HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-(Octyloxy)benzoic acid
OOBA · TIMTEC-BB SBB008044 · RARECHEM AL BO 0490 · octyloxybenzoicacid · 4-octoxybenzoic acid · p-Octoxybenzoic acid · 4-OCTYLOXYBENZOIC ACID · LABOTEST-BB LT00114432
Identifikatoren & physikalische Daten
| CAS No. | 2493-84-7 |
|---|---|
| Summenformel | C15H22O3 |
| Durchschnittliche Molmasse | 250,33 g/mol |
| Monoisotopische Masse | 250,15689456 g/mol |
| SMILES | CCCCCCCCOc1ccc(C(=O)O)cc1 |
| InChIKey | IALWCYFULVHLEC-UHFFFAOYSA-N |
| PubChem CID | 17231 |
| ChEMBL | CHEMBL1328156 |
| ChEBI | CHEBI:170073 |
| EC No. | 607-462-8 |
| DTXSID | DTXSID1025807 |
Chemische & physikalische Eigenschaften
| XLogP | 5 |
|---|---|
| Polarare Oberfläche (TPSA) | 46,5 |
| H-Brücken-Donoren | 1 |
| H-Brücken-Akzeptoren | 3 |
| Frei drehbare Bindungen | 9 |
| Schwere Atome | 18 |
| Formalladung | 0 |
| Komplexität | 220 |
| Stoffklassen | Liquid Crystal (LCM) Monomers |
| SpringerMaterials Properties | Chemical diffusion |
| Löslichkeit | less than 1 mg/mL at 68 °F (NTP, 1992)almost transparency in hot Methanol |
| Schmelzpunkt | 226 °F (Turbid) (NTP, 1992)101-105 °C (lit.) |
| Physical Description | P-n-octyloxybenzoic acid is a white powder. (NTP, 1992) |
| Siedepunkt | 353.47°C (rough estimate) |
| Dichte | 1.0589 (rough estimate) |
| Brechungsindex | 1.5600 (estimate) |
| Lagerbedingungen | Sealed in dry,Room Temperature |
| Aggregatzustand | powder to crystal |
| pKa (Säurekonstante) | 4.48±0.10(Predicted) |
| Farbe | White to Almost white |
| CAS Datenbank | 2493-84-7(CAS DataBase Reference) |
| EPA chemische Informationen | p-(Octyloxy)benzoic acid (2493-84-7) |
Sicherheit & Vorschriften
| GHS-Einstufung | WarningH315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]P264, P264+P265, P280, P302+P352, P305+P351+P338, P321, P332+P317, P337+P317, and P362+P364 (click each P-code to see the statement)The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory. |
|---|---|
| Brandgefahren | Flash point data for this chemical are not available, however it is probably combustible. (NTP, 1992) |
| Reaktive Gruppe | Acids, Carboxylic |
| Reactivity Profile | P-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 waterthose 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 it 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 |
Anwendungen & Verwendung
Verwenden
Intermediate for the synthesis of liquid crystals including chiral ferroelectric benzoates. Used in the preparation of medicinal compounds.
Herstellung & Synthese
synthetische
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.