Determine the necessary mass, volume, or concentration for preparing a solution.
UltraBio™, ≥99%(HPLC) UltraBio™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal 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 6 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| PH | 3.5-6.0 (25 °C, 0.5 M in H 2 O) |
|---|---|
| Sonrisas canónicas | O.OC[C@@H](O)[C@@H](O[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O)[C@H](O)[C@@H](O)C=O |
| IUPAC Name | (2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol;hydrate |
| InChIKey | WSVLPVUVIUVCRA-KPKNDVKVSA-N |
| INCHI | 1S/C12H22O11.H2O/c13-1-3-5(15)6(16)9(19)12(22-3)23-10-4(2-14)21-11(20)8(18)7(10)17;/h3-20H,1-2H2;1H2/t3-,4-,5+,6+,7-,8-,9-,10-,11+,12+;/m1./s1 |
| Isómeros SMILES | C([C@@H]1[C@@H]([C@@H]([C@H]([C@@H](O1)O[C@@H]2[C@H](O[C@@H]([C@@H]([C@H]2O)O)O)CO)O)O)O)O.O |
| WGK Alemania | 3 |
| CAS alternativo | 10039-26-6 |
| Peso molecular | 360.31 |
| Beilstein | 3768231 |
| Reaxy-Rn | 38095197 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=38095197&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 | Carbohydrates and carbohydrate conjugates |
| Intermediate Tree Nodes | Glycosyl compounds |
| Direct Parent | O-glycosyl compounds |
| Alternative Parents | Disaccharides Oxanes Secondary alcohols Hemiacetals Polyols Oxacyclic compounds Acetals Primary alcohols Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | O-glycosyl compound - Disaccharide - Oxane - Secondary alcohol - Hemiacetal - Oxacycle - Organoheterocyclic compound - Polyol - Acetal - Organic oxide - 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 | H 2 O: 0.5 M at 20 °C, clear, colorless |
|---|---|
| Rotación específica [α] | 52.5 ° (C=10, H2O) |
| Punto de fusión (°C) | 219°C |
| Peso molecular | 360.310 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 9 |
| Hydrogen Bond Acceptor Count | 12 |
| Rotatable Bond Count | 4 |
| Exact Mass | 360.127 Da |
| Monoisotopic Mass | 360.127 Da |
| Topological Polar Surface Area | 191.000 Ų |
| Heavy Atom Count | 24 |
| Formal Charge | 0 |
| Complexity | 382.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 10 |
| 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. Bin Ma, Jiafeng Niu, Hao Zhu, Huibing Chi, Zhaoxin Lu, Fengxia Lu, Ping Zhu. (2024) Engineering substrate specificity of quinone-dependent dehydrogenases for efficient oxidation of deoxynivalenol to 3-keto-deoxynivalenol. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, [PMID:38431002] [10.1016/j.ijbiomac.2024.130484] |
| 2. Tengjing Gong, Danting Shi, Zhigao Zhu, Bin Liu, Senlin Shao. (2022) Polyamide Thin-Film Composite Janus Membranes Avoiding Direct Contact between Feed Liquid and Hydrophobic Pores for Excellent Wetting Resistance in Membrane Distillation. ACS ES&T Water, [PMID:] [10.1021/acsestwater.2c00475] |
| 3. Guanyu Chi, Yinghua Lv, Shuang Chao, Chenxi Hou, Yuxin Pei, Zhichao Pei. (2022) Glyconanoparticles with Activatable Near-Infrared Probes for Tumor-Cell Imaging and Targeted Drug Delivery. International Journal of Nanomedicine, [PMID:35401000] [10.2147/IJN.S337082] |
| 4. Pengxuan Xi, Wanxue Cao, Li Li, Weimin Shi, Fuxin Li, Haitao Xu, Xiaojie Xu, Yu Ke, Jianye Zhang. (2021) Identification of related impurities in an oral pharmaceutical formulation of tebipenem pivoxil using ultra-high-performance liquid chromatography/electrospray ionization quadrupole time-of-flight tandem mass spectrometry. RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 35 (16): (e9129). [PMID:34097785] [10.1002/rcm.9129] |
| 5. Yinga Wu, Jia Cai, Jingfen Han, Huricha Baigude. (2015) Cell Type-Specific Delivery of RNAi by Ligand-Functionalized Curdlan Nanoparticles: Balancing the Receptor Mediation and the Charge Motivation. ACS Applied Materials & Interfaces, [PMID:26345600] [10.1021/acsami.5b06792] |
| 6. Lu Zewei, Lv Changhui, Chen Zhuoer, Zhu Zhiwei, Ma Xiaoqiang. (2026) A modular single- and dual-gene expression toolkit for Kluyveromyces marxianus. WORLD JOURNAL OF MICROBIOLOGY & BIOTECHNOLOGY, 42 (2): (54). [PMID:41571921] [10.1007/s11274-026-04794-4] |
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