Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

46017

Supelco

Fenpropidin

PESTANAL®, analytical standard

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Empirical Formula (Hill Notation):
C19H31N
CAS Number:
67306-00-7
Molecular Weight:
273.46
Beilstein:
5336091
MDL number:
MFCD00242960
UNSPSC Code:
41116107
PubChem Substance ID:
329757057
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

CC(CN1CCCCC1)Cc2ccc(cc2)C(C)(C)C

InChI

1S/C19H31N/c1-16(15-20-12-6-5-7-13-20)14-17-8-10-18(11-9-17)19(2,3)4/h8-11,16H,5-7,12-15H2,1-4H3

InChI key

MGNFYQILYYYUBS-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

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

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Sens. 1B - STOT RE 2 - STOT SE 3

Target Organs

Central nervous system, Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCF5286
BCBS9747V
SZBF243XV
SZBB294XV
SZB7019XV

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.

Search for a COA

Already Own This Product?

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

Visit the Document Library

C Marcireau et al.
Current genetics, 22(4), 267-272 (1992-10-01)
We have transformed Saccharomyces cerevisiae with a genomic library contained in the replicative vector pFL44. The resulting transformants were screened for resistance to fenpropidin, a specific inhibitor of sterol 14-reductase. A plasmid was isolated that transformed yeast both to resistance
Carole Bedos et al.
Environmental science & technology, 44(7), 2522-2528 (2010-03-05)
Few data sets of pesticide volatilization from plants at the field scale are available. In this work, we report measurements of fenpropidin and chlorothalonil volatilization on a wheat field using the aerodynamic gradient (AG) method and an inverse dispersion modeling
Huiyu Zhao et al.
Ecotoxicology and environmental safety, 77, 52-56 (2011-11-15)
The residue levels and dissipation rate of fenpropidin in wheat and soil were investigated by LC-MS/MS and GC-MS, respectively. The dissipation rates of fenpropidin were described using first-order kinetics and its half-life ranged from 3.1 to 3.3 days in wheat
C C Steel
Journal of chromatography, 566(2), 435-443 (1991-05-31)
An enzyme assay for inhibitors of fungal sterol delta 14-reductase employing isocratic reversed-phase high-performance liquid chromatography is described. A Hypersil 5-microns octadecylsilyl (ODS) column (250 mm x 4.6 mm I.D.) was used and a mobile phase consisting of methanol-water-ethanol (86:4:10
Xin Liu et al.
Microbiology (Reading, England), 157(Pt 6), 1665-1675 (2011-03-26)
Fusarium graminearum, the causal agent of wheat head blight, shows intrinsic resistance to amine fungicides. It is commonly accepted that the amines target sterol C-14 reductase and sterol Δ(8)-Δ(7) isomerase of ergosterol biosynthesis, encoded by the genes ERG24 and ERG2
View All Related Papers

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