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Trietazin
PESTANAL®, analytical standard
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About This Item
Empirische Formel (Hill-System):
C9H16ClN5
CAS-Nummer:
Molekulargewicht:
229.71
Beilstein:
16028
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24
Empfohlene Produkte
Qualität
analytical standard
Qualitätsniveau
Produktlinie
PESTANAL®
Haltbarkeit
limited shelf life, expiry date on the label
Methode(n)
HPLC: suitable
gas chromatography (GC): suitable
Anwendung(en)
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)
InChIKey
HFBWPRKWDIRYNX-UHFFFAOYSA-N
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Allgemeine Beschreibung
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.
Anwendung
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.
Rechtliche Hinweise
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
Signalwort
Warning
H-Sätze
Gefahreneinstufungen
Acute Tox. 4 Oral - Aquatic Acute 1
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
dust mask type N95 (US), Eyeshields, Gloves
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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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