One further fact respecting these compounds of carbon, oxygen and hydrogen, should be mentioned; namely, that they are divisible into two classes—the one consisting of substances that result from the destructive decomposition of organic matter, and the other consisting of substances that exist as such in organic matter. These two classes of substances exhibit, in different degrees, the properties to which we have been directing our attention. The lower alcohols, their allies and derivatives, which possess greater molecular mobility and chemical stability than the rest of these triatomic compounds, are rarely found in animal or vegetal bodies. While the sugars and amylaceous substances, the fixed oils and fats, the gums and resins, which have all of them much less molecular mobility, and are, chemically considered, more unstable and inert, are components of the living tissues of plants and animals.

§ 4. Among compounds containing all the four chief organic elements, a division analogous to that just named may be made. There are some which result from the decomposition of living tissues; there are others which make parts of living tissues in their state of integrity; and these two groups are contrasted in their properties in the same way as are the parallel groups of triatomic compounds.

Of the first division, certain products found in the animal excretions are the most important, and the only ones that need be noted; such, namely, as urea, kreatine, kreatinine. These animal-bases exhibit much less molecular mobility than the average of the substances treated of in the last section: being solid at ordinary temperatures, fusing, where fusible at all, at temperatures above that of boiling water, and having no power to assume a gaseous state. Chemically considered, their stability is low, and their activity but small, in comparison with the stabilities and activities of the simpler compounds.

It is, however, the nitrogenous constituents of living tissues, that display most markedly those characteristics of which we have been tracing the growth. Albumen, fibrin, casein, and their allies, are bodies in which that molecular mobility exhibited by three of their components in so high a degree is reduced to a minimum. These substances are known only in the solid state. That is to say, when deprived of the water usually mixed with them, they do not admit of fusion, much less of volatilization. To which add, that they have not even that molecular mobility which solution in water implies; since, though they form viscid mixtures with water, they do not dissolve in the same perfect way as do inorganic compounds. The chemical characteristics of these substances are instability and inertness carried to the extreme. How rapidly albumenoid matters decompose under ordinary conditions, is daily seen: the difficulty of every housewife being to prevent them from decomposing. It is true that when desiccated and kept from contact with air, they may be preserved unchanged for long periods; but the fact that they can be only thus preserved, proves their great instability. It is true, also, that these most complex nitrogenous principles are not absolutely inert, since they enter into combinations with some bases; but their unions are very feeble.

It should be noted, too, of these bodies, that though they exhibit in the lowest degree that kind of molecular mobility which implies facile vibration of the molecules as wholes, they exhibit in high degrees that kind of molecular mobility resulting in isomerism, which implies permanent changes in the positions of adjacent atoms with respect to each other. Each of them has a soluble and an insoluble form. In some cases there are indications of more than two such forms. And it appears that their metamorphoses take place under very slight changes of conditions.

In these most unstable and inert organic compounds, we find that the molecular complexity reaches a maximum: not only since the four chief organic elements are here united with small proportions of sulphur and sometimes phosphorus; but also since they are united in high multiples. The peculiarity which we found characterized even diatomic compounds of the organic elements, that their molecules are formed not of single equivalents of each component, but of two, three, four, and more equivalents, is carried to the greatest extreme in these compounds, which take the leading part in organic actions. According to Lieberkühn, the formula of albumen is C72H112SN18O22. That is to say, with the sulphur there are united seventy-two atoms of carbon, one hundred and twelve of hydrogen, eighteen of nitrogen, and twenty-two of oxygen: the molecule being thus made up of more than two hundred ultimate atoms.

§ 5. Did space permit, it would be useful here to consider in detail the interpretations that may be given of the peculiarities we have been tracing: bringing to their solution, the general mechanical principles which are now found to hold true of molecules as of masses. But it must suffice briefly to indicate the conclusions which such an inquiry promises to bring out.

Proceeding on these principles, it may be argued that the molecular mobility of a substance must depend partly on the inertia of its molecules; partly on the intensity of their mutual polarities; partly on their mutual pressures, as determined by the density of their aggregation; and (where the molecules are compound) partly on the molecular mobilities of their component molecules. Whence it is to be inferred that any three of these remaining constant, the molecular mobility will vary as the fourth. Other things equal, therefore, the molecular mobility of molecules must decrease as their masses increase; and so there must result that progression we have traced, from the high molecular mobility of the uncombined organic elements, to the low molecular mobility of those large-moleculed substances into which they are ultimately compounded.

Applying to molecules the mechanical law which holds of masses, that since inertia and gravity increase as the cubes of the dimensions while cohesion increases as their squares, the self-sustaining power of a body becomes relatively smaller as its bulk becomes greater; it might be argued that these large, aggregate molecules which constitute organic substances, are mechanically weak—are less able than simpler molecules to bear, without alteration, the forces falling on them. That very massiveness which renders them less mobile, enables the physical forces acting on them more readily to change the relative positions of their component atoms; and so to produce what we know as re-arrangements and decompositions.

Further, it seems a not improbable conclusion, that this formation of large aggregates of elementary atoms and resulting diminution of self-sustaining power, must be accompanied by a decrease of those dimensional contrasts to which polarity is ascribable. A sphere is the figure of equilibrium which any aggregate of units tends to assume, under the influence of simple mutual attraction. Where the number of units is small and their mutual polarities are decided, this proclivity towards spherical grouping will be overcome by the tendency towards some more special form, determined by their mutual polarities. But it is manifest that in proportion as an aggregate molecule becomes larger, the effects of simple mutual attraction must become relatively greater; and so must tend to mask the effects of polar attraction. There will consequently be apt to result in highly compound molecules like these organic ones, containing hundreds of elementary atoms, such approximation to the spherical form as must involve a less distinct polarity than in simpler molecules. If this inference be correct, it supplies us with an explanation both of the chemical inertness of these most complex organic substances, and of their inability to crystallize.