CHEMICAL AND PHYSICAL PROPERTIES
Physical Description | White solid; [Merck Index] White crystalline solid; [MSDSonline] |
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Color/Form | White crystalline solid |
Melting Point | 116 °C |
Solubility | Solubility (g/L, 20 °C): hexane 0.057, n-octanol 1.4, methanol 20, toluene 55, acetone 86, ethyl acetate 130, acetonitrile 340, dichloromethane 400 |
Density | 1.33 |
Vapor Pressure | 8.3X10-13 mm Hg at 25 °C |
LogP | log Kow = 2.50 at 20 °C |
Stability/Shelf Life | Photostable. |
Decomposition | When heated to decomposition it emits toxic vapors of /nitrogen oxides/. |
Ionization Efficiency | Positive |
Collision Cross Section | 195.75 Ų [M+H]+ [CCS Type: TW] |
Kovats Retention Index | 3083 3047.2 3076.2 |
Other Experimental Properties | Color: Beige solid /Heritage fungicide/ |
Chemical Classes | Pesticides -> Fungicides |
SAFETY INFORMATION
Signal word | Danger |
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Pictogram(s) |
Skull and Crossbones Acute Toxicity GHS06 Environment GHS09 |
GHS Hazard Statements |
H331:Acute toxicity,inhalation H410:Hazardous to the aquatic environment, long-term hazard |
Precautionary Statement Codes |
P261:Avoid breathing dust/fume/gas/mist/vapours/spray. P271:Use only outdoors or in a well-ventilated area. P273:Avoid release to the environment. P391:Collect spillage. Hazardous to the aquatic environment P403+P233:Store in a well-ventilated place. Keep container tightly closed. |
COMPUTED DESCRIPTORS
Molecular Weight | 403.4 g/mol |
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XLogP3 | 3.7 |
Hydrogen Bond Donor Count | 0 |
Hydrogen Bond Acceptor Count | 8 |
Rotatable Bond Count | 8 |
Exact Mass | 403.11682065 g/mol |
Monoisotopic Mass | 403.11682065 g/mol |
Topological Polar Surface Area | 104 Ų |
Heavy Atom Count | 30 |
Formal Charge | 0 |
Complexity | 646 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 1 |
Undefined Bond Stereocenter Count | 0 |
Covalently-Bonded Unit Count | 1 |
Compound Is Canonicalized | Yes |
PRODUCT INTRODUCTION
description
Azoxystrobin is an aryloxypyrimidine having a 4,6-diphenoxypyrimidine skeleton in which one of the phenyl rings is cyano-substituted at C-2 and the other carries a 2-methoxy-1-(methoxycarbonyl)vinyl substituent, also at C-2. An inhibitor of mitochondrial respiration by blocking electron transfer between cytochromes b and c1, it is used widely as a fungicide in agriculture. It has a role as a mitochondrial cytochrome-bc1 complex inhibitor, a xenobiotic, an environmental contaminant, an antifungal agrochemical and a quinone outside inhibitor. It is a nitrile, an aryloxypyrimidine, an enoate ester, an enol ether, a methyl ester and a methoxyacrylate strobilurin antifungal agent.