(1S)-()-10-Camphorsulfonic acid
10mM in DMSO
- Product Code: 232990
Alias:
D(+) Camphorsulfonic acid; D- Camphor-10-sulfonic acid, dextrocamphorsulfonic acid, (1S)-7,7-dimethyl-2-oxo-dicyclo[2.2.1]heptane-1-methanesulfonic acid
CAS:
3144-16-9
| Molecular Weight: | 232.3 g./mol | Molecular Formula: | C₁₀H₁₆O₄S |
|---|---|---|---|
| EC Number: | 221-554-1 | MDL Number: | MFCD00064157 |
| Melting Point: | 196-200 °C (dec.)(lit.) | Boiling Point: | |
| Density: | Storage Condition: | -20°C, Inert Gas |
Product Description:
Widely used in chiral resolution and asymmetric synthesis, this compound serves as a chiral resolving agent for separating enantiomers of basic organic molecules, especially amines and amino derivatives. Its sulfonic acid group provides strong acidity and good solubility in polar solvents, making it effective in salt formation with racemic mixtures. The rigid camphor backbone ensures high stereoselectivity during crystallization processes. It is also employed as a chiral dopant in studies of chiral recognition and in the preparation of chiral stationary phases for chromatography. Additionally, it finds use in organic synthesis as a catalyst or auxiliary due to its stability and well-defined stereochemistry.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1ml | 10-20 days | ฿6,190.00 |
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(1S)-()-10-Camphorsulfonic acid
Widely used in chiral resolution and asymmetric synthesis, this compound serves as a chiral resolving agent for separating enantiomers of basic organic molecules, especially amines and amino derivatives. Its sulfonic acid group provides strong acidity and good solubility in polar solvents, making it effective in salt formation with racemic mixtures. The rigid camphor backbone ensures high stereoselectivity during crystallization processes. It is also employed as a chiral dopant in studies of chiral recognition and in the preparation of chiral stationary phases for chromatography. Additionally, it finds use in organic synthesis as a catalyst or auxiliary due to its stability and well-defined stereochemistry.
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