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CAS No 502-65-8 , Lycopene Search by region : China

  • Name: Lycopene
  • Synonyms: PSI,PSI-CAROTENE; LYCOSOURCE;Lycopene Beadlet;Lycopene; 4,4-CAROTENE; 2,6,10,14,19,23,27,31-OCTAMETHYL-DOTRIACONTA-2,6,8,10,12,14,16,18,20,22,24,26,30-TRIDECAENE; E 160d; JARCOPENE(TM); Y,Y-CAROTENE; LYCOPENE;
  • CAS Registry Number:
  • Melting Point: 172-173 ºC
  • Flash Point: 350.7 ºC
  • Boiling Point: 660.9 ºC
  • Density: 0.888 g/cm3
  • Refractive index: 1.53
  • Water Solubility: Stability
  • Safety Statements: 26-36/37/39
  • Hazard Symbols: Xi: Irritant;
  • Flash Point: 350.7 ºC
  • EINECS: 207-949-1
  • Molecular Weight: 536.88
  • InChI: InChI=1/C40H56/c1-33(2)19-13-23-37(7)27-17-31-39(9)29-15-25-35(5)21-11-12-22-36(6)26-16-30-40(10)32-18-28-38(8)24-14-20-34(3)4/h11-12,15-22,25-32H,13-14,23-24H2,1-10H3/b12-11+,25-15+,26-16+,31-17+,32-18+,35-21+,36-22+,37-27+,38-28+,39-29+,40-30+
  • Risk Statements: 36/37/38
  • Molecular Formula: C40H56
  • Molecular Structure:CAS No:502-65-8 Lycopene

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  • Botanical Resource:. Lycopersicon esculentum Mill Part of the Plant Used: Fruit Active Ingredients: lycopene Molecular formula: C40H56 Molecular weight: 536.88 CAS No.: 502-65-8 EC No.: 207-949-1 Appearance & Color: Deep red solid powder or oil Solub...
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References of Lycopene
Title: Lycopene
CAS Registry Number: 502-65-8
CAS Name: y,y-Carotene
Synonyms: (all-trans)-lycopene
Molecular Formula: C40H56
Molecular Weight: 536.87
Percent Composition: C 89.49%, H 10.51%
Literature References: Carotenoid antioxidant occurring in ripe fruit, especially in tomatoes. One kg of fresh ripe tomatoes yields 0.02 g lycopene. Isoln procedure: R. Willst?tter, H. H. Escher, Z. Physiol. Chem. 64, 47 (1910). Chromatographic sepn from other carotenoids: A. Winterstein, ibid. 215, 51 (1933); A. Winterstein, G. Stein, ibid. 220, 247 (1933). HPLC determn in plasma: M. V. Vertzoni et al., J. Chromatogr. B 819, 149 (2005). Structure: Willst?tter, Escher, loc. cit.; Karrer and collaborators: Helv. Chim. Acta 11, 751, 1201 (1928); 12, 285 (1929); 13, 1084 (1930); 14, 435 (1931); Kuhn, Grundmann, Ber. 65, 898, 1880 (1932). Synthesis: P. Karrer et al., Helv. Chim. Acta 33, 1349 (1950); O. Isler et al., ibid. 39, 463 (1956). Commercial prepn: Kabbe et al., DE 1168890 (1964 to Bayer). Oral toxicity study: W. Mellert et al., Food Chem. Toxicol. 40, 1581 (2002). Review of antioxidant activity and role in human health: A. V. Rao, S. Agarwal, Nutr. Res. 19, 305-323 (1999).
Properties: Long, deep red needles from carbon disulfide + ethanol, from methylene chloride + methanol, mp 172-173°. Absorption max, trans-form (petroleum ether): 446, 472, 505 nm (E1%1cm 2250, 3450, 3150). One gram dissolves in 50 ml carbon disulfide, in 3 l boiling ether, in 12 l boiling petr ether, in 14 l hexane at 0°. Sol in chloroform, benzene. Almost insol in methanol, ethanol, water.
Melting point: mp 172-173°
Absorption maximum: Absorption max, trans-form (petroleum ether): 446, 472, 505 nm (E1%1cm 2250, 3450, 3150)
 
Derivative Type: 15,15￠-cis-Form
CAS Registry Number: 59092-07-8
Properties: mp ~105° then solidifies again. Absorption max (petroleum ether): 361, 444, 470, 502 nm (E1%1cm 1110, 1280, 1660, 1280).
Melting point: mp ~105° then solidifies again
Absorption maximum: Absorption max (petroleum ether): 361, 444, 470, 502 nm (E1%1cm 1110, 1280, 1660, 1280)