𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The acid-binding properties of long-chain aliphatic amines

✍ Scribed by Smith, E. Lester ;Page, J. E.


Publisher
Wiley (John Wiley & Sons)
Year
1948
Weight
481 KB
Volume
67
Category
Article
ISSN
0368-4075

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Long‐chain aliphatic tertiary amines such as methyldioctylamine can be used as anion exchangers. Tertiary amines are much more efficient as acid‐binders than primary or secondary amines. The acid‐binding efficiency of tertiary amines improves as the length of the carbon chain increases. Strong acids are extracted more readily than weak acids and can be removed from mixtures with weak acids. Methyldioctylamine and the anion‐exchange resin De‐acidite C have acid‐binding capacities of the same order. The technique can be used to remove mineral acids from acid hydrolysates of protein, but is not of much value for the extraction or purification of penicillin.


📜 SIMILAR VOLUMES


The acylation of long chain aliphatic pr
✍ Macgregor, J. H. ;Ward, F. 📂 Article 📅 1947 🏛 Wiley (John Wiley & Sons) ⚖ 272 KB

## Abstract A method of acylating long chain primary aliphatic amines is described. Representative series of N‐monoalkylstearamides, N,N′‐dialkyladipamides and N,N′‐dialkylsebacamides, in which each alkyl radical contains between 8 and 18 carbon atoms, have been prepared by acylating the long chain

Reactions of aliphatic methanesulfonates
✍ Friedrich Spener; Helmut K. Mangold 📂 Article 📅 1972 🏛 Elsevier Science 🌐 English ⚖ 164 KB

Esters of long-chain alcohols with long-chain acids, i.e., the wax esters, are obtained in high yields by the reaction of alkyl mcthanesulfonates with the sodium or potassium salts of fatty acids. The procedure is applicable to the preparation of saturated as well as unsaturated esters.