CA2182011C - Combinaisons de principes actifs utilises pour inhiber ou reguler la nitrification - Google Patents
Combinaisons de principes actifs utilises pour inhiber ou reguler la nitrificationInfo
- Publication number
- CA2182011C CA2182011C CA002182011A CA2182011A CA2182011C CA 2182011 C CA2182011 C CA 2182011C CA 002182011 A CA002182011 A CA 002182011A CA 2182011 A CA2182011 A CA 2182011A CA 2182011 C CA2182011 C CA 2182011C
- Authority
- CA
- Canada
- Prior art keywords
- active ingredients
- alone
- soil
- triazole
- dcd
- 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 - Fee Related
Links
- 230000002401 inhibitory effect Effects 0.000 title claims description 5
- 239000013543 active substance Substances 0.000 title claims 3
- 230000001105 regulatory effect Effects 0.000 title 1
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims abstract description 32
- 239000004480 active ingredient Substances 0.000 claims abstract description 28
- SOIFLUNRINLCBN-UHFFFAOYSA-N ammonium thiocyanate Chemical compound [NH4+].[S-]C#N SOIFLUNRINLCBN-UHFFFAOYSA-N 0.000 claims abstract description 14
- 150000001875 compounds Chemical class 0.000 claims abstract description 9
- 150000003839 salts Chemical class 0.000 claims abstract description 7
- XYXNTHIYBIDHGM-UHFFFAOYSA-N ammonium thiosulfate Chemical compound [NH4+].[NH4+].[O-]S([O-])(=O)=S XYXNTHIYBIDHGM-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000003112 inhibitor Substances 0.000 claims abstract description 4
- NOIXNOMHHWGUTG-UHFFFAOYSA-N 2-[[4-[4-pyridin-4-yl-1-(2,2,2-trifluoroethyl)pyrazol-3-yl]phenoxy]methyl]quinoline Chemical compound C=1C=C(OCC=2N=C3C=CC=CC3=CC=2)C=CC=1C1=NN(CC(F)(F)F)C=C1C1=CC=NC=C1 NOIXNOMHHWGUTG-UHFFFAOYSA-N 0.000 claims abstract description 3
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 claims description 47
- 239000002689 soil Substances 0.000 claims description 29
- 238000000034 method Methods 0.000 claims description 21
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 17
- 239000003337 fertilizer Substances 0.000 claims description 10
- 229910052757 nitrogen Inorganic materials 0.000 claims description 9
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 4
- 239000011707 mineral Substances 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 239000003905 agrochemical Substances 0.000 claims 2
- NSPMIYGKQJPBQR-CVMUNTFWSA-N 1h-1,2,4-triazole Chemical class [13CH]=1[15N]=[13CH][15NH][15N]=1 NSPMIYGKQJPBQR-CVMUNTFWSA-N 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 239000012141 concentrate Substances 0.000 claims 1
- 239000000839 emulsion Substances 0.000 claims 1
- 239000003630 growth substance Substances 0.000 claims 1
- 239000004009 herbicide Substances 0.000 claims 1
- 239000000575 pesticide Substances 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 239000000725 suspension Substances 0.000 claims 1
- 230000002195 synergetic effect Effects 0.000 abstract description 4
- XKVUYEYANWFIJX-UHFFFAOYSA-N 5-methyl-1h-pyrazole Chemical compound CC1=CC=NN1 XKVUYEYANWFIJX-UHFFFAOYSA-N 0.000 description 17
- 238000007405 data analysis Methods 0.000 description 15
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 8
- 229960005419 nitrogen Drugs 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 7
- 241000196324 Embryophyta Species 0.000 description 6
- 229910002651 NO3 Inorganic materials 0.000 description 6
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 6
- 101150054830 S100A6 gene Proteins 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 239000004202 carbamide Substances 0.000 description 4
- 235000013877 carbamide Nutrition 0.000 description 4
- 230000005764 inhibitory process Effects 0.000 description 4
- FMCUPJKTGNBGEC-UHFFFAOYSA-N 1,2,4-triazol-4-amine Chemical compound NN1C=NN=C1 FMCUPJKTGNBGEC-UHFFFAOYSA-N 0.000 description 3
- 150000003868 ammonium compounds Chemical class 0.000 description 3
- 150000002823 nitrates Chemical class 0.000 description 3
- 239000000618 nitrogen fertilizer Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 230000001580 bacterial effect Effects 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- SFDJOSRHYKHMOK-UHFFFAOYSA-N nitramide Chemical compound N[N+]([O-])=O SFDJOSRHYKHMOK-UHFFFAOYSA-N 0.000 description 2
- 150000003217 pyrazoles Chemical class 0.000 description 2
- 150000003852 triazoles Chemical class 0.000 description 2
- WCRAKJMHCWUABB-UHFFFAOYSA-N 1,2,4-triazol-1-ylmethanol Chemical compound OCN1C=NC=N1 WCRAKJMHCWUABB-UHFFFAOYSA-N 0.000 description 1
- CDIOIIJXUJXYPB-UHFFFAOYSA-N 1,2,4-triazole-1-carboximidamide Chemical compound NC(=N)N1C=NC=N1 CDIOIIJXUJXYPB-UHFFFAOYSA-N 0.000 description 1
- PNZZQMXKKNDHNS-UHFFFAOYSA-N 3-methylpyrazole-1-carboxamide Chemical compound CC=1C=CN(C(N)=O)N=1 PNZZQMXKKNDHNS-UHFFFAOYSA-N 0.000 description 1
- GWLRCPBBLXQXRZ-UHFFFAOYSA-N 3-methylpyrazole-1-carboximidamide Chemical compound CC=1C=CN(C(N)=N)N=1 GWLRCPBBLXQXRZ-UHFFFAOYSA-N 0.000 description 1
- 229910000497 Amalgam Inorganic materials 0.000 description 1
- 239000002028 Biomass Substances 0.000 description 1
- 101000713575 Homo sapiens Tubulin beta-3 chain Proteins 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- 101100409194 Rattus norvegicus Ppargc1b gene Proteins 0.000 description 1
- 102100036790 Tubulin beta-3 chain Human genes 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000004459 forage Substances 0.000 description 1
- 239000003673 groundwater Substances 0.000 description 1
- 239000003864 humus Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 125000001477 organic nitrogen group Chemical group 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- WRHZVMBBRYBTKZ-UHFFFAOYSA-N pyrrole-2-carboxylic acid Chemical compound OC(=O)C1=CC=CN1 WRHZVMBBRYBTKZ-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P60/00—Technologies relating to agriculture, livestock or agroalimentary industries
- Y02P60/20—Reduction of greenhouse gas [GHG] emissions in agriculture, e.g. CO2
- Y02P60/21—Dinitrogen oxide [N2O], e.g. using aquaponics, hydroponics or efficiency measures
Landscapes
- Fertilizers (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Des inhibiteurs de la nitrification se caractérisent en ce qu'ils contiennent comme principes actifs 1H-1,2-4-triazol substitué ou non, ses sels ou ses complexes métalliques, et au moins un autre composé tel qu'un pyrazol substitué, ses sels ou ses complexes métalliques, dicyanodiamide, guanylthiourée, thiourée, thiosulfate d'ammonium, thiocyanate d'ammonium. Ces agents présentent des effets synergiques considérables et sont, par rapport aux composés isolés, plus économiques, d'une efficacité accrue, et ils peuvent être utilisés en quantités réduites.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEP4405392.4 | 1994-02-21 | ||
| DE4405392A DE4405392C1 (de) | 1994-02-21 | 1994-02-21 | Wirkstoffkombinationen zur Hemmung bzw. Regelung der Nitrifikation |
| PCT/DE1995/000248 WO1995022515A1 (fr) | 1994-02-21 | 1995-02-20 | Combinaisons de principes actifs utilises pour inhiber ou reguler la nitrification |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2182011A1 CA2182011A1 (fr) | 1995-08-24 |
| CA2182011C true CA2182011C (fr) | 2001-06-05 |
Family
ID=25933964
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002182011A Expired - Fee Related CA2182011C (fr) | 1994-02-21 | 1995-02-20 | Combinaisons de principes actifs utilises pour inhiber ou reguler la nitrification |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA2182011C (fr) |
-
1995
- 1995-02-20 CA CA002182011A patent/CA2182011C/fr not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CA2182011A1 (fr) | 1995-08-24 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| MKLA | Lapsed |