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Supelco

Ametryn

PESTANAL®, analytical standard

Synonym(s):

2-Ethylamino-4-isopropylamino-6-methylthio-1,3,5-triazine

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About This Item

Empirical Formula (Hill Notation):
C9H17N5S
CAS Number:
Molecular Weight:
227.33
Beilstein:
613099
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(NC(C)C)nc(SC)n1

InChI

1S/C9H17N5S/c1-5-10-7-12-8(11-6(2)3)14-9(13-7)15-4/h6H,5H2,1-4H3,(H2,10,11,12,13,14)

InChI key

RQVYBGPQFYCBGX-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.

Legal Information

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

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

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

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Renato Grillo et al.
Journal of hazardous materials, 186(2-3), 1645-1651 (2011-01-11)
The purpose of this work was to develop a modified release system for the herbicide ametryn by encapsulating the active substance in biodegradable polymer microparticles produced using the polymers poly(hydroxybutyrate) (PHB) or poly(hydroxybutyrate-valerate) (PHBV), in order to both improve the
Dimuth Navaratna et al.
Bioresource technology, 113, 191-200 (2012-01-17)
A lab-scale membrane bioreactor (MBR) was used to remove Ametryn from synthetic wastewater. It was found that concentrations of MLSS and extra-cellular polymeric substances (EPS) in MBR mixed liquor fluctuated (production and decay) differently for about 40 days (transition period)
Nai-Yun Gao et al.
Journal of hazardous materials, 164(2-3), 640-645 (2008-10-01)
Ultraviolet (UV) irradiation (253.7nm) in the presence of hydrogen peroxide (H(2)O(2)) was used to decompose aqueous ametryn. The concentrations of ametryn were measured with time under various experiment conditions. The investigated factors included H(2)O(2) dosages, initial pH, initial ametryn concentrations
Bin Xu et al.
Journal of hazardous materials, 169(1-3), 586-592 (2009-05-09)
The chemical oxidation of the herbicide ametryn was investigated by aqueous chlorination between pH 4 and 10 at a temperature of 25 degrees C. Ametryn was found to react very rapidly with aqueous chlorine. The reaction kinetics can be well
Djavanshir Djozan et al.
Journal of chromatography. A, 1216(12), 2211-2219 (2009-02-03)
A monolithic ametryn molecular-imprinted polymer based on a simple polymerization method was fabricated for use as new solid-phase microextraction (SPME) fiber, which can be coupled with GC and GC/MS for selective extraction and analysis of triazine herbicides. Methacrylic acid (MAA)

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