4,13-Diaza-18-crown 6-ether

CAS : 23978-55-4

Ref. 3D-FD62081

Informations sur le produit

• Nom: 4,13-Diaza-18-crown 6-ether
• Synonymes: 1,4,10,13-Tetraoxa-7,16-diazacyclooctadecane, 1,10-Diaza-18-crown ether, 1,10-Diaza-18-crown-6, 1,10-Diaza-4,7,13,16-tetraoxa-18-crown-6, 1,10-Diaza-4,7,13,16-tetraoxacyclooctadecane, 1,4,10,13-Tetraoxa-7,16-Diazaciclooctadecano, 1,4,10,13-Tetraoxa-7,16-diazacyclooctadecan, 1,7,10,16-Tetraoxa-4,13-diazacyclooctadecane, 2,2'-Kryptofix, 4,13-Diaza-18-crown-6, 4,13-Diaza-18-crown-6-ether, 4,7,13,16-Tetraoxa-1,10-diazacyclooctadecane, 7,16-Diaza-1,4,10,13-tetraoxacyclooctadecane, 7,16-Diaza-18-crown-6, Cryptand 22, Cryptand(2.2), Crytand[2,2], Cyclooctadecane, 1,4,10,13-Tetraoxa-7,16-Diaza-, Diaza crown ether 22, Diaza-18-crown-6, Kryptand[2.2], Kryptofix 22, Kryptofix[2.2], Nsc 339325

Description

4,13-Diaza-18-crown 6-ether belongs to the class of crown ethers. It is a synthetic compound that has been shown to form stable complexes with metal ions such as copper and sodium. 4,13-Diaza-18-crown 6-ether has been shown to be effective in treating urinary tract infections, and it is also used as a membrane system for separation of organic compounds. 4,13-Diaza-18-crown 6-ether has been shown to have a transport rate through membranes that is 10 times faster than traditional crown ethers. This rate can be increased by adding metal hydroxides or salts such as sodium chloride or potassium chloride. The mechanism for this transport may be due to intramolecular hydrogen bonding between the nitrogen atoms in 4,13-diazacrown 6 and the hydrogen atom on the metal hydroxide molecule. The photochemical properties of 4,13 diazacrown 6 can

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 262.35 g/mol
• Formule: C₁₂H₂₆N₂O₄
• Degré de pureté: Min. 95%
• InChI: InChI=1S/C12H26N2O4/c1-5-15-9-10-17-7-3-14-4-8-18-12-11-16-6-2-13-1/h13-14H,1-12H2
• Code InChI: InChIKey=NLMDJJTUQPXZFG-UHFFFAOYSA-N
• SMILES: C1COCCOCCNCCOCCOCCN1