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Supelco

Ethirimol

PESTANAL®, analytical standard

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About This Item

Empirische Formel (Hill-System):
C11H19N3O
CAS-Nummer:
23947-60-6
Molekulargewicht:
209.29
Beilstein:
882476
EG-Nummer:
245-949-3
MDL-Nummer:
MFCD00055519
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329756770
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

agriculture
environmental

Format

neat

SMILES String

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)

InChIKey

BBXXLROWFHWFQY-UHFFFAOYSA-N

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Anwendung

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

Rechtliche Hinweise

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

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

H-Sätze

H312

Gefahreneinstufungen

Acute Tox. 4 Dermal

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Analysenzertifikate (COA)

Lot/Batch Number
BCCK6073
BCBX5666
BCBV3230
SZBC048XV
SZB7318XV

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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
[Chromatographic determination of Milgo in water, soil, and plants].
A A Krasnykh et al.
Gigiena i sanitariia, (6)(6), 69-70 (1980-06-01)
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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