D-Camphorsulfnic acid CAS#3144-16-9

Chiral Synthesis Capability: D-Camphor Sulfonic Acid is a chiral organic sulfonic acid that can induce asymmetric reactions, helping synthesize compounds with specific chiral configurations.

Important Organic Synthesis Intermediate: It serves as a valuable intermediate in organic synthesis and is widely applied in pharmaceutical development and advanced chemical research.

Excellent Application in Asymmetric Catalysis: With unique chiral properties, D-Camphor Sulfonic Acid is widely used in asymmetric catalysis to improve the selectivity and efficiency of chemical reactions.

Good Acidic Properties and Salt-Forming Ability: It exhibits certain acidity and can react with bases to form corresponding salts, providing versatility in various chemical processes.

D-Camphorsulfonic Acid CAS#3144-16-9

D-Camphorsulfonic Acid is a chiral organic sulfonic acid featuring a unique molecular structure and distinctive chemical properties. As an important intermediate in organic synthesis, it is widely utilized in pharmaceutical synthesis, asymmetric catalysis, and other advanced chemical applications.

Owing to its chiral characteristics, D-Camphorsulfonic Acid can serve as a chiral inducer in asymmetric reactions, facilitating the preparation of compounds with specific stereochemical configurations. Additionally, it exhibits acidic properties and can react with bases to form corresponding salts, further expanding its versatility in chemical processes.

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(1S)-(+)-Camphor-10-sulphonic acid Chemical Properties

Product Name:

(1S)-(+)-Camphor-10-sulphonic acid

Synonyms:

D-CAMPHORSULFONIC ACID;D(-)-CAMPHORSULPHONIC ACID;D-CAMPHORSULPHONIC ACID;CSA;D-REYCHLER'S ACID;D-OXO-10-BORNANESULFONIC ACID;(+)-BETA-CAMPHORSULFONIC ACID;(+)-CAMPHOR-10-SULFONIC ACID (BETA)

CAS:

3144-16-9

MF:

C10H16O4S

MW:

232.3

EINECS:

221-554-1

Product Categories:

chiral;Pharmaceutical Intermediates;FINE Chemical & INTERMEDIATES;Chiral Compounds;Bicyclic Monoterpenes;Biochemistry;for Resolution of Bases;Optical Resolution;Reagents for Oligosaccharide Synthesis;Synthetic Organic Chemistry;Terpenes;Peptide;Sulfur & Selenium Compounds;3144-16-9;3597-91-9;11

Mol File:

3144-16-9.mol

Melting point 

196-200 °C (dec.)(lit.)

alpha 

22 º (589nm, c=20, H2O 25 ºC)

Boiling point 

344.46°C (rough estimate)

density 

1.2981 (rough estimate)

refractive index 

21.5 ° (C=5, H2O)

storage temp. 

Store below +30°C.

solubility 

Exhibit moderate solubility in HCCl.

form 

Crystalline Powder

pka

1.17±0.50(Predicted)

color 

White to off-white

PH

0.3 (200g/l, H2O)

optical activity

[α]20/D +21.5±1°, c = 10% in H2O

biological source

human

Water Solubility 

SOLUBLE

Sensitive 

Hygroscopic

Merck 

141734

BRN 

2809675

Stability:

Stable. Protect from moisture. Incompatible with strong oxidizing agents, strong bases.

InChIKey

MIOPJNTWMNEORI-GMSGAONNSA-N

CAS DataBase Reference

3144-16-9(CAS DataBase Reference)

EPA Substance Registry System

Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S,4R)- (3144-16-9)

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(1S)-(+)-Camphor-10-sulfonic acid is widely used as a stabilizing agent and an effective chiral resolving agent. Due to its excellent chiral recognition ability, it is commonly applied in the resolution of enantiomers and asymmetric synthesis processes.

It can also be used as a dopant in the template-free potentiostatic electropolymerization of chiral polyaniline (PANI) nanofibers, where (1S)-(+)-camphor-10-sulfonic acid (D-CSA) or (1R)-(-)-camphor-10-sulfonic acid (L-CSA) is introduced to induce chirality. In addition, it serves as an important raw material for the synthesis of quaternary ammonium compounds (QUATs) derived from (1S)-(+)-camphor-10-sulfonic acid.

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