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| | 3,6-DIAMINOACRIDINE HYDROCHLORIDE Basic information |
| Product Name: | 3,6-DIAMINOACRIDINE HYDROCHLORIDE | | Synonyms: | 3,6-diaminoacridinehydrochloridehemihydrate;3,6-diamino-acridinmonohydrochloride;nci-c04137;PROFLAVINE HYDROCHLORIDE;PROFLAVINE MONOHYDROCHLORIDE;PROFLAVIN MONOHYDROCHLORIDE;TIMTEC-BB SBB003182;EUFLAVIN | | CAS: | 952-23-8 | | MF: | C13H12ClN3 | | MW: | 245.71 | | EINECS: | 213-459-9 | | Product Categories: | | | Mol File: | 952-23-8.mol |  |
| | 3,6-DIAMINOACRIDINE HYDROCHLORIDE Chemical Properties |
| WGK Germany | 3 | | RTECS | AR9064000 |
| | 3,6-DIAMINOACRIDINE HYDROCHLORIDE Usage And Synthesis |
| Uses | Acridine-3,6-diamine hydrochloride, canbe used for studying cation transfer at the liquid–liquid interface. | | Definition | ChEBI: A hydrochloride resulting from the reaction of equimolar amounts of 3,6-diaminoacridine and hydrogen chloride. | | General Description | Brown powder. | | Air & Water Reactions | Slightly soluble in water. | | Reactivity Profile | 3,6-DIAMINOACRIDINE HYDROCHLORIDE is amphoteric. Reacts both as a weak acid and as a weak base. | | Safety Profile | Poison by
subcutaneous route. Questionable
carcinogen. Mutation data reported. When
heated to decomposition it emits very toxic
fumes of NOx and HCl. Used as a drug, as a
Isinfectant, and as a topical antiseptic. | | Purification Methods | It is first purified by precipitation of the free base by adding aqueous NH3 solution to an aqueous solution of the hydrochloride or hydrogen sulfate (see below), drying the precipitate and subliming at 0.01mm Hg [Müller & Crothers Eur J Biochem, 54 267 1975]. [Beilstein 22 H 487.] |
| | 3,6-DIAMINOACRIDINE HYDROCHLORIDE Preparation Products And Raw materials |
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