(+)-Camphoric Acid TCI C0012

Chemical Identity

CAS No.: 124-83-4
PubChem: CID 101807·SID 87565223
Formula: C10H16O4
Molecular weight: 200.23 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ChEBI·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: trans-(1R,3S)-1,2,2-trimethylcyclopentane-1,3-dicarboxylic acid
SMILES: CC1(C(CCC1(C)C(=O)O)C(=O)O)C
InChIKey: LSPHULWDVZXLIL-LDWIPMOCSA-N
MDL: MDL00001375

Rp 1.220.100,00

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TCI C0012 (+)-Camphoric Acid, CAS 124-83-4, is an optically active dicarboxylic acid derived from the camphor skeleton. Its two carboxyl groups and rigid carbon framework make it a practical chiral building block for asymmetric synthesis. The compound is commonly employed as a resolving agent for racemic bases and as a precursor to chiral ligands, esters, and amides. AMI Scientific offers this TCI product in 25 g and 100 g pack sizes for flexible laboratory use.

TCI brochures (PDF)

Chiral Auxiliaries and Optical Resolving Agents 2025-06-17 · p. 7
Terpenes 2025-09-22 · p. 4
Chiral Building Blocks 2025-04-14 · p. 14

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Baur et al. (2000). Quantitation and validation of cis-camphoric acid 3-methyl ester and cis-camphoric acid 1-methyl ester using CE. Journal of Pharmaceutical and Biomedical Analysis doi:10.1016/s0731-7085(99)00313-1
Dmowski et al. (1997). Selective fluorination of (1R,3S)-(+)-camphoric acid with sulphur tetrafluoride. Preparation of fluorinated optically active derivatives of 1,2,2-trimethylcyclopentane. Journal of Fluorine Chemistry doi:10.1016/s0022-1139(97)00016-x
Moloney et al. (1996). Chiral carboxylic acid ligands derived from camphoric acid. Tetrahedron: Asymmetry doi:10.1016/0957-4166(96)00328-x

References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.