4-n-Octyloxybenzoic acid Property

Melting point:

101-105 °C (lit.)

Boiling point:

353.47°C (rough estimate)

Density 

1.0589 (rough estimate)

refractive index 

1.5600 (estimate)

storage temp. 

Sealed in dry,Room Temperature

solubility 

almost transparency in hot Methanol

form 

powder to crystal

pka

4.48±0.10(Predicted)

color 

White to Almost white

CAS DataBase Reference

2493-84-7(CAS DataBase Reference)

EPA Substance Registry System

p-(Octyloxy)benzoic acid (2493-84-7)

Safety

Safety Statements 

24/25

WGK Germany 

3

TSCA 

Yes

HS Code 

29189990

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

4-n-Octyloxybenzoic acid Chemical Properties,Usage,Production

Chemical Properties

White to light yellow crystal powder

Uses

Intermediate for the synthesis of liquid crystals including chiral ferroelectric benzoates. Used in the preparation of medicinal compounds.

Definition

ChEBI: 4-(octyloxy)benzoic acid is a member of benzoic acids.

Preparation

Synthesis of 4-(Octyloxy)benzoic acid: 1-bromooctane was synthesised using n-octanol as raw material and 1-bromooctane was reacted with methyl p-hydroxybenzoate and then hydrolysed to obtain 4-(Octyloxy)benzoic acid.

General Description

P-n-octyloxybenzoic acid is a white powder. (NTP, 1992)

Air & Water Reactions

Insoluble in water.

Reactivity Profile

4-N-OCTYLOXYBENZOIC ACID is a carboxylic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in 4-N-OCTYLOXYBENZOIC ACID to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions.

Fire Hazard

Flash point data for 4-N-OCTYLOXYBENZOIC ACID are not available, however 4-N-OCTYLOXYBENZOIC ACID is probably combustible.

References

[1] F. A. KOLOKOLOV O. A R A V Shokurov. Ultrathin films based on luminescent complexes of 4-n-octyloxybenzoic acid with lanthanides[J]. Russian Chemical Bulletin, 2019, 67 12: 2230-2233. DOI:10.1007/s11172-018-2360-8.
[2] M. PETROV. Surface induced transitions in the nematic phase of 4-n octyloxybenzoic acid[J]. Journal De Physique Ii, 1992, 4 1: 1159-1193. DOI:10.1051/JP2:1992194.