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

CAS: 110-72-5 Cat. No.: N138023 Peso molecular: 88.15 Beilstein Registry Number: 1098272 Número EC: 203-795-4

GRADE & PURITY ≥99%(GC)

Synonyms

eTILAMINOETILAMINA | ETILTILENEDIAMINA, N- | (2-aminoetil)(etil)amina | 2-Aminoetil(etil)amina | EINECS 203-795-4 | AKOS005206991 | ETILENEDIAMINA | 2-Etilaminoetilamina | N-Etil etilendiamina | UNII-941MVD708N | AI3-26672 | J-523392 | ETILAMINOETILAMINA

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

La N-etiletilendiamina es un agente quelante utilizado en estudios de investigación sobre mutagénesis. La N-etiletilendiamina se condensa con el 2-hidroxi-3-metoxi-benzaldehído. También forma complejos organometálicos de rutenio(II) que inhiben el crecimiento de líneas celulares de cáncer de ovario humano
Un agente quelante utilizado en estudios de investigación sobre mutagénesis

Specifications

Sinónimos

eTILAMINOETILAMINA | ETILTILENEDIAMINA, N- | (2-aminoetil)(etil)amina | 2-Aminoetil(etil)amina | EINECS 203-795-4 | AKOS005206991 | ETILENEDIAMINA | 2-Etilaminoetilamina | N-Etil etilendiamina | UNII-941MVD708N | AI3-26672 | J-523392 | ETILAMINOETILAMINA

Especificaciones y pureza

≥99%(GC)

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥99%(GC)

Nombres e identificadores

• Pubchem Sid: 488183719
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488183719
• Sonrisas canónicas: 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
• Isómeros SMILES: CCNCCN
• WGK Alemania: 3
• Número ONU: 2734
• Grupo de embalaje: II
• Peso molecular: 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
    • Clase Organonitrogen compounds
      • Subclass Amines
        • Level5 Secondary amines
          • Level6 Dialkylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: 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
• Descripción: 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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Solubility in water: Completely soluble
• Sensibilidad: Air & Moisture sensitive
• Índice de refracción: 1.44
• Punto de inflamación (°F): 50 °F
• Punto de inflamación (°C): 10 °C
• Punto de ebullición (°C): 128-130°C
• Peso molecular: 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

Referencias

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]