≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature,Argon charged 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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 504751196 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504751196 |
| Sonrisas canónicas | C(C(C(C(C(=O)CO)O)O)O)O |
| IUPAC Name | (3S,4R,5S)-1,3,4,5,6-pentahydroxyhexan-2-one |
| InChIKey | BJHIKXHVCXFQLS-OTWZMJIISA-N |
| INCHI | 1S/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3,5-9,11-12H,1-2H2/t3-,5+,6+/m0/s1 |
| Isómeros SMILES | C([C@@H]([C@H]([C@@H](C(=O)CO)O)O)O)O |
| WGK Alemania | 3 |
| RTECS | WG3195025 |
| Peso molecular | 180.16 |
| Beilstein | 1724554 |
| Reaxy-Rn | 2207947 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2207947&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 | Not available |
| Direct Parent | Monosaccharides |
| Alternative Parents | Beta-hydroxy ketones Acyloins Alpha-hydroxy ketones Secondary alcohols Polyols Primary alcohols Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Monosaccharide - Beta-hydroxy ketone - Acyloin - Alpha-hydroxy ketone - Secondary alcohol - Ketone - Polyol - Organic oxide - Hydrocarbon derivative - Primary alcohol - Carbonyl group - Alcohol - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as monosaccharides. These are compounds containing one carbohydrate unit not glycosidically linked to another such unit, and no set of two or more glycosidically linked carbohydrate units. Monosaccharides have the general formula CnH2nOn. |
| External Descriptors | L-sorbose |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 F1501119 | Certificate of Analysis | Feb 06, 2023 | S111850 |
| A2621117 | Certificate of Analysis | Dec 06, 2022 | S111850 |
| B2307675 | Certificate of Analysis | Dec 06, 2022 | S111850 |
| B2307698 | Certificate of Analysis | Dec 06, 2022 | S111850 |
| B2307745 | Certificate of Analysis | Dec 06, 2022 | S111850 |
| B2307829 | Certificate of Analysis | Dec 06, 2022 | S111850 |
| F2527069 | Certificate of Analysis | Dec 06, 2022 | S111850 |
| K2308162 | Certificate of Analysis | Dec 06, 2022 | S111850 |
| K2429131 | Certificate of Analysis | Dec 06, 2022 | S111850 |
| K2506056 | Certificate of Analysis | Dec 06, 2022 | S111850 |
| Solubilidad | Soluble in water |
|---|---|
| Sensibilidad | Moisture sensitive. |
| Rotación específica [α] | -43 ° (C=1, H2O) |
| Punto de fusión (°C) | 158-160°C |
| Peso molecular | 180.160 g/mol |
| XLogP3 | -3.200 |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 5 |
| Exact Mass | 180.063 Da |
| Monoisotopic Mass | 180.063 Da |
| Topological Polar Surface Area | 118.000 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 147.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 3 |
| 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. Xia Hua, GenLai Du, Jian Han, Yong Xu. (2020) Bioprocess Intensification for Whole-Cell Catalysis of Catabolized Chemicals with 2,4-Dinitrophenol Uncoupling. ACS Sustainable Chemistry & Engineering, [PMID:] [10.1021/acssuschemeng.0c06466] |
| 2. Shi Ning, Liu Qiying, Cen Hu, Ju Rongmei, He Xiong, Ma Longlong. (2019) Formation of humins during degradation of carbohydrates and furfural derivatives in various solvents. Biomass Conversion and Biorefinery, 10 (2): (277-287). [PMID:] [10.1007/s13399-019-00414-4] |
| 3. Yao Huang, Fang Feng, Zhi-Gang Chen, Tao Wu, Zi-Han Wang. (2017) Green and efficient removal of cadmium from rice flour using natural deep eutectic solvents. FOOD CHEMISTRY, [PMID:29120780] [10.1016/j.foodchem.2017.10.060] |
| 4. Lili Lv, Lijuan Wang, Yanan Zou, Rui Chen, Jiaojiao Yu. (2016) Chiral separation by nonaqueous capillary electrophoresis using L-sorbose–boric acid complexes as chiral ion-pair selectors. RSC Advances, 6 (106): (104193-104200). [PMID:] [10.1039/C6RA21806G] |
