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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:
200-659-6
Beilstein/REAXYS Number:
747081
MDL number:
InChI key
WJNRPILHGGKWCK-UHFFFAOYSA-N
InChI
1S/C9H16ClN5/c1-5(2)11-8-13-7(10)14-9(15-8)12-6(3)4/h5-6H,1-4H3,(H2,11,12,13,14,15)
SMILES string
CC(C)Nc1nc(Cl)nc(NC(C)C)n1
grade
analytical standard
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
concentration
100 μg/mL in methanol
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
application(s)
agriculture
cleaning products
cosmetics
food and beverages
personal care
format
single component solution
storage temp.
2-8°C
General description
用于 Supelco MIP SPE 滤芯的标准品。欲知更多信息,请索取 Supelco 资料 T407075、T706023
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
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1
target_organs
Eyes
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
51.8 °F
flash_point_c
11 °C
ppe
Eyeshields, Faceshields, Gloves
法规信息
危险化学品
此项目有
R Carabias-Martínez et al.
Journal of chromatography. A, 1122(1-2), 194-201 (2006-05-13)
A method of capillary electrophoresis (CE) for the determination of triazine herbicides and some of their main metabolites in water samples has been developed. The proposed CE method includes an off-line solid-phase extraction (SPE) procedure with LiChrolut EN sorbent coupled
A Ghauch et al.
Chemosphere, 41(12), 1835-1843 (2000-11-04)
Atrazine, propazine and simazine were tested separately and in mixture by batch procedure in a laboratory-constructed apparatus. 3.75 l of a buffered s-triazines pesticide solution was treated at room temperature by 325-mesh zero-valent iron powder (ZVIP) (20 g/l). High performance
N Hanioka et al.
Toxicology and applied pharmacology, 156(3), 195-205 (1999-05-01)
The in vitro metabolism of chlorotriazines, simazine (SIZ), atrazine (ATZ), and propazine (PRZ) was studied using control, 3-methylcholanthrene-, phenobarbital-, pyridine-, dexamethasone-, and clofibrate-treated rat liver microsomes. The metabolites were determined by HPLC. The principal reactions by cytochrome P450 (P450) system
"Does atrazine transform to propazine in aquatic sediments?": Comment on "biological and chemical transformations of atrazine in coastal aquatic sediments" by Kelly L. Smalling and C. Marjorie Aelion [Chemosphere 62 (2006) 188-196].
E Michael Thurman
Chemosphere, 65(8), 1440-1441 (2006-06-10)
Rita Carabias-Martínez et al.
Electrophoresis, 27(2), 423-432 (2005-12-13)
CE in nonaqueous media was used to study the migrating behavior of two weakly basic s-triazine pesticides and one of their metabolites. The target pesticides were selected to be representative for each of the two main groups: propazine and deethylatrazine
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