DINOBUTON

DINOBUTON Basic information
Product Name:DINOBUTON
Synonyms:ACREX;ACARELTE UO;2-SEC-BUTYL-4,6-DINITROPHENYLISO-PROPYLCARBONATE;TALAN;DRAWINOL;DINOBUTON;Dinobuton(content>10%);Dinobuton liquid(content>2%)
CAS:973-21-7
MF:C14H18N2O7
MW:326.3
EINECS:213-546-1
Product Categories:D;DAlphabetic;DID - DINPesticides;Dinitrophenol compounds;Fungicides;Pesticides;AcaricidesPesticides&Metabolites;Alpha sort;Pesticides&Metabolites
Mol File:973-21-7.mol
DINOBUTON Structure
DINOBUTON Chemical Properties
Melting point 61-62℃
Boiling point 464.35°C (rough estimate)
density 1.2731 (rough estimate)
refractive index 1.5110 (estimate)
Water Solubility Insoluble in water
form neat
Merck 13,3315
BRN 2065340
CAS DataBase Reference973-21-7
EPA Substance Registry SystemDinobuton (973-21-7)
Safety Information
Hazard Codes T,N
Risk Statements 25-50/53
Safety Statements 37-45-60-61
RIDADR 2779
WGK Germany 3
RTECS FF9100000
HazardClass 6.1(b)
PackingGroup III
HS Code 29209090
Hazardous Substances Data973-21-7(Hazardous Substances Data)
ToxicityLD50 in male, female rats (mg/kg): 59, 71 orally (Gaines)
MSDS Information
DINOBUTON Usage And Synthesis
UsesMiticide.
UsesDinobuton is a non-systemic fungicide, active against powdery mildews in apples, cotton and vegetables.
DefinitionChEBI: Dinobuton is a C-nitro compound.
Metabolic pathwayDinobuton is metabolised in plants and animals via common metabolic pathways. The primary reaction is hydrolytic cleavage of the carbonate-dinitrophenyl linkage to yield dinoseb. Further reduction of the nitro-groups of dinoseb yields the corresponding monoamino and diamino analogues. Acetylation and deamination via hydroxylation/ elimination, and oxidation of the sec-butyl moiety also occurred. N- and O-Conjugation as glucosides and glucuronides occurred in both plants and animals. The metabolic pathways of dinobuton are presented in Scheme 1.
DegradationThere is limited information on the hydrolytic stability of dinobuton (1). Marchenko and Vakulenko (1983) reported that the hydrolysis DT50 values of dinobuton in pH 2, 7 and 11 buffer solutions at 22 °C were 15 days, 17 days and 4 hours, respectively. In vitro studies showed the rapid hydrolysis of dinobuton to dinoseb [ 2-sec-butyl-4,6-dinitrophenol (2)] by tissue homogenates of spider mites and animal tissues. Once generated, dinoseb was stable to hydrolytic and photolytic degradation under acidic condition but was readily degraded under alkaline conditions (Brestkin et al., 1978; Molnar, 1935). Uncharacterised complex polar materials were reported as photodecomposition products of dinoseb (Matsuo and Casida, 1970). Grechko et al. (1986) reported that the DTW for dinobuton in aqueous solution under UV light irradiation (365 nm) was <30 min.
DINOBUTON Preparation Products And Raw materials
DINOBUTON 2-Methyl-6-nitroanisole Phenol, 2-amino-6-(1-methylethyl)- (9CI) Fast Scarlet RC Base 2-sec-Butylphenol DNPP 2-Methyl-4,6-dinitrophenol 5-NITRO-2-METHOXY-1-ISOPROPYLBENZOL 1-Methoxy-2,4-dinitrobenzene 2-ISOPROPYL-4-NITROPHENOL DINOSEB METHYL ETHER 1-ISOPROPYL-4-NITROBENZENE o-Anisidine, 3-isopropyl- (5CI) 2-METHYL-4,6-DINITROANISOLE 4-AMINO-2-ISOPROPYLANISOL METHYL ISOPROPYL CARBONATE 4-METHOXY-3-NITROANILINE 4,6-Dinitro-2-sec-butylphenol

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