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CAS No 60-32-2 , 6-aminohexanoic acid

  • Name: 6-aminohexanoic acid
  • Synonyms: aminocaproic acid; 6-Aminocaproic acid; Hemocaprol; Caprocid;6-aminohexanoic acid; amicar; Epsamon; Acepramin; Epsikapron; Capramol;
  • CAS Registry Number:
  • Melting Point: 204-209 ºC
  • Density: 1.03 g/mL at 20 °C
  • Safety Statements: R36/37/38
  • Hazard Symbols: Xi: Irritant;
  • EINECS: 200-469-3
  • Molecular Weight: 131.17292
  • InchiKey: SLXKOJJOQWFEFD-UHFFFAOYSA-N
  • InChI: InChI=1S/C6H13NO2/c7-5-3-1-2-4-6(8)9/h1-5,7H2,(H,8,9)
  • Risk Statements: S26;S36
  • Molecular Formula: C6H13NO2
  • Molecular Structure:CAS No:60-32-2 6-aminohexanoic acid

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60-32-2 6-Aminocaproic acid

  • 6-Aminocaproic acid Name:6-Aminocaproic acid Synonym:6-Aminohexanoic acid; H-EAhx-OH; H-6-Ahx-OH; H-6-Aca-OH; epsilon-Aminocaproic acid; 6-Aminohexanoic acid; EACA; 6-aminohexanoate; E-AMINOCAPROIC ACID; Aminocaproic acid CAS: 60-32-2 EINECS:200-469-...
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60-32-2 e- Aminocaproic acid

  • e- Aminocaproic acid
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60-32-2 6-Aminocaproic acid

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60-32-2 6-Aminocaproic acid

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60-32-2 6-Aminocaproic acid

  • United States HBCChem, Inc. [Manufacturers]
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60-32-2 6-Aminohexanoic acid

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60-32-2 6-Aminocaproic acid

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60-32-2 6-Aminocaproic acid

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60-32-2 H-epsilon-Acp-OH

  • H-epsilon-Acp-OH
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60-32-2 Aminocaproic acid (epsilon-)

  • Aminocaproic acid (epsilon-)
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References of 6-aminohexanoic acid
Title: e-Aminocaproic Acid
CAS Registry Number: 60-32-2
CAS Name: 6-Aminohexanoic acid
Synonyms: epsilon-aminocaproic acid; epsilcapramin; EACA
Manufacturers' Codes: CY-116
Trademarks: Amicar (Wyeth); Epsikapron (Pharmacia); Hemocaprol (Sanofi-Aventis)
Molecular Formula: C6H13NO2
Molecular Weight: 131.17
Percent Composition: C 54.94%, H 9.99%, N 10.68%, O 24.39%
Line Formula: H2N(CH2)5COOH
Literature References: Antifibrinolytic; inhibits the activity of plasmin and plasminogen, q.q.v. Prepn: S. Gabriel, T. A. Maass, Ber. 32, 1266 (1899); A. Galat, S. Mallin, J. Am. Chem. Soc. 68, 2729 (1946); C. Y. Meyers, L. E. Miller, Org. Synth. coll. vol. IV, 39 (1963). Toxicity data: D. W. Hallesy et al., Pharmacologist 3, 62 (1961). Crystal structure: G. Bodor et al., Acta Crystallogr. 23, 482 (1967). Clinical trial and mode of action study: T. J. Vander Salm et al., J. Thorac. Cardiovasc. Surg. 112, 1098 (1996).
Properties: Crystals from alcohol, mp 202-203°. pK1 4.43; pK2 10.75. Freely sol in water; sparingly in methanol. Practically insol in ethanol, chloroform. LD50 in rats (g/kg): 7.0 i.p.; ~3.3 i.v. (Hallesy).
Melting point: mp 202-203°
pKa: pK1 4.43; pK2 10.75
Toxicity data: LD50 in rats (g/kg): 7.0 i.p.; ~3.3 i.v. (Hallesy)
 
Derivative Type: Hydrochloride
CAS Registry Number: 4321-58-8
Molecular Formula: C6H13NO2.HCl
Molecular Weight: 167.63
Percent Composition: C 42.99%, H 8.42%, N 8.36%, O 19.09%, Cl 21.15%
Properties: mp 128-129°.
Melting point: mp 128-129°
 
Therap-Cat: Hemostatic.
Keywords: Hemostatic.