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N,N-Dimethyl-4-nitrosoaniline - >98.0%, high purity , CAS No.138-89-6

7 Citations COA COA
    Grade & Purity:
  • ≥98%
In stock
Item Number
N159022
Grouped product items
SKU Size
Availability
 Price Qty
N159022-5g
5g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$10.90
N159022-25g
25g
1
$38.90
N159022-100g
100g
1
$119.90
N159022-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$458.90
Wish List
Bulk Order  SDS  DATASHEET  Specification Sheet
View related series
Nitrogenous compounds (2445) Non heterocyclic block (8163)

Basic Description

Synonyms AKOS005208791 | NCGC00091697-01 | NCGC00091697-05 | Tox21_202129 | Ultra Brilliant Blue P | EINECS 205-343-1 | NCGC00091697-04 | NSC2775 | NSC-2775 | A50923 | Benzenamine,N-dimethyl-4-nitroso- | N,N-Dimethyl-4-nitrosoaniline, 97% | N0262 | p-nitrosodimeth
Specifications & Purity ≥98%
Biochemical and Physiological Mechanisms N,N-Dimethyl-4-nitrosoaniline is used for the detection of singlet oxygen. Singlet oxygen reacts with imidazole and thereby bleaches N,N-Dimethyl-4-nitrosoaniline via oxidation. Bleaching of N,N-Dimethyl-4-nitrosoaniline is observed as reduction in the ab
Storage Temp Store at 2-8°C,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic nitrogen compounds
Class Organonitrogen compounds
Subclass Amines
Intermediate Tree Nodes Tertiary amines - Tertiary alkylarylamines
Direct Parent Dialkylarylamines
Alternative Parents Aniline and substituted anilines  Propargyl-type 1,3-dipolar organic compounds  C-nitroso compounds  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Aniline or substituted anilines - Dialkylarylamine - Benzenoid - Monocyclic benzene moiety - Organic nitroso compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - C-nitroso compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as dialkylarylamines. These are aliphatic aromatic amines in which the amino group is linked to two aliphatic chains and one aromatic group.
External Descriptors a small molecule

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
NR3C1 Tclin Glucocorticoid receptor (14987 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
VDR Tclin Vitamin D receptor (26531 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TSHR Tclin Thyroid stimulating hormone receptor (29986 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
THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
RXRA Tclin Retinoid X receptor alpha (3637 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CXCL8 Tchem Interleukin-8 (642 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AHR Tclin Aryl hydrocarbon receptor (1071 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NR1H4 Tclin Bile acid receptor FXR (6228 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NFKB1 Tclin Nuclear factor NF-kappa-B p105 subunit (1459 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TP53 Tchem Cellular tumor antigen p53 (48468 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
Lymphoblastoid cell (5959 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
FEN1 Tchem Flap endonuclease 1 (12055 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HIF1A Tchem Hypoxia-inducible factor 1 alpha (6027 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
POLI Tchem DNA polymerase iota (116820 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SNCA Tchem Alpha-synuclein (10960 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
SMAD3 Tchem Mothers against decapentaplegic homolog 3 (68039 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Cruzipain (33337 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
lef Anthrax lethal factor (7585 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 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
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Impa1 Inositol monophosphatase 1 (16203 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

IUPAC Name N,N-dimethyl-4-nitrosoaniline
INCHI InChI=1S/C8H10N2O/c1-10(2)8-5-3-7(9-11)4-6-8/h3-6H,1-2H3
InChIKey CMEWLCATCRTSGF-UHFFFAOYSA-N
Smiles CN(C)C1=CC=C(C=C1)N=O
Isomeric SMILES CN(C)C1=CC=C(C=C1)N=O
RTECS BX7175000
UN Number 1369
Packing Group II
Molecular Weight 150.18
Beilstein 12677
Reaxy-Rn 607293
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=607293&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.

7 results found

Lot Number Certificate Type Date Item
K2422101 Certificate of Analysis Aug 11, 2022 N159022
J2229365 Certificate of Analysis Aug 11, 2022 N159022
J2229366 Certificate of Analysis Aug 11, 2022 N159022
J2229367 Certificate of Analysis Aug 11, 2022 N159022
J2229370 Certificate of Analysis Aug 11, 2022 N159022
K2411132 Certificate of Analysis Apr 10, 2021 N159022
G2404071 Certificate of Analysis Apr 10, 2021 N159022

Chemical and Physical Properties

Solubility Insoluble in water; Soluble in Alcohol,Ether
Sensitivity Light sensitive;Air sensitive;Heat sensitive
Melt Point(°C) 84.0-87°C
Molecular Weight 150.180 g/mol
XLogP3 1.800
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 1
Exact Mass 150.079 Da
Monoisotopic Mass 150.079 Da
Topological Polar Surface Area 32.700 Ų
Heavy Atom Count 11
Formal Charge 0
Complexity 128.000
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. Jingsong Lu, Jing Yu, Wensheng Xie, Xiaohan Gao, Zhenhu Guo, Zeping Jin, Ying Li, Abdul Fahad, Neema Ufurahi Pambe, Shenglei Che, Yen Wei, Lingyun Zhao.  (2023)  Physical Dissolution Combined with Photodynamic Depletion: A Two-Pronged Nanoapproach for Deoxygenation-Driven and Hypoxia-Activated Prodrug Therapy.  ACS Applied Bio Materials,     
2. Ying Zhang, Ting-Ting Li, Zhike Wang, Bing-Chiuan Shiu, Jia-Horng Lin, Ching-Wen Lou.  (2023)  Coaxial microfluidic spinning design produced high strength alginate membranes for antibacterial activity and drug release.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,  243  (124956). 
3. Yan Yan, Xiangjuan Ma, Yijing Xia, Huajun Feng, Shengjue Liu, Cong He, Yangcheng Ding.  (2023)  Mechanism of highly efficient electrochemical degradation of antibiotic sulfadiazine using a layer-by-layer GNPs/PbO2 electrode.  ENVIRONMENTAL RESEARCH,  217  (114778). 
4. Xiaolei Zhang, Zhiquan Wang, Jialin Huang, Huihui Chen, Qiang Liu, Ping Yao, Hao H. Ngo, Long D. Nghiem.  (2022)  A novel membrane photo-electro oxidizer for advanced treatment of coal processing wastewater: Fouling control and permeate quality.  Journal of Cleaner Production,  378  (134573). 
5. Shengli Wang, Shuzhao Pei, Jinna Zhang, Junqiang Huang, Shijie You.  (2022)  Flow-through electrochemical removal of benzotriazole by electroactive ceramic membrane.  WATER RESEARCH,  218  (118454). 
6. Xiangjuan Ma, Yan Yan, Qizhou Dai, Jianxian Gao, Shengjue Liu, Yijing Xia.  (2021)  Energy-efficient pulse electrochemical oxidation of Acid Blue 9 using a Ti/SnO2-Sb/α,β-Polytetrafluoroethylene-Fe-PbO2 electrode: Kinetics, mass transfer and mechanism.  SEPARATION AND PURIFICATION TECHNOLOGY,  279  (119775). 
7. Ting-Ting Li, Bing-Bing Shou, Lu Yang, Hai-Tao Ren, Xian-Jin Hu, Jia-Horng Lin, Tao Cai, Ching-Wen Lou.  (2024)  Modification of traditional composite nonwovens with stable storage of light absorption transients and photodynamic antibacterial effect.  PHOTOCHEMISTRY AND PHOTOBIOLOGY,     

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