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Merck

45643

Supelco

Propineb

PESTANAL®, analytical standard

Synonym(e):

Zink-propylenbis-(dithiocarbamat)

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About This Item

Lineare Formel:
[C5H8N2S4Zn]n
CAS-Nummer:
Beilstein:
2360676
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Beschreibung

technical mixture

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Mol-Gew.

Mw 289.78 g/mol

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

agriculture
environmental

Format

neat

SMILES String

CC1CNC(=S)S[Zn]SC(=S)N1

InChI

1S/C5H10N2S4.Zn/c1-3(7-5(10)11)2-6-4(8)9;/h3H,2H2,1H3,(H2,6,8,9)(H2,7,10,11);/q;+2/p-2

InChIKey

KKMLIVYBGSAJPM-UHFFFAOYSA-L

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Allgemeine Beschreibung

Propineb belongs to the dithiocarbamates (DTCs) class of fungicides, widely used in agriculture and horticulture. It has an additional advantage of low production cost, broad-spectrum of chemical and biological reactivity.

Anwendung

Propineb may be used as an analytical reference standard for the quantification of the analyte in environmental samples and vegetable 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.

Empfohlene Produkte

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Rechtliche Hinweise

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Piktogramme

Health hazardEnvironment

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Aquatic Chronic 2 - STOT RE 2

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves


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Analysenzertifikate (COA)

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Kunden haben sich ebenfalls angesehen

Slide 1 of 5

1 of 5

Marina Marinovich et al.
Chemical research in toxicology, 15(1), 26-32 (2002-01-22)
Dithiocarbamates (DTCs) are used mainly in agriculture as pesticides and as alcohol deterrent drugs. Neurological complications as well as movement disorders characterized by plastic rigidity, muscle twitch and paralysis are the prevailing symptoms in chronically exposed animals and humans. We
A T Wojdyła
Communications in agricultural and applied biological sciences, 69(4), 705-715 (2005-03-11)
Chitosan, (Biochikol 020 PC) a potential elicitor of plant defence and also an active inhibitor of fungal growth was used in experiments. The compound was used at concentrations 0.01 to 0.2% as a plant spray for rose protection against Sphaerotheca
M Yaldiz et al.
Clinical and experimental obstetrics & gynecology, 27(3-4), 235-237 (2001-02-24)
The dithiocarbamates are known to cause dermatitis, conjunctivitis, rhinitis, pharyngitis and bronchitis in humans. The experimental group received Propineb (obtained from Bayer) concentrations of 400 ppm in distilled water five days a week (treatment time three weeks) administered orally by
Kelly Flampouri et al.
Talanta, 80(5), 1799-1804 (2010-02-16)
Two of the most important categories of pesticides used in agricultural practice are organophosphates and dithiocarbamates. Their extensive and inappropriate use has rendered their reliable monitoring at trace levels more and more necessary. This study presents the construction of a
E Deveci et al.
The Journal of toxicological sciences, 24(2), 79-85 (1999-06-01)
Dithiocarbamate propineb and maneb are organometal fungicides, which are widely used for the control of diseases in plants. Female Wistar rats were exposed orally to 200 and 400 ppm propineb (Zn-containing dithiocarbamate) and 250 ppm maneb (Mn-containing dithiocarbamate), from the

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