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Diaminocaproic acid

Drechsel gave it the formula CsHi4N202 and regarded it as a diaminocaproic acid Ellinger proved in 1899 that it possessed this constitution, by obtaining cadaverine from it by putrefaction, which showed that the two amino groups were in the a, e-positions —... [Pg.59]

Henderson s experiments also showed that lysine must have this constitution, namely, o, e-diaminocaproic acid. Its constitution was only definitely determined by synthesis by Fischer and Weigert by the following method —... [Pg.59]

When y-cyanopropylmalonic ester is treated with nitrous acid, it loses one of its carboxethyl groups and is converted into a-oximido-8-cyanovalerianic acid, which on reduction with sodium amalgam yields a, e-diaminocaproic acid, thus —... [Pg.59]

SYNS AhQNUTRIN (X,e-DIAMINOCAPROIC ACID 2,6-DIAMINOHEXANOIC ACID 1-LYSINE (9CI) -(+)-LYSINE LYSINE ACID... [Pg.848]

Ornithine, NH2.CH2.CH2.CH2.CHNH2.COOH, a, 5-di-aminovaleric acid, and lysine, a, e-diaminocaproic acid, are obtained from proteins. The former is converted into putrescine, NH2(CH2)4NH2, and the latter into cadaverine, NH2(CH2)sNH2, by putrefactive bacteria. [Pg.319]

In Reference 107, the effect of grafting of a polar group (MAH) onto LDPE chains and the chemical modification of clay particles with 2,6-diaminocaproic acid (L-lysine monohydrochloride) to produce nanocomposites with a matrix composed of a ternary blend of PEs (LDPE, LLDPE, and HDPE) was studied in detail. X-ray diffraction was used to determine the exfoliation degree of the clay. Morphological features were revealed by scanning electron microscopy and thermal analysis disclosed the thermal stability of the samples. Comparative analyses of the mechanical (under tension) and rheological properties of the nanocomposites were carried out as well. [Pg.592]

CAS 56-87-1 EINECS/ELINCS 200-294-2 Synonyms a,e-Diaminocaproic acid L-a,e-Diaminocaproic acid 2,6-Diaminohexanoic acid Lys Lysine (INCI)... [Pg.2437]

Group IV, Diamino, Monocarboxylic Acids. Lysine (a, -diaminocaproic acid) is distinguished by the extra amino group in its side chain which imparts basic properties to it. Depending on the pH of the solution, lysine may bear various charges. Furthermore, hydroxylysine has been discovered in collagen. [Pg.28]

See other pages where Diaminocaproic acid is mentioned: [Pg.244]    [Pg.3]    [Pg.1611]    [Pg.600]    [Pg.539]    [Pg.384]    [Pg.773]    [Pg.887]    [Pg.595]    [Pg.209]    [Pg.27]    [Pg.1202]    [Pg.644]    [Pg.449]    [Pg.6]    [Pg.7]    [Pg.73]    [Pg.74]   
See also in sourсe #XX -- [ Pg.319 ]



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