Antifungal drugs

(R)-(+)-Limonene is the R- and the predominant enantiomer of the cyclic monoterpene, limonene. It is present as the major constituent of essential oils extracted from oranges, grapefruits, and lemons.

(R)-(+)-Limonene is the R- and the predominant enantiomer of the cyclic monoterpene, limonene. It is present as the major constituent of essential oils extracted from oranges, grapefruits, and lemons.

( R )-(+)-Limonene is an optically active ( R ) form of limonene. Limonene is a 10-carbon cyclohexanoid monoterpene.

( R )-(+)-Limonene is an optically active ( R ) form of limonene. Limonene is a 10-carbon cyclohexanoid monoterpene.

Analysis Note Assay (GC, area%): &#8805 94.0 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 0.

Analysis Note Assay (GC, area%): &#8805 94.0 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 0.

Application Refer to the product&#8242s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

(R)-(-)-1,3-Butanediol

Application This product is Informer compound X7 of the Aryl Halide Chemistry Informer Library developed by chemists at Merck &amp Co., Inc.

( S )-(-)-1,2,4-Butanetriol can be prepared via reduction of ( S )-malic acid in the presence of borane-dimethyl sulfide. Application ( S )-(-)-1,2,4-Butanetriol may be used as a starting material in the enantioselective total syntheses of

( S )-(-)-1,2,4-Butanetriol can be prepared via reduction of ( S )-malic acid in the presence of borane-dimethyl sulfide. Application ( S )-(-)-1,2,4-Butanetriol may be used as a starting material in the enantioselective total syntheses of

Analysis Note Assay (GC, area%): &#8805 98.0 % (a/a) Melting range (lower value): &#8805 117 &#176C Melting range (upper value): &#8804 121 &#176C Identity (IR): passes test