Butylamine Hydroiodide - ≥97%(T) , CAS No.36945-08-1

CAS: 36945-08-1 Cat. No.: B152886 Peso molecular: 201.05 Número EC: 807-963-3

GRADE & PURITY ≥97%(T)

Synonyms

SCHEMBL7019492 | n-butylammonium iodide | butan-1-amine;hydroiodide | AS-57718 | A928455 | Butylamine Hydroiodide | 1-Butanamine Hydroiodide | butan-1-amine hydroiodide | AKOS037645152 | MFCD28100822 | B4433 | T70838 | SY117090

Storage

Store at 2-8°C,Protected from light,Argon charged

Shipped In

Wet ice

Descripción general

The iodide and bromide based alkylated halides find applications as precursors for fabrication of perovskites for photovoltaic applications.

Specifications

Sinónimos

SCHEMBL7019492 | n-butylammonium iodide | butan-1-amine;hydroiodide | AS-57718 | A928455 | Butylamine Hydroiodide | 1-Butanamine Hydroiodide | butan-1-amine hydroiodide | AKOS037645152 | MFCD28100822 | B4433 | T70838 | SY117090

Especificaciones y pureza

≥97%(T)

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Protected from light, Argon charged

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥97%(T)

Nombres e identificadores

• Sonrisas canónicas: CCCCN.I
• IUPAC Name: butan-1-amine;hydroiodide
• InChIKey: CALQKRVFTWDYDG-UHFFFAOYSA-N
• INCHI: 1S/C4H11N.HI/c1-2-3-4-5;/h2-5H2,1H3;1H
• Isómeros SMILES: CCCCN.I
• Peso molecular: 201.05
• Reaxy-Rn: 3905443
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3905443&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Clase Organonitrogen compounds
      • Subclass Quaternary ammonium salts

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Clase: Organonitrogen compounds
• Subclass: Quaternary ammonium salts
• Intermediate Tree Nodes: Not available
• Direct Parent: Quaternary ammonium salts
• Alternative Parents: Organic iodide salts Monoalkylamines Hydrocarbon derivatives Organic cations
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Quaternary ammonium salt - Hydrocarbon derivative - Organic iodide salt - Organic salt - Primary amine - Primary aliphatic amine - Amine - Organic cation - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as quaternary ammonium salts. These are compounds containing positively charged polyatomic ion of the structure NR4+, R being an alkyl group or an aryl group.
• 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

• Solubilidad: Soluble in water
• Sensibilidad: Moisture,light,air sensitive
• Punto de fusión (°C): 173 °C (exp.)
• Peso molecular: 201.050 g/mol
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 201.001 Da
• Monoisotopic Mass: 201.001 Da
• Topological Polar Surface Area: 26.000 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 13.100
• 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: 2

XLogP3

Referencias

1. Zhangxin Chen, Ning Xu, Weijun Li, Ruiyang Zhao, Yujie Dong, Junlei Liu, Chang Su, Jianli Wang, Cheng Zhang.  (2019)  Effect of trace hydrofluoric acid in a LiPF6 electrolyte on the performance of a Li–organic battery with an N-heterocycle based conjugated microporous polymer as the cathode.  Journal of Materials Chemistry A,  7  (27): (16347-16355).  [PMID:] [10.1039/C9TA01810G]