US2021380522A1PendingUtilityA1

Ethyl Benzyl Quaternary Amines of Amido Amines for Improved Antifungal properties

Individually held — no corporate assignee on recordPriority: Dec 19, 2014Filed: Jul 8, 2021Published: Dec 9, 2021
Est. expiryDec 19, 2034(~8.4 yrs left)· nominal 20-yr term from priority
Inventors:Thomas Daly
C07C 211/63C07C 233/36C11D 1/62
74
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Claims

Abstract

Ethyl benzyl quaternaries having superior anti-fungal properties versus their benzyl quaternary analogs. The ethylbenzyl amidoamine quaternaries of the present invention are easily produced without significant waste and with minimal capital, while possessing improved antimicrobial properties.

Claims

exact text as granted — not AI-modified
1 . The salt of the quaternary ammonium compound of the following structure: 
       
         
           
           
               
               
           
         
         wherein R and R 1  are independently chosen from alkyl, alkenyl, alkynyl, branched or linear, cyclic or acyclic from 1-22 carbons wherein Q is chosen from —CH 3 , —CH 2 CH 3 , —CH 2 —C 6 H 5 , or —CH(CH 2 —CH 3 )—C 6 H 5 . 
       
     
     
         2 . The salt of the quaternary ammonium compound of  claim 1  wherein Q=—CH 3 . 
     
     
         3 . The salt of the quaternary ammonium compound of  claim 1  wherein Q=—CH 2 CH 3 . 
     
     
         4 . The salt of the quaternary ammonium compound of  claim 1  wherein Q=—CH 2 —C 6 H 5 . 
     
     
         5 . The salt of the quaternary ammonium compound of  claim 1  wherein Q=—CH(CH 2 —CH 3 )—C 6 H 5 . 
     
     
         6 . The salt of the quaternary ammonium compound of  claim 1  wherein Q=—CH 3  and one of R or R′ is alkyl. 
     
     
         7 . The salt of the quaternary ammonium compound of  claim 1  wherein Q=—CH 2 CH 3  and at least one of R or R′ is alkyl. 
     
     
         8 . The salt of the quaternary ammonium compound of  claim 1  wherein Q=—CH 2 —C 6 H 5  and at least one of R or R′ is alkyl. 
     
     
         9 . The salt of the quaternary ammonium compound of  claim 1  wherein Q=—CH(CH 2 —CH 3 )—C 6 H 5  and at least one of R or R′ is alkyl. 
     
     
         10 . The salt of the quaternary ammonium compound of  claim 1  wherein Q=—CH 3  and R is not equal to R′. 
     
     
         11 . The salt of the quaternary ammonium compound of  claim 1  wherein Q=—CH 2 CH 3  and R is not equal to R′. 
     
     
         12 . The salt of the quaternary ammonium compound of  claim 1  wherein Q=—CH 2 —C 6 H 5  and R is not equal to R′. 
     
     
         13 . The salt of the quaternary ammonium compound of  claim 1  wherein Q=—CH(CH 2 —CH 3 )—C 6 H 5  and R is not equal to R′. 
     
     
         14 . The salt of the quaternary ammonium compound of  claim 1  wherein R═R′. 
     
     
         15 . The salt of the quaternary ammonium compound of the following structure: 
       
         
           
           
               
               
           
         
         wherein R and R 1  are independently chosen from alkyl, alkenyl, alkynyl, branched or linear, cyclic or acyclic from 1-22 carbons wherein Q is chosen from —CH 3 , —CH 2 CH 3 , —CH 2 —C 6 H 5 , or —CH(CH 2 —CH 3 )—C 6 H 5 . 
       
     
     
         16 . The salt of the quaternary ammonium compound of  claim 15  wherein Q=—CH 3 . 
     
     
         17 . (The salt of the quaternary ammonium compound of  claim 15  wherein Q=—CH 2 CH 3 . 
     
     
         18 . The salt of the quaternary ammonium compound of  claim 15  wherein Q=—CH 2 —C 6 H 5 . 
     
     
         19 . The salt of the quaternary ammonium compound of  claim 15  wherein Q=—CH(CH 2 —CH 3 )—C 6 H 5 .

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