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Details

Stereochemistry ACHIRAL
Molecular Formula C8H12N2
Molecular Weight 136.1943
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIMETHYL-P-PHENYLENEDIAMINE

SMILES

CN(C)C1=CC=C(N)C=C1

InChI

InChIKey=BZORFPDSXLZWJF-UHFFFAOYSA-N
InChI=1S/C8H12N2/c1-10(2)8-5-3-7(9)4-6-8/h3-6H,9H2,1-2H3

HIDE SMILES / InChI
Molecular Formula C8H12N2
Molecular Weight 136.1943
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
139594
PubMed

PubMed

TitleDatePubMed
A novel mixed valence form of Rhus vernicifera laccase and its reaction with dioxygen to give a peroxide intermediate bound to the trinuclear center.
2001 Jun
Antiradical efficiency of Maillard reaction mixtures in a hydrophilic media.
2002 May 8
Anion- and pH-dependent activation of the soluble form of dopamine beta-hydroxylase.
2003 Feb 1
Enzymological characterization of EpoA, a laccase-like phenol oxidase produced by Streptomyces griseus.
2003 May
A multisyringe flow injection method for the automated determination of sulfide in waters using a miniaturised optical fiber spectrophotometer.
2004 Dec 15
Biochemical and molecular characterization of an azoreductase from Staphylococcus aureus, a tetrameric NADPH-dependent flavoprotein.
2005 May
Flow-through optical fiber sensor for automatic sulfide determination in waters by multisyringe flow injection analysis using solid-phase reflectometry.
2005 May
Synthesis and antibacterial activity of some imidazole-5-(4H)one derivatives.
2005 Oct
Microbial conversion of selected azo dyes and their breakdown products.
2006
Enzymatic and spectroscopic studies on the activation or inhibition effects by substituted phenolic compounds in the oxidation of aryldiamines and catechols catalyzed by Rhus vernicifera laccase.
2006 Dec
Sequential determination of trace amounts of iron and copper in water samples by flow injection analysis with catalytic spectrophotometric detection.
2006 Jan
Determination of total and dissolved amount of iron in water samples using catalytic spectrophotometric flow injection analysis.
2006 Jan 15
Antioxidant profile of red wines evaluated by total antioxidant capacity, scavenger activity, and biomarkers of oxidative stress methodologies.
2007 Jul 11
Conformational analysis of the electron-transfer kinetics across oligoproline peptides using N,N-dimethyl-1,4-benzenediamine donors and pyrene-1-sulfonyl acceptors.
2007 Jun 21
The effect of substituent groups on the reductive degradation of azo dyes by zerovalent iron.
2007 Jun 25
Metabolism of azo dyes by Lactobacillus casei TISTR 1500 and effects of various factors on decolorization.
2007 Mar
Antioxidant and radical scavenging properties of curcumin.
2008 Jul 10
Covalently modified graphitic carbon-based stationary phases for anion chromatography.
2009 Nov
Polyphenol contents and antioxidant activity of lyophilized aqueous extract of propolis from Erzurum, Turkey.
2010 Aug-Sep
Antioxidant activity of bisbenzylisoquinoline alkaloids from Stephania rotunda: cepharanthine and fangchinoline.
2010 Feb
Metabolism of azo dyes by human skin microbiota.
2010 Jan
Evaluation of antioxidant capacity and phenol content in jackfruit (Artocarpus heterophyllus Lam.) fruit pulp.
2010 Jun
Non-invasive index of liver fibrosis induced by alcohol, thioacetamide and Schistosomal infection in mice.
2010 Jun 1
Effects of organic solvents on the activity of free and immobilised laccase from Rhus vernicifera.
2010 Nov 1
Synthesis and antioxidant properties of diphenylmethane derivative bromophenols including a natural product.
2010 Oct
Patents

Patents

05585394
5
07375101
9
08691979
9
JP2000119515A
1
JP2000136267A
1
JP2002363316A
1
JP2003127302A
1
JP2004231731A
1
JP2005162621A
1
JP2006280335A
1
JP2010007055A
1
JPH01315405A
1
JPH0284470A
3
JPH03203933A
1
JPH037253A
1
JPH06172525A
1
JPH06172526A
1
JPH06271762A
1
JPH06329958A
1
JPH07224152A
1
JPH07242822A
1
JPH08225797A
1
JPH083312A
1
JPH09104751A
1
JPS54111547A
1
JPS5626965A
1
JPS562941A
1
JPS5698215A
1
JPS57117505A
1
JPS57207603A
1
JPS5851898A
1
JPS5993721A
1
JPS60223876A
1
JPS62135528A
1
JPS62223261A
1
JPS63301264A
1
Substance Class Chemical
Created
by admin
on Sat Dec 16 20:11:07 GMT 2023
Edited
by admin
on Sat Dec 16 20:11:07 GMT 2023
Record UNII
7GZH2FMK7X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIMETHYL-P-PHENYLENEDIAMINE
MI  
Common Name English
CI 76075
Common Name English
P-AMINO-N,N-DIMETHYLANILINE
Common Name English
NSC-1493
Code English
P-AMINODIMETHYLANILINE
Common Name English
DIMETHYL-P-PHENYLENEDIAMINE [MI]
Common Name English
DIMETHYL-P-PHENYLENEDIAMINE, N,N-
Common Name English
N,N-DIMETHYL-1,4-BENZENEDIAMINE
Systematic Name English
N,N-DIMETHYL-P-PHENYLENEDIAMINE
INCI  
INCI  
Official Name English
N1,N1-DIMETHYL-1,4-BENZENEDIAMINE
Systematic Name English
N,N-DIMETHYL-P-BENZENEDIAMINE [HSDB]
Common Name English
1,4-BENZENEDIAMINE, N,N-DIMETHYL-
Systematic Name English
N,N-DIMETHYL-P-PHENYLENEDIAMINE [INCI]
Common Name English
4-(DIMETHYLAMINO)ANILINE
Systematic Name English
Code System Code Type Description
MERCK INDEX
m4548
Created by admin on Sat Dec 16 20:11:07 GMT 2023 , Edited by admin on Sat Dec 16 20:11:07 GMT 2023
PRIMARY Merck Index
PUBCHEM
7472
Created by admin on Sat Dec 16 20:11:07 GMT 2023 , Edited by admin on Sat Dec 16 20:11:07 GMT 2023
PRIMARY
HSDB
5330
Created by admin on Sat Dec 16 20:11:07 GMT 2023 , Edited by admin on Sat Dec 16 20:11:07 GMT 2023
PRIMARY
CHEBI
15783
Created by admin on Sat Dec 16 20:11:07 GMT 2023 , Edited by admin on Sat Dec 16 20:11:07 GMT 2023
PRIMARY
NSC
1493
Created by admin on Sat Dec 16 20:11:07 GMT 2023 , Edited by admin on Sat Dec 16 20:11:07 GMT 2023
PRIMARY
WIKIPEDIA
Dimethyl-4-phenylenediamine
Created by admin on Sat Dec 16 20:11:07 GMT 2023 , Edited by admin on Sat Dec 16 20:11:07 GMT 2023
PRIMARY
ECHA (EC/EINECS)
202-807-5
Created by admin on Sat Dec 16 20:11:07 GMT 2023 , Edited by admin on Sat Dec 16 20:11:07 GMT 2023
PRIMARY
EPA CompTox
DTXSID6025149
Created by admin on Sat Dec 16 20:11:07 GMT 2023 , Edited by admin on Sat Dec 16 20:11:07 GMT 2023
PRIMARY
FDA UNII
7GZH2FMK7X
Created by admin on Sat Dec 16 20:11:07 GMT 2023 , Edited by admin on Sat Dec 16 20:11:07 GMT 2023
PRIMARY
MESH
C004781
Created by admin on Sat Dec 16 20:11:07 GMT 2023 , Edited by admin on Sat Dec 16 20:11:07 GMT 2023
PRIMARY
CAS
99-98-9
Created by admin on Sat Dec 16 20:11:07 GMT 2023 , Edited by admin on Sat Dec 16 20:11:07 GMT 2023
PRIMARY
Related Record Type Details
Structure of N,N-DIMETHYL-P-PHENYLENEDIAMINE SULFATE
SALT/SOLVATE -> PARENT
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