GB918365A - Fungicidal and acaricidal compositions - Google Patents
Fungicidal and acaricidal compositionsInfo
- Publication number
- GB918365A GB918365A GB1075561A GB1075561A GB918365A GB 918365 A GB918365 A GB 918365A GB 1075561 A GB1075561 A GB 1075561A GB 1075561 A GB1075561 A GB 1075561A GB 918365 A GB918365 A GB 918365A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dodecyl
- glycine
- amino
- sulphate
- ester
- 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
- 230000000855 fungicidal effect Effects 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 title abstract 2
- 230000000895 acaricidal effect Effects 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 5
- -1 aliphatic amino acid derivative Chemical class 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- FXHYAXBIUKRLLT-UHFFFAOYSA-N 2-(decylazaniumyl)acetate Chemical compound CCCCCCCCCCNCC(O)=O FXHYAXBIUKRLLT-UHFFFAOYSA-N 0.000 abstract 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 abstract 2
- 239000004480 active ingredient Substances 0.000 abstract 2
- ZPCQJJNJMGCLSC-UHFFFAOYSA-L 2-(dodecylamino)acetic acid nickel(2+) sulfate Chemical compound S(=O)(=O)([O-])[O-].[Ni+2].C(CCCCCCCCCCC)NCC(=O)O ZPCQJJNJMGCLSC-UHFFFAOYSA-L 0.000 abstract 1
- LNPHVNNRZGCOBK-UHFFFAOYSA-N 2-(dodecylazaniumyl)acetate Chemical compound CCCCCCCCCCCCNCC(O)=O LNPHVNNRZGCOBK-UHFFFAOYSA-N 0.000 abstract 1
- KDJPMXHQWRVTNV-UHFFFAOYSA-N 2-(pentadecylamino)acetic acid Chemical compound CCCCCCCCCCCCCCCNCC(O)=O KDJPMXHQWRVTNV-UHFFFAOYSA-N 0.000 abstract 1
- VIQOQTJPKVEXGN-UHFFFAOYSA-N 2-chloroethyl 2-(dodecylamino)acetate Chemical compound ClCCOC(CNCCCCCCCCCCCC)=O VIQOQTJPKVEXGN-UHFFFAOYSA-N 0.000 abstract 1
- BDFNILJADJYEMA-UHFFFAOYSA-N 2-hydroxyethyl 2-(dodecylamino)acetate Chemical compound OCCOC(CNCCCCCCCCCCCC)=O BDFNILJADJYEMA-UHFFFAOYSA-N 0.000 abstract 1
- CIFUPJOZATUHPX-UHFFFAOYSA-N 3-(dodecylamino)-N,N-diethylpropanamide Chemical compound C(CCCCCCCCCCC)NCCC(=O)N(CC)CC CIFUPJOZATUHPX-UHFFFAOYSA-N 0.000 abstract 1
- VIRQROAUBXZBES-UHFFFAOYSA-N 3-(dodecylamino)-N-methyl-N-phenylpropanamide Chemical compound C(CCCCCCCCCCC)NCCC(=O)N(C1=CC=CC=C1)C VIRQROAUBXZBES-UHFFFAOYSA-N 0.000 abstract 1
- KYWAPQHHSJWEFV-UHFFFAOYSA-N 3-(dodecylamino)-N-phenylpropanamide Chemical compound C(CCCCCCCCCCC)NCCC(=O)NC1=CC=CC=C1 KYWAPQHHSJWEFV-UHFFFAOYSA-N 0.000 abstract 1
- LIYJMWCISHOVHW-UHFFFAOYSA-N 3-(dodecylamino)-n,n-dimethylpropanamide Chemical compound CCCCCCCCCCCCNCCC(=O)N(C)C LIYJMWCISHOVHW-UHFFFAOYSA-N 0.000 abstract 1
- DOGYIROFDHBQIA-UHFFFAOYSA-N 3-(dodecylamino)-n-methylpropanamide Chemical compound CCCCCCCCCCCCNCCC(=O)NC DOGYIROFDHBQIA-UHFFFAOYSA-N 0.000 abstract 1
- FUJYDOUXZQBAAO-UHFFFAOYSA-N 3-(dodecylamino)propanamide Chemical compound CCCCCCCCCCCCNCCC(N)=O FUJYDOUXZQBAAO-UHFFFAOYSA-N 0.000 abstract 1
- AEDQNOLIADXSBB-UHFFFAOYSA-N 3-(dodecylazaniumyl)propanoate Chemical compound CCCCCCCCCCCCNCCC(O)=O AEDQNOLIADXSBB-UHFFFAOYSA-N 0.000 abstract 1
- HGMDJWDKKALQSH-UHFFFAOYSA-N N-cyclohexyl-3-(dodecylamino)propanamide Chemical compound C(CCCCCCCCCCC)NCCC(=O)NC1CCCCC1 HGMDJWDKKALQSH-UHFFFAOYSA-N 0.000 abstract 1
- NELAPBZQCTWNLI-UHFFFAOYSA-L S(=O)(=O)([O-])[O-].[Cu+2].C(CCCCCCCCCCCCCC)NCC(=O)O Chemical compound S(=O)(=O)([O-])[O-].[Cu+2].C(CCCCCCCCCCCCCC)NCC(=O)O NELAPBZQCTWNLI-UHFFFAOYSA-L 0.000 abstract 1
- NMJBOZIPKCOSBU-UHFFFAOYSA-L S(=O)(=O)([O-])[O-].[Mn+2].C(CCCCCCCCCCC)NCC(=O)O Chemical compound S(=O)(=O)([O-])[O-].[Mn+2].C(CCCCCCCCCCC)NCC(=O)O NMJBOZIPKCOSBU-UHFFFAOYSA-L 0.000 abstract 1
- BYGHIKGYROQYLN-UHFFFAOYSA-L S(=O)(=O)([O-])[O-].[Zn+2].C(CCCCCCCCC)NCC(=O)O Chemical compound S(=O)(=O)([O-])[O-].[Zn+2].C(CCCCCCCCC)NCC(=O)O BYGHIKGYROQYLN-UHFFFAOYSA-L 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 1
- 125000005907 alkyl ester group Chemical group 0.000 abstract 1
- 125000000068 chlorophenyl group Chemical group 0.000 abstract 1
- ONCOFZBSYDRWRI-UHFFFAOYSA-N copper 2-(decylamino)acetic acid dinitrate Chemical compound [N+](=O)([O-])[O-].[Cu+2].C(CCCCCCCCC)NCC(=O)O.[N+](=O)([O-])[O-] ONCOFZBSYDRWRI-UHFFFAOYSA-N 0.000 abstract 1
- 239000003995 emulsifying agent Substances 0.000 abstract 1
- QOLIMOFOWZLWMG-UHFFFAOYSA-N ethyl 2-(dodecylamino)acetate Chemical compound CCCCCCCCCCCCNCC(=O)OCC QOLIMOFOWZLWMG-UHFFFAOYSA-N 0.000 abstract 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- JGNBZFBRQBHXJV-UHFFFAOYSA-N methyl 2-(dodecylamino)acetate Chemical compound CCCCCCCCCCCCNCC(=O)OC JGNBZFBRQBHXJV-UHFFFAOYSA-N 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- BESHWCKETUYIAZ-UHFFFAOYSA-N propyl 2-(dodecylamino)acetate Chemical compound C(CC)OC(CNCCCCCCCCCCCC)=O BESHWCKETUYIAZ-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 229910021653 sulphate ion Inorganic materials 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- ZCECQBSDGGHLAR-UHFFFAOYSA-L zinc 2-(dodecylamino)acetic acid sulfate Chemical compound S(=O)(=O)([O-])[O-].[Zn+2].C(CCCCCCCCCCC)NCC(=O)O ZCECQBSDGGHLAR-UHFFFAOYSA-L 0.000 abstract 1
- UIZPBSBXWXXVPD-UHFFFAOYSA-L zinc 2-(pentadecylamino)acetic acid dichloride Chemical compound [Cl-].[Zn+2].C(CCCCCCCCCCCCCC)NCC(=O)O.[Cl-] UIZPBSBXWXXVPD-UHFFFAOYSA-L 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF30810A DE1125713B (de) | 1960-03-23 | 1960-03-23 | Schaedlingsbekaempfungsmittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB918365A true GB918365A (en) | 1963-02-13 |
Family
ID=7093928
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1075561A Expired GB918365A (en) | 1960-03-23 | 1961-03-23 | Fungicidal and acaricidal compositions |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE601542A (enrdf_load_stackoverflow) |
| DE (1) | DE1125713B (enrdf_load_stackoverflow) |
| GB (1) | GB918365A (enrdf_load_stackoverflow) |
| NL (1) | NL262748A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4077941A (en) | 1974-03-11 | 1978-03-07 | Ciba-Geigy Corporation | Metal salts of N,N-disubstituted β-alanines and stabilized compositions |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1191629B (de) * | 1962-03-16 | 1965-04-22 | Basf Ag | Fungizide Mittel |
| US4126700A (en) * | 1977-05-13 | 1978-11-21 | Block Drug Company, Inc., Reed & Carnrich Division | Aminopropionic-acids as ectoparasiticides |
| CH650768A5 (de) * | 1982-08-27 | 1985-08-15 | Pharmaton Sa | Basische acetanilide, verfahren zu deren herstellung und arzneimittel, die diese acetanilide enthalten. |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2293034A (en) * | 1941-05-22 | 1942-08-18 | American Cyanamid Co | Pest control composition |
| US2653895A (en) * | 1949-01-11 | 1953-09-29 | Nathan L Drake | Insect repellents |
-
0
- NL NL262748D patent/NL262748A/xx unknown
- BE BE601542D patent/BE601542A/xx unknown
-
1960
- 1960-03-23 DE DEF30810A patent/DE1125713B/de active Pending
-
1961
- 1961-03-23 GB GB1075561A patent/GB918365A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4077941A (en) | 1974-03-11 | 1978-03-07 | Ciba-Geigy Corporation | Metal salts of N,N-disubstituted β-alanines and stabilized compositions |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1125713B (de) | 1962-03-15 |
| BE601542A (enrdf_load_stackoverflow) | |
| NL262748A (enrdf_load_stackoverflow) |
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