Enantiomer separation is indispensable for the production of many pharmaceuticals.
From the sciencedaily.com
The infamous case of thalidomide arose from the effects of the unwanted enantiomer.
From the en.wikipedia.org
Each enantiomer will rotate the light in a different sense, clockwise or counterclockwise.
From the en.wikipedia.org
An enantiomer can be named by the direction in which it rotates the plane of polarized light.
From the en.wikipedia.org
This kind of light can destroy one enantiomer of an amino acid while leaving the other unscathed.
From the newscientist.com
One enantiomer smells like orange and the other like lemon.
From the sciencedaily.com
In chemistry, such a molecule is called an enantiomer or is said to exhibit chirality or enantiomerism.
From the en.wikipedia.org
For example, one enantiomer of the chiral molecule limonene smells of lemon, the other smells of orange.
From the sciencedaily.com
Identification, chemical proof, and biological characterization of the biologically active species and its enantiomer.
From the nature.com
More examples
Enantiomorph: either one of a pair of compounds (crystals or molecules) that are mirror images on each other but are not identical
One of a pair of stereoisomers that is the mirror image of the other, but may not be superimposed on this other stereoisomer. Almost always, a pair of enantiomers contain at least one chiral center, and a sample of either enantiomer will be optically active
(enantiomers) Molecules which exist in two nonsuperimposable mirror images, analogous to human hands. ...
(Enantiomers) have - when present in a symmetric environment - identical chemical and physical properties except for their ability to rotate plane-polarized light by equal amounts but in opposite directions.
Is a molecule that is not superimposable on its mirror image, related to chirality
ICH Draft Guideline on Impurities in Drug Substances, FR V.59, No. 183, Sept. 22, 1994: Means compounds with the same molecular formula as the drug substance, which differ in the arrangement of atoms within the molecule and are nonsuperimposable mirror images.
One of the two mirror-image forms of an optically active molecule.
In chemistry, a special class of stereoisomers whose structure is not superimposable on its mirror image; a chiral molecule. Two enantiomers of a compound have identical chemical properties, but differ in a characteristic physical property, the ability to rotate the plane of plane-polarized light.