≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 8 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Na+ ionophore; blocks glycoprotein secretion; may induce catecholamine secretion from chromaffin cells. Useful in potentiometric and spectroscopic studies of alkali metal ion complexes.
| Sonrisas canónicas | CCC1(CCC(O1)C2(CCC3(O2)CC(C(C(O3)C(C)C(C(C)C(=O)[O-])OC)C)O)C)C4C(CC(O4)C5C(CC(C(O5)(CO)O)C)C)C.[Na+] |
|---|---|
| IUPAC Name | sodium;(2S,3R,4S)-4-[(2S,5R,7S,8R,9S)-2-[(2R,5S)-5-ethyl-5-[(2R,3S,5R)-5-[(2S,3S,5R,6R)-6-hydroxy-6-(hydroxymethyl)-3,5-dimethyloxan-2-yl]-3-methyloxolan-2-yl]oxolan-2-yl]-7-hydroxy-2,8-dimethyl-1,10-dioxaspiro[4.5]decan-9-yl]-3-methoxy-2-methylpentanoate |
| InChIKey | XOIQMTLWECTKJL-FBZUZRIGSA-M |
| INCHI | 1S/C36H62O11.Na/c1-10-34(31-20(3)16-26(43-31)28-19(2)15-21(4)36(41,18-37)46-28)12-11-27(44-34)33(8)13-14-35(47-33)17-25(38)22(5)30(45-35)23(6)29(42-9)24(7)32(39)40;/h19-31,37-38,41H,10-18H2,1-9H3,(H,39,40);/q;+1/p-1/t19-,20-,21+,22+,23-,24-,25-,26+,27+,28-,29+,30-,31+,33-,34-,35+,36-;/m0./s1 |
| Isómeros SMILES | CC[C@]1(CC[C@@H](O1)[C@@]2(CC[C@@]3(O2)C[C@@H]([C@H]([C@H](O3)[C@@H](C)[C@H]([C@H](C)C(=O)[O-])OC)C)O)C)[C@H]4[C@H](C[C@@H](O4)[C@@H]5[C@H](C[C@H]([C@@](O5)(CO)O)C)C)C.[Na+] |
| WGK Alemania | 3 |
| RTECS | JH2830000 |
| CAS alternativo | 17090-79-8 |
| Peso molecular | 692.85 |
| Beilstein | 4122200 |
| Reaxy-Rn | 4122200 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4122200&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Clase | Organooxygen compounds |
| Subclass | Ethers |
| Intermediate Tree Nodes | Acetals |
| Direct Parent | Ketals |
| Alternative Parents | Fatty acids and conjugates Oxanes Oxolanes Carboxylic acid salts Hemiacetals Secondary alcohols Oxacyclic compounds Monocarboxylic acids and derivatives Dialkyl ethers Carboxylic acids Organic zwitterions Organic sodium salts Organic oxides Hydrocarbon derivatives Carbonyl compounds Primary alcohols |
| Molecular Framework | Aliphatic heteropolycyclic compounds |
| Substituents | Ketal - Oxane - Fatty acid - Oxolane - Carboxylic acid salt - Hemiacetal - Secondary alcohol - Carboxylic acid derivative - Carboxylic acid - Dialkyl ether - Monocarboxylic acid or derivatives - Oxacycle - Organic alkali metal salt - Organoheterocyclic compound - Alcohol - Hydrocarbon derivative - Organic oxide - Primary alcohol - Organic sodium salt - Organic zwitterion - Organic salt - Carbonyl group - Aliphatic heteropolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as ketals. These are acetals derived from ketones by replacement of the oxo group by two hydrocarbyloxy groups R2C(OR)2 ( R not Hydrogen ). This term, once abandoned, has been reinstated as a subclass of acetals. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 C2226649 | Certificate of Analysis | Jan 19, 2026 | M118287 |
| L2518040 | Certificate of Analysis | Dec 29, 2025 | M118287 |
| A1809060 | Certificate of Analysis | Aug 18, 2025 | M118287 |
| A1809059 | Certificate of Analysis | Aug 18, 2025 | M118287 |
| B2512064 | Certificate of Analysis | Feb 15, 2025 | M118287 |
| C2226606 | Certificate of Analysis | May 23, 2022 | M118287 |
| Sensibilidad | Heat Sensitive |
|---|---|
| Punto de fusión (°C) | 264 °C(dec.) |
| Peso molecular | 692.900 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 11 |
| Rotatable Bond Count | 10 |
| Exact Mass | 692.411 Da |
| Monoisotopic Mass | 692.411 Da |
| Topological Polar Surface Area | 156.000 Ų |
| Heavy Atom Count | 48 |
| Formal Charge | 0 |
| Complexity | 1110.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 17 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 2 |
| 1. Liping Zhang, Yuan Xu, Wenjuan Cao, Shibao Xie, Lu Wen, Gang Chen. (2023) Understanding the translocation mechanism of PLGA nanoparticles across round window membrane into the inner ear: a guideline for inner ear drug delivery based on nanomedicine. International Journal of Nanomedicine, [PMID:29403277] [10.2147/IJN.S154968] |
| 2. Enqi He, Wei Quan, Jie Luo, Chuxin Liu, Wanting Zheng, Qingwu Shen. (2023) Absorption and Transport Mechanism of Red Meat-Derived N-glycolylneuraminic Acid and Its Damage to Intestinal Barrier Function through the NF-κB Signaling Pathway. Toxins, 15 (2): (132). [PMID:36828446] [10.3390/toxins15020132] |
| 3. Junjie Zhao, Yehui Luan, Yanan Chen, Linli Cheng, Qianxi Qin. (2022) Toxicological and transcriptomic-based analysis of monensin and sulfamethazine co-exposure on male SD rats. ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, [PMID:36155339] [10.1016/j.ecoenv.2022.114110] |
| 4. Xu Li, Rui Zhao, Di Shao, Yue Yuan, Shuyun Bi. (2022) Multispectral and molecular modeling investigations on the binding behaviors of two anticoccidials with serum albumins. JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, [PMID:33583333] [10.1080/07391102.2021.1886173] |
| 5. Wangjing Zhai, Qiqi Guo, Nan Wang, Xueke Liu, Donghui Liu, Zhiqiang Zhou, Peng Wang. (2024) Antibiotics alter the metabolic profile of metolachlor in soil–plant system by disturbing the detoxifying process and oxidative stress. BIORESOURCE TECHNOLOGY, [PMID:38851596] [10.1016/j.biortech.2024.130855] |
| 6. Xiang-Xing Kong, Jia-Sheng Xu, Ye-Ting Hu, Yu-Rong Jiao, Sheng Chen, Cheng-Xuan Yu, Si-Qi Dai, Zong-Bao Gao, Xu-Ran Hao, Jun Li, Ke-Feng Ding. (2024) Circulation immune cell landscape in canonical pathogenesis of colorectal adenocarcinoma by CyTOF analysis. iScience, [PMID:38455977] [10.1016/j.isci.2024.109229] |
| 7. Hu Songliu, Zhan Ning, Li Jian, Wang Liqun, Liu Yiyan, Jin Ke, Wang Yixuan, Zhang Juxuan, Chen Yiyang, Bai Yang, Wang Yichong, Qi Lishuang, Liu Shilong. (2025) RBM15 recruits myeloid-derived suppressor cells via the m6A-IGF2BP3/CBR3-AS1/miR-409-3p/CXCL1 axis, facilitating radioresistance in non-small-cell lung cancer. Journal of Translational Medicine, 23 (1): (1-19). [PMID:39962467] [10.1186/s12967-025-06205-y] |
| 8. Dingsheng Wen, Liping Zhang, Peiwen Deng, Huaan Li, Xiaohua Feng, Lu Wen, Gang Chen. (2026) Tracking the Spatiotemporal Journey of Chitosan Nanoparticles Across Ear Physiological Barriers: Mechanisms and Pathways. DRUG METABOLISM AND DISPOSITION, [PMID:41764965] [10.1016/j.dmd.2026.100233] |
