Basic Info.

Model NO.

EC

Model NO.

EC

Product Desciption

Herbicide Pesticide Propisochlor 720g/L EC

Description: Pre-emergence or pre-plant herbicide for control of annual grasses and some broad leaved weeds
Example pests controlled: Cockspur grass; goose grass; Green bristlegrass; Goosefoot grass; Black nightshade
Example applications: Maize; Potatoes; Soybean; Corn; Peanuts; Rice; Spring OSR; Sunflower; peas; Wheat; Barley

Chemical structure: 

Isomerism	A chiral molecule with two enantiomers - S- and R-. The technical material is an isomeric mixture but it is the R-isomer that exhibits the strongest herbicidal activity.
Chemical formula	C15H22ClNO2
Canonical SMILES	CCC1=CC=CC(=C1N(COC(C)C)C(=O)CCl)C
Isomeric SMILES	No data
International Chemical Identifier key (InChIKey)	KZNDFYDURHAESM-UHFFFAOYSA-N
International Chemical Identifier (InChI)	InChI=1S/C15H22ClNO2/c1-5-13-8-6-7-12(4)15(13)17(14(18)9-16)10-19-11(2)3/h6-8,11H,5,9-10H2,1-4H3

General status: 

Pesticide type	Herbicide
Substance group	Chloroacetanilide
Minimum active substance purity	943 g/kg
Known relevant impurities	EU dossier - none declared
Substance origin	Synthetic
Mode of action	Inhibits protein synthesis and so blocks cell division, selective, absorbed by shoots of germinating plants. Inhibition of VLCFA (inhibition of cell division).
CAS RN	86763-47-5
EC number	-
CIPAC number	-
US EPA chemical code	-
PubChem CID	167454
Molecular mass (g mol-1)	283.80
PIN (Preferred Identification Name)	2-chloro-N-(2-ethyl-6-methylphenyl)-N-[(propan-2-yloxy)methyl]acetamide
IUPAC name	2-chloro-6'-ethyl-N-isopropoxymethylacet-ortho-toluidide
CAS name	2-chloro-N-(2-ethyl-6-methylphenyl)-N-((1-methylethoxy)methyl)acetamide
Other status information	Chemical subject to PIC regulations
Relevant Environmental Water Quality Standards	-
Herbicide Resistance Classification (HRAC)	K3
Herbicide Resistance Classification (WSSA)	15