Ethylamine hydrobromide

Base Information

• Chemical Name: Ethylamine hydrobromide
• CAS No.: 593-55-5
• Molecular Formula: C2H7N.BrH
• Molecular Weight: 125.996
• European Community (EC) Number: 209-797-1
• NSC Number: 4117
• UNII: 10430J81ZZ
• DSSTox Substance ID: DTXSID1060475
• Wikidata: Q27251104
• Mol file: 593-55-5.mol

Synonyms:ethylamine;ethylamine hydrobromide;ethylamine hydrochloride;ethylamine, 14C-labeled

Chemical Property of Ethylamine hydrobromide

Chemical Property:

• Vapor Pressure: 1130mmHg at 25°C
• Melting Point: 160 °C
• Refractive Index: 1.4800 (estimate)
• Boiling Point: 14.2 °C at 760mmHg
• PSA: 26.02000
• Density: 0.691g/cm³
• LogP: 1.62340
• Water Solubility.: almost transparency
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 124.98401
• Heavy Atom Count: 4
• Complexity: 2.8

Purity/Quality:

98%,99%, ^*data from raw suppliers

Ethylamine Hydrobromide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCN.Br
• Description: Ethylammonium bromide (EABr) has been used as a precursor for the?alteration of crystallite structure, evolution of film morphology, and fine-tuning optical properties of perovskitematerials to improve the efficiency of hybrid electronic devices.
• Uses: Ethylamine Hydrobromide can be used as intermediate (where liquid ethylamine or liquid hydrobromic acid cannot be used). Organohalide based perovskites have emerged as an important class of material for solar cell applications. Our perovskites precursors are useful for synthesizing mixed cation or anion perovskites needed for the optimization of the band gap, carrier diffusion length and power conversion efficiency of perovskites based solar cells.

Technology Process of Ethylamine hydrobromide

There total 6 articles about Ethylamine hydrobromide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

ethyl-carboximidoyl bromide (115197-42-7) + water (7732-18-5) → carbon dioxide (124-38-9,18923-20-1) + hydrogen bromide (10035-10-6,12258-64-9) + ethylamine hydrobromide (593-55-5)

Guidance literature:

Reference yield:

ethyl-carboximidoyl bromide (115197-42-7) → carbon dioxide (124-38-9,18923-20-1) + hydrogen bromide (10035-10-6,12258-64-9) + ethylamine hydrobromide (593-55-5)

Guidance literature:

Reference yield:

carbon disulfide (75-15-0,12122-00-8) + ethyl-carboximidoyl bromide (115197-42-7) + ethanol (64-17-5) → ethyl bromide (74-96-4) + hydrogen bromide (10035-10-6,12258-64-9) + ethylamine hydrobromide (593-55-5)

Guidance literature:

upstream raw materials:

1,1,2,2-tetrabromoethane

diethyl ether

ethylamine

2-bromoheptanal

Downstream raw materials:

3-phenyl-2-ethyl-5-chloro-1-oxo-2,3-dihydropyrrolo<3,4-b>indole

2-Ethyl-1-(4-nitro-phenyl)-1,4-dihydro-2H-pyrrolo[3,4-b]indol-3-one

2-Ethyl-7-methoxy-1-(4-nitro-phenyl)-1,4-dihydro-2H-pyrrolo[3,4-b]indol-3-one

Refernces