3007-70-3

Basic information

• Product Name: N-heptylaniline
• Synonyms: N-heptylaniline;N-Heptylbenzenamine;Phenylheptylamine
• CAS NO: 3007-70-3
• Molecular Formula: C₁₃H₂₁N
• Molecular Weight: 191.3125
• Mol File: 3007-70-3.mol
• Article Data: 42

Chemical Properties

• Boiling Point: 293.4°Cat760mmHg
• Flash Point: 131.5°C
• Appearance: /
• Density: 0.92g/cm³
• Vapor Pressure: 0.00173mmHg at 25°C
• Refractive Index: 1.524
• PKA: 5.05±0.50(Predicted)
• CAS DataBase Reference: N-heptylaniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-heptylaniline(3007-70-3)
• EPA Substance Registry System: N-heptylaniline(3007-70-3)

Safety Data

• Hazardous Substances Data: 3007-70-3(Hazardous Substances Data)

Usage

General Description

N-heptylaniline is a chemical compound composed of a heptyl group and an aniline group. It is a clear to pale yellow liquid with a molecular formula of C13H19N and a molecular weight of 193.29 g/mol. N-heptylaniline is commonly used in the manufacturing of dyes, pigments, and pharmaceuticals. It is also utilized in the production of rubber and plastic chemicals, as well as in the synthesis of other organic compounds. N-heptylaniline is considered to be a hazardous substance and should be handled with care, as it can cause skin and eye irritation upon contact.

InChI:InChI=1/C13H21N/c1-2-3-4-5-9-12-14-13-10-7-6-8-11-13/h6-8,10-11,14H,2-5,9,12H2,1H3

Upstream product

• 111-71-7 heptanal 
• 98-95-3 nitrobenzene 
• 62-53-3 aniline 
• 629-04-9 1-Bromoheptane 
• 1227476-15-4 Azobenzene 
• 64-17-5 ethanol 
• 127-09-3 sodium acetate 
• 4282-40-0 1-Iodoheptane 
• 111-68-2 1-Heptylamine 
• 98-80-6 phenylboronic acid 
• 369360-94-1 N-heptyl-N-phenylhydrazine 
• 135-19-3 β-naphthol 
• 142-82-5 n-heptane 
• 591-50-4 iodobenzene 

Downstream Products

• 37529-27-4 4-heptylaniline 
• 62-53-3 aniline 
• 20330-65-8 N-(4-heptylphenyl)acetamide 
• 132902-66-0 N-heptyl-N-methylaniline 
• 37877-51-3 N-heptyl-toluene-4-sulfonanilide 

Relevant articles and documents

Reusable Co-nanoparticles for general and selectiveN-alkylation of amines and ammonia with alcohols

A general cobalt-catalyzedN-alkylation of amines with alcohols by borrowing hydrogen methodology to prepare different kinds of amines is reported. The optimal catalyst for this transformation is prepared by pyrolysis of a specific templated material, which is generatedin situby mixing cobalt salts, nitrogen ligands and colloidal silica, and subsequent removal of silica. Applying this novel Co-nanoparticle-based material, >100 primary, secondary, and tertiary amines includingN-methylamines and selected drug molecules were conveniently prepared starting from inexpensive and easily accessible alcohols and amines or ammonia.

A base-free Chan–Lam reaction catalyzed by an easily assembled Cu(II)-carboxylate metal-organic framework

A new copper(II) metal-organic framework is constructed as a sustainable copper heterogeneous catalyst. Cu-DPTCA, with high catalytic activity, can effectively promote the Chan–Lam coupling reaction of arylboronic acids and amines without adding any base or additive.

Atomically dispersed Rh on hydroxyapatite as an effective catalyst for tandem hydroaminomethylation of olefins

Tandem hydroaminomethylation is an efficient and green route for one-pot synthesis of amines directly from olefins. Herein, heterogeneous hydroxyapatite (HAP) supported single-atom Rh catalyst was prepared and used for tandem hydroaminomethylation of olefins. Characterization techniques confirmed the atomic dispersion of Rh species on HAP. Up to 99% conversion of 1-hexene with high selectivity to the desired amines (93.2%) was obtained over 0.5Rh1/HAP catalyst. Mechanism study demonstrated that the first hydroformylation step during the tandem catalytic process was rate-determining. Compared with the Rh nanoparticles on other oxide supports (Mg3Al, MgO and Al2O3), the atomically dispersed Rh sites on HAP ensured the high hydroformylation activity, thereby guaranteed the outstanding catalytic performance for the total tandem process. Furthermore, various corresponding amines can be obtained with satisfactory yields over 0.5Rh1/HAP catalyst from a wide scope of olefins or amines substrates.