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45898

Supelco

Propham solution

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

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About This Item

CAS Number:
122-42-9
Beilstein:
2209666
EC Number:
200-659-6
MDL number:
MFCD00026382
UNSPSC Code:
41116107
PubChem Substance ID:
329757007
NACRES:
NA.24

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

concentration

100 μg/mL in methanol

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture

format

single component solution

storage temp.

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)

InChI key

VXPLXMJHHKHSOA-UHFFFAOYSA-N

Application

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

Legal Information

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

Signal Word

Danger

Hazard Classifications

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

Target Organs

Eyes

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

49.5 °F - closed cup

Flash Point(C)

9.7 °C - closed cup

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Certificates of Analysis (COA)

Lot/Batch Number
BCBT9431
SZBE129XV
SZBA200X
2158X
6300X

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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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