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 |
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≥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 21 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 528753764 |
|---|---|
| Canonical Smiles | C(C(=O)CO)O |
| IUPAC Name | 1,3-dihydroxypropan-2-one |
| InChIKey | RXKJFZQQPQGTFL-UHFFFAOYSA-N |
| INCHI | 1S/C3H6O3/c4-1-3(6)2-5/h4-5H,1-2H2 |
| Isomeric SMILES | C(C(=O)CO)O |
| Molecular Weight | 90.08 |
| Reaxy-Rn | 1740268 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1740268&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 |
| Class | Organooxygen compounds |
| Subclass | Carbohydrates and carbohydrate conjugates |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Monosaccharides |
| Alternative Parents | Glycerone and derivatives Alpha-hydroxy ketones Primary alcohols Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Glycerone or derivatives - Monosaccharide - Alpha-hydroxy ketone - Ketone - Organic oxide - Hydrocarbon derivative - Primary alcohol - Carbonyl group - Alcohol - Aliphatic acyclic compound |
| Description | 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 | a small molecule |
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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 | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Mar 16, 2026 | D189238 | |
| Certificate of Analysis | Mar 16, 2026 | D189238 | |
| Certificate of Analysis | Mar 16, 2026 | D189238 | |
| Certificate of Analysis | Mar 16, 2026 | D189238 | |
| Certificate of Analysis | Nov 13, 2025 | D189238 | |
| Certificate of Analysis | Nov 13, 2025 | D189238 | |
| Certificate of Analysis | Nov 13, 2025 | D189238 | |
| Certificate of Analysis | Apr 26, 2025 | D189238 | |
| Certificate of Analysis | Apr 26, 2025 | D189238 | |
| Certificate of Analysis | Apr 26, 2025 | D189238 | |
| Certificate of Analysis | Apr 26, 2025 | D189238 | |
| Certificate of Analysis | Apr 26, 2025 | D189238 | |
| Certificate of Analysis | Apr 26, 2025 | D189238 | |
| Certificate of Analysis | Apr 26, 2025 | D189238 | |
| Certificate of Analysis | Apr 16, 2024 | D189238 | |
| Certificate of Analysis | Apr 16, 2024 | D189238 | |
| Certificate of Analysis | Apr 16, 2024 | D189238 | |
| Certificate of Analysis | Apr 16, 2024 | D189238 | |
| Certificate of Analysis | Apr 16, 2024 | D189238 |
| Solubility | Soluble in methanol |
|---|---|
| Sensitivity | heat sensitive |
| Boil Point(°C) | 188℃ |
| Melt Point(°C) | 75.0-96.5℃ |
| Molecular Weight | 90.080 g/mol |
| XLogP3 | -1.400 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 2 |
| Exact Mass | 90.0317 Da |
| Monoisotopic Mass | 90.0317 Da |
| Topological Polar Surface Area | 57.500 Ų |
| Heavy Atom Count | 6 |
| Formal Charge | 0 |
| Complexity | 44.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| 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. Ruite Lai, Qidong Hou, Guanjie Yu, Chao Xie, Hengli Qian, Tianliang Xia, Xinyu Bai, Yao Tang, Mian Laiq Ur Rehman, Meiting Ju. (2023) Incorporation of tin into zirconium phosphate to boost efficient conversion of trioses to lactic acid. CATALYSIS COMMUNICATIONS, [PMID:] [10.1016/j.catcom.2023.106803] |
| 2. Mingyu Guo, Chengfeng Zhou, Yuandong Cui, Wei Jiang, Guangting Han, Zhan Jiang, Haoxi Ben, Xiaoli Yang. (2023) Sustainable Production of Lactic Acid from Cellulose Using Au/W-ZnO Catalysts. Polymers, 15 (21): (4235). [PMID:37959915] [10.3390/polym15214235] |
| 3. Dan Luo, Qin Wang, Jiansu Ran, Ruixue Yangcheng, Yuntong Cui, Shuang Luo, Jianjian Wang. (2023) Boosting the aqueous-phase production of lactic acid via dual-site activation of carbohydrates. CATALYSIS COMMUNICATIONS, [PMID:] [10.1016/j.catcom.2023.106701] |
| 4. Yi-fan Miao, Qing Ye, Ming-yang Zhang, Lin Gao, Xi-yan Wang, Wen-xin Zhong, Zi-xuan Wang, Zhong-gui He, Chu-tong Tian, Jin Sun. (2023) Enhancing Oral Performance of Paclitaxel Lipid-Mimic Prodrug via Modulating Type of Fatty Acids. Advanced Healthcare Materials, 12 (19): (2203118). [PMID:36929289] [10.1002/adhm.202203118] |
| 5. Yongfang Zhou, Thomas J.A. Slater, Xuanli Luo, Yi Shen. (2022) A versatile single-copper-atom electrocatalyst for biomass valorization. APPLIED CATALYSIS B-ENVIRONMENTAL, [PMID:] [10.1016/j.apcatb.2022.122218] |
| 6. Bo Tang, Di Wang, Ang Li, Hui-Min Tang, En-Cui Yang, Weili Dai. (2022) Constructing core-shell structured Au/Snβ@mesosilica composite for one-pot base-free conversion of glycerol to methyl lactate. MICROPOROUS AND MESOPOROUS MATERIALS, [PMID:] [10.1016/j.micromeso.2022.112348] |
| 7. Qin Wang, Dan Luo, Jiansu Ran, Jie Zheng, Yuntong Cui, Ruixue Yangcheng, Shuang Luo, Jianjian Wang. (2022) Solvent-free synthesis of a zirconium-carbon coordination catalyst for efficient aqueous-phase production of lactic acid from xylose. APPLIED CATALYSIS A-GENERAL, [PMID:] [10.1016/j.apcata.2022.118871] |
| 8. Miao Zuo, Xinyu Wang, Wenlong Jia, Yanzhong Zhu, Xianhai Zeng, Lu Lin. (2022) Efficient 5-hydroxymethylfurfural synthesis from carbohydrates and food wastes in aqueous-natural deep eutectic solvent (A-NADES) with robust Al2O3 or Al(OH)3. FUEL, [PMID:] [10.1016/j.fuel.2022.125062] |
| 9. Xiaomei Ning, Xiaosong Zhou, Jin Luo, Liang Zhan. (2021) PtBi on carbon cloth as efficient flexible electrode for electro-oxidation of liquid fuels. JOURNAL OF ELECTROANALYTICAL CHEMISTRY, [PMID:] [10.1016/j.jelechem.2021.115958] |
| 10. Miao Zuo, Xinyu Wang, Qian Wang, Xianhai Zeng, Lu Lin. (2021) Aqueous-Natural Deep Eutectic Solvent-Enhanced 5-Hydroxymethylfurfural Production from Glucose, Starch, and Food Wastes. ChemSusChem, 15 (13): (e202101889). [PMID:34730878] [10.1002/cssc.202101889] |
| 11. Zhiyan He, Guangxing Yang, Hongjuan Wang, Fengying Dai, Feng Peng, Hao Yu. (2020) Co–N–C-Supported Platinum Catalyst: Synergistic Effect on the Aerobic Oxidation of Glycerol. ACS Sustainable Chemistry & Engineering, [PMID:] [10.1021/acssuschemeng.0c07332] |
| 12. Haiyong Wang, Haosheng Xin, Chiliu Cai, Changhui Zhu, Zhongxun Xiu, Qiying Liu, Yujing Weng, Chenguang Wang, Xinghua Zhang, Shijun Liu, Zifang Peng, Longlong Ma. (2020) Selective C3-C4 Keto-Alcohol Production from Cellulose Hydrogenolysis over Ni-WOx/C Catalysts. ACS Catalysis, [PMID:] [10.1021/acscatal.0c02375] |
| 13. Ning Shi, Qiying Liu, Xiong He, Gui Wang, Ni Chen, Jiayu Peng, Longlong Ma. (2019) Molecular Structure and Formation Mechanism of Hydrochar from Hydrothermal Carbonization of Carbohydrates. ENERGY & FUELS, [PMID:] [10.1021/acs.energyfuels.9b02174] |
| 14. Yan Yan, Jinyao Sun, Xianting Xie, Pengchong Wang, Ying Sun, Yalin Dong, Jianfeng Xing. (2018) Colon-targeting mutual prodrugs of 5-aminosalicylic acid and butyrate for the treatment of ulcerative colitis. RSC Advances, 8 (5): (2561-2574). [PMID:35541446] [10.1039/C7RA13011B] |
| 15. Jie Wang, Guodong Yao, Fangming Jin. (2017) One-pot catalytic conversion of carbohydrates into alkyl lactates with Lewis acids in alcohols. Molecular Catalysis, [PMID:] [10.1016/j.mcat.2017.03.021] |
| 16. Xiaomei Ning, Yuhang Li, Hao Yu, Feng Peng, Hongjuan Wang, Yanhui Yang. (2016) Promoting role of bismuth and antimony on Pt catalysts for the selective oxidation of glycerol to dihydroxyacetone. JOURNAL OF CATALYSIS, [PMID:] [10.1016/j.jcat.2015.12.020] |
| 17. Wenxin Zhong, Yalin Xu, Zixuan Wang, Xiyan Wang, Yaqi Li, Jinrui Liu, Can Zhao, Xianbao Shi, Zhonggui He, Bingjun Sun, Chutong Tian. (2024) Dual role of triglyceride structures facilitates anti-tumor drug delivery: Both as a self-assembling module and a responsive module. JOURNAL OF COLLOID AND INTERFACE SCIENCE, [PMID:39277950] [10.1016/j.jcis.2024.09.096] |
| 18. Jinyan Tan, Fan Liu, Xiaoxue He, Lin Gao, Linsheng Wu, Xianbao Shi, Jing Li, Yanfei Chen, Yanhua Liu, Yongbing Sun, Zhixiao Zhang, Zhonggui He, Qikun Jiang, Jin Sun. (2024) Probing Different Lengths of the Tertiary Amine Head Group on Triglyceride-Mimetic Ionizable Lipid-Mediated siRNA Delivery. JOURNAL OF MEDICINAL CHEMISTRY, [PMID:39589900] [10.1021/acs.jmedchem.4c02239] |
| 19. Haichao Zhou, Jianglin Liu, Dalang Chen, Yanlin Qin, Tiejun Wang, Xueqing Qiu, Xuliang Lin. (2025) Boosting middle hydroxyl adsorption on lignin-derived carbon loaded MnO–Ni for glycerol conversion to dihydroxyacetone. AICHE JOURNAL, [PMID:] [10.1002/aic.70012] |
| 20. Liu Yang, Shang Huishan, Zhang Bing, Yan Dongpeng, Xiang Xu. (2024) Surface fluorination of BiVO4 for the photoelectrochemical oxidation of glycerol to formic acid. Nature Communications, 15 (1): (1-12). [PMID:39289360] [10.1038/s41467-024-52161-4] |
| 21. Chen-Xi Li, Qian Ren, Feng Peng, Ming-Fei Li. (2026) Lignin-tailored synergistic catalyst with cobalt single-atom and zinc clusters dual-site for conversion of hemicellulose to lactic acid. BIORESOURCE TECHNOLOGY, [PMID:] [10.1016/j.biortech.2026.134908] |