CHRYSOIDINE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C12H12N4.ClH
Molecular Weight	248.711
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	1
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

Cl.NC1=CC(N)=C(C=C1)\N=N\C2=CC=CC=C2

InChI

InChIKey=MCTQNEBFZMBRSQ-GEEYTBSJSA-N

InChI=1S/C12H12N4.ClH/c13-9-6-7-12(11(14)8-9)16-15-10-4-2-1-3-5-10;/h1-8H,13-14H2;1H/b16-15+;

HIDE SMILES / InChI

Molecular Formula	C12H12N4
Molecular Weight	212.2505
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	1
Optical Activity	NONE

Molecular Formula	ClH
Molecular Weight	36.461
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
Degradation of textile dyes mediated by plant peroxidases.	2002 Jul-Dec	12396133
Highly sensitive indirect photometric detection of cations by capillary electrophoresis with the cationic dye chrysoidine.	2003 May 16	12830880
Performance of TX-100 and TX-114 for the separation of chrysoidine dye using cloud point extraction.	2006 Sep 21	16600488
Extracellular terbium and divalent cation effects on the red blood cell Na pump and chrysoidine effects on the renal Na pump.	2007 Jul-Aug	17459735
Role of polyfunctional organic molecules in the synthesis and assembly of metal nanoparticles.	2007 Jun	17655007
Adsorption of Chrysoidine R by using fly ash in batch process.	2007 Jun 25	17141408
Chelating compound, chrysoidine, is more effective in both antiprion activity and brain endothelial permeability than quinacrine.	2007 May	17235694
[Simultaneous determination of chrysoidine and auramine O in bean products by HPLC].	2007 Sep	18161341
Identification of inorganic improvised explosive devices by analysis of postblast residues using portable capillary electrophoresis instrumentation and indirect photometric detection with a light-emitting diode.	2007 Sep 15	17705451
Cloud point extraction and flame atomic absorption spectrometry combination for copper(II) ion in environmental and biological samples.	2008 Dec 30	18433996
Induction of DNA strand breaks by genotoxicants in the alga Chlamydomonas reinhardtii.	2009 Sep	19385715
Large impact of the apoplast on somatic embryogenesis in Cyclamen persicum offers possibilities for improved developmental control in vitro.	2010 Apr 28	20426818
Rapid method for the confirmatory analysis of chrysoidine in aquaculture products by ultra-performance liquid chromatography-tandem mass spectrometry.	2010 Sep	20082281

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 17:32:16 GMT 2023` Edited by `admin` on `Fri Dec 15 17:32:16 GMT 2023`
Record UNII	2431787HMZ
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

CHRYSOIDINE

Common Name

English

4-(2-PHENYLDIAZENYL)-1,3-BENZENEDIAMINE HYDROCHLORIDE (1:1)

Systematic Name

English

C.I. BASIC ORANGE 2

Common Name

English

CHRYSOIDINE ORANGE

Common Name

English

2,4-DIAMINOAZOBENZENE HYDROCHLORIDE

Systematic Name

English

TERTROPHENE BROWN CG

Common Name

English

CHRYSOIDINE [IARC]

Common Name

English

C.I. 11270

Common Name

English

BASIC ORANGE 2

Official Name

English

NSC-152834

Code

English

BASIC ORANGE 2 [INCI]

Common Name

English

CHRYSOIDINE HYDROCHLORIDE

Common Name

English

CHRYSOIDINE [MI]

Common Name

English

CHRYSOIDINE Y

Common Name

English

4-PHENYLAZO-M-PHENYLENEDIAMINE HYDROCHLORIDE

Systematic Name

English

Code System Code Type Description

ECHA (EC/EINECS)

208-545-8