Application：
(R)-(−)-Hexahydromandelic acid can be used:
As an intermediate in the synthesis of antimycobacterial compound pyridomycin analogs.
As a model α-hydroxy acid compound in the chirality sensing studies of organic probes using circular dichroism technique.
As a starting material in the synthesis of chiral ionic liquids, which are applicable as chiral solvents in asymmetric synthesis and as chiral stationary phases in chromatographic separations.
| Pubchem Sid | 488191550 |
|---|---|
| Sonrisas canónicas | C1CCC(CC1)C(C(=O)O)O |
| IUPAC Name | (2R)-2-cyclohexyl-2-hydroxyacetic acid |
| InChIKey | RRDPWAPIJGSANI-SSDOTTSWSA-N |
| INCHI | 1S/C8H14O3/c9-7(8(10)11)6-4-2-1-3-5-6/h6-7,9H,1-5H2,(H,10,11)/t7-/m1/s1 |
| Isómeros SMILES | C1CCC(CC1)[C@H](C(=O)O)O |
| WGK Alemania | 3 |
| Peso molecular | 158.19 |
| Reaxy-Rn | 3196810 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3196810&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 | Alpha hydroxy acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Alpha hydroxy acids and derivatives |
| Alternative Parents | Secondary alcohols Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | Alpha-hydroxy acid - Secondary alcohol - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic homomonocyclic compound |
| Descripción | 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 | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 C2303498 | Certificate of Analysis | Jan 05, 2026 | C348615 |
| C2303320 | Certificate of Analysis | Jan 05, 2026 | C348615 |
| C2303319 | Certificate of Analysis | Jan 05, 2026 | C348615 |
| C2303318 | Certificate of Analysis | Jan 05, 2026 | C348615 |
| C2303317 | Certificate of Analysis | Jan 05, 2026 | C348615 |
| C2303315 | Certificate of Analysis | Jan 05, 2026 | C348615 |
| C2303314 | Certificate of Analysis | Jan 05, 2026 | C348615 |
| C2303509 | Certificate of Analysis | Dec 09, 2025 | C348615 |
| C2525406 | Certificate of Analysis | Jan 03, 2023 | C348615 |
| Rotación específica [α] | [α]18/D −23°, c = 1 in acetic acid |
|---|---|
| Punto de fusión (°C) | 127-129 °C |
| Peso molecular | 158.190 g/mol |
| XLogP3 | 1.500 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 2 |
| Exact Mass | 158.094 Da |
| Monoisotopic Mass | 158.094 Da |
| Topological Polar Surface Area | 57.500 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 138.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| 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 |
