Name: 2-(2-Iodoethyl-[13C2])-2-methyl-[13C]-dioxolane-2-[13C]
Brand: BOC Sciences
Rating: 5 (1 reviews)

General Information

Catalog: BLP-005626

CAS: 101025-40-5

Molecular Formula: [13C]4C2H11IO2

Molecular Weight: 246.03

Chemical Structure

Description	2-(2-Iodoethyl-[13C2])-2-methyl-[13C]-dioxolane-2-[13C] is intended for use as an internal standard for 2-(2-iodoethyl)-2-methyl-1,3-dioxolane. 2-(2-Iodoethyl-13C2)-2-methyl-[13C]-dioxolane-2-[13C], as an ethylene glycol protected short chain alkehyde, can be readily convert to relative complicated chemical via nucleophilic substitution reactions.
Related CAS	53750-51-9 (unlabelled)
Canonical SMILES	CC1(OCCO1)CCI
InChI	InChI=1S/C6H11IO2/c1-6(2-3-7)8-4-5-9-6/h2-5H2,1H3/i1+1,2+1,3+1,6+1
InChI Key	SXVDTZCWOQEFBN-HDPXQERQSA-N
Purity	≥98% by CP; 99% atom 13C
Appearance	Clear Colorless Liquid

2-(2-Iodoethyl-[13C2])-2-methyl-[13C]-dioxolane-2-[13C] is a labeled chemical compound often used in research and industrial applications. Here are some key applications of this compound:

Isotope Labeling for NMR Studies: The carbon-13 labels in 2-(2-Iodoethyl-[13C2])-2-methyl-[13C]-dioxolane-2-[13C] make it an excellent candidate for nuclear magnetic resonance (NMR) spectroscopy studies. Researchers use this compound to investigate the structural and dynamic properties of complex molecules. Its distinct isotopic composition provides valuable insights into reaction mechanisms and intermolecular interactions.

Tracer Studies in Metabolic Research: The labeled nature of 2-(2-Iodoethyl-[13C2])-2-methyl-[13C]-dioxolane-2-[13C] makes it useful for tracing metabolic pathways in biological systems. By incorporating this compound into metabolic studies, scientists can follow the fate of molecules through different biochemical pathways. This application assists in understanding metabolic fluxes and exploring potential metabolic engineering approaches.

Chemical Synthesis: In organic synthesis, 2-(2-Iodoethyl-[13C2])-2-methyl-[13C]-dioxolane-2-[13C] can be used to introduce iodoethyl groups into target molecules. Its isotopic labeling also allows for the precise monitoring of reactions and product formation. This capability is crucial for developing synthetic routes and optimizing reaction conditions in the pharmaceutical and chemical industries.

Environmental Fate Studies: The labeled compound is employed in environmental chemistry to study the fate and transport of organic molecules. It helps researchers trace the movement and transformation of chemicals in various ecosystems. This information is vital for assessing the environmental impact of pollutants and developing strategies for remediation and sustainability.