6697-12-7

Basic information

• Product Name: N-HEXADECANOPHENONE
• Synonyms: 1-Hexadecanone, 1-phenyl-;1-Phenyl-1-hexadecanone;Pentadecyl phenyl ketone;PALMITOPHENONE;N-HEXADECANOPHENONE;N-PENTADECYL PHENYL KETONE;HEXADECANOPHENONE;HEXADECANOPHENONE 95%
• CAS NO: 6697-12-7
• Molecular Formula: C₂₂H₃₆O
• Molecular Weight: 316.52
• Product Categories: C15 to C38;Carbonyl Compounds;Ketones
• Mol File: 6697-12-7.mol
• Article Data: 7

Chemical Properties

• Melting Point: 61-65 °C(lit.)
• Boiling Point: 248 °C12 mm Hg(lit.)
• Flash Point: 155.8°C
• Appearance: /
• Density: 0.8692
• Vapor Pressure: 8.95E-07mmHg at 25°C
• Refractive Index: 1.4675 (estimate)
• CAS DataBase Reference: N-HEXADECANOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: N-HEXADECANOPHENONE(6697-12-7)
• EPA Substance Registry System: N-HEXADECANOPHENONE(6697-12-7)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 6697-12-7(Hazardous Substances Data)

Usage

General Description

N-HEXADECANOPHENONE is a chemical compound with the formula C22H34O. It is a white solid with a strong odor, and it is commonly found in perfumes and fragrances due to its pleasant aroma. N-HEXADECANOPHENONE is also used as a flavoring agent in the food industry, providing a sweet, fruity taste. Additionally, it is a key intermediate in the production of various organic compounds, such as pesticides and pharmaceuticals. Due to its versatile properties, N-HEXADECANOPHENONE is widely used in industrial applications and consumer products. However, it is important to handle this chemical with care, as it can be irritating to the skin, eyes, and respiratory system.

InChI:InChI=1/C22H36O/c1-2-3-4-5-6-7-8-9-10-11-12-13-17-20-22(23)21-18-15-14-16-19-21/h14-16,18-19H,2-13,17,20H2,1H3

Upstream product

• 629-79-8 palmitonitrile 
• 629-54-9 Palmitamide 
• 57-10-3 1-hexadecylcarboxylic acid 
• 65-85-0 benzoic acid 
• 112-67-4 n-hexadecanoyl chloride 
• 98-80-6 phenylboronic acid 
• 603-33-8 triphenylbismuthane 
• 100663-86-3 C₂₈H₄₀N₂O₂ 
• 71-43-2 benzene 

Downstream Products

• 26174-65-2 N'-[1-Phenyl-hexadec-(E)-ylidene]-hydrazinecarbodithioic acid methyl ester 
• 1120-36-1 1-tetradecene 
• 98-86-2 acetophenone 
• 125520-15-2 1-Phenylhexadecylacetat 
• 1271732-53-6 (R)-1-phenyl-1-hexadecanol 
• 79098-13-8 4-hexadecylaniline 
• 1306630-59-0 C₆₄H₈₅N₅O₆ 
• 1223591-64-7 C₂₈H₄₂N₂O 
• 1271732-58-1 (S)-1-phenyl-1-hexadecanol 
• 65-85-0 benzoic acid 
• 26173-53-5 N'-[1-Phenyl-hexadec-(E)-ylidene]-hydrazinecarbodithioic acid hexadecyl ester 
• 26174-72-1 N'-[1-Phenyl-hexadec-(E)-ylidene]-hydrazinecarbodithioic acid dodecyl ester 
• 1851-97-4 1-Phenyl-1-hexadecanol 
• 1459-09-2 1-phenylhexadecane 

Relevant articles and documents

PROCESS FOR THE PREPARATION OF ALKOXYLATES COMPOSITIONS

A mixture of two alkoxylates surfactants, one being an aryl aliphatic carbinol alkoxylate, the other one being a dialiphatic carbinol alkoxylate, said mixture being useful for stabilizing emulsions and dispersions used in agricultural or pharmaceutical formulations. The alkoxylates surfactants may serve as substitutes for nonylphenol ethoxylates (NPE) and tristyrylphenol ethoxylates (TSE).

Liquid-crystalline polymorphism of symmetrical azobananas: Bis(4-(4-alkylphenyl)azophenyl) 2-nitroisophtalates

In this paper we present a series of novel compounds, bis(4-(4-alkylphenyl) azophenyl) 2-nitroisophtalates, which exhibit nematic and banana-type liquidcrystalline phases. The alkyl chain length varies from 1 to 18 carbons. The first ten members of this series exhibit nematic phase. The last eleven compounds exhibit banana-type liquid crystalline phases. The propyl and pentyl derivatives have extra second type of banana mesophase. Copyright Taylor & Francis Group, LLC.

A new ketone synthesis by palladium-catalyzed cross-coupling reactions of esters with organoboron compounds

(Chemical Equation Presented) The palladium-catalyzed coupling reaction of 2-pyridyl esters with organoboron compounds is described. The reaction is compatible with various functional groups and proceeds under mild reaction conditions. The coordination of the nitrogen atom to Pd is a key step for efficient reaction.