Online Database of Chemicals from Around the World

N-(2-Hydroxyethyl)piperazine
[CAS# 103-76-4]

Top Active Suppliers
Shanghai Worldyang Chemical Co., Ltd. China Inquire  
+86 13651600618
+86 (21) 5679-5779
sales7777@worldyachem.com
QQ chat
WeChat: 13651600618
WhatsApp: +86 13651600618
Chemical manufacturer since 2012
chemBlink premium supplier since 2023
down More Suppliers...
Identification
Classification API >> Antiparasitic drug >> Anthelmintic
Name N-(2-Hydroxyethyl)piperazine
Synonyms 1-Piperazineethanol
Molecular Structure CAS # 103-76-4, N-(2-Hydroxyethyl)piperazine, 1-Piperazineethanol
Molecular Formula C6H14N2O
Molecular Weight 130.19
CAS Registry Number 103-76-4
EC Number 203-142-3
SMILES C1CN(CCN1)CCO
Properties
Density 1.061 g/mL (Expl.)
Melting point -38.5 ºC (Expl.)
Boiling point 246 ºC (Expl.)
Refractive index 1.506 (Expl.)
Flash point 135 ºC (Expl.)
Water solubility MISCIBLE
Safety Data
Hazard Symbols symbol symbol   GHS05;GHS07 Danger    Details
Hazard Statements H315-H318-H319-H335    Details
Precautionary Statements P261-P264-P264+P265-P271-P280-P302+P352-P304+P340-P305+P351+P338-P305+P354+P338-P317-P319-P321-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Serious eye damageEye Dam.1H318
Specific target organ toxicity - single exposureSTOT SE3H335
Eye irritationEye Irrit.2H319
Skin corrosionSkin Corr.1BH314
Acute toxicityAcute Tox.1H310
Chronic hazardous to the aquatic environmentAquatic Chronic3H412
Acute toxicityAcute Tox.1H300
Skin sensitizationSkin Sens.1H317
SDS Available
up Discovory and Applicatios
N-(2-Hydroxyethyl)piperazine, also known as HEPP, is an organic compound widely used in various applications due to its versatile properties. It belongs to the class of piperazine derivatives, which are characterized by a six-membered heterocyclic structure containing two nitrogen atoms. The addition of a hydroxyethyl group to the piperazine ring imparts both hydrophilic and lipophilic characteristics to the molecule, making it useful in a broad range of chemical and industrial processes.

The discovery of N-(2-Hydroxyethyl)piperazine dates back to the early 20th century, as researchers began to explore the chemical properties and potential applications of piperazine derivatives. Piperazine itself had already found applications in medicinal chemistry, and the introduction of functional groups like the hydroxyethyl group enhanced its properties, leading to further investigation into its utility in various fields.

In terms of its applications, N-(2-Hydroxyethyl)piperazine is primarily used as a building block in the synthesis of other chemicals. It serves as an intermediate in the preparation of surfactants, chelating agents, and corrosion inhibitors. Its ability to form stable complexes with metal ions makes it particularly useful in the formulation of agents for water treatment and industrial cleaning. These complexes can effectively prevent the deposition of minerals and help control scale formation in water systems, making HEPP valuable in the maintenance of industrial equipment, such as boilers and cooling systems.

Additionally, N-(2-Hydroxyethyl)piperazine has found significant use in the pharmaceutical and biotechnology industries. It can be used to prepare derivatives with enhanced biological activity. The compound's amine functionality allows it to participate in reactions that yield biologically active molecules, such as antimicrobial agents and anticancer compounds. By modifying the hydroxyethyl group or introducing other substituents onto the piperazine ring, researchers can tailor the compound's properties to suit specific therapeutic needs.

Another notable application of N-(2-Hydroxyethyl)piperazine is in the synthesis of polymeric materials. It can be used to prepare polyamine-based polymers that have desirable properties such as flexibility, adhesion, and resistance to various environmental factors. These polymers are utilized in coatings, adhesives, and sealants, where chemical resistance and durability are critical.

N-(2-Hydroxyethyl)piperazine also plays a role in the development of ion exchange resins. Its ability to interact with various ions makes it useful in creating resins for water purification, which are widely applied in both domestic and industrial water treatment systems.

In summary, N-(2-Hydroxyethyl)piperazine is a valuable chemical with diverse applications across industries such as pharmaceuticals, water treatment, polymer production, and more. Its unique combination of functional groups enhances its chemical reactivity, making it a versatile component in the synthesis of a variety of useful compounds and materials.
Market Analysis Reports
List of Reports Available for N-(2-Hydroxyethyl)piperazine
Related Products
4-(2-Hydroxyethyl)oxyindole  N-(2-Hydroxyethyl)-1,5-pentanediamine  N-(2-Hydroxyethyl)perfluorobutanesulfonamide  3-(1-Hydroxyethyl)phenol  4-(1-Hydroxyethyl)phenol  [3-(1-Hydroxyethyl)phenyl]boronic acid  2-(2-Hydroxy)ethyl-p-phenylene diamino sulfate  N-[4-(2-Hydroxyethyl)phenyl]-2-[(4-nitrobenzoyl)amino]benzamide  1-(2-Hydroxyethyl)-5-phenyl-1H-pyrazole-4-carbonitrile  N-Hydroxyethylphthalimide  N-(2-Hydroxyethyl)piperazine-N'-(4-butanesulfonic acid)  (3S)-3-(2-Hydroxyethyl)-1-piperazinecarboxylic acid 1,1-dimethylethyl ester  (3R)-3-(2-Hydroxyethyl)-1-piperazinecarboxylic acid 1,1-dimethylethyl ester  (S)-2-(2-Hydroxyethyl)piperazine-1-carboxylic acid tert-butyl ester  N-(2-Hydroxyethyl)-1-[(6-methoxy-5-methylpyrimidin-4-yl)methyl]-6-methyl-1H-pyrrolo[3,2-b]pyridine-3-carboxamide  4-(4-(1-Hydroxyethyl)-2-methoxy-5-nitrophenoxy)butanoic acid  1-[5-(2-Hydroxyethyl)-2-methoxyphenyl]ethanone  N-(2-Hydroxyethyl)-N-methylaniline  1-(2-Hydroxyethyl)-4-[3-(3-methyl-2(3H)-benzothiazolylidene)-1-propenyl]quinolinium tetrafluoroborate  (3S,4R)-3-[(1R)-1-Hydroxyethyl]-4-[(1R)-1-methyl-3-diazo-3-(4-nitrobenzyloxycarbonyl)-2-oxopropyl]azetidin-2-one