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Merck

31761

Supelco

Trietazin

PESTANAL®, analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C9H16ClN5
Número de CAS:
Peso molecular:
229.71
Beilstein/REAXYS Number:
16028
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(Cl)nc(n1)N(CC)CC

InChI

1S/C9H16ClN5/c1-4-11-8-12-7(10)13-9(14-8)15(5-2)6-3/h4-6H2,1-3H3,(H,11,12,13,14)

InChI key

HFBWPRKWDIRYNX-UHFFFAOYSA-N

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General description

Trietazine is a triazine herbicide primarily applied as pre- and post- emergent chemical for the control of annual and perennial grass and broad-leaved weeds.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Trietazine may be used as a herbicide reference standard for the determination of the analyte:
  • In milk samples based on microwave-assisted ionic liquid microextraction (MAILME) coupled with high-performance liquid chromatography (HPLC).
  • In traditional Chinese medicines (TCMs) by liquid chromatography combined with ultra fast electrospray ionization tandem mass spectrometry (UFLC-ESI-MS/MS) method.

Legal Information

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

pictograms

Exclamation markEnvironment

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Certificados de análisis (COA)

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Visite la Librería de documentos

Sung-Ben Huang et al.
Journal of agricultural and food chemistry, 54(3), 713-719 (2006-02-02)
A method is reported for the determination of atrazine, simazine, and their respective dealkylated chlorotriazine metabolites in ground, surface, and finished drinking water. Water samples are diluted 1:4 in an injection vial prior to analysis using liquid chromatography/electrospray ionization-mass spectrometry/mass
B A Kurliandskiĭ et al.
Gigiena truda i professional'nye zabolevaniia, (3)(3), 15-18 (1990-01-01)
The article presents research data related to the biotransformation, intoxication mechanisms and pathogenic properties of chlortriazine dye-stuffs. All the dye-stuffs studies were characterized by similar intoxication properties and pathogenesis, and were related to the 3rd class of hazardous substances. The
Tami S McMullin et al.
Toxicology in vitro : an international journal published in association with BIBRA, 21(3), 492-501 (2006-12-26)
This study estimated the kinetic constants for oxidative metabolism of atrazine (ATRA) and its chlorotriazine (Cl-TRI) metabolites, 2-chloro-4-ethylamino-6-amino-1,3,5-triazine (ETHYL), 2-chloro-4-amino-6-isopropylamino-1,3,5-triazine (ISO), and diaminochlorotriazine (DACT), using freshly isolated rat hepatocytes. Hepatocytes were incubated with 1.74, 44, 98, and 266 microM ATRA.
Susan C Laws et al.
Toxicological sciences : an official journal of the Society of Toxicology, 112(1), 78-87 (2009-08-20)
Previously, we reported that atrazine (ATR) alters steroidogenesis in male Wistar rats resulting in elevated serum corticosterone (CORT), progesterone, and estrogens. The increase in CORT indicated that this chlorotriazine herbicide may alter the hypothalamic-pituitary-adrenal axis. This study characterizes the temporal
Determination of triazine herbicides and their metabolites in multiple medicinal parts of traditional Chinese medicines using streamlined pretreatment and UFLC-ESI-MS/MS.
Liu C, et al.
Chemosphere, 190(4), 103-113 (2018)

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