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Moligand™,≥97% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Protected from light,Store at -20°C,Argon charged Ships Ice chest + Ice pads 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Sonrisas canónicas | CCOC1C(C(C(C(O1)CO)O)O)O |
|---|---|
| IUPAC Name | (2R,3R,4S,5S,6R)-2-ethoxy-6-(hydroxymethyl)oxane-3,4,5-triol |
| InChIKey | WYUFTYLVLQZQNH-JAJWTYFOSA-N |
| INCHI | 1S/C8H16O6/c1-2-13-8-7(12)6(11)5(10)4(3-9)14-8/h4-12H,2-3H2,1H3/t4-,5-,6+,7-,8-/m1/s1 |
| Isómeros SMILES | CCO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O |
| CAS alternativo | 30285-48-4,3198-49-0 |
| Términos de entrada MeSH | alpha-ethylglucoside;ethyl glucoside;ethyl glucoside hexadecanoate, (D)-isomer;ethyl glucoside, (alpha-D)-isomer;ethyl glucoside, (beta-D)-isomer;ethyl glucoside, (D)-isomer |
| Peso molecular | 208.21 |
| Reaxy-Rn | 34589062 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=34589062&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Clase | Organooxygen compounds |
| Subclass | Carbohydrates and carbohydrate conjugates |
| Intermediate Tree Nodes | Glycosyl compounds |
| Direct Parent | O-glycosyl compounds |
| Alternative Parents | Hexoses Oxanes Secondary alcohols Polyols Oxacyclic compounds Acetals Primary alcohols Hydrocarbon derivatives |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Hexose monosaccharide - O-glycosyl compound - Oxane - Monosaccharide - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. |
| External Descriptors | Not available |
| Solubilidad | heat sensitive;Moisture sensitive |
|---|---|
| Punto de fusión (°C) | 81 °C |
| Peso molecular | 208.210 g/mol |
| XLogP3 | -1.800 |
| Hydrogen Bond Donor Count | 4 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 3 |
| Exact Mass | 208.095 Da |
| Monoisotopic Mass | 208.095 Da |
| Topological Polar Surface Area | 99.400 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 175.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 5 |
| 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 | 1 |
| 1. Jinghua Wang, Jiangang Wang, Hongyou Cui. (2025) Formylation-mediated pretreatment: Enabling high-yield production of methyl levulinate from cellulose at high substrate loading. CHEMICAL ENGINEERING JOURNAL, [PMID:] [10.1016/j.cej.2025.167667] |
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