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Propamocarb

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C9H20N2O2
CAS Number:
24579-73-5
Molecular Weight:
188.27
Beilstein/REAXYS Number:
2080745
MDL number:
MFCD00078717
UNSPSC Code:
41116107
PubChem Substance ID:
329756852
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

storage temp.

2-8°C

SMILES string

CCCOC(=O)NCCCN(C)C

InChI

1S/C9H20N2O2/c1-4-8-13-9(12)10-6-5-7-11(2)3/h4-8H2,1-3H3,(H,10,12)

InChI key

WZZLDXDUQPOXNW-UHFFFAOYSA-N

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General description

Propamocarb is a systemic fungicide, widely used for greenhouse vegetables and agricultural commodities, which shows protective action against phycomycetous diseases (Phythium, Phytophthora spp.).

application

Propamocarb may be used as an analytical reference standard for the quantification of the analyte in vegetables and fruits samples using different chromatography techniques.
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

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk_germany

WGK 2

flash_point_f

212.0 °F

flash_point_c

> 100 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM1414
BCCK0091
BCCH0552
BCCG4029
BCBW7547

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Nilüfer Aydemir et al.
Toxicology letters, 147(1), 73-78 (2004-01-01)
In this study, we aimed to evaluate the genotoxic effects of fungicides fenarimol and propamocarb which are used to protect crops from fungi. For this reason, bone-marrow micronucleus and chromosome aberration tests were carried out in Swiss albino mice. Mice
J C Taylor et al.
Food additives and contaminants, 21(6), 572-577 (2004-06-19)
A simple, sensitive and reliable liquid chromatography-mass spectrometry method with direct injection of diluted samples is reported for the determination of propamocarb residues in wine. Red and white wines were diluted 40- and 20-fold, respectively, using water. Liquid chromatography was
Gabriele Schmuck et al.
Archives of toxicology, 78(6), 330-337 (2004-02-27)
Carbamates belonged to an older insecticide group, with propoxur being representative of this group. However, today carbamates with hormonal effects on insects, like fenoxycarb, or with fungicide properties, like propamocarb, are also used. The goal was a comparison of three
Sherif H Abd-Alrahman et al.
Bulletin of environmental contamination and toxicology, 89(2), 302-305 (2012-06-16)
Propamocarb-hydrochloride is a widely used fungicide around the world. The dissipation of propamocarb-hydrochloride in tomatoes, potatoes and cucumber were evaluated. QuEChERS methodology before quantification using HPLC-DAD was used. Preharvest interval and maximum residue limit were 4 days and 1.0 mg
Rui Zhang et al.
Acta biochimica et biophysica Sinica, 51(1), 88-96 (2018-12-14)
Propamocarb (PM) is a pesticide that is widely used to protect cucumbers and other plants from downy mildew. Recently, some studies indicated that PM exposure had potential toxic effects in animals. In this study, adult male zebrafish were exposed to
View All Related Papers

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