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

CAS: 35963-20-3 | C10H16O4S | 232.29 g/mol
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Catalog NumberQuantity
ALFB21553.22100 g
Catalog number ALFB21553.22
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Quantity:
100 g
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Chemical Identifiers
CAS78-83-1
IUPAC Name2-methylpropan-1-ol
Molecular FormulaC4H10O
InChI KeyZXEKIIBDNHEJCQ-UHFFFAOYSA-N
SMILESCC(C)CO
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless
FormLiquid
Assay (GC)≥98.5% (non-U.S. Specification)
Assay from Supplier's CofA≥98.5% (U.S. Specification)
CommentPurchased in the U.S. and in other countries
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(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.