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Supelco

Propazine

PESTANAL®, analytical standard

Synonym(s):

2,4-Bis(isopropylamino)-6-chloro-1,3,5-triazine

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About This Item

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

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable
solid phase extraction (SPE): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

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

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General description

Propazine is a triazine herbicide, used in controlling broad-leaved weeds and annual grasses in sweet sorghum.
Propazine is a triazine herbicide, used in controlling broad-leaved weeds and annual grasses in sweet sorghum.

Application

Propazine may be used as a reference standard for the determination of propazine in water samples using enzyme-linked Immunosorbent assay (ELISA) and gas chromatography-mass spectrometry detection (GC-MS).
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

Pictograms

Health hazardEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Enzyme-linked immunosorbent assay compared with gas chromatography/mass spectrometry for the determination of triazine herbicides in water.
Thurman ME, et al.
Analytical Chemistry, 62(18), 2043-2048 (1990)
Pesticide Profiles: Toxicity, Environmental Impact, and Fate (1997)
Pesticide Profiles: Toxicity, Environmental Impact, and Fate (1997)
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:
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

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