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CAS No 334-48-5 , decanoic acid Search by region : Spain

  • Name: decanoic acid
  • Synonyms: Caprinic acid; Decylic acid;decanoic acid; n-Decoic acid; n-Decylic acid; 334-48-5; n-Capric acid; n-Decanoic acid;CAPRIC ACID;
  • CAS Registry Number:
  • Melting Point: 30-32 ºC
  • Boiling Point: 268-270 ºC
  • Density: 0.89
  • Refractive index: 1.4169
  • Water Solubility: 0.15 G/L (20 º C)
  • Safety Statements: R36/38
  • Hazard Symbols: Xi: Irritant;
  • HS Code: 29159080
  • EINECS: 206-376-4
  • Molecular Weight: 172.2646
  • InchiKey: GHVNFZFCNZKVNT-UHFFFAOYSA-N
  • InChI: InChI=1S/C10H20O2/c1-2-3-4-5-6-7-8-9-10(11)12/h2-9H2,1H3,(H,11,12)
  • Risk Statements: S26;S37/39
  • Molecular Formula: C10H20O2
  • Molecular Structure:CAS No:334-48-5 decanoic acid

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334-48-5 DECANOIC ACID, 98% PS

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References of decanoic acid
Title: n-Capric Acid
CAS Registry Number: 334-48-5
CAS Name: Decanoic acid
Molecular Formula: C10H20O2
Molecular Weight: 172.26
Percent Composition: C 69.72%, H 11.70%, O 18.58%
Line Formula: CH3(CH2)8COOH
Literature References: Prepn from octyl bromide: Shishido et al., J. Am. Chem. Soc. 81, 5817 (1959); Closson, De Pree, US 2918494 (1959 to Ethyl Corp.). Recovery from Cuphea llavea Llave et Lex, Lythaceae seed oil: Miwa et al., US 2964546 (1960 to U.S.D.A.). Toxicity study: L. Or?, A. Wretlind, Acta Pharmacol. Toxicol. 18, 141 (1961). Review: Fatty Acids Part I, K. S. Markley, Ed. (Interscience, New York, 2nd ed., 1960) pp 34, 39.
Properties: Crystalline solid, mp 31.4°. Rancid odor. bp 270°. d450 0.8782. nD40 1.4288. Practically insol in water (0.015 g/100 g at 20°). Sol in ethanol, ether, chloroform, benzene, carbon disulfide. Also sol in dil HNO3 from which it precipitates unchanged by addition of water. LD50 i.v. in mice: 129 ±5.4 mg/kg (Or?, Wretlind).
Melting point: mp 31.4°
Boiling point: bp 270°
Index of refraction: nD40 1.4288
Density: d450 0.8782
Toxicity data: LD50 i.v. in mice: 129 ±5.4 mg/kg (Or?, Wretlind)
Use: Manuf of esters for artificial fruit flavors and perfumes; as an intermediate in other chemical syntheses.