Skip to Content
Merck
All Photos(2)

Documents

32461

Supelco

Ametoctradin

PESTANAL®, analytical standard

Synonym(s):

5-Ethyl-6-octyl[1,2,4]triazolo[1,5-a]pyrimidin-7-amine

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C15H25N5
CAS Number:
Molecular Weight:
275.39
MDL number:
UNSPSC Code:
41116107
NACRES:
NA.24

grade

analytical standard

Quality Level

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

SMILES string

CCCCCCCCc1c(CC)nc2cnnn2c1N

InChI

1S/C15H25N5/c1-3-5-6-7-8-9-10-12-13(4-2)19-15-17-11-18-20(15)14(12)16/h11H,3-10,16H2,1-2H3

InChI key

GGKQIOFASHYUJZ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Ametoctradin is a novel triazolopyrimidine fungicide, considered as effective agricultural fungicide. It is also an oomycete-specific fungicide, as it is potent inhibitor of mitochondrial bc1 complex of oomycetes in mitochondrial respiration.

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

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Synthesis of Ametoctradin and Its Bioactivity.
Chai, B. S., et al.
Agrochemicals, 51, 645-674 (2012)
Ametoctradin is a Potent Q o Site Inhibitor of the Mitochondrial Respiration Complex III
Zhu, Xiaolei, et al.
Journal of Agricultural and Food Chemistry, 63 (13), 3377-3386 (2015)
Binding of the respiratory chain inhibitor ametoctradin to the mitochondrial bc1 complex.
Fehr, Marcus, Antje Wolf, and Gerd Stammler
Pest Management Science, 72 (3), 591-602 (2016)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service