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45883

Supelco

Metolachlor solution

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

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About This Item

Empirical Formula (Hill Notation):
C15H22ClNO2
CAS Number:
Molecular Weight:
283.79
Beilstein:
8396147
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

concentration

100 μg/mL in acetonitrile

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

single component solution

storage temp.

2-8°C

SMILES string

CCc1cccc(C)c1N(C(C)COC)C(=O)CCl

InChI

1S/C15H22ClNO2/c1-5-13-8-6-7-11(2)15(13)17(14(18)9-16)12(3)10-19-4/h6-8,12H,5,9-10H2,1-4H3

InChI key

WVQBLGZPHOPPFO-UHFFFAOYSA-N

Related Categories

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

Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

35.6 °F - closed cup

Flash Point(C)

2 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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J Restivo et al.
Journal of hazardous materials, 239-240, 249-256 (2012-09-27)
The catalytic ozonation of the herbicide metolachlor (MTLC) was tested using carbon nanomaterials as catalysts. Multiwalled carbon nanotubes were used in semi-batch experiments and carbon nanofibres grown on a honeycomb cordierite monolith were tested in continuous experiments. The application of
M T Moore et al.
Bulletin of environmental contamination and toxicology, 89(2), 292-295 (2012-06-02)
Phytotoxicity assessments were performed to compare responses of Typha latifolia (L.) seeds to atrazine (only) and atrazine + S-metolachlor exposure concentrations of 0.03, 0.3, 3, and 30 mg L(-1), as well as permethrin exposure concentrations of 0.008, 0.08, 0.8, and
Zisis Vryzas et al.
Chemosphere, 89(11), 1330-1338 (2012-06-29)
Biotransformation studies of atrazine, metolachlor and evolution of their metabolites were carried out in soils and subsoils of Northern Greece. Trace atrazine, its metabolites and metolachlor residues were detected in field soil samples 1 year after their application. The biotransformation
Yongnian Ni et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 97, 753-761 (2012-08-18)
Enantioselective binding interaction of the pesticides, metolachlor (RAC-metolachlor) and its S-enantiomer (S-metolachlor), with bovine serum albumin (BSA) was investigated by fluorescence and UV-vis absorption spectroscopy. Both RAC- and S-metolachlors quenched the intrinsic fluorescence of BSA via a static mechanism, and
Hui J Liu et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 47(5), 410-419 (2012-03-20)
The toxicity of Rac-metolachlor and S-metolachlor on rice (IIYou92, Oryza sativa L.) seedlings was determined and compared in a hydroponics experiment. The elongation of shoot, main root, and the number of lateral roots were inhibited in both Rac- and S-metolachlor

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