160563-01-9

Basic information

• Product Name: 10,19-BIS[(OCTADECYLCARBAMOYL)METHOXY-ACETYL]-1,4,7,13,16-PENTAOXA-10,19-DIAZACYCLOHENEICOSANE
• Synonyms: 10,19-BIS[(OCTADECYLCARBAMOYL)METHOXY-ACETYL]-1,4,7,13,16-PENTAOXA-10,19-DIAZACYCLOHENEICOSANE;K23E1;CALCIUM IONOPHORE V;4,16-Bis[(N-octadecylcarbamoyl)-3-oxabutyryl]-1,7,10,13,19-pentaoxa-4,16-diazacyclohenicosane;K23E1, 10,19-Bis[(octadecylcarbamoyl)methoxyacetyl]-1,4,7,13,16-pentaoxa-10,19-diazacycloheneicosane;K23E1, 10,19-Bis[(octadecylcarbamoyl)met
• CAS NO: 160563-01-9
• Molecular Formula: C58H112N4O11
• Molecular Weight: 1041.53008
• Mol File: 160563-01-9.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 1052.7°C at 760 mmHg
• Flash Point: 590.4°C
• Appearance: /
• Density: 0.985g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.468
• PKA: 14.53±0.46(Predicted)
• CAS DataBase Reference: 10,19-BIS[(OCTADECYLCARBAMOYL)METHOXY-ACETYL]-1,4,7,13,16-PENTAOXA-10,19-DIAZACYCLOHENEICOSANE(CAS DataBase Reference)
• NIST Chemistry Reference: 10,19-BIS[(OCTADECYLCARBAMOYL)METHOXY-ACETYL]-1,4,7,13,16-PENTAOXA-10,19-DIAZACYCLOHENEICOSANE(160563-01-9)
• EPA Substance Registry System: 10,19-BIS[(OCTADECYLCARBAMOYL)METHOXY-ACETYL]-1,4,7,13,16-PENTAOXA-10,19-DIAZACYCLOHENEICOSANE(160563-01-9)

Safety Data

• Safety Statements: 22-24/25
• WGK Germany: 3
• Hazardous Substances Data: 160563-01-9(Hazardous Substances Data)

Usage

Molecular structure

A complex chemical compound with a long and precise molecular structure.

Acetyl and carbamoyl groups

Contains multiple acetyl and carbamoyl groups.

Ether and diaza rings

Contains ether and diaza rings.

Surfactant and emulsifying properties

Likely to have surfactant and emulsifying properties due to its long hydrophobic chains and polar functional groups.

Industrial and commercial applications

May be used in industrial and commercial applications as a surfactant, detergent, or emulsifier.

Potential uses in pharmaceuticals or biotechnology research

Could potentially have uses in pharmaceuticals or biotechnology research.

InChI:InChI=1/C58H112N4O11/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-59-55(63)51-72-53-57(65)61-37-41-67-45-46-68-42-38-62(40-44-70-48-50-71-49-47-69-43-39-61)58(66)54-73-52-56(64)60-36-34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-54H2,1-2H3,(H,59,63)(H,60,64)

Upstream product

• 124-30-1 1-aminooctadecane 
• 23978-10-1 kryptofix 23 

Relevant articles and documents

Design and synthesis of calcium and magnesium ionophores based on double-armed diazacrown ether compounds and their application to an ion-sensing component for an ion-selective electrode

The double-armed diazacrown ethers, which have a base diazacrown ether ring with two diamide-type side chains, were designed and synthesized on the basis of the proposed molecular model for the novel neutral Ca2+ and Mg2+ ionophores. The potentiometric ion-selective electrodes were prepared with over 20 kinds of systematically synthesized diazacrown ether derivatives. The relationship between the molecular structures of the ionophores and the ion selectivities was fully discussed. The electrodes based on the 21- and 18-membered diazacrown ether derivatives possessing a glycolic diamide and malonic diamide in their side chains (K23E1 and K22B5) exhibited excellent Ca2+ and Mg2+ selectivities, respectively. The ion-selectivity features of the novel Ca2+ and Mg2+ ionophores supply important structural information about the design of host molecules for alkaline earth metal cations.