103037-27-0

Basic information

• Product Name: 3-Heptylpyridine
• Synonyms: 3-Heptylpyridine;Pyridine, 3-heptyl;pyridine, 3-heptyl-
• CAS NO: 103037-27-0
• Molecular Formula: C₁₂H₁₉N
• Molecular Weight: 177.28596
• Mol File: 103037-27-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 258.5 °C at 760 mmHg
• Flash Point: 123.1 °C
• Appearance: /
• Density: 0.895g/cm³
• Vapor Pressure: 0.0221mmHg at 25°C
• Refractive Index: 1.488
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3-Heptylpyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Heptylpyridine(103037-27-0)
• EPA Substance Registry System: 3-Heptylpyridine(103037-27-0)

Safety Data

• Hazardous Substances Data: 103037-27-0(Hazardous Substances Data)

Usage

General Description

3-Heptylpyridine is a chemical compound with the molecular formula C12H21N. It is a colorless to pale yellow liquid with a strong, unpleasant odor. 3-Heptylpyridine is mainly used as a flavor and fragrance ingredient due to its strong, roasted coffee-like odor. It is commonly found in food and beverage products, as well as in cosmetic and personal care products. Additionally, 3-Heptylpyridine has been studied for its potential antimicrobial and insecticidal properties, making it a versatile compound with various industrial applications. However, it is important to handle this chemical with care, as it has been identified as a skin and eye irritant and may have harmful effects if ingested or inhaled in large quantities.

InChI:InChI=1/C12H19N/c1-2-3-4-5-6-8-12-9-7-10-13-11-12/h7,9-11H,2-6,8H2,1H3

Upstream product

• 108-99-6 3-Methylpyridine 
• 638-45-9 1-Iodohexane 
• 110-86-1 pyridine 
• 107264-14-2 diphenylmethanone O-octanoyl oxime 

Relevant articles and documents

AGENT FOR IMPROVING PERMEATION OF A DRUG INTO A NAIL AND AN EXTERNAL TREATING AGENT CONTAINING THE SAME

The present invention herein provides a compound which promotes drug-permeation into nails. A penetrating promoter comprises, for instance, the following formulas. R1, R2 and R3 are alkyl groups having a carbon number of 1 to 15 and have OH groups at their ends.

Surprising substituent effects on the self-assembly of helicates from bis(bipyridyl) BINOL ligands

(Figure Presented) A number of different bis(bipyridyl) BINOL ligands were prepared using a convergent building block approach. These were studied with regard to their ability to undergo self-assembly to dinuclear helicates upon coordination to suitable late-transition-metal ions. Surprisingly, the substituents at the periphery of the ligand structure were found to have a marked influence on the outcome of the self-assembly processes with regard to the helicates composition, the stereoselectivity of the helicate formation, their redox reactivity, and their electronical properties as scrutinized by NMR- and CD-spectroscopic methods as well as ESI-mass spectrometric methods.

Synthesis of substituted 2,2′-bipyridines from 2-bromo- or 2-chloropyridines using tetrakis(triphenylphosphine)palladium(0) as a catalyst in a modified Negishi cross-coupling reaction

A protocol for an efficient, modified Negishi cross-coupling strategy for substituted 2,2′-bipyridines employing tetrakis(triphenylphosphine) palladium(0) as a simple, commercially available, and relatively inexpensive catalyst for both 2-bromo- and 2-chl