N,N-Dimethylallylamine - ≥98% , CAS No.2155-94-4

CAS: 2155-94-4 Cat. No.: D117859 Peso molecular: 85.15 Beilstein Registry Number: 1734044 Número EC: 218-458-7

GRADE & PURITY ≥98%

Synonyms

Allyldimethylamine | N,N-DIMETHYL-2-PROPENYLAMINE | FT-0629518 | N-Allyl-N,N-dimethylamine | 2',6'-Dihydroxy-4'methoxyacetophenone | N,N-dimethyl allyl amine | Q23638211 | NSC 32615 | allyl dimethylamine | Titantetrachlorid | 5-vinyl-pyrrolidin-2-one | N,

Storage

Protected from light,Argon charged,Room temperature

Shipped In

Normal

Specifications

Sinónimos

Allyldimethylamine | N, N-DIMETHYL-2-PROPENYLAMINE | FT-0629518 | N-Allyl-N, N-dimethylamine | 2', 6'-Dihydroxy-4'methoxyacetophenone | N, N-dimethyl allyl amine | Q23638211 | NSC 32615 | allyl dimethylamine | Titantetrachlorid | 5-vinyl-pyrrolidin-2-one | N,

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Protected from light, Argon charged, Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488185031
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488185031
• Sonrisas canónicas: CN(C)CC=C
• IUPAC Name: N,N-dimethylprop-2-en-1-amine
• InChIKey: GBCKRQRXNXQQPW-UHFFFAOYSA-N
• INCHI: 1S/C5H11N/c1-4-5-6(2)3/h4H,1,5H2,2-3H3
• Isómeros SMILES: CN(C)CC=C
• WGK Alemania: 3
• Peso molecular: 85.15
• Beilstein: 1734044
• Reaxy-Rn: 1734044
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1734044&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: Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Tertiary 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

Propiedades químicas y físicas

• Sensibilidad: light sensitive；air sensitive
• Índice de refracción: 1.4
• Punto de inflamación (°F): -20 °C
• Punto de inflamación (°C): -20°C
• Punto de ebullición (°C): 64°C
• Peso molecular: 85.150 g/mol
• XLogP3: 0.900
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 85.0891 Da
• Monoisotopic Mass: 85.0891 Da
• Topological Polar Surface Area: 3.200 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 39.200
• 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. Xue-Li Liu, Yi-Fan Chen, Yi-Wen Chen, Wei-Kang Peng, Han-Chun Liu.  (2022)  Preparation of carbosilane quaternary ammonium surfactants and surface activity.  TENSIDE SURFACTANTS DETERGENTS,  59  (5): (424-432).  [PMID:] [10.1515/tsd-2022-2428]

2. Peixian Huo, Hongyao Ding, Ziqing Tang, Xiaoxu Liang, Jianyu Xu, Miaomiao Wang, Rui Liang, Guoxing Sun.  (2022)  Conductive silk fibroin hydrogel with semi-interpenetrating network with high toughness and fast self-recovery for strain sensors.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:35577196] [10.1016/j.ijbiomac.2022.05.084]

3. Yuan-Yuan Yu, Zhong-Qiu Liu, Guo-Qiang Zhang, Yu-Jing Liu, An-Guo Ying.  (2021)  Rationally designed novel multifunctional poly(ionic liquid)s for ultra-selective valorization of Yiwu lignite to monocyclic aromatic compounds.  Journal of Cleaner Production,      [PMID:] [10.1016/j.jclepro.2021.129775]

4. 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]

5. Mingzhu Liu, Biyu Jin, Qinghua Zhang, Xiaoli Zhan, Fengqiu Chen.  (2018)  High-performance solid polymer electrolytes for lithium ion batteries based on sulfobetaine zwitterion and poly (ethylene oxide) modified polysiloxane.  JOURNAL OF ALLOYS AND COMPOUNDS,      [PMID:] [10.1016/j.jallcom.2018.01.263]

6. Jia-Liang Guo, Qing-Qing Sun, Zhong-Qiu Liu, Feng-Xiang Wang, Tingjun Fu, Yujing Liu, Anguo Ying.  (2024)  An intelligent dual stimuli-responsive Pickering emulsion for highly efficiently producing waste frying oil-based biodiesel.  Journal of Cleaner Production,      [PMID:] [10.1016/j.jclepro.2024.140638]

7. Jiale Sun, Yanan Liu, Junjie Wei, Peng Wei, Tao Chen.  (2024)  Pseudo-photoelectric cascade conversion endowing photosensitive Janus ionogel for solar energy harvesting and sensing.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.149836]