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经验公式(希尔记法):
C14H13N3
化学文摘社编号:
分子量:
223.27
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
41116107
EC Number:
432-140-7
MDL number:
InChI key
CIFWZNRJIBNXRE-UHFFFAOYSA-N
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)
SMILES string
CC#Cc1cc(C)nc(Nc2ccccc2)n1
grade
analytical standard
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
Quality Level
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相关类别
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
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
267.8 °F
flash_point_c
131 °C
ppe
Eyeshields, Faceshields, Gloves
法规信息
农药列管产品
此项目有
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
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.
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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