DINOCAP
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
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)
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
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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DINOCAP(131-72-6)Related Product Information
- 1-ISOPROPYL-4-NITROBENZENE
- DINOSEB ACETATE
- 2-METHYL-4,6-DINITROANISOLE
- 1-Methoxy-2,4-dinitrobenzene
- 2-sec-Butylphenol
- Fast Scarlet RC Base
- DINOCAP
- 2-Methyl-4,6-dinitrophenol
- 2,4-DINITROPHENETOLE
- 2-ISOPROPYL-6-NITROPHENOL
- DINOSEB METHYL ETHER
- ETHOXYPHENYLENE-2,4-DIAMINE
- 4,6-Dinitro-2-sec-butylphenol
- 4-METHOXY-3-NITROANILINE
- 2-(1-METHYLHEPTYL)-4,6-DINITROPHENYL CROTONATE,2-METHYLHEPTYL-4,6-DINITROPHENYL CROTONATE
- 2-NITROPHENYL ACETATE
- 4-(ALLYLOXY)ANILINE
- Phenol, 2-amino-6-(1-methylethyl)- (9CI)