DIPEA consists of a central nitrogen atom that is bonded to an ethyl group and two isopropyl groups. A lone pair of electrons resides on the nitrogen atom, which can react with electrophiles.

N,N-Diisopropylethylamine ReagentPlus®, ≥99%; CAS Number: 7087-68-5; EC Number: 230-392-0; Synonyms: N-Ethyldiisopropylamine,DIPEA,Ethyldiisopropylamine,‘Hünig’s base’; Linear Formula: [(CH3)2CH]2NC2H5 at Sigma-Aldrich

N,N-Diisopropylethylamine (DIPEA) is a tertiary amino compound. ChEBI. 1 Structures. 1.1 2D Structure. Structure Search. Get Image. Download Coordinates. Chemical Structure Depiction. Full screen Zoom in Zoom out. PubChem. 1.2 3D Conformer. PubChem. 2 Names and Identifiers. 2.1 Computed Descriptors.

Feb 8, 2025 · 二异丙基乙胺(dipea)为无色透明液体，不溶于水，易溶于丙酮等有机溶剂。dipea是重要的农药医药中间体，可以用来合成麻醉剂、除草剂，也可作为位阻胺参与各类催化反应。

Apr 10, 2025 · N,N-Diisopropylethylamine is also known as Hunig's base and abbreviated as DIPEA or DIEA, It is a sterically hindered amine and an organic compound. The colourless liquid was named as Hung’s base after Siegfried Hunig, a German chemist. It is noteworthy that the compound is commercially available.

DIPEA diisopropylethylamine | C16H38N2 | CID 19871184 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.

Apr 11, 2023 · N,N-Diisopropylethylamine (DIPEA) is an organic compound and an amine. It is named after the German chemist Siegfried Hünig. It is used in organic chemistry as a base. N,N-Diisopropylethylamine consists of a central nitrogen that is bonded to an ethyl group and two isopropyl groups.

N, N-Diisopropylethylamine is a hindered non-nucleophilic amine base used in alkylation, aldol-like reactions, eliminations, and selective generation of enolates.It is widely used as a proton scavenger in organic synthesis. Due to its less nucleophilic nature, it produces less byproducts.

N,N-Diisopropylethylamine Revision Date 06-Jan-2023 Mutagenic Effects No information available Reproductive Effects No information available. Developmental Effects No information available. Teratogenicity No information available. STOT - single exposure Respiratory system STOT - repeated exposure None known Aspiration hazard No information available Symptoms …

N,N-Diisopropylethylamine (DIPEA), also known as Hünig's base, is a widely used non-nucleophilic base in organic synthesis reactions. This compound is particularly valuable in deprotonation and acid-base reactions, making it suitable for substitution reactions.