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2.6- Dihydroxy-3-phenylazo

Chlorpromazine reacts with 9-bromomethylacridine in acetonitrile to give a quaternary ammonium derivative, which on subsequent photolysis yields fluorescent products [136]. The fluorescence is linear over the analyte range of 0.05 to 1 pg. Lumogallion 5-chloro-3-(2,4-dihydroxy-phenylazo)-2-hydroxybenzenesulfonic acid forms a fluorescent ion-pair complex with chlorpromazine in the presence of Al(III) which is extracted (without interference from primary or secondary amines) up to equimolar concentrations [137,138]. [Pg.136]

Das Diazonium-Salz von l,2-Bis-[4-diazoniono-3-sulfonio-phenyl]-ethen reagiert jedoch mit Brenzcatechin zum /,2-Bis-[4-(3,4-dihydroxy-phenylazo)-3-sulfophenyl]-ethen, das mit Kupfer blaue Losnngen bildet und zu dessen quantitativer Bestimmung verwendet werden kann3 ... [Pg.26]

Bis-[4-nitro-phenylazo]-l, 3-dihydroxy-benzol 20% Schmp. 290-292° (Zers.)... [Pg.27]

Sodium 2-(Parasulfo phenylazo)- , 8-dihydroxy- 3,6-naphthalene disulfonate] also called [4, 5 dihydroxy-3-(para-sulfophenylazo)-2, 7-napthalenedisulfonic acid trisodium salt]. [Pg.128]

Sodium 4-[2,4-dihydroxy-3-(2,4-dimethylphenylazo) phenylazo] benzenesulfonate. See Acid orange 24 Sodium dihydroxyethylglycinate CAS 139-41-3 EINECS/ELINCS 205-360-4 Synonyms Bicine N,N-Bis (2-hydroxyethyl) glycine, monosodium salt N,N-Bis (2-hydroxyethyl) glycine, sodium salt DHEG DHEGNa... [Pg.4015]

It has been found by experiment that substances of the type RX, containing two different haptenic groups, do not form precipitates with either anti-R serum or anti-X serum Alone, but do form precipitates with a mixture of the two specific antisera. This provides proof of the effective bivalence of the dihaptenic precipitating antigen, and thus furnishes further evidence for e framework theory of antigen-antibody precipitation. In these experiments tiie anti-R serum and anti-X serum were made by injecting rabbits with sheep serum coupled with diazotized p-arsanilic add and diazotized p-aminobenzoic acid, respectively, and the RX substances used were l-amino-2-/>-(p-azophenylazo)-phenylarsonic acid-3,6-disul-fonic add 7-p-(p-azophenylazo)-benzoic acid-8-hy-droxynaphthalene and l,8-dihydroxy-2-/>-azo-phenylarsonic acid-3,6-disulfonic acid-7-p-(p-azo-phenylazo)-benzoic acid-naphthalene. [Pg.117]

Chloro-2-hydroxy-3-sulfophenyI) azol-6-phenylazo-4,5-dihydroxy-2,7-naphthalenedisulfonic acid, 9CI... [Pg.231]

Carboxy-4-sulfophenylazo)-4,5-dihydroxy-6-[4-(phenylazo)phenylazo]-2,7-naphthalenedisulfonic acid... [Pg.375]


See other pages where 2.6- Dihydroxy-3-phenylazo is mentioned: [Pg.43]    [Pg.1183]    [Pg.2553]    [Pg.275]    [Pg.26]    [Pg.43]    [Pg.338]    [Pg.152]    [Pg.1110]    [Pg.338]    [Pg.354]    [Pg.354]    [Pg.79]    [Pg.1162]    [Pg.855]    [Pg.333]    [Pg.346]    [Pg.1182]    [Pg.1183]    [Pg.1197]    [Pg.1197]    [Pg.1723]    [Pg.1723]    [Pg.1953]    [Pg.2553]    [Pg.2557]    [Pg.2622]    [Pg.2662]    [Pg.2674]    [Pg.2784]    [Pg.77]    [Pg.82]    [Pg.368]    [Pg.368]    [Pg.383]   
See also in sourсe #XX -- [ Pg.43 ]




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2-[4- phenylazo

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