N-Ethyldiisopropylamine solution - suitable for peptide synthesis, ~2 M in 1-methyl-2-pyrrolidinone , CAS No.7087-68-5

CAS: 7087-68-5 Cat. No.: N433364 Formula: C₈H₁₉N Molecular Weight: 129.24 Beilstein Registry Number: 4124745 EC Number: 230-392-0

GRADE & PURITY Suitable for peptide synthesis, ~2 M in 1-methyl-2-pyrrolidinone

Synonyms

diisopropylethylarnine | diisoproplyethylamine | EtNiPr2 | i-Pr2EtN | N-(4-chlorobenzyl)piperazine | N-ethyidiisopropylamine | N-ethyl-N-isopropyl-propan-2-amine | N-ethyl-N-isopropylpropan-2-amine | 1H-Imidazol-2-amine xsulfate | (S)-2-((S)-2-Amino-3-phe

Storage

Protected from light,Room temperature,Argon charged

Shipped In

FedEx DG Service

Overview

N -Ethyldiisopropylamine (EDIA) reacts with monoactivated Michael acceptors to afford symmetrical sulfones.

Application：

N,N-Diisopropylethylamine (DIPEA), also known as Hünig′s base, is a sterically hindered amine. It is commonly employed as a base in peptide synthesis. Additionally, DIPEA is also used in the Pd-catalyzed cross-coupling reactions, which include Heck coupling and Sonagashira coupling reactions.

Specifications

Synonyms

diisopropylethylarnine | diisoproplyethylamine | EtNiPr2 | i-Pr2EtN | N-(4-chlorobenzyl)piperazine | N-ethyidiisopropylamine | N-ethyl-N-isopropyl-propan-2-amine | N-ethyl-N-isopropylpropan-2-amine | 1H-Imidazol-2-amine xsulfate | (S)-2-((S)-2-Amino-3-phe

Specifications & Purity

suitable for peptide synthesis, ~2 M in 1-methyl-2-pyrrolidinone

Storage

Protected from light,Room temperature,Argon charged

Shipped In

FedEx DG Service

Grade

Suitable for peptide synthesis

Names and Identifiers

Pubchem Sid

508810894

Canonical Smiles

CCN(C(C)C)C(C)C

IUPAC Name

N-ethyl-N-propan-2-ylpropan-2-amine

InChIKey

JGFZNNIVVJXRND-UHFFFAOYSA-N

INCHI

1S/C8H19N/c1-6-9(7(2)3)8(4)5/h7-8H,6H2,1-5H3

Isomeric SMILES

CCN(C(C)C)C(C)C

WGK Germany

2

UN Number

UN 3384

Packing Group

I

Molecular Weight

129.24

Beilstein

4124745

Reaxy-Rn

605301

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=605301&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Class Organonitrogen compounds
      • Subclass Amines
        • Level5 Tertiary amines
          • Level6 Trialkylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Class: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Tertiary amines
• Direct Parent: Trialkylamines
• Alternative Parents: Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tertiary aliphatic amine - Organopnictogen compound - Hydrocarbon derivative - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as trialkylamines. These are organic compounds containing a trialkylamine group, characterized by exactly three alkyl groups bonded to the amino nitrogen.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Sensitivity: Light sensitive；Air sensitive；Hygroscopic
• Refractive Index: 1.414
• Flash Point(°F): 51.08 ℉
• Flash Point(°C): 10.6°C
• Boil Point(°C): 127°C
• Melt Point(°C): -45 °C
• Molecular Weight: 129.240 g/mol
• XLogP3: 2.200
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 129.152 Da
• Monoisotopic Mass: 129.152 Da
• Topological Polar Surface Area: 3.200 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 59.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1