(1R)-(-)-Camphor-10-sulfonic acid, 98%, Thermo Scientific Chemicals
(1R)-(-)-Camphor-10-sulfonic acid, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

(1R)-(-)-Camphor-10-sulfonic acid, 98%, Thermo Scientific Chemicals

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500 g
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100 g
Catalog number B21553.36
also known as B21553-36
Price (EUR)/ Each
357,78
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402.00 
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Quantity:
500 g
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Price (EUR)/ Each
357,78
Online exclusive
402.00 
Save 44,22 (11%)
Add to cart
(1R)-(-)-Camphor-10-sulfonic acid, 98%, Thermo Scientific Chemicals
Catalog numberB21553.36
Price (EUR)/ Each
357,78
Online exclusive
402.00 
Save 44,22 (11%)
-
Add to cart
Chemical Identifiers
CAS35963-20-3
IUPAC Name[(1R)-7,7-dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl]methanesulfonic acid
Molecular FormulaC10H16O4S
InChI KeyMIOPJNTWMNEORI-MHPPCMCBSA-N
SMILESCC1(C)C2CC[C@]1(CS(O)(=O)=O)C(=O)C2
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SpecificationsSpecification SheetSpecification Sheet
FormCrystals or powder or crystalline powder
Assay (Aqueous acid-base Titration)≥97.5 to ≤102.5%
Identification (FTIR)Conforms
Optical Rotation-21.0? ? 2.5? (c=20 in water)
Appearance (Color)White to cream
(1R)-(-)-Camphor-10-sulfonic acid, is used as a pharamaceutical intermediate and also used as a chiral derivative of Camp. It can also be used as resolving agents for chiral amines and other cations.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
(1R)-(-)-Camphor-10-sulfonic acid, is used as a pharamaceutical intermediate and also used as a chiral derivative of Camp. It can also be used as resolving agents for chiral amines and other cations.

Solubility
Soluble in water, and a wide variety of organic substances.

Notes
Hygroscopic. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Stable under recommended storage conditions. Keep away strong oxidizing agents, strong acids and bases.
RUO – Research Use Only

General References:

  1. W Oppolzer.; P Dudfield. Asymmetric halogenation of camphor-10-sulfonic acid derived esters: an efficient new route to enantiomerically pure halohydrins and epoxides. Tetrahedron letters. 198526 (41), 5036-5040.
  2. M Vandewalle.; J Van der Eycken.; W Oppolzer. Iridoids: enantioselective synthesis of loganin via an asymmetric diels-alder reaction. Tetrahedron. 198642 (14), 4035-4043.