphorodithioate | |
Other names
O-Ethyl-S,S-diphenyldithiophosphate; EDDP
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.037.420 |
KEGG | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C14H15O2PS2 | |
Molar mass | 310.37 g·mol−1 |
Density | 1.23 g/cm3 [1] |
Melting point | −25 °C (−13 °F; 248 K) [1] |
56 mg/L (20 °C) [1] | |
Hazards | |
GHS labelling: | |
[1] | |
Danger | |
H301, H311, H317, H331, H410 [1] | |
P261, P273, P280, P301+P310, P311, P501 [1] | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Edifenphos (O-ethyl-S,S-diphenyldithiophosphate, EDDP) is a systemic fungicide that inhibits phosphatidylcholine biosynthesis. [2] [3] It was introduced in 1966 by Bayer to combat blast fungus and Pellicularia sasakii in rice cultivation. [3] It was never authorized for use in the EU. [4]
Names | |
---|---|
Preferred IUPAC name
O-Ethyl S,S-diphenyl phosphorodithioate | |
Other names
O-Ethyl-S,S-diphenyldithiophosphate; EDDP
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.037.420 |
KEGG | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C14H15O2PS2 | |
Molar mass | 310.37 g·mol−1 |
Density | 1.23 g/cm3 [1] |
Melting point | −25 °C (−13 °F; 248 K) [1] |
56 mg/L (20 °C) [1] | |
Hazards | |
GHS labelling: | |
[1] | |
Danger | |
H301, H311, H317, H331, H410 [1] | |
P261, P273, P280, P301+P310, P311, P501 [1] | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Edifenphos (O-ethyl-S,S-diphenyldithiophosphate, EDDP) is a systemic fungicide that inhibits phosphatidylcholine biosynthesis. [2] [3] It was introduced in 1966 by Bayer to combat blast fungus and Pellicularia sasakii in rice cultivation. [3] It was never authorized for use in the EU. [4]