(1R)-(+)-Camphor, 98%, Thermo Scientific Chemicals
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(1R)-(+)-Camphor, 98%, Thermo Scientific Chemicals
(1R)-(+)-Camphor, 98%, Thermo Scientific Chemicals
(1R)-(+)-Camphor, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

(1R)-(+)-Camphor, 98%, Thermo Scientific Chemicals

CAS: 464-49-3 | C10H16O | 152.24 g/mol
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100 g
25 g
Catalog number ALFA10708.22
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Specifications
Chemical Name or Material(1R)- (+)-Camphor
CAS464-49-3
Health Hazard 1H228-H302-H315-H319-H335-H500
Health Hazard 2GHS H Statement
H228-H315-H319
Flammable solid.
Causes skin irritation.
Causes serious eye irritation.
Health Hazard 3P210-P240-P241-P261-P264b-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P362-P370+P378q-P501c
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(1R)-(+)-Camphor is used as a chiral intermediate and auxiliary. It is also used as a skin antipruritic and as an anti-infective agent.

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 is used as a chiral intermediate and auxiliary. It is also used as a skin antipruritic and as an anti-infective agent.

Solubility
Soluble in water (0.1 g/L at 20°C).

Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. G. Grogan.; G. Roberts.; S. Parsons, N. Turner.; S. Flitsch. P450camr, a cytochrome P450 catalysing the stereospecific 6-endo-hydroxylation of (1R)-(+)-camphor. Applied Microbiology and Biotechnology. 2002, 59, (4), 449-454.
  2. V Santhi.; J.Madhusudana Rao. Asymmetric reduction of prochiral ketones using in situ generated oxazaborolidines derived from amino alcohols of (1R)-camphor as catalysts. Tetrahedron: Asymmetry. 2000, 11 (17), 3553-3560.