(1S)-()-10-Camphorsulfonic acid

99%

Reagent Code: #71180
label
Alias D(+)camphorsulfonic acid; D-camphor-10-sulfonic acid, D-camphorsulfonic acid, (1S)-7,7-dimethyl-2-oxo-bicyclo[2.2.1]heptane- 1-Methanesulfonic acid
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CAS Number 3144-16-9

science Other reagents with same CAS 3144-16-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.3 g/mol
Formula C₁₀H₁₆O₄S
badge Registry Numbers
EC Number 221-554-1
MDL Number MFCD00064157
thermostat Physical Properties
Melting Point 196-200 °C (dec.)(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used as a chiral resolving agent in organic synthesis to separate enantiomers of racemic mixtures. It is particularly effective in resolving amines and amino acids, making it valuable in pharmaceutical research for producing enantiomerically pure compounds. Also employed as a catalyst in asymmetric synthesis reactions, enhancing the efficiency and selectivity of the process. In the field of materials science, it is utilized in the preparation of conductive polymers due to its ability to dope and improve the electrical properties of materials like polyaniline. Additionally, it serves as a key component in the formulation of certain electrolytes for electrochemical applications.

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Test Parameter Specification
Loss on Drying 0-2%
Melting point 197-202
Purity (Neutralization Titration) 98.5-101.5%
Specific Rotation (α20/D c=5 H2O) 20-23
Appearance White to off-white powder
Solubility (5 in H2O) Clear colorless to light yellow solution

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 2.5kg
10-20 days ฿12,830.00
inventory 25g
10-20 days ฿350.00
inventory 100g
10-20 days ฿720.00
inventory 500g
10-20 days ฿2,770.00

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(1S)-()-10-Camphorsulfonic acid
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Used as a chiral resolving agent in organic synthesis to separate enantiomers of racemic mixtures. It is particularly effective in resolving amines and amino acids, making it valuable in pharmaceutical research for producing enantiomerically pure compounds. Also employed as a catalyst in asymmetric synthesis reactions, enhancing the efficiency and selectivity of the process. In the field of materials science, it is utilized in the preparation of conductive polymers due to its ability to dope and improve

Used as a chiral resolving agent in organic synthesis to separate enantiomers of racemic mixtures. It is particularly effective in resolving amines and amino acids, making it valuable in pharmaceutical research for producing enantiomerically pure compounds. Also employed as a catalyst in asymmetric synthesis reactions, enhancing the efficiency and selectivity of the process. In the field of materials science, it is utilized in the preparation of conductive polymers due to its ability to dope and improve the electrical properties of materials like polyaniline. Additionally, it serves as a key component in the formulation of certain electrolytes for electrochemical applications.

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