| Identification | Back Directory | [Name]
DITALIMFOS | [CAS]
5131-24-8 | [Synonyms]
re199
sf101
O 199
Farmil
leucon
M 2452
m-2452
Millie
Laptran
PLONDREL
Dowco 199
dowco-199
frutogard
Ortho 199
italimfos
DITALIMFOS
LAPTRAN(R)
Ditalimphos
PLONDREL(R)
DOWCO(R) 199
DITALIMFOS STANDARD
DITALIMFOS PESTANAL
ditalimfos (bsi,iso,ansi)
Ditalimfos Solution, 100ppm
Ditalimfos(100ug/mlinHexane)
Ditalimfos @100 μg/mL in MeOH
DitalimfosSolutions,100mg/L,1ml
o,o-diethylphthalimidothiophosphate
Diethyl phthalimidophosphonothioate
O,O-Diethyl phthalimidothiophosphate
O,O-Diaethyl-N-phtalimido-thiophosphat
O,O-DIETHYL PHTALIMIDOPHOSPHONOTHIOATE
O,O-DIETHYL PHTHALIMIDO-PHOSPHONOTHIOATE
O,O-Diethyl phthalimidophosphonothionate
Phthalimide, N-(diethoxyphosphinothioyl)-
2-diethoxyphosphinothioylisoindole-1,3-dione
2-diethoxythiophosphorylisoindoline-1,3-quinone
phosphonothioicacid,phthalimido-,o,o-diethylester
O,O-diethyl phthalimidophosphonothioate ditalimfos
Phosphonothioic acid, phthalimido-, O,O-diethyl ester
o,o-Diethyl 1,3-dioxo-1,3-dihydro-2H-isoindol-2-ylphosphonothioate
o,o-diethyl(1,2-dihydro-1,3-dioxo-2h-isoindol-2-yl)phosphonothioate
O,O-Diethyl (1,2-dihydro-1,3-dioxo-2H-isoindol-2-yl)phosphonothioate
O,O-Diethyl (1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)phosphonothioate
phosphonothioicacid,(1,2-dihydro-1,3-dioxo-2h-isoindol-2-yl)-,o,o-diethyl
Phosphonothioic acid, (1,2-dihydro-1,3-dioxo-2H-isoindol-2-yl)-, O,O-diethyl ester
Phosphonothioic acid, (1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-, O,O-diethyl ester
Phosphonothioic acid, P-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-, O,O-diethyl ester | [EINECS(EC#)]
225-875-8 | [Molecular Formula]
C12H14NO4PS | [MDL Number]
MFCD00055502 | [MOL File]
5131-24-8.mol | [Molecular Weight]
299.28 |
| Chemical Properties | Back Directory | [Melting point ]
85-86℃ | [Boiling point ]
400.3±28.0 °C(Predicted) | [density ]
1.38±0.1 g/cm3(Predicted) | [Fp ]
>100 °C | [storage temp. ]
APPROX 4°C
| [form ]
solid | [pka]
-3.08±0.20(Predicted) | [Water Solubility ]
133mg/L(room temperature) | [BRN ]
1542822 | [Henry's Law Constant]
2.3×103 mol/(m3Pa) at 25℃, Ebert et al. (2023) | [Major Application]
agriculture | [InChI]
1S/C12H14NO4PS/c1-3-16-18(19,17-4-2)13-11(14)9-7-5-6-8-10(9)12(13)15/h5-8H,3-4H2,1-2H3 | [InChIKey]
MTBZIGHNGSTDJV-UHFFFAOYSA-N | [SMILES]
CCOP(=S)(OCC)N1C(=O)c2ccccc2C1=O | [EPA Substance Registry System]
Ditalimfos (5131-24-8) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi,Xn,F | [Risk Statements ]
38-43-36-20/21/22-11 | [Safety Statements ]
36/37-16 | [RIDADR ]
UN2811 6.1/PG 3 | [WGK Germany ]
2 | [RTECS ]
TB2050000 | [HS Code ]
29337900 | [Storage Class]
3 - Flammable liquids | [Hazard Classifications]
Acute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Eye Irrit. 2
Flam. Liq. 2 | [Toxicity]
LD50 oral in rabbit: 1gm/kg |
| Hazard Information | Back Directory | [Uses]
Ditalimfos is an organophosphorus pesticide. | [Definition]
ChEBI: Ditalimfos is a member of isoindoles and a phthalimide fungicide. | [Production Methods]
Ditalimfos is commercially synthesised through esterification of phthalimidophosphonothioic acid with ethanol. The production process begins with the formation of phthalimidophosphonothioic acid, which involves reacting phthalic anhydride with aminothiophosphonic acid derivatives under controlled conditions. This intermediate is then esterified with ethanol or other short-chain alcohols in the presence of an acid catalyst to yield the diethyl ester form of ditalimfos. The reaction is typically conducted under reflux with solvent control to ensure high yield and purity. | [Mechanism of action]
Non-systemtic with protective and curative action. Thought to disrupt fungal respiration and growth. | [Pesticide Type]
Fungicide |
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