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Thifensulfuron-methyl

PESTANAL®, analytical standard

Synonyme(s) :

Harmony

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About This Item

Formule empirique (notation de Hill):
C12H13N5O6S2
Numéro CAS:
79277-27-3
Poids moléculaire :
387.39
Numéro Beilstein :
7448062
Numéro MDL:
MFCD00468118
Code UNSPSC :
41116107
ID de substance PubChem :
329757063
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Chaîne SMILES 

COC(=O)c1sccc1S(=O)(=O)NC(=O)Nc2nc(C)nc(OC)n2

InChI

1S/C12H13N5O6S2/c1-6-13-10(16-12(14-6)23-3)15-11(19)17-25(20,21)7-4-5-24-8(7)9(18)22-2/h4-5H,1-3H3,(H2,13,14,15,16,17,19)

Clé InChI

AHTPATJNIAFOLR-UHFFFAOYSA-N

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Description générale

Thifensulfuron-methyl belongs to the class of sulfonylurea pesticides, generally employed for controlling many grasses and broadleaved weed species, affecting cultivation of crops such as corn, potatoes, tomatoes, citrus, vines and rice.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Thifensulfuron-methyl may be used as an analytical reference standard for the quantification of the analyte in environmental matrices using various chromatography techniques.

Informations légales

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

Pictogrammes

Environment
GHS09

Mention d'avertissement

Warning

Mentions de danger

H410

Conseils de prudence

P273 - P391 - P501

Classification des risques

Aquatic Acute 1 - Aquatic Chronic 1

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves

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Certificats d'analyse (COA)

Lot/Batch Number
BCCJ8999
BCBZ1910
SZBD339XV
SZBD221XV
SZB8203XV

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Journal of Chromatography A, 855(2), 575-582 (1999)
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BMC oral health, 8, 5-5 (2008-02-13)
Xylitol chewing gum has been shown to reduce Streptococcus mutans levels and decay. Two studies examined the presence and time course of salivary xylitol concentrations delivered via xylitol-containing pellet gum and compared them to other xylitol-containing products. A within-subjects design
Qing-Zhi Zhu et al.
Environmental science & technology, 36(24), 5411-5420 (2003-01-11)
A molecularly imprinted polymer (MIP) was synthesized using the herbicide metsulfuron-methyl (MSM) as a template, 2-(trifluoromethyl)acrylic acid as a functional monomer, divinylbenzene as a cross-linker, and dichloromethane as a porogen. This polymer was used as a solid-phase extraction material for
Allan J Cessna et al.
Journal of environmental quality, 35(6), 2395-2401 (2006-10-31)
Sulfonylurea herbicides are applied at relatively low rates (3 to 40 g ha(-1)) to control weeds in a variety of crops across the Canadian prairies. Because of their high phytotoxicity and the likelihood of their transport in surface runoff, there
Cheng-gen Xie et al.
Luminescence : the journal of biological and chemical luminescence, 26(4), 271-279 (2010-07-16)
Uniform molecular imprinting microspheres were prepared using precipitation polymerization with thifensulfuron-methyl (TFM) as template, acrylamide as functional monomer and ethylene glycol dimethacrylate as cross-linker. TFM could be selectively adsorbed on the molecularly imprinted polymers (MIPs) matrix through the hydrogen bonding
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