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Merck

34045

Supelco

氧环唑

PESTANAL®, analytical standard

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

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About This Item

经验公式(希尔记法):
C12H11Cl2N3O2
CAS号:
分子量:
300.14
EC號碼:
MDL號碼:
分類程式碼代碼:
41116107
PubChem物質ID:
NACRES:
NA.24

等級

analytical standard

品質等級

產品線

PESTANAL®

儲存期限

limited shelf life, expiry date on the label

技術

HPLC: suitable
gas chromatography (GC): suitable

應用

agriculture
environmental

格式

neat

SMILES 字串

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 密鑰

AKNQMEBLVAMSNZ-UHFFFAOYSA-N

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相关类别

一般說明

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).

應用

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.

推薦產品

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.

法律資訊

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

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

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


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分析证书(COA)

Lot/Batch Number

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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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