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Propineb

PESTANAL®, analytical standard

Synonyme(s) :

Zinc propylenebis(dithiocarbamate)

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About This Item

Formule linéaire :
[C5H8N2S4Zn]n
Numéro CAS:
Numéro Beilstein :
2360676
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Description

technical mixture

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Poids mol.

Mw 289.78 g/mol

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Chaîne SMILES 

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

Clé InChI

KKMLIVYBGSAJPM-UHFFFAOYSA-L

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Description générale

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.

Application

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.

Produits recommandés

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.

Informations légales

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

Pictogrammes

Health hazardEnvironment

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Aquatic Chronic 2 - STOT RE 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves


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Certificats d'analyse (COA)

Lot/Batch Number

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Les clients ont également consulté

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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
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
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
Barbara Viviani et al.
Toxicology letters, 182(1-3), 63-68 (2008-09-30)
Neurological complications as well as movement disorders are relevant symptoms in animals and humans chronically exposed to dithiocarbamates. Using rat pheochromocytoma cells differentiated by NGF (PC12), we investigated whether propineb affects acetylcholine (Ach) release and the molecular mechanisms involved. Propineb

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