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| | 3,6-diamino-2,7,10-trimethylacridinium chloride Basic information |
| Product Name: | 3,6-diamino-2,7,10-trimethylacridinium chloride | | Synonyms: | 3,6-diamino-2,7,10-trimethylacridinium chloride;BASIC ORANGE 4-11( C.I. 46035);Basic Orange 4;C.I.Basic Orange 4:C.I.46035;3,6-Diamino-2,7,10-trimethylacridin-10-ium chloride;Acridinium, 3,6-diamino-2,7,10-trimethyl-, chloride (1:1);C.I.Basic Yellow 5 | | CAS: | 6441-73-2 | | MF: | C16H18N3.Cl | | MW: | 287.79 | | EINECS: | 229-224-9 | | Product Categories: | | | Mol File: | 6441-73-2.mol |  |
| | 3,6-diamino-2,7,10-trimethylacridinium chloride Chemical Properties |
| | 3,6-diamino-2,7,10-trimethylacridinium chloride Usage And Synthesis |
| Preparation | Basic dye C.I. 46025 (by Formaldehydeand 4-Methylbenzene-1,3-diaminereaction, product and amino reaction hydrochloric acid and ammonium chloride heating or remove ammonia, melting with ferric chloride and oxidation) and Dimethyl sulfateor and Methyl 4-methylbenzenesulfonatereaction. Note: the market many similar Basic dye, they are through the Basic dye C.I. 46025 or 46065 (from Benzaldehyde and 4-Methylbenzene-1,3-diaminediazo, cyclization, and then by oxidation with ferric chloride into a base derived. When alcohol and mineral acid or halide burning reaction, amino group is alkylated, but the use of Dimethyl sulfate or Methyl 4-methylbenzenesulfonateor Ethyl p-toluenesulfonate, the resulting formation of a real acridine heterocyclic compounds. | | Properties and Applications | yellow orange
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| | 3,6-diamino-2,7,10-trimethylacridinium chloride Preparation Products And Raw materials |
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