14426-20-1

Basic information

• Product Name: 2-DIETHYLAMINOETHANOL HYDROCHLORIDE
• Synonyms: 2-(diethylamino)-ethanohydrochloride;2-diethylamino-ethanohydrochloride;dehydrasal;diethylaminoethanolhydrochloride;N,N-DiethylethanolamineHCl;2-DIETHYLAMINOETHANOL HYDROCHLORIDE 98+%;N N-(DIETHYLAMINO)ETHANOL HYDROCHLORIDE;N,N-DIETHYLAMINOETHANOL HCL
• CAS NO: 14426-20-1
• Molecular Formula: C₆H₁₅NO*ClH
• Molecular Weight: 153.65
• EINECS: 238-395-9
• Product Categories: Aliphatics;Amines;Miscellaneous Reagents
• Mol File: 14426-20-1.mol
• Article Data: 2

Chemical Properties

• Melting Point: 133°C
• Boiling Point: 478.8°Cat760mmHg
• Flash Point: 243.4°C
• Appearance: /
• Density: 1.52g/cm³
• Storage Temp.: Refrigerator
• Solubility: Chloroform (Slightly), Methanol (Slightly), Water (Slightly)
• Sensitive: Moisture Sensitive
• CAS DataBase Reference: 2-DIETHYLAMINOETHANOL HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-DIETHYLAMINOETHANOL HYDROCHLORIDE(14426-20-1)
• EPA Substance Registry System: 2-DIETHYLAMINOETHANOL HYDROCHLORIDE(14426-20-1)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-37/39
• RTECS: KK5553400
• TSCA: Yes
• Hazardous Substances Data: 14426-20-1(Hazardous Substances Data)

Usage

Description

2-Diethylaminoethanol Hydrochloride, with the CAS number 14426-20-1, is a white solid compound that is primarily utilized in the field of organic synthesis. It is known for its unique chemical properties that make it a valuable component in various chemical reactions and processes.

Uses

Used in Organic Synthesis:
2-Diethylaminoethanol Hydrochloride is used as a reagent in organic synthesis for its ability to facilitate a range of chemical reactions. Its presence can enhance the efficiency and selectivity of these reactions, making it a crucial component in the synthesis of various organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Diethylaminoethanol Hydrochloride is used as an intermediate in the production of certain medications. Its unique chemical properties allow it to be a key component in the development of new drugs, contributing to the advancement of medical treatments.
Used in Chemical Research:
2-Diethylaminoethanol Hydrochloride is also used as a research tool in chemical laboratories. Its properties make it an interesting subject for study, and it can be used to explore various aspects of chemical reactions and mechanisms, furthering our understanding of organic chemistry.
Used in Material Science:
In the field of material science, 2-Diethylaminoethanol Hydrochloride can be used to develop new materials with specific properties. Its unique chemical characteristics can contribute to the creation of materials with enhanced performance in various applications, such as in electronics or coatings.
Overall, 2-Diethylaminoethanol Hydrochloride is a versatile compound with a wide range of applications across different industries, from pharmaceuticals to material science, due to its unique chemical properties and its role in organic synthesis.

InChI:InChI=1/C6H15NO.ClH/c1-3-7(4-2)5-6-8;/h8H,3-6H2,1-2H3;1H

Upstream product

• 100-37-8 2-(Diethylamino)ethanol 
• 78853-39-1 Cyclodrinhydrochlorid 

Downstream Products

• 806658-11-7 2-hydroxy-4-nitro-benzoic acid-(2-diethylamino-ethyl ester) 
• 100-35-6 2-(diethylamino)ethyl chloride 
• 102708-87-2 3,4,5-triethoxy-benzoic acid-(2-diethylamino-ethyl ester) 
• 7110-01-2 (4-nitro-phenyl)-acetic acid-(2-dimethylamino-ethyl ester) 
• 233753-19-0 2,5-bis[3-(N,N-diethylamino)-1-oxapropyl]-1,4-dibromobenzene 
• 120-72-9 indole 
• 99872-70-5 [2-(2-Benzyl-4-chloro-5-methyl-phenoxy)-ethyl]-diethyl-amine 
• 16545-00-9 bis[2-(diethylamino)ethyl] adipate 
• 10368-09-9 3,4,5-Trimethoxy-benzoesaeure-<2-diaethylamino-aethylester> 
• 122473-06-7 3,4,5-tributoxy-benzoic acid-(2-diethylamino-ethyl ester) 
• 102703-42-4 3,4,5-tripropoxy-benzoic acid-(2-diethylamino-ethyl ester) 
• 3858-89-7 chloroprocaine hydrochloride 
• 443-20-9 4-amino-2-fluoro-benzoic acid-(2-diethylamino-ethyl ester); hydrochloride 
• 105539-04-6 2-(diethylamino)ethyl (S)-(-)-tropate 

Relevant articles and documents

Diethanolamine and N,N-diethylethanolamine ionic liquids as precatalyst-precursors and reaction media in green Heck reaction protocol

It was found that Heck reaction with PdCl2 in diethanolamine and N,N-diethylethanolamine ionic liquids (ILs) is more efficient than analogous reactions performed in classical organic solvents. The used ILs facilitate solubility of the Pd(II) precatalysts, increase catalyst stability during the reaction, and function as reaction media, bases, precatalyst-precursors, good coordinating ligands, and mobile support for active Pd species. Thus, Heck reaction occurs without additional solvents, ligands and bases, that makes experimental procedure much simpler. Our DFT investigation provides mechanistic insight into the formation of the trans-[PdCl2(DEA)2] complex that acts as a precatalyst.