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Phthalein purple

Oxo-I 3H)- isobenzofuranylidene)bis[(6-hydroxy-5-methyl 3,I-phenylene)methylene]]bis[ -(carboxymethyl) glycine],9CI. 3,3 -Bis[N,l di(carboxymethyl)aminomethyl]-o-cresolphthalein. Phthalein complexone. Metal phthalein. 0-Cresolphthalein complexone. Phthalein purple [2411-89-4]... [Pg.256]

Phthalein complexone, see C-00308 Phthalein purple, see C-00308 Phthalein violet, P-00220... [Pg.1048]

Phthaleins (Phthalic anhydride TH SO.) red green fluorescence usually blue purple red blue- purple — green faint green fluorescence... [Pg.410]

Similarly o-sulphobeiizoic anhydride and o-cresol yields o-cresolsulphone-phthalein (o-cresol red) dibromination of the last-named gives dibromo-o-sulphonephthaleln (bromocresol purple) ... [Pg.989]

The arsanilic acid can be obtained from the aqueous alkaline solution either as the free acid or as the sodium salt. To obtain the free acid the solution is acidified with concentrated hydrochloric acid until the purple color of tetrabromophenolsulfon-phthalein is changed to a faint yellow. Care should be taken, in the addition of the acid, not to overstep the end-point (Note 4). Crystallization is stimulated by scratching and the flask is allowed to stand over night to complete the precipitation. The crystals are filtered off and recrystallized once from water (about 2500 cc.) in order to obtain a white product. If the initial crystals obtained have an appreciable pink tinge, it is advisable to remove most of the color by digesting with a small volume of warm alcohol before crystallization from water is attempted (Note 5). [Pg.14]

Meta cresol purple m-Cresolsulphone-phthalein Red Yellow 1-2-2-8... [Pg.54]

The pH required for the precipitation of C is about 5-5 this can be more conveniently achieved by the use of either nitrazine (sodium dinitrophenyl-azo-naphthol sulphonate) or bromocresol purple (dibromo-o-cresol-sulphone-phthalein) test-papers. All that is necessary is to add the sodium hydroxide solution until the appropriate colour change is produced it is best to use a... [Pg.451]

F) Preparation of Sulfonphthaleins. The preparations described involve (1) hydrolysis of o-sulfobenzoic imide (saccharin) to the ammonium salt of o-sulfobenzoic acid (2) preparation of o-sulfo-benzoic anhydride (3) preparation of phenolsulfonphthalein (phenol red) (4) bromination of phenolsulfonphthalein to tetrabromo derivative (bromophenol blue) (5) preparation of o-cresolsulfon-phthalein (cresol red) (6) bromination of o-cresolsulfonphthalein to the dibromo derivative (bromocresol purple)The equations for the steps are ... [Pg.337]

See other pages where Phthalein purple is mentioned: [Pg.196]    [Pg.557]    [Pg.1202]    [Pg.1163]    [Pg.572]    [Pg.597]    [Pg.1204]    [Pg.100]    [Pg.1100]    [Pg.1501]    [Pg.1505]    [Pg.1238]    [Pg.1439]    [Pg.1443]    [Pg.1502]    [Pg.1506]    [Pg.2833]    [Pg.1163]    [Pg.196]    [Pg.557]    [Pg.1202]    [Pg.1163]    [Pg.572]    [Pg.597]    [Pg.1204]    [Pg.100]    [Pg.1100]    [Pg.1501]    [Pg.1505]    [Pg.1238]    [Pg.1439]    [Pg.1443]    [Pg.1502]    [Pg.1506]    [Pg.2833]    [Pg.1163]    [Pg.943]    [Pg.72]    [Pg.1212]    [Pg.17]    [Pg.180]    [Pg.124]    [Pg.314]    [Pg.390]    [Pg.28]    [Pg.40]    [Pg.1166]   


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