Kmuh (N-(κ-maleimidoundecanoic acid) hydrazide, trifluoroacetic acid salt)

Molecular Weight: 0
Update Date: 2026-09-12 18:51:19

What is Kmuh (N-(κ-maleimidoundecanoic acid) hydrazide, trifluoroacetic acid salt)?

General Description

BMPH, EMCH and KMUH are heterobifunctional crosslinkers containing sulfhydryl-reactive maleimide and carbonyl-reactive hydrazide moieties. Maleimides react with free sulfhydryls (-SH) to form stable thioether bonds. Hydrazide groups react with carbonyls (aldehydes and ketones) to form stable hydrazone bonds. Aldehyde groups can be created by periodate-oxidation of sialic acid and other sugar components of glycoprotein polysaccharides. Thus, these crosslinkers are useful for conjugating glycoproteins and sulfhydryl-containing peptides or proteins. Alternatively, the amine of the hydrazide moiety can be reacted to carboxyl groups using the crosslinker EDC.

Properties of Kmuh (N-(κ-maleimidoundecanoic acid) hydrazide, trifluoroacetic acid salt)

storage temp.	2-8°C
form	powder

Safety information for Kmuh (N-(κ-maleimidoundecanoic acid) hydrazide, trifluoroacetic acid salt)

Computed Descriptors for Kmuh (N-(κ-maleimidoundecanoic acid) hydrazide, trifluoroacetic acid salt)

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