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Details

Stereochemistry ACHIRAL
Molecular Formula C6H7N3O2.ClH
Molecular Weight 189.6
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-NITRO-O-PHENYLENEDIAMINE HYDROCHLORIDE

SMILES

Cl.NC1=CC=C(C=C1N)[N+]([O-])=O

InChI

InChIKey=IFTLGFVLGVXRBT-UHFFFAOYSA-N
InChI=1S/C6H7N3O2.ClH/c7-5-2-1-4(9(10)11)3-6(5)8;/h1-3H,7-8H2;1H

HIDE SMILES / InChI

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

Molecular Formula C6H7N3O2
Molecular Weight 153.1387
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Modulatory effect of phenolic fractions of Terminalia arjuna on the mutagenicity in Ames assay.
2002
Antimutagenic activities of acetone and methanol fractions of Terminalia arjuna.
2002 Oct
Antimutagenic activity of spearmint.
2004
Enhancement of the morphological transformation of Syrian hamster embryo (SHE) cells by reducing incubation time of the target cells.
2004 Apr 14
Antimutagenicity of herbal detoxification formula Smoke Shield against environmental mutagens.
2004 Mar
Evaluation of the cytotoxicity, genotoxicity, mutagenicity, and antimutagenicity of propolis from Tucuman, Argentina.
2005 Nov 16
Antimutagenic and anti-oxidant activities of the non-steroidal anti-inflammatory drug celecoxib.
2005 Oct
Evaluation of comparative and combined antimutagenic potential of vitamin C and vitamin E using histidine mutant Salmonella typhimurium strains.
2008 Jan
Determination of genotoxic, antigenotoxic and cytotoxic potential of the extract from lichen Cetraria aculeata (Schreb.) Fr. in vitro.
2008 Jan
Antioxidant and antimutagenic activities of Mexican oregano (Lippia graveolens Kunth).
2008 Mar
1-Methyl-6-nitro-1H-benzimidazole.
2008 Mar 5
Phytochemical, antibacterial, antiproliferative, and antioxidant potentials and DNA damage-protecting activity of Acacia salicina extracts.
2009 Jun
Microwave assisted, one-pot synthesis of 5-nitro- 2-aryl substituted-1H-benzimidazole libraries: screening in vitro for antimicrobial activity.
2009 Oct
Validation of an in vitro screening test for predicting the tumor promoting potential of chemicals based on gene expression.
2010 Apr
Determination of Se(IV) in natural waters by adsorptive stripping voltammetry of 5-nitropiazselenol.
2010 Feb 15
Modulatory role of alizarin from Rubia cordifolia L. against genotoxicity of mutagens.
2010 Jan
Antimutagenic and antioxidant potentials of Teucrium ramosissimum essential oil.
2010 Jul
Phlomis mauritanica extracts reduce the xanthine oxidase activity, scavenge the superoxide anions, and inhibit the aflatoxin B1-, sodium azide-, and 4-nitrophenyldiamine-induced mutagenicity in bacteria.
2010 Jun
Antioxidant, antimutagenic, and antidiabetic activities of edible leaves from Cnidoscolus chayamansa Mc. Vaugh.
2010 Mar
Oxidative Stress Mechanisms Do Not Discriminate between Genotoxic and Nongenotoxic Liver Carcinogens.
2015 Aug 17
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 00:09:41 GMT 2023
Edited
by admin
on Sat Dec 16 00:09:41 GMT 2023
Record UNII
R6FRD37482
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-NITRO-O-PHENYLENEDIAMINE HYDROCHLORIDE
Common Name English
O-PHENYLENEDIAMINE, 4-NITRO-, HYDROCHLORIDE
Common Name English
4-NITRO-O-PHENYLENEDIAMINE HCL [INCI]
Common Name English
1,2-BENZENEDIAMINE, 4-NITRO-, HYDROCHLORIDE (1:1)
Systematic Name English
4-NITRO-O-PHENYLENEDIAMINE HCL
INCI  
INCI  
Official Name English
1,2-BENZENEDIAMINE, 4-NITRO-, MONOHYDROCHLORIDE
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
258-429-6
Created by admin on Sat Dec 16 00:09:41 GMT 2023 , Edited by admin on Sat Dec 16 00:09:41 GMT 2023
PRIMARY
CAS
53209-19-1
Created by admin on Sat Dec 16 00:09:41 GMT 2023 , Edited by admin on Sat Dec 16 00:09:41 GMT 2023
PRIMARY
PUBCHEM
5743500
Created by admin on Sat Dec 16 00:09:41 GMT 2023 , Edited by admin on Sat Dec 16 00:09:41 GMT 2023
PRIMARY
FDA UNII
R6FRD37482
Created by admin on Sat Dec 16 00:09:41 GMT 2023 , Edited by admin on Sat Dec 16 00:09:41 GMT 2023
PRIMARY
EPA CompTox
DTXSID70201289
Created by admin on Sat Dec 16 00:09:41 GMT 2023 , Edited by admin on Sat Dec 16 00:09:41 GMT 2023
PRIMARY
Related Record Type Details
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