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N,N′-Dimethyl-9,9′-biacridinium dinitrate - ≥97.0%, high purity , CAS No.2315-97-1
Basic Description
Synonyms
Bis(N-methylacridinium) Nitrate | HY-D0720 | 10,10'-Dimethyl-9,9'-biacridinium nitrate | Dimethyl biacridinium dinitrate | 10,10'-Dimethyl-9,9'-biacridinium Dinitrate [for Chemiluminescence Research] | EINECS 219-023-4 | L 6868 | Lucigenin | NSC 151912 |
Specifications & Purity
≥97%
Storage Temp
Room temperature,Argon charged
Shipped In
Normal
Product Description
Applications： diagnostic assay manufacturing;hematology;histology
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Quinolines and derivatives
Subclass
Benzoquinolines
Intermediate Tree Nodes
Not available
Direct Parent
Acridines
Alternative Parents
Bipyridines and oligopyridines Pyridinium derivatives Benzenoids Organic nitrates Heteroaromatic compounds Organic nitro compounds Organic nitric acids Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic salts Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Acridine - 4,4p-bipyridinium - Bipyridine - Pyridine - Pyridinium - Benzenoid - Organic nitrate - Heteroaromatic compound - Organic nitric acid - Organic nitric acid or derivatives - Organic nitro compound - Azacycle - Allyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic oxygen compound - Hydrocarbon derivative - Organonitrogen compound - Organic nitrogen compound - Organic oxide - Organopnictogen compound - Organic salt - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as acridines. These are organic compounds containing the acridine moiety, a linear tricyclic heterocycle which consists of two benzene rings joined by a pyridine ring.
External Descriptors
Not available
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Names and Identifiers
IUPAC Name
10-methyl-9-(10-methylacridin-10-ium-9-yl)acridin-10-ium;dinitrate
INCHI
InChI=1S/C28H22N2.2NO3/c1-29-23-15-7-3-11-19(23)27(20-12-4-8-16-24(20)29)28-21-13-5-9-17-25(21)30(2)26-18-10-6-14-22(26)28;2*2-1(3)4/h3-18H,1-2H3;;/q+2;2*-1
InChIKey
KNJDBYZZKAZQNG-UHFFFAOYSA-N
Smiles
C[N+]1=C2C=CC=CC2=C(C3=CC=CC=C31)C4=C5C=CC=CC5=[N+](C6=CC=CC=C64)C.[N+](=O)([O-])[O-].[N+](=O)([O-])[O-]
Isomeric SMILES
C[N+]1=C2C=CC=CC2=C(C3=CC=CC=C31)C4=C5C=CC=CC5=[N+](C6=CC=CC=C64)C.[N+](=O)([O-])[O-].[N+](=O)([O-])[O-]
WGK Germany
3
Molecular Weight
510.51
Beilstein
3901768
Reaxy-Rn
3901768
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3901768&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
acetic acid: 10 mg/mL
Sensitivity
Moisture sensitive.
Melt Point(°C)
245-250 °C
Molecular Weight
510.500 g/mol
XLogP3
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
6
Rotatable Bond Count
1
Exact Mass
510.154 Da
Monoisotopic Mass
510.154 Da
Topological Polar Surface Area
134.000 Ų
Heavy Atom Count
38
Formal Charge
0
Complexity
522.000
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
3
Citations of This Product
1.
Guo Jian-Shuang, Li Juan-Juan, Wang Ze-Han, Liu Yang, Yue Yu-Xin, Li Hua-Bin, Zhao Xiu-He, Sun Yuan-Jun, Ding Ya-Hui, Ding Fei, Guo Dong-Sheng, Wang Liang, Chen Yue.
(2023)
Dual hypoxia-responsive supramolecular complex for cancer target therapy. Nature Communications,
14
(1):
(1-13).
2.
Weike Shaoyong, Hongli Jin, Xiao Jiang, Bocheng Xu, Yalin Liu, Yizhen Wang, Mingliang Jin.
(2023)
Benzo [a] pyrene-loaded aged polystyrene microplastics promote colonic barrier injury via oxidative stress-mediated notch signalling. JOURNAL OF HAZARDOUS MATERIALS,
457
(131820).
3.
Shuai Quan, Kaixiang Ji, Fangshuo Liu, Tesfaye Hailemariam Barkae, Mohamed Ibrahim Halawa, Saima Hanif, Baohua Lou, Jianping Li, Guobao Xu.
(2022)
Chemiluminescence of lucigenin-tetracycline and its application for sensitive determination of procyanidin. JOURNAL OF FOOD AND DRUG ANALYSIS,
30
(2):
( 293–302).
4.
Yi Wang, Chengpei Du, Ze Liu, Kanglin Pei, Yan Zhang, Wenjing Qi.
(2022)
Chemiluminescence “turn-on” detection of tyrosinase activity via in situ generation of dopamine based on a lucigenin and riboflavin system. NEW JOURNAL OF CHEMISTRY,
46
(9):
(4156-4161).
5.
Xiaojie Chai, Yan Cui, Wencai Xu, Lingce Kong, Yanjun Zuo, Ling Yuan, Wenming Chen.
(2021)
Degradation of malathion in the solution of acetyl peroxyborate activated by carbonate: Products, kinetics and mechanism. JOURNAL OF HAZARDOUS MATERIALS,
407
(124808).
6.
Huijuan Yu, Wen-Chao Geng, Zhe Zheng, Jie Gao, Dong-Sheng Guo, Yuefei Wang.
(2019)
Facile Fluorescence Monitoring of Gut Microbial Metabolite Trimethylamine N-oxide via Molecular Recognition of Guanidinium-Modified Calixarene. Theranostics,
9
(16):
( 4624–4632).
7.
Di Wu, Yi Wang, Wenjing Qi, Jianyang Xu, Kanglin Pei, Lingyan Ma, Lin Qi.
(2024)
Long-lasting chemiluminescence of lucigenin/p-aminophenol system for detection of p-aminophenol in environmental water. DYES AND PIGMENTS,
223
(111959).
8.
Weike Shaoyong, Lu Sun, Yujie Gan, Hongli Jin, Wusu Wang, Lin Yin, Yizhen Wang, Mingliang Jin.
(2024)
Sight of Aged Microplastics Adsorbing Heavy Metal Exacerbated Intestinal Injury: A Mechanistic Study of Autophagy-Mediated Toxicity Response. ACS Nano,
18
(42):
(28849-28865).
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8 Citations
C2521407