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Pirimicarb

PESTANAL®, analytical standard

Synonyme(s) :

2-Dimethylamino-5,6-dimethyl-4-pyrimidinyl dimethylcarbamate

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About This Item

Formule empirique (notation de Hill):
C11H18N4O2
Numéro CAS:
23103-98-2
Poids moléculaire :
238.29
Numéro Beilstein :
663442
Numéro CE :
245-430-1
Numéro MDL:
MFCD00055520
Code UNSPSC :
41116107
ID de substance PubChem :
329756842
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Gamme de produits

PESTANAL®

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Application(s)

agriculture
environmental

Format

neat

Chaîne SMILES 

CN(C)C(=O)Oc1nc(nc(C)c1C)N(C)C

InChI

1S/C11H18N4O2/c1-7-8(2)12-10(14(3)4)13-9(7)17-11(16)15(5)6/h1-6H3

Clé InChI

YFGYUFNIOHWBOB-UHFFFAOYSA-N

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Catégories apparentées

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Informations légales

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

Produit(s) apparenté(s)

Réf. du produit
Description
Tarif

Pictogrammes

Skull and crossbonesHealth hazardEnvironment
GHS06,GHS08,GHS09

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Skin Sens. 1

Code de la classe de stockage

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Choose from one of the most recent versions:

Certificats d'analyse (COA)

Lot/Batch Number
BCCL4153
BCCK5301
BCBZ9642
BCBW4813
BCBW3080

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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Fabienne Dulin et al.
Parasitology research, 113(12), 4601-4610 (2014-11-02)
Varroa destructor is the main concern related to the gradual decline of honeybees. Nowadays, among the various acaricides used in the control of V. destructor, most presents increasing resistance. An interesting alternative could be the identification of existent molecules as
Andrea X Silva et al.
PloS one, 7(6), e36366-e36366 (2012-06-12)
Insecticide resistance is one of the best examples of rapid micro-evolution found in nature. Since the development of the first synthetic insecticide in 1939, humans have invested considerable effort to stay ahead of resistance phenotypes that repeatedly develop in insects.
Anneli Widenfalk et al.
Environmental pollution (Barking, Essex : 1987), 152(3), 576-584 (2007-09-08)
A freshwater sediment was exposed to the pesticides captan, glyphosate, isoproturon, and pirimicarb at environmentally relevant and high concentrations. Effects on sediment microorganisms were studied by measuring bacterial activity, fungal and total microbial biomass as community-level endpoints. At the sub-community
Guowen Zhang et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 78(2), 687-694 (2010-12-24)
The interaction between pirimicarb and calf thymus DNA in physiological buffer (pH 7.4) was investigated with the use of Neutral Red (NR) dye as a spectral probe by UV-vis absorption, fluorescence and circular dichroism (CD) spectroscopy, as well as viscosity
Andrea X Silva et al.
PloS one, 7(6), e36810-e36810 (2012-06-12)
Among herbivorous insects that have exploited agro-ecosystems, the peach-potato aphid, Myzus persicae, is recognized as one of the most important agricultural pests worldwide. Uses over 400 plant species and has evolved different insecticides resistance mechanisms. As M. persicae feeds upon
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