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HomeProduct name listPyraclostrobin

Pyraclostrobin

Synonym(s):Methyl {2-[1-(4-chlorophenyl)-1H-pyrazol-3-yloxymethyl]phenyl}methoxycarbamate

  • CAS NO.:175013-18-0
  • Empirical Formula: C19H18ClN3O4
  • Molecular Weight: 387.82
  • MDL number: MFCD03792774
  • EINECS: 605-747-1
  • SAFETY DATA SHEET (SDS)
  • Update Date: 2024-12-18 14:07:02
Pyraclostrobin Structural

What is Pyraclostrobin?

The Uses of Pyraclostrobin

Pyraclostrobin is a fungicide for use in seed grass and food crops.

The Uses of Pyraclostrobin

Agricultural fungicide.

What are the applications of Application

Pyraclostrobin is a fungicide

Definition

ChEBI: Pyraclostrobin is a carbamate ester that is the methyl ester of [2-({[1-(4-chlorophenyl)-1H-pyrazol-3-yl]oxy}methyl)phenyl]methoxycarbamic acid. A fungicide used to control major plant pathogens including Septoria tritici, Puccinia spp. and Pyrenophora teres. It has a role as a mitochondrial cytochrome-bc1 complex inhibitor, a xenobiotic, an environmental contaminant and an antifungal agrochemical. It is a member of pyrazoles, a carbamate ester, an aromatic ether, a member of monochlorobenzenes, a methoxycarbanilate strobilurin antifungal agent and a carbanilate fungicide.

Agricultural Uses

Pyraclostrobin (trade names: Cabrio®, Headline®) primed the tobacco cv. Xanthi nc for more rapid accumulation of antimicrobial PR-1 defence proteins after infection with Tobacco mosaic virus and the wildfire pathogen Ps pv. tabaci. The Pyraclostrobininduced priming for enhanced PR-1 accumulation in response to pathogen attack was associated with enhanced disease resistance (Herms et al. 2002). The enhanced resistance to pathogenic viruses and bacteria in Pyraclostrobin-treated plants was also seen on various crops and ornamental plants in both the greenhouse and field (Koehle et al. 2003, 2006). It is interesting that in the field, Pyraclostrobin-induced priming was associated with enhanced resistance also to abiotic stresses, including drought. In addition, treatment with Pyraclostrobin increased crop yield in the field. Also, in various crops Pyraclostrobin and other strobilurin fungicides induce a ‘greening effect.’ The term refers to the phenomenon of delayed leaf senescence and an increased grain-filling period resulting in enhanced biomass and yield (Bartlett et al. 2002). Together, the findings made with Pyraclostrobin suggest that this chemistry, in addition to exerting direct antifungal activity, may also protect plants by priming them for a boosted activation of subsequently stress-induced defence responses. This conclusion is consistent with an earlier report demonstrating that another commercial fungicide, Oryzemate®, enhanced the resistance to Tobacco mosaic virus in tobacco (Koganezawa et al. 1998) and to a bacterial and an oomycete pathogen in Arabidopsis (Yoshioka et al. 2001). Oryzemate® contains Probenazole as the active ingredient which is metabolized to saccharin in treated plants (Koganezawa et al. 1998). The latter compound seems to elicit priming in Oryzemate®-treated plants (Siegrist et al. 1998).

Properties of Pyraclostrobin

Melting point: 63.7-65.2°
Boiling point: 501.1±60.0 °C(Predicted)
Density  1.27±0.1 g/cm3(Predicted)
storage temp.  0-6°C
solubility  DMSO: 250 mg/mL (644.63 mM)
form  neat
pka -0.23±0.10(Predicted)
form  Solid
color  Off-white to light yellow
Stability: Toxic
NIST Chemistry Reference Pyraclostrobine(175013-18-0)
EPA Substance Registry System Pyraclostrobin (175013-18-0)

Safety information for Pyraclostrobin

Signal word Danger
Pictogram(s)
ghs
Skull and Crossbones
Acute Toxicity
GHS06
ghs
Environment
GHS09
GHS Hazard Statements H315:Skin corrosion/irritation
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.
P264:Wash hands thoroughly after handling.
P264:Wash skin thouroughly after handling.
P271:Use only outdoors or in a well-ventilated area.
P273:Avoid release to the environment.
P302+P352:IF ON SKIN: wash with plenty of soap and water.

Computed Descriptors for Pyraclostrobin

InChIKey HZRSNVGNWUDEFX-UHFFFAOYSA-N

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