Determine the necessary mass, volume, or concentration for preparing a solution.
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
≥99% 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.
| Pubchem Sid | 488186810 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488186810 |
| Sonrisas canónicas | C(C(C(C(CO)O)O)O)O |
| IUPAC Name | (2R,4R)-pentane-1,2,3,4,5-pentol |
| InChIKey | HEBKCHPVOIAQTA-QWWZWVQMSA-N |
| INCHI | 1S/C5H12O5/c6-1-3(8)5(10)4(9)2-7/h3-10H,1-2H2/t3-,4-/m1/s1 |
| Isómeros SMILES | C([C@H](C([C@@H](CO)O)O)O)O |
| WGK Alemania | 3 |
| Peso molecular | 152.15 |
| Beilstein | 1720520 |
| Reaxy-Rn | 1902256 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1902256&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 | Sugar alcohols |
| Alternative Parents | Monosaccharides Secondary alcohols Polyols Primary alcohols Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Sugar alcohol - Monosaccharide - Secondary alcohol - Polyol - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as sugar alcohols. These are hydrogenated forms of carbohydrate in which the carbonyl group (aldehyde or ketone, reducing sugar) has been reduced to a primary or secondary hydroxyl group. |
| External Descriptors | arabinitol |
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
| Certificate of Analysis | Jul 10, 2025 | A111948 | |
| Certificate of Analysis | Jul 10, 2025 | A111948 | |
| Certificate of Analysis | Jun 09, 2025 | A111948 | |
| Certificate of Analysis | Jun 29, 2024 | A111948 | |
| Certificate of Analysis | Jun 29, 2024 | A111948 | |
| Certificate of Analysis | Oct 12, 2022 | A111948 | |
| Certificate of Analysis | Oct 12, 2022 | A111948 | |
| Certificate of Analysis | Oct 12, 2022 | A111948 | |
| Certificate of Analysis | Oct 12, 2022 | A111948 | |
| Certificate of Analysis | Oct 12, 2022 | A111948 |
| Rotación específica [α] | 12° (C=5,Sodium borate(8%)) |
|---|---|
| Punto de fusión (°C) | 97-105°C |
| Peso molecular | 152.150 g/mol |
| XLogP3 | -2.500 |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 4 |
| Exact Mass | 152.068 Da |
| Monoisotopic Mass | 152.068 Da |
| Topological Polar Surface Area | 101.000 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 76.100 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| 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. Hengtao Tang, Zhi Chen, Yu Shao, Xin Ju, Liangzhi Li. (2022) Development of an enzymatic cascade to systematically utilize lignocellulosic monosaccharide. JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, 103 (4): (1974-1980). [PMID:36448581] [10.1002/jsfa.12364] |
| 2. Xiaolan Li, Yufei Zhang, Hossain M. Zabed, Junhua Yun, Guoyan Zhang, Mei Zhao, Yuvaraj Ravikumar, Xianghui Qi. (2022) High-level production of d-arabitol by Zygosaccharomyces rouxii from glucose: Metabolic engineering and process optimization. BIORESOURCE TECHNOLOGY, [PMID:36334865] [10.1016/j.biortech.2022.128251] |
| 3. Liangqing Zhang, Jiarong Qiu, Xing Tang, Yong Sun, Xianhai Zeng, Lu Lin. (2021) Efficient Synthesis of Sugar Alcohols over a Synergistic and Sustainable Catalyst. CHINESE JOURNAL OF CHEMISTRY, 39 (9): (2467-2476). [PMID:] [10.1002/cjoc.202100140] |
| 4. Gan Xiaorong, Zhao Huimin, Schirhagl Romana, Quan Xie. (2019) Non enzymatic fluorometric determination of glucose by using quenchable g-C3N4 quantum dots. MICROCHIMICA ACTA, 186 (12): (1-10). [PMID:31728637] [10.1007/s00604-019-3990-8] |
| 5. Xue-Feng Shao, Chao Wang, Yong-Jian Yang, Biao Feng, Zi-Qin Zhu, Wu-Jun Wang, Yi Zeng, Li-Wu Fan. (2018) Screening of sugar alcohols and their binary eutectic mixtures as phase change materials for low-to-medium temperature latent heat storage. (Ⅰ): Non-isothermal melting and crystallization behaviors. ENERGY, [PMID:] [10.1016/j.energy.2018.07.081] |
| 6. Feng Sha, Yucong Zheng, Jiao Chen, Kequan Chen, Fei Cao, Ming Yan, Pingkai Ouyang. (2018) D-Tagatose manufacture through bio-oxidation of galactitol derived from waste xylose mother liquor. GREEN CHEMISTRY, 20 (10): (2382-2391). [PMID:] [10.1039/C8GC00091C] |
| 7. Rui Jia, Keyan Sun, Rongchun Li, Youyou Zhang, Wenxia Wang, Heng Yin, Dawei Fang, Quan Shi, Zhicheng Tan. (2017) Heat capacities of some sugar alcohols as phase change materials for thermal energy storage applications. JOURNAL OF CHEMICAL THERMODYNAMICS, [PMID:] [10.1016/j.jct.2017.08.004] |
| 8. Yongchun Huang, Jie Bai, Jinman Shui, Zhanhai Su, Chengzhu Cao, Haiyan Wang, Qiong Wu, Shoude Zhang. (2025) Simultaneous determination of the monosaccharide types and their absolute configurations in polysaccharides based on UPLC-MS/MS. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, [PMID:39788268] [10.1016/j.ijbiomac.2025.139647] |