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

Details

Stereochemistry ACHIRAL
Molecular Formula C14H16N2O2
Molecular Weight 244.289
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIANISIDINE

SMILES

COC1=C(N)C=CC(=C1)C2=CC(OC)=C(N)C=C2

InChI

InChIKey=JRBJSXQPQWSCCF-UHFFFAOYSA-N
InChI=1S/C14H16N2O2/c1-17-13-7-9(3-5-11(13)15)10-4-6-12(16)14(8-10)18-2/h3-8H,15-16H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C14H16N2O2
Molecular Weight 244.289
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Efficacy of 101 antimicrobials and other agents on the development of Cryptosporidium parvum in vitro.
1996 Dec
Using base-specific Salmonella tester strains to characterize the types of mutation induced by benzidine and benzidine congeners after reductive metabolism.
2001 Dec
Rapid screening of H(2)O(2) production by Mycoplasma mycoides and differentiation of European subsp. mycoides SC (small colony) isolates.
2001 Feb 26
Recombinant expression of N-terminal truncated mutants of the membrane bound mouse, rat and human flavoenzyme dihydroorotate dehydrogenase. A versatile tool to rate inhibitor effects?
2001 Mar
Dyes metabolized to 3,3'-dimethoxybenzidine (3,3'-dimethoxybenzidine dye class).
2002
Optimisation of the enzyme-based determination of hydrogen peroxide using the quartz crystal microbalance.
2002 Sep
Synthesis and evaluation of analogues of Congo red as potential compounds against transmissible spongiform encephalopathies.
2003 Jun
Simplified method to assay total plasma peroxidase activity and ferriheme products in sickle cell anemia, with initial results in assessing clinical severity in a trial with citrulline therapy.
2003 Oct
Dyes metabolized to 3,3'-dimethoxybenzidine (3,3'-dimethoxybenzidine dye class).
2004
Spectrophotometric determination of leukocytes in urine.
2004
Oxidation of benzidine and its derivatives by thyroid peroxidase.
2004 Feb
A novel automated method to measure total antioxidant response against potent free radical reactions.
2004 Feb
Enzymes in the cavity of hollow silica nanoparticles.
2005 Apr 1
A new automated colorimetric method for measuring total oxidant status.
2005 Dec
LC-MS/MS method for the confirmatory determination of aromatic amines and its application in textile analysis.
2005 Jan
Precise method for the measurement of catalase activity in honey.
2005 May-Jun
Hollow gold nanoparticles encapsulating horseradish peroxidase.
2005 Nov
Characterization of peroxidase in buckwheat seed.
2006 Feb
Improved analytical sensitivity reveals the occurrence of gender-related variability in diamine oxidase enzyme activity in healthy individuals.
2007 Nov
Screening of 397 chemicals and development of a quantitative structure--activity relationship model for androgen receptor antagonism.
2008 Apr
Hemozymes peroxidase activity of artificial hemoproteins constructed from the Streptomyces lividans xylanase A and iron(III)-carboxy-substituted porphyrins.
2008 Apr
Metabolic adaptations to ammonia-induced oxidative stress in leaves of the submerged macrophyte Vallisneria natans (Lour.) Hara.
2008 Apr 28
Sequential and simultaneous determination of bromate and chlorite (DBPs) by flow techniques: kinetic differentiation.
2008 Aug 15
Effect of Zofenopril on regeneration of sciatic nerve crush injury in a rat model.
2009 Jun 9
Inter-laboratory evaluation of the bioluminescent Salmonella reverse mutation assay using 10 model chemicals.
2009 Sep
[New approaches to the measurement of the concentration and peroxidase activity of myeloperoxidase in human blood plasma].
2009 Sep-Oct
Non-linear effects of macromolecular crowding on enzymatic activity of multi-copper oxidase.
2010 Apr
Effects of oxygen, growth state, and senescence on the antioxidant responses of WI-38 fibroblasts.
2010 Dec
Optimization of media components for laccase production by litter dwelling fungal isolate Fusarium incarnatum LD-3.
2010 Feb
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:13:07 GMT 2023
Edited
by admin
on Fri Dec 15 17:13:07 GMT 2023
Record UNII
MJY508JZXV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIANISIDINE
MI  
Common Name English
3,3'-DIMETHOXY-4,4'-DIAMINOBIPHENYL
Systematic Name English
3,3'-DIMETHOXYBENZIDINE
HSDB  
Systematic Name English
DIANISIDINE [MI]
Common Name English
DIMETHOXYBENZIDINE, 3,3'-
Systematic Name English
3,3'-DIMETHOXYBENZIDINE [HSDB]
Common Name English
NSC-3168
Code English
3,3'-DIMETHOXYBENZIDINE [IARC]
Common Name English
3,3'-DIMETHOXY-(1,1'-BIPHENYL)-4,4'-DIAMINE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C45178
Created by admin on Fri Dec 15 17:13:07 GMT 2023 , Edited by admin on Fri Dec 15 17:13:07 GMT 2023
NCI_THESAURUS C461
Created by admin on Fri Dec 15 17:13:07 GMT 2023 , Edited by admin on Fri Dec 15 17:13:07 GMT 2023
Code System Code Type Description
ECHA (EC/EINECS)
204-355-4
Created by admin on Fri Dec 15 17:13:07 GMT 2023 , Edited by admin on Fri Dec 15 17:13:07 GMT 2023
PRIMARY
HSDB
1627
Created by admin on Fri Dec 15 17:13:07 GMT 2023 , Edited by admin on Fri Dec 15 17:13:07 GMT 2023
PRIMARY
NSC
3168
Created by admin on Fri Dec 15 17:13:07 GMT 2023 , Edited by admin on Fri Dec 15 17:13:07 GMT 2023
PRIMARY
CAS
119-90-4
Created by admin on Fri Dec 15 17:13:07 GMT 2023 , Edited by admin on Fri Dec 15 17:13:07 GMT 2023
PRIMARY
EPA CompTox
DTXSID3025091
Created by admin on Fri Dec 15 17:13:07 GMT 2023 , Edited by admin on Fri Dec 15 17:13:07 GMT 2023
PRIMARY
NCI_THESAURUS
C44365
Created by admin on Fri Dec 15 17:13:07 GMT 2023 , Edited by admin on Fri Dec 15 17:13:07 GMT 2023
PRIMARY
PUBCHEM
8411
Created by admin on Fri Dec 15 17:13:07 GMT 2023 , Edited by admin on Fri Dec 15 17:13:07 GMT 2023
PRIMARY
MERCK INDEX
m4262
Created by admin on Fri Dec 15 17:13:07 GMT 2023 , Edited by admin on Fri Dec 15 17:13:07 GMT 2023
PRIMARY Merck Index
MESH
D003962
Created by admin on Fri Dec 15 17:13:07 GMT 2023 , Edited by admin on Fri Dec 15 17:13:07 GMT 2023
PRIMARY
FDA UNII
MJY508JZXV
Created by admin on Fri Dec 15 17:13:07 GMT 2023 , Edited by admin on Fri Dec 15 17:13:07 GMT 2023
PRIMARY
WIKIPEDIA
o-Dianisidine
Created by admin on Fri Dec 15 17:13:07 GMT 2023 , Edited by admin on Fri Dec 15 17:13:07 GMT 2023
PRIMARY