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CAS No 50-56-6 , Oxtocin

  • Name: Oxtocin
  • Synonyms: (2S)-1-[(4R,7S,10S,13S,16S,19R)-19-amino-13-[(2S)-butan-2-yl]-10-(2-carbamoylethyl)-7-(carbamoylmethyl)-16-[(4-hydroxyphenyl)methyl]-6,9,12,15,18-pentaoxo-1,2-dithia-5,8,11,14,17-pentazacycloicosane-4-carbonyl]-N-[(1S)-1-(carbamoylmethylcarbamoyl)-3-methyl-butyl]pyrrolidine-2-carboxamide;Oxtocin; (2s)-1-[(4r,7s,10s,13s,16s,19r)-19-amino-13-[(2s)-butan-2-yl]-10-(2-carbamoylethyl)-7-(carbamoylmethyl)-16-[(4-hydroxyphenyl)methyl]-6,9,12,15,18-pentaoxo-1,2-dithia-5,8,11,14,17-pentazacycloicosane-4-carbonyl]-n-[(1s)-1-(carbamoylmethylcarbamoyl)-3-methyl-butyl]pyrrolidine-2-carboxamide; oxytocin acetate;oxytocin lyophilized; oxtocin; H-Cys-Tyr-Ile-Gln-Asn-Cys-Pro-Leu-Gly-NH2 (Disulfide bond); Oxytocin Solution; H-Cys-Tyr-Ile-Gln-Asn-Cys-Pro-Leu-Gly-NH2 Disulfide bond;
  • CAS Registry Number:
  • Transport: UN 3249
  • Flash Point: 881.1 °C
  • Boiling Point: 1533.3 °C at760mmHg
  • Density: 1.27 g/cm3
  • Safety Statements: 26-36
  • Hazard Symbols: Xi: Irritant;
  • Flash Point: 881.1 °C
  • EINECS: 200-048-4
  • Molecular Weight: 1007.19
  • InChI: InChI=1/C43H66N12O12S2/c1-5-22(4)35-42(66)49-26(12-13-32(45)57)38(62)51-29(17-33(46)58)39(63)53-30(20-69-68-19-25(44)36(60)50-28(40(64)54-35)16-23-8-10-24(56)11-9-23)43(67)55-14-6-7-31(55)41(65)52-27(15-21(2)3)37(61)48-18-34(47)59/h8-11,21-22,25-31,35,56H,5-7,12-20,44H2,1-4H3,(H2,45,57)(H2,46,58)(H2,47,59)(H,48,61)(H,49,66)(H,50,60)(H,51,62)(H,52,65)(H,53,63)(H,54,64)
  • Risk Statements: 36/37/38
  • Molecular Formula: C43H66N12O12S2
  • Molecular Structure:CAS No:50-56-6 Oxtocin

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References of Oxtocin
Title: Oxytocin
CAS Registry Number: 50-56-6
Synonyms: Alpha-hypophamine; ocytocin
Trademarks: Intertocine-S (Veterinaria); Perlacton (Chassot); Pitocin (Monarch); Syntocinon (Novartis); Orasthin (Aventis); Partocon (Ferring); Synpitan (Werfft); Uteracon (National)
Molecular Formula: C43H66N12O12S2
Molecular Weight: 1007.19
Percent Composition: C 51.28%, H 6.60%, N 16.69%, O 19.06%, S 6.37%
Literature References: The principal uterus-contracting and lactation-stimulating hormone of the posterior pituitary gland. Isoln: Pierce et al., J. Biol. Chem. 199, 929 (1952). Structure and synthesis: Tuppy, Michl, Monatsh. Chem. 84, 1011 (1953); Tuppy, Biochim. Biophys. Acta 11, 449 (1953); du Vigneaud et al., J. Am. Chem. Soc. 75, 4879 (1953); 76, 3115 (1954); Bodanszky, du Vigneaud, ibid. 81, 2504 (1959); Cash et al., J. Med. Pharm. Chem. 5, 413 (1962); Sakakibara et al., Bull. Chem. Soc. Jpn. 38, 120 (1965). Solid phase synthesis: Bayer, Hagenmaier, Tetrahedron Lett. 1968, 2037; Ives, Can. J. Chem. 46, 2318 (1968). Synthesis of D-oxytocin: Flouret, du Vigneaud, J. Am. Chem. Soc. 87, 3775 (1965). Description of commercial process: Velluz et al., US 2938891 and US 3076797 (1960, 1963, both to Roussel-UCLAF). Radioimmunoassay: T. Chard, Clin. Biochem. Anal. 5, 209 (1977). Review: du Vigneaud, Experientia Suppl. II (14th Intl. Congr. Pure and Appl. Chem.), 9-26 (1955); R. Caldeyro-Barcia, H. Heller, Proc. Intl. Symp. on Oxytocin (Montevideo 1959) 443 pp; several authors, Adv. Exp. Med. Biol. 2, 53-104 (1968); C. R. W. Edwards in Hormones in Blood vol. 2, C. H. Gray, V. James, Ed. (Academic Press, New York, 3rd ed., 1979) pp 401-421. Review of role in parturition: A.-R. Fuchs, F. Fuchs, Adv. Exp. Med. 1980, 403-428. Comprehensive description: F. Nachtmann et al., Anal. Profiles Drug Subs. 10, 563-600 (1981). Book: Oxytocin: Cellular and Molecular Approaches in Medicine and Research, R. Ivell, J. A. Russell, Eds. (Plenum Press, New York, 1995) 673 pp.
Properties: White powder. [a]D22 -26.2° (c = 0.53). Sol in water, 1-butanol, 2-butanol.
Optical Rotation: [a]D22 -26.2° (c = 0.53)
Therap-Cat: Oxytocic.
Therap-Cat-Vet: Stimulates milk let-down, uterine contraction.
Keywords: Oxytocic.