N-(2-(2-(2-(2-Aminoethoxy)ethoxy)ethoxy)ethyl) -5-(dimethylamino)naphthalene-1-sulfonamide (99%) 

Catalog#: AMTGC1582-AN26

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Name: N-(2-(2-(2-(2-Aminoethoxy)ethoxy)ethoxy)ethyl)-5-(dimethylamino)naphthalene-1-sulfonamide

Molecular Formula: C20H31N3O5S 

CAS#: 914311-67-4 

SMILES: NCCOCCOCCOCCNS(=O)(C1=CC=CC2=C1C=CC=C2N(C)C)=O 

MDL#: none 

Catalog#: AMTGC1582-AN26 

Molecular weight: 424.54 g/mol 

Other names: 

  • Dansyl-PEG4-amine  
  • PEG4 fluorescent amine linker  
  • Dansyl-functionalized PEG amine 
  • 5-(Dimethylamino)-N-(2-(2-(2-(2-aminoethoxy)ethoxy)ethoxy)ethyl)naphthalene-1-sulfonamide 

Fields of Interest: bioconjugation, fluorescent labeling, and chemical probe development 

Background & Applications:  

Background 

N-(2-(2-(2-(2-Aminoethoxy)ethoxy)ethoxy)ethyl)-5-(dimethylamino)naphthalene-1-sulfonamide is a multifunctional amine-functionalized PEG conjugate featuring a PEG4 spacer linked to a dansyl (dimethylaminonaphthalene sulfonamide) fluorophore. The polyethylene glycol segment provides hydrophilicity, flexibility, and improved solubility, while spatially separating the fluorescent moiety from the reactive terminal primary amine. The amine functionality enables efficient coupling to activated carboxylic acids, NHS esters, isocyanates, and related electrophiles, supporting site-specific conjugation. The dansyl group is a well-known environment-sensitive fluorophore widely used in fluorescence labeling and sensing applications. This compound serves as a versatile intermediate within a comprehensive portfolio of functionalized PEGs designed for modular conjugation and optical probe development. 

Applications 

This Dansyl-PEG4-amine derivative is commonly used in bioconjugationfluorescent labeling, and chemical probe development applications where both conjugation capability and optical detection are required. Typical uses include preparation of fluorescently labeled biomolecules, polymers, and surfaces, synthesis of imaging probes and diagnostics, and incorporation into materials for sensing or mechanistic studies. The combination of a reactive primary amine, a hydrophilic PEG spacer, and a fluorescent dansyl reporter enables controlled assembly of multifunctional probes with improved solubility and reduced nonspecific interactions. As part of a robust functionalized PEG product line, this compound supports advanced strategies in diagnostics, biomaterials, imaging, and specialty chemical synthesis. 

Appearance: Orange, viscous liquid 

Purity: 99% 

Storage: Room Temp 

Solubility: Dichloromethane, Chloroform, Methanol 

 

Literature: 

  • Tetrahedron Letters, 2013, vol. 54, # 49, p. 6682 – 6686 
  • Organic and Biomolecular Chemistry, 2015, vol. 13, # 12, p. 3648 – 3653 
  • Journal of the American Chemical Society, 2011, vol. 133, # 32, p. 12382 – 12385 
Categories

Functionalized PEGs

CAS #

[914311-67-4]

Purity %

99%

Smiles

NCCOCCOCCOCCNS(=O)(C1=CC=CC2=C1C=CC=C2N(C)C)=O

Molecular Weight

424.54

Molecular Formula

C20H31N3O5S

Functional Groups

Amine, Sulfonamide

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