US2017313920A1PendingUtilityA1

Biological Buffers with Wide Buffering Ranges

Individually held — no corporate assignee on recordPriority: Oct 6, 2010Filed: Jul 14, 2017Published: Nov 2, 2017
Est. expiryOct 6, 2030(~4.2 yrs left)· nominal 20-yr term from priority
Inventors:Thomas Daly
C07F 9/3817C07C 229/12C07C 205/40C07C 219/22C07C 229/22C07F 9/58C07C 217/08C07C 215/10C07D 295/15C07D 213/74C07C 205/15C07C 309/14C07C 219/06C09K 3/00C07C 217/28C07F 9/091C11D 1/66C07F 9/3808C07D 295/088C07C 215/08C07C 217/48C07F 9/588
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Claims

Abstract

Amines and amine derivatives that improve the buffering range, and/or reduce the chelation and other negative interactions of the buffer and the system to be buffered. The reaction of amines or polyamines with various molecules to form polyamines with differing pKa's will extend the buffering range, derivatives that result in polyamines that have the same pKa yields a greater buffering capacity. Derivatives that result in zwitterionic buffers improve yield by allowing a greater range of stability.

Claims

exact text as granted — not AI-modified
I claim: 
     
         1 . The biological buffer of the following structure and its salts: 
       
         
           
           
               
               
           
         
         where A and D are independently chosen from —H, —CH3, —CH2CH3, —CH2CH2CH3, —CH2OH, —CH2O(CH2CH2CH2N) n H, and where n and m are integers greater than zero. 
       
     
     
         2 . The biological buffer and its salts of  claim 1  wherein A=D=—CH3 and m=1. 
     
     
         3 . The biological buffer and its salts of  claim 1  wherein A=D=—CH2OH and m=1. 
     
     
         4 . The biological buffer and its salts of  claim 1  wherein A=D-CH2O(CH2CH2CH2N) n H and n=m=1. 
     
     
         5 . The biological buffer and its salts of  claim 1  wherein A=—CH2CH3, D=—CH2O(CH2CH2CH2N) n H and n=m=1. 
     
     
         6 . The biological buffer and its salts of  claim 1  wherein A=—CH3, D=—CH2O(CH2CH2CH2N) n H and n=m=1. 
     
     
         7 . The biological buffer and its salts of  claim 1  wherein A is —CH3 and D is —CH2CH3. 
     
     
         8 . The quaternary ammonium compound and its salts of the following structure: 
       
         
           
           
               
               
           
         
         where A, D, and E are independently chosen from, —H, —CH3, —CH2CH3, —CH2OH; G is chosen from —H, or —CH2CH3; R and R′ are chosen independently and selected from the group alkyl, alkenal, or alkynal, linear or branched, saturated or unsaturated. 
       
     
     
         9 . The quaternary ammonium compound and its salts of  claim 8  wherein A=D=—CH3, E=—CH2OH, R=R′=—CH3 and G=—H. 
     
     
         10 . The quaternary ammonium compound and its salts of  claim 8  wherein A=D=E=—CH2OH, R=R′=—CH3 and G=—H. 
     
     
         11 . The quaternary ammonium compound and its salts of  claim 8  wherein A=D=—CH3, E=—CH2OH, R=R′=—CH3 and G=—CH2CH3. 
     
     
         12 . The quaternary ammonium compound and its salts of  claim 8  wherein A=D=E=—CH2OH, R=R′=—CH3 and G=—CH2CH3. 
     
     
         13 . The surfactant of the following structure: 
       
         
           
           
               
               
           
         
         where R is alkyl, saturated or unsaturated, cyclic or acyclic, branched or linear from 2-22 carbons; A and D are independently chosen from —H, —CH3, —CH2CH3, —CH2CH2CH3, —CH2OH. 
       
     
     
         14 . The surfactant of  claim 13  wherein A is —H and D is —CH3. 
     
     
         15 . The surfactant of  claim 13  wherein A is —CH3 and D is chosen from —CH3, —CH2CH3, —CH2CH2CH3, —CH2OH. 
     
     
         16 . The surfactant of  claim 13  wherein A is —CH3 and D is chosen from —CH2CH2CH3, —CH2OH. 
     
     
         17 . The surfactant of  claim 13  wherein A is —CH3 and D is —CH2OH.

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