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755842

Sigma-Aldrich

6-Maleimidohexanoic acid

90% (GC)

Synonym(s):

2,5-Dihydro-2,5-dioxo-1H-pyrrole-1-hexanoic acid, 6-Maleimide hexanoic acid, MCA, Maleimidocaproic acid, 6-Maleimidocaproic acid, N-Maleoyl-6-aminocaproic acid, N-(5-Carboxypentyl)maleimide

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About This Item

Empirical Formula (Hill Notation):
C10H13NO4
CAS Number:
55750-53-3
Molecular Weight:
211.21
Beilstein:
1532405
MDL number:
MFCD00043140
UNSPSC Code:
12162002
PubChem Substance ID:
329766144
NACRES:
NA.23

Quality Level

100

Assay

90% (GC)

form

powder

mp

87-92 °C

storage temp.

2-8°C

SMILES string

OC(=O)CCCCCN1C(=O)C=CC1=O

InChI

1S/C10H13NO4/c12-8-5-6-9(13)11(8)7-3-1-2-4-10(14)15/h5-6H,1-4,7H2,(H,14,15)

InChI key

WOJKKJKETHYEAC-UHFFFAOYSA-N

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Application

Probe for thiol groups (SH-groups) in membrane proteins.
Intermediate for ester and amide linked maleimide monomers

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H335

Hazard Classifications

Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

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Certificates of Analysis (COA)

Lot/Batch Number
MKCP0799
MKCP0797
MKCP0796
MKCL8961
MKCH5159

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D B R K Gupta Udatha et al.
Journal of structural biology, 190(3), 314-327 (2015-04-25)
The catalytic residues in carbohydrate esterase enzyme families constitute a highly conserved triad: serine, histidine and aspartic acid. This catalytic triad is generally located in a very sharp turn of the protein backbone structure, called the nucleophilic elbow and identified
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