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4-Nitrodiphenylamine - 98%, high purity , CAS No.836-30-6

1 Citations COA COA
    Grade & Purity:
  • ≥98%
In stock
Item Number
N133610
Grouped product items
SKU Size
Availability
 Price Qty
N133610-250mg
250mg
2
$14.90
N133610-1g
1g
1
$43.90
N133610-5g
5g
1
$158.90
N133610-25g
25g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$639.90
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View related series
Benzene ring compounds (72)

Basic Description

Synonyms AI3-02915 | 4-Nitrodiphenylamine, 99% | DTXCID107323 | NCGC00164030-01 | SR-01000421153-1 | EINECS 212-646-2 | FT-0619232 | SMR000203627 | 4-12-00-01619 (Beilstein Handbook Reference) | MLS000584664 | WLN: WNR DMR | BRN 2051910 | N-(4-Nitrophenyl)-N-pheny
Specifications & Purity ≥98%
Shipped In Normal
Product Description

4-Nitrodiphenylamine undergoes heterogeneous catalytic transfer hydrogenation to form p-phenylenediamines. 4-Nitrodiphenylamine is used as stabilizer for propellants and explosives
4-Nitrodiphenylamine was used to study reduction of nitrated diphenylamine derivatives in sediment water batch enrichments and dense cell suspensions of anaerobic, aromatic-compound-mineralizing pure bacterial cultures

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Nitrobenzenes
Intermediate Tree Nodes Not available
Direct Parent Nitrobenzenes
Alternative Parents Nitroaromatic compounds  Aniline and substituted anilines  Secondary amines  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Nitrobenzene - Nitroaromatic compound - Aniline or substituted anilines - C-nitro compound - Organic nitro compound - Organic oxoazanium - Secondary amine - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic nitrogen compound - Organonitrogen compound - Organic oxygen compound - Amine - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as nitrobenzenes. These are compounds containing a nitrobenzene moiety, which consists of a benzene ring with a carbon bearing a nitro group.
External Descriptors Not available

Associated Targets(Human)

ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALOX12 Tchem Arachidonate 12-lipoxygenase (3262 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HepG2 (196354 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
L3MBTL1 Tchem Lethal(3)malignant brain tumor-like protein 1 (14536 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HPGD Tchem 15-hydroxyprostaglandin dehydrogenase [NAD+] (24926 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ATAD5 Tbio ATPase family AAA domain-containing protein 5 (122566 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
BAZ2B Tchem Bromodomain adjacent to zinc finger domain protein 2B (56204 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
FTL Ferritin light chain (43324 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nr1i2 Nuclear receptor subfamily 1 group I member 2 (14 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
skn-1 Protein skinhead-1 (1832 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
hsp-16.2 Heat shock protein Hsp-16.2 (213 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 488181827
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488181827
IUPAC Name 4-nitro-N-phenylaniline
INCHI InChI=1S/C12H10N2O2/c15-14(16)12-8-6-11(7-9-12)13-10-4-2-1-3-5-10/h1-9,13H
InChIKey XXYMSQQCBUKFHE-UHFFFAOYSA-N
Smiles C1=CC=C(C=C1)NC2=CC=C(C=C2)[N+](=O)[O-]
Isomeric SMILES C1=CC=C(C=C1)NC2=CC=C(C=C2)[N+](=O)[O-]
WGK Germany 3
Molecular Weight 214.22
Reaxy-Rn 2051910
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2051910&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

18 results found

Lot Number Certificate Type Date Item
K2222588 Certificate of Analysis Mar 10, 2025 N133610
B2521522 Certificate of Analysis Feb 27, 2025 N133610
B2521518 Certificate of Analysis Feb 27, 2025 N133610
B2521519 Certificate of Analysis Feb 27, 2025 N133610
B2521520 Certificate of Analysis Feb 27, 2025 N133610
B2521521 Certificate of Analysis Feb 27, 2025 N133610
K2222577 Certificate of Analysis Sep 18, 2024 N133610
K2222584 Certificate of Analysis Sep 18, 2024 N133610
K2222586 Certificate of Analysis Sep 18, 2024 N133610
F2404397 Certificate of Analysis Jun 12, 2024 N133610
F2404398 Certificate of Analysis Jun 12, 2024 N133610
F2404396 Certificate of Analysis Jun 12, 2024 N133610
J2424250 Certificate of Analysis Jun 12, 2024 N133610
K2111483 Certificate of Analysis Aug 07, 2023 N133610
K2222593 Certificate of Analysis Nov 07, 2022 N133610
K2222587 Certificate of Analysis Nov 07, 2022 N133610
K2021107 Certificate of Analysis Sep 16, 2022 N133610
K2021105 Certificate of Analysis Sep 16, 2022 N133610

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Chemical and Physical Properties

Solubility Soluble in Acetone, Acetonitrile, DMF, DMSO and Ethyl Acetate, Soluble in Acetone, Acetonitrile, DMF, DMSO and Ethyl Acetate.Insoluble in water
Flash Point(°F) 374°F
Flash Point(°C) 190℃
Boil Point(°C) 211°/30mm
Melt Point(°C) 132-135℃
Molecular Weight 214.220 g/mol
XLogP3 3.700
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 2
Exact Mass 214.074 Da
Monoisotopic Mass 214.074 Da
Topological Polar Surface Area 57.900 Ų
Heavy Atom Count 16
Formal Charge 0
Complexity 226.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

How to Cite Aladdin Scientific Products?
1. Juanjuan Yao, Huiying Zhang, Longfu Chen, Wei Liu, Naiyun Gao, Shiyi Liu, Xiangyu Chen, Fanghui Rao.  (2021)  The Roles of Sono-induced Nitrosation and Nitration in the Sono-degradation of Diphenylamine in Water: Mechanisms, Kinetics and Impact Factors.  JOURNAL OF HAZARDOUS MATERIALS,  402  (123720). 

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