1219798-96-5

Basic information

• Product Name: 4-Fluorobenzyl--d4-aMine
• Synonyms: 4-Fluorobenzyl--d4-aMine
• CAS NO: 1219798-96-5
• Molecular Formula: C7H4D4FN
• Molecular Weight: 129.168170312
• Mol File: 1219798-96-5.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-Fluorobenzyl--d4-aMine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Fluorobenzyl--d4-aMine(1219798-96-5)
• EPA Substance Registry System: 4-Fluorobenzyl--d4-aMine(1219798-96-5)

Safety Data

• Hazardous Substances Data: 1219798-96-5(Hazardous Substances Data)

Usage

Description

4-Fluorobenzyl--d4-amine, also known as 4-Fluorobenzyl-2,3,5,6-d4-amine, is an isotopically labeled research compound with a unique molecular structure. It consists of a benzyl group with a fluorine atom at the 4-position and four deuterium atoms attached to the carbon atoms of the benzyl group. 4-Fluorobenzyl--d4-amine is characterized by its stable isotope labeling, which allows for enhanced detection and tracking in various analytical techniques.

Uses

Used in Chemical Synthesis:
4-Fluorobenzyl--d4-amine is used as a building block in the synthesis of various organic compounds, particularly those requiring stable isotope labeling for analytical purposes. Its unique structure and deuterium labeling make it a valuable tool for studying reaction mechanisms and monitoring the incorporation of labeled compounds into complex molecules.
Used in Analytical Chemistry:
In analytical chemistry, 4-Fluorobenzyl--d4-amine is employed as an internal standard or a reference compound for mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy. Its stable isotope labeling provides a distinct signature, allowing for accurate quantification and identification of target analytes in complex samples.
Used in Pharmaceutical Research:
4-Fluorobenzyl--d4-amine is utilized in pharmaceutical research as a labeled analog of active pharmaceutical ingredients (APIs). This allows researchers to study the pharmacokinetics, metabolism, and biodistribution of drug candidates, as well as to investigate the mechanisms of drug action and resistance.
Used in Environmental Studies:
In environmental studies, 4-Fluorobenzyl--d4-amine can be used as a tracer compound to track the fate and transport of pollutants or contaminants in various ecosystems. Its stable isotope labeling enables the differentiation between naturally occurring and anthropogenic sources of the compound, providing valuable insights into environmental processes and pollution control strategies.
Used in Material Science:
4-Fluorobenzyl--d4-amine can be incorporated into the synthesis of novel materials, such as polymers, coatings, and sensors, with enhanced properties due to the presence of stable isotopes. This allows for the development of advanced materials with improved performance characteristics and applications in various industries, including electronics, energy, and healthcare.