Determine the necessary mass, volume, or concentration for preparing a solution.
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inherent viscosity 1.4dL/g for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Protected from light 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 504750411 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504750411 |
| Canonical Smiles | C(C(=O)O)O |
| IUPAC Name | 2-hydroxyacetic acid |
| InChIKey | AEMRFAOFKBGASW-UHFFFAOYSA-N |
| INCHI | 1S/C2H4O3/c3-1-2(4)5/h3H,1H2,(H,4,5) |
| Isomeric SMILES | C(C(=O)O)O |
| Reaxy-Rn | 1209322 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1209322&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 acids and derivatives |
| Class | Hydroxy acids and derivatives |
| Subclass | Alpha hydroxy acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Alpha hydroxy acids and derivatives |
| Alternative Parents | Monocarboxylic acids and derivatives Carboxylic acids Primary alcohols Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Alpha-hydroxy acid - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as alpha hydroxy acids and derivatives. These are organic compounds containing a carboxylic acid substituted with a hydroxyl group on the adjacent carbon. |
| External Descriptors | primary alcohol - 2-hydroxy monocarboxylic acid |
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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 | May 12, 2026 | P477164 | |
| Certificate of Analysis | May 12, 2026 | P477164 | |
| Certificate of Analysis | May 12, 2026 | P477164 | |
| Certificate of Analysis | Apr 03, 2026 | P477164 | |
| Certificate of Analysis | Apr 03, 2026 | P477164 | |
| Certificate of Analysis | Jan 20, 2026 | P477164 | |
| Certificate of Analysis | Dec 12, 2025 | P477164 | |
| Certificate of Analysis | Dec 12, 2025 | P477164 | |
| Certificate of Analysis | Jul 14, 2025 | P477164 | |
| Certificate of Analysis | Aug 19, 2023 | P477164 | |
| Certificate of Analysis | Aug 19, 2023 | P477164 | |
| Certificate of Analysis | Jan 07, 2023 | P477164 | |
| Certificate of Analysis | Jan 07, 2023 | P477164 |
| Solubility | hexafluoroisopropanol: soluble |
|---|---|
| Sensitivity | Light & Moisture & Heat sensitive |
| Melt Point(°C) | 225 - 230 °C |
| Molecular Weight | 76.050 g/mol |
| XLogP3 | -1.100 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 1 |
| Exact Mass | 76.016 Da |
| Monoisotopic Mass | 76.016 Da |
| Topological Polar Surface Area | 57.500 Ų |
| Heavy Atom Count | 5 |
| Formal Charge | 0 |
| Complexity | 40.200 |
| 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. Jiuli Chang, Lili Wang, Zhanqiang Hu, Songsong Zhi, Dapeng Wu, Kai Jiang, Zhiyong Gao. (2025) Concurrent production of glycolate and H2 via paired electrolysis: Ethylene glycol oxidation and hydrogen evolution from polyethylene terephthalate hydrolysate. CHEMICAL ENGINEERING JOURNAL, [PMID:] [10.1016/j.cej.2025.166475] |