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46028

Supelco

Thifensulfuron-methyl

PESTANAL®, analytical standard

Synonym(s):

Harmony

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About This Item

Empirical Formula (Hill Notation):
C12H13N5O6S2
CAS Number:
79277-27-3
Molecular Weight:
387.39
Beilstein:
7448062
MDL number:
MFCD00468118
UNSPSC Code:
41116107
PubChem Substance ID:
329757063
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

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)

InChI key

AHTPATJNIAFOLR-UHFFFAOYSA-N

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General description

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.

Legal Information

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

Pictograms

Environment
GHS09

Signal Word

Warning

Hazard Statements

H410

Precautionary Statements

P273 - P391 - P501

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

46028-1EA:
46028-BULK:
46028-VAR:
46028-100MG:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ8999
BCBZ1910
SZBD339XV
SZBD221XV
SZB8203XV

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Determination of sulfonylurea degradation products in soil by liquid chromatography-ultraviolet detection followed by confirmatory liquid chromatography-tandem mass spectrometry
Bossi R, et al.
Journal of Chromatography A, 855(2), 575-582 (1999)
Christine A Riedy et al.
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
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
J J Stry et al.
Journal of AOAC International, 83(3), 651-659 (2000-06-27)
Size-exclusion chromatography (SEC) was coupled to reversed-phase liquid chromatography/mass spectrometry for the determination of thifensulfuron-methyl and tribenuron-methyl in cottonseed and cotton gin trash. The limit of quantitation was 20 parts per billion (ppb), and the limit of detection was 6
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
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