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Details

Stereochemistry ACHIRAL
Molecular Formula C9H20N2O2.ClH
Molecular Weight 224.728
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PROPAMOCARB HYDROCHLORIDE

SMILES

Cl.CCCOC(=O)NCCCN(C)C

InChI

InChIKey=MKIMSXGUTQTKJU-UHFFFAOYSA-N
InChI=1S/C9H20N2O2.ClH/c1-4-8-13-9(12)10-6-5-7-11(2)3;/h4-8H2,1-3H3,(H,10,12);1H

HIDE SMILES / InChI

Molecular Formula C9H20N2O2
Molecular Weight 188.2673
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Use of semipermeable membrane devices for monitoring pesticides in indoor air.
2009-11-18
Carbamates synergize the toxicity of acrinathrin in resistant western flower thrips (Thysanoptera: Thripidae).
2009-02
Different responses of biochemical markers in frogs (Rana ridibunda) from urban and rural wetlands to the effect of carbamate fungicide.
2008-09
Towards minimization of chlorinated solvents consume in Fourier transform infrared spectroscopy determination of Propamocarb in pesticide formulations.
2008-04-15
Modification and re-validation of the ethyl acetate-based multi-residue method for pesticides in produce.
2007-11
Selection for Fungicide Resistance Within a Growing Season in Field Populations of Phytophthora infestans at the Center of Origin.
2006-12
Pesticide exposure: the hormonal function of the female reproductive system disrupted?
2006-05-31
Downy mildews on ornamental plants and their control.
2006
Effect of pesticides on estrogen receptor transactivation in vitro: a comparison of stable transfected MVLN and transient transfected MCF-7 cells.
2005-12-01
Determination of residues of propamocarb in wine by liquid chromatography-electrospray mass spectrometry with direct injection.
2004-06
Effects of the carbamates fenoxycarb, propamocarb and propoxur on energy supply, glucose utilization and SH-groups in neurons.
2004-06
The investigation of the genotoxic effects of fenarimol and propamocarb in mouse bone marrow in vivo.
2004-02-28
A Rapid Microbioassay for Discovery of Novel Fungicides for Phytophthora spp.
2003-01
Detection of organophosphate and carbamate pesticides in vegetable samples by a photothermal biosensor.
2003-01
Determination of propamocarb in vegetables using polymer-based high-performance liquid chromatography coupled with electrospray mass spectrometry.
2002-10-04
[Field test and lab experiment on control efficacy of the pathogen of opium poppy mildew].
2002-07
[Multiresidue analysis of nitrogen-containing and sulfur-containing pesticides in agricultural products using dual-column GC-NPD/FPD].
2002-04
Effects of currently used pesticides in assays for estrogenicity, androgenicity, and aromatase activity in vitro.
2002-02-15
Suppression of Pythium spp. by Trichoderma spp. during germination of tomato seeds in soilless growing media.
2002
The influence of fungicides on the growth of Trichoderma asperellum.
2002
Immunotoxicity of cupravit and previcur fungicides in mice.
2001-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 20:03:28 GMT 2025
Edited
by admin
on Mon Mar 31 20:03:28 GMT 2025
Record UNII
V39TC0925S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PROPAMOCARB HYDROCHLORIDE
ISO   MI  
Common Name English
BANOL
Preferred Name English
PROPYL 3-(DIMETHYLAMINO)PROPYLCARBAMATE MONOHYDROCHLORIDE
Systematic Name English
CARBAMIC ACID, (3-(DIMETHYLAMINO)PROPYL)-, PROPYL ESTER, MONOHYDROCHLORIDE
Common Name English
SN-66752
Code English
PROPLANT
Brand Name English
PROPAMOCARB HYDROCHLORIDE [MI]
Common Name English
PREVICUR
Brand Name English
PROPAMOCARB HYDROCHLORIDE [ISO]
Common Name English
AE-B066752
Code English
HOE-102791
Code English
Classification Tree Code System Code
EPA PESTICIDE CODE 119302
Created by admin on Mon Mar 31 20:03:28 GMT 2025 , Edited by admin on Mon Mar 31 20:03:28 GMT 2025
Code System Code Type Description
CHEBI
82090
Created by admin on Mon Mar 31 20:03:28 GMT 2025 , Edited by admin on Mon Mar 31 20:03:28 GMT 2025
PRIMARY
MERCK INDEX
m9182
Created by admin on Mon Mar 31 20:03:28 GMT 2025 , Edited by admin on Mon Mar 31 20:03:28 GMT 2025
PRIMARY Merck Index
CAS
25606-41-1
Created by admin on Mon Mar 31 20:03:28 GMT 2025 , Edited by admin on Mon Mar 31 20:03:28 GMT 2025
PRIMARY
ECHA (EC/EINECS)
247-125-9
Created by admin on Mon Mar 31 20:03:28 GMT 2025 , Edited by admin on Mon Mar 31 20:03:28 GMT 2025
PRIMARY
FDA UNII
V39TC0925S
Created by admin on Mon Mar 31 20:03:28 GMT 2025 , Edited by admin on Mon Mar 31 20:03:28 GMT 2025
PRIMARY
PUBCHEM
33112
Created by admin on Mon Mar 31 20:03:28 GMT 2025 , Edited by admin on Mon Mar 31 20:03:28 GMT 2025
PRIMARY
EPA CompTox
DTXSID6034849
Created by admin on Mon Mar 31 20:03:28 GMT 2025 , Edited by admin on Mon Mar 31 20:03:28 GMT 2025
PRIMARY
ALANWOOD
propamocarb hydrochloride
Created by admin on Mon Mar 31 20:03:28 GMT 2025 , Edited by admin on Mon Mar 31 20:03:28 GMT 2025
PRIMARY