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45660

Supelco

Simetryn

PESTANAL®, analytical standard

Synonym(s):

2,4-Bis(ethylamino)-6-methylthio-1,3,5-triazine

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About This Item

Empirical Formula (Hill Notation):
C8H15N5S
CAS Number:
Molecular Weight:
213.30
Beilstein:
11728
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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

CCNc1nc(NCC)nc(SC)n1

InChI

1S/C8H15N5S/c1-4-9-6-11-7(10-5-2)13-8(12-6)14-3/h4-5H2,1-3H3,(H2,9,10,11,12,13)

InChI key

MGLWZSOBALDPEK-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Legal Information

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

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Lucas S Machado et al.
Journal of chromatography. A, 1651, 462260-462260 (2021-06-06)
Monolithic polymers are described as continuous and highly porous materials. They have been gaining popularity as an effective extracting phase for some sample preparation methods, due to their variety of functionalities, such as wide pH range tolerance, good permeability, and
G J Hughes et al.
The Biochemical journal, 199(1), 61-67 (1981-10-01)
Native rat haemoglobins were found to bind simetryn sulphoxide to an extent 40-fold greater than human haemoglobin. This specific behaviour was studied by using only high-pressure ('performance') liquid chromatography for the preparative separation of globin chains and the isolation of
Fate and behavior of herbicides, butachlor, CNP, chlomethoxynil, and simetryne in river water, shellfish, and sediments of the Ishikari River.
T Ohyama et al.
Bulletin of environmental contamination and toxicology, 39(4), 555-562 (1987-10-01)
Dang Thi Tuyet Nhung et al.
Chemosphere, 77(10), 1393-1399 (2009-10-09)
A set of packed micro paddy lysimeters, placed in a greenhouse, was used to simulate the dissipation of two herbicides, simetryn and thiobencarb, in a controlled environment. Data from a field monitoring study in 2003, including the soil condition and
Kosuke Nishi et al.
Journal of agricultural and food chemistry, 53(13), 5096-5104 (2005-06-23)
A monoclonal antibody (mab) selective for the thiomethyl-s-triazine herbicide simetryn was obtained and characterized in enzyme-linked immunosorbent assay (ELISA). An IC(50) value for simetryn was 8.5 ng/mL, and the detection range extended from 1.1 to 70 ng/mL in ELISA. The

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