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Detail of "13881-91-9"

  • CAS Number:
  • 13881-91-9
  • Name:

  • Methanesulfonic acid,1-amino-

  • Superlist Name:
  • Aminomethanesulfonic acid
  • Molecular Structure:
  • Formula:
  • CH5NO3S
  • Molecular Weight:
  • 111.11
  • Synonyms:
  • Methanesulfonicacid, amino- (6CI,7CI,8CI,9CI);(Aminomethyl)sulfonic acid;Aminomethanesulphonic acid;NSC 209983;
  • EINECS:
  • 237-649-6
  • Density:
  • 1.652 g/cm3
  • Melting Point:
  • 184 °C (dec.)(lit.)
  • Appearance:
  • White powder
  • Hazard Symbols:
  • CorrosiveC
  • Risk Codes:
  • 34
  • Safety:
  • 26-36/37/39-45 Details
  • Transport Information:
  • UN 2585 8/PG 3
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CAS No.13881-91-9 Aminomethanesulfonic acidCompetitive Product

Assay:≥98.0%  Appearance:White crysta...  Package:10kg/25kg

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CAS No.13881-91-9 Aminomethanesulfonic acid

Assay:99%

Molecular Formula:CH5NO3S Molecular Weight:111.11 EINECS NO.:237-649-6 Grade Standard: Medicine Grade

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CAS No.13881-91-9 Aminomethanesulfonic acid

Assay:98%  Appearance:White crysta...

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Aminomethanesulfonic acid

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Aminomethanesulfonic Acid

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Reference

Antifibrinolytic agents
Antifibrinolytic agents. Cook, Elton S.; Tanaka, Kinji; Fujii, Akira (Stanley Drug Products, Inc., USA). Fr. Demande FR 2321285 18 Mar 1977, 9 pp. (French). (France). CODEN: FRXXBL. CLASS: IC: A61K031-185. APPLICATION: FR 75-25473 18 Aug 1975. DOCUMENT TYPE: Patent CA Section: 63 (Pharmaceuticals) Antifibrinolytic tablets and injectable solns. comprise a prepd. w-aminoalkylsulfonic acid (H2N-(CH2)n-SO3H; n <5) plasmin [9001-90-5] inhibitor. For example, aminomethylsulfonic acid [13881-91-9] was prepd. by adding NH4OH, 61.5 g in a 28% aq. soln., to NaHSO3 111, H2O 139, and HCHO 85.2 g at 75°. After cooling and treatment with concd. H2SO4 aminomethylsulfonic acid 20.4 g crystals pptd. Tablets and injectable saline solns. contain aminoalkylsulfonic acid for a dose of 10-500 mg/kg.
Inhibition of the synthesis of taurocholic acid by structural analogs of taurine
Inhibition of the synthesis of taurocholic acid by structural analogs of taurine. Lombardini, John B. (Sch. Med., Texas Tech Univ., Lubbock, Tex., USA). Biochem. Pharmacol., 26(12), 1175-7 (English) 1977. CODEN: BCPCA6. DOCUMENT TYPE: Journal CA Section: 3 (Biochemical Interactions) Isethionic acid [107-36-8] and aminomethanesulfonic acid [13881-91-9] were potent inhibitors of rat liver microsomal formation of taurocholic acid [81-24-3] from taurine [107-35-7] with 50% inhibitory concns. (I50) of 110 and 688.mu.M resp. Hydroxypropanesulfonic acid [15909-83-8] and aminoethanesulfuric acid [926-39-6] were less potent with I50 3125 and 3750.mu.M resp. Hypotaurine [300-84-5] and glycine [56-40-6] decreased taurocholate formation at high concns. with I50 7500 and 8800.mu.M resp.
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