4209-22-7

Usage

Uses

Used in Surfactant Production:
1-Bromotriacontane is used as a raw material for the production of surfactants, which are essential in various industries for their ability to reduce surface tension and stabilize emulsions.
Used in Lubricant Production:
As a component in the formulation of lubricants, 1-bromotriacontane contributes to the development of products that reduce friction and wear in mechanical systems.
Used in Coating Industry:
1-Bromotriacontane is utilized as a component in the production of coatings, enhancing their properties such as durability and resistance to environmental factors.
Used in Medicine:
Although not extensively detailed in the provided materials, 1-bromotriacontane has potential applications in the medical field, possibly due to its chemical properties and ability to interact with biological systems.
Used in Organic Synthesis:
1-Bromotriacontane serves as a chemical intermediate in organic synthesis, enabling the creation of a variety of complex organic compounds for different applications.
Used in Nanotechnology:
Leveraging its capacity to form self-assembled monolayers, 1-bromotriacontane is applied in nanotechnology to develop materials and devices with unique properties at the nanoscale.
It is crucial to exercise caution when handling 1-bromotriacontane due to its hazardous nature, ensuring that proper safety measures are implemented to protect individuals and the environment.

InChI:InChI=1/C30H61Br/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30-31/h2-30H2,1H3

Upstream product

• 593-50-0 melissyl alcohol 

Downstream Products

• 167026-72-4 4'-Hentriacontyl-2,2':6',2''-terpyridine 
• 145315-01-1 1-octatetracontanol 
• 1061586-94-4 hexakis(triacontyloxy)hexadehydrotribenzo[12]annulene 
• 1386991-54-3 4-(triacontyloxy)salicylaldehyde 

Relevant academic research and scientific papers

Correlation of anti-HIV potency with lipophilicity in a series of cosalane analogs having normal alkenyl and phosphodiester chains as cholestane replacements

In order to define the role of the cholestane moiety in the anti-HIV agent cosalane, a series of cosalane analogs was synthesized in which the cholestane ring system was replaced by normal alkenyl and phosphodiester substituents having varied chain lengths and lipophilicities. The compounds containing simple alkenyl substituents were found to be more potent as inhibitors of the cytopathic effect of HIV-1 in cell culture than the phosphodiesters. In addition, the potencies of the alkene congeners correlated positively with chain length and lipophilicity of the alkene. The results indicate that the cholestane moiety of cosalane functions as a lipophilic accessory appendage to escort the dichlorodisalicylmethane pharmacophore to a lipid environment.

Quantitative Treatment of the Rotational Dynamics of Flexible-Chain Molecules. 13C NMR Relaxation Study of Hydrocarbon Chains Attached to the Fluorene Anchor

13C spin-lattice relaxation times (T1) and nuclear Overhauser enhancements (NOEs) were measured for individual carbons in flexible-chain molecules consisting of a hydrocarbon chain attached to fluorene moiety at position 3 through an ester bond.Quantitative treatment of the relaxation data of the ring carbons revealed an anisotropic motion for all the molecules studied.The relaxation times of the chain carbons were analysed in terms of a correlation function describing multiple internal rotations about successive C-C bonds.The results (rotational diffusion constants) were used to discuss features of the chain mobility as a function of chain length and chain unsaturation.The assumptions involved in the quantitative treatment were examined and the values were compared with those of n-alkanes and lipid bilayers. - Keywords: 13C NMR spin-lattice relaxation times Rotational diffusion constants Rotational dynamics Overall and internal motions Hydrocarbon-chain esters of fluorene-3-carboxylic acid