Diisopropylamine, hydrochloride

Base Information

• Chemical Name: Diisopropylamine, hydrochloride
• CAS No.: 819-79-4
• Molecular Formula: C6H15 N . Cl H
• Molecular Weight: 137.653
• Hs Code.: 2921199990
• Mol file: 819-79-4.mol

Synonyms:Disopromine hydrochloride;Diisopropylammonium chloride;Bis(isopropyl)ammonium chloride;NSC 1808;DIISOPROPYLAMINE, HYDROCHLORIDE;1,1-Dimethyldiethylamine hydrochloride;Diethylamine, dimethyl-, hydrochloride;Ethylamine, N-t-butyl-, hydrochloride;B-26;tert-Butylamine, N-ethyl-, hydrochloride;2-Propanamine, N-(1-methylethyl)-, hydrochloride;DIETHYLAMINE, 1,1-DIMETHYL-, HYDROCHLORIDE;N-(1-Methylethyl)-2-propanamine Hydrochloride;Disotat (TN);Diisopropylammoniumchlorid;LS-61859;LS-61992;D07842

Chemical Property of Diisopropylamine, hydrochloride

Chemical Property:

• Vapor Pressure: 74mmHg at 25°C
• Melting Point: 216-218 ºC(lit.)
• Boiling Point: 83.9°C at 760 mmHg
• Flash Point: 41.3°C
• PSA: 12.03000
• LogP: 2.58570
• Storage Temp.: Inert atmosphere,Room Temperature
• Water Solubility.: almost transparency
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 137.0971272
• Heavy Atom Count: 8
• Complexity: 33.4

Purity/Quality:

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

Diisopropylamine Hydrochloride ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)[NH2+]C(C)C.[Cl-]
• Chemical Composition and Structure: Diisopropylamine hydrochloride is a salt compound composed of diisopropylamine (C6H15N) and hydrochloric acid (HCl), resulting in the formation of a salt.
• Uses: Organic Synthesis:; Utilized in organic synthesis as a reactant or catalyst.; ; Pharmaceuticals:; Used as an intermediate in the synthesis of pharmaceutical compounds.; ; Surfactant Production:; Employed in the production of surfactants.; ; Catalytic Processes:; Participates in catalytic processes, such as the magnesium-promoted synthesis of hindered non-nucleophilic amines.
• Production Methods: Synthesized through chemical reactions involving the reaction of diisopropylamine with hydrochloric acid.

Technology Process of Diisopropylamine, hydrochloride

There total 15 articles about Diisopropylamine, hydrochloride 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: 100.0%

P-(chloromethyl)-N,N,N',N'-tetraisopropylphosphonous diamide (124862-12-0) → dichloro(chloromethyl)phosphine (2155-78-4) + diisopropylamine hydrochloride (819-79-4)

Guidance literature:

With hydrogenchloride; In diethyl ether; -70 deg C --> room temperature;

Reference yield: 98.0%

diisopropylamine (108-18-9) + tris(dimethylamino)isothiocyanatophosphonium chloride → diisopropylamine hydrochloride (819-79-4) + C13H32N5PS

Guidance literature:

for 6h;

Reference yield: 83.0%

boron trichloride (10294-34-5) + diisopropylamine (108-18-9) → bis(diisopropylamino)chloroborane (28049-80-1) + diisopropylamine hydrochloride (819-79-4)

Guidance literature:

In light petroleum; -78°C; sepn. of (C3H7)2NH*HCl ppt.;

DOI:10.1039/jr9620001786

upstream raw materials:

piperidine hydrochloride

N,N-diisopropyl-1-amino-2-(methylsulfonyl)-3-phenyl-2-propene

P-(chloromethyl)-N,N,N',N'-tetraisopropylphosphonous diamide

N-(pentafluorophenyl)carbonimidoyl dichloride

Downstream raw materials:

N,N-Diisopropyl-guanidin

piperidine hydrochloride

N,N-diisopropyl-1-amino-2-(methylsulfonyl)-3-phenyl-2-propene

triisopropylamine

Refernces

• 1、 -. "HERBICIDAL COMPOUNDS". Page/Page column 28. . Retrieved 2021/10/22.
• 2、 Yoshida, Suguru,Igawa, Kazunobu,Tomooka, Katsuhiko. "Nucleophilic substitution reaction at the nitrogen of arylsulfonamides with phosphide anion". supporting information. p. 19358 - 19361. Retrieved 2013/02/22.