Difference between revisions of "Alizarin blue"
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5,6-dihydroxynaphtho[2,3-f]-quinoline-7,12-dione; 7,8-dihydroxy-5,6-phthaloquinoline; CI 67410; bleu d'alizarine (Fr.); blu d' alizarina (It.); azul de alizarina (Port.); Alizarine Blue R; | 5,6-dihydroxynaphtho[2,3-f]-quinoline-7,12-dione; 7,8-dihydroxy-5,6-phthaloquinoline; CI 67410; bleu d'alizarine (Fr.); blu d' alizarina (It.); azul de alizarina (Port.); Alizarine Blue R; | ||
| − | == | + | == Physical and Chemical Properties == |
Soluble in glacial acetic acid, amyl alcohol and hot benzene. Slightly soluble in ethanol, ether and cold benzene. Insoluble in water. | Soluble in glacial acetic acid, amyl alcohol and hot benzene. Slightly soluble in ethanol, ether and cold benzene. Insoluble in water. | ||
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! scope="row"| Melting Point | ! scope="row"| Melting Point | ||
| − | | 268-270 | + | | 268-270 C |
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! scope="row"| Molecular Weight | ! scope="row"| Molecular Weight | ||
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| − | == | + | ==Resources and Citations== |
* Richard S. Lewis, ''Hawley's Condensed Chemical Dictionary'', Van Nostrand Reinhold, New York, 10th ed., 1993 | * Richard S. Lewis, ''Hawley's Condensed Chemical Dictionary'', Van Nostrand Reinhold, New York, 10th ed., 1993 | ||
Latest revision as of 08:23, 26 April 2022
Description
Alizarine blue crystallizes in brownish-violet needles from a benzene solution. When prepared in a saturated alcoholic solution, alizarin blue is used as an acid-base indicator. It changes from pink at pH 0.0 to yellow at pH 2.6. It also changes from yellow at pH 6.0 to green at pH 7.6.
See also Alizarin.
Synonyms and Related Terms
5,6-dihydroxynaphtho[2,3-f]-quinoline-7,12-dione; 7,8-dihydroxy-5,6-phthaloquinoline; CI 67410; bleu d'alizarine (Fr.); blu d' alizarina (It.); azul de alizarina (Port.); Alizarine Blue R;
Physical and Chemical Properties
Soluble in glacial acetic acid, amyl alcohol and hot benzene. Slightly soluble in ethanol, ether and cold benzene. Insoluble in water.
| Composition | C17H9NO4 |
|---|---|
| Melting Point | 268-270 C |
| Molecular Weight | 291.25 |
Resources and Citations
- Richard S. Lewis, Hawley's Condensed Chemical Dictionary, Van Nostrand Reinhold, New York, 10th ed., 1993
- The Merck Index, Susan Budavari (ed.), Merck Research Labs, Whitehouse Station, NJ, 12th Edition, 1996 Comment: entry 234