33970
嘧菌胺
PESTANAL®, analytical standard
别名:
4-甲基-N-苯基-6-(1-丙炔基)-2-嘧啶胺
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关于此项目
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:
产品名称
嘧菌胺, PESTANAL®, analytical standard
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
Toshihiro Nagata et al.
Pest management science, 60(4), 399-407 (2004-05-04)
A series of 2-anilinopyrimidines was prepared and their fungicidal activities against Botrytis cinerea Pers were examined. The activity fell sharply with any substitution on the anilinobenzene ring. Substituents at the 5-position of the pyrimidine ring greatly reduced the activity. Substituents
I Miura et al.
Bioscience, biotechnology, and biochemistry, 60(10), 1690-1697 (1996-10-01)
Mepanipyrim, N-(4-methyl-6-prop-1-ynylpyrimidin-2-yl)aniline, diminished the cell surface expression of envelope glycoproteins of Newcastle disease and vesicular stomatitis viruses at concentrations where their synthesis was not profoundly affected. Intoxication by diphtheria toxin and ricin and recycling of transferrin were not affected even
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