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33970

Supelco

Mepanipyrim

PESTANAL®, analytical standard

Synonym(e):

4-Methyl-N-phenyl-6-(1-propinyl)-2-pyrimidinamin

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About This Item

Empirische Formel (Hill-System):
C14H13N3
CAS-Nummer:
110235-47-7
Molekulargewicht:
223.27
EG-Nummer:
432-140-7
MDL-Nummer:
MFCD01656050
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329754711
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

CC#Cc1cc(C)nc(Nc2ccccc2)n1

InChI

1S/C14H13N3/c1-3-7-13-10-11(2)15-14(17-13)16-12-8-5-4-6-9-12/h4-6,8-10H,1-2H3,(H,15,16,17)

InChIKey

CIFWZNRJIBNXRE-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

Piktogramme

Health hazardEnvironment
GHS08,GHS09

Signalwort

Warning

H-Sätze

H351,H410

Gefahreneinstufungen

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

267.8 °F

Flammpunkt (°C)

131 °C

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
BCCH0493
BCCG4986
BCCD3770
BCBZ5180
SZBE094XV

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Die Dokumentenbibliothek aufrufen

Paola Calza et al.
Journal of chromatography. A, 1049(1-2), 115-125 (2004-10-27)
Mepanipyrim, a widely used pyrimidinic fungicide, has been photocatalytically degraded in aqueous solution on TiO2. The purpose of this study is to artificially produce degradation compounds similar to those formed in the environment. Numerous intermediates have been identified and characterised
M Terada et al.
The Journal of toxicological sciences, 23(3), 223-234 (1998-10-21)
Mepanipyrim, a new fungicide, was administered orally to rats, mice and dogs for 13 weeks to clarify its toxic profiles. Hepatotoxicities were observed characteristically in these species with high concentrations of mepanipyrim; more than 200 ppm in rats, more than
M Terada et al.
Toxicology and applied pharmacology, 154(1), 1-11 (1999-01-12)
We have previously reported that ingestion of mepanipyrim induces fatty liver in rats due to the inhibitory effect on the synthesis or secretion of hepatocytic very low density lipoproteins (VLDL). To clarify the mechanism by which mepanipyrim induces fatty liver
Virgínia C Fernandes et al.
Environmental science and pollution research international, 19(9), 4184-4192 (2012-05-09)
Pesticides are among the most widely used chemicals in the world. Because of the widespread use of agricultural chemicals in food production, people are exposed to low levels of pesticide residues through their diets. Scientists do not yet have a
Michiko Nakamura et al.
Bioscience, biotechnology, and biochemistry, 67(1), 139-150 (2003-03-07)
Mepanipyrim inhibited retrograde Golgi-to-ER trafficking induced by brefeldin A (BFA), nordihydroguaiaretic acid, clofibrate, and arachidonyltrifluoromethyl ketone in NRK and other types of cells, but did not inhibit anterograde trafficking of Golgi-resident proteins translocated to ER by BFA and newly synthesized
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