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CAS No 19767-45-4 , sodium

  • Name: sodium
  • Synonyms: Mistabron;2-sulfanylethanesulfonate; Mitexan; Sodium 2-mercaptoethanesulfonate; Mesnum; Uromitexan;Mesnex; 19767-45-4;sodium; 2-Mercaptoethanesulfonic acid sodium salt;
  • CAS Registry Number:
  • Safety Statements: R36/37/38
  • Hazard Symbols: Xi: Irritant;
  • EINECS: 243-285-9
  • Molecular Weight: 164.179069
  • InchiKey: XOGTZOOQQBDUSI-UHFFFAOYSA-M
  • InChI: InChI=1S/C2H6O3S2.Na/c3-7(4,5)2-1-6;/h6H,1-2H2,(H,3,4,5);/q;+1/p-1
  • Risk Statements: S26;S36
  • Molecular Formula: C2H5NaO3S2
  • Molecular Structure:CAS No:19767-45-4 sodium

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19767-45-4 MESNA

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19767-45-4 MESNA

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19767-45-4 sodium 2-mercaptoethanesulfonate

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19767-45-4 sodium 2-mercaptoethanesulfonate

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References of sodium
Title: Mesna
CAS Registry Number: 19767-45-4
CAS Name: 2-Mercaptoethanesulfonic acid sodium salt
Synonyms: sodium mercaptoethanesulfonate
Manufacturers' Codes: D-7093; UCB-3983
Trademarks: Mesnex (Baxter); Mistabron (UCB); Mistabronco (UCB); Mucofluid (UCB); Uromitexan (Baxter)
Molecular Formula: C2H5NaO3S2
Molecular Weight: 164.18
Percent Composition: C 14.63%, H 3.07%, Na 14.00%, O 29.24%, S 39.06%
Line Formula: [HSCH2CH2SO3]-Na+
Literature References: Sulfhydryl donor used to reduce the urotoxic effects of antineoplastic alkylating agents; also has mucolytic activity. Prepn: I. M. Lipovich, J. Appl. Chem. USSR 18, 718 (1945); C. H. Schramm et al., J. Am. Chem. Soc. 77, 6231 (1955). Synthesis and properties: V. E. Petrun'kin, C.A. 51, 5693a (1957); ibid. 54, 24379c (1960). Use as mucolytic: NL 6605816; H. Morren, US 3567835 (1966, 1971 both to U.C.B.); as uroprotective agent: N. Brock, DE 2756018; idem, US 4220660 (1979, 1980 both to Asta-Werke AG). Pharmacology, toxicity, and uroprotective effects in animals: N. Brock et al., Eur. J. Cancer Clin. Oncol. 18, 1377 (1982). HPLC determn in plasma and urine: C. A. James, H. J. Rogers, J. Chromatogr. 382, 394 (1986). Clinical pharmacokinetics: C. A. James et al., Br. J. Clin. Pharmacol. 23, 561 (1987). Clinical study of mucolytic effects: M. Tekeres et al., Clin. Ther. 4, 56 (1981). Symposium on pharmacology, toxicity and clinical uroprotective efficacy: Cancer Treat. Rev. 10, Suppl. A, 1-192 (1983). Reviews: I. C. Shaw, M. I. Graham, ibid. 14 67-86 (1987); S. E. Schoenike, W. J. Dana, Clin. Pharm. 9, 179-191 (1990).
Properties: Freely sol in water, sparingly sol in organic solvents. LD50 in male, female mice, male, female rats (mg/kg): 1887, 2048, 2098, 1683 i.v.; 2005, 2098, 1529, 1251 i.p.; 6102, >7200, 4440, 4679 orally (Brock).
Toxicity data: LD50 in male, female mice, male, female rats (mg/kg): 1887, 2048, 2098, 1683 i.v.; 2005, 2098, 1529, 1251 i.p.; 6102, >7200, 4440, 4679 orally (Brock)
Therap-Cat: Mucolytic; antineoplastic adjunct (uroprotective).
Keywords: Antineoplastic Adjunct; Uroprotective; Mucolytic.