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36587

Supelco

Propazine solution

100 μg/mL in methanol, PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C9H16ClN5
CAS Number:
Molecular Weight:
229.71
Beilstein/REAXYS Number:
747081
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

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

SMILES string

CC(C)Nc1nc(Cl)nc(NC(C)C)n1

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)

InChI key

WJNRPILHGGKWCK-UHFFFAOYSA-N

General description

Standard for Supelco MIP SPE cartridges. For more information request Supelco Literature 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

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

51.8 °F

flash_point_c

11 °C

ppe

Eyeshields, Faceshields, Gloves


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R Carabias-Martínez et al.
Journal of chromatography. A, 1085(2), 199-206 (2005-08-19)
A molecularly imprinted polymer (MIP) obtained by precipitation polymerisation using propazine as template has been employed as sorbent for the solid phase extraction of triazines and some of their hydroxylated and dealkylated metabolites from river water. Three configurations were studied:
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
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
L Guzzella et al.
Water science and technology : a journal of the International Association on Water Pollution Research, 57(1), 139-144 (2008-01-15)
A MIP (molecularly imprinted polymer) was synthesized and evaluated for its use as sorbent for solid phase extraction (MISPE) of common used triazines (atrazine and terbuthylazine) and their widespread metabolites (desethyl-atrazine and desethyl-terbuthylazine) in water samples. MIP was produced by
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

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