CAS 4461-39-6

N-(2-Hydroxyethyl)-1,3-propanediamine

Description:

N-(2-Hydroxyethyl)-1,3-propanediamine, also known as HEPA, is an organic compound characterized by its amine functional groups and a hydroxyl group. It features a three-carbon chain with two amine groups (-NH2) and one hydroxyl group (-OH) attached to it, which contributes to its hydrophilicity and ability to form hydrogen bonds. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is soluble in water and various organic solvents, making it versatile for different applications. HEPA is often used in the synthesis of surfactants, chelating agents, and as a building block in the production of polymers and pharmaceuticals. Its amine groups can participate in various chemical reactions, including acylation and alkylation, which further enhances its utility in organic synthesis. Additionally, due to its structure, it may exhibit biological activity, making it of interest in medicinal chemistry. Safety precautions should be taken when handling this compound, as it may cause irritation to the skin and eyes.

Formula: C₅H₁₄N₂O

InChI: InChI=1/C5H14N2O/c6-2-1-3-7-4-5-8/h7-8H,1-6H2/p+2

InChI key: InChIKey=GHKSKVKCKMGRDU-UHFFFAOYSA-N

SMILES: C(NCCO)CCN

Synonyms:

• 1,3-Diamino-N-(2-hydroxyethyl)propane
• 1,3-Diamino-N-(hydroxyethyl)propane
• 2-(3-Aminopropylamino)Ethanol
• 2-Hydroxyethylamino Propylamine
• 2-[(3-Aminopropyl)amino]ethan-1-ol
• 2-[(3-Aminopropyl)amino]ethanol
• 3-(2-Hydroxyethylamino)propylamine
• 3-(Hydroxyethylamino)propanamine
• Ethanol, 2-[(3-aminopropyl)amino]-
• Heapa
• Koei 3311
• N-(2-Hydroxyethyl)-1,3-Diaminopropane
• N-(2-Hydroxyethyl)-Propanediamine-1,3
• N-(2-Hydroxyethyl)Trimethylenediamine
• N-(2-Hydroxyethyl)propan-1,3-diamine
• N-(2-hydroxyethyl)propane-1,3-diaminium
• N-(3-Aminopropyl)-2-aminoethanol
• N-(Aminopropyl)ethanolamine
• N-(Hydroxyethyl)propane-1,3-diamine
• N-(β-Hydroxyethyl)-1,3-diaminopropane
• N-(2-Hydroxyethyl)-1,3-propanediamine

N-(2-Hydroxyethyl)-1,3-propanediamine

CAS: 4461-39-6

Formula: C₅H₁₄N₂O

Purity: 95%

Color and Shape: Liquid

Molecular weight: 118.1775

Ref: IN-DA0071K0

2-(3-Aminopropylamino)ethanol

CAS: 4461-39-6

Formula: NH₂CH₂CH₂CH₂NHCH₂CH₂OH

Molecular weight: 118.18

Ref: 7W-GL3189

N-(2-Hydroxyethyl)-1,3-propanediamine

CAS: 4461-39-6

N-(2-Hydroxyethyl)-1,3-propanediamine

Purity: 98%

Molecular weight: 118.18g/mol

Ref: 54-OR80807

2-[(3-Aminopropyl)amino]ethanol

CAS: 4461-39-6

Formula: C₅H₁₄N₂O

Purity: >95.0%(T)

Color and Shape: Colorless to Light yellow clear liquid

Molecular weight: 118.18

Ref: 3B-H1817

2-(3-Aminopropylamino)ethanol

CAS: 4461-39-6

Formula: C₅H₁₄N₂O

Purity: 95%

Color and Shape: Liquid, Clear

Molecular weight: 118.18

Ref: 10-F048142

2-(3-Aminopropylamino)ethanol

Controlled Product

CAS: 4461-39-6

Applications 2-(3-Aminopropylamino)ethanol is the hydroxy analogue of WR-1065 (A576820), a metabolite of Amifostine (A576810). Amifostine is an organic thiophosphate that has the ability to protect a broad range of tissues from cytotoxicity (e.g. from chemotherapeutic agents) without inducing an antitumour response. 2-(3-Aminopropylamino)ethanol is also used as an nucleophilic tag in the detection of human butyrylcholinesterase adducts.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Antonadou, D., et al.: Int. J. Rad. Oncol. Biol. Phys., 52, 739 (2002); Kemp, G., et al.: J. Clin. Oncol., 14, 2101 (1996)

Formula: C₅H₁₄N₂O

Color and Shape: Neat

Molecular weight: 118.18

Ref: TR-A628205