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Merck

45660

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:
1014-70-6
Molecular Weight:
213.30
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329756874
EC Number:
213-801-7
Beilstein/REAXYS Number:
11728
MDL number:
MFCD00078720

Key Documents

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Product Name

Simetryn, PESTANAL®, analytical standard

InChI key

MGLWZSOBALDPEK-UHFFFAOYSA-N

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)

SMILES string

CCNc1nc(NCC)nc(SC)n1

grade

analytical standard

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

Quality Level

100

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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.

Other Notes

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.

Legal Information

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

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

hcodes

H302,H410

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ1046
BCBW8487

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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
Russel C G Chidya et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 53(9), 602-614 (2018-07-24)
This study investigated spatio-temporal variations of selected pesticide residues in the Kurose River in Higashi-Hiroshima city (Hiroshima Prefecture), Japan. Water samples were collected from the river at seven sites every month for 1 year (March 2016 to February 2017). Pesticide residues
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
Haruyo Sambe et al.
Journal of chromatography. A, 1152(1-2), 130-137 (2006-09-27)
Uniformly-sized, molecularly imprinted polymers (MIPs) for atrazine, ametryn and irgarol were prepared by a multi-step swelling and polymerization method using ethylene glycol dimethacrylate as a cross-linker and methacrylic acid (MAA), 2-(trifluoromethyl) acrylic acid (TFMAA) or 4-vinylpyridine either as a functional
Md Abul Kashem et al.
Biosensors, 9(4) (2019-11-16)
A microalgae (Pseudokirchneriella subcapitata) biosensor chip for pesticide sensing has been developed by attaching the immobilized microalgae biofilm pon the microarray dye spots (size 100 μm and pitch 200 μm). The dye spots (ruthenium complex) were printed upon SO3-modified glass
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