504-57-4

Basic information

• Product Name: 10-NONADECANONE
• Synonyms: DI-N-NONYL KETONE;DINONYL KETONE;DI-N-DINONYL KETONE;CAPRINONE;10-NONADECANONE;nonadecan-10-one;10-NONADECANONE 99%;10-Nonadecanone,99%
• CAS NO: 504-57-4
• Molecular Formula: C₁₉H₃₈O
• Molecular Weight: 282.5
• EINECS: 207-994-7
• Product Categories: Aromatic Ketones (substituted)
• Mol File: 504-57-4.mol
• Article Data: 14

Chemical Properties

• Melting Point: 58°C
• Boiling Point: 156 °C / 1.1mmHg
• Flash Point: 81.6°C
• Appearance: /
• Density: 0.8512 (estimate)
• Vapor Pressure: 4.17E-05mmHg at 25°C
• Refractive Index: 1.4513 (estimate)
• Storage Temp.: Refrigerator
• Solubility: Chloroform (Sparingly), Methanol (Slightly)
• CAS DataBase Reference: 10-NONADECANONE(CAS DataBase Reference)
• NIST Chemistry Reference: 10-NONADECANONE(504-57-4)
• EPA Substance Registry System: 10-NONADECANONE(504-57-4)

Safety Data

• Safety Statements: 22-24/25
• Hazardous Substances Data: 504-57-4(Hazardous Substances Data)

Usage

General Description

10-Nonadecanone is a long-chain fatty acid derived from natural sources such as coconut oil or beeswax. It is a colorless liquid with a faint sweet, floral odor, and is commonly used as a flavoring agent in food and beverages. It also has insecticidal properties, making it an effective natural repellent for various pests, including mosquitoes and fruit flies. Due to its low toxicity and pleasant fragrance, 10-Nonadecanone is often used in insect repellent products for personal use as well as in agricultural settings. It is also used in the manufacturing of perfumes and other fragranced products. Overall, 10-Nonadecanone is a versatile chemical with applications in both the food and fragrance industries, as well as in pest control.

InChI:InChI=1/C19H38O/c1-3-5-7-9-11-13-15-17-19(20)18-16-14-12-10-8-6-4-2/h3-18H2,1-2H3

Upstream product

• 56-23-5 tetrachloromethane 
• 112-13-0 n-decanoyl chloride 
• 121-44-8 triethylamine 
• 75-36-5 acetyl chloride 
• 60-29-7 diethyl ether 
• 67-64-1 acetone 
• 108-88-3 toluene 
• 58712-53-1 4-nonylidene-3-octyl-oxetan-2-one 
• 111-83-1 1-bromo-octane 
• 6407-36-9 N-isopropyliden-cyclohexyl amine 
• 334-48-5 1-decanoic acid 
• 1264-57-9 decanoyl coenzyme A 
• 1763-10-6 S-palmitoyl-coenzyme A 
• 18198-76-0 Palmitoleoyl-Coenzyme A 

Downstream Products

• 3241-23-4 nonadecan-10-amine 
• 334-48-5 1-decanoic acid 
• 119621-19-1 benzyl-(3-hydroxy-2-octyl-dodecyl)-dimethyl-ammonium; chloride 
• 1440632-75-6 1-(6-Hydroxymethyl-2,2-dinonyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-5-methyl-3-(3,7,11-trimethyldodeca-2,6,10-trienyl)-1H-pyrimidin-2,4-dione 
• 1440632-26-7 1-((3aR,4R,6R,6aR)-6-(hydroxymethyl)-2,2-dinonyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)-3-((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl)pyrimidin-2,4(1H,3H)-dione 
• 1590381-23-9 5’-{4-[3-(ethoxycarbonyl)-7,8-dihydro-6,8,8-trimethyl-2-oxo-2H-pyrano[3,2-g]quinolin-9(6H)-yl]butanoyl}-5-fluoro-2’,3’-O-(1-nonyldecylidene)uridine 
• 1440631-78-6 1-((3aR,4R,6R,6aR)-6-(hydroxymethyl)-2,2-dinonyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)pyrimidin-2,4(1H,3H)-dione 
• 1440632-40-5 1-(6-hydroxymethyl-2,2-dinonyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-5-methyl-1H-pyrimidin-2,4-dione 
• 1416474-23-1 3-nonyldodecyl p-toluenesulfonate 
• 113550-13-3 2,6-dioctyl-[1,4]benzoquinone 
• 115207-22-2 2,6-dioctyl-hydroquinone 
• 111-66-0 oct-1-ene 
• 101829-05-4 4,4-dimethyl-2,2-dinonyloxazolidine-N-oxyl 
• 112-12-9 methyl nonyl ketone 

Relevant articles and documents

Characterization of uranyl soaps by spectroscopic and thermal measurements

The infrared and visible spectrophotometric data of uranyl soaps showed that metal-oxygen bonds in uranyl soaps are not purely ionic but are partially covalent in character.The X-ray diffraction patterns confirmed the double-layer structure with molecular

Direct conversion of carboxylic acids (Cn) to alkenes (C2n - 1) over titanium oxide in absence of noble metals

Carbon-carbon bond formations and deoxygenation reactions are important for biomass up-grading. The classical ketonic decarboxylation of carboxylic acids provides symmetrical ketones with 2n + 1 carbon atoms and eliminates three oxygen atoms. Herein, this reaction is carried out with titanium oxide at 400°C, and an olefin with 2n + 1 carbon atoms is obtained instead of the ketone. For olefin formation hydrogen transfer reactions are required from suitable precursors to form aromatics and coke. Additional aldol condensation reactions increase further molecular weight in the product mixture. Hence, a combination of titanium oxide with a hydrodeoxygenation bed provides double amount of diesel fuel as the combination with zirconium oxide when reacting hexose-derived pentanoic acid.

TREHALOSE COMPOUND, METHOD FOR PRODUCING SAME, AND PHARMACEUTICAL PRODUCT CONTAINING THE COMPOUND

It is an object of the present invention to provide a trehalose compound having high immunopotentiating activity and low toxicity. The trehalose compound is represented by formula (1). (In the formula, X and X' each represents a phenyl, a naphtyl, R1-CHR1- (wherein R1 and R2 each represents a C7-C21 alkyl group or the like) or the like; and n and n' each independently represents an integer of 0-3). The compound exhibits a high activating effect on macrophages and neutrophils.