1632-98-0 Usage
Description
ACETALDEHYDE-13C2 99 ATOM % 13C2, also known as Acetaldehyde-13C2 labelled analog of Acetaldehyde (A132600), is a compound that contains two stable isotopes of carbon, 13C, in its molecular structure. This isotopic labeling allows for the tracking and analysis of the compound's behavior in various chemical reactions and processes.
Uses
Used in Organic and Polymer Chemical Reactions:
ACETALDEHYDE-13C2 99 ATOM % 13C2 is used as a general solvent for facilitating and enhancing the efficiency of various organic and polymer chemical reactions. The isotopic labeling of the compound enables researchers to monitor and study the reaction pathways and mechanisms more effectively.
Used in Fruit and Food Quality:
ACETALDEHYDE-13C2 99 ATOM % 13C2 plays a significant role in the quality, ripening, and deterioration of fruits and other food products. The compound's presence can be used to study and understand the biochemical processes involved in fruit maturation and spoilage, leading to the development of better preservation techniques and improved food quality.
Used in Pharmaceutical Research:
ACETALDEHYDE-13C2 99 ATOM % 13C2 can be employed in pharmaceutical research as a labeled analog for studying the metabolism and pharmacokinetics of acetaldehyde, a compound that is often associated with alcohol consumption and has been linked to various health issues. The isotopic labeling allows for a more accurate tracking of acetaldehyde's behavior in the body, which can be crucial for the development of new drugs and therapies.
Used in Environmental Studies:
In environmental science, ACETALDEHYDE-13C2 99 ATOM % 13C2 can be utilized as a labeled compound to study the fate and transport of acetaldehyde in the environment, such as in soil, water, and air. This information can be valuable for understanding the impact of acetaldehyde on ecosystems and human health, as well as for developing strategies to mitigate its negative effects.
Used in Industrial Processes:
ACETALDEHYDE-13C2 99 ATOM % 13C2 can be employed in various industrial processes, such as the production of chemicals, materials, and pharmaceuticals, where the isotopic labeling of the compound can provide valuable insights into reaction mechanisms, process optimization, and product development.
Check Digit Verification of cas no
The CAS Registry Mumber 1632-98-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,3 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1632-98:
(6*1)+(5*6)+(4*3)+(3*2)+(2*9)+(1*8)=80
80 % 10 = 0
So 1632-98-0 is a valid CAS Registry Number.
InChI:InChI=1/C2H4O/c1-2-3/h2H,1H3/i1+1,2+1
1632-98-0Relevant articles and documents
Structure, dynamics, and reactivity of an alkoxy intermediate formed from acetylene on zeolite catalysts: An in situ solid-state NMR study
Lazo, Noel D.,White, Jeffery L.,Munson, Eric J.,Lambregts, Marsha,Haw, James F.
, p. 4050 - 4052 (1990)
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Synthesis of aldehydic ribonucleotide and amino acid precursors by photoredox chemistry
Ritson, Dougal J.,Sutherland, John D.
supporting information, p. 5845 - 5847 (2013/07/11)
Light work: UV irradiation of a system formed by adding copper(I) cyanide to an aqueous solution of glycolonitrile, sodium phosphate, and hydrogen sulfide efficiently generates aldehyde precursors to the building blocks of RNA and proteins. Copyright
