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

Details

Stereochemistry ACHIRAL
Molecular Formula C9H6F3N3O
Molecular Weight 229.1586
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FLONICAMID

SMILES

FC(F)(F)C1=C(C=NC=C1)C(=O)NCC#N

InChI

InChIKey=RLQJEEJISHYWON-UHFFFAOYSA-N
InChI=1S/C9H6F3N3O/c10-9(11,12)7-1-3-14-5-6(7)8(16)15-4-2-13/h1,3,5H,4H2,(H,15,16)

HIDE SMILES / InChI
Molecular Formula C9H6F3N3O
Molecular Weight 229.1586
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description

FLONICAMID, a nicotinamide derivative, is an insecticide used to control aphids, thrips, and whitefly in a range of situations including glasshouses. It is a xenobiotic that is thought to disturb insect feeding pattern. FLONICAMID is suggested to be a possible human carcinogen.

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Amplification of a cytochrome P450 gene is associated with resistance to neonicotinoid insecticides in the aphid Myzus persicae.
2010-06-24
Choosing organic pesticides over synthetic pesticides may not effectively mitigate environmental risk in soybeans.
2010-06-22
Fifty years of the integrated control concept: moving the model and implementation forward in Arizona.
2009-12
Effect of pesticides on adult rove beetle Atheta coriaria (Coleoptera: Staphylinidae) survival in growing medium.
2009-10
Teppeki, selective insecticide about Bombus terrestris.
2009
Evaluation of the susceptibility of the pea aphid, Acyrthosiphon pisum, to a selection of novel biorational insecticides using an artificial diet.
2009
Analysis of flonicamid and its metabolites in dried hops by liquid chromatography-tandem mass spectrometry.
2007-10-03
Flonicamid, a novel insecticide with a rapid inhibitory effect on aphid feeding.
2007-10
Effect of insecticides on mealybug destroyer (Coleoptera: Coccinellidae) and parasitoid Leptomastix dactylopii (Hymenoptera: Encyrtidae), natural enemies of citrus mealybug (Homoptera: Pseudococcidae).
2006-10
Patents

Patents

JP2006131526A
1
JP2008509189A
189
JP2010524483A
52
JP2011506567A
10
JP2011509971A
151
JP2011526599A
45
JP2011527307A
41
JP2012500817A
2
JP2012500824A
79
JP4705585B2
2
JP4829882B2
10
JP5313146B2
1
JPH06321903A
1

Sample Use Guides

In Vivo Use Guide
Curator's Comment: Toxicity data.
Acute oral LD50 in rat: 884 mg/kg.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:07:38 GMT 2025
Edited
by admin
on Mon Mar 31 19:07:38 GMT 2025
Record UNII
9500W2Z53J
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ARIA
Preferred Name English
FLONICAMID
ISO   MI  
Common Name English
TURBINE
Brand Name English
FLONICAMID [MI]
Common Name English
F-1785
Code English
FLONICAMID [ISO]
Common Name English
CARBINE
Brand Name English
IKI-220
Code English
N-CYANOMETHYL-4-(TRIFLUOROMETHYL)NICOTINAMIDE
Systematic Name English
N-(CYANOMETHYL)-4-(TRIFLUOROMETHYL)NICOTINAMIDE
Systematic Name English
BELEAF
Brand Name English
N-(CYANOMETHYL)-4-(TRIFLUOROMETHYL)-3-PYRIDINECARBOXAMIDE
Systematic Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 128016
Created by admin on Mon Mar 31 19:07:38 GMT 2025 , Edited by admin on Mon Mar 31 19:07:38 GMT 2025
Code System Code Type Description
PUBCHEM
9834513
Created by admin on Mon Mar 31 19:07:38 GMT 2025 , Edited by admin on Mon Mar 31 19:07:38 GMT 2025
PRIMARY
MERCK INDEX
m5407
Created by admin on Mon Mar 31 19:07:38 GMT 2025 , Edited by admin on Mon Mar 31 19:07:38 GMT 2025
PRIMARY Merck Index
WIKIPEDIA
Flonicamid
Created by admin on Mon Mar 31 19:07:38 GMT 2025 , Edited by admin on Mon Mar 31 19:07:38 GMT 2025
PRIMARY
EPA CompTox
DTXSID8034611
Created by admin on Mon Mar 31 19:07:38 GMT 2025 , Edited by admin on Mon Mar 31 19:07:38 GMT 2025
PRIMARY
CAS
158062-67-0
Created by admin on Mon Mar 31 19:07:38 GMT 2025 , Edited by admin on Mon Mar 31 19:07:38 GMT 2025
PRIMARY
FDA UNII
9500W2Z53J
Created by admin on Mon Mar 31 19:07:38 GMT 2025 , Edited by admin on Mon Mar 31 19:07:38 GMT 2025
PRIMARY
ALANWOOD
flonicamid
Created by admin on Mon Mar 31 19:07:38 GMT 2025 , Edited by admin on Mon Mar 31 19:07:38 GMT 2025
PRIMARY
CHEBI
39291
Created by admin on Mon Mar 31 19:07:38 GMT 2025 , Edited by admin on Mon Mar 31 19:07:38 GMT 2025
PRIMARY
HSDB
7937
Created by admin on Mon Mar 31 19:07:38 GMT 2025 , Edited by admin on Mon Mar 31 19:07:38 GMT 2025
PRIMARY
MESH
C524822
Created by admin on Mon Mar 31 19:07:38 GMT 2025 , Edited by admin on Mon Mar 31 19:07:38 GMT 2025
PRIMARY
NIH
NCATS
PRIVACY NOTICE
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966