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CAS No 544-63-8 , tetradecanoic acid

  • Name: tetradecanoic acid
  • Synonyms: 1-Tridecanecarboxylic acid;tetradecanoic acid; n-Tetradecan-1-oic acid; n-Tetradecoic acid; 544-63-8;Tetradecanoic acid; Crodacid; n-Tetradecanoic acid; MYRISTIC ACID;
  • CAS Registry Number:
  • Melting Point: 54-55 ºC
  • Boiling Point: 326 ºC
  • Density: 0.862
  • Refractive index: 1.4305 (20 C)
  • Water Solubility: <0.1 G/100 ML AT 18 ºC
  • Safety Statements: 24/25
  • HS Code: 29159080
  • EINECS: 208-875-2
  • Molecular Weight: 228.37092
  • InchiKey: TUNFSRHWOTWDNC-UHFFFAOYSA-N
  • InChI: InChI=1S/C14H28O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14(15)16/h2-13H2,1H3,
    (H,15,16)
  • Risk Statements: S24/25
  • Molecular Formula: C14H28O2
  • Molecular Structure:CAS No:544-63-8 tetradecanoic acid
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544-63-8 Myristic acid

  • United States Bedoukian Research, Inc. [Manufacturers]
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544-63-8 Myristic acid

  • China Maxim Group Co,.Ltd [Manufacturers]
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544-63-8 Myristic acid

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544-63-8 Myristic acid

  • United States SRS Aromatics Ltd [Importer/Exporter]
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544-63-8 Myristic acid

  • United States Procter & Gamble Chemicals [Manufacturer]
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544-63-8 MYRISTIC ACID

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References of tetradecanoic acid
Title: Myristic Acid
CAS Registry Number: 544-63-8
CAS Name: Tetradecanoic acid
Molecular Formula: C14H28O2
Molecular Weight: 228.37
Percent Composition: C 73.63%, H 12.36%, O 14.01%
Line Formula: CH3(CH2)12COOH
Literature References: Occurs in nutmeg butter (Myristica fragrans Houtt.) to the extent of 70-80%; predominates in the fats of the Myristicaceae; in palm seed fats it may comprise 20% of the total fatty acids; in milk fats between 8-12% of the total acids. Occurs in most animal and vegetable fats; has been found in considerable amounts (up to 15%) in sperm whale oil, see Markley, Fatty Acids (New York, 1947). Prepn: G. D. Beal, Org. Synth. coll. vol. I, 379 (2nd ed., 1941). Prepn from tall-oil fatty acids: Segessmann, Molnar, US 2481356 (1949); from 9-ketotetradecanoic acid: Ames et al., J. Chem. Soc. 1950, 174; by electrolysis of methyl hydrogen adipate + decanoic acid: Greaves et al., ibid. 1950, 3326; by Maurer oxidation of myristyl alc: Langenbeck, Richter, Ber. 89, 202 (1956); from cetanol: Selwitz, US 2969380 (1961 to Gulf). Wide-line NMR spectrum: A. V. Bailey, R. A. Pittman, J. Am. Oil Chem. Soc. 48, 775 (1971). Toxicity study: L. Or?, A. Wretlind, Acta Pharmacol. Toxicol. 18, 141 (1961).
Properties: Crystals from methanol, mp 58.5°. bp100 250.5°; bp16 199°; bp4 184°. d454 0.8622. d470 0.8528. d490 0.8394. nD60 1.4305; nD70 1.4273. Soluble in abs alcohol, methanol, ether, petr ether, benzene, chloroform. Neutralization value: 245.68. Absorption spectrum: Markley, op. cit. LD50 i.v. in mice: 432.6 mg/kg (Or?, Wretlind).
Melting point: mp 58.5°
Boiling point: bp100 250.5°; bp16 199°; bp4 184°
Index of refraction: nD60 1.4305; nD70 1.4273
Density: d454 0.8622; d470 0.8528; d490 0.8394
Toxicity data: LD50 i.v. in mice: 432.6 mg/kg (Or?, Wretlind)
 
Derivative Type: Ethyl ester
Synonyms: Ethyl myristate
Molecular Formula: C16H32O2
Molecular Weight: 256.42
Percent Composition: C 74.94%, H 12.58%, O 12.48%
Properties: Liquid, mp 12°; bp 295°; bp30 195°. d420 0.856. Insol in water. Sol in alcohol; slightly sol in ether.
Melting point: mp 12°
Boiling point: bp 295°; bp30 195°
Density: d420 0.856
 
Use: As ingredient in soaps and shaving creams; in lubricants; in coatings for anodized aluminum.