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Details

Stereochemistry ABSOLUTE
Molecular Formula C10H14O4.2Na
Molecular Weight 244.1953
Optical Activity ( + )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Disodium (+)-camphorate

SMILES

[Na+].[Na+].CC1(C)[C@H](CC[C@@]1(C)C([O-])=O)C([O-])=O

InChI

InChIKey=HTBITCNUUYEGAB-YJGIZBEXSA-L
InChI=1S/C10H16O4.2Na/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);;/q;2*+1/p-2/t6-,10+;;/m1../s1

HIDE SMILES / InChI

Molecular Formula C10H14O4
Molecular Weight 198.2158
Charge -2
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula Na
Molecular Weight 22.98976928
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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
Multifunctional homochiral lanthanide camphorates with mixed achiral terephthalate ligands.
2010-10-18
Chiral gels derived from secondary ammonium salts of (1R,3S)-(+)-camphoric acid.
2010-09-21
Progresses in TCM metal-based antitumour agents.
2010-06
Synthesis of (1R,4S,6R)-5,5,6-trimethyl-2-phosphabicyclo[2.2.2]octane and derivatives.
2010-04-28
Poly[(μ(3)-camphorato-κO:O':O'')(2-methyl-1H-imidazole-κN)zinc(II)].
2010-03-03
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.
2009-05-18
Ionothermal synthesis of homochiral framework with acetate-pillared cobalt-camphorate architecture.
2008-07-07
2-Amino-pyrimidinium picrate.
2007-12-06
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.
2007-11-07
(1R,3S)-Camphoric acid as a building block in supramolecular chemistry: adducts with organic polyamines.
2003-02
(1R,3S)-Camphoramic acid.
2002-02
Patents
Substance Class Chemical
Created
by admin
on Wed Apr 02 11:19:39 GMT 2025
Edited
by admin
on Wed Apr 02 11:19:39 GMT 2025
Record UNII
CE3TBG9T8N
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,3-Cyclopentanedicarboxylic acid, 1,2,2-trimethyl-, disodium salt, (1R,3S)-
Preferred Name English
Disodium (+)-camphorate
Systematic Name English
1,3-Cyclopentanedicarboxylic acid, 1,2,2-trimethyl-, sodium salt (1:2), (1R,3S)-
Systematic Name English
Code System Code Type Description
FDA UNII
CE3TBG9T8N
Created by admin on Wed Apr 02 11:19:39 GMT 2025 , Edited by admin on Wed Apr 02 11:19:39 GMT 2025
PRIMARY
CAS
508-36-1
Created by admin on Wed Apr 02 11:19:39 GMT 2025 , Edited by admin on Wed Apr 02 11:19:39 GMT 2025
PRIMARY
EPA CompTox
DTXSID10965030
Created by admin on Wed Apr 02 11:19:39 GMT 2025 , Edited by admin on Wed Apr 02 11:19:39 GMT 2025
PRIMARY
PUBCHEM
102175596
Created by admin on Wed Apr 02 11:19:39 GMT 2025 , Edited by admin on Wed Apr 02 11:19:39 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE