Merck
CN
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文件

安全信息

34045

Supelco

氧环唑

PESTANAL®, analytical standard

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别名:
1-[2-(2,4-二氯苯基)-1,3-二氧戊环-2-基甲基]-1H-1,2,4-三唑
经验公式（希尔记法）:
C12H11Cl2N3O2
CAS号:
60207-31-0
分子量:
300.14
EC 号:
262-102-3
MDL编号:
MFCD00865600
PubChem化学物质编号:
329754779
NACRES:
NA.24

等级

analytical standard

质量水平

100

产品线

PESTANAL®

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

应用

agriculture
environmental

格式

neat

SMILES字符串

Clc1ccc(c(Cl)c1)C3(Cn2cncn2)OCCO3

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

InChI key

AKNQMEBLVAMSNZ-UHFFFAOYSA-N

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相关类别

一般描述

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).

应用

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.

推荐产品

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.

法律信息

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H302

危险分类

Acute Tox. 4 Oral

储存分类代码

11 - Combustible Solids

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

法规信息

农药列管产品

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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
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)
Roberts RT and Hutson HD
Metabolic Pathways of Agrochemicals: Herbicides and plant growth regulators; (1998)
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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