NO742668L - - Google Patents

Info

Publication number: NO742668L
Authority: NO; Norway
Prior art keywords: carbon atoms; alkyl group; hydrogen; compound according; sodium
Prior art date: 1973-07-23

Application number

NO742668A

Other languages

English (en)

Norwegian (no)

Inventor

C L Mcintosh

Original Assignee

Du Pont

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1973-07-23

Filing date

1974-07-22

Publication date

1975-01-24

1974-05-30 Priority claimed from US05/474,536 external-priority patent/US3943201A/en

1974-07-22 Application filed by Du Pont filed Critical Du Pont

1975-01-24 Publication of NO742668L publication Critical patent/NO742668L/no

Links

150000001875 compounds Chemical class 0.000 claims description 64
125000004432 carbon atom Chemical group C* 0.000 claims description 55
229910052739 hydrogen Inorganic materials 0.000 claims description 34
239000001257 hydrogen Substances 0.000 claims description 34
125000000217 alkyl group Chemical group 0.000 claims description 32
150000002431 hydrogen Chemical class 0.000 claims description 26
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 17
229910052801 chlorine Inorganic materials 0.000 claims description 15
239000000460 chlorine Substances 0.000 claims description 15
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 14
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 13
229910052700 potassium Inorganic materials 0.000 claims description 13
239000011591 potassium Substances 0.000 claims description 13
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 12
125000002768 hydroxyalkyl group Chemical group 0.000 claims description 12
229910052760 oxygen Inorganic materials 0.000 claims description 12
239000001301 oxygen Substances 0.000 claims description 12
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 11
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 11
230000008635 plant growth Effects 0.000 claims description 11
229910052708 sodium Inorganic materials 0.000 claims description 11
239000011734 sodium Substances 0.000 claims description 11
239000005864 Sulphur Substances 0.000 claims description 9
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 8
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical compound BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 8
229910052744 lithium Inorganic materials 0.000 claims description 8
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 7
125000003342 alkenyl group Chemical group 0.000 claims description 7
239000011701 zinc Substances 0.000 claims description 7
229910052725 zinc Inorganic materials 0.000 claims description 7
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 6
CROOPQURPKJTOH-UHFFFAOYSA-N COC(=O)P(O)(O)=O.C(C)[Na] Chemical group COC(=O)P(O)(O)=O.C(C)[Na] CROOPQURPKJTOH-UHFFFAOYSA-N 0.000 claims description 6
NOSMQIYCWDWLIL-UHFFFAOYSA-N COC(=O)P(O)(O)=O.C[Na] Chemical group COC(=O)P(O)(O)=O.C[Na] NOSMQIYCWDWLIL-UHFFFAOYSA-N 0.000 claims description 6
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 6
229910052788 barium Inorganic materials 0.000 claims description 6
DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 6
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
239000011575 calcium Substances 0.000 claims description 6
229910052791 calcium Inorganic materials 0.000 claims description 6
229910052740 iodine Inorganic materials 0.000 claims description 6
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 5
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 5
239000011777 magnesium Substances 0.000 claims description 5
229910052749 magnesium Inorganic materials 0.000 claims description 5
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 5
BGYPJLADNCZNGX-UHFFFAOYSA-N methoxycarbonylphosphonic acid Chemical group COC(=O)P(O)(O)=O BGYPJLADNCZNGX-UHFFFAOYSA-N 0.000 claims description 5
239000011593 sulfur Substances 0.000 claims description 5
229910052717 sulfur Inorganic materials 0.000 claims description 5
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 4
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 4
229910052794 bromium Inorganic materials 0.000 claims description 4
YPJQMKNLYYYMOM-UHFFFAOYSA-N diazanium;methyl phosphonatoformate Chemical group [NH4+].[NH4+].COC(=O)P([O-])([O-])=O YPJQMKNLYYYMOM-UHFFFAOYSA-N 0.000 claims description 4
229910052731 fluorine Inorganic materials 0.000 claims description 4
239000011737 fluorine Substances 0.000 claims description 4
230000002401 inhibitory effect Effects 0.000 claims description 4
DFHAXXVZCFXGOQ-UHFFFAOYSA-K trisodium phosphonoformate Chemical group [Na+].[Na+].[Na+].[O-]C(=O)P([O-])([O-])=O DFHAXXVZCFXGOQ-UHFFFAOYSA-K 0.000 claims description 4
PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 3
FUKBGYXHGNWHFP-UHFFFAOYSA-L [Na+].[Na+].COP(O)(=O)C([O-])=O.COP(O)(=O)C([O-])=O Chemical group [Na+].[Na+].COP(O)(=O)C([O-])=O.COP(O)(=O)C([O-])=O FUKBGYXHGNWHFP-UHFFFAOYSA-L 0.000 claims description 3
ICSHUPSUGZYMFT-UHFFFAOYSA-L disodium;carboxy(ethoxy)phosphinate Chemical group [Na+].[Na+].CCOP([O-])(=O)C(O)=O.CCOP([O-])(=O)C(O)=O ICSHUPSUGZYMFT-UHFFFAOYSA-L 0.000 claims description 3
229910052748 manganese Inorganic materials 0.000 claims description 3
239000011572 manganese Substances 0.000 claims description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
FFCBLGDWKJHVHG-UHFFFAOYSA-N CSC(=O)P(O)(O)=O.C[Na] Chemical group CSC(=O)P(O)(O)=O.C[Na] FFCBLGDWKJHVHG-UHFFFAOYSA-N 0.000 claims 1
241000196324 Embryophyta Species 0.000 description 45
239000000243 solution Substances 0.000 description 23
150000003839 salts Chemical class 0.000 description 21
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
239000000463 material Substances 0.000 description 14
230000012010 growth Effects 0.000 description 13
-1 alkali metal salt Chemical class 0.000 description 12
238000000034 method Methods 0.000 description 10
239000000203 mixture Substances 0.000 description 10
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
230000000694 effects Effects 0.000 description 9
238000005342 ion exchange Methods 0.000 description 9
FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 9
239000004480 active ingredient Substances 0.000 description 8
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 7
239000004615 ingredient Substances 0.000 description 7
239000002253 acid Substances 0.000 description 6
239000007864 aqueous solution Substances 0.000 description 6
239000003085 diluting agent Substances 0.000 description 6
239000002245 particle Substances 0.000 description 6
239000004563 wettable powder Substances 0.000 description 6
150000007513 acids Chemical class 0.000 description 5
239000002585 base Substances 0.000 description 5
239000002904 solvent Substances 0.000 description 5
239000004094 surface-active agent Substances 0.000 description 5
239000000725 suspension Substances 0.000 description 5
230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 5
239000004552 water soluble powder Substances 0.000 description 5
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
235000014441 Prunus serotina Nutrition 0.000 description 4
241001278079 Salix nigra Species 0.000 description 4
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
238000002156 mixing Methods 0.000 description 4
239000002373 plant growth inhibitor Substances 0.000 description 4
239000000843 powder Substances 0.000 description 4
159000000000 sodium salts Chemical class 0.000 description 4
239000007787 solid Substances 0.000 description 4
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
XLWYFERKZNPRDR-UHFFFAOYSA-N CSC(=S)P(O)(O)=O.C(C)[Na] Chemical compound CSC(=S)P(O)(O)=O.C(C)[Na] XLWYFERKZNPRDR-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
241000220225 Malus Species 0.000 description 3
UEZVMMHDMIWARA-UHFFFAOYSA-N Metaphosphoric acid Chemical compound OP(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-N 0.000 description 3
244000046052 Phaseolus vulgaris Species 0.000 description 3
235000010627 Phaseolus vulgaris Nutrition 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
230000002378 acidificating effect Effects 0.000 description 3
239000000908 ammonium hydroxide Substances 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
238000010790 dilution Methods 0.000 description 3
239000012895 dilution Substances 0.000 description 3
235000013399 edible fruits Nutrition 0.000 description 3
235000009518 sodium iodide Nutrition 0.000 description 3
238000005507 spraying Methods 0.000 description 3
238000003756 stirring Methods 0.000 description 3
239000000080 wetting agent Substances 0.000 description 3
240000008027 Akebia quinata Species 0.000 description 2
235000007756 Akebia quinata Nutrition 0.000 description 2
235000007320 Avena fatua Nutrition 0.000 description 2
241000735234 Ligustrum Species 0.000 description 2
241000220296 Malus sp. Species 0.000 description 2
RHUODGTXEYJWLD-UHFFFAOYSA-N NC(=O)OP(O)=O Chemical class NC(=O)OP(O)=O RHUODGTXEYJWLD-UHFFFAOYSA-N 0.000 description 2
240000008296 Prunus serotina Species 0.000 description 2
241001412173 Rubus canescens Species 0.000 description 2
241000921305 Salix sp. Species 0.000 description 2
244000062793 Sorghum vulgare Species 0.000 description 2
238000005054 agglomeration Methods 0.000 description 2
230000002776 aggregation Effects 0.000 description 2
238000013019 agitation Methods 0.000 description 2
235000021016 apples Nutrition 0.000 description 2
150000001768 cations Chemical class 0.000 description 2
230000001276 controlling effect Effects 0.000 description 2
239000000428 dust Substances 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
239000008187 granular material Substances 0.000 description 2
239000003906 humectant Substances 0.000 description 2
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 2
229910000043 hydrogen iodide Inorganic materials 0.000 description 2
230000007062 hydrolysis Effects 0.000 description 2
238000006460 hydrolysis reaction Methods 0.000 description 2
239000007788 liquid Substances 0.000 description 2
229910000000 metal hydroxide Inorganic materials 0.000 description 2
150000004692 metal hydroxides Chemical class 0.000 description 2
VITRIUYHBVKBDH-UHFFFAOYSA-N methyl dimethoxyphosphorylformate Chemical compound COC(=O)P(=O)(OC)OC VITRIUYHBVKBDH-UHFFFAOYSA-N 0.000 description 2
238000006386 neutralization reaction Methods 0.000 description 2
231100001184 nonphytotoxic Toxicity 0.000 description 2
239000008188 pellet Substances 0.000 description 2
ZJAOAACCNHFJAH-UHFFFAOYSA-N phosphonoformic acid Chemical class OC(=O)P(O)(O)=O ZJAOAACCNHFJAH-UHFFFAOYSA-N 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
238000013138 pruning Methods 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
239000002689 soil Substances 0.000 description 2
238000001228 spectrum Methods 0.000 description 2
239000007858 starting material Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
238000012360 testing method Methods 0.000 description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
239000002023 wood Substances 0.000 description 2
MAUMSNABMVEOGP-UHFFFAOYSA-N (methyl-$l^{2}-azanyl)methane Chemical compound C[N]C MAUMSNABMVEOGP-UHFFFAOYSA-N 0.000 description 1
NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 1
235000009051 Ambrosia paniculata var. peruviana Nutrition 0.000 description 1
235000003097 Artemisia absinthium Nutrition 0.000 description 1
240000001851 Artemisia dracunculus Species 0.000 description 1
235000017731 Artemisia dracunculus ssp. dracunculus Nutrition 0.000 description 1
235000003261 Artemisia vulgaris Nutrition 0.000 description 1
241000209764 Avena fatua Species 0.000 description 1
244000075850 Avena orientalis Species 0.000 description 1
RACPNRHEFWJTJX-UHFFFAOYSA-N CSC(=O)P(O)(O)=O.C(C)[Na] Chemical compound CSC(=O)P(O)(O)=O.C(C)[Na] RACPNRHEFWJTJX-UHFFFAOYSA-N 0.000 description 1
244000201986 Cassia tora Species 0.000 description 1
235000014552 Cassia tora Nutrition 0.000 description 1
235000007516 Chrysanthemum Nutrition 0.000 description 1
240000005250 Chrysanthemum indicum Species 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
244000075634 Cyperus rotundus Species 0.000 description 1
235000016854 Cyperus rotundus Nutrition 0.000 description 1
235000012827 Digitaria sp Nutrition 0.000 description 1
QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
241000192043 Echinochloa Species 0.000 description 1
244000078127 Eleusine coracana Species 0.000 description 1
235000013499 Eleusine coracana subsp coracana Nutrition 0.000 description 1
241000555682 Forsythia x intermedia Species 0.000 description 1
244000068988 Glycine max Species 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
240000002024 Gossypium herbaceum Species 0.000 description 1
235000004341 Gossypium herbaceum Nutrition 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
241000208422 Rhododendron Species 0.000 description 1
241000218998 Salicaceae Species 0.000 description 1
241000124033 Salix Species 0.000 description 1
235000011684 Sorghum saccharatum Nutrition 0.000 description 1
241000218636 Thuja Species 0.000 description 1
240000003243 Thuja occidentalis Species 0.000 description 1
235000008109 Thuja occidentalis Nutrition 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
244000098338 Triticum aestivum Species 0.000 description 1
235000005373 Uvularia sessilifolia Nutrition 0.000 description 1
241001506773 Xanthium sp. Species 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
239000002250 absorbent Substances 0.000 description 1
230000002745 absorbent Effects 0.000 description 1
239000011149 active material Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
238000005904 alkaline hydrolysis reaction Methods 0.000 description 1
150000001450 anions Chemical class 0.000 description 1
239000001138 artemisia absinthium Substances 0.000 description 1
OTSAMNSACVKIOJ-UHFFFAOYSA-N azane;carbamoyl(ethoxy)phosphinic acid Chemical compound [NH4+].CCOP([O-])(=O)C(N)=O OTSAMNSACVKIOJ-UHFFFAOYSA-N 0.000 description 1
AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
MZJUGRUTVANEDW-UHFFFAOYSA-N bromine fluoride Chemical compound BrF MZJUGRUTVANEDW-UHFFFAOYSA-N 0.000 description 1
UHURJXXAXXMMLW-UHFFFAOYSA-N but-3-en-1-yl radical Chemical compound [CH2]CC=C UHURJXXAXXMMLW-UHFFFAOYSA-N 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000012876 carrier material Substances 0.000 description 1
238000003889 chemical engineering Methods 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 description 1
229930002875 chlorophyll Natural products 0.000 description 1
235000019804 chlorophyll Nutrition 0.000 description 1
ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 1
239000004927 clay Substances 0.000 description 1
238000003776 cleavage reaction Methods 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
230000003111 delayed effect Effects 0.000 description 1
239000003599 detergent Substances 0.000 description 1
238000011161 development Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
NWVQNVFVBMFHHI-UHFFFAOYSA-N ethoxy(methoxycarbonyl)phosphinic acid Chemical compound CCOP(O)(=O)C(=O)OC NWVQNVFVBMFHHI-UHFFFAOYSA-N 0.000 description 1
NOJFJZZMRDSOLM-UHFFFAOYSA-N ethyl diethoxyphosphorylformate Chemical compound CCOC(=O)P(=O)(OCC)OCC NOJFJZZMRDSOLM-UHFFFAOYSA-N 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000006260 foam Substances 0.000 description 1
230000005094 fruit set Effects 0.000 description 1
238000000227 grinding Methods 0.000 description 1
208000006278 hypochromic anemia Diseases 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
239000003456 ion exchange resin Substances 0.000 description 1
229920003303 ion-exchange polymer Polymers 0.000 description 1
239000011133 lead Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
MLJVWFGPQCOELH-UHFFFAOYSA-N methyl diethoxyphosphorylformate Chemical compound CCOP(=O)(OCC)C(=O)OC MLJVWFGPQCOELH-UHFFFAOYSA-N 0.000 description 1
BMPFQUFNKSYHME-UHFFFAOYSA-N methyl diethoxyphosphorylmethanedithioate Chemical compound CCOP(=O)(OCC)C(=S)SC BMPFQUFNKSYHME-UHFFFAOYSA-N 0.000 description 1
YHCFHHZOOKYAEO-UHFFFAOYSA-N methylazanium;methyl phosphonatoformate Chemical compound [NH3+]C.[NH3+]C.COC(=O)P([O-])([O-])=O YHCFHHZOOKYAEO-UHFFFAOYSA-N 0.000 description 1
230000002906 microbiologic effect Effects 0.000 description 1
235000019713 millet Nutrition 0.000 description 1
239000012053 oil suspension Substances 0.000 description 1
238000004806 packaging method and process Methods 0.000 description 1
238000012856 packing Methods 0.000 description 1
238000010422 painting Methods 0.000 description 1
235000020030 perry Nutrition 0.000 description 1
238000005191 phase separation Methods 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
239000002243 precursor Substances 0.000 description 1
238000012545 processing Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
239000004576 sand Substances 0.000 description 1
230000007017 scission Effects 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
230000000638 stimulation Effects 0.000 description 1
239000000758 substrate Substances 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
239000004546 suspension concentrate Substances 0.000 description 1
GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
GETQZCLCWQTVFV-UHFFFAOYSA-O trimethylammonium Chemical compound C[NH+](C)C GETQZCLCWQTVFV-UHFFFAOYSA-O 0.000 description 1
238000009966 trimming Methods 0.000 description 1
ILRVASBWNRYBFD-UHFFFAOYSA-K trisodium phosphonoformate hexahydrate Chemical compound O.O.O.O.O.O.[Na+].[Na+].[Na+].[O-]C(=O)P([O-])([O-])=O ILRVASBWNRYBFD-UHFFFAOYSA-K 0.000 description 1
238000009736 wetting Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4062—Esters of acids containing the structure -C(=X)-P(=X)(XR)2 or NC-P(=X)(XR)2, (X = O, S, Se)
- C07F9/4065—Esters of acids containing the structure -C(=X)-P(=X)(XR)2, (X = O, S, Se)

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Chemical & Material Sciences (AREA)
Crystallography & Structural Chemistry (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Biochemistry (AREA)
General Health & Medical Sciences (AREA)
Molecular Biology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

NO742668A 1973-07-23 1974-07-22 NO742668L (da)

Applications Claiming Priority (5)

Application Number	Priority Date	Filing Date	Title
US38161973A	1973-07-23	1973-07-23
US38162073A	1973-07-23	1973-07-23
US39772373A	1973-09-17	1973-09-17
US47453774A	1974-05-30	1974-05-30
US05/474,536 US3943201A (en)	1973-07-23	1974-05-30	Alkoxy carboxycarbonylphosphonic acid esters

Publications (1)

Publication Number	Publication Date
NO742668L true NO742668L (da)	1975-01-24

Family

ID=27541382

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO742668A NO742668L (da)	1973-07-23	1974-07-22

Country Status (22)

Country	Link
JP (1)	JPS5069236A (da)
AR (1)	AR214853A1 (da)
BE (1)	BE817918A (da)
BR (1)	BR7405998D0 (da)
CH (1)	CH591209A5 (da)
CS (1)	CS180016B2 (da)
DD (1)	DD111789A5 (da)
DE (1)	DE2435407A1 (da)
DK (1)	DK395274A (da)
FR (1)	FR2238432B1 (da)
GB (1)	GB1469136A (da)
HU (1)	HU171255B (da)
IE (1)	IE39635B1 (da)
IL (1)	IL45303A (da)
IT (1)	IT1049202B (da)
LU (1)	LU70581A1 (da)
MY (1)	MY8000218A (da)
NL (1)	NL7409943A (da)
NO (1)	NO742668L (da)
PL (1)	PL98264B1 (da)
SE (1)	SE422269B (da)
SU (1)	SU671704A3 (da)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA1140049A (en) *	1977-12-22	1983-01-25	Dke J.E. Helgstran	Pharmaceutical preparations from derivatives of hydroxycarbonylphosphonic acid
DE3607445A1 (de) *	1986-03-07	1987-09-10	Hoechst Ag	Verfahren zur herstellung von alkali-phosphonoformiaten

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3033891A (en) *	1959-11-27	1962-05-08	Monsanto Chemicals	Mono salts of o-hydrocarbyl-carboalkylthiol phosphonic acids

1974
- 1974-06-22 HU HU74DU00000226A patent/HU171255B/hu unknown
- 1974-06-22 BR BR5998/74A patent/BR7405998D0/pt unknown
- 1974-06-27 SE SE7408487A patent/SE422269B/xx unknown
- 1974-07-19 CS CS7400005165A patent/CS180016B2/cs unknown
- 1974-07-19 IL IL45303A patent/IL45303A/en unknown
- 1974-07-19 DD DD180007A patent/DD111789A5/xx unknown
- 1974-07-22 JP JP49083332A patent/JPS5069236A/ja active Pending
- 1974-07-22 NO NO742668A patent/NO742668L/no unknown
- 1974-07-22 IT IT25437/74A patent/IT1049202B/it active
- 1974-07-22 BE BE146790A patent/BE817918A/xx unknown
- 1974-07-22 DK DK395274A patent/DK395274A/da unknown
- 1974-07-22 LU LU70581A patent/LU70581A1/xx unknown
- 1974-07-22 FR FR7425333A patent/FR2238432B1/fr not_active Expired
- 1974-07-22 AR AR254812A patent/AR214853A1/es active
- 1974-07-22 SU SU742044846A patent/SU671704A3/ru active
- 1974-07-22 GB GB3238374A patent/GB1469136A/en not_active Expired
- 1974-07-23 PL PL1974172929A patent/PL98264B1/pl unknown
- 1974-07-23 DE DE2435407A patent/DE2435407A1/de not_active Withdrawn
- 1974-07-23 CH CH1016174A patent/CH591209A5/xx not_active IP Right Cessation
- 1974-07-23 IE IE1560/74A patent/IE39635B1/xx unknown
- 1974-07-23 NL NL7409943A patent/NL7409943A/xx unknown
1980
- 1980-12-30 MY MY218/80A patent/MY8000218A/xx unknown

Also Published As

Publication number	Publication date
CS180016B2 (en)	1977-12-30
IE39635L (en)	1975-01-23
GB1469136A (en)	1977-03-30
AU7146674A (en)	1976-01-22
FR2238432B1 (da)	1978-07-13
BR7405998D0 (pt)	1975-05-13
CH591209A5 (da)	1977-09-15
SE7408487L (da)	1975-01-24
AR214853A1 (es)	1979-08-15
IL45303A (en)	1977-07-31
DK395274A (da)	1975-03-10
IT1049202B (it)	1981-01-20
IL45303A0 (en)	1974-10-22
FR2238432A1 (da)	1975-02-21
DD111789A5 (da)	1975-03-12
LU70581A1 (da)	1974-11-28
MY8000218A (en)	1980-12-31
IE39635B1 (en)	1978-11-22
SU671704A3 (ru)	1979-06-30
JPS5069236A (da)	1975-06-10
NL7409943A (nl)	1975-01-27
SE422269B (sv)	1982-03-01
DE2435407A1 (de)	1975-02-13
PL98264B1 (pl)	1978-04-29
HU171255B (hu)	1977-12-28
BE817918A (fr)	1974-11-18

Publication	Publication Date	Title
KR860002169B1 (ko)	1986-12-22	N-포스포노메틸글리신의 트리알킬술포늄 염류의 제조방법
EP0109314B1 (en)	1986-09-03	Aluminum n-phosphonomethylglycine and its use as a herbicide
US3799758A (en)	1974-03-26	N-phosphonomethyl-glycine phytotoxicant compositions
NO830500L (no)	1983-09-09	N-fosfonometylglycin-derivater og fremgangsmaate til fremstilling derav
NO141090B (no)	1979-10-01	N-fosfonmetylglyciner for anvendelse som herbicid og/eller fytotoksisk middel
EP0054382B1 (en)	1985-04-24	Triethylsulfonium salts of n-phosphonomethylglycine, production thereof, their use as plant growth regulators, herbicides and compositions containing them
EP0073574B1 (en)	1985-11-13	Phosphonium salts of n-phosphonomethylglycine, preparation and compositions thereof and the use thereof as herbicides and plant growth regulants
DK142056B (da)	1980-08-18	N-organo-N-phosphonomethylglycin-N-oxid-forbindelser til anvendelse som herbicider eller plantevækstregulerende midler.
CA1118784A (en)	1982-02-23	Glycylmethylphosphinic acid derivatives, process for their production and use thereof
US4341549A (en)	1982-07-27	Phosphonium salts of N-phosphonomethylglycine and their use as herbicides and plant growth regulants
US3943201A (en)	1976-03-09	Alkoxy carboxycarbonylphosphonic acid esters
US4018854A (en)	1977-04-19	Carboxyphosphonates
WO1983003608A1 (en)	1983-10-27	Tetra-substituted ammonium salt of n-phosphonomethylglycine and their uses as herbicides and plant growth regulants
NO742668L (da)	1975-01-24
SU1486049A3 (ru)	1989-06-07	Способ регулирования роста сельскохозяйственных культур
EP0115176B1 (en)	1986-08-06	Stannic n-phosphonomethylglycine compounds and their use as herbicides
AU614730B2 (en)	1991-09-12	Compositions including herbicidal combinations of the glyphosate type and the phenoxybenzoic type
NO860068L (no)	1986-07-15	Herbicide forbindelser og preparater.
HU184234B (en)	1984-07-30	Preparations for controlling the plant growth
US4106923A (en)	1978-08-15	Phosphonomethyl glycine ester anhydrides, herbicidal composition containing same and use thereof
US4033749A (en)	1977-07-05	Alkoxycarbonylphosphonic acid derivative brush control agents
US4328027A (en)	1982-05-04	Di-triethylamine salt of N,N'-bis-carboethoxymethyl-N,N'-bis-phosphonomethylurea and its use as a plant growth regulator
US4108626A (en)	1978-08-22	Alkoxycarbonylphosphonic acid derivative brush control agents
US4095970A (en)	1978-06-20	2,6-Dichlorothiolbenzoates and use thereof as plant growth regulators
US4701211A (en)	1987-10-20	Substituted benzyltriethylammonium salts and their use as plant growth enhancers