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Detail of > 60-32-2

  • MSDS Download
  • CAS Number:
  • 60-32-2
  • Name:
  • Hexanoicacid, 6-amino-

  • Superlist Name:
  • 6-Aminocaproic acid
  • Formula:
  • C6H13NO2
  • Molecular Structure:
  • Synonyms:
  • Caproicacid, e-amino- (3CI);6-Amino-n-hexanoic acid;6-Aminocaproic acid;6-Aminohexanoic acid;ACS;Acepramin;Amicar;Amikar;CL10304;CY 116;Caplamin;Capramol;Caprolisin;EACA;Epsamon;Epsicapron;Epsilon S;Hemocaprol;Hemopar;Hepin;NSC 212532;NSC 26154;NSC 400230;e-Amino-n-hexanoic acid;e-Aminocaproic acid;e-Leucine;e-Norleucine;w-Aminocaproic acid;w-Aminohexanoic acid;
  • Molecular Weight:
  • 131.20
  • EINECS:
  • 200-469-3
  • Density:
  • 1.042 g/cm3
  • Melting Point:
  • 207-209 °C (dec.)(lit.)
  • Boiling Point:
  • 255.6 °C at 760 mmHg
  • Flash Point:
  • 108.4 °C
  • Solubility:
  • soluble in water
  • Appearance:
  • white crystalline powder
  • Hazard Symbols:
  • IrritantXi
  • Risk Codes:
  • 36/37/38
  • Safety:
  • 26-36Details
  • Deleted CAS:
  • 93208-38-9|87867-96-7
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    Reference

    Hardenable coating composition
    Hardenable coating composition. Traenckner, Hans Joachim; Fuhr, Karl; Rosenkranz, Hans Juergen; Patheiger, Manfred; Rudolph, Hans (Bayer A.-G., Ger.). Ger. Offen. DE 2534012 17 Feb 1977, 43 pp. (German). (Germany). CODEN: GWXXBX. CLASS: IC: C08G059-56. APPLICATION: DE 75-2534012 30 Jul 1975. DOCUMENT TYPE: Patent CA Section: 42 (Coatings, Inks, and Related Products) Section cross-reference(s): 43 Resins with high reactivity to radiation in the form of coatings but which can be stored with a min. amt. of increase in viscosity are manufd. by reaction of bisphenol A diglycidyl ether (I) [1675-54-3] with 0.Some commonly used reagents like 98-89-5 and 124-09-4 are used in this experiment.01-0.5 NH equivs. NH3(g), hexamethylenediamine [124-09-4], or .epsilon.-aminocaproic acid [60-32-2], 0.40-0.90 carboxy equivs. acrylic acid (II) [79-10-7], and 0.09-0.50 carboxy equivs. satd. aliphatic or cycloaliph. carboxylic acids per epoxy equiv. of I. Thus, 42.5 g NH3(g) was introduced in 20 h into 6800 g I at 60.degree.. Thiodiglycol catalyst (68.4 g) was then added and in 2 hrs 1386 g II was added and in an addnl. 30 min 340 g AcOH [64-19-7] was added. The mixt. was stirred at 60.degree. until an acid value of 0 was observed and then mixed with 0.05% p-methoxyphenol to give a stabilized resin. Paper and carton were coated with 8-10 .mu.m high-gloss, colorless, non-yellow coatings using the above prepd. resin in EtOAc or BuOAc as solvents, benzophenone as photosensitizer and 30-80 watt high-pressure Hg-vapor UV lamps as a drying app. .
    Effect of antikinin drugs on the course of experimental myocarditis
    Effect of antikinin drugs on the course of experimental myocarditis. Surovikina, M. S.; Odinokova, V. A.; Paleev, N. R.; Gurevich, M. A.; Yankovskaya, M. O. (Mosk. Obl. Nauchno-Issled. Klin. Inst. im. Vladimirskogo, Moscow, USSR). Kardiologiya, (9), 84-9 (Russian) 1976. CODEN: KARDA2.Several substances with their cas registry numbers 11096-15-4 and 53-86-1 may be metioned in this study. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacodynamics) The specific antikinins, anginin [1882-26-4] (6 or 10 mg/kg, orally) and contrical [11096-15-4] (3000-6000 units/kg, i.p. or i.v.) given daily to rabbits with allergic myocarditis decreased activation of the plasma kinin system. The nonspecific .epsilon.-aminocaproic acid [60-32-2] (400 mg/kg/day, orally) had similar but weaker effects. The nonspecific aspirin [50-78-2] (50 mg/kg/day, orally) and indomethacin [53-86-1] (2 mg/kg/day, orally) had no effect on the degree of activation of the plasma kinin system but decreased the duration of the inflammatory-allergic process and inhibited the amt. of circulating kininogen. All 5 compds. normalized morphol. of the heart during myocarditis, esp. the specific antikinins. .

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