40933-03-7

Usage

Explanation

The compound is named based on its structure, which includes an adamantane backbone with two deuterium atoms (D2) attached to the nitrogen atom.

Explanation

This name is derived from the adamantane structure and the presence of a deuterium-labeled amine group.

Explanation

The adamantane structure is characterized by its cage-like arrangement of three interconnected cyclohexane rings.

Explanation

The deuterium atoms replace the hydrogen atoms in the parent compound, specifically at the nitrogen atom of the amine group.

Explanation

The presence of deuterium atoms in the compound leads to increased stability compared to the non-deuterated parent compound.

Explanation

The replacement of hydrogen atoms with deuterium atoms results in altered chemical properties, such as changes in reactivity and reduced exchange rates.

Explanation

1-Aminoadamantane-N,N-D2 is used as an internal standard in mass spectrometry and NMR spectroscopy for the quantification and identification of related compounds.

Explanation

The compound is utilized in a wide range of research and analytical applications, including pharmaceutical, environmental, and biochemical studies.

Explanation

1-Aminoadamantane-N,N-D2 aids in the accurate measurement and identification of structurally similar compounds in complex samples.

Structure

Adamantane backbone with three fused cyclohexane rings

Deuterium Labeling

N,N-D2

Improved Stability

Due to deuterium atoms

Different Chemical Properties

Compared to the parent compound

Application

Stable isotope-labeled internal standard

Research and Analytical Applications

Various fields

Quantification and Identification

Related compounds