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Merck

46120

Supelco

Clomazon

PESTANAL®, analytical standard

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100 MG
CHF 136.00

CHF 136.00


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100 MG
CHF 136.00

About This Item

Empirische Formel (Hill-System):
C12H14ClNO2
CAS-Nummer:
Molekulargewicht:
239.70
Beilstein:
7480026
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

CHF 136.00


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Qualität

analytical standard

Qualitätsniveau

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Anwendung(en)

agriculture
environmental

Format

neat

Lagertemp.

2-8°C

SMILES String

CC1(C)CON(Cc2ccccc2Cl)C1=O

InChI

1S/C12H14ClNO2/c1-12(2)8-16-14(11(12)15)7-9-5-3-4-6-10(9)13/h3-6H,7-8H2,1-2H3

InChIKey

KIEDNEWSYUYDSN-UHFFFAOYSA-N

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Anwendung


  • Ecological risk assessment of Clomazone in Northeast China: A study analyzed the presence and distribution of herbicide residues, including Clomazone, in soils across the Mollisols region, assessing their ecological risks. This research highlights the environmental impact of such herbicides and informs crop safety protocols and regulatory standards (Li et al., 2024).

  • Characterization of Clomazone sorption in agricultural soils: This research characterized the sorption behavior of Clomazone in various agricultural soils using different kinetic models, contributing to a better understanding of its environmental interactions and aiding in the improvement of its application strategies for effective weed control (Ðurović-Pejčev et al., 2023).

  • Bioassay assessment of water toxicity including Clomazone: A study utilized bioassays to assess the toxicity of water samples from Brazilian rural areas, implicating several contaminants including Clomazone. The findings are crucial for evaluating the safety of drinking water and the implications of herbicide runoff in agricultural settings (Brucker et al., 2021).

Rechtliche Hinweise

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

Piktogramme

Exclamation markEnvironment

Signalwort

Warning

Gefahreneinstufungen

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

314.6 °F

Flammpunkt (°C)

157 °C

Persönliche Schutzausrüstung

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


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Kunden haben sich ebenfalls angesehen

Márcia Crestani et al.
Chemosphere, 67(11), 2305-2311 (2007-02-07)
The effects of the herbicide, clomazone, on acetylcholinesterase (AChE), catalase and TBARS formation in teleost fish (Rhamdia quelen) were studied. The fish were exposed to 0.5 or 1.0 mg L(-1) of clomazone for 12, 24, 48, 96 and 192 h.
Sergiane Souza Caldas et al.
Analytica chimica acta, 665(1), 55-62 (2010-04-13)
In this study, a simple, rapid and efficient method has been developed for the extraction and preconcentration of different classes of pesticides, carbofuran (insecticide), clomazone (herbicide) and tebuconazole (fungicide) in aqueous samples by dispersive liquid-liquid microextraction (DLLME) coupled with liquid
Patrick L Tomco et al.
Pest management science, 68(8), 1141-1147 (2012-03-31)
Clomazone is a popular herbicide used on California rice fields and exhibits rapid anaerobic microbial degradation (t(1/2) = 7.9 days). To test the potential of direct and indirect photolytic degradation as a cofactor in the overall degradation rate, sacrificial time-series
Biljana F Abramović et al.
Chemosphere, 93(1), 166-171 (2013-06-19)
The photocatalytic degradation of the herbicide clomazone (0.05mM) in aqueous suspensions of TiO2 Degussa P25 was examined as a function of the different operational parameters. The optimum concentration of the catalyst was found to be 0.50mgmL(-1) under UV light at
Mei Han et al.
PloS one, 8(5), e62467-e62467 (2013-05-08)
In Catharanthus roseus, the monoterpene moiety exerts a strong flux control for monoterpene indole alkaloid (MIA) formation. Monoterpene synthesis depends on the methyl-D-erythritol 4-phosphate (MEP) pathway. Here, we have explored the regulation of this pathway in response to developmental and

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