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Merck
CN

36587

Propazine solution

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

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About This Item

Empirical Formula (Hill Notation):
C9H16ClN5
CAS Number:
139-40-2
Molecular Weight:
229.71
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329755410
EC Number:
200-659-6
Beilstein/REAXYS Number:
747081
MDL number:
MFCD00047341

Key Documents

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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

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

WGK 2

flash_point_f

51.8 °F

flash_point_c

11 °C

ppe

Eyeshields, Faceshields, Gloves

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCBS2259V

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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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