4815-57-0

Basic information

• Product Name: 1,4-DIPROPYLBENZENE
• Synonyms: 1,4-DI-N-PROPYLBENZENE;1,4-DIPROPYLBENZENE;Benzene, p-dipropyl-;benzene,1,4-dipropyl-;p-Dipropylbenzene
• CAS NO: 4815-57-0
• Molecular Formula: C₁₂H₁₈
• Molecular Weight: 162.27
• Mol File: 4815-57-0.mol
• Article Data: 3

Chemical Properties

• Melting Point: -25.43°C (estimate)
• Boiling Point: 221 °C / 746mmHg
• Flash Point: 84.3°C
• Appearance: /
• Density: 0.86
• Vapor Pressure: 0.132mmHg at 25°C
• Refractive Index: 1.4880-1.4920
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 1,4-DIPROPYLBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-DIPROPYLBENZENE(4815-57-0)
• EPA Substance Registry System: 1,4-DIPROPYLBENZENE(4815-57-0)

Safety Data

• Hazardous Substances Data: 4815-57-0(Hazardous Substances Data)

Usage

General Description

1,4-Dipropylbenzene is a chemical compound with the molecular formula C15H20. It belongs to the class of organic compounds known as alkylbenzenes, which are compounds containing a benzene ring substituted with at least one alkyl group. 1,4-Dipropylbenzene is a colorless, flammable liquid with a faint, sweet odor, and it is insoluble in water. It is primarily used as a solvent in various industrial applications, including the manufacturing of paints, coatings, and adhesives. Additionally, it is also used as a fragrance ingredient in perfumes and personal care products. However, it can pose health risks if inhaled or ingested in large quantities, and it is also a potential environmental hazard due to its toxicity to aquatic organisms.

InChI:InChI=1/C12H18/c1-3-5-11-7-9-12(6-4-2)10-8-11/h7-10H,3-6H2,1-2H3

Upstream product

• 106-94-5 propyl bromide 
• 71-43-2 benzene 
• 64-67-5 diethyl sulfate 
• 106-42-3 para-xylene 
• 28785-06-0 4-n-propylbenzaldehyde 
• 103-65-1 phenylpropane 
• 623-27-8 terephthalaldehyde, 
• 107549-75-7 1,4-bis(1-hydroxypropyl)benzene 
• 56147-30-9 1-(4-propyl-phenyl)-propan-1-one 

Downstream Products

• 857565-87-8 1-(2,5-dipropyl-phenyl)-ethanone 
• 103-65-1 phenylpropane 
• 17171-72-1 1,3-dipropyl-benzene 
• 40820-32-4 1,4-dibromo-2,5-dipropylbenzene 
• 1070768-73-8 1,4-diiodo-2,5-di(n-propyl)benzene 
• 64357-36-4 (2,5-Dipropyl-phenyl)-phenyl-methanone 
• 15181-14-3 1,3,5-tri(1-propyl)benzene 
• 41898-97-9 1,2,4-tri-n-propylbenzene 
• 857982-87-7 1-(2,5-dipropyl-phenyl)-propan-1-one 

Relevant articles and documents

Regioselective differentiation of vicinal methylene C-H bonds enabled by silver-catalysed nitrene transfer

Silver-catalyzed nitrene insertion enables the formation of benzosultams in good yield and with regioselectivity complementary to other transition metal nitrene-transfer catalysts. Preferential formation of six-membered benzosultam rings predominates for alkyl-substituted benzenesulphonamide precursors. Ligand-controlled tunability is also achieved for benzenesulphonamides with γ-branched alkyl substituents. Mechanistic probes suggest that the reaction pathway differs depending on whether a α (benzylic) or β (homobenzylic) C-H bond undergoes amidation, as well as the catalyst identity.

Photoelectron Spectra of Paracyclophane and Paracyclophane-4-ene. An Estimation of Inductive and Hyperconjugative Effect for Paracyclophanes

Based on the split of the first two bands in the photoelectron(PE)spectra of paracyclophane, paracyclophane-4-ene, 1,4-di-n-butyl-, 1,4-di-n-propyl- and 1,4-diethylbenzene as well as p-xylene it is shown that the inductive and hyperconjugative effec