CAS 140-31-8

1-Piperazineethanamine

Description:

1-Piperazineethanamine, also known as N-(2-aminoethyl)piperazine, is an organic compound characterized by its piperazine ring structure with an ethylamine side chain. It is a colorless to pale yellow liquid at room temperature and is soluble in water and various organic solvents, which enhances its utility in chemical synthesis and formulations. The compound exhibits basic properties due to the presence of both the piperazine nitrogen atoms and the amino group, allowing it to participate in various chemical reactions, including nucleophilic substitutions and complexation with metal ions. It is often used as a building block in the synthesis of pharmaceuticals, agrochemicals, and surfactants. Additionally, 1-Piperazineethanamine can act as a ligand in coordination chemistry. Safety data indicates that it may cause irritation upon contact with skin or eyes, and appropriate handling precautions should be taken. Overall, its unique structure and reactivity make it a valuable compound in both industrial and research applications.

Formula: C₆H₁₅N₃

InChI: InChI=1S/C6H15N3/c7-1-4-9-5-2-8-3-6-9/h8H,1-7H2

InChI key: InChIKey=IMUDHTPIFIBORV-UHFFFAOYSA-N

SMILES: C(CN)N1CCNCC1

Synonyms:

• 1-(2-Aminomethyl)piperazine
• 1-(2-Ammonioethyl)Piperazinediium
• 1-(Piperazin-1-Yl)Ethanamine
• 1-(β-Aminoethyl)piperazine
• 1-Aminoethylpiperazine
• 1-Piperazineethanamine
• 1-Piperazineethylamine
• 2-(1-Piperazino)ethylamine
• 2-(1-Piperazinyl)ethanamine
• 2-(1-Piperazinyl)ethylamine
• 2-(Piperazin-1-Yl)Ethanamine
• 2-(Piperazin-1-Yl)Ethanamine Acetate (1:1)
• 2-(Piperazin-1-yl)ethan-1-amine
• 2-(Piperazin-1-yl)ethaneamine
• 2-(Piperazinyl-1-yl)ethanamine
• 2-Piperazin-1-Iletilamina
• 2-Piperazin-1-Ylethylamine
• 2-Piperazin-1-ylethylamin
• 2-Piperazine-1-Ylethylamine
• 2-Piperazinoethylamine
• 2-Piperazinylethylamine
• 4-(2-Aminoethyl)piperazine
• AEP
• Ancamine AEP
• Epicure 3200
• Epikure 3202
• N-(2-Aminoaethyl)-Piperazin
• N-(2-Aminoethyl)piperazine
• N-(β-Aminoethyl)piperazine
• N-Aep
• N-Aminoethylpiperazine
• Nsc 38968
• Piperazine, 1-(2-aminoethyl)-
• Piperazine, N-Aminoethyl-

N-(2-Aminoethyl)piperazine

CAS: 140-31-8

Formula: C₆H₁₅N₃

Purity: >99.0%(GC)(T)

Color and Shape: Colorless to Light yellow to Light orange clear liquid

Molecular weight: 129.21

Ref: 3B-A0304

1-(2-Aminoethyl)piperazine, 98%

CAS: 140-31-8

1-(2-Aminoethyl)piperazine is utilized in a variety of reactions for studying corrosion inhibition, biological activity and metal ligand effects on catalysis. It is used for epoxy curing, surface activation, and as an asphalt additive. It is used in lube oil and fuel additives, mineral processing ai

Formula: C₆H₁₅N₃

Purity: 98%

Color and Shape: Liquid, Clear colorless

Molecular weight: 129.21

Ref: 02-A10154

N-(2-Aminoethyl)piperazine

CAS: 140-31-8

N-(2-Aminoethyl)piperazine

Purity: >99.0%

Ref: 54-OR1079016

1-(2-Aminoethyl) Piperazine

CAS: 140-31-8

Formula: C₆H₁₅N₃

Molecular weight: 129.21

Ref: 4Z-P-228044

N-(2-Aminoethyl)piperazine

Controlled Product

CAS: 140-31-8

Formula: C₆H₁₅N₃

Color and Shape: Neat

Molecular weight: 129.2034

Ref: 04-C10202360

Trientine Impurity 3

CAS: 140-31-8

Formula: C₆H₁₅N₃

Molecular weight: 129.21

Ref: ST-EA-CP-T50008

2-(Piperazin-1-yl)ethanamine

CAS: 140-31-8

Formula: C₆H₁₅N₃

Purity: 95.0%

Color and Shape: Liquid

Molecular weight: 129.207

Ref: 10-F079259

N-(2-Aminoethyl)piperazine

CAS: 140-31-8

N-(2-Aminoethyl)piperazine (NAPE) is a chemical compound that can be used as an environmentally friendly catalyst for the degradation of ethylene diamine and other amines. NAPE has been shown to be stable under alkaline conditions, and its fluorescence probe has been used to monitor the progress of the reaction. This compound is a coordination complex with nitrogen atoms at the corners of a square and two amines at opposite corners of the square. The amine groups are coordinated to metal ions in a geometry that is determined by the atomic number of the metal ion. Disulfide bonds form between two cysteine residues on adjacent chains. Glycol ethers can also form disulfide bonds with NAPE, forming glycol ether-NAPE complexes. Antibodies have been shown to bind to glycol ether-NAPE complexes, suggesting that these complexes may play a role in antibody response, although experimental solubility data have not yet confirmed this

Formula: C₆H₁₅N₃

Purity: Min. 95%

Molecular weight: 129.2 g/mol

Ref: 3D-FA75429