GB1308951A - Stabilization of phosphoric acid pesticides - Google Patents
Stabilization of phosphoric acid pesticidesInfo
- Publication number
- GB1308951A GB1308951A GB1172670A GB1172670A GB1308951A GB 1308951 A GB1308951 A GB 1308951A GB 1172670 A GB1172670 A GB 1172670A GB 1172670 A GB1172670 A GB 1172670A GB 1308951 A GB1308951 A GB 1308951A
- Authority
- GB
- United Kingdom
- Prior art keywords
- carbon atoms
- rings
- groups
- radical
- alkyl
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 title abstract 6
- 229910000147 aluminium phosphate Inorganic materials 0.000 title abstract 3
- 239000000575 pesticide Substances 0.000 title abstract 2
- 230000006641 stabilisation Effects 0.000 title 1
- 238000011105 stabilization Methods 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 32
- -1 carbocyclic radicals Chemical class 0.000 abstract 21
- 150000003254 radicals Chemical group 0.000 abstract 12
- 125000000217 alkyl group Chemical group 0.000 abstract 8
- 125000003118 aryl group Chemical group 0.000 abstract 6
- 150000001875 compounds Chemical class 0.000 abstract 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 5
- 239000004215 Carbon black (E152) Substances 0.000 abstract 4
- 229930195733 hydrocarbon Natural products 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 2
- 125000004423 acyloxy group Chemical group 0.000 abstract 2
- 125000005236 alkanoylamino group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 2
- 150000005840 aryl radicals Chemical class 0.000 abstract 2
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 abstract 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 2
- 229910052794 bromium Inorganic materials 0.000 abstract 2
- 125000001589 carboacyl group Chemical group 0.000 abstract 2
- 125000002837 carbocyclic group Chemical group 0.000 abstract 2
- 229910052801 chlorine Inorganic materials 0.000 abstract 2
- 239000000460 chlorine Substances 0.000 abstract 2
- 150000004696 coordination complex Chemical class 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 abstract 2
- 229910052731 fluorine Inorganic materials 0.000 abstract 2
- 239000011737 fluorine Substances 0.000 abstract 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 125000001624 naphthyl group Chemical group 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 230000000361 pesticidal effect Effects 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- RAPBNVDSDCTNRC-UHFFFAOYSA-N Chlorobenzilate Chemical compound C=1C=C(Cl)C=CC=1C(O)(C(=O)OCC)C1=CC=C(Cl)C=C1 RAPBNVDSDCTNRC-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005864 Sulphur Substances 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 239000000654 additive Substances 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- AXGUBXVWZBFQGA-UHFFFAOYSA-N chloropropylate Chemical compound C=1C=C(Cl)C=CC=1C(O)(C(=O)OC(C)C)C1=CC=C(Cl)C=C1 AXGUBXVWZBFQGA-UHFFFAOYSA-N 0.000 abstract 1
- 230000009918 complex formation Effects 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000003381 stabilizer Substances 0.000 abstract 1
- 230000000087 stabilizing effect Effects 0.000 abstract 1
- 239000000341 volatile oil Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B50/00—Formazane dyes; Tetrazolium dyes
-
- 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
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
-
- 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
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/113—Esters of phosphoric acids with unsaturated acyclic alcohols
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B45/00—Complex metal compounds of azo dyes
Landscapes
- Chemical & Material Sciences (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)
Abstract
1308951 Stabilizing phosphoric acid pesticides CIBA-GEIGY AG 11 March 1970 [19 March 1969 12 March 1969 (2)] 11726/70 Heading ASE A pesticidal composition comprises (A) at least one pesticidal ester of phosphoric acid containing at least one alkyl group containing 1-3 carbon atoms; (B) as stabilizing agent, 0.1-10% by weight, based on the weight of (A), of at least one (i) compound of formula: or tautomer thereof of formula: or compound of formula wherein R represents a radical of hydroaromatic or of aromatic character comprising one, two or three rings, each having 5 or 6 ring members and when said radical contains two or three rings, the rings are condensed together or bound to each other, directly or via an oxygen atom or an -NH-, -CH 2 , or -CH=CH- group; the radical R being selected from (a) carbocyclic radicals of aromatic character having 1-3 rings and heterocyclic radicals of aromatic character having from 1-3 rings one of which rings contains one or two ring hetero atoms chosen from nitrogen, oxygen and sulphur; (b) carbocyclic character having two or three carbocyclic or heterocyclic radicals with hydroaromatic rings each of 5 or 6 ring members and at least two of these rings are condensed together, wherein two or four carbon atoms in one of the rings are saturated and at least one other ring is aromatic; (c) radicals as defined under (a) or (b) substituted by one or two phenylazo, napthylazo and/or arylazoarylazo (in which each of the aryl radicals is phenyl or naphthyl) groups; and (d) a radical as defined under (a), (b) or (c) with at least one of its rings bearing one to four substituents selected from fluorine, chlorine, bromine, iodine, keto oxygen, hydroxy, carboxy, alkyl having from one to six carbon atoms, alkenyl having from two to five carbon atoms, cycloalkyl having five or six carbon atoms, amino, alkanoylamino having up to five carbon atoms, mono-benzylamino, alkoxy having from one to five carbon atoms, benzyloxy, nitro, sulpho, cyano, amino substituted by one or two groups selected from alkyl groups having one to four carbon atoms, phenyl groups and benzyl groups, alkoxycarbonyl having from two to six carbon atoms, alkylsulphonyl having from one to five carbon atoms, sulphamoyl the nitrogen atom of which is unsubstituted or substituted by one or two hydrocarbon radicals having a total of one to eight carbon atoms, alkanoyloxy having at most eighteen carbon atoms, and alkenoyloxy having at most eighteen carbon atoms, alkanoyl having up to five carbon atoms and dialkylamino-alkyl having a total of from three to nine carbon atoms; and of 5 or 6 ring members and at least two of these rings are condensed together, wherein two or four carbon atoms in one of the rings are saturated and at least one other ring is aromatic; (c) radicals as defined under (a) or (b) substituted by one or two phenylazo, naphthylazo and/or arylazoarylazo (in which each of the aryl radicals is phenyl or naphthyl) groups; and (d) a radical as defined under (a), (b) or (c) with at least one of its rings bearing one to four substituents selected from fluorine, chlorine, bromine, iodine, keto oxygen, hydroxy, carboxy, alkyl having from one to six carbon atoms, alkenyl having from two to five carbon atoms, cycloalkyl having five or six carbon atoms, amino, alkanoylamino having up to five carbon atoms, mono-benzoylamino, alkoxy having from one to five carbon atoms, benzyloxy, nitro, sulpho, cyano, amino substituted by one or two groups selected from alkyl groups having one to four carbon atoms, phenyl groups and benzyl groups, alkoxycarbonyl having from two to six carbon atoms, alkylsulphonyl having from one to five carbon atoms, sulphamoyl the nitrogen atom of which is unsubstituted or substituted by one or two hydrocarbon radicals having a total of one to eight carbon atoms, alkanoyloxy having at most eighteen carbon atoms, and alkenoyloxy having at most eighteen carbon atoms, alkanoyl having up to five carbon atoms and dialkylamino-alkyl having a total of from three to nine carbon atoms; and R<SP>1</SP> is benzyl, alkyl of from H7 carbon atoms, alkenyl of two to eight carbon atoms or a radical R is defined under any one of (a) to (d) as defined above and R" is a radical R' as defined above, an unsubstituted phenylazo or naphthylazo group or a phenylazo or naphthylazo group substituted by methyl or ethyl; or R' and R" taken together represent a divalent hydrocarbon radical having a total of four to fourteen carbon atoms which is a straight or branched chain radical or a chain radical containing an aryl ring condensed to the chain, any substituent of said hydrocarbon radical being selected from the substituents defined under (d), and groups of the formula = NX (in which X represents hydrogen, alkyl having from one to five carbon atoms or phenyl), and the group of formula: represents a radical R as defined under (a) to (d) above other than a group at defined above wherein R' and R" are taken together, or (ii) salt of a compound as defined under (i) above bearing at least one group capable of salt formation, or (iii) metal complex of a compound or salt as defined under (i) or (ii) bearing one or two groups capable of metal complex formation selected from hydroxy, carboxy, amino, mono (C 1 -C 4 ) alkyl amino, phenylamino, phenylsulphonamido and (C 1 -C 4 alkyl) sulphonamido groups and, optionally (C) a solid or liquid solvent which is a solvent for component (A) and/or (B), component (B) being soluble in component (A) and/or (if present) component (C). The compositions may also contain other additives and active ingredients and many suitable compounds are specified, including essential oils, chlorbenzilate and chlorpropylate.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR6906862A FR2036342A5 (en) | 1969-03-12 | 1969-03-12 | Insecticidal phosphoric ester compositions stabilised - against humidity |
FR6906861A FR2036341A5 (en) | 1969-03-12 | 1969-03-12 | Insecticidal phosphoric ester compositions stabilised - against humidity |
FR6906860A FR2036340A5 (en) | 1969-03-12 | 1969-03-12 | Insecticidal phosphoric ester compositions stabilised - against humidity |
LU60052 | 1969-12-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1308951A true GB1308951A (en) | 1973-03-07 |
Family
ID=27446008
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1172670A Expired GB1308951A (en) | 1969-03-12 | 1970-03-11 | Stabilization of phosphoric acid pesticides |
Country Status (5)
Country | Link |
---|---|
AT (1) | AT309896B (en) |
CA (1) | CA931502A (en) |
CH (1) | CH582477A5 (en) |
GB (1) | GB1308951A (en) |
NL (1) | NL143935B (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2552901A1 (en) * | 1974-11-27 | 1976-06-10 | Ciba Geigy Ag | DEVICE FOR INDICATING ACTIVE INGREDIENT VACUUM |
DE2552902A1 (en) * | 1975-09-05 | 1977-03-17 | Ciba Geigy Ag | ELECTRICAL DEVICE DISPENSING ACTIVE INGREDIENTS |
WO2000069260A1 (en) * | 1999-05-14 | 2000-11-23 | Bayer Aktiengesellschaft | Dyed compositions containing insecticides |
AU760406B2 (en) * | 1998-11-03 | 2003-05-15 | Montech Usa Inc. | Polyolefin composition having a high balance of stiffness and impact strength |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2498201A2 (en) * | 1980-06-11 | 1982-07-23 | Roussel Uclaf | LIGHT STABLE COMPOSITIONS CONTAINING PYRETHRINOID COMPOUNDS AND DYES |
-
1970
- 1970-03-05 CH CH321070A patent/CH582477A5/xx not_active IP Right Cessation
- 1970-03-11 AT AT621271A patent/AT309896B/en not_active IP Right Cessation
- 1970-03-11 NL NL7003492A patent/NL143935B/en unknown
- 1970-03-11 CA CA077062A patent/CA931502A/en not_active Expired
- 1970-03-11 GB GB1172670A patent/GB1308951A/en not_active Expired
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2552901A1 (en) * | 1974-11-27 | 1976-06-10 | Ciba Geigy Ag | DEVICE FOR INDICATING ACTIVE INGREDIENT VACUUM |
DE2552902A1 (en) * | 1975-09-05 | 1977-03-17 | Ciba Geigy Ag | ELECTRICAL DEVICE DISPENSING ACTIVE INGREDIENTS |
AU760406B2 (en) * | 1998-11-03 | 2003-05-15 | Montech Usa Inc. | Polyolefin composition having a high balance of stiffness and impact strength |
WO2000069260A1 (en) * | 1999-05-14 | 2000-11-23 | Bayer Aktiengesellschaft | Dyed compositions containing insecticides |
US6706761B1 (en) * | 1999-05-14 | 2004-03-16 | S. C. Johnson & Son, Inc. | Dyed compositions containing insecticides |
Also Published As
Publication number | Publication date |
---|---|
NL7003492A (en) | 1970-09-15 |
NL143935B (en) | 1974-11-15 |
CH582477A5 (en) | 1976-12-15 |
AT309896B (en) | 1973-09-10 |
CA931502A (en) | 1973-08-07 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
IL62110A (en) | Pharmaceutical compositions containing(substituted)phenyl alkyl imidazole derivatives,some new such compounds and their preparation | |
RU94011232A (en) | Alkaline-earth metal salts, transient metal salts and ketocarboxylic acid transient metal complexes as corrosion inhibitors | |
IE782115L (en) | Imidazole derivatives | |
GB1441056A (en) | Phenyl-pyridazines their preparation and use as herbicides | |
GB1308951A (en) | Stabilization of phosphoric acid pesticides | |
GB1392100A (en) | Insecticides | |
IE35434B1 (en) | Benzene derivatives | |
GB1353399A (en) | N,n-disubstituted amidoximes and their derivatives | |
GB1318136A (en) | Phenyl carbamate compounds their preparation and their insecticidal use | |
GB1296799A (en) | ||
NZ189091A (en) | Prostaglandin derivatives | |
IE791036L (en) | Thienopyridines and furanopyridines | |
ES8704460A1 (en) | 2-Pyridine-thiol derivatives, processes for their preparation and pharmaceutical compositions containing them. | |
IE810120L (en) | Imidazole hydrazone derivatives | |
GB1350286A (en) | Herbicidal composition | |
GB1348856A (en) | Insecticidal phosphoroamidothioates and compositions containing them | |
GB1315541A (en) | P-trifluoro-methylphenylimino compounds their manufacture and their use as active substances in pesticides | |
GB1054347A (en) | ||
KR850001180A (en) | Method for preparing an aryloxybenzoic acid derivative | |
DK602383D0 (en) | 1,1-DIPHENYLPROPANOL DERIVATIVES | |
GB1315552A (en) | Fungicidal insecticidal and miticidal compositions comprising organophosphates and method for using said compositions | |
ES319090A1 (en) | Carbamic acid (fluoroacetamido-trichloro)ethyl esters | |
SE425539B (en) | HERBICIDAL COMPOSITION CONTAINING A MIXTURE OF A 2-PICOLIC ACID COMPOUND AND A BENZOTIAZOLINE COMPOUND AND USING THESE COMPOSITION TO CONTROL GROWTH OF VEGETABLES | |
GB1470012A (en) | Ketone peroxide composition | |
GB1199857A (en) | o-Substituted 2-Phenylimino-1-Azacycloheptanes and their production |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |