ChemicalBook >> CAS DataBase List >>4-n-Octyloxybenzoic acid

4-n-Octyloxybenzoic acid

CAS No.
2493-84-7
Chemical Name:
4-n-Octyloxybenzoic acid
Synonyms
OOBA;TIMTEC-BB SBB008044;RARECHEM AL BO 0490;octyloxybenzoicacid;p-Octoxybenzoic acid;4-octoxybenzoic acid;4-OCTYLOXYBENZOIC ACID;LABOTEST-BB LT00114432;4-(octyloxy)-benzoicaci;p-n-octyloxybenzoicacid
CBNumber:
CB7169458
Molecular Formula:
C15H22O3
Molecular Weight:
250.33
MDL Number:
MFCD00013993
MOL File:
2493-84-7.mol
Last updated:2024-12-18 14:15:30

4-n-Octyloxybenzoic acid Properties

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)
FDA UNII 04GD4OJ7FU
EPA Substance Registry System p-(Octyloxy)benzoic acid (2493-84-7)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
Safety Statements  24/25
WGK Germany  3
TSCA  Yes
HS Code  29189990
NFPA 704
0
0 0

4-n-Octyloxybenzoic acid price More Price(12)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 363200 4-(Octyloxy)benzoic acid 98% 2493-84-7 10g $90.4 2023-06-20 Buy
TCI Chemical O0117 4-n-Octyloxybenzoic Acid >98.0%(GC)(T) 2493-84-7 25g $89 2024-03-01 Buy
Alfa Aesar B22659 4-n-Octyloxybenzoic acid, 98% 2493-84-7 10g $41.3 2021-12-16 Buy
Alfa Aesar B22659 4-n-Octyloxybenzoic acid, 98% 2493-84-7 50g $164 2021-12-16 Buy
TRC O148550 4-n-Octyloxybenzoic Acid 2493-84-7 500mg $60 2021-12-16 Buy
Product number Packaging Price Buy
363200 10g $90.4 Buy
O0117 25g $89 Buy
B22659 10g $41.3 Buy
B22659 50g $164 Buy
O148550 500mg $60 Buy

4-n-Octyloxybenzoic acid Chemical Properties,Uses,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.

4-n-Octyloxybenzoic acid Preparation Products And Raw materials

Raw materials

Preparation Products

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4-OCTYLOXYBENZOIC ACID 4-N-OCTYLOXYBENZOIC ACID PARA-N-OCTYLOXYBENZOICACID 4-[(Oct-1-yl)oxy]benzoic acid 4-n-Octyloxybenzoic Acid LABOTEST-BB LT00114432 RARECHEM AL BO 0490 P-(OCTYLOXY)BENZOIC ACID TIMTEC-BB SBB008044 4-n-Octyloxybenzoicacid,99% 4-Octyloxybenzoic acid,98% 4-(octyloxy)-benzoicaci Benzoic acid, 4-(octyloxy)- Benzoic acid, p-(octyloxy)- octyloxybenzoicacid OOBA p-n-Octyloxybenzoic acid p-n-octyloxybenzoicacid p-Octoxybenzoic acid 4-octoxybenzoic acid 4-n-OctyloxybenzoicAcid> 2493-84-7 CH3CH27OC6H4CO2H Benzoic Acids (Building Blocks for Liquid Crystals) Building Blocks for Liquid Crystals Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts Benzoic acid Acids & Esters Anisoles, Alkyloxy Compounds & Phenylacetates Benzoic Acids (Building Blocks for Liquid Crystals) Building Blocks for Liquid Crystals Functional Materials Building block Liquid Crystals Organic Electronics and Photonics