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Merck
CN

37087

氟醚唑

PESTANAL®, analytical standard

别名:

(RS)-2-(2,4-Dichlorophenyl)-3-(1H-1,2,4-triazolyl)propyl 1,1,2,2-tetrafluoroethyl ether, (±)-1-[2-(2,4-Dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]-1H-1,2,4-triazole

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关于此项目

经验公式（希尔记法）:
C13H11Cl2F4N3O
化学文摘社编号:
112281-77-3
分子量:
372.15
NACRES:
NA.24
PubChem Substance ID:
329755623
UNSPSC Code:
41116107
EC Number:
407-760-6
MDL number:
MFCD01632314

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产品名称

氟醚唑, PESTANAL®, analytical standard

InChI key

LQDARGUHUSPFNL-UHFFFAOYSA-N

InChI

1S/C13H11Cl2F4N3O/c14-9-1-2-10(11(15)3-9)8(4-22-7-20-6-21-22)5-23-13(18,19)12(16)17/h1-3,6-8,12H,4-5H2

SMILES string

FC(F)C(F)(F)OCC(Cn1cncn1)c2ccc(Cl)cc2Cl

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
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

Quality Level

100

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相关类别

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

General description

Tetraconazole is a systemicbroad spectrum triazole fungicide, which can be used to control a large number of fungi like Ascomycetes, Basidiomycetes, and Deuteromycetes especially Sphaerotheca fuliginea on cucumber and Erysiphe graminis on wheat. It can be prepared, via stereoselective lipase-catalyzed hydrolysis of the racemic precursor (R,S)-2-(2,4-dichlorophenyl)-3-(1H-1,2,4-triazol-l-y1)-prop-l-yl acetate.

Legal Information

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

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

农药列管产品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
BCCN7933
BCCK3695
BCCJ8998
BCCD5820
BCBZ8225

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Chemoenzymic synthesis and biological activity of both enantiomeric forms of tetraconazole, a new antifungal triazole
Bianchi D, et al.
Journal of Agricultural and Food Chemistry, 39, 197-201 (1991)
Ultrastructural studies of the effects of tetraconazole on the barley-powdery mildew host pathogen complex
Maffi.D, et al.
Mycological research, 99, 799-805 (1995)

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