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CAS No 546-88-3 , N-hydroxyacetamide Search by region : Germany

  • Name: N-hydroxyacetamide
  • Synonyms: Lithostat;N-hydroxyacetamide; Acetic acid;N-Hydroxyacetamide; oxime; Methylhydroxamic acid; Acetylhydroxamic acid; 546-88-3; Acetohydroximic acid;
  • CAS Registry Number:
  • Transport: OTH
  • Melting Point: 86-90 ºC
  • Density: 1.155g/cm3
  • Refractive index: 1.42
  • Safety Statements: R61
  • Hazard Symbols: T: Toxic;
  • EINECS: 208-913-8
  • Molecular Weight: 75.0666
  • InchiKey: RRUDCFGSUDOHDG-UHFFFAOYSA-N
  • InChI: InChI=1S/C2H5NO2/c1-2(4)3-5/h5H,1H3,(H,3,4)
  • Risk Statements: S45;S53
  • Molecular Formula: C2H5NO2
  • Molecular Structure:CAS No:546-88-3 N-hydroxyacetamide

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546-88-3 Acetohydroxamic acid

  • Acetohydroxamic acid
  • Germany VeZerf Laborsynthesen GmbH [Manufacturer]
  • Tel: +49 (0)6784 903764
  • Fax: +49 (0)6784 903765
  • Address: Langenfelder Strasse 1255743 Idar-ObersteinGERMANY Idar-Oberstein,nullGermany
Contact Supplier

546-88-3 Acetohydroxamic acid; 98%

  • Acetohydroxamic acid; 98%
  • Germany ABCR GmbH & Co KG [Manufacturer]
  • Tel: +49 721 95061-0
  • Fax: +49 721 95061-80
  • Address: Im Schlehert 10
    76187 Karlsruhe
    Germany null,nullGermany
Contact Supplier

546-88-3 Acetohydroxamic acid

  • Acetohydroxamic acid
  • Germany CHEMOS GmbH [Manufacturer]
  • Tel: 0049 9402/9336 0
  • Fax: 0049 9402/9336 13
  • Address: CHEMOS GmbH
    Werner-von-Siemensstr. 3
    93128 Regenstauf
    Germany null,nullGermany
Contact Supplier

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References of N-hydroxyacetamide
Title: Acetohydroxamic Acid
CAS Registry Number: 546-88-3
CAS Name: N-Hydroxyacetamide
Synonyms: N-acetylhydroxylamine; acetic acid oxime; AHA
Trademarks: Lithostat (Mission Pharmacal)
Molecular Formula: C2H5NO2
Molecular Weight: 75.07
Percent Composition: C 32.00%, H 6.71%, N 18.66%, O 42.63%
Line Formula: CH3CONHOH
Literature References: Urease inhibitor. Prepn: A. Miolati, Ber. 25, 699 (1892); W. M. Wise, W. W. Brandt, J. Am. Chem. Soc. 77, 1058 (1955); H. A. Staab et al., Ber. 95, 1275 (1962); G. Sosnovsky, J. A. Krogh, Synthesis 1980, 654. Inhibition of urease activity: K. Kobashi et al., Biochim. Biophys. Acta 65, 380 (1962); W. N. Fishbein et al., Nature 208, 46 (1965); W. N. Fishbein, P. P. Carbone, J. Biol. Chem. 240, 2407 (1965); D. P. Griffith et al., Invest. Urol. 11, 234 (1973). Metabolism: E. Wolpert et al., Proc. Soc. Exp. Biol. Med. 136, 592 (1971); W. N. Fishbein et al., J. Pharmacol. Exp. Ther. 186, 173 (1973). Pharmacokinetics: S. Feldman et al., Invest. Urol. 15, 498 (1978). Clinical studies in treatment of kidney stones: D. B. Griffith et al., J. Urol. 119, 9 (1978); A. Martelli et al., Urology 17, 320 (1981).
Properties: mp 89-92°. pKa 8.70. pH (aq soln): 9.39.
Melting point: mp 89-92°
pKa: pKa 8.70
Therap-Cat: Antiurolithic. Antibacterial adjunct (urinary tract infection).
Keywords: Antiurolithic.