IL37651A - Stabilised pesticidal compositions containing phosphoric esters - Google Patents

Stabilised pesticidal compositions containing phosphoric esters

Info

Publication number: IL37651A
Authority: IL; Israel
Prior art keywords: phosphate; phosphoric; vinyl; composition according; ester
Prior art date: 1970-09-11

Application number

IL37651A

Other languages

English (en)

Other versions

IL37651A0 (en

Original Assignee

Ciba Geigy Ag

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.)

1970-09-11

Filing date

1971-09-03

Publication date

1974-09-10

1971-09-03 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1971-11-29 Publication of IL37651A0 publication Critical patent/IL37651A0/xx

1974-09-10 Publication of IL37651A publication Critical patent/IL37651A/en

Links

239000000203 mixture Substances 0.000 title claims description 47
150000002148 esters Chemical class 0.000 title claims description 36
230000000361 pesticidal effect Effects 0.000 title claims description 11
239000002904 solvent Substances 0.000 claims description 20
239000003381 stabilizer Substances 0.000 claims description 19
150000001875 compounds Chemical class 0.000 claims description 18
239000007787 solid Substances 0.000 claims description 14
-1 vinyl phosphate vinyl dipropyl phosphate Chemical compound 0.000 claims description 13
238000000034 method Methods 0.000 claims description 11
125000001931 aliphatic group Chemical group 0.000 claims description 9
229910019142 PO4 Inorganic materials 0.000 claims description 7
239000010452 phosphate Substances 0.000 claims description 7
230000003019 stabilising effect Effects 0.000 claims description 7
239000002671 adjuvant Substances 0.000 claims description 6
239000001913 cellulose Substances 0.000 claims description 6
229920002678 cellulose Polymers 0.000 claims description 6
229920002554 vinyl polymer Polymers 0.000 claims description 6
238000000354 decomposition reaction Methods 0.000 claims description 5
229920005989 resin Polymers 0.000 claims description 5
239000011347 resin Substances 0.000 claims description 5
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 4
239000005977 Ethylene Substances 0.000 claims description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 4
239000003795 chemical substances by application Substances 0.000 claims description 4
238000009833 condensation Methods 0.000 claims description 4
230000005494 condensation Effects 0.000 claims description 4
229920001577 copolymer Polymers 0.000 claims description 4
150000002367 halogens Chemical group 0.000 claims description 4
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 4
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
125000003118 aryl group Chemical group 0.000 claims description 3
229910052801 chlorine Inorganic materials 0.000 claims description 3
239000000460 chlorine Substances 0.000 claims description 3
150000002118 epoxides Chemical class 0.000 claims description 3
239000011521 glass Substances 0.000 claims description 3
229910052500 inorganic mineral Inorganic materials 0.000 claims description 3
239000007788 liquid Substances 0.000 claims description 3
239000011707 mineral Substances 0.000 claims description 3
239000002023 wood Substances 0.000 claims description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
229910052794 bromium Inorganic materials 0.000 claims description 2
239000011575 calcium Substances 0.000 claims description 2
229910052791 calcium Inorganic materials 0.000 claims description 2
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical class O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 claims description 2
150000003839 salts Chemical class 0.000 claims description 2
239000000377 silicon dioxide Substances 0.000 claims description 2
239000003784 tall oil Substances 0.000 claims description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 3
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims 2
239000012528 membrane Substances 0.000 claims 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
239000004264 Petrolatum Substances 0.000 claims 1
239000004698 Polyethylene Substances 0.000 claims 1
239000004743 Polypropylene Substances 0.000 claims 1
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 1
229910000147 aluminium phosphate Inorganic materials 0.000 claims 1
150000001721 carbon Chemical class 0.000 claims 1
238000006243 chemical reaction Methods 0.000 claims 1
FXBLJWDJXBQLEL-UHFFFAOYSA-N ethenyl dimethyl phosphate Chemical group COP(=O)(OC)OC=C FXBLJWDJXBQLEL-UHFFFAOYSA-N 0.000 claims 1
125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 claims 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
229930195733 hydrocarbon Natural products 0.000 claims 1
150000002430 hydrocarbons Chemical class 0.000 claims 1
229940066842 petrolatum Drugs 0.000 claims 1
235000019271 petrolatum Nutrition 0.000 claims 1
125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 claims 1
229920000573 polyethylene Polymers 0.000 claims 1
229920001155 polypropylene Polymers 0.000 claims 1
KYKNRZGSIGMXFH-ZVGUSBNCSA-M potassium bitartrate Chemical compound [K+].OC(=O)[C@H](O)[C@@H](O)C([O-])=O KYKNRZGSIGMXFH-ZVGUSBNCSA-M 0.000 claims 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
239000008262 pumice Substances 0.000 claims 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 19
239000005864 Sulphur Substances 0.000 description 19
OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 6
238000002474 experimental method Methods 0.000 description 6
230000000295 complement effect Effects 0.000 description 5
230000007062 hydrolysis Effects 0.000 description 5
238000006460 hydrolysis reaction Methods 0.000 description 5
239000003921 oil Substances 0.000 description 4
239000000843 powder Substances 0.000 description 4
239000005995 Aluminium silicate Substances 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
125000000217 alkyl group Chemical group 0.000 description 3
235000012211 aluminium silicate Nutrition 0.000 description 3
238000009472 formulation Methods 0.000 description 3
230000000749 insecticidal effect Effects 0.000 description 3
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
229940099259 vaseline Drugs 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
AHIBWURJLGCHAY-UHFFFAOYSA-N [S].C1=CC=CC=C1 Chemical compound [S].C1=CC=CC=C1 AHIBWURJLGCHAY-UHFFFAOYSA-N 0.000 description 2
XAQHXGSHRMHVMU-UHFFFAOYSA-N [S].[S] Chemical compound [S].[S] XAQHXGSHRMHVMU-UHFFFAOYSA-N 0.000 description 2
239000013078 crystal Substances 0.000 description 2
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
DMCJFWXGXUEHFD-UHFFFAOYSA-N pentatriacontan-18-one Chemical compound CCCCCCCCCCCCCCCCCC(=O)CCCCCCCCCCCCCCCCC DMCJFWXGXUEHFD-UHFFFAOYSA-N 0.000 description 2
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
230000006641 stabilisation Effects 0.000 description 2
239000000126 substance Substances 0.000 description 2
150000003505 terpenes Chemical class 0.000 description 2
235000007586 terpenes Nutrition 0.000 description 2
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
AMLFJZRZIOZGPW-NSCUHMNNSA-N (e)-prop-1-en-1-amine Chemical compound C\C=C\N AMLFJZRZIOZGPW-NSCUHMNNSA-N 0.000 description 1
QNRATNLHPGXHMA-XZHTYLCXSA-N (r)-(6-ethoxyquinolin-4-yl)-[(2s,4s,5r)-5-ethyl-1-azabicyclo[2.2.2]octan-2-yl]methanol;hydrochloride Chemical compound Cl.C([C@H]([C@H](C1)CC)C2)CN1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OCC)C=C21 QNRATNLHPGXHMA-XZHTYLCXSA-N 0.000 description 1
RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 description 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
240000004307 Citrus medica Species 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
241000196324 Embryophyta Species 0.000 description 1
244000068988 Glycine max Species 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
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 description 1
239000005642 Oleic acid Substances 0.000 description 1
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
239000005662 Paraffin oil Substances 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
241000607479 Yersinia pestis Species 0.000 description 1
SZGPJHJDNRNHIP-UHFFFAOYSA-N [Cr].[Na].[Na] Chemical compound [Cr].[Na].[Na] SZGPJHJDNRNHIP-UHFFFAOYSA-N 0.000 description 1
238000009825 accumulation Methods 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000013543 active substance Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
150000001344 alkene derivatives Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
BBBFJLBPOGFECG-VJVYQDLKSA-N calcitonin Chemical group N([C@H](C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)NCC(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H]([C@@H](C)O)C(=O)N1[C@@H](CCC1)C(N)=O)C(C)C)C(=O)[C@@H]1CSSC[C@H](N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H]([C@@H](C)O)C(=O)N1 BBBFJLBPOGFECG-VJVYQDLKSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
238000004040 coloring Methods 0.000 description 1
CXUDZCXFKWLXIX-UHFFFAOYSA-N cyclohexyl-(1-phenylcyclohexyl)diazene Chemical compound C1CCC(CC1)N=NC2(CCCCC2)C3=CC=CC=C3 CXUDZCXFKWLXIX-UHFFFAOYSA-N 0.000 description 1
230000001066 destructive effect Effects 0.000 description 1
238000001514 detection method Methods 0.000 description 1
229950001327 dichlorvos Drugs 0.000 description 1
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical class OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
SWSFKKWJEHRFFP-UHFFFAOYSA-N dihexadecyl(dimethyl)azanium Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCC SWSFKKWJEHRFFP-UHFFFAOYSA-N 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
239000003205 fragrance Substances 0.000 description 1
230000008014 freezing Effects 0.000 description 1
238000007710 freezing Methods 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
230000003993 interaction Effects 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000000463 material Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
125000005395 methacrylic acid group Chemical group 0.000 description 1
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
NFBAXHOPROOJAW-UHFFFAOYSA-N phenindione Chemical compound O=C1C2=CC=CC=C2C(=O)C1C1=CC=CC=C1 NFBAXHOPROOJAW-UHFFFAOYSA-N 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920001225 polyester resin Polymers 0.000 description 1
239000004645 polyester resin Substances 0.000 description 1
229920001228 polyisocyanate Polymers 0.000 description 1
239000005056 polyisocyanate Substances 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
229920005749 polyurethane resin Polymers 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
230000003014 reinforcing effect Effects 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
235000000346 sugar Nutrition 0.000 description 1
150000008163 sugars Chemical class 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
229920005992 thermoplastic resin Polymers 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 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
- C07F9/06—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
- 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
- C07F9/091—Esters of phosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
- 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
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
- C07F9/173—Esters of thiophosphoric acids with unsaturated acyclic alcohols

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)

IL37651A 1970-09-11 1971-09-03 Stabilised pesticidal compositions containing phosphoric esters IL37651A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR707033012A FR2104969B1 (fr)	1970-09-11	1970-09-11

Publications (2)

Publication Number	Publication Date
IL37651A0 IL37651A0 (en)	1971-11-29
IL37651A true IL37651A (en)	1974-09-10

Family

ID=9061187

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL37651A IL37651A (en)	1970-09-11	1971-09-03	Stabilised pesticidal compositions containing phosphoric esters

Country Status (17)

Country	Link
US (1)	US3832464A (fr)
AR (1)	AR192584A1 (fr)
AT (1)	AT310504B (fr)
BE (1)	BE772455A (fr)
BR (1)	BR7105976D0 (fr)
CA (1)	CA979356A (fr)
CH (1)	CH573706A5 (fr)
DE (1)	DE2145318A1 (fr)
ES (1)	ES394951A1 (fr)
FR (1)	FR2104969B1 (fr)
GB (1)	GB1320635A (fr)
IL (1)	IL37651A (fr)
IT (1)	IT942167B (fr)
LU (1)	LU63880A1 (fr)
NL (1)	NL149178B (fr)
OA (1)	OA03868A (fr)
ZA (1)	ZA715997B (fr)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5133933A (en) *	1983-08-16	1992-07-28	Interface Research Corporation	Microbiocidal preservative
US5474739A (en) *	1978-02-04	1995-12-12	Interface, Inc.	Microbiocidal composition
US5032310A (en) *	1983-08-16	1991-07-16	Interface, Inc.	Microbiocidal cleansing and disinfecting formulations and preparation thereof
AU3707100A (en) *	1999-02-25	2000-09-14	Van Kampen Group, Inc., The	The use of specific terpenes to kill, impede, render inactive, or inhibit the growth of plants, bacteria, fungi, yeasts, viruses, and insects, parasites
US10238685B2 (en) *	2015-12-02	2019-03-26	Johnson & Johnson Consumer Inc.	Compositions containing polymeric sulfur and uses thereof
US10261244B2 (en) *	2016-02-15	2019-04-16	Nxgen Partners Ip, Llc	System and method for producing vortex fiber

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3116201A (en) *	1952-02-29	1963-12-31	Shell Oil Co	Organo-phosphorus insecticide
NL273220A (fr) *	1961-01-06
NL276695A (fr) *	1961-04-05

1970
- 1970-09-11 FR FR707033012A patent/FR2104969B1/fr not_active Expired
1971
- 1971-09-03 IL IL37651A patent/IL37651A/en unknown
- 1971-09-08 ZA ZA715997A patent/ZA715997B/xx unknown
- 1971-09-09 LU LU63880A patent/LU63880A1/xx unknown
- 1971-09-10 OA OA54361A patent/OA03868A/fr unknown
- 1971-09-10 NL NL717112507A patent/NL149178B/xx unknown
- 1971-09-10 ES ES394951A patent/ES394951A1/es not_active Expired
- 1971-09-10 AT AT789471A patent/AT310504B/de not_active IP Right Cessation
- 1971-09-10 BE BE772455A patent/BE772455A/fr unknown
- 1971-09-10 DE DE2145318A patent/DE2145318A1/de active Pending
- 1971-09-10 BR BR5976/71A patent/BR7105976D0/pt unknown
- 1971-09-10 GB GB4240071A patent/GB1320635A/en not_active Expired
- 1971-09-10 CH CH1331671A patent/CH573706A5/xx not_active IP Right Cessation
- 1971-09-10 CA CA122,521A patent/CA979356A/en not_active Expired
- 1971-09-10 IT IT52803/71A patent/IT942167B/it active
- 1971-09-10 AR AR237868A patent/AR192584A1/es active
- 1971-09-13 US US00180135A patent/US3832464A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
IT942167B (it)	1973-03-20
AR192584A1 (es)	1973-02-28
BE772455A (fr)	1972-03-10
NL7112507A (fr)	1972-03-14
CH573706A5 (fr)	1976-03-31
NL149178B (nl)	1976-04-15
FR2104969A1 (fr)	1972-04-28
FR2104969B1 (fr)	1973-08-10
ES394951A1 (es)	1974-03-16
AT310504B (de)	1973-10-10
GB1320635A (en)	1973-06-20
CA979356A (en)	1975-12-09
OA03868A (fr)	1971-12-24
DE2145318A1 (de)	1974-08-08
ZA715997B (en)	1972-08-30
US3832464A (en)	1974-08-27
BR7105976D0 (pt)	1973-04-05
LU63880A1 (fr)	1973-03-09
AU3325571A (en)	1973-03-15
IL37651A0 (en)	1971-11-29

Publication	Publication Date	Title
US2685552A (en)	1954-08-03	Dimethyl 1-carbomethoxy-1-propen-2-yl phosphate
US3133808A (en)	1964-05-19	Herbicide composition
US3112244A (en)	1963-11-26	Method for controlling nematodes with phosphorothioites and phosphorothioates
IL37651A (en)	1974-09-10	Stabilised pesticidal compositions containing phosphoric esters
US2906661A (en)	1959-09-29	Treating agricultural soils with propargyl phosphorothioates
US3867526A (en)	1975-02-18	Stabilized compositions containing a phosphoric acid ester pesticide and an alcoholic compound
US3781428A (en)	1973-12-25	Hydrophobic insecticidal compositions
US2861912A (en)	1958-11-25	Method for combating pests and preparations suitable therefor
US3806560A (en)	1974-04-23	O-ethyl-s-propyl-s-alkoxy-or substituted amino-carbonylmethyl-phosphorodithiolates
US3102842A (en)	1963-09-03	Dialkyl alpha-(trihalophenyl)-beta-(halo)-vinyl phosphates
CA1076476A (fr)	1980-04-29	Procede pour accroitre la puissance d'insecticides de type esters phosphoriques et nouveaux produits insecticides
US3099597A (en)	1963-07-30	Halophenyl arylphosphonothioates
US2864741A (en)	1958-12-16	Di (alkylmercapto) substituted vinyl, dialkyl phosphate and thiophosphate insecticides
US2523114A (en)	1950-09-19	Methoxy dicyclopentadiene mercuric chloride for controlling parasites
GB1168644A (en)	1969-10-29	Pesticidal Compositions
US2358925A (en)	1944-09-26	Insecticide
US3174990A (en)	1965-03-23	O-[2-halo-1-(polyhalophenyl) vinyl] esters of o, o-dialkyl phosphorothioic and oalkyl alkylphosphonothioic acids
Dyte et al.	1972	Laboratory evaluation of organophosphorus insecticides against susceptible and malathion-resistant strains of Tribolium castaneum (Herbst)(Coleoptera, Tenebrionidae)
US3450713A (en)	1969-06-17	Cyclic dicarboximido-substituted phosphonothioates
US3279983A (en)	1966-10-18	Halophenyl phosphonothioates
US3258394A (en)	1966-06-28	Dimethyl-1-methyl-2-(methylcarbamoyl) vinyl phosphate insecticide and method of use
US3116335A (en)	1963-12-31	Organic sulfur-containing compounds
US4067990A (en)	1978-01-10	Process for the preparation of insecticidal compositions based on carbamic esters
US3077431A (en)	1963-02-12	Phosphinothioates
US3428655A (en)	1969-02-18	Controlling insects and other pests with phosphonothioates