2-[2-(2-Aminoethoxy)ethoxy]ethanol (99%)

Catalog#: AMTGC598-AE20-99

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Name: 2-[2-(2-Aminoethoxy)ethoxy]ethanol (99% purity) 

Molecular Formula: C6H15NO3 

CAS#: 6338-55-2

SMILES: C(O)COCCOCCN 

MDL#: MFCD07367495 

Catalog#: AMTGC598-AE20-99 

Molecular weight: 149.19g/mol 

Other names: 

  • NH2-PEG3-OH 
  • (PEO)3-monoamine 
  • Triethylene glycol monoamine 

Fields of Interest: PEGylating reagents, medicinal chemistry, organic synthesis 

Background & Applications: 

Background
2-[2-(2-Aminoethoxy)ethoxy]ethanol (CAS 6338-55-2) is a monofunctional amine-functionalized PEG derivative based on a PEG2 backbone, featuring a terminal primary amine and a hydroxyl group at the opposite end. The polyethylene glycol chain provides hydrophilicity, flexibility, and compatibility with aqueous and biological environments. The primary amine enables efficient coupling to activated carboxylic acids, NHS esters, isocyanates, and related electrophiles, while the hydroxyl group offers additional derivatization options or can remain unreactive for controlled, single-point functionalization. This compact PEG intermediate is a useful member of a versatile portfolio of functionalized PEGs designed for predictable molecular modification. 

Applications
2-[2-(2-Aminoethoxy)ethoxy]ethanol is commonly used in bioconjugationdrug delivery, and materials science applications where short linker length and monofunctional amine reactivity are desired. Typical uses include PEGylation of small molecules and polymers to enhance solubility and stability, preparation of multifunctional intermediates, and surface or nanoparticle modification. As part of a comprehensive functionalized PEG product line, this amine–alcohol PEG supports modular design strategies in pharmaceutical research, biomaterials development, and specialty chemical synthesis. 

Appearance: Colorless Liquid 

Purity: 99% 

Storage: 0-3 °C for long term storage  

Solubility: Soluble in DMF, DMSO, ethanol, and buffer solutions (e.g., PBS). 

Literature:

Used in linker design and PEGylation strategies for research reagents and biochemical applications. Typical references in chemistry and bioconjugation literature. 

  1. Tetrahedron, 1982, vol. 38, # 22, p. 3359 – 3362, https://doi.org/10.1016/0040-4020(82)80119-1
  2. Journal of Chemical Research, Miniprint, 1984, # 9, p. 2672 – 2691
Categories

Functionalized PEGs

Scaffold/Subcategory

Functionalized PEGs

CAS #

[6338-55-2]

Purity %

99%

Smiles

C(O)COCCOCCN

Molecular Weight

149.19

Molecular Formula

C6H15NO3

Functional Groups

Amine, Hydroxyl

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