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Amino-Tri-(Propargyl-PEG2-ethoxymethyl)-methane TFA Salt
| Catalog Number | R01-0071 |
| Category | Alkynes |
| Molecular Formula | C34H56N4O12 |
| Molecular Weight | 712.84 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
Amino-Tri-(Propargyl-PEG2-ethoxymethyl)-methane TFA Salt is a crosslinker containing an amino group with three propargyl groups. The amino group is reactive with carboxylic acids, activated NHS esters, and carbonyls. The propargyl groups can form triazole linkage with azide-bearing compounds or biomolecules via copper catalyzed click chemistry.
Chemical Information
Product Specification
Application
Computed Properties
| Purity | 98% |
| IUPAC Name | 3-[2-amino-3-[3-oxo-3-[2-(2-prop-2-ynoxyethoxy)ethylamino]propoxy]-2-[[3-oxo-3-[2-(2-prop-2-ynoxyethoxy)ethylamino]propoxy]methyl]propoxy]-N-[2-(2-prop-2-ynoxyethoxy)ethyl]propanamide |
| Canonical SMILES | C#CCOCCOCCNC(=O)CCOCC(COCCC(=O)NCCOCCOCC#C)(COCCC(=O)NCCOCCOCC#C)N |
| InChI | InChI=1S/C34H56N4O12/c1-4-13-42-22-25-45-19-10-36-31(39)7-16-48-28-34(35,29-49-17-8-32(40)37-11-20-46-26-23-43-14-5-2)30-50-18-9-33(41)38-12-21-47-27-24-44-15-6-3/h1-3H,7-30,35H2,(H,36,39)(H,37,40)(H,38,41) |
| InChIKey | ZDSGMMNTGVDLQW-UHFFFAOYSA-N |
| Storage | -20 °C |
Amino-Tri-(Propargyl-PEG2-ethoxymethyl)-methane TFA Salt, a specialized reagent in chemical biology and medicinal chemistry, is a versatile tool with diverse applications.
Click Chemistry: This compound shines in click chemistry, serving as a potent agent for bioorthogonal labeling and biomolecule modification. By integrating propargyl groups, it facilitates seamless reactions with azides under gentle conditions, forming durable triazole linkages. This capability is invaluable for tagging proteins, nucleotides, and other biomolecules for intricate imaging and functional exploration.
Drug Conjugation: Leveraging Amino-Tri-(Propargyl-PEG2-ethoxymethyl)-methane TFA Salt, researchers can craft drug conjugates endowed with enhanced solubility and targeted delivery prowess. The polyethylene glycol (PEG) component boosts solubility and biocompatibility of drug entities, ideal for crafting precision therapies that reach specific cell populations, curtailing undesired side effects with precision.
Surface Modification: In the domains of material science and bioengineering, this compound finds utility in surface modification, empowering researchers to imbue surfaces with tailored functional groups. By grafting onto surfaces, it enables the creation of bioactive coatings, amping up cell adhesion, protein binding, or antimicrobial attributes.
Polymer Conjugates: Capitalizing on the PEGylated structure of this reagent, scientists can forge polymer conjugates that elevate their utility for biomedical applications. Through conjugation to diverse polymers, it enhances their stability, circulation duration, and functionalization capabilities. This prowess makes it a prime candidate for augmenting drug delivery systems, diagnostic mediators, and other advanced biotechnological instruments.
| XLogP3 | -4.1 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 13 |
| Rotatable Bond Count | 36 |
| Exact Mass | 712.38947323 g/mol |
| Monoisotopic Mass | 712.38947323 g/mol |
| Topological Polar Surface Area | 196Ų |
| Heavy Atom Count | 50 |
| Formal Charge | 0 |
| Complexity | 907 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
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