N-Ethylethylenediamine - ≥99%(GC) , CAS No.110-72-5

CAS: 110-72-5 Cat. No.: N138023 Molecular Weight: 88.15 Beilstein Registry Number: 1098272 EC Number: 203-795-4

GRADE & PURITY ≥99%(GC)

Synonyms

ethylaminoethylamine | ETHYLETHYLENEDIAMINE, N- | (2-aminoethyl)(ethyl)amine | 2-Aminoethyl(ethyl)amine | EINECS 203-795-4 | AKOS005206991 | ethylethylenediamine | 2-Ethylaminoethylamine | N-Ethyl ethylenediamine | UNII-941MVD708N | AI3-26672 | J-523392 |

Storage

Argon charged,Room temperature

Shipped In

Normal

Overview

N-Ethylethylenediamine is a chelating agent used in mutagenesis research studies. N-Ethylethylenediamine undergoes condensation with 2-hydroxy-3-methoxybenzaldehyde. It also forms organometallic ruthenium(II) complexes that inhibit the growth in human ovarian cancer cell lines
A chelating agent used in mutagenesis research studies

Specifications

Synonyms

ethylaminoethylamine | ETHYLETHYLENEDIAMINE, N- | (2-aminoethyl)(ethyl)amine | 2-Aminoethyl(ethyl)amine | EINECS 203-795-4 | AKOS005206991 | ethylethylenediamine | 2-Ethylaminoethylamine | N-Ethyl ethylenediamine | UNII-941MVD708N | AI3-26672 | J-523392 |

Specifications & Purity

≥99%(GC)

Storage

Argon charged, Room temperature

Shipped In

Normal

Purity

≥99%(GC)

Names and Identifiers

• Pubchem Sid: 488183719
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488183719
• Canonical Smiles: CCNCCN
• IUPAC Name: N'-ethylethane-1,2-diamine
• InChIKey: SCZVXVGZMZRGRU-UHFFFAOYSA-N
• INCHI: 1S/C4H12N2/c1-2-6-4-3-5/h6H,2-5H2,1H3
• Isomeric SMILES: CCNCCN
• WGK Germany: 3
• UN Number: 2734
• Packing Group: II
• Molecular Weight: 88.15
• Beilstein: 1098272
• Reaxy-Rn: 1098272
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1098272&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Class Organonitrogen compounds
      • Subclass Amines
        • Level5 Secondary amines
          • Level6 Dialkylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Class: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Secondary amines
• Direct Parent: Dialkylamines
• Alternative Parents: Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Secondary aliphatic amine - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Primary aliphatic amine - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as dialkylamines. These are organic compounds containing a dialkylamine group, characterized by two 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

Mechanisms of Action

Chemical and Physical Properties

• Solubility: Solubility in water: Completely soluble
• Sensitivity: Air & Moisture sensitive
• Refractive Index: 1.44
• Flash Point(°F): 50 °F
• Flash Point(°C): 10 °C
• Boil Point(°C): 128-130°C
• Molecular Weight: 88.150 g/mol
• XLogP3: -0.800
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 88.1 Da
• Monoisotopic Mass: 88.1 Da
• Topological Polar Surface Area: 38.100 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 21.500
• 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

References

1. Jenaidullah Batur, Zunbin Duan, Ruipeng Jin, Rui Li, Yabo Xie, Xue-Feng Yu, Jian-Rong Li.  (2024)  Enhanced Catalytic Activity of Crystalline Phosphorus Nanosheets Fabricated via Solvothermal Phase Transformation.  INORGANIC CHEMISTRY,      [PMID:38861347] [10.1021/acs.inorgchem.4c01757]

2. Zunbin Duan, Rui Li, He Bian, Yanfang Wang, Xue Zhang, Ziqiang Cheng, Danni Liu, Yang Li, Shuai Zhang, Guangbo Qu, Paul K. Chu, Jiahong Wang.  (2025)  Large-Scale synthesis of crystalline phosphorus nanosheets with superior air-water stability and flame-retardancy ability.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.159566]

3. Xi Tang, Ge Gao, Wufeng Jiang, Bin Xu, Fan Wu, Cong Luo, Xiaoshan Li, Liqi Zhang.  (2025)  The structure–activity relationship for CO2 absorption heat of chain diamines: Effects of amino types, methyl/ethyl groups, and chain lengths.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.160838]