Summary

1911 Encyclopædia Britannica, Volume 10… (1911)

By heating the coloured dimethyl ether with caustic soda, the monomethyl ether is obtained (O. Fischer and E. Hepp, Ber., 1895, 28, p. 397) ; this crystallizes in triclinic tables, and melts at 262° C. It is to be noted that the colourless monomethyl ether fluoresces strongly in alkaline solution, the dimethyl ether of melting point 208° fluoresces only in neutral solution (e.g., in alcoholic solution) , and the dimethyl ether of melting point 198° C. only in concentrated hydrochloric or sulphuric acid solution (Fischer and Hepp) .
Source: Wikisource

1911 Encyclopædia Britannica, Volume 10… (1911)

It crystallizes from alcohol in yellowish red needles, and dyes silk, wool, and mordanted cotton a fine pink colour. When heated with caustic alkalis it yields dibromresorcin and dibrommonoresorcin-phthalein. The corresponding iodo compound is known as erythrosin. Fluorescein is readily nitrated, yielding a di- or tetra-nitro compound according to conditions.
Source: Wikisource

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