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Merck
CN

45883

异丙甲草胺 溶液

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

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经验公式(希尔记法):
C15H22ClNO2
化学文摘社编号:
分子量:
283.79
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
200-835-2
Beilstein/REAXYS Number:
8396147
MDL number:
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InChI key

WVQBLGZPHOPPFO-UHFFFAOYSA-N

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

SMILES string

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

grade

analytical standard

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

Quality Level

相关类别

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

signalword

Danger

Hazard Classifications

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

存储类别

3 - Flammable liquids

wgk

WGK 2

flash_point_f

35.6 °F - closed cup

flash_point_c

2 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

农药列管产品
危险化学品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
Megha Thakkar et al.
Aquatic toxicology (Amsterdam, Netherlands), 126, 198-206 (2012-12-12)
Metolachlor, a chloroacetanilide herbicide, has been frequently detected in coastal waters. This study examined the growth, photosynthesis, and detoxification responses of chlorophyte Dunaliella tertiolecta (DT) and brown tide alga Aureococcus anophagefferens (AA) upon 5-day exposure to 0.5-5 mg L(-1) metolachlor.
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
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

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