37593-06-9

Basic information

• Product Name: 1-(4-DECYLPHENYL)ETHAN-1-ONE
• Synonyms: 1-(4-DECYLPHENYL)ETHAN-1-ONE;LABOTEST-BB LT00000233;4-N-DECYLACETOPHENONE;1-[4-(Dec-1-yl)phenyl]ethan-1-one, 1-(4-Acetylphenyl)decane;4'-(Dec-1-yl)acetophenone;1-(4-decylphenyl)ethanone
• CAS NO: 37593-06-9
• Molecular Formula: C₁₈H₂₈O
• Molecular Weight: 260.41
• Mol File: 37593-06-9.mol
• Article Data: 6

Chemical Properties

• Melting Point: 33 °C
• Boiling Point: 371.4 °C at 760 mmHg
• Flash Point: 156.6 °C
• Appearance: /
• Density: 0.911 g/cm³
• Vapor Pressure: 1.04E-05mmHg at 25°C
• Refractive Index: 1.491
• CAS DataBase Reference: 1-(4-DECYLPHENYL)ETHAN-1-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-DECYLPHENYL)ETHAN-1-ONE(37593-06-9)
• EPA Substance Registry System: 1-(4-DECYLPHENYL)ETHAN-1-ONE(37593-06-9)

Safety Data

• Safety Statements: S24/25:Avoid contact with skin and eyes.
• Hazardous Substances Data: 37593-06-9(Hazardous Substances Data)

Usage

General Description

1-(4-decylphenyl)ethan-1-one, also known as p-decylphenyl ethanone, is a chemical compound with the molecular formula C18H28O. It is a ketone with a 4-decylphenyl group attached to the carbon chain. 1-(4-DECYLPHENYL)ETHAN-1-ONE is often used in the production of perfumes and fragrances due to its pleasant and long-lasting odor. It is also used in the synthesis of various pharmaceuticals and as a flavoring agent in food products. In addition, it has potential applications in the field of organic synthesis and material science. Overall, 1-(4-decylphenyl)ethan-1-one has versatile industrial and commercial uses due to its unique chemical properties and applications in different industries.

InChI:InChI=1/C18H28O/c1-3-4-5-6-7-8-9-10-11-17-12-14-18(15-13-17)16(2)19/h12-15H,3-11H2,1-2H3

Upstream product

• 104-72-3 decylbenzene 
• 75-36-5 acetyl chloride 
• 107678-20-6 2-(4-Decyl-phenyl)-2-methyl-[1,3]dithiane 
• 108-24-7 acetic anhydride 

Downstream Products

• 38300-04-8 4-decylbenzoic acid 
• 69511-08-6 1-(4-decylphenyl)ethan-1-ol 
• 78450-46-1 1,3-Di(p-n-decylphenyl)propane-1,3-dione 
• 134444-34-1 1-(p-n-decylphenyl)3-(p-n-decyloxyphenyl)propane-1,3-dione 
• 37593-13-8 N-(4-decylphenyl)acetamide 
• 16877-72-8 4-n-decyl-α-bromoacetophenone 
• 53097-42-0 3-(4-Decyl-phenyl)-3-oxo-propionic acid methyl ester 
• 46926-59-4 1-decyl-4-vinylbenzene 
• 78575-35-6 (4-Decyl-phenyl)-[(E)-hydroxyimino]-acetaldehyde oxime 
• 94775-85-6 3-(4-Decyl-phenyl)-6-propyl-pyridazine 
• 94775-75-4 1-(4-Decyl-phenyl)-2-hydroxy-heptane-1,4-dione 
• 94775-66-3 Potassium; 2-[2-(4-decyl-phenyl)-1-hydroxy-2-oxo-ethyl]-3-oxo-hexanoate 
• 83471-22-1 4-decyl-3-nitro-benzoic acid 

Relevant articles and documents

Syndiospecific synthesis of longer p-n-alkyl-substituted polystyrenes using monocyclopentadienyl-type titanium catalysts

Substituted styrenes with linear alkyl substituents (C6 to C12) at the para position on the ring were synthesized and polymerized using the (Me)5CpTi(OMe)3/MAO catalytic system. Increased polymerization activiti

DETHIOACETALISATION DE DITHIANNES-1,3 PAR DES TRIBROMURES DE PHOSPHONIUM

Methyltriphenylphosphonium tribromide 1 acts as an efficient mild dethioketalization reagent with high selectivity for 2-phenyl and 2-vinyl 1,3-dithiannes 2 versus 2-alkyl 1,3-dithiannes and without any secondary bromination reaction of the investigated substrates.The reaction was also succesful with trimethylphenylammonium tribromide.

Multiple Melting Behaviour in Square-planar trans-Bis-(1-p-n-alkylphenylbutane-1,3-dionato)copper(II) - The Effect of Alkyl Chain Length

The title complexes having different n-alkyl groups from methyl to dodecyl have synthesized.All these complexes exhibit solid polymorphism.The number of polymorphs depends on the length of the alkyl chain: two for n (the number of carbon atoms) = 0-2, three for n = 3-5 and 12, and four for n = 6-11, respectively.Each polymorphic form except those with the highest m.p.s. exhibits multiple melting behaviour: double melting for n = 0-5,8, and 12, and triple melting for n = 6-11 except 8.The m.p.s. of the complexes with alkyl groups of odd carbon atoms are higher than those with even atoms, while the respective ligand solids show the opposit e even-odd effect in their m.p.s.