| Identification | More | [Name]
Diafenthiuron | [CAS]
80060-09-9 | [Synonyms]
1-tert-butyl-3-(2,6-diisopropyl-4-phenoxyphenyl)thiourea
3-(2,6-diisopropyl-4-phenoxyphenyl)-1-tert-butyl-thiourea
DIAFENTHIURON
PEGASUS
POLO
cga106630
n-(2,6-bis(1-methylethyl)-4-phenoxyphenyl)-n’-(1,1-dimethylethyl)-thioure
n-(2,6-bis(1-methylethyl)-4-phenoxyphenyl)-n’-(1,1-dimethylethyl)thiourea
DIAFENTHIURON PESTANAL, 250 MG
diafenthiuron (bsi, draft e-iso)
1-tert-bytyl-3-(2,6-di-iso-propyl-4-phenoxyphenyl) thiourea
3-tert-Butyl-1-(4-phenoxy-2,6-diisopropylphenyl)thiourea | [Molecular Formula]
C23H32N2OS | [MDL Number]
MFCD01311814 | [Molecular Weight]
384.58 | [MOL File]
80060-09-9.mol |
| Chemical Properties | Back Directory | [Melting point ]
144.6-147.7°C | [Boiling point ]
448.8±55.0 °C(Predicted) | [density ]
1.0367 (rough estimate) | [refractive index ]
1.5950 (estimate) | [Fp ]
149 °C | [storage temp. ]
0-6°C | [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
neat | [pka]
12?+-.0.70(Predicted) | [color ]
White to Off-White | [Water Solubility ]
Water: < 0.1 mg/mL (insoluble) | [Merck ]
13,2988 | [BRN ]
8343025 | [Major Application]
agriculture
environmental | [InChI]
1S/C23H32N2OS/c1-15(2)19-13-18(26-17-11-9-8-10-12-17)14-20(16(3)4)21(19)24-22(27)25-23(5,6)7/h8-16H,1-7H3,(H2,24,25,27) | [InChIKey]
WOWBFOBYOAGEEA-UHFFFAOYSA-N | [SMILES]
CC(C)c1cc(Oc2ccccc2)cc(C(C)C)c1NC(=S)NC(C)(C)C | [CAS DataBase Reference]
80060-09-9(CAS DataBase Reference) | [EPA Substance Registry System]
80060-09-9(EPA Substance) |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H332 | [Precautionary statements ]
P261-P271-P304+P340+P312 | [Hazard Codes ]
Xn | [Risk Statements ]
R20:Harmful by inhalation. | [Safety Statements ]
S22:Do not breathe dust . | [RIDADR ]
UN 2811 | [WGK Germany ]
2 | [RTECS ]
XN9100000 | [HazardClass ]
6.1(a) | [PackingGroup ]
II | [HS Code ]
29309090 | [Storage Class]
6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects | [Hazard Classifications]
Acute Tox. 3 Inhalation
Aquatic Acute 1
Aquatic Chronic 1
STOT RE 2 | [Toxicity]
LD50 in rats (mg/kg): 2068 orally; >2000 dermally; LC50 (14 hr) in rats: 558 mg/m3 by inhalation (Streibert, 1988) |
| Hazard Information | Back Directory | [Description]
Diafenthiuron is a broad spectrum acaricide and insecticide, diafenthiuron is registered for use on cotton, soybeans, vegetables, fruit and ornamentals. It controls all post-hatch stages of mites, whiteflies and aphids. Its ability to control all sucking pests of cotton as well as mites, with no known toxicity to beneficial insects, is unique and very valuable in cotton integrated pest management (IPM) programs. | [Uses]
Diafenthiuron is an insecticide. | [Definition]
ChEBI: Diafenthiuron is an aromatic ether that is 1,3-diisopropyl-5-phenoxybenzene in which the hydrogen atom at position 2 is substituted by a (tert-butylcarbamothioyl)nitrilo group. An agricultural proinsecticide which is used to control mites, aphids and whitefly in cotton. It has a role as an oxidative phosphorylation inhibitor and a proinsecticide. It is a thiourea acaricide, a thiourea insecticide and an aromatic ether. It is functionally related to a diphenyl ether. | [Production Methods]
Diafenthiuron is commercially produced through a multi-step synthesis that begins with the preparation of key intermediates such as 2,6-diisopropyl-4-phenoxyaniline. This compound undergoes a condensation reaction with tert-butyl isothiocyanate to form the final active ingredient. | [Toxicology]
Diafenthiuron has low toxicity to birds, mammals and beneficial insects, and is only slightly toxic to predatory mites. It is toxic to fish, but presents little hazard because it is rapidly degraded. | [Mode of action]
Diafenthiuron is a proinsecticide, which means that it must be converted to another compound – the drug – in order to be toxic. Activation of diafenthiuron to its carbodiimide drug occurs on the leaf surface, catalyzed by light, or in the insect, catalyzed by P450 monooxygenases. Diafenthiuron carbodiimide binds to the glutamate residue in the transmembrane F0 subunit of ATP synthase where protons from the intermembrane space dock to begin their journey across the inner mitochondrial membrane. Binding of diafenthiuron carbodiimide to this site blocks proton transport and ATP synthesis. Diafenthiuron was launched in 1991 and resistance has not yet been reported. | [Pesticide Type]
Insecticide; Acaricide; Miticide |
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| Company Name: |
J & K SCIENTIFIC LTD.
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| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
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