U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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 of CHRYSOIDINE

SMILES

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

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

PubMed

TitleDatePubMed
Rapid method for the confirmatory analysis of chrysoidine in aquaculture products by ultra-performance liquid chromatography-tandem mass spectrometry.
2010-09
[Removal of chrysoidine from water by functionalized mesoporous material SBA-16].
2010-06
Large impact of the apoplast on somatic embryogenesis in Cyclamen persicum offers possibilities for improved developmental control in vitro.
2010-04-28
Removal and recovery of Chrysoidine Y from aqueous solutions by waste materials.
2010-04-15
Investigation on the toxic interaction of chrysoidine hydrochloride-CTMAB combined contamination with calf thymus DNA.
2010-01
Induction of DNA strand breaks by genotoxicants in the alga Chlamydomonas reinhardtii.
2009-09
Lobar pneumonia treated by Musgrave Park physicians.
2009-05
Cloud point extraction and flame atomic absorption spectrometry combination for copper(II) ion in environmental and biological samples.
2008-12-30
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.
2007-09-15
[Simultaneous determination of chrysoidine and auramine O in bean products by HPLC].
2007-09
Adsorption of Chrysoidine R by using fly ash in batch process.
2007-06-25
Role of polyfunctional organic molecules in the synthesis and assembly of metal nanoparticles.
2007-06
Chelating compound, chrysoidine, is more effective in both antiprion activity and brain endothelial permeability than quinacrine.
2007-05
Extracellular terbium and divalent cation effects on the red blood cell Na pump and chrysoidine effects on the renal Na pump.
2007-02-15
Performance of TX-100 and TX-114 for the separation of chrysoidine dye using cloud point extraction.
2006-09-21
Highly sensitive indirect photometric detection of cations by capillary electrophoresis with the cationic dye chrysoidine.
2003-05-16
Degradation of textile dyes mediated by plant peroxidases.
2002-10-25
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:47:51 GMT 2025
Edited
by admin
on Mon Mar 31 18:47:51 GMT 2025
Record UNII
2431787HMZ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHRYSOIDINE
MI  
Common Name English
BASIC ORANGE 2
INCI  
INCI  
Preferred 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
NSC-152834
Code 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
Created by admin on Mon Mar 31 18:47:51 GMT 2025 , Edited by admin on Mon Mar 31 18:47:51 GMT 2025
PRIMARY
FDA UNII
2431787HMZ
Created by admin on Mon Mar 31 18:47:51 GMT 2025 , Edited by admin on Mon Mar 31 18:47:51 GMT 2025
PRIMARY
MERCK INDEX
m3531
Created by admin on Mon Mar 31 18:47:51 GMT 2025 , Edited by admin on Mon Mar 31 18:47:51 GMT 2025
PRIMARY Merck Index
NSC
152834
Created by admin on Mon Mar 31 18:47:51 GMT 2025 , Edited by admin on Mon Mar 31 18:47:51 GMT 2025
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CAS
532-82-1
Created by admin on Mon Mar 31 18:47:51 GMT 2025 , Edited by admin on Mon Mar 31 18:47:51 GMT 2025
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HSDB
5491
Created by admin on Mon Mar 31 18:47:51 GMT 2025 , Edited by admin on Mon Mar 31 18:47:51 GMT 2025
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MESH
C005562
Created by admin on Mon Mar 31 18:47:51 GMT 2025 , Edited by admin on Mon Mar 31 18:47:51 GMT 2025
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EPA CompTox
DTXSID0024559
Created by admin on Mon Mar 31 18:47:51 GMT 2025 , Edited by admin on Mon Mar 31 18:47:51 GMT 2025
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