AbstractEven chain sodium alkanesulfonates from the Strecker reaction, odd chain sodium alkanesulfonates from the alkaline decarboxylation of ॅ‐sulfo acids, and sodium 1‐hydroxy‐2‐alkanesulfonates from the reduction of esters of ॅ‐sulfo acids were compared with respect to Krafft point, critical micelle concentration, detergency and foam height. Sodium alkanesulfonates and crude fusion products from the ॅ‐sulfo acids (mixtures of alkanesulfonates of one less carbon atom with a lesser amount of a soap of two less carbon atoms) are more soluble and have better detergent and foaming properties. Sodium 1‐hydroxy‐2‐alkanesulfonates resemble monosodium salts of ॅ‐sulfo acids.Alkanesulfonic acids and 1‐hydroxy‐2‐alkane‐sulfonic acids obtained from the sodium salts by ion exchange have lower Krafft points and are more readily soluble. The critical micelle concentrations of 1‐hydroxy‐2‐alkanesulfonic acids and ॅ‐sulfo acids are nearly the same and about equal to those of alkanesulfonic acids of one less carbon atom.