(+)-(18-Crown-6)-2,3,11,12-tetracarboxylic Acid
| Product Name | (+)-(18-Crown-6)-2,3,11,12-tetracarboxylic Acid |
|---|---|
| CAT No. | CS-T-13484 |
| CAS No. | 61696-54-6 |
| Category | Impurities |
| Stock | Enquire |
| Mol. Wt. | Not Available |
| Mol. For. | Not Available |
| Hazardous | This is not a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Canonical Smiles | C1COC(C(OCCOCCOC(C(OCCO1)C(=O)O)C(=O)O)C(=O)O)C(=O)O |
| InchIKey | FZERLKNAJSFDSQ-DDHJBXDOSA-N |
| Inchl | InChI=1S/C16H24O14/c17-13(18)9-10(14(19)20)29-7-3-26-4-8-30-12(16(23)24)11(15(21)22)28-6-2-25-1-5-27-9/h9-12H,1-8H2,(H,17,18)(H,19,20)(H,21,22)(H,23,24)/t9-,10-,11-,12-/m1/s1 |
| IUPAC | (2R,3R,11R,12R)-1,4,7,10,13,16-hexaoxacyclooctadecane-2,3,11,12-tetracarboxylic acid |
| Controlled | No |
| Shipping | Free for purchase above 1000$ |
| Delivery | In-Stock, products will be dispatched within 24 hours via FedEx for USA, Europe, and other countries. |
| Return | Returns/replacement accepted if you are not satisfied with the quality of the product, (please send us an email with the reason/issues which are facing, within 15 days, after receipt of the product). |
| Ordering | Place your order online or by email sales@clearsynth.com |
(+)-(18-Crown-6)-2,3,11,12-tetracarboxylic acid is a complex organic compound with the chemical formula C20H24O10. It is a chiral molecule, meaning it exists in two enantiomeric forms, which have identical physical and chemical properties except for their interaction with polarized light. The compound is commonly used as a ligand in coordination chemistry, where it forms complexes with metal ions.
The crown ether moiety of (+)-(18-Crown-6)-2,3,11,12-tetracarboxylic acid provides a cavity that is the perfect size to encapsulate metal ions such as potassium, sodium, or lithium. The tetracarboxylic acid groups can then form strong coordination bonds with the metal ions, stabilizing the complex. These complexes have a range of potential applications, including ion sensing, catalysis, and separation techniques.
In addition to its use as a ligand
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