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Pirimicarb

PESTANAL®, analytical standard

Synonym(e):

(2-Dimethylamino-5,6-dimethyl-4-pyrimidinyl)-dimethylcarbamat

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About This Item

Empirische Formel (Hill-System):
C11H18N4O2
CAS-Nummer:
23103-98-2
Molekulargewicht:
238.29
Beilstein:
663442
EG-Nummer:
245-430-1
MDL-Nummer:
MFCD00055520
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329756842
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Produktlinie

PESTANAL®

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

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

InChIKey

YFGYUFNIOHWBOB-UHFFFAOYSA-N

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Anwendung

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

Rechtliche Hinweise

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

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34209

Pirimicarb-d6, PESTANAL®, analytical standard

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

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

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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

Choose from one of the most recent versions:

Analysenzertifikate (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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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
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
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.
Frank Seitz et al.
Environmental toxicology and chemistry, 31(3), 518-523 (2011-12-16)
Titanium dioxide nanoparticles (nTiO₂) form reactive oxygen species (ROS) under irradiation by ultraviolet light (UV). This known photocatalytic activity may finally affect the presence and toxicity of organic environmental chemicals, which have not yet been studied at ambient UV intensity.
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