CAS 23978-55-4
:Diaza-18-crown-6
Description:
Diaza-18-crown-6 is a synthetic macrocyclic compound belonging to the crown ether family, characterized by its ability to selectively bind cations, particularly alkali and alkaline earth metals. Its structure features a cyclic arrangement of six ether linkages, with two nitrogen atoms incorporated into the ring, enhancing its chelating properties. This compound exhibits a high degree of solubility in polar organic solvents, making it useful in various applications, including ion-selective electrodes, extraction processes, and as a phase transfer catalyst. The presence of nitrogen atoms in the crown structure allows for stronger interactions with cations compared to its oxygen-only counterparts, leading to increased selectivity and binding strength. Diaza-18-crown-6 can also form stable complexes with metal ions, which can be exploited in analytical chemistry for the detection and separation of specific ions. Additionally, its unique properties make it a subject of interest in supramolecular chemistry and materials science, where it can be utilized in the development of new functional materials and sensors.
Formula:C12H26N2O4
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
InChI key:InChIKey=NLMDJJTUQPXZFG-UHFFFAOYSA-N
SMILES:C1COCCOCCNCCOCCOCCN1
Synonyms:- 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
- 1,4,10,13-Tetraoxa-7,16-diazacyclooctadecane
- See more synonyms
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Found 6 products.
4,13-Diaza-18-crown 6-Ether
CAS:Formula:C12H26N2O4Purity:>98.0%(T)Color and Shape:White to Almost white powder to crystalMolecular weight:262.351,10-Diaza-18-crown-6, 96%
CAS:<p>1,10-Diaza-18-crown-6 are starting materials to produce macrocyclic polyamine metal-complexing agents. It is used as a ligand in chemistry for the applications of diagnostic imaging technique to identify medical condition or disease and for the development of medication as a therapeutic agent and ph</p>Formula:C12H28N2O4Purity:96%Color and Shape:Powder or crystals or crystalline powder, White to pale creamMolecular weight:264.371,4,10,13-Tetraoxa-7,16-diazacyclooctadecane
CAS:Formula:C12H26N2O4Purity:97%Color and Shape:SolidMolecular weight:262.3458Ref: IN-DA003DLI
1g70.00€5g205.00€15g583.00€25g534.00€250gTo inquire500gTo inquire100mg26.00€250mg38.00€4,13-Diaza-18-crown-6-ether
CAS:4,13-Diaza-18-crown-6-etherFormula:C12H26N2O4Purity:98%Color and Shape: white crystalsMolecular weight:262.35g/mol4,13-Diaza-18-crown 6-ether
CAS:<p>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</p>Formula:C12H26N2O4Purity:Min. 95%Molecular weight:262.35 g/mol





