4-Nitroquinoline N-oxide - 10mM in DMSO , CAS No.56-57-5

CAS: 56-57-5 Cat. No.: N424788 Peso molecular: 190.16 Beilstein Registry Number: 165756 Número EC: 200-281-1
Disponible para pedir
GRADE & PURITY 10mM in DMSO
Synonyms
4-NQO | Quinoline, 4-nitro-, 1-oxide (6CI,8CI,9CI) | AB4039 | DTXSID5025780 | Quinoline, 4-nitro-, oxide | 4-Nitroquinoline-1-oxide | 4-nitroquinoline1-oxide | 4-Nitrochinolin N-oxid | AC-907/25014229 | SCHEMBL105454 | 4-nitroquinolin-1-ol | X5081510EV |
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1ml
N424788-1ml
2
38,90US$
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 6 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
4-NQO | Quinoline, 4-nitro-, 1-oxide (6CI, 8CI, 9CI) | AB4039 | DTXSID5025780 | Quinoline, 4-nitro-, oxide | 4-Nitroquinoline-1-oxide | 4-nitroquinoline1-oxide | 4-Nitrochinolin N-oxid | AC-907/25014229 | SCHEMBL105454 | 4-nitroquinolin-1-ol | X5081510EV |
Especificaciones y pureza
10mM in DMSO
Mecanismos bioquímicos y fisiológicos
Skin and lung tumor initiator under experimental conditions.
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores
Sonrisas canónicasC1=CC=C2C(=C1)C(=CC=[N+]2[O-])[N+](=O)[O-]
IUPAC Name4-nitro-1-oxidoquinolin-1-ium
InChIKeyYHQDZJICGQWFHK-UHFFFAOYSA-N
INCHI1S/C9H6N2O3/c12-10-6-5-9(11(13)14)7-3-1-2-4-8(7)10/h1-6H
Isómeros SMILES C1=CC=C2C(=C1)C(=CC=[N+]2[O-])[N+](=O)[O-]
WGK Alemania 3
RTECS VC2100000
Número ONU 2811
Grupo de embalaje I
Peso molecular 190.16
Beilstein 165756
Reaxy-Rn 165756
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=165756&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseQuinolines and derivatives
SubclassNitroquinolines and derivatives
Intermediate Tree Nodes Not available
Direct Parent4-nitroquinoline N-oxides
Alternative Parents Nitroaromatic compounds  Pyridinium derivatives  Benzenoids  Heteroaromatic compounds  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents 4-nitroquinoline n-oxide - Nitroaromatic compound - Pyridine - Pyridinium - Benzenoid - Heteroaromatic compound - C-nitro compound - Organic nitro compound - Organic oxoazanium - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Azacycle - Organic oxide - Organopnictogen compound - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as 4-nitroquinoline n-oxides. These are nitroquinoline derivative bearing a nitro group at ring position 4 and N-oxide group at ring position 1.
External Descriptors a small molecule
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (no humanos)
Salmonella typhimurium (15756 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bacillus subtilis (32866 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Saccharomyces cerevisiae (19171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHO-AA8 (574 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Vibrio harveyi (399 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
SensibilidadLight sensitive,Hygroscopic
Punto de fusión (°C)154-156°C
Peso molecular190.160 g/mol
XLogP31.100
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count3
Rotatable Bond Count0
Exact Mass190.038 Da
Monoisotopic Mass190.038 Da
Topological Polar Surface Area71.300 Ų
Heavy Atom Count14
Formal Charge0
Complexity229.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Hui Zhang, Yanjing Ji, Changqing Yuan, Pei Sun, Quanchen Xu, Dongliang Lin, Zeyu Han, Xinkai Xu, Qihui Zhou, Jing Deng.  (2022)  Fabrication of astaxanthin-loaded electrospun nanofiber-based mucoadhesive patches with water‐insoluble backing for the treatment of oral premalignant lesions.  MATERIALS & DESIGN,      [PMID:] [10.1016/j.matdes.2022.111131]
2. Yuanyuan Niu, Jianfeng Zhou, Haohong Lai, Qing Zhou, Shumei Wang, Haiyun Zhai.  (2021)  An UiO-66/P-L-histidine composite film fabricated by electropolymerization and electrodeposition for sensing biomarker 4-nitroquinoline N-oxide.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2021.106925]
3. Jiashu Liu, Jianhui Chen, Kangjia Zuo, Huanan Li, Fang Peng, Qiuping Ran, Rui Wang, Zhengbing Jiang, Huiting Song.  (2021)  Chemically induced oxidative stress improved bacterial laccase-mediated degradation and detoxification of the synthetic dyes.  ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY,      [PMID:34597843] [10.1016/j.ecoenv.2021.112823]
4. Shushu Ding, Chunyan Liu, Yue Zhu, Jinlong Li, Guoyue Shi, Anwei Zhu.  (2024)  Rare Earth-Carbon Dots Nanocomposite-Modified Glass Nanopipettes: Electro-Optical Detection of Bacterial ppGpp.  ANALYTICAL CHEMISTRY,      [PMID:38442333] [10.1021/acs.analchem.3c05211]
5. Dan Wan, Xihong Zhou, Chunyan Xie, Xugang Shu, Xin Wu, Yulong Yin.  (2015)  Toxicological evaluation of ferrous N-carbamylglycinate chelate: Acute, Sub-acute toxicity and mutagenicity.  REGULATORY TOXICOLOGY AND PHARMACOLOGY,      [PMID:26364753] [10.1016/j.yrtph.2015.09.013]
6. Xiyuan Qin, Kai Kang, Bowen Zhu, Yujie Shi, Shoushan Bu.  (2025)  C1QBP Drives M2 Macrophage Polarization Via TRAF2-CCL2 to Promote Oral Squamous Cell Carcinoma Progression.  INTERNATIONAL DENTAL JOURNAL,      [PMID:41160931] [10.1016/j.identj.2025.103938]
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