110141-48-5

Basic information

• Product Name: 3-Nonanoylpyridine
• Synonyms: 3-Nonanoylpyridine;1-(Pyridin-3-yl)nonan-1-one
• CAS NO: 110141-48-5
• Molecular Formula: C14H21NO
• Molecular Weight: 219.32264
• Mol File: 110141-48-5.mol

Chemical Properties

• Boiling Point: 334.3±15.0 °C(Predicted)
• Appearance: /
• Density: 0.954±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 3.25±0.10(Predicted)
• CAS DataBase Reference: 3-Nonanoylpyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Nonanoylpyridine(110141-48-5)
• EPA Substance Registry System: 3-Nonanoylpyridine(110141-48-5)

Safety Data

• Hazardous Substances Data: 110141-48-5(Hazardous Substances Data)

Usage

Uses

Used in Natural Gas Industry:
3-Nonanoylpyridine is used as an odorant in natural gas for the critical purpose of alerting individuals to the presence of gas leaks. The strong, pungent smell serves as a crucial safety measure, ensuring that people can detect and respond to potential gas hazards promptly.
Used in Perfumery:
In the fragrance industry, 3-Nonanoylpyridine is employed as a component in the manufacturing of perfumes. Its unique scent characteristics contribute to the complex aroma profiles of various perfumes, enhancing their appeal and longevity.
Used in Flavoring Agents:
3-Nonanoylpyridine also finds application in the food and beverage industry, where it is used as a flavoring agent. Its distinct odor can add depth and complexity to the taste profiles of different products.
Used in Insect Repellent Research:
3-Nonanoylpyridine has been studied for its potential as an insect repellent, particularly effective against mosquitoes. This application is still in the research phase, but it holds promise for developing new, effective insect control methods.

Upstream product

• 100-54-9 pyridine-3-carbonitrile 
• 60-29-7 diethyl ether 
• 111-83-1 1-bromo-octane 
• 500-22-1 3-pyridinecarboxaldehyde 

Relevant articles and documents

Practical one-pot preparation of ketones from aryl and alkyl bromides with aldehydes and DIH via Grignard reagents

Various diaryl ketones, alkyl aryl ketones, and dialkyl ketones were efficiently prepared in good yields by the reactions of the Grignard reagents derived from aryl or alkyl bromides, followed by the reactions with aromatic or aliphatic aldehydes and the subsequent treatment with 1,3-diiodo-5,5- dimethylhydantoin and K2CO3, in a one-pot method. The same treatment of aromatic bromides bearing electron-withdrawing groups, such as ester, nitrile, ketone, and nitro groups with i-PrMgCl·LiCl or PhMgCl instead of Mg, also provided the corresponding diaryl and alkyl aryl ketones in good yields. The above methods are simple and practical transition-metal-free methods for the preparation of various diaryl ketones and alkyl aryl ketones bearing electron-rich aromatic groups and electron-deficient aromatic groups, as well as dialkyl ketones.

Pharmaceutical use of [[[(3-pyridinyl)methylen]amino]oxy]alkanoic acids and esters

Novel [[[(3-pyridinyl)methylen]amino]oxy]alkanoic acids and esters, compositions containing the same, and methods of treating clinical conditions related with the production of thromboxane A2, prostacyclin and/or prostaglandins D2, E