Homoanisic Acid Ethyl Ester 99% see COA kanbei

(4-Methoxyphenyl)acetic acid

Benzeneacetic acid,4-methoxy-;Acetic acid,(p-methoxyphenyl)-;4-Methoxybenzeneacetic acid;Homoanisic acid;(p-Methoxyphenyl)acetic acid;(4-Methoxyphenyl)acetic acid;2-(p-Anisyl)acetic acid;p-Anisylacetic acid;2-(p-Methoxyphenyl)acetic acid;NSC 27799;NSC 65597;2-(4-Methoxyphenyl)acetic acid;4-Methoxyphenacetic acid

104-01-8

C9H10O3

InChIKey=NRPFNQUDKRYCNX-UHFFFAOYSA-N

166.17400

166.17

203-166-4

AJP2V8U5K6

65597|27799

3261

DTXSID1059288

29189090

Bulk Drug Intermediates

46.53000

1.4

4-methoxyphenylacetic acid appears as pale yellow or off white colored flakes. Severely irritates skin and eyes. May be toxic by ingestion.

1.2±0.1 g/cm3

87 °C

138 °C

124.3ºC

1.502

H2O: 6 g/L (20 ºC)

Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.

0.143mmHg at 25°C

137.4 Ų [M+H]+ [CCS Type: DT, Method: single field calibrated with Agilent tune mix (Agilent)]

No rapid reaction with air. No rapid reaction with water.

Acids, Carboxylic

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 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; like other acids, they often catalyze (increase the rate of) chemical reactions.