U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS
This repository is under review for potential modification in compliance with Administration directives.

Details

Stereochemistry RACEMIC
Molecular Formula C10H16O4
Molecular Weight 200.2316
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CAMPHORIC ACID

SMILES

CC1(C)[C@H](CC[C@@]1(C)C(O)=O)C(O)=O

InChI

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

HIDE SMILES / InChI

Molecular Formula C10H16O4
Molecular Weight 200.2316
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Camphoric acid is a product of oxidation of camphor, naturally occurring in rosemary. In the early twentieth century, camphoric acid was used in the night-sweats of phthisis and was also employed in solution as a local antiseptic to the nose, throat, and bladder. Camphoric acid was found to induce the expression of glutamate receptors NMDAR1, GluR3/4, and mGluR8.

Approval Year

PubMed

PubMed

TitleDatePubMed
(1R,3S)-Camphoramic acid.
2002 Feb
(1R,3S)-Camphoric acid as a building block in supramolecular chemistry: adducts with organic polyamines.
2003 Feb
2-Amino-pyrimidinium picrate.
2007 Dec 6
Assembly of a homochiral, body-centered cubic network composed of vertex-shared Mg12 cages: use of electrospray ionization mass spectrometry to monitor metal carboxylate nucleation.
2007 Nov 7
Ionothermal synthesis of homochiral framework with acetate-pillared cobalt-camphorate architecture.
2008 Jul 7
Alteration of molecular conformations, coordination modes, and architectures for a novel 3,8-diimidazol-1,10-phenanthroline compound in the construction of cadmium(II) and zinc(II) homochiral coordination polymers involving an auxiliary chiral camphorate ligand.
2009 May 18
Synthesis of (1R,4S,6R)-5,5,6-trimethyl-2-phosphabicyclo[2.2.2]octane and derivatives.
2010 Apr 28
Progresses in TCM metal-based antitumour agents.
2010 Jun
Poly[(μ(3)-camphorato-κO:O':O'')(2-methyl-1H-imidazole-κN)zinc(II)].
2010 Mar 3
Multifunctional homochiral lanthanide camphorates with mixed achiral terephthalate ligands.
2010 Oct 18
Chiral gels derived from secondary ammonium salts of (1R,3S)-(+)-camphoric acid.
2010 Sep 21
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:24:04 GMT 2025
Edited
by admin
on Mon Mar 31 18:24:04 GMT 2025
Record UNII
32K0C7JGCJ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CAMPHORIC ACID
MI   WHO-DD  
Common Name English
NSC-174634
Preferred Name English
DL-CAMPHORIC ACID
Common Name English
Camphoric acid [WHO-DD]
Common Name English
1,2,2-TRIMETHYL-1,3-CYCLOPENTANECARBOXYLIC ACID
Common Name English
CAMPHORIC ACID [MI]
Common Name English
CAMPHORIC ACID, DL-
Common Name English
CIS-(1)-CAMPHORIC ACID
Systematic Name English
NSC-60219
Code English
CAMPHORIC ACID, (±)-
Common Name English
1,3-CYCLOPENTANEDICARBOXYLIC ACID, 1,2,2-TRIMETHYL-, (1R,3S)-REL-
Common Name English
Code System Code Type Description
NCI_THESAURUS
C45678
Created by admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
CONCEPT Industrial Aid
ECHA (EC/EINECS)
226-404-9
Created by admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
PRIMARY
CAS
560-05-4
Created by admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
SUPERSEDED
SMS_ID
100000076604
Created by admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
PRIMARY
EPA CompTox
DTXSID301021163
Created by admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
PRIMARY
MERCK INDEX
m3005
Created by admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
PRIMARY Merck Index
WIKIPEDIA
CAMPHORIC ACID
Created by admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
PRIMARY
NSC
60219
Created by admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
PRIMARY
NSC
174634
Created by admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
PRIMARY
FDA UNII
32K0C7JGCJ
Created by admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
PRIMARY
EVMPD
SUB13219MIG
Created by admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
PRIMARY
ChEMBL
CHEMBL1205405
Created by admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
PRIMARY
CAS
5394-83-2
Created by admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
PRIMARY
NCI_THESAURUS
C87257
Created by admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP