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DINOCAP

Basic information Safety Supplier Related

DINOCAP Basic information

Product Name:
DINOCAP
Synonyms:
  • 2(OR 4)-ISO-OCTYL-4,6-(OR 2,6)-DINITROPHENYL 2-BUTENOATE
  • KARATHAN
  • KARATHANE
  • KARATHANE(R)
  • (RS)-2-(1-Methylheptyl)-4,6-dinitrophenyl crotonate
  • 2-(1-Methylheptyl)-4,6-dinitrophenyl (2E)-2-butenoate
  • 2-(1-METHYLHEPTYL)-4,6-DINITROPHENYL CROTONATE
  • 2-METHYLHEPTYL-4,6-DINITROPHENYL CROTONATE
CAS:
131-72-6
MF:
C18H24N2O6
MW:
364.39
EINECS:
679-522-1
Mol File:
131-72-6.mol
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DINOCAP Chemical Properties

Boiling point:
473.7±45.0 °C(Predicted)
Density 
1.175±0.06 g/cm3(Predicted)
vapor pressure 
7.5 x 10-5 Pa (25 °C)
storage temp. 
0-6°C
solubility 
DMSO (Slightly), Methanol (Slightly)
Water Solubility 
<0.1 mg l-1
form 
Oil
color 
Light yellow to yellow
LogP
6.477 (est)
EPA Substance Registry System
(E)-2-(1-Methylheptyl)-4,6-dinitrophenyl 2-butenoate (131-72-6)
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Safety Information

Hazard Codes 
T,N
Risk Statements 
61-20/22-38-43-48/22-50/53
Safety Statements 
53-36/37-45-60-61
RIDADR 
UN 3082 9 / PGIII
WGK Germany 
3
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DINOCAP Usage And Synthesis

Uses

Dinocap is a contact fungicide which provides both protective and curative activities against powdery mildews, fruit rots, stem rots, leaf spots, brown rots, etc., in a wide range of crops including pome fruits, stone fruits, citrus, vines, hops, ornamentals and berries.

Definition

ChEBI: 2,4-dinitro-6-(octan-2-yl)phenyl (E)-but-2-enoate is an enoate ester obtained by formal condensation of the carboxy group of 3-methylacrylic acid with the phenolic hydroxy group of 2,4-dinitro-6-(octan-2-yl)phenol. It is a C-nitro compound and an enoate ester.

Metabolic pathway

Dinocap is a mixture 2,4- and 2,6-dinitro isomers of octylphenyl crotonate. Limited data are available in the open literature. Information presented in this summary is abstracted from the data evaluation published by the Pesticide Safety Directorate (PSD). Degradation and metabolism studies were conducted mainly with the 2,4-dinitro isomer. Hydrolytic cleavage of the crotonate to yield the corresponding phenol is the primary pathway in soil, plants and animals. β-Hydroxylation and/or carboxylation of the octyl moiety is a minor pathway in animals (Scheme 1).

Degradation

The hydrolytic degradation of dinocap [1,(2,4-dinitro-6-octylphenyl crotonate)] was examined at 25 °C. The estimated DT50 values of [14C-phenyl]dinocap in pH 5, 7 and 9 buffer solution were 229 days, 56 days and 17 hours, respectively. Cleavage of the crotonate moiety yielded 2,4-dinitro-6-octylphenol(2) as the major product.

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