US2023202941A1PendingUtilityA1

Nitrification inhibitors

65
Assignee: LINCOLN UNIVPriority: May 25, 2020Filed: Feb 13, 2023Published: Jun 29, 2023
Est. expiryMay 25, 2040(~13.9 yrs left)· nominal 20-yr term from priority
C09K 15/30C05G 3/80C07D 237/14C07D 241/18C07D 239/34C05C 3/00B09C 1/08C05C 9/00C02F 2103/20C02F 1/68C05G 3/90B09C 2101/00Y02P60/21
65
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Claims

Abstract

Nitrification inhibitors and uses of same to prevent nitrate leaching or nitrous oxide emissions as well as increase pasture or crop production. The nitrification inhibitors and formulations including same may be used for direct or indirect application to soil or pasture.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of manufacturing a nitrification-inhibiting composition comprising introducing into a carrier at least one nitrification inhibitor compound of Formula 1:
                       wherein X 1  and X 5  ═ N; X 2  and X 4  ═ CH; and X 3  ═ C—R; wherein R is selected from the group consisting of H and OMe; or   wherein X 1  and X 5  ═ CH; X 2  and X 4  ═ N; and X 3  ═ C—R; wherein R is selected from the group consisting of H and OMe; or   wherein X 1  and X 3  ═ N; and X 2 , X 4  and X 5  ═ CH; or   wherein X 1 , X 4 , and X 5  ═ CH; X 2  is selected from the group consisting of N and N═O; and X 3  ═ C—R; and wherein if X 2  is N═O R is H; and wherein if X 2  is N then R is OMe; or   wherein X 1  ═ N, X 2 , X 4  and X 5  ═ CH; and X 3  ═ C—R; wherein R is OMe; or   wherein X 1  and X 2  ═ N; X 3  ═ C—R; and X 4  and X 5  ═ CH; wherein R is selected from the group consisting of H and OMe; or   wherein X 1  and X 4  ═ N; X 2  and X 5  ═ CH; and X 3  ═ C—R; wherein R is selected from the group consisting of H and OMe; or   wherein X 1 , X 2 , X 4  and X 5  ═ CH; X 3  ═ C—R; wherein R is selected from the group consisting of OMe, OEt, and C≡CH.   
     
     
         2 . The method as claimed in  claim 1  wherein the carrier is a solid or liquid carrier. 
     
     
         3 . The method as claimed in  claim 2  wherein the carrier is water, effluent, animal urine or manure. 
     
     
         4 . The method as claimed in  claim 2  wherein the carrier is a solid or liquid fertilizer. 
     
     
         5 . The method as claimed in  claim 4  wherein the fertilizer comprises urea or another fertilizer that contains ammonium (or ammonia) or produces ammonium (or ammonia). 
     
     
         6 . The method as claimed in  claim 1 , wherein the compound is selected from the group consisting of:
 2-Ethynyl 1,3 Diazine;   3-Ethynyl 1,5 Diazine;   4-Ethynylpyrimidine;   2-Ethynyl-5-methoxypyrimidine;   5-Ethynyl-2-methoxypyrimidine;   2-ethynyl-5-methoxypyridine;   5-ethynyl-2-methoxypyridine;   3-ethynylpyridine 1-oxide;   2,5-diethynylpyridine;   3-Ethynylpyridazine;   3-Ethynyl-6-methoxypyridazine;   2-ethynylpyrazine;   2-Ethynyl-5-methoxypyrazine;   4-Ethynylanisole;   1-ethoxy-4-ethynylbenzene;   1,4-diethynylbenzene;   and has a dosage rate between substantially 1 kg/ha to 9 kg/ha.   
     
     
         7 . A method, as claimed in  claim 6 , wherein the compound is selected from the group consisting of:
 2-Ethynyl 1,3 Diazine;   3-Ethynyl 1,5 Diazine;   4-Ethynylpyrimidine;   2-Ethynyl-5-methoxypyrimidine;   5-Ethynyl-2-methoxypyrimidine;   2-ethynyl-5-methoxypyridine;   3-ethynylpyridine 1-oxide;   3-Ethynylpyridazine;   3-Ethynyl-6-methoxypyridazine;   2-Ethynyl-5-methoxypyrazine;   4-Ethynylanisole.   
     
     
         8 . A method, as claimed in  claim 6 , wherein the compound is selected from the group consisting of:
 2-Ethynyl 1,3 Diazine;   3-Ethynyl 1,5 Diazine;   2-ethynyl-5-methoxypyridine;   3-ethynylpyridine 1-oxide;   3-Ethynylpyridazine.

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