U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C19H31N
Molecular Weight 273.4561
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FENPROPIDIN

SMILES

CC(CN1CCCCC1)CC2=CC=C(C=C2)C(C)(C)C

InChI

InChIKey=MGNFYQILYYYUBS-UHFFFAOYSA-N
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

HIDE SMILES / InChI

Molecular Formula C19H31N
Molecular Weight 273.4561
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Fenpropidin is a piperidine contact fungicide used to control a range of diseases in cereals. Example pests controlled: powdery mildew, rhynchosporium, brown and yellow rusts, leaf spots. Fenpropidin inhibits sterol biosynthesis in membranes. It is a specific inhibitor of sterol 14-reductase.

Approval Year

PubMed

PubMed

TitleDatePubMed
Pesticide cocktails can interact synergistically on aquatic crustaceans.
2010-05
Fungicide volatilization measurements: inverse modeling, role of vapor pressure, and state of foliar residue.
2010-04-01
Baseline sensitivity to proquinazid in Blumeria graminis f. sp. tritici and Erysiphe necator and cross-resistance with other fungicides.
2009-08
Investigations into the source of two fungicides measured in the air for 24 hours following application to a cereal crop.
2009
Performance of the Chemcatcher passive sampler when used to monitor 10 polar and semi-polar pesticides in 16 Central European streams, and comparison with two other sampling methods.
2008-05
Determination of 10 particle-associated multiclass polar and semi-polar pesticides from small streams using accelerated solvent extraction.
2008-02
Antifungals: need to search for a new molecular target.
2006-04-17
Molar absorptivities of 2,4-D, cymoxanil, fenpropidin, isoproturon and pyrimethanil in aqueous solution in the near-UV.
2006-01
Evidence of differences in the biotransformation of organic contaminants in three species of freshwater invertebrates.
2002
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:04:54 GMT 2025
Edited
by admin
on Mon Mar 31 22:04:54 GMT 2025
Record UNII
845XW54F31
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FENPROPIDIN
ISO   MI  
Common Name English
PATROL
Preferred Name English
FENPROPIDIN [ISO]
Common Name English
FENPROPIDIN [MI]
Common Name English
PIPERIDINE, 1-(3-(4-(1,1-DIMETHYLETHYL)PHENYL)-2-METHYLPROPYL)-
Systematic Name English
Code System Code Type Description
PUBCHEM
91694
Created by admin on Mon Mar 31 22:04:54 GMT 2025 , Edited by admin on Mon Mar 31 22:04:54 GMT 2025
PRIMARY
FDA UNII
845XW54F31
Created by admin on Mon Mar 31 22:04:54 GMT 2025 , Edited by admin on Mon Mar 31 22:04:54 GMT 2025
PRIMARY
ALANWOOD
fenpropidin
Created by admin on Mon Mar 31 22:04:54 GMT 2025 , Edited by admin on Mon Mar 31 22:04:54 GMT 2025
PRIMARY
CAS
67306-00-7
Created by admin on Mon Mar 31 22:04:54 GMT 2025 , Edited by admin on Mon Mar 31 22:04:54 GMT 2025
PRIMARY
CHEBI
81917
Created by admin on Mon Mar 31 22:04:54 GMT 2025 , Edited by admin on Mon Mar 31 22:04:54 GMT 2025
PRIMARY
EPA CompTox
DTXSID9058157
Created by admin on Mon Mar 31 22:04:54 GMT 2025 , Edited by admin on Mon Mar 31 22:04:54 GMT 2025
PRIMARY
MERCK INDEX
m5290
Created by admin on Mon Mar 31 22:04:54 GMT 2025 , Edited by admin on Mon Mar 31 22:04:54 GMT 2025
PRIMARY Merck Index
DRUG BANK
DB12728
Created by admin on Mon Mar 31 22:04:54 GMT 2025 , Edited by admin on Mon Mar 31 22:04:54 GMT 2025
PRIMARY