N-Methylethylenediamine - ≥97%(T) , CAS No.109-81-9

CAS: 109-81-9 Cat. No.: N159347 Peso molecular: 74.13 Beilstein Registry Number: 878141 Número EC: 203-707-4

GRADE & PURITY ≥97%(T)

Synonyms

methylethylenediamine | N-methylethylene diamine | V3P6B23FWK | MFCD00008165 | N-methyl ethylenediamine | N-methyl-1,2-diaminoethane | 2-Aminoethylmethylamine | KFIGICHILYTCJF-UHFFFAOYSA- | N-Methylethylidenediamine | FT-0631611 | N-Methyl-1,2 diaminoetha

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

General description
N-Methylethylenediamine undergoes condensation with pyridine-2-carboxaldehyde to form an imine. It reacts with isoquinoline-5-sulfonyl chloride to form N-(2-aminoethyl)-N-methyl-isoquinoline-5-sulfonamide.

Specifications

Sinónimos

methylethylenediamine | N-methylethylene diamine | V3P6B23FWK | MFCD00008165 | N-methyl ethylenediamine | N-methyl-1, 2-diaminoethane | 2-Aminoethylmethylamine | KFIGICHILYTCJF-UHFFFAOYSA- | N-Methylethylidenediamine | FT-0631611 | N-Methyl-1, 2 diaminoetha

Especificaciones y pureza

≥97%(T)

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥97%(T)

Nombres e identificadores

• Pubchem Sid: 488180650
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488180650
• Sonrisas canónicas: CNCCN
• IUPAC Name: N'-methylethane-1,2-diamine
• InChIKey: KFIGICHILYTCJF-UHFFFAOYSA-N
• INCHI: 1S/C3H10N2/c1-5-3-2-4/h5H,2-4H2,1H3
• Isómeros SMILES: CNCCN
• WGK Alemania: 3
• RTECS: KV5250500
• Número ONU: 2734
• Grupo de embalaje: II
• Peso molecular: 74.13
• Beilstein: 878141
• Reaxy-Rn: 878141
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=878141&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

Propiedades químicas y físicas

• Sensibilidad: Air sensitive,Moisture sensitive.
• Índice de refracción: 1.44
• Punto de inflamación (°F): 105.8 °F
• Punto de inflamación (°C): 41 °C
• Punto de ebullición (°C): 116 °C
• Peso molecular: 74.130 g/mol
• XLogP3: -1.100
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 74.0844 Da
• Monoisotopic Mass: 74.0844 Da
• Topological Polar Surface Area: 38.100 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 14.400
• 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. Mingzhen Quan, Yan Xiong, Yiliang Xu, Mingyang Li, Mingyue Chen, Jindong Cao, Jing Zhao, Quanlin Liu.  (2023)  Structural diversity and photoluminescence enhancement of indium-based hybrid metal halides.  JOURNAL OF ALLOYS AND COMPOUNDS,      [PMID:] [10.1016/j.jallcom.2023.172818]

2. Yalin Niu, Peng Jiang, Tianying Guo.  (2024)  A MOFs/MIPs@GAs Ternary Composite Catalytic System with Graphene Oxide Aerogels as the Multifunctional Skeleton for High-Efficiency Detoxification of Organophosphate Nerve Agents in Pure Water.  ACS Applied Materials & Interfaces,      [PMID:39239733] [10.1021/acsami.4c08332]

3. Yalin Niu, Peng Jiang, Tianying Guo.  (2024)  Facile preparation of UiO-66-NH2-stabilized high internal phase molecularly imprinted polymers for synergistic catalytic hydrolysis detoxification of organophosphate nerve agents.  Journal of Materials Chemistry A,  12  (37): (25465-25474).  [PMID:] [10.1039/D4TA04230A]

4. Wang Tang, Tianxiong Liu, Hongxia Gao, Shaofei Wang, Min Zhou, Ningbo Yu, Zhiwu Liang.  (2025)  Study on artificial neural networks and structure–activity relationship for constructing viscosity correlations of amine aqueous solutions based on chemical structure information.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2025.131912]

5. Wang Feifei, Wang Xinling, Wang Yu, Zhang Yin, Liu Tianxiang, Sun Jian.  (2025)  In situ formation of fluorescent non-conjugated polymer dots for α-glucosidase activity assay and inhibitor screening.  MICROCHIMICA ACTA,  192  (9): (1-10).  [PMID:40779177] [10.1007/s00604-025-07417-1]