Diisopropylethylamine

　　Main Uses

　　Non-nucleophilic base in organic synthesis:

　　In peptide synthesis, used to neutralize acids generated during amino group protection reactions (such as Boc and Fmoc protection), avoiding side reactions caused by excessive nucleophilicity of the amino group;

　　Used as a base in coupling reactions (such as Suzuki and Heck reactions) to adjust the pH of the reaction system and promote catalyst activity;

　　Used in the preparation of carboxylic esters and amides, etc., to neutralize acids generated during the reaction (such as hydrochloric acid and hydrobromic acid), while minimizing the impact on sensitive functional groups.

　　Pharmaceutical and agrochemical intermediates:

　　Acting as a basic catalyst or acid scavenger, participating in the synthesis processes of antibiotics, antiviral drugs, herbicides, etc.

　　Other fields:

　　Used in the synthesis of surfactants to adjust the alkalinity of the reaction system;

　　Used as an extractant to assist in the separation of certain organic compounds or metal ions.

CAS NO: 7087-68-5

EC NO: 230-392-0

Molecular Formula: C₈H₁₉N

Molecular Weight: 129.2432

Synonyms: N-Ethyldiisopropylamine; N-Ethyldiisopropylamine; Diisopropylethylamine; N,N'-Diisopropylethylamine; N,N-Diisopropylethylamine;

Structure: