2-Ethylhexylammonium chloride

Base Information

• Chemical Name: 2-Ethylhexylammonium chloride
• CAS No.: 26392-49-4
• Molecular Formula: C8H19 N . Cl H
• Molecular Weight: 165.706
• Hs Code.: 2921199090
• Mol file: 26392-49-4.mol

Synonyms:2-ethylhexylammonium chloride;SCHEMBL8967683

Chemical Property of 2-Ethylhexylammonium chloride

Chemical Property:

• Vapor Pressure: 1.71mmHg at 25°C
• Boiling Point: 167.3°Cat760mmHg
• Flash Point: 52.2°C
• PSA: 26.02000
• Density: g/cm³
• LogP: 3.66380
• Water Solubility.: very faint turbidity
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 5
• Exact Mass: 165.1284273
• Heavy Atom Count: 10
• Complexity: 52.5

Purity/Quality:

97% ^*data from raw suppliers

2-Ethylhexylamine Hydrochloride >97.0%(N)(T) ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn
• Hazard Codes: Xn
• Statements: 36/37/38-36-22
• Safety Statements: 26-36/37/39

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCC(CC)C[NH3+].[Cl-]
• Uses: 2-Ethylhexylamine Hydrochloride is used as a reactant or reagent in preparation of N-alkyl carbamates.

Technology Process of 2-Ethylhexylammonium chloride

There total 5 articles about 2-Ethylhexylammonium chloride 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: 92.0%

3-(nitromethyl)heptane (3457-56-5) → 2-ethyl-hexylamine hydrochloride (26392-49-4)

Guidance literature:

3-(nitromethyl)heptane; With C₃₆H₅₆Cl₃CrN₂O; magnesium; 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane; In tetrahydrofuran; at 60 ℃; for 24h; Inert atmosphere; Schlenk technique;

With hydrogenchloride; In tetrahydrofuran; water; ethyl acetate; at 20 ℃;

DOI:10.1021/jacs.0c12318

Reference yield: 39.0%

2-((2R)-ethylhexyl)isoindoline-1,3-dione (1443771-66-1) → (R)-2-ethylhexylamine hydrochloride (26392-49-4)

Guidance literature:

2-((2R)-ethylhexyl)isoindoline-1,3-dione; With hydrazine hydrate; In ethanol; for 0.25h; Reflux;

With hydrogenchloride; In water;

DOI:10.1016/j.bmc.2013.09.057

Reference yield: 28.0%

2-((2S)-ethylhexyl)isoindoline-1,3-dione → (S)-2-ethylhexylamine hydrochloride (26392-49-4)

Guidance literature:

2-((2S)-ethylhexyl)isoindoline-1,3-dione; With hydrazine hydrate; In ethanol; for 0.25h; Reflux;

With hydrogenchloride; In water;

DOI:10.1016/j.bmc.2013.09.057

upstream raw materials:

2-((2R)-ethylhexyl)isoindoline-1,3-dione

3-bromomethylheptane

3-(nitromethyl)heptane

Downstream raw materials:

alexidine

2,9-bis(2-ethylhexyl)anthra[2,1,9-def:6,5,10-d',e',f']diisoquinoline-1,3,8,10(2H,9H)-tetraone