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46120

Supelco

Clomazone

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C12H14ClNO2
Número de CAS:
81777-89-1
Peso molecular:
239.70
Beilstein/REAXYS Number:
7480026
MDL number:
MFCD00072457
UNSPSC Code:
41116107
PubChem Substance ID:
329757073
NACRES:
NA.24

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

application(s)

agriculture
environmental

format

neat

storage temp.

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

InChI key

KIEDNEWSYUYDSN-UHFFFAOYSA-N

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Categorías relacionadas

Application


  • 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).

Legal Information

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

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

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

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

314.6 °F

flash_point_c

157 °C

ppe

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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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
Márcia Crestani et al.
Ecotoxicology and environmental safety, 65(1), 48-55 (2005-08-16)
The effects of clomazone (0.5 and 1.0 mg/L) according to nominal concentrations used in paddy rice fields (0.4-0.7 mg/L) on protein and carbohydrate metabolism and haematological parameters were evaluated in silver catfish (Rhamdia quelen) after 12, 24, 48, 96 and
Roberta Cattaneo et al.
Archives of environmental contamination and toxicology, 62(1), 97-106 (2011-04-22)
Field and laboratory experiments were performed to evaluate toxicological responses of Cyprinus carpio exposed to the commercial herbicide clomazone (500 mg l(-1)). Fish were exposed to 0.5 mg l(-1) of the formulated herbicide for 7, 30, and 90 days. Fish were exposed to clomazone in
Marc Clastre et al.
Experimental parasitology, 116(4), 375-384 (2007-04-03)
The apicoplast is a recently discovered, plastid-like organelle present in most apicomplexa. The methylerythritol phosphate (MEP) pathway involved in isoprenoid biosynthesis is one of the metabolic pathways associated with the apicoplast, and is a new promising therapeutic target in Plasmodium
Pedro M David Gara et al.
Photochemistry and photobiology, 85(3), 686-692 (2008-12-11)
The photodegradation of the herbicide clomazone in the presence of S(2)O(8) (2-) or of humic substances of different origin was investigated. A value of (9.4 +/- 0.4) x 10(8) m(-1) s(-1) was measured for the bimolecular rate constant for the
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