≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
(1S,3R)-(−)-Camphoric acid can be used:
As an enantiomeric linker in the preparation of chiral surface-anchored metal-organic frameworks (MOFs).
To prepare porous MOFs having multifunctional properties; used in gas adsorption and separation of racemic alcohols.
To prepare a cobalt(II) coordination polymer named {Co(phen)(H2O)[C8H14(COO)2]}n·(CH3OH)n , wherein “phen” is 1,10-phenanthroline and C8H14(COOH)2 is (1S,3R)-camphoric acid.
| Pubchem Sid | 504757879 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504757879 |
| Sonrisas canónicas | CC1(C(CCC1(C)C(=O)O)C(=O)O)C |
| IUPAC Name | (1S,3R)-1,2,2-trimethylcyclopentane-1,3-dicarboxylic acid |
| InChIKey | LSPHULWDVZXLIL-QUBYGPBYSA-N |
| INCHI | 1S/C10H16O4/c1-9(2)6(7(11)12)4-5-10(9,3)8(13)14/h6H,4-5H2,1-3H3,(H,11,12)(H,13,14)/t6-,10+/m0/s1 |
| Isómeros SMILES | C[C@@]1(CC[C@H](C1(C)C)C(=O)O)C(=O)O |
| WGK Alemania | 3 |
| Peso molecular | 200.23 |
| Beilstein | 1874670 |
| Reaxy-Rn | 2050202 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2050202&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 | Carboxylic acids and derivatives |
| Subclass | Dicarboxylic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Dicarboxylic acids and derivatives |
| Alternative Parents | Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic homomonocyclic compounds |
| Substituents | Dicarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups. |
| 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 |
|---|---|---|---|
 H2508777 | Certificate of Analysis | Jul 05, 2025 | S161035 |
| H2508778 | Certificate of Analysis | Jul 05, 2025 | S161035 |
| H2508779 | Certificate of Analysis | Jul 05, 2025 | S161035 |
| L2509009 | Certificate of Analysis | Jul 05, 2025 | S161035 |
| H2507644 | Certificate of Analysis | Jul 01, 2024 | S161035 |
| K1827036 | Certificate of Analysis | Sep 19, 2022 | S161035 |
| K1827037 | Certificate of Analysis | Sep 19, 2022 | S161035 |
| Rotación específica [α] | -48° (C=4,MeOH) |
|---|---|
| Punto de fusión (°C) | 188 °C |
| Peso molecular | 200.230 g/mol |
| XLogP3 | 1.300 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 2 |
| Exact Mass | 200.105 Da |
| Monoisotopic Mass | 200.105 Da |
| Topological Polar Surface Area | 74.600 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 282.000 |
| 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. Duo Xu, Bowen Du, Yantian Ji, Huimin Sun, Tiecheng Wang, Xianqiang Yin. (2024) Stereoselective transport of 2-aryl propionic acid enantiomers in porous media subjected to chiral organic acids. JOURNAL OF HAZARDOUS MATERIALS, [PMID:38377915] [10.1016/j.jhazmat.2024.133824] |
| 2. Jifeng Gao, Yuansen Zhi, Xuemei Yang, Guiyang Yan, Jianshe Hu, Xiaozhi He, Baoyan Zhang. (2025) Synthesis and properties of chiral liquid crystal compounds containing cinnamic acid groups. LIQUID CRYSTALS, [PMID:] [10.1080/02678292.2025.2548266] |
