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Merck
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重要文件

45478

Supelco

乙嘧酚

PESTANAL®, analytical standard

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About This Item

經驗公式(希爾表示法):
C11H19N3O
CAS號碼:
分子量::
209.29
Beilstein:
882476
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

形式

neat

SMILES 字串

CCCCc1c(C)nc(NCC)nc1O

InChI

1S/C11H19N3O/c1-4-6-7-9-8(3)13-11(12-5-2)14-10(9)15/h4-7H2,1-3H3,(H2,12,13,14,15)

InChI 密鑰

BBXXLROWFHWFQY-UHFFFAOYSA-N

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相關類別

應用

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

法律資訊

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

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象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Dermal

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, Gloves


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分析證明 (COA)

Lot/Batch Number

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[Chromatographic determination of Milgo in water, soil, and plants].
A A Krasnykh et al.
Gigiena i sanitariia, (6)(6), 69-70 (1980-06-01)
P Proença et al.
Forensic science international, 133(1-2), 95-100 (2003-05-14)
Fenarimol (Rubigan) is a pyrimidine ergosterol biosynthesis inhibitor used as a systemic fungicide. The authors present a fatal fenarimol intoxication case analysed in the Forensic Toxicology Service of the National Institute of Legal Medicine. The results were used to compare
L J Fitzpatrick et al.
Journal of chromatography. A, 918(2), 429-433 (2001-06-16)
This paper assesses the effect of pressurised fluid extraction (PFE) on the recovery of bupirimate and its degradation product, ethirimol from a range of soil types. The analytes were extracted under standard conditions (pressure, 2000 p.s.i.; temperature, 100 degrees C;
Shagufta Khan et al.
Food chemistry, 199, 870-875 (2016-01-19)
In the present communication, a non-covalent fenarimol-imprinted polymer was synthesized by precipitation polymerization technique using methacrylic acid (MAA) as a functional monomer, ethylene glycol dimethacrylate (EGDMA) as a cross-linker, and azobisisobutyronitrile (AIBN) as an initiator in different porogenic solvent. Binding
Alexander I Vardavas et al.
Mutation research, 829-830, 26-32 (2018-05-01)
Imidacloprid (IMI) is a systemic, chloro-nicotinyl insecticide classified in Regulation N° 1272/2008 of the European Commision as "harmful if swallowed and very toxic to aquatic life, with long-lasting effects". IMI is metabolized in vitro both by aldehyde oxidase (AOX) (reduction)

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