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CAS No 72-18-4 , (2S)-2-amino-3-methylbutanoic acid

  • Name: (2S)-2-amino-3-methylbutanoic acid
  • Synonyms: 2-Amino-3-methylbutyric acid; 2-Amino-3-methylbutanoic acid;(2S)-2-amino-3-methylbutanoic acid; (S)-2-Amino-3-methylbutyric acid; valine; (S)-Valine;L-valine; 72-18-4;
  • CAS Registry Number:
  • Melting Point: 315 ºC
  • Density: 1.23
  • Refractive index: 28 ° (C=8, HCl)
  • Alpha: 28 º (C=8, 6N HCL)
  • Water Solubility: 85 G/L (20 ºC)
  • Safety Statements: 24/25-36-22
  • Hazard Symbols: Xn: Harmful;
  • EINECS: 200-773-6
  • Molecular Weight: 117.14634
  • InchiKey: KZSNJWFQEVHDMF-BYPYZUCNSA-N
  • InChI: InChI=1S/C5H11NO2/c1-3(2)4(6)5(7)8/h3-4H,6H2,1-2H3,(H,7,8)/t4-/m0/s1
  • Risk Statements: S24/25:Avoidcontactwithskinandeyes.;
  • Molecular Formula: C5H11NO2
  • Molecular Structure:CAS No:72-18-4 (2S)-2-amino-3-methylbutanoic acid

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    • 72-18-4 L-Valine

    • Name L-Valine Other Name H-L-VAL-OH CAS NO. 72-18-4 Purity 99% Merck? 149,909 Molecular Formula C5H11NO2 Molecular Weight 117.15 Apperance White crystalline powder Usage ?used in studies to attenuate arrhythmias and induce hypotensive effects.
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    References of (2S)-2-amino-3-methylbutanoic acid
    Title: Valine
    CAS Registry Number: 72-18-4
    CAS Name: L-Valine
    Synonyms: Val; V; 2-aminoisovaleric acid; 2-amino-3-methylbutyric acid; a-aminoisovaleric acid; (S)-2-amino-3-methylbutanoic acid
    Molecular Formula: C5H11NO2
    Molecular Weight: 117.15
    Percent Composition: C 51.26%, H 9.46%, N 11.96%, O 27.31%
    Literature References: An essential amino acid for human development. Identified from organ extracts in 1856 by von Group-Besanez; isolated from proteins in 1879 by Schützenberger who proposed that it was aminovaleric acid. Structure confirmation: E. Fischer, Ber. 39, 2320 (1906). Early chemistry and biochemistry: Amino Acids and Proteins, D. M. Greenberg, Ed. (Charles C. Thomas, Springfield, IL, 1951) 950 pp., passim; J. P. Greenstein, M. Winitz, Chemistry of the Amino Acids vols 1-3 (John Wiley and Sons, Inc., New York, 1961) pp. 2368-2380, passim. Conformation study: R. H. Yun, J. Hermans, Protein Eng. 4, 761 (1991). Nutritional assessment study: V. R. Young et al., J. Nutr. 102, 1159 (1972); in parenteral nutrition: P. Reiderer et al., Nutr. Metab. 24, 209 (1980); in hemodialysis patients: G. A. Young et al., Kidney Int. 21, 492 (1982). Brief review of metabolism: P. Kamoun, Trends Biochem. Sci. 17, 175-176 (1992).
    Properties: Leaflets from water + alcohol, mp 315° (closed capillary). d 1.230. Sublimes. [M]D +33.1° (5N HCl); +72.6° (glacial acetic acid); [a]D23 +22.9° (c = 0.8 in 20% HCl). pK1 2.32; pK2 9.62. Soly in water at 0°: 83.4 g/l; at 25°: 88.5 g/l; at 50°: 96.2 g/l; at 65°: 102.4 g/l. Insol in common neutral solvents.
    Melting point: mp 315° (closed capillary)
    pKa: pK1 2.32; pK2 9.62
    Optical Rotation: [a]D23 +22.9° (c = 0.8 in 20% HCl)
    Density: d 1.230
     
    Derivative Type: DL-Form
    Properties: Sublimes without melting at ordinary speed of heating. Dec 298° (closed capillary, very rapid heating). One part dissolves in 11.7 parts of water at 15°, in 14.1 parts of water at 25°. Insol in common neutral solvents.