Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C15H17N4O7S.Na |
| Molecular Weight | 420.373 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].CCCOC1=NN(C(=O)[N-]S(=O)(=O)C2=CC=CC=C2C(=O)OC)C(=O)N1C
InChI
InChIKey=JRQGDDUXDKCWRF-UHFFFAOYSA-M
InChI=1S/C15H18N4O7S.Na/c1-4-9-26-14-16-19(15(22)18(14)2)13(21)17-27(23,24)11-8-6-5-7-10(11)12(20)25-3;/h5-8H,4,9H2,1-3H3,(H,17,21);/q;+1/p-1
| Molecular Formula | C15H18N4O7S |
| Molecular Weight | 398.391 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | Na |
| Molecular Weight | 22.98976928 |
| Charge | 1 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Propoxycarbazone-Sodium (also known as BAY MKH 6561) is asulfonylaminocarbonyltriazolinone derivative patented by German multinational pharmaceutical and life sciences company Bayer A.-G. as herbicide Propoxycarbazone inhibits acetolactate synthase (ALS), and has selectivity on spring, winter, and durum varieties. The spectrum of control includes several species of monocot and dicot weeds at the application rates of 30 to 45 g/ha. Bromus control is the primary target since existing herbicides have limited timing, selectivity, and use patterns which reduce usefulness. Propoxycarbazone applied postemergence between the 1- to 2-leaf stage and shoot elongation has provided economic control of the following Bromus species: B. tectorum, B. secalinus, B. mollis, B. rigidus, and B. japonicus. Side effects, and sometimes control, was also noted on Aegilops tauschii for which there is no selective control outside genetically altered wheat cultivars. Broadleaf control was obtained primarily on the mustard family, including species in the genera Sisymbrium, Brassica, Descurainia, Chorispora, Camelina, Capsella, and Thlaspi. Propoxycarbazone provides control for adequate weed spectrum, however, considerations of resistance management, difficult and diverse weed pressure, and extended growing seasons will sometimes necessitate the use of sequential herbicides or mix partners.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:50:32 GMT 2025
by
admin
on
Mon Mar 31 22:50:32 GMT 2025
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| Record UNII |
B7Z8Z1D27B
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| Record Status |
Validated (UNII)
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| Record Version |
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EPA PESTICIDE CODE |
122019
Created by
admin on Mon Mar 31 22:50:32 GMT 2025 , Edited by admin on Mon Mar 31 22:50:32 GMT 2025
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B7Z8Z1D27B
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propoxycarbazone-sodium
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admin on Mon Mar 31 22:50:32 GMT 2025 , Edited by admin on Mon Mar 31 22:50:32 GMT 2025
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12056759
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admin on Mon Mar 31 22:50:32 GMT 2025 , Edited by admin on Mon Mar 31 22:50:32 GMT 2025
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m9221
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admin on Mon Mar 31 22:50:32 GMT 2025 , Edited by admin on Mon Mar 31 22:50:32 GMT 2025
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PRIMARY | Merck Index | ||
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DTXSID9034864
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7891
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181274-15-7
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