139554-72-6

Basic information

• Product Name: N-BIOTINYL-N'-MALEIMIDO-ETHYLENEDIAMINE
• Synonyms: N-BIOTINYL-N'-MALEIMIDO-ETHYLENEDIAMINE;(3aS,4S,6aR)-N-[2-(2,5-Dihydro-2,5-dioxo-1H-pyrrol-1-yl)ethyl]hexahydro-2-oxo-1H-thieno[3,4-d]iMidazole-4-pentanaMide;5-(2-Oxo-hexahydro-thieno[3,4-d]iMidazol-6-yl)-pentanoic acid [2-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-ethyl]-aMide;N-Biotinyl-Na€-maleimido-ethylenediamine
• CAS NO: 139554-72-6
• Molecular Formula: C16H23N5O4S
• Molecular Weight: 381.45
• Product Categories: Biotin Derivatives;Maleimide Derivatives;MTS & Sulfhydryl Active Reagents
• Mol File: 139554-72-6.mol
• Article Data: 3

Chemical Properties

• Melting Point: 123-129°C
• Boiling Point: 743.543°C at 760 mmHg
• Flash Point: 403.48°C
• Appearance: /
• Density: 1.313g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.574
• Storage Temp.: -20°C Freezer, Under Inert Atmosphere
• Solubility: DMSO (Slightly, Heated), Methanol (Slightly, Heated, Sonicated)
• CAS DataBase Reference: N-BIOTINYL-N'-MALEIMIDO-ETHYLENEDIAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: N-BIOTINYL-N'-MALEIMIDO-ETHYLENEDIAMINE(139554-72-6)
• EPA Substance Registry System: N-BIOTINYL-N'-MALEIMIDO-ETHYLENEDIAMINE(139554-72-6)

Safety Data

• Hazardous Substances Data: 139554-72-6(Hazardous Substances Data)

Usage

Chemical Properties

White Solid

InChI:InChI=1/C16H22N4O4S/c21-12(17-7-8-20-13(22)5-6-14(20)23)4-2-1-3-11-15-10(9-25-11)18-16(24)19-15/h5-6,10-11,15H,1-4,7-9H2,(H,17,21)(H2,18,19,24)/t10?,11-,15?/m0/s1

Upstream product

• 58-85-5 biotin 
• 146474-00-2 N-(2-aminoethyl)maleimide trifluoroacetic acid salt 
• 35013-72-0 biotin N-Hydroxysuccinimide ester 
• 125923-10-6 1-(2-aminoethyl)-1H-pyrrole-2,5-dione 
• 215654-55-0 C₁₁H₁₈N₂O₅ 
• 134272-63-2 N-[2-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-ethyl]-carbamic acid tert-butyl ester 
• 146474-00-2 N-(2-aminoethyl)maleimide trifluoroacetate 

Relevant articles and documents

Sequential DNA-Encoded Building Block Fusion for the Construction of Polysubstituted Pyrazoline Core Libraries

The construction of chemical libraries containing polysubstituted pyrazoline scaffolds is highly desirable for the discovery of novel chemical ligands for biological targets. Herein, we report a sequential DNA-encoded synthesis strategy for polysubstitute

ANTIBODY CONJUGATES AND METHODS OF MAKING THE ANTIBODY CONJUGATES

Described herein are antibody conjugates and methods of making antibody conjugates.