≥98% 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 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Sodium glycocholate hydrate is a conjugated bile salt and an ionic biologic detergent.
Sodium glycocholate hydrate has been used in a study to assess serum total bile acids via a fluorimetric and enzymatic method. It has also been used in a study to investigate its effect on micelle formation and solubilization of testosterone.
| Pubchem Sid | 504769702 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504769702 |
| Sorrisi canonici | CC(CCC(=O)NCC(=O)[O-])C1CCC2C1(C(CC3C2C(CC4C3(CCC(C4)O)C)O)O)C.O.[Na+] |
| IUPAC Name | sodium;2-[[(4R)-4-[(3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,7,12-trihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoyl]amino]acetate;hydrate |
| InChIKey | YWROUPFMHKARON-HJRQWJHVSA-M |
| INCHI | 1S/C26H43NO6.Na.H2O/c1-14(4-7-22(31)27-13-23(32)33)17-5-6-18-24-19(12-21(30)26(17,18)3)25(2)9-8-16(28)10-15(25)11-20(24)29;;/h14-21,24,28-30H,4-13H2,1-3H3,(H,27,31)(H,32,33);;1H2/q;+1;/p-1/t14-,15+,16-,17-,18+,19+,20-,21+,24+,25+,26-;;/m1../s1 |
| Isomeri SMILES | C[C@H](CCC(=O)NCC(=O)[O-])[C@H]1CC[C@@H]2[C@@]1([C@H](C[C@H]3[C@H]2[C@@H](C[C@H]4[C@@]3(CC[C@H](C4)O)C)O)O)C.O.[Na+] |
| CAS alternativo | 863-57-0 |
| PubChem CID | 23702132 |
| Peso molecolare | 487.6 |
| Beilstein | 3854517 |
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 | Lipids and lipid-like molecules |
| Classe | Steroids and steroid derivatives |
| Subclass | Bile acids, alcohols and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Glycinated bile acids and derivatives |
| Alternative Parents | Trihydroxy bile acids, alcohols and derivatives 12-hydroxysteroids 3-alpha-hydroxysteroids 7-hydroxysteroids N-acyl-alpha amino acids N-acyl amines Secondary carboxylic acid amides Secondary alcohols Carboxylic acid salts Cyclic alcohols and derivatives Polyols Carboxylic acids Monocarboxylic acids and derivatives Organic sodium salts Organopnictogen compounds Organic zwitterions Carbonyl compounds Hydrocarbon derivatives Organonitrogen compounds Organic oxides |
| Molecular Framework | Aliphatic homopolycyclic compounds |
| Substituents | Glycinated bile acid - Trihydroxy bile acid, alcohol, or derivatives - Hydroxy bile acid, alcohol, or derivatives - 3-hydroxysteroid - 12-hydroxysteroid - Hydroxysteroid - 7-hydroxysteroid - 3-alpha-hydroxysteroid - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Alpha-amino acid or derivatives - Fatty amide - Fatty acyl - N-acyl-amine - Cyclic alcohol - Secondary alcohol - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid salt - Polyol - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Carboxylic acid - Organic alkali metal salt - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Organic sodium salt - Organic salt - Organic zwitterion - Organonitrogen compound - Carbonyl group - Organic oxygen compound - Alcohol - Aliphatic homopolycyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as glycinated bile acids and derivatives. These are compounds with a structure characterized by the presence of a glycine linked to a bile acid skeleton. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
 J2122364 | Certificate of Analysis | Aug 11, 2025 | S101417 |
| J2122365 | Certificate of Analysis | Aug 11, 2025 | S101417 |
| J2122366 | Certificate of Analysis | Aug 11, 2025 | S101417 |
| F1728047 | Certificate of Analysis | Jan 08, 2025 | S101417 |
| G2013080 | Certificate of Analysis | Apr 07, 2024 | S101417 |
| G2013079 | Certificate of Analysis | Apr 07, 2024 | S101417 |
| G2013081 | Certificate of Analysis | Apr 07, 2024 | S101417 |
| I2314053 | Certificate of Analysis | Sep 19, 2023 | S101417 |
| I2314054 | Certificate of Analysis | Sep 19, 2023 | S101417 |
| I2314055 | Certificate of Analysis | Sep 19, 2023 | S101417 |
| I2314056 | Certificate of Analysis | Sep 19, 2023 | S101417 |
| I2314057 | Certificate of Analysis | Sep 19, 2023 | S101417 |
| I2314058 | Certificate of Analysis | Sep 19, 2023 | S101417 |
| I2314059 | Certificate of Analysis | Sep 19, 2023 | S101417 |
| I1412127 | Certificate of Analysis | Jul 12, 2022 | S101417 |
| Sensibilità | Heat sensitive |
|---|---|
| Rotazione specifica [α] | 30 ° (C=1, H2O) |
| Punto di fusione (°C) | 210-215°C |
| Peso molecolare | 505.600 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 6 |
| Exact Mass | 505.302 Da |
| Monoisotopic Mass | 505.302 Da |
| Topological Polar Surface Area | 131.000 Ų |
| Heavy Atom Count | 35 |
| Formal Charge | 0 |
| Complexity | 766.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 11 |
| 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 | 3 |
| 1. Yunhui Liao, Feng Chen, Haishan Tang, Wubliker Dessie, Zuodong Qin. (2024) Combination of a Deep Eutectic Solvent and Macroporous Resin for Green Recovery of Iridoids, Chlorogenic Acid, and Flavonoids from Eucommia ulmoides Leaves. MOLECULES, 29 (3): (737). [PMID:38338480] [10.3390/molecules29030737] |
| 2. Zijun Tao, Jian Zhang, Fuge Niu, Huien Zhang, Zhongfa Chen, Shanfu Wang, Yuli Zhang, Jie Li, Peng Liu. (2024) Polygonati rhizoma fermentation by Monascus ruber and evaluation of fermentation products in vitro. PROCESS BIOCHEMISTRY, [PMID:] [10.1016/j.procbio.2024.07.013] |
| 3. Jin Wang, Jie Li, Xiao Luo, Mei-Mei Qu Mo, Jing Feng, Wen-Bing Li, Huiling Yan, Yi-Chen Hu, Liang Zou, Ding-Tao Wu. (2024) Structural properties and biological effects of pectic polysaccharides extracted from Tartary buckwheat sprouts by high pressure-assisted deep eutectic solvent extraction. LWT-FOOD SCIENCE AND TECHNOLOGY, [PMID:] [10.1016/j.lwt.2024.116397] |
| 4. Ying You, Chen Song, Yinghuan Fu, Yujiao Sun, Chengrong Wen, Beiwei Zhu, Shuang Song. (2024) Structure-activity relationship of Caulerpa lentillifera polysaccharide in inhibiting lipid digestion. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, [PMID:38228205] [10.1016/j.ijbiomac.2024.129435] |
| 5. Wanjun Ma, Honger Yao, Li Zhao, Haipeng Lv. (2026) Effects of the flowering process on the metabolite profiles and bioactivities of Shaanxi Fu brick tea. Food Chemistry-X, [PMID:41853609] [10.1016/j.fochx.2026.103741] |
