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CAS No 57-00-1 , 2-[carbamimidoyl(methyl)amino]acetic acid Search by region : China

  • Name: 2-[carbamimidoyl(methyl)amino]acetic acid
  • Synonyms: Krebiozon; N-amidinosarcosine; N-methyl-N-guanylglycine; Kreatin; hydrate; Pyrolysate; (alpha-Methylguanido)acetic acid; Creatine;Creatin;2-[carbamimidoyl(methyl)amino]acetic acid;
  • CAS Registry Number:
  • Melting Point: ~295 °C (dec.)
  • Flash Point: 118.1°C
  • Boiling Point: 271.6°Cat760mmHg
  • Density: 1,33 g/cm3
  • Refractive index: 1.506 (20 C)
  • Safety Statements: R36/37/38
  • Hazard Symbols: Xi: Irritant;
  • Flash Point: 118.1°C
  • EINECS: 200-306-6
  • Molecular Weight: 131.13316
  • InchiKey: CVSVTCORWBXHQV-UHFFFAOYSA-N
  • InChI: InChI=1S/C4H9N3O2/c1-7(4(5)6)2-3(8)9/h2H2,1H3,(H3,5,6)(H,8,9)
  • Risk Statements: S26;S36
  • Molecular Formula: C4H9N3O2
  • Molecular Structure:CAS No:57-00-1 2-[carbamimidoyl(methyl)amino]acetic acid

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57-00-1 CAS 57-00-1 Creatine

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  • Alias: Creatine anhydrous; Creatine preparation; N-amidinosarcosine; 5-Chloro-2-Maino Benzotrifluoride; N-carbamimidoyl-N-methylglycine Molecular Formule: C4H9N3O2 Molecular Weight: 131.1332 CAS: 57-00-1 EINECS: 200-306-6
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57-00-1 Creatine CAS: 57-00-1

  • Creatine Alias: Creatine anhydrous; Creatine preparation; N-amidinosarcosine; 5-Chloro-2-Maino Benzotrifluoride; N-carbamimidoyl-N-methylglycine Molecular Formule: C4H9N3O2 Molecular Weight: 131.1332 Molecular Structure: CAS: 57-00-1 EINECS: 200-306-...
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    • Creatine is a naturally occurring amino acid (protein building block) found mainly in muscles. Fifty percent of creatine in our bodies is ingested through the foods we eat while the other 50% is made in the liver, kidney, and pancreas. Roughly one-th...
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    References of 2-[carbamimidoyl(methyl)amino]acetic acid
    Title: Creatine
    CAS Registry Number: 57-00-1
    CAS Name: N-(Aminoiminomethyl)-N-methylglycine
    Synonyms: N-amidinosarcosine; (a-methylguanido)acetic acid; N-methyl-N-guanylglycine; methylglycocyamine
    Molecular Formula: C4H9N3O2
    Molecular Weight: 131.13
    Percent Composition: C 36.64%, H 6.92%, N 32.04%, O 24.40%
    Literature References: Amino acid that participates in the transfer of high energy phosphate in muscle cells. Predominantly found in skeletal and cardiac muscle; occurring also in its phosphorylated form, see phosphocreatine. Produced by liver, pancreas and kidneys by the transfer of the guanidine moiety of arginine to glycine which is then methylated to give creatine. First identified in meat extracts by Chevreul in 1835; name derived from the Greek "kreas," meaning flesh. Synthesis by heating cyanamide with sarcosine: Strecker, Jahresber. Chem. 1868, 686; cf. Volhard, Z. Chem. 5, 318 (1869); Paulmann, Arch. Pharm. 232, 638 (1894); Bergmann, Zervas, Z. Physiol. Chem. 173, 80 (1928); King J. Chem. Soc. 1930, 2374. Use in diagnosis of myocardial infarction: J. Delanghe et al., Ann. Clin. Biochem. 25, 383 (1988). HPLC determn in cardiac muscle: T. Teerlink et al., Anal. Biochem. 214, 278 (1993). Review of role in energy metabolism: S. P. Bessman, C. L. Carpenter, Annu. Rev. Biochem. 54, 831-862 (1985). Review of efficacy and safety as nutritional supplement: A. S. Graham, R. C. Hatton, J. Am. Pharm. Assoc. 39, 803-810 (1999); of effects of dietary supplementation on exercise performance: T. W. Demant, E. C. Rhodes, Sports Med. 28, 49-60 (1999); A. Casey, P. L. Greenhaff, Am. J. Clin. Nutr. 72, Suppl., 607S-617S (2000).
    Properties: Monoclinic prisms from water as the monohydrate. Becomes anhydr at 100°; dec 303°. Neutral reaction to litmus. pKb (20°) 11.02. Adsorption on various chromatographic agents: Grettie, Williams, J. Am. Chem. Soc. 50, 671 (1928). Absorption spectrum: Abderhalden, Haas, Z. Physiol. Chem. 164, 7 (1927). One gram of the monohydrate dissolves in 75 ml water, in about 9 liters alcohol. Insol in ether.
    pKa: pKb (20°) 11.02