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Supelco

Propham -Lösung

100 μg/mL in methanol, PESTANAL®, analytical standard

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About This Item

CAS-Nummer:
122-42-9
Beilstein:
2209666
EG-Nummer:
200-659-6
MDL-Nummer:
MFCD00026382
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329757007
NACRES:
NA.24

Qualität

analytical standard

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Konzentration

100 μg/mL in methanol

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

agriculture

Format

single component solution

Lagertemp.

2-8°C

SMILES String

CC(C)OC(=O)Nc1ccccc1

InChI

1S/C10H13NO2/c1-8(2)13-10(12)11-9-6-4-3-5-7-9/h3-8H,1-2H3,(H,11,12)

InChIKey

VXPLXMJHHKHSOA-UHFFFAOYSA-N

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

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Zielorgane

Eyes

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 1

Flammpunkt (°F)

49.5 °F - closed cup

Flammpunkt (°C)

9.7 °C - closed cup

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
BCBT9431
SZBE129XV
SZBA200X
2158X
6300X

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Die Dokumentenbibliothek aufrufen

H Beernaert et al.
Zeitschrift fur Lebensmittel-Untersuchung und -Forschung, 193(5), 433-435 (1991-11-01)
This study describes a gas chromatographic method for the quantitative determination of residual propham and chlorpropham in potatoes. Both herbicides are extracted from the foodstuff with methylene chloride. After centrifugation and concentration, propham and chlorpropham are quantitatively determined by gas
Ali Ozcan et al.
Chemosphere, 73(5), 737-744 (2008-07-31)
The removal of a carbamate herbicide, propham, from aqueous solution has been carried out by the electro-Fenton process. Hydroxyl radical, a strong oxidizing agent, was generated catalytically and used for the oxidation of propham aqueous solutions. The degradation kinetics of
Ali Ozcan et al.
Water research, 42(12), 2889-2898 (2008-04-02)
This study aims the removal of a carbamate herbicide, propham, from aqueous solution by direct electrochemical advanced oxidation process using a boron-doped diamond (BDD) anode. This electrode produces large quantities of hydroxyl radicals from oxidation of water, which leads to
D G Hoover et al.
Applied and environmental microbiology, 51(2), 226-232 (1986-02-01)
The rates of mineralization of nitrilotriacetic acid (NTA), 2,4-dichlorophenoxyacetic acid (2,4-D), p-nitrophenol, aniline, and isopropyl N-phenylcarbamate (IPC) at one or more concentrations ranging from 100 pg/ml to 1.0 microgram/ml were proportional to chemical concentrations in samples of three lakes. The
B Caporiccio et al.
Comptes rendus des seances de la Societe de biologie et de ses filiales, 175(4), 496-500 (1981-01-01)
The bibliographic data dealing with the acute toxicity of two phenylcarbamates, propham and chloropropham, are not very precise an often contradictory. This work is a restatement and also a demonstration of the high sensitivity of the aquatic animals that we
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