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45627

Supelco

Pirimicarb

PESTANAL®, analytical standard

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C11H18N4O2
CAS Number:
23103-98-2
Molecular Weight:
238.29
Beilstein:
663442
EC Number:
245-430-1
MDL number:
MFCD00055520
UNSPSC Code:
41116107
PubChem Substance ID:
329756842
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

SMILES string

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

InChI key

YFGYUFNIOHWBOB-UHFFFAOYSA-N

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Application

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

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Product No.
Description
Pricing

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

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

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)

Lot/Batch Number
BCCL4153
BCCK5301
BCBZ9642
BCBW4813
BCBW3080

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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.
Michael J Smirle et al.
Journal of economic entomology, 103(2), 374-378 (2010-05-01)
Green apple aphid, Aphis pomi De Geer, and Aphis spiraecola Patch (both Hemiptera: Aphididae), are sympatric aphid species that are pests of apples (Malus spp.) and other crops. A. spiraecola has been shown to be significantly more tolerant to several
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
Encarnación Rodríguez-Gonzalo et al.
Electrophoresis, 29(19), 4066-4077 (2008-10-30)
CZE was assayed for the separation of carbamate pesticides susceptible to protonation (Pirimicarb, Carbendazim). Different electrophoretic media with high organic contents were explored, adequate separation and resolution being achieved when a BGE based on ACN with acetic acid in the
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