n-Tetradecoic acid

Myristic acid

Tetradecanoic acid;Myristic acid;Neo-Fat 14;Univol U 316S;n-Tetradecoic acid;1-Tridecanecarboxylic acid;n-Tetradecanoic acid;n-Tetradecan-1-oic acid;Prifac 2942;NAA 142;NAA 104;Emery 655;Hystrene 9014;Edenor C 14;Kortacid 1499;Philacid 1400;NSC 5028;Lunac MY 98;Prifrac 2942;Edenor C 14/98-100;1-Tetradecanoic acid;MY 98;Imex C 1499;Palmac 98-14;Lunac M 98;Edenor C14-99 (C);Sinar FA 1499;Myristates;Edenor C14-99;POFAC 1498;45184-05-2

544-63-8

C14H28O2

InChIKey=TUNFSRHWOTWDNC-UHFFFAOYSA-N

228.37

228.37

508624

208-875-2

0I3V7S25AW

5028

DTXSID6021666

C68393

Oily, white, crystalline solid|Crystals from methanol|Leaflets from ethyl ether

29159080

Bulk Drug Intermediates

37.3

5.3

White Flakes, Powder, Chunks or Crystalline Mass

0.8622 g/cm³ @ Temp: 54 °C

58.5 °C

326.2 °C

>230 °F

1.451

H2O: <0.1 g/100 mL at 18 ºC

−20°C

<0.01 hPa (20 °C)

LD50 i.v. in mice: 432.6 mg/kg (Or, Wretlind)

Combustible

The odor should be faint with no rancidity.

Henry's Law constant = 4.95X10-7 atm-cu m/mol at 25 °C (est)

pKa = 4.90

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

Neutralization value: 245.68|Heat of fusion = 44.8 kJ/mol; specific heat = 1.60 J/g (for the solid)|Hydroxyl radical reaction rate constant = 1.68X10-11 cu-cm/molec sec at 25 °C (est)

Insoluble in water.

Acids, Carboxylic

TETRADECANOIC 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 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.

-8,721.4 kJ/mol