N-Alilmetilamina - ≥96% , CAS No.627-37-2

CAS: 627-37-2 Cat. No.: I136680 Peso molecular: 71.12 Beilstein Registry Number: 1098387 Número EC: 210-996-0

GRADE & PURITY ≥96%

Synonyms

Allylamine, N-methyl- | allylmethyl amine | EINECS 210-996-0 | (Methyl)(prop-2-en-1-yl)amine | Allyl methyl amine | MFCD00008641 | N-Methyl-2-propen-1-amine | 2-Propen-1-amine, N-methyl- | F21270 | N-Methylallylamine | n-methyl-allylamine | N-Allylmethyla

Storage

Conservar a 2-8°C,cargado con argón

Shipped In

Hielo húmedo

Descripción general

aplicación：

La N-alilmetilamina se utiliza en la producción de N-alil-alfa,alfa-dicloro-N-metilacetamida. Se utiliza como monómero funcional para coordinar con iones Cd(II)/Zn(II) para obtener las películas de polimetacrilato de metilo - metacrilato de butilo - N-alilmetilamina (PMBA), que es útil como bloques de construcción para fabricar una célula fotocatalítica.

Specifications

Sinónimos

Allylamine, N-methyl- | allylmethyl amine | EINECS 210-996-0 | (Methyl)(prop-2-en-1-yl)amine | Allyl methyl amine | MFCD00008641 | N-Methyl-2-propen-1-amine | 2-Propen-1-amine, N-methyl- | F21270 | N-Methylallylamine | n-methyl-allylamine | N-Allylmethyla

Especificaciones y pureza

≥96%

Condiciones de almacenamiento de almacenamiento

Conservar a 2-8°C, cargado con argón

Enviado en

Hielo húmedo

Pureza

≥96%

Nombres e identificadores

• Pubchem Sid: 504754381
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504754381
• Sonrisas canónicas: CNCC=C
• IUPAC Name: N-methylprop-2-en-1-amine
• InChIKey: IOXXVNYDGIXMIP-UHFFFAOYSA-N
• INCHI: 1S/C4H9N/c1-3-4-5-2/h3,5H,1,4H2,2H3
• Isómeros SMILES: CNCC=C
• WGK Alemania: 3
• RTECS: UC6632500
• Número ONU: 3286
• Grupo de embalaje: II
• Peso molecular: 71.12
• Beilstein: 1098387
• Reaxy-Rn: 1098387
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1098387&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 Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Secondary aliphatic amine - Organopnictogen compound - Hydrocarbon derivative - 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: CO2 sensitive；Air sensitive；Heat sensitive
• Índice de refracción: 1.41
• Punto de inflamación (°F): -18.4 °F
• Punto de inflamación (°C): -28 °C
• Punto de fusión (°C): 66℃
• Peso molecular: 71.120 g/mol
• XLogP3: 0.400
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 71.0735 Da
• Monoisotopic Mass: 71.0735 Da
• Topological Polar Surface Area: 12.000 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 24.800
• 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. Ting-ting Bai, Ming-yan Cong, Yu-xiang Jia, Ke-ke Ma, Meng Wang.  (2020)  Preparation of self-crosslinking anion exchange membrane with acid block performance from side-chain type polysulfone.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2020.117831]

2. Jiye Teng, Tao Zhang, Hongbo Zhao, Peiling Zhang, Zhengzhe Wu, Zhiwei Chang, Ming Li, Chenjie Zhu.  (2025)  Dual-functionalization of lignin towards superior reinforcement for styrene-butadiene rubber.  INDUSTRIAL CROPS AND PRODUCTS,      [PMID:] [10.1016/j.indcrop.2025.120500]

3. Xiuqin Fang, Chang Wang, Hong-Hui Shu, Sheng-Li Han, Cheng-Mei Liu.  (2024)  Improving the removal rate of bisphenol A and Cu2+ from water using P/N coexisting β-cyclodextrin-based adsorbents by enhancing adsorbents-pollutants interactions.  CARBOHYDRATE POLYMERS,      [PMID:39174082] [10.1016/j.carbpol.2024.122437]

4. Nianming Jiao, Zhang Jiang, Yuan Yao, Long Liu, Yanqiang Zhang.  (2025)  Multicyclopropyl-functionalized hypergolic ionic liquids with enhanced energetic performance.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2025.128777]