952-23-8 Usage
Uses
Used in Chemical Research:
3,6-DIAMINOACRIDINE HYDROCHLORIDE is used as a research compound for studying cation transfer at the liquid-liquid interface. This application is valuable for understanding the behavior of cations in different environments and can contribute to the development of new chemical processes and technologies.
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.]
Check Digit Verification of cas no
The CAS Registry Mumber 952-23-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,5 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 952-23:
(5*9)+(4*5)+(3*2)+(2*2)+(1*3)=78
78 % 10 = 8
So 952-23-8 is a valid CAS Registry Number.
InChI:InChI=1/2C13H11N3.2ClH.H2O/c2*14-10-3-1-8-5-9-2-4-11(15)7-13(9)16-12(8)6-10;;;/h2*1-7H,14-15H2;2*1H;1H2
952-23-8Relevant academic research and scientific papers
Chemical oxidative degradation of acridine orange dye in aqueous solution by Fenton's reagent
Chen, Chiing-Chang,Wu, Ren-Jang,Tzeng, Yi-You,Lu, Chung-Shin
experimental part, p. 1147 - 1155 (2010/08/13)
Degradation of acridine orange (AO) in aqueous solution by Fenton's reagent (Fe2+ and H2O2) was investigated. The effects of different reaction parameters such as initial AO concentration, pH value of solution, ferrous con
Aminoacridine-α, β-(D)- or -(L)-N-glycoside derivatives, the salts thereof and a process for the preparation of such compounds
-
, (2008/06/13)
The invention relates to novel aminoacridine-α,β-(D)- and -(L)-N-glycoside derivatives, the salts thereof and to a novel process for the preparation of such compounds and salts. The novel compounds have the formula I STR1 wherein R is hydrogen or a group of the formula II STR2 wherein n=0 or 1, p=1 or 2, A-p is an anion, preferably halogenide, R1 is hydrogen or a methyl group and R2 is hydrogen or a sugar residue, or R is dimethylamine, and the two substituents X and X1 are identical or different and stand for hydrogen, a group of the formula II, dimethylamine, halogen, a C1-4 alkyl group, a C1-4 alkoxy group, for a nitro-, cyano-, carbomethoxy-, carbamoyl-, phenyl- or a C1-4 alkylphenyl group, with the restriction that at least one of the substituents R, X and X1 represents a group of formula II with R2 =sugar residue, and R3 is hydrogen or a C1-5 alkyl group.
