Homobifunctional Carboxyl Reactive – VectorLabs https://staging.vectorlabs.com From linker design and synthesis, bioconjugated design and manufacturing, biomolecule labeling and functionalization, and detection system and solutions, our team is here to help you move forward, with impact. Wed, 22 Oct 2025 17:17:45 +0000 en-US hourly 1 https://wordpress.org/?v=6.8.3 https://staging.vectorlabs.com/wp-content/uploads/2024/11/V-favicon-02-100x100.png Homobifunctional Carboxyl Reactive – VectorLabs https://staging.vectorlabs.com 32 32 Diamido-dPEG®₁₁-diamine https://staging.vectorlabs.com/products/diamido-dpeg11-diamine/ Sat, 24 Feb 2024 02:10:15 +0000 https://staging.vectorlabs.com/?post_type=product&p=36077 Diamido-dPEG®11-diamine, product number QBD-10361, is a water-soluble, homobifunctional, single molecular weight, discrete chain length polyethylene glycol (dPEG®) crosslinker that is 49 atoms (57.1 Å) long. Both ends of the crosslinker terminate with amino groups that react with activated carboxylates or their active esters to form stable amide bonds. Aldehydes and ketones react to form labile Schiff bases that are reducible to secondary amines for improved bond stability. This molecule is useful for modifying carboxylic acid-functionalized surfaces, small molecules with reactive carbonyl groups, and carbohydrates containing reducing sugars.

The use of Diamido-dPEG®11-diamine appears in several patents. Moreover, researchers at the Karolinska Institutet, Stockholm, Sweden, reported the use of Diamido-dPEG®11-diamine in an investigation of γ-secretase and its role in Alzheimer’s Disease. Furthermore, Diamido-dPEG®11-diamine may prove useful in the following applications:
Crosslinking peptides or other small biomolecules using available carboxylic acids, aldehydes, or ketones;
Introducing a dPEG® amine onto reducing sugars of a glycoprotein’s carbohydrate coat;
Passivating nanoparticle surfaces coated with carboxylic acids or their active esters; and,
Adding a medium-length dPEG® amine at the carboxyl terminus of a peptide.

Specifications

Unit Size 100 mg, 1000 mg
Molecular Weight 742.94; single compound
Chemical formula C₃₄H₇₀N₄O₁₃
CAS 1224728-09-9
Purity > 97%
Spacers dPEG® Spacer is 49 atoms and 57.1 Å
Shipping Ambient
Typical solubility properties (for additional information contact Customer Support) Methylene chloride, Acetontrile, DMAC, DMSO or water.
Storage and handling -20°C; Always let come to room temperature before opening; be careful to limit exposure to moisture and restore under an inert atmosphere; stock solutions can be prepared with dry solvent and kept for several days (freeze when not in use). dPEG® pegylation compounds are generally hygroscopic and should be treated as such. This will be less noticeable with liquids, but the solids will become tacky and difficult to manipulate, if care is not taken to minimize air exposure.

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Description

Diamido-dPEG®11-diamine, product number QBD-10361, is a water-soluble, homobifunctional, single molecular weight, discrete chain length polyethylene glycol (dPEG®) crosslinker that is 49 atoms (57.1 Å) long. Both ends of the crosslinker terminate with amino groups that react with activated carboxylates or their active esters to form stable amide bonds. Aldehydes and ketones react to form labile Schiff bases that are reducible to secondary amines for improved bond stability. This molecule is useful for modifying carboxylic acid-functionalized surfaces, small molecules with reactive carbonyl groups, and carbohydrates containing reducing sugars.

The use of Diamido-dPEG®11-diamine appears in several patents. Moreover, researchers at the Karolinska Institutet, Stockholm, Sweden, reported the use of Diamido-dPEG®11-diamine in an investigation of γ-secretase and its role in Alzheimer’s Disease. Furthermore, Diamido-dPEG®11-diamine may prove useful in the following applications:
Crosslinking peptides or other small biomolecules using available carboxylic acids, aldehydes, or ketones;
Introducing a dPEG® amine onto reducing sugars of a glycoprotein’s carbohydrate coat;
Passivating nanoparticle surfaces coated with carboxylic acids or their active esters; and,
Adding a medium-length dPEG® amine at the carboxyl terminus of a peptide.

Specifications

Unit Size100 mg, 1000 mg
Molecular Weight742.94; single compound
Chemical formulaC₃₄H₇₀N₄O₁₃
CAS1224728-09-9
Purity> 97%
SpacersdPEG® Spacer is 49 atoms and 57.1 Å
ShippingAmbient
Typical solubility properties (for additional information contact Customer Support)Methylene chloride, Acetontrile, DMAC, DMSO or water.
Storage and handling-20°C; Always let come to room temperature before opening; be careful to limit exposure to moisture and restore under an inert atmosphere; stock solutions can be prepared with dry solvent and kept for several days (freeze when not in use). dPEG® pegylation compounds are generally hygroscopic and should be treated as such. This will be less noticeable with liquids, but the solids will become tacky and difficult to manipulate, if care is not taken to minimize air exposure.



Documents

References

Greg T. Hermanson, Bioconjugate Techniques, 3rd Edition, Elsevier, Waltham, MA 02451, 2013, ISBN 978-0-12-382239-0; See Chapter 18, Discrete PEG Reagents, pp. 787-821, for a full overview of the dPEG® products.

Visualizing Active Enzyme Complexes Using a Photoreactive Inhibitor for Proximity Ligation – Application on y-Secretase. Sophia Schedin-Weiss, Mitsuhiro Inoue, Yasuhiro Teranishi, Natsuko Goto Yamamoto, Helena Karlstrom, Bengt Winblad, Lars O. Tjernberg. PLoS ONE 2013, 8 (5) e63962. May 24, 2013. DOI:10.1371/journal.pone.0063962.

Teranishi, Y.; Hur, J.-Y.; Welander, H.; Frånberg, J.; Aoki, M.; Winblad, B.; Frykman, S.; Tjernberg, L. O. Affinity Pulldown of γ-Secretase and Associated Proteins from Human and Rat Brain. Journal of Cellular and Molecular Medicine 2010, 14 (11), 2675–2686. https://doi.org/10.1111/j.1582-4934.2009.00907.x.

Teranishi, Y. Identification and Investigation of Gamma-Secretase Associated Proteins from Brain. Doctoral Dissertation, Inst för neurobiologi, vårdvetenskap och samhälle / Dept of Neurobiology, Care Sciences and Society: Stockholm, Sweden, 2012.

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