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关于此项目
经验公式(希尔记法):
C12H11Cl2N3O2
化学文摘社编号:
分子量:
300.14
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
41116107
EC Number:
262-102-3
MDL number:
产品名称
氧环唑, PESTANAL®, analytical standard
InChI key
AKNQMEBLVAMSNZ-UHFFFAOYSA-N
InChI
1S/C12H11Cl2N3O2/c13-9-1-2-10(11(14)5-9)12(18-3-4-19-12)6-17-8-15-7-16-17/h1-2,5,7-8H,3-4,6H2
SMILES string
Clc1ccc(c(Cl)c1)C3(Cn2cncn2)OCCO3
grade
analytical standard
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
application(s)
agriculture
environmental
format
neat
Quality Level
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相关类别
Application
Azaconazole, is an agricultural fungicide, which shows activity against wood destroying fungi and sapstain fungi. It can also play the role of a disinfectant in mushroom cultivation and in the storage of fruits and vegetables.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
General description
Azaconazole has been used as an internal standard in the determination of propiconazole, a fungistatic agent in white spruce, using gas chromatography/mass spectrometry (GC/MS).
Other Notes
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
农药列管产品
此项目有
G O Rankin et al.
Toxicology, 34(1), 1-11 (1985-01-01)
Azaconazole is an experimental agricultural fungicide which has shown promise for use in controlling powdery mildew on crops and bean rust. This study examined the nephrotoxic potential of a single intraperitoneal azaconazole injection (0.4 or 0.6 mmol/kg) or daily azaconazole
Roberts RT and Hutson HD
Metabolic Pathways of Agrochemicals: Herbicides and plant growth regulators; (1998)
Interaction of azole derivatives with cytochrome P-450 isozymes in yeast, fungi, plants and mammalian cells.
Bossche VH, et al.
Pest Management Science, 21.4, 289-306 (1987)
Raman microscopy for the quantitation of propiconazole in white spruce
Kurti E, et al.
Wood Science and Technology, 39.8, 618-629 (2005)
Bryce E Mansfield et al.
PLoS pathogens, 6(9), e1001126-e1001126 (2010-10-14)
Despite the wealth of knowledge regarding the mechanisms of action and the mechanisms of resistance to azole antifungals, very little is known about how the azoles are imported into pathogenic fungal cells. Here the in-vitro accumulation and import of Fluconazole
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