≥99% 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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Camphor acid is a type of dicarboxylic acid, usually prepared by the oxidation of terpenes (+) - camphor. It can be used as a chiral inducer in some organic reactions. It is slightly soluble in cold water and soluble in hot water, ethanol, ether, esters, trichloromethane, fats, and oils. Solubility: 1g/125ml water, 1g/1ml ethanol, 1g/20ml glycerol.
Application
(1R,3S)-(+)-Camphoric acid may be used in the preparation (1R,2S,3R,5S)-2,3-dibenzyl-1,8,8-trimethyl-3-thianiumbicyclo[3.2.1]octane perchlorate. It reacts with uranyl nitrate in pyridine(py) or py/methanol(MeOH) to form novel uranyl-organic assemblages.
| Pubchem Sid | 504756494 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504756494 |
| Sorrisos canónicos | CC1(C(CCC1(C)C(=O)O)C(=O)O)C |
| IUPAC Name | (1R,3S)-1,2,2-trimethylcyclopentane-1,3-dicarboxylic acid |
| InChIKey | LSPHULWDVZXLIL-LDWIPMOCSA-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+/m1/s1 |
| SMILES isoméricas | C[C@]1(CC[C@@H](C1(C)C)C(=O)O)C(=O)O |
| WGK Alemanha | 2 |
| Peso molecular | 200.23 |
| Beilstein | 9745 |
| 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 |
| Classe | 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 |
| Descrição | 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 | Data | Item |
|---|---|---|---|
 J2226306 | Certificate of Analysis | Aug 04, 2026 | C107293 |
| J2424532 | Certificate of Analysis | Oct 15, 2024 | C107293 |
| J2424533 | Certificate of Analysis | Oct 15, 2024 | C107293 |
| J2424534 | Certificate of Analysis | Oct 15, 2024 | C107293 |
| H2321108 | Certificate of Analysis | Sep 28, 2022 | C107293 |
| J2226304 | Certificate of Analysis | Sep 28, 2022 | C107293 |
| J2226307 | Certificate of Analysis | Sep 28, 2022 | C107293 |
| Solubilidade | DMSO (Slightly), Ethanol (Slightly), Methanol (Slightly) |
|---|---|
| Rotação específica [α] | 46 ° (C=5, EtOH) |
| Ponto de fusão (°C) | 183-187°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. Cai-Fang Liu, Xiao-Yan Ran, Cheng Liu, Yu-lan Zhu, Yan-Rui Lu, Yu-Ping Yang, Bang-Jin Wang, Jun-Hui Zhang, Sheng-Ming Xie, Li-Ming Yuan:. (2023) Chiral metal–organic framework [Zn2(D-Cam)2(4,4′-bpy)]n@SiO2 core–shell composite for HPLC separation. MICROCHEMICAL JOURNAL, [PMID:] [10.1016/j.microc.2023.109569] |
| 2. Miao Pandeng, Li Yuchen, Du Yingxiang. (2023) Dual-ligand 3D lammelar chiral metal–organic framework for capillary electrochromatographic enantioseparations. MICROCHIMICA ACTA, 190 (8): (1-11). [PMID:37464133] [10.1007/s00604-023-05890-0] |
| 3. Huijuan Han, Shujun Chao, Xiaoli Yang, Xiaobing Wang, Kui Wang, Zhengyu Bai, Lin Yang. (2017) Ni nanoparticles embedded in N doped carbon nanotubes derived from a metal organic framework with improved performance for oxygen evolution reaction. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, [PMID:] [10.1016/j.ijhydene.2017.05.043] |
| 4. 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] |
