2348-19-8

Usage

Uses

Used in Analytical Chemistry:
NONANAL (DNPH DERIVATIVE) is used as a chemical reagent for the detection and measurement of carbonyl compounds in various samples. It forms a colored complex with these compounds, facilitating their analysis using spectrophotometry and chromatography.
Used in Environmental Analysis:
In the environmental sector, NONANAL (DNPH DERIVATIVE) is used as an analytical tool for the identification and quantification of carbonyl compounds in pollutants, helping to assess and monitor air and water quality.
Used in Food Industry:
NONANAL (DNPH DERIVATIVE) is employed in the food industry as a means to analyze and quantify carbonyl compounds in food additives, ensuring the safety and quality of food products.
Used in Industrial Chemical Analysis:
This DNPH derivative is also utilized in the industrial chemical sector for the analysis of carbonyl compounds in various chemicals, contributing to the development and quality control of industrial products.

InChI:InChI=1/C15H22N4O4/c1-2-3-4-5-6-7-8-11-16-17-14-10-9-13(18(20)21)12-15(14)19(22)23/h9-12,17H,2-8H2,1H3/b16-11+

Upstream product

• 54815-13-3 pelargonaldehyde diethyl acetal 
• 119-26-6 (2,4-dinitro-phenyl)-hydrazine 
• 132724-54-0 9-(1-Benzotriazol-1-yl-nonyl)-9H-carbazole 
• 111-83-1 1-bromo-octane 
• 862672-34-2 (R,7E,16Z)-pentacosa-7,16-dien-2,4-diyne-1,6-diol 
• 122-32-7 trioleoylglycerol 
• 124-19-6 nonan-1-al 
• 101170-73-4 5-butyl-thiophene-2-carbaldehyde-diethylacetal 
• 98954-25-7 5-n-butylthiophene-2-carbaldehyde 
• 120-87-6 Dihydroxystearic Acid 
• 33472-14-9 (1-hydroxy-nonyl)-phosphonic acid di-sec-butyl ester 
• 14596-80-6 octyl-[1,3,5]trioxane 
• 5432-30-4 2-octyl-1,3-dioxolane 

Downstream Products

• 79348-63-3 C₁₅H₂₁BrN₄O₄ 

Relevant academic research and scientific papers

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.

Acetylenic strongylodiols from a Petrosia (Strongylophora) Okinawan marine sponge

Seven new long-chain acetylenic alcohols, strongylodiols D-J, were isolated from an Okinawan marine sponge of the genus Petrosia (Strongylophora). The structures of these compounds were elucidated on the basis of the results of spectroscopic analysis and

1-(Carbazol-9-ylmethyl)benzotriazole Anion: A Formyl Anion Equivalent

The title anion, readily available as its lithium derivative, smoothly reacts with a wide range of electrophiles to give well-characterized products which are easily hydrolyzed to the corresponding aldehydes in high overall yields.The method is compared with currently available routes.