3663-23-8

Basic information

• Product Name: 4-butylbenzene-1,2-diamine
• Synonyms: 4-butylbenzene-1,2-diamine;3,4-Diamino-1-butylbenzene;4-Butyl-1,2-benzenediamine;4-butylbenzene-1,2-diamine C10H16N2 164.25
• CAS NO: 3663-23-8
• Molecular Formula: C₁₀H₁₆N₂
• Molecular Weight: 164.24744
• EINECS: 222-917-7
• Mol File: 3663-23-8.mol

Chemical Properties

• Boiling Point: 302.3 °C at 760 mmHg
• Flash Point: 161.7 °C
• Appearance: /
• Density: 1.027 g/cm³
• Vapor Pressure: 0.000998mmHg at 25°C
• Refractive Index: 1.584
• CAS DataBase Reference: 4-butylbenzene-1,2-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-butylbenzene-1,2-diamine(3663-23-8)
• EPA Substance Registry System: 4-butylbenzene-1,2-diamine(3663-23-8)

Safety Data

• Hazardous Substances Data: 3663-23-8(Hazardous Substances Data)

Usage

Uses

Used in Chemical Production:
4-butylbenzene-1,2-diamine is utilized as a key intermediate in the synthesis of various chemical products, including dyes, pharmaceuticals, and polymers. Its presence in these industries is crucial for the development of a wide range of applications, from colorants to medicinal compounds.
Used as a Curing Agent in Epoxy Resins:
In the manufacturing sector, 4-butylbenzene-1,2-diamine serves as an effective curing agent for epoxy resins. Its role in this application is to facilitate the hardening and cross-linking of the resin, which is essential for producing strong and durable materials used in coatings, adhesives, and composites.
Used in Pharmaceutical Industry:
4-butylbenzene-1,2-diamine is used as a building block in the development of pharmaceuticals. Its chemical structure allows for the creation of various drug molecules, contributing to the advancement of medicinal chemistry and the treatment of different health conditions.
Used in Dye Industry:
In the dye industry, 4-butylbenzene-1,2-diamine is employed as a precursor for the production of dyes. Its chemical properties enable the creation of dyes with specific color characteristics, which are vital for applications in textiles, plastics, and printing inks.
Used in Polymer Industry:
4-butylbenzene-1,2-diamine is used as a monomer in the polymer industry. It contributes to the formation of polymers with unique properties, such as enhanced strength, flexibility, or chemical resistance, which are essential for various industrial and consumer applications.

InChI:InChI=1/C10H16N2/c1-2-3-4-8-5-6-9(11)10(12)7-8/h5-7H,2-4,11-12H2,1H3

Upstream product

• 3663-22-7 4-n-butyl-2-nitroaniline 
• 1126-78-9 N-(n-butyl)aniline 
• 62-53-3 aniline 
• 104-13-2 4-Butylaniline 
• 3663-21-6 N-(4-butyl-2-nitrophenyl)acetamide 
• 3663-20-5 N-(4-butylphenyl)acetamide 

Downstream Products

• 103853-61-8 5-butyl-1,3-dihydro-benzimidazol-2-one 
• 35198-65-3 C₁₈H₂₆N₄O₄S₂ 
• 35198-64-2 1,2-bis-(3-methoxycarbonyl-2-thioureido)-4-n-butylbenzene 
• 35266-34-3 1-methoxycarbonyl-3-(2-amino-4-n-butylphenyl)thiourea 
• 3663-24-9 5-n-butyl-1H-benzotriazole 

Relevant articles and documents

4-butylbenzene-1,2-diamine synthesis method

The invention discloses 4-butylbenzene-1,2-diamine synthesis method. The method includes steps: dissolving 4-butyl-2-nitroaniline into a solvent, adding aqueous solution which contains sodium sulfide,sodium thiosulfate and sodium hydrosulfite, performing heating reaction and TLC detection, filtering after reaction is finished, performing organic solvent extraction, and evaporating organic solventextract liquid to dry to obtain 4-butylbenzene-1,2-diamine. The method is low in equipment requirement, simple in operation, low in cost and suitable for industrial production, the reaction yield reaches 89.2%, and the crude product purity reaches 97% or above.

5-n-butyl-1H-benzotriazole synthesis process

The present invention discloses a 5-n-butyl-1H-benzotriazole synthesis process, which comprises: adding concentrated sulfuric acid to acetic anhydride in a dropwise manner, and adding 4-n-butyl aniline in a dropwise manner to prepare 4-n-butyl acetanilide; adding a mixed acid solution comprising 65% concentrated nitric acid and acetic anhydride to the 4-n-butyl acetanilide in a dropwise manner to synthesize 4-n-butyl-2-nitro acetanilide; synthesizing 4-n-butyl-2-nitroaniline by using the 4-n-butyl-2-nitro acetanilide, 95% ethanol and 40% sodium hydroxide as raw materials; under the effect of a catalyst, using the 4-n-butyl-2-nitroaniline and dehydrated alcohol and sequentially using nitrogen and hydrogen to convert under a closed condition to prepare 4-n-butyl-o-phenylenediamine; and adding the 4-n-butyl-o-phenylenediamine, water and sodium nitrite to an autoclave to synthesize the 5-n-butyl-1H-benzotriazole. According to the present invention, the process equipment is simple, and the product yield is high.

BENZIIMIDAZOLE AND IMIDAZOPYRIDINE DERIVATIVES AS SODIUM CHANNEL MODULATORS

The invention relates to benzimidazole and imidazopyridine derivatives, to their use in medicine, to compositions containing them, to processes for their preparation and to intermediates used in such processes. More particularly the invention relates to new Nav1.8 modulators of formula (I) or pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, R5, R6, R7. X and Y are as defined in the description. Nav1.8 modulators are potentially useful in the treatment of a wide range of disorders, particularly pain.

Quinoxaline compound, liquid crystal composition containing the compound, liquid crystal device using the composition, display apparatus and display method

A quinoxaline compound of the formula (I) according to claim 1 characterized by having at least one quinoxaline-2,6 (or 2,7)-diyl group is suitable as a component for a liquid crystal composition providing improved response characteristics and a high contrast. A liquid crystal device is constituted by disposing the liquid crystal composition between a pair of electrode plates. The liquid crystal device is used as a display panel constituting a display apparatus providing good display characteristics.

Organo-metal compositions, preparation and use

Complexes of a transition metal and a tetrasubstituted aromatic compound which contain at least two transition metal atoms. At least two of the substituents are -SH groups, the other two substituents being -SH, -OH and -NHR. The complexes are prepared by reacting the tetrasubstituted aromatic compound with a transition metal compound in the presence of a disubstituted aromatic compound. Depending on the relative proportions of the di- and tetra--substituted compounds, the resulting complex may contain more than one residue from the tetra-substituted compound and more than two transition metal atoms. The complexes possess infra-red absorbing properties which vary in dependence on the particular complex, the complexes with more than one residue from the tetrasubstituted compound absorbing radiation of longer wavelength. The compounds can be used to provide infra-red absorbing compositions, for example as a coating or inter-layer for glass. The complexes may be used together with one or more different infra-red absorbing materials. The tetra-substituted aromatic compound may be a tetra-thiol and this can be prepared from an aromatic compound containing at least four halogen substituents by reaction with an alkaline thiol compound in the presence of iron and sulphur in a polar solvent such as dimethyl formamide.

Nouveaux diamino-3,4 phenylalcanes et leur transformation en benzimidazolemethanethiols-2

We report five o-phenylenediamines which are substituted by an aliphatic chain containing n carbon atoms (n = 4, 6, 8, 10, 12).We describe a well adapted general synthetic method using Schmidt's reaction.The diamines were then transformed into 2-benzimidazolemethanethiols and their related S-methyl derivatives which structures were checked by (1)H NMR.

Perfluoroalkyl benzodiazepines

New perfluoroalkyl derivatives of benzodiazepine are prepared by reacting an orthophenylenediamine with a beta-diketone at least one of whose alkyls is a C1 - C15 perfluoroalkyl. The stable products are useful as heat-exchange substances and as surfactants in organic solution.

Alkyl 4-(o-aminophenyl)-3-thioallophanates

Various alkyl 4-(o-aminophenyl)-3-thioallophanates and alkyl 4-(o-alkylaminophenyl)-3-thioallophanates are useful as fungicides and mite ovicides. The compounds are prepared by reacting an o-phenylenediamine with the appropriate alkoxycarbonylisothiocyanate and an exemplary species is methyl 4-(o-aminophenyl)-3-thioallophanate.