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Merck
CN

33970

Mepanipyrim

PESTANAL®, analytical standard

Synonym(s):

4-Methyl-N-phenyl-6-(1-propynyl)-2-pyrimidinamine

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About This Item

Empirical Formula (Hill Notation):
C14H13N3
CAS Number:
110235-47-7
Molecular Weight:
223.27
NACRES:
NA.24
PubChem Substance ID:
329754711
UNSPSC Code:
41116107
EC Number:
432-140-7
MDL number:
MFCD01656050

Key Documents

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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

100

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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

pictograms

Health hazardEnvironment
GHS08,GHS09

signalword

Warning

hcodes

H351,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

267.8 °F

flash_point_c

131 °C

ppe

Eyeshields, Faceshields, Gloves

Regulatory Information

农药列管产品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCH0493
BCCG4986
BCCD3770
BCBZ5180

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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
Thais Sieiro-Sampedro et al.
Food chemistry, 300, 125223-125223 (2019-07-31)
The impact of fungicides mepanipyrim (Mep) and tetraconazole (Tetra) and their corresponding commercial formulations (Mep-Form and Tetra-Form) on the aroma composition of wines was assessed. Fungicide residues can affect the biotransformation of aroma precursors from grapes and/or the yeast metabolism.
M Terada et al.
The Journal of toxicological sciences, 23(3), 235-241 (1998-10-21)
Our preceding paper reported that mepanipyrim, a new fungicide, induced fatty liver in the rat. This study was undertaken to examine this phenomenon further on hepatic triglyceride (TG) synthesis, on liver and serum lipid concentrations, and on concentration of serum
P Cabras et al.
Journal of agricultural and food chemistry, 47(9), 3854-3857 (1999-12-20)
The influence of six fungicides (azoxystrobin, cyprodinil, fludioxonil, mepanipyrim, pyrimethanil, and tetraconazole) on the fermentative activity of two yeasts (Saccharomyces cerevisiae and Kloeckeraapiculata) and two lactic bacteria (Leuconostoc oenos and Lactobacillus plantarum) was studied. The possibility of their being degraded
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
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