Determine the necessary mass, volume, or concentration for preparing a solution.
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≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Product Application:
6-Hydroxyhexanoic acid acts as a useful reagent in synthetic chemistry. It is used as a precursor to prepare surface active monomers.
| Sonrisas canónicas | C(CCC(=O)O)CCO |
|---|---|
| IUPAC Name | 6-hydroxyhexanoic acid |
| InChIKey | IWHLYPDWHHPVAA-UHFFFAOYSA-N |
| INCHI | 1S/C6H12O3/c7-5-3-1-2-4-6(8)9/h7H,1-5H2,(H,8,9) |
| Isómeros SMILES | C(CCC(=O)O)CCO |
| Peso molecular | 132.16 |
| Reaxy-Rn | 1236785 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1236785&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 |
| Clase | Hydroxy acids and derivatives |
| Subclass | Medium-chain hydroxy acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Medium-chain hydroxy acids and derivatives |
| Alternative Parents | Medium-chain fatty acids Hydroxy fatty acids Straight chain fatty acids Monocarboxylic acids and derivatives Carboxylic acids Primary alcohols Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Medium-chain hydroxy acid - Medium-chain fatty acid - Hydroxy fatty acid - Straight chain fatty acid - Fatty acyl - Fatty acid - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Carbonyl group - Organic oxide - Organic oxygen compound - Alcohol - Organooxygen compound - Primary alcohol - Hydrocarbon derivative - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as medium-chain hydroxy acids and derivatives. These are hydroxy acids with a 6 to 12 carbon atoms long side chain. |
| External Descriptors | Hydroxy fatty acids |
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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 | Dec 12, 2025 | H302536 | |
| Certificate of Analysis | Aug 20, 2025 | H302536 | |
| Certificate of Analysis | Apr 13, 2024 | H302536 | |
| Certificate of Analysis | Jan 14, 2022 | H302536 | |
| Certificate of Analysis | Jan 14, 2022 | H302536 | |
| Certificate of Analysis | Jan 14, 2022 | H302536 | |
| Certificate of Analysis | Jan 14, 2022 | H302536 | |
| Certificate of Analysis | Jan 14, 2022 | H302536 | |
| Certificate of Analysis | Jan 14, 2022 | H302536 | |
| Certificate of Analysis | Jan 14, 2022 | H302536 | |
| Certificate of Analysis | Jan 14, 2022 | H302536 | |
| Certificate of Analysis | Jan 14, 2022 | H302536 |
| Sensibilidad | Hygroscopic |
|---|---|
| Índice de refracción | 1.456 |
| Punto de inflamación (°F) | 230°F |
| Punto de inflamación (°C) | >110° |
| Punto de ebullición (°C) | 113-116℃ |
| Punto de fusión (°C) | 38-40° |
| Peso molecular | 132.160 g/mol |
| XLogP3 | -0.400 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 5 |
| Exact Mass | 132.079 Da |
| Monoisotopic Mass | 132.079 Da |
| Topological Polar Surface Area | 57.500 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 80.400 |
| 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 |