6-Azido-hexanoic acid

6-Azido-hexanoic acid

Product Number: 4066756

CAS Number: 79598-53-1

€ 267.50 – € 1,071.10

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Product Description

Building block for Staudinger ligation as well as for “click chemistry”. This highly selective reaction can be applied for the conjugation of peptides with various molecules and for the cyclization of peptides. The azido moiety may also be considered as a protected amino group which is deblocked under reductive conditions.

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Isolation and primary structure of novel neurointermediate pituitary peptides derived from the C-terminal of the rat vasopressin-neurophysin precursor (propressophysin).

J.P.H.Burbach et al., Eur. J. Biochem., 156, 137 (1986)

Versatile conjugation of octreotide to dendrimers by cycloaddition ("click") chemistry to yield high-affinity multivalent cyclic Peptide dendrimers.

C.-B.Yim et al., Bioconjug. Chem., 20, 1323 (2009)

A generic building block for C- and N-terminal protein-labeling and protein-immobilization.

A.Watzke et al., Bioorg. Med. Chem., 14, 6288 (2006)

Efficiency and fidelity in a click-chemistry route to triazole dendrimers by the copper(i)-catalyzed ligation of azides and alkynes.

P.Wu et al., Angew. Chem. Int. Ed. Engl., 43, 3928 (2004)

Identification of protein targets of 4-hydroxynonenal using click chemistry for ex vivo biotinylation of azido and alkynyl derivatives.

A.Vila et al., Chem. Res. Toxicol., 21, 432 (2008)

Molecular weight: 157.17

Chemical Formula: C₆H₁₁N₃O₂

Storage Temperature: < -15°C

Synonyms: ε-Azidocaproic acid

Old Product Number: Q-2740

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