255062-85-2

Basic information

• Product Name: Methyl 2-(octyloxy)benzoate
• Synonyms: Methyl 2-(octyloxy)benzoate
• CAS NO: 255062-85-2
• Molecular Formula: C₁₆H₂₄O₃
• Molecular Weight: 264.35996
• EINECS: 1806241-263-5
• Mol File: 255062-85-2.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 356.4 °C at 760 mmHg
• Flash Point: 148.5 °C
• Appearance: /
• Density: 0.99g/cm³
• Vapor Pressure: 2.93E-05mmHg at 25°C
• Refractive Index: 1.489
• CAS DataBase Reference: Methyl 2-(octyloxy)benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 2-(octyloxy)benzoate(255062-85-2)
• EPA Substance Registry System: Methyl 2-(octyloxy)benzoate(255062-85-2)

Safety Data

• Hazardous Substances Data: 255062-85-2(Hazardous Substances Data)

Usage

General Description

Methyl 2-(octyloxy)benzoate, also known as Octyl Salicylate, is a chemical compound commonly used in the production of sunscreen and other cosmetic products. It belongs to the family of organic esters and is derived from salicylic acid. Its primary function is to absorb and filter UVB rays from the sun, providing protection to the skin from sunburn and sun damage. It is easily absorbed by the skin and is known for its non-greasy and lightweight texture, making it a popular ingredient in sunscreen lotions and creams. Additionally, it is commonly used in hair care products, lip balms, and other personal care items for its UV protection properties.

InChI:InChI=1/C16H24O3/c1-3-4-5-6-7-10-13-19-15-12-9-8-11-14(15)16(17)18-2/h8-9,11-12H,3-7,10,13H2,1-2H3

Upstream product

• 111-83-1 1-bromo-octane 
• 119-36-8 methyl salicylate 

Downstream Products

• 26095-59-0 otilonium bromide 
• 26090-29-9 4-(2-Octyloxy-benzoylamino)-benzoic acid 2-diethylamino-ethyl ester 
• 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 
• 416899-33-7 5-(aminomethylcarbonylamino)-2-octyloxy-N-hexylbenzamide 
• 416899-32-6 5-(((phenylmethoxy)carbonyl)aminomethylcarbonylamino)-2-octyloxy-N-hexylbenzamide 
• 787629-33-8 C₅₇H₇₈N₈O₁₂ 
• 787629-32-7 2-methoxy-3-{N'-[5-(N'-{2-methoxy-3-[N'-(2-octyloxy-benzoyl)-hydrazinocarbonyl]-benzoyl}-hydrazinocarbonyl)-2,4-bis-octyloxy-benzoyl]-hydrazinocarbonyl}-benzoic acid methyl ester 
• 787629-28-1 5-(N'-{2-Methoxy-3-[N'-(2-octyloxy-benzoyl)-hydrazinocarbonyl]-benzoyl}-hydrazinocarbonyl)-2,4-bis-octyloxy-benzoic acid hydrazide 
• 787629-31-6 5-(N'-{2-methoxy-3-[N'-(2-octyloxy-benzoyl)-hydrazinocarbonyl]-benzoyl}-hydrazinocarbonyl)-2,4-bis-octyloxy-benzoic acid methyl ester 
• 787629-30-5 2-Methoxy-3-[N'-(2-octyloxy-benzoyl)-hydrazinocarbonyl]-benzoic acid hydrazide 
• 787629-29-2 2-methoxy-3-[N'-(2-octyloxy-benzoyl)-hydrazinocarbonyl]-benzoic acid methyl ester 
• 774236-33-8 5-(3-hydroxy-3-methyl-but-1-ynyl)-2-octyloxy-benzoic acid methyl ester 
• 774236-34-9 5-(3-hydroxy-3-methylbut-1-ynyl)-2-(n-octyloxy)benzoic acid 

Relevant articles and documents

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.

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 highly stable, six-hydrogen-bonded molecular duplex

This paper describes the design, synthesis, and characterization of a hydrogen-bonded molecular duplex (3·4). Two oligoamide molecular strands, 3 and 4, with the complementary hydrogen-bonding sequences ADAADA and DADDAD, respectively, were found to form