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经验公式(希尔记法):
C9H16ClN5
化学文摘社编号:
分子量:
229.71
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
217-618-3
Beilstein/REAXYS Number:
16028
MDL number:
产品名称
草达津, PESTANAL®, analytical standard
InChI key
HFBWPRKWDIRYNX-UHFFFAOYSA-N
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)
SMILES string
CCNc1nc(Cl)nc(n1)N(CC)CC
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
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相关类别
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.
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.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
农药列管产品
此项目有
Süleyman Aşır et al.
Electrophoresis, 36(23), 2888-2895 (2015-08-08)
Trietazine was selectively separated from aqueous solution containing the competitor molecule cyanazine, which is similar in size and shape to the template molecule. Structural features of the molecularly imprinted column were figured out by SEM. The influence of the mobile-phase
Determination of phenylurea and triazine herbicides in milk by microwave assisted ionic liquid microextraction high-performance liquid chromatography.
Gao S, et al.
Talanta, 82(4), 1371-1377 (2010)
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
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
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.
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