1527-95-3

Basic information

• Product Name: DECYL ALDEHYDE (DNPH DERIVATIVE)
• Synonyms: DECYL ALDEHYDE (DNPH DERIVATIVE);Caprinaldehyde-2,4-DNPH, Decyl aldehyde-2,4-DNPH;Decanal 2,4-dinitrophenylhydrazone;Decanal-DNPH solution,10ppm;Decanal-DNPH solution,15ppm;Decanal-DNPH solution,3ppm
• CAS NO: 1527-95-3
• Molecular Formula: C₁₆H₂₄N₄O₄
• Molecular Weight: 336.39
• Mol File: 1527-95-3.mol
• Article Data: 4

Chemical Properties

• Melting Point: 100-104 °C
• Appearance: /
• CAS DataBase Reference: DECYL ALDEHYDE (DNPH DERIVATIVE)(CAS DataBase Reference)
• NIST Chemistry Reference: DECYL ALDEHYDE (DNPH DERIVATIVE)(1527-95-3)
• EPA Substance Registry System: DECYL ALDEHYDE (DNPH DERIVATIVE)(1527-95-3)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 1527-95-3(Hazardous Substances Data)

Upstream product

• 122-32-7 trioleoylglycerol 
• 119-26-6 (2,4-dinitro-phenyl)-hydrazine 
• 255370-46-8 C₁₈H₂₉N₂⁽¹⁺⁾*I^(1-) 
• 111-83-1 1-bromo-octane 
• 97-00-7 1-chloro-2,4-dinitro-benzene 
• 13372-74-2 n-decanal oxime 
• 61668-40-4 1-ethoxydec-1-ene 
• 112-31-2 caprinaldehyde 

Relevant articles and documents

Formation of potentially toxic carbonyls during oxidation of triolein in the presence of alimentary antioxidants

Abstract: A relation between oil uptake and cancer as well as induction of hepatic inflammation was shown earlier. It is discussed that the main oil oxidation products—hydroperoxides and carbonyls—might be the reason for the mentioned diseases. In this manuscript quantitative determination of aldehydes which are formed during oxidation of triolein—as a model substance—using the Rancimat 679 is described. The oxidation of 11?g of triolein is carried out at 120?°C sparging air with a flow of 20?dm3/h for 10?h. A series of aliphatic aldehydes starting from hexanal to decanal as well as decenal was identified by LC–MS/MS and quantified as DNPH derivatives. In addition, the total amount of carbonyls was determined. Based on the calibration with hexanal, all other dominant substances were in the similar concentration range with maximum concentrations of 1.6?μmol/cm3 of hexanal, 2.3?μmol/cm3 of heptanal, 2.5?μmol/cm3 of octanal, 3.2?μmol/cm3 of nonanal, 4.0?μmol/cm3 of decanal after 6?h. The total amount of carbonyls reached a maximum after 6?h being 27?μmol/cm3 for triolein without antioxidant. The results of this investigation will be a basis for further toxicological studies on oxidized oils.

Analysis of carbonyl compounds in sea buckthorn for the evaluation of triglyceride oxidation, by enzymatic hydrolysis and derivatisation methodology

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