IL27826A - Stabilized compositions of 2-alkoxycarbonylaminobenzimidazole-n-carboxylic acid esters - Google Patents

Stabilized compositions of 2-alkoxycarbonylaminobenzimidazole-n-carboxylic acid esters

Info

Publication number: IL27826A
Authority: IL; Israel
Prior art keywords: acid; compositions; acidic; water; pesticidal
Prior art date: 1966-05-06

Application number

IL27826A

Other languages

English (en)

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.)

1966-05-06

Filing date

1967-04-19

Publication date

1971-08-25

1967-04-19 Application filed by Du Pont filed Critical Du Pont

1971-08-25 Publication of IL27826A publication Critical patent/IL27826A/en

Links

239000000203 mixture Substances 0.000 title claims description 61
230000002378 acidificating effect Effects 0.000 claims description 27
239000000463 material Substances 0.000 claims description 23
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239000002253 acid Substances 0.000 claims description 15
230000000361 pesticidal effect Effects 0.000 claims description 12
239000004094 surface-active agent Substances 0.000 claims description 12
239000003921 oil Substances 0.000 claims description 10
150000001875 compounds Chemical class 0.000 claims description 9
239000007921 spray Substances 0.000 claims description 9
239000003085 diluting agent Substances 0.000 claims description 7
230000000087 stabilizing effect Effects 0.000 claims description 6
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239000003456 ion exchange resin Substances 0.000 claims description 5
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150000001720 carbohydrates Chemical class 0.000 claims description 4
239000003906 humectant Substances 0.000 claims description 4
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 claims description 3
150000007524 organic acids Chemical class 0.000 claims description 3
125000000217 alkyl group Chemical group 0.000 claims description 2
125000004432 carbon atom Chemical group C* 0.000 claims description 2
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KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
235000019198 oils Nutrition 0.000 description 9
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DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 5
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IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 3
WEYSQARHSRZNTC-UHFFFAOYSA-N 1h-benzimidazol-2-ylcarbamic acid Chemical compound C1=CC=C2NC(NC(=O)O)=NC2=C1 WEYSQARHSRZNTC-UHFFFAOYSA-N 0.000 description 3
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239000005642 Oleic acid Substances 0.000 description 3
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 3
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230000000855 fungicidal effect Effects 0.000 description 3
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VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
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VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
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150000007513 acids Chemical class 0.000 description 2
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229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
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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 2
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239000002904 solvent Substances 0.000 description 2
150000005846 sugar alcohols Polymers 0.000 description 2
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
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JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 1
GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 1
HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
YYYOQURZQWIILK-UHFFFAOYSA-N 2-[(2-aminophenyl)disulfanyl]aniline Chemical compound NC1=CC=CC=C1SSC1=CC=CC=C1N YYYOQURZQWIILK-UHFFFAOYSA-N 0.000 description 1
KWVPFECTOKLOBL-KTKRTIGZSA-N 2-[(z)-octadec-9-enoxy]ethanol Chemical compound CCCCCCCC\C=C/CCCCCCCCOCCO KWVPFECTOKLOBL-KTKRTIGZSA-N 0.000 description 1
GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
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RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
241000221785 Erysiphales Species 0.000 description 1
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical class OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
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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
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230000007797 corrosion Effects 0.000 description 1
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PYRZPBDTPRQYKG-UHFFFAOYSA-N cyclopentene-1-carboxylic acid Chemical class OC(=O)C1=CCCC1 PYRZPBDTPRQYKG-UHFFFAOYSA-N 0.000 description 1
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239000000243 solution Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
230000006641 stabilisation Effects 0.000 description 1
238000011105 stabilization Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
150000003440 styrenes Chemical class 0.000 description 1
239000000126 substance Substances 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 description 1
235000015523 tannic acid Nutrition 0.000 description 1
229920002258 tannic acid Polymers 0.000 description 1
229940033123 tannic acid Drugs 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
230000005945 translocation Effects 0.000 description 1
238000011282 treatment Methods 0.000 description 1
150000003626 triacylglycerols Chemical class 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
238000009736 wetting Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D235/30—Nitrogen atoms not forming part of a nitro radical
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D235/30—Nitrogen atoms not forming part of a nitro radical
- C07D235/32—Benzimidazole-2-carbamic acids, unsubstituted or substituted; Esters thereof; Thio-analogues thereof

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Disintegrating Or Milling (AREA)

IL27826A 1966-05-06 1967-04-19 Stabilized compositions of 2-alkoxycarbonylaminobenzimidazole-n-carboxylic acid esters IL27826A (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US54774166A	1966-05-06	1966-05-06
US62990867A	1967-04-11	1967-04-11

Publications (1)

Publication Number	Publication Date
IL27826A true IL27826A (en)	1971-08-25

Family

ID=27068639

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL27826A IL27826A (en)	1966-05-06	1967-04-19	Stabilized compositions of 2-alkoxycarbonylaminobenzimidazole-n-carboxylic acid esters

Country Status (19)

Country	Link
US (1)	US3454700A (de)
AT (1)	AT289458B (de)
BE (1)	BE698070A (de)
BR (1)	BR6789195D0 (de)
CH (1)	CH485409A (de)
CY (1)	CY632A (de)
DE (1)	DE1642321A1 (de)
DK (1)	DK114518B (de)
DO (1)	DOP1967001357A (de)
ES (1)	ES339902A1 (de)
FI (1)	FI43369B (de)
GB (1)	GB1190401A (de)
GR (1)	GR34612B (de)
IL (1)	IL27826A (de)
LU (1)	LU53599A1 (de)
MY (1)	MY7300060A (de)
NL (1)	NL6706333A (de)
NO (1)	NO117094B (de)
OA (1)	OA02424A (de)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3930010A (en) *	1972-06-06	1975-12-30	Du Pont	Fungicidal formulations of 2-benzimidazolecarbamic acid, alkyl esters
JPS5799505A (en) *	1980-12-12	1982-06-21	Kumiai Chem Ind Co Ltd	Fungicidal composition for agricultural and horticultural use

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2933502A (en) *	1958-02-12	1960-04-19	Du Pont	Benzimidazolone derivatives
US2933504A (en) *	1959-08-10	1960-04-19	Du Pont	Derivatives of polyalkoxycarbonyl imine
US3010968A (en) *	1959-11-25	1961-11-28	Du Pont	Process for manufacture of certain alkyl esters of benzimidazole carbamic acids

1967
- 1967-04-11 US US629908A patent/US3454700A/en not_active Expired - Lifetime
- 1967-04-19 IL IL27826A patent/IL27826A/en unknown
- 1967-04-27 ES ES339902A patent/ES339902A1/es not_active Expired
- 1967-04-27 GR GR670134612A patent/GR34612B/el unknown
- 1967-05-02 DO DO1967001357A patent/DOP1967001357A/es unknown
- 1967-05-02 CH CH625767A patent/CH485409A/de not_active IP Right Cessation
- 1967-05-03 DE DE19671642321 patent/DE1642321A1/de active Pending
- 1967-05-03 AT AT412967A patent/AT289458B/de not_active IP Right Cessation
- 1967-05-05 BE BE698070D patent/BE698070A/xx unknown
- 1967-05-05 DK DK239167AA patent/DK114518B/da unknown
- 1967-05-05 FI FI1302/67A patent/FI43369B/fi active
- 1967-05-05 OA OA52922A patent/OA02424A/xx unknown
- 1967-05-05 BR BR189195/67A patent/BR6789195D0/pt unknown
- 1967-05-05 LU LU53599D patent/LU53599A1/xx unknown
- 1967-05-05 NO NO168007A patent/NO117094B/no unknown
- 1967-05-05 GB GB21058/67A patent/GB1190401A/en not_active Expired
- 1967-05-05 NL NL6706333A patent/NL6706333A/xx unknown
1972
- 1972-02-19 CY CY63272A patent/CY632A/xx unknown
1973
- 1973-12-31 MY MY197360A patent/MY7300060A/xx unknown

Also Published As

Publication number	Publication date
MY7300060A (en)	1973-12-31
FI43369B (de)	1970-11-30
DK114518B (da)	1969-07-07
GB1190401A (en)	1970-05-06
CY632A (en)	1972-02-19
ES339902A1 (es)	1968-08-16
LU53599A1 (de)	1967-09-04
GR34612B (el)	1968-05-27
BR6789195D0 (pt)	1973-06-05
DOP1967001357A (es)	1972-03-29
AT289458B (de)	1971-04-26
US3454700A (en)	1969-07-08
NL6706333A (de)	1967-11-07
DE1642321A1 (de)	1971-05-06
CH485409A (de)	1970-02-15
NO117094B (de)	1969-06-30
BE698070A (de)	1967-10-16
OA02424A (fr)	1970-05-05

Publication	Publication Date	Title
US3657443A (en)	1972-04-18	2-benzimidazolecarbamic acid alkyl esters as foliar fungicides
EP0236272B1 (de)	1991-06-12	Fungizide Verwendung eines Cyanopyrrol-Derivates
EP0126254A1 (de)	1984-11-28	N-(2-Nitrophenyl)-4-aminopyrimidin-Derivate als Mikrobizide
EP0133247B1 (de)	1989-12-13	N-Aminomethyl-3-phenyl-4-cyanopyrrol-Derivate, deren Herstellung und Verwendung als Mikrobizide
US3932168A (en)	1976-01-13	Substituted aryloxyacetamido nitrile derivatives as carbohydrate deposition agents
EP3308647A1 (de)	2018-04-18	Agrochemische zusammensetzungen zur reduzierung agrochemischer reste
EP0346841A2 (de)	1989-12-20	1-Aryl-naphthoesäureamide und diese enthaltende mikrobizide Mittel
PL202065B1 (pl)	2009-05-29	Solwat pimetrozyny, sposób wytwarzania solwatu pimetrozyny oraz kompozycja pestycydowa
EP0163606B1 (de)	1989-09-06	Mikrobizide 1-Fluor-1-azolyl-2,2-diarylethanderivate
US3454700A (en)	1969-07-08	Methods for stabilizing pesticidal compositions of 2 - alkoxycarbonylaminobenzimidazolecarboxylic esters
JPH08337505A (ja)	1996-12-24	水溶性粒状除草剤組成物
HU213638B (en)	1997-08-28	Method for producing herbicidal granular compositions
KR930005279B1 (ko)	1993-06-17	무수 살충제 조성물의 제조방법
KR880002613B1 (ko)	1988-12-07	살균제 조성물 및 균류 억제방법
EP0068296B1 (de)	1985-12-11	Eine fungizide Zusammensetzung, Verfahren zu deren Herstellung und Anwendung
US3427388A (en)	1969-02-11	Esters of benzimidazolecarbamic acid as mite ovicides
US3662069A (en)	1972-05-09	Alkyl 1-(n-substituted thiocarbamoyl)-2-benzimidazolecarbamates as fungicides and mite ovicides
DE2123830A1 (de)	1971-12-02	Neue Thiocyanatomethylhydantoinverbindungen
US3279982A (en)	1966-10-18	Fungicidal mixture of thiuram sulfides and oxidizing agent
HU198603B (en)	1989-11-28	Stable, fenarimol-containing, powdered fungicide
IL33014A (en)	1972-06-28	Fungicidal compositions comprising sucrose and 1-alkylaminocarbonyl-2-alkoxycarbonylaminobenzimidazoles
EP0215307B1 (de)	1991-07-24	Pyrimiden-Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Mikrobizide
US3472936A (en)	1969-10-14	Synergistic fungicidal composition
EP0439426A1 (de)	1991-07-31	Mikrobizide Mittel
CH663612A5 (de)	1987-12-31	N-substituierte aminopropansulfonsaeure-derivate.