725-00-8 Usage
Description
PROPIONALDEHYDE 2,4-DINITROPHENYLHYDRAZONE is a dinitrophenylhydrazone (DNPH) derivative of an aliphatic aldehyde. It is identified in mainstream cigarette smoke and is also a byproduct of lipid peroxidation. PROPIONALDEHYDE 2,4-DINITROPHENYLHYDRAZONE is characterized by its role as a dye and a metabolite.
Uses
Used in Chemical Analysis:
PROPIONALDEHYDE 2,4-DINITROPHENYLHYDRAZONE is used as a chemical marker for the detection and analysis of aldehydes, particularly in the context of cigarette smoke and lipid peroxidation processes. Its presence helps researchers understand the chemical composition and potential health implications of exposure to cigarette smoke and oxidative stress.
Used in Environmental Monitoring:
In the environmental sector, PROPIONALDEHYDE 2,4-DINITROPHENYLHYDRAZONE is used as an indicator of air pollution and tobacco smoke exposure. Monitoring the levels of this compound can provide insights into the quality of air and the potential health risks associated with smoking or secondhand smoke exposure.
Used in Pharmaceutical Research:
PROPIONALDEHYDE 2,4-DINITROPHENYLHYDRAZONE serves as a valuable compound in pharmaceutical research, particularly in the development of drugs targeting aldehyde-related pathways. Its unique chemical properties make it a useful tool for studying the mechanisms of action and potential therapeutic applications in various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 725-00-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 725-00:
(5*7)+(4*2)+(3*5)+(2*0)+(1*0)=58
58 % 10 = 8
So 725-00-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H10N4O4/c1-2-5-10-11-8-4-3-7(12(14)15)6-9(8)13(16)17/h3-6,11H,2H2,1H3
725-00-8Relevant articles and documents
Effect of CHAPS and CPC micelles on Ir(III) catalyzed Ce(IV) oxidation of aliphatic alcohols at room temperature and pressure
Ghosh, Aniruddha,Saha, Rumpa,Saha, Bidyut
, p. 223 - 237 (2014/05/06)
Kinetics of cerium(IV) oxidation of aliphatic alcohols: ethanol, propanol, propan-2-ol, 1-butanol and 2-butanol were studied at 30 °C in the presence and absence of surfactants in acidic medium. The reaction was studied under pseudo-first-order conditions
Revisiting the reaction of hydroxyl radicals with vicinal diols in water
Jiang, Dong,Barata-Vallejo, Sebastian,Golding, Bernard T.,Ferreri, Carla,Chatgilialoglu, Chryssostomos
supporting information; experimental part, p. 1102 - 1107 (2012/04/04)
The carbonyl products of the reactions of hydroxyl radicals with three vicinal diols (ethane-1,2-diol, propane-1,2-diol and butane-2,3-diol) have been identified and quantified. Hydroxyl radicals were produced by γ-radiolysis of N2O-saturated aqueous solutions. The reactions result in the formation of alkoxyl radicals (～15%) followed by β-fragmentation, and α-hydroxyl alkyl radicals that undergo H2O elimination. The latter process is part of a radical chain reaction at higher diol concentrations.
Analysis of carbonyl compounds in sea buckthorn for the evaluation of triglyceride oxidation, by enzymatic hydrolysis and derivatisation methodology
Mathew, Sindhu,Grey, Carl,Rumpunen, Kimmo,Adlercreutz, Patrick
experimental part, p. 1399 - 1405 (2012/02/03)
Carbonyl compounds formed in sea buckthorn berry (Hippophae rhamnoides) and oil samples as a result of lipid oxidation were determined by enzymatic hydrolysis followed by derivatisation with 2,4-dinitrophenylhydrazine and analysed by LC-UV and electrospra
