Cas No.: 1422540-88-2
PRODUCT INFORMATION
Description
This is a heterobifunctional, hydrophilic linker for 'Click Chemistry' and thiol-based conjugations. It contains: 1) A terminal alkyne group for Copper(I)-catalyzed (CuAAC) click reactions with azides. 2) An S-acetyl-protected thiol group. This thioester is stable to click conditions but can be selectively cleaved with a mild base (e.g., hydroxylamine) to reveal a free sulfhydryl group. This free thiol can then be used for a subsequent conjugation, such as reacting with a maleimide or immobilizing onto a gold surface. The 4-unit PEG spacer adds hydrophilicity.
Molecular Weight
290.37
Purity
>98.0%
Formula
C₁₃H₂₂O₅S
Product Type
Heterobifunctional Crosslinkers
Group 1
Alkyne
Group 2
Other
Form (20 deg.C)
Liquid
Storage Condition
Store under inert gas, -20°C
Molecular Structure
For Research Use Only | Not For Clinical Use
Related products
- 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide (CAT#: OLY-1023-YS284)
- N-([ε-Maleimidocaproyloxy)sulfosuccinimide Ester (Sulfo-EMCS) (CAT#: OLY-1023-YS88)
- m-PEG4-amine PEGylation Crosslinker (CAT#: OLY-1023-YS234)
- 3-Maleimido-propionic NHS (BMPS) Heterobifunctional Crosslinker (CAT#: OLY-1023-YS108)
- t-Boc-N-amido-PEG4-acid PEGylation Crosslinker (CAT#: OLY-1023-YS116)
- (R)-α-Lipoic Acid Heterobifunctional Crosslinker (CAT#: OLY-1023-YS8)
- Biotin-LC-NHS Ester Biotins Conjugation Reagent (CAT#: OLY-1023-YS192)
- Sulfosuccinimidyl-4-(N-maleimidomethyl)cyclohexane-1-carboxylate (Sulfo-SMCC) (CAT#: OLY-1023-YS104)
Online Inquiry
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
