1571-86-4

Basic information

• Product Name: 1,4-DI-N-BUTYLBENZENE
• Synonyms: 1,4-DIBUTYLBENZENE;1,4-DI-N-BUTYLBENZENE;Benzene, 1,4-dibutyl;benzene,1,4-dibutyl-;p-dibutylbenzene;1,4-DI-N-BUTYLBENZENE 97%;1,4-Di-n-butylbenzene, 97+%
• CAS NO: 1571-86-4
• Molecular Formula: C₁₄H₂₂
• Molecular Weight: 190.32
• Mol File: 1571-86-4.mol
• Article Data: 9

Chemical Properties

• Melting Point: -31--30°C
• Boiling Point: 97-99°C 3mm
• Flash Point: 110°(230°F)
• Appearance: /
• Density: 0,856 g/cm3
• Vapor Pressure: 0.0167mmHg at 25°C
• Refractive Index: 1.4890
• CAS DataBase Reference: 1,4-DI-N-BUTYLBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-DI-N-BUTYLBENZENE(1571-86-4)
• EPA Substance Registry System: 1,4-DI-N-BUTYLBENZENE(1571-86-4)

Safety Data

• Safety Statements: 24/25
• Hazardous Substances Data: 1571-86-4(Hazardous Substances Data)

Usage

General Description

1,4-DI-N-BUTYLBENZENE is a colorless liquid chemical with a distinct sweet odor that is used as a solvent in industrial processes. It is primarily used as an intermediate in the production of other chemicals and as a solvent in the manufacturing of adhesives, coatings, and sealants. It is classified as a hazardous substance due to its flammability and potential to cause irritation to the skin, eyes, and respiratory system. 1,4-DI-N-BUTYLBENZENE is not known to be carcinogenic, but precautions should be taken to avoid prolonged exposure and inhalation. It should be handled and stored in accordance with strict safety guidelines to minimize the risk of accidents and environmental harm.

InChI:InChI=1/C14H22/c1-3-5-7-13-9-11-14(12-10-13)8-6-4-2/h9-12H,3-8H2,1-2H3

Upstream product

• 149834-47-9 1,4-Bis-((E)-but-1-enyl)-benzene 
• 85732-07-6 1,4-Bis(1-butenyl)benzol 
• 122-56-5 tributyl borane 
• 17763-88-1 1,4-phenylene bis(trifluoromethanesulfonate) 
• 92273-73-9 n-butylzinc bromide 
• 624-38-4 para-diiodobenzene 
• 589-87-7 1,4-bromoiodobenzene 
• 106-37-6 1.4-dibromobenzene 
• 106-38-7 para-bromotoluene 
• 106-46-7 para-dichlorobenzene 
• 106-39-8 bromochlorobenzene 
• 13505-46-9 1,4-bis-(3-oxo-but-1-enyl)-benzene 
• 495-40-9 propiophenone 
• 104-51-8 1-butylbenzene 

Downstream Products

• 85-01-8 phenanthrene 
• 37920-25-5 1-(4-butylphenyl)ethanone 
• 78210-22-7 1,4-dibutyl-2-nitro-benzene 
• 683239-08-9 1,4-dibutyl-2,3,5,6-tetrabromobenzene 
• 108-88-3 toluene 
• 200713-92-4 1,4-Dibromo-2,5-di-n-butylbenzene 
• 107917-05-5 1,4-Dibutyl-cyclohexan 
• 32937-58-9 1-(2,5-dibutyl-phenyl)-ethanone 
• 20062-04-8 2,5-dibutylbenzene-1-sulfonyl chloride 
• 200713-94-6 2,5-dibutylbenzene-1,4-dicarbaldehyde 
• 1373042-26-2 2,2'-(2,5-dibutylbenzene-1,4-diyl)bis(5,5-dimethyl-1,3-dioxane) 
• 64357-70-6 (2,5-Dibutyl-phenyl)-phenyl-methanone 
• 32917-60-5 2,5-Di-n-butylstyrol 
• 32917-54-7 2,5-Di-n-butylphenyl-methylcarbinol 

Relevant articles and documents

Molecular rods based on oligo-spiro-thioketals

We report on an extension of the previously established concept of oligospiroketal (OSK) rods by replacing a part or all ketal moieties by thioketals leading to oligospirothioketal (OSTK) rods. In this way, some crucial problems arising from the reversible formation of ketals are circumvented. Furthermore, the stability of the rods toward hydrolysis is considerably improved. To successfully implement this concept, we first developed a number of new oligothiol building blocks and improved the synthetic accessibility of known oligothiols, respectively. Another advantage of thioacetals is that terephthalaldehyde (TAA) sleeves, which are too flexible in the case of acetals can be used in OSTK rods. The viability of the OSTK approach was demonstrated by the successful preparation of some OSTK rods with a length of some nanometers.

Palladium-catalyzed cross-coupling alkylation of arenediazonium o-benzenedisulfonimides

Arenediazonium o-benzenedisulfonimides were reacted with tetramethyltin, tetrabutyltin or trialkylboranes. The reactions, carried out in the presence of palladium(II) derivatives as precatalysts, gave the methylation and alkylation products with good over

Tetraorganoindates as Nucleophilic Coupling Partners in Pd-Catalyzed Cross-Coupling Reactions

(Equation presented) In situ generated ate complex In situ-generated tetraorganoindate complexes from the reaction of 1 equiv of indium trichloride with 4 equiv of appropriate organometallics are efficient nucleophiles in Pd-catalyzed cross-coupling reactions. In this novel reaction tetraorganoindates containing methyl, 1°- and 2°-alkyl, vinyl, alkynyl, and aryl groups transfer the four organic groups to a variety of electrophiles with high atom efficiency.