27830-12-2

Usage

Uses

Used in Sunscreen and Cosmetic Products:
2-n-Octyloxybenzoic acid is used as a UV filter for its capacity to absorb and dissipate UV radiation, providing protection against skin damage and premature aging. It is particularly valued for its low skin irritation potential, making it suitable for sensitive skin types.
Used in Waterproof and Sweat-Resistant Sunscreens:
2-n-Octyloxybenzoic acid is used as an ingredient in waterproof and sweat-resistant sunscreens, ensuring effective protection during outdoor and water activities. Its ability to maintain its protective properties under such conditions makes it a preferred choice for active individuals.
Used in Antioxidant and Antimicrobial Applications:
2-n-Octyloxybenzoic acid is being studied for its potential antioxidant properties, which could contribute to the prevention of oxidative stress and related skin conditions. Additionally, its antimicrobial properties are of interest for applications that require protection against microbial infections and contamination.

InChI:InChI=1/C15H22O3/c1-2-3-4-5-6-9-12-18-14-11-8-7-10-13(14)15(16)17/h7-8,10-11H,2-6,9,12H2,1H3,(H,16,17)

Upstream product

• 119-36-8 methyl salicylate 
• 111-83-1 1-bromo-octane 
• 255062-85-2 2-octyloxybenzoic acid methyl ester 

Downstream Products

• 13736-58-8 2-(octyloxy)-5-nitro-benzoic acid 
• 62435-37-4 methyl 4-(octyloxy)benzoate 
• 26090-29-9 4-(2-Octyloxy-benzoylamino)-benzoic acid 2-diethylamino-ethyl ester 
• 26095-59-0 otilonium bromide 
• 267897-55-2 N-(carboxymethyl)-5-acetamido-2-(octyloxy)benzamide 
• 267897-54-1 N-((ethoxycarbonyl)methyl)-5-acetamido-2-(octyloxy)benzamide 
• 267897-52-9 N-((ethoxycarbonyl)methyl)-5-amino-2-(octyloxy)benzamide 
• 416899-35-9 5-((((5-hydroxycarbonyl-2,4-dioctyloxy)phenylcarbonyl)aminomethylcarbonyl)ammino)-2-octyloxy-N-hexylbenzamide 
• 416899-34-8 5-((((5-methoxycarbonyl-2,4-dioctyloxy)phenylcarbonyl)aminomethylcarbonyl)amino)-2-octyloxy-N-hexylbenzamide 
• 267897-50-7 N-((ethoxycarbonyl)methyl)-2-(octyloxy)-5-nitrobenzamide 
• 416899-33-7 5-(aminomethylcarbonylamino)-2-octyloxy-N-hexylbenzamide 
• 416899-32-6 5-(((phenylmethoxy)carbonyl)aminomethylcarbonylamino)-2-octyloxy-N-hexylbenzamide 
• 267897-53-0 N-hexyl-5-amino-2-(octyloxy)benzamide 
• 267897-51-8 N-hexyl-2-(octyloxy)-5-nitrobenzamide 

Relevant academic research and scientific papers

ANTIBIOTIC AMMONIUM COMPOUNDS AND METHODS FOR THE TREATMENT OF BACTERIAL INFECTIONS

The present disclosure provides ammonium compounds, e.g., compounds according to Formula I as set forth herein, which are useful as antimicrobial agents. Methods for the treatment of bacterial infections and associated conditions, e.g., gastrointestinal conditions, are also described, as well as methods for altering the microbiome of subjects such as humans.

Preparation method of octylonium bromide

The invention belongs to the field of drug synthesis, and provides a preparation method of octylonium bromide. The preparation method of the octylonium bromide comprises the following steps: synthesizing methyl o-octyloxybenzoate from methyl salicylate as

Highly Ordered Nanoporous Films from Supramolecular Diblock Copolymers with Hydrogen-Bonding Junctions

We designed efficient precursors that combine complementary associative groups with exceptional binding affinities and thiocarbonylthio moieties enabling precise RAFT polymerization. Well defined PS and PMMA supramolecular polymers with molecular weights up to 30 kg mol?1are synthesized and shown to form highly stable supramolecular diblock copolymers (BCPs) when mixed, in non-polar solvents or in the bulk. Hierarchical self-assembly of such supramolecular BCPs by thermal annealing affords morphologies with excellent lateral order, comparable to features expected from covalent diblock copolymer analogues. Simple washing of the resulting materials with protic solvents disrupts the supramolecular association and selectively dissolves one polymer, affording a straightforward process for preparing well-ordered nanoporous materials without resorting to crosslinking or invasive chemical degradations.

A branched, hydrogen-bonded heterodimer: a novel system for achieving high stability and specificity

Presented is a description of the design, synthesis, and characterization of a novel, branched, six hydrogen-bonded heterodimer termed 'trident'. Two branched oligoamide molecules, 1 and 2, with complementary hydrogen-bonding sequences 3(AD) and 3(DA), re

Cyclic hexapeptide compounds

Compounds of the formula STR1 wherein R1 is hydrogen or hydroxyl; R2 is hydrogen; hydroxyl or methyl, R3 is hydrogen or hydroxyl; R4 is C5 -C23 alkyl, C5 -C23 alkenyl, aryl or substituted aryl; R5 is --CH2 OH, --CH(CH3)OH, --CH(CH2 CONH2)OH; R6 is --CH2 OH or --CH(CH3)OH; R is --CH2 OH or --CH(CH3)OH; provided that when R4 is --(CH2)8 CH(CH3)CH2 CH(CH3)C2 H5, R5 is --CH2 OH or --CH(CH3)OH. The compounds are useful as antimicrobial agents, especially as antifungal agents.

Alkylphenyl 3-cyano or fluoro-4-alkyloxybenzoates and mesomorphic mixtures thereof

An organic compound having a high negative dielectric anisotropy is capable, by mixing with a nematic liquid crystal, of improving the dynamic scattering effect of the liquid crystal. The organic compounds have the formula: STR1 in which R is either a flu