mPEG8-amine - CAS 869718-81-0

mPEG8-amine - CAS 869718-81-0 Catalog number: BADC-01177

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m-PEG8-Amine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).

Category
ADCs Linker
Product Name
mPEG8-amine
CAS
869718-81-0
Catalog Number
BADC-01177
Molecular Formula
C17H37NO8
Molecular Weight
383.48
Purity
≥95%
mPEG8-amine

Ordering Information

Catalog Number Size Price Quantity
BADC-01177 -- $-- Inquiry
Description
m-PEG8-Amine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
Synonyms
m-PEG8-amine; 2,5,8,11,14,17,20,23-Octaoxapentacosan-25-amine; mPEG8-NH2; 3,6,9,12,15,18,21,24-Octaoxapentacosan-1-amine; 3,6,9,12,15,18,21,24-octaoxa-pentacosylamine; methyl-PEG8-amine
IUPAC Name
2-[2-[2-[2-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanamine
Canonical SMILES
COCCOCCOCCOCCOCCOCCOCCOCCN
InChI
InChI=1S/C17H37NO8/c1-19-4-5-21-8-9-23-12-13-25-16-17-26-15-14-24-11-10-22-7-6-20-3-2-18/h2-18H2,1H3
InChIKey
YXWBFPPGROXJLL-UHFFFAOYSA-N
Density
1.054±0.06 g/cm3 (Predicted)
Solubility
Soluble in DMSO, Water
Flash Point
213.9°C
LogP
0.40800
PSA
99.86000
Appearance
Pale Yellow Oily Matter
Shipping
Room temperature
Storage
Store at 2-8°C
Boiling Point
448.0±40.0°C (Predicted)
Form
Solid
Biological Activity
m-PEG8-Amine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1] . In Vitro: ADCs are comprised of an antibody to which is attached an ADC cytotoxin through an ADC linker.

mPEG8-amine, a derivative of polyethylene glycol, boasts unique properties that make it a versatile choice for diverse biomedical and chemical applications. Explore four key applications of mPEG8-amine:

Drug Delivery: Powering the advancement of drug delivery systems, mPEG8-amine is instrumental in enhancing the solubility and stability of pharmaceutical compounds. Through the strategic conjugation of drugs with mPEG8-amine, researchers can extend their circulation time and mitigate immunogenicity, ultimately revolutionizing drug delivery efficiency and elevating therapeutic outcomes to new heights.

Bioconjugation: In the intricate domain of bioconjugation, mPEG8-amine emerges as a crucial player, facilitating the modification of proteins, peptides, and other biomolecules. Leveraging its amine functional group, mPEG8-amine enables stable covalent attachment to diverse targets, amplifying their solubility and biocompatibility. This crucial modification serves as a catalyst for enhancing the pharmacokinetics and efficacy of biologically active compounds.

Surface Modification: Delving into surface modification applications, mPEG8-amine takes center stage in the coating of medical devices and nanoparticles. By grafting mPEG8-amine onto surfaces, a hydrophilic layer is crafted, curbing protein adsorption and cell adhesion. This quality is pivotal in sculpting biocompatible surfaces that mitigate immune responses and optimize implant performance.

Diagnostics: Stepping into the realm of diagnostics, mPEG8-amine assumes a crucial role in steering the development of imaging agents and biosensors. The versatility of mPEG8-amine in conjugating with an array of probes or markers facilitates the creation of targeted diagnostics with exquisite specificity and sensitivity.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Historical Records: mPEG8-amine
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