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131860-33-8

131860-33-8 structural image
Product Name: Azoxystrobin
Formula: C22H17N3O5
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CHEMICAL AND PHYSICAL PROPERTIES

Physical Description White solid; [Merck Index] White crystalline solid; [MSDSonline]
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
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
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.

RELATED SUPPLIERS

Indofil Industries Limited

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product:131860-33-8 Azoxystrobin 99%
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