4434-66-6

Usage

Uses

Used in Organic Synthesis:
1-Bromononadecane is used as a chemical intermediate for the synthesis of various organic compounds. Its reactivity allows it to participate in a range of chemical reactions, making it a valuable component in the production of specialty chemicals.
Used in Surfactant Production:
In the surfactant industry, 1-Bromononadecane is utilized as a raw material to produce surfactants that lower the surface tension between liquids and solids, enhancing the effectiveness of cleaning and emulsifying agents.
Used in Lubricant Formulation:
1-Bromononadecane serves as a component in the formulation of lubricants, contributing to their viscosity and performance characteristics, which are essential for reducing friction and wear in mechanical applications.
Used as a Dispersant:
In the production of dispersants, 1-Bromononadecane is used to improve the distribution of particles in a medium, preventing the formation of agglomerates and ensuring a uniform mixture.
Used in Pharmaceutical Manufacturing:
1-Bromononadecane is employed in the synthesis of pharmaceuticals, where its unique chemical properties contribute to the development of new drugs and active pharmaceutical ingredients.
Used in Agrochemical Production:
1-BROMONONADECANE also finds application in the agrochemical industry, where it is used in the synthesis of various agrochemicals, including pesticides and herbicides, to enhance crop protection and yield.
Given the potential health hazards associated with 1-Bromononadecane, it is crucial to handle this chemical with care, adhering to safety guidelines and regulations to ensure the well-being of individuals and the environment.

InChI:InChI=1/C19H39Br/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20/h2-19H2,1H3

Upstream product

• 3344-77-2 12-bromododecanol 
• 51795-88-1 1-bromo-10-(tetrahydropyranyloxy)decane 
• 53463-68-6 1-bromo-10-decanol 
• 112-47-0 1,10-Decanediol 
• 646-30-0 nonadecanoic acid 
• 629-04-9 1-Bromoheptane 
• 1454-84-8 nonadecan-1-ol 

Downstream Products

• 55791-69-0 4-(n-nonadecylamino)benzoic acid 
• 1254966-90-9 5-(nonadecane-1-sulfonyl)-1-phenyl-1H-tetrazole 
• 593-50-0 melissyl alcohol 
• 55791-68-9 4-Nonadecylamino-benzoic acid ethyl ester 

Relevant academic research and scientific papers

The synthesis of single enantiomers of a meromycolic acid

3-Oxa-2,4-dioxobicyclo[3.1.0]hexane provides a flexible starting material for the preparation of single enantiomers of a meromycolic acid, a long chain fatty acid containing two remote cis-cyclopropanes. (C) 2000 Elsevier Science Ltd.

Microwave and ultrasound assisted first synthesis of 12-hydroxyhentriacontane

An aliphatic alcohol 12-hydroxyhentriacontane has been synthesised for the first time. The synthetic route of this naturally occurring alcohol adopts the techniques of microwave and ultrasonic irradiation. The synthetic approach provided enough material to corroborate the structure of the target molecule which had been isolated from leaves of Ziziphus mauritiana and exhibits excellent anti-inflammatory, antibacterial and antimicrobial properties.

The synthesis of a single enantiomer of a major α-mycolic acid of M. tuberculosis

We report a synthesis of a single enantiomer of a mycolic acid from Mycobacterium tuberculosis containing a di-cis-cyclopropane. The method can be simply varied to modify the chain lengths or the absolute stereochemistry of either cyclopropane.

Anti-mycobacterial compositions and their use for the treatment of tuberculosis and related diseases

Compounds, pharmaceutical compositions, and methods for the treatment of mycobacterial diseases, such as tuberculosis and leprosy, are provided. Use of the compounds for promoting an antiseptic condition of a surface are also included. Some of the preferred compounds include thiatetracosanoic acids, esters, and fluorinated analogs.

UNSATURATED ANALOGUES OF 1-TRIACONTANOL

A simple regio- and stereoselective synthesis of unsaturated analogues of the plant growth stimulator 1-triacontanol from ω-alkyn-1-ols is reported.Starting from the easily accessible 10-undecyn-1-ol, eight n-C30 alcohols containing , (E) -C=C- or (Z) -C=C- group in the position 21 and/or 10 have been prepared.Spectral and gas-chromatographic properties (Kovats retention indices) of the novel compounds are described.