N,N,N′-Trimetiletilendiamina - ≥97%(GC)(T) , CAS No.142-25-6

CAS: 142-25-6 Cat. No.: N159374 Peso molecular: 102.18 Beilstein Registry Number: 505989 Número EC: 205-529-2

GRADE & PURITY ≥97%(GC)(T)

Synonyms

F0001-0495 | N1,N1,N2-trimethyl-1,2-ethanediamine | AMY10373 | N,N,N'-Trimethyl ethylenediamine | N,N,N-TRIMETHYL ETHYLENEDIAMINE | N,N,N'-Trimethylethylene diamine | N,N'-trimethylethylenediamine | AS-20039 | MFCD00014874 | N,N',N'-trimethylethylenediami

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

Se sintetiza mediante un haz molecular supersónico de vaporización por láser. Se ha estudiado mediante ionización de campo pulsado con energía cinética de electrones cero.
Se ha utilizado en la preparación de un nuevo tensioactivo gemini, N,N-dimetil-N-{2-[N′-metil-N′-(3-sulfopropil)-alquilamonio]etil}-1-bromuros de alquilamonio (2C(n)AmSb, donde n representa longitudes de cadena de hidrocarburos de 8, 10, 12 y 14), haciéndolo reaccionar con bromuro de n-alquilo. También se ha utilizado como componente amínico para la formación in situ de α-aminoalcóxidos.

Specifications

Sinónimos

F0001-0495 | N1, N1, N2-trimethyl-1, 2-ethanediamine | AMY10373 | N, N, N'-Trimethyl ethylenediamine | N, N, N-TRIMETHYL ETHYLENEDIAMINE | N, N, N'-Trimethylethylene diamine | N, N'-trimethylethylenediamine | AS-20039 | MFCD00014874 | N, N', N'-trimethylethylenediami

Especificaciones y pureza

≥97%(GC)(T)

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥97%(GC)(T)

Nombres e identificadores

• Pubchem Sid: 504754149
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504754149
• Sonrisas canónicas: CNCCN(C)C
• IUPAC Name: N,N',N'-trimethylethane-1,2-diamine
• InChIKey: HVOYZOQVDYHUPF-UHFFFAOYSA-N
• INCHI: 1S/C5H14N2/c1-6-4-5-7(2)3/h6H,4-5H2,1-3H3
• Isómeros SMILES: CNCCN(C)C
• WGK Alemania: 3
• CAS alternativo: 142-25-6
• Número ONU: 2733
• Grupo de embalaje: II
• Peso molecular: 102.18
• Beilstein: 505989
• Reaxy-Rn: 505989
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=505989&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Tertiary amines
• Direct Parent: Trialkylamines
• Alternative Parents: Dialkylamines Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tertiary aliphatic amine - Secondary amine - Secondary aliphatic amine - Organopnictogen compound - Hydrocarbon derivative - Aliphatic acyclic compound
• Descripción: 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

Objetivos asociados (humanos)

PRMT1 Tchem Protein-arginine N-methyltransferase 1 (867 Activities)

Discover Target: PRMT1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PRMT3 Tchem Protein arginine N-methyltransferase 3 (219 Activities)

Discover Target: PRMT3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PRMT6 Tchem Protein arginine N-methyltransferase 6 (321 Activities)

Discover Target: PRMT6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PRMT5 Tchem Protein arginine N-methyltransferase 5 (1273 Activities)

Discover Target: PRMT5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

PRMT8 Tchem Protein arginine N-methyltransferase 8 (122 Activities)

Discover Target: PRMT8

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Objetivos asociados (no humanos)

Carm1 Histone-arginine methyltransferase CARM1 (53 Activities)

Discover Target: Carm1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Sensibilidad: Moisture sensitive
• Índice de refracción: 1.42
• Punto de inflamación (°F): 57.2 °F
• Punto de inflamación (°C): 14 °C
• Punto de ebullición (°C): 116 °C
• Peso molecular: 102.180 g/mol
• XLogP3: -0.200
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 102.116 Da
• Monoisotopic Mass: 102.116 Da
• Topological Polar Surface Area: 15.300 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 35.100
• 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. Jindong Cao, Jiawei Lin, Kunjie Liu, Yan Xiong, Na Wang, Shihui He, Xusheng Zhang, Zhongnan Guo, Xin Chen, Jing Zhao, Quanlin Liu.  (2022)  Antimony and bismuth cooperation to enhance the broad yellow photoluminescence of zero-dimensional hybrid halide.  Journal of Materials Chemistry C,  10  (26): (9841-9848).  [PMID:] [10.1039/D2TC01672A]

2. 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]