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Merck

CRM18124

Supelco

Mesotrion Metabolite AMBA

certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Sinónimos:

2-Amino-4-(methylsulfonyl)benzoic acid

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10 MG
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10 MG
US$ 96,50

About This Item

Fórmula empírica (notación de Hill):
C8H9NO4S
Número de CAS:
Peso molecular:
215.23
Número MDL:
Código UNSPSC:
41116107
NACRES:
NA.24

US$ 96,50

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grado

certified reference material
TraceCERT®

Nivel de calidad

Línea del producto

TraceCERT®

caducidad

limited shelf life, expiry date on the label

fabricante / nombre comercial

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Formato

neat

temp. de almacenamiento

−20°C

cadena SMILES

[S](=O)(=O)(C)c1cc(c(cc1)C(=O)O)N

InChI

1S/C8H9NO4S/c1-14(12,13)5-2-3-6(8(10)11)7(9)4-5/h2-4H,9H2,1H3,(H,10,11)

Clave InChI

KFOGGDGNOLZBNY-UHFFFAOYSA-N

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Descripción general

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com

AMBA (2-amino-4-methylsulfonylbenzoic acid) is one of the metabolites formed from biodegradation of parent Mesotrione. Mesotrione is a selective herbicide that belongs to the triketone family, developed for use in maize culture as a substitute for atrazine. It is used for pre- and post-emergence control of common broad-leaved weeds, primarily in corn (maize). It acts by inhibiting the p-hydroxyphenylpyruvate dioxygenase (HPPD) enzyme, thus, blocking the production of carotenoid pigments in susceptible plants.

Mesotrion is currently approved for its use in the European Union. Maximum residue levels (MRLs) have been set according to Reg (EU) 2017/626 for mesotrione for various products of plant and animal origin from 0.01 to 0.05 mg/kg. Compared to the parent compound, AMBA metabolite is more persistent in soil and possess greater toxicity in selected microorganisms.

Aplicación

The certified reference material (CRM) is intended to be used as a calibrant for chromatography and other analytical techniques. The CRM may also find following uses:
  • Study the biodegradation and toxicity of herbicide mixtures mesotrione, nicosulfuron, and S-metolachlor by a bacterial strain, Bacillus sp. Mes11
  • Isolation and characterization of a Bacillus sp. from cloud water for rapid biotransformation of mesotrione herbicide
  • Investigation of mesotrione biodegradation products by the bacterial strain Bacillus sp. 3B6 using liquid chromatography/electrospray ionization quadrupole time-of-flight mass spectrometry (LC/ESI-QTOF-MS)
  • Qualitative and quantitative metabolic profiling of mesotrione, by the bacterial strain Bacillus sp. 3B6 using NMR, LC-NMR, and LC-MS
  • Method development for the determination of the mesotrione and its two metabolites, MNBA and AMBA in rice, rice plants, rice hulls, water, and soil using UPLC and triple-quadrupole tandem mass spectrometry

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Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Información legal

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

Pictogramas

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Palabra de señalización

Warning

Clasificaciones de peligro

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Órganos de actuación

Respiratory system

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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S Durand et al.
Letters in applied microbiology, 43(2), 222-228 (2006-07-28)
The aim of this study was to find and characterize a fungal or bacterial strain capable of metabolizing mesotrione, a new selective herbicide for control of broad-leaved weeds in maize. This strain was isolated from cloud water and showed close
Pengqiang Du et al.
Food chemistry, 229, 260-267 (2017-04-05)
In this study, an efficient and fast method for the determination of the herbicide mesotrione and its two metabolites [4-methylsulfonyl-2-nitrobenzoic acid (MNBA) and 2-amino-4-methylsulfonylbenzoic acid (AMBA)] in rice, rice plants, rice hulls, water, and soil was developed, using ultra performance
Louis Carles et al.
Journal of hazardous materials, 354, 42-53 (2018-05-05)
The prediction of chemical mixture toxicity is a major concern regarding unintentional mixture of pesticides from agricultural lands treated with various such compounds. We focused our work on a mixture of three herbicides commonly applied on maize crops within a
Kassio Ferreira Mendes et al.
Environmental science and pollution research international, 24(9), 8425-8435 (2017-02-12)
The effects of mesotrione, S-metolachlor, and terbuthylazine, applied in mixture, on soil biodegradation remain insufficiently researched. However, herbicide mixtures have been a common practice in agricultural systems in the last years. Understanding the fate of soil-applied herbicides may help on
Stéphanie Durand et al.
Rapid communications in mass spectrometry : RCM, 20(17), 2603-2613 (2006-08-01)
The metabolic pathway involved in the biotransformation of the herbicide mesotrione by the bacterial strain Bacillus sp. 3B6 was investigated by a reliable liquid chromatography/electrospray ionization quadrupole time-of-flight mass spectrometry (LC/ESI-QTOF-MS) method. The LC/ESI-MS method, both in positive and negative

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