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Leucocrystal Violet - analytical standard, high purity , CAS No.603-48-5
Basic Description
Synonyms
LCV | 3vw1 | 4,4''-Methylidynetris(N,N-dimethylaniline) | 4-[bis[4-(dimethylamino)phenyl]methyl]-N,N-dimethylaniline | AS-66577 | CI BASIC VIOLET 3, LEUCO | PD065506 | A-DMA | AI3-19978 | LCV | Tris(4-(dimethylamino)phenyl)methane | AKOS015903459 | STL416
Specifications & Purity
analytical standard
Storage Temp
Protected from light
Shipped In
Normal
Grade
analytical standard
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Triphenyl compounds
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Triphenyl compounds
Alternative Parents
Dialkylarylamines Aniline and substituted anilines Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Triphenyl compound - Aniline or substituted anilines - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Monocyclic benzene moiety - Tertiary amine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as triphenyl compounds. These are aromatic compounds containing a triphenyl moiety.
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.
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
4-[bis[4-(dimethylamino)phenyl]methyl]-N,N-dimethylaniline
INCHI
InChI=1S/C25H31N3/c1-26(2)22-13-7-19(8-14-22)25(20-9-15-23(16-10-20)27(3)4)21-11-17-24(18-12-21)28(5)6/h7-18,25H,1-6H3
InChIKey
OAZWDJGLIYNYMU-UHFFFAOYSA-N
Smiles
CN(C)C1=CC=C(C=C1)C(C2=CC=C(C=C2)N(C)C)C3=CC=C(C=C3)N(C)C
Isomeric SMILES
CN(C)C1=CC=C(C=C1)C(C2=CC=C(C=C2)N(C)C)C3=CC=C(C=C3)N(C)C
WGK Germany
3
Molecular Weight
373.53
Beilstein
13315
Reaxy-Rn
2222570
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2222570&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Sensitivity
Light sensitive.
Melt Point(°C)
175-177°C
Molecular Weight
373.500 g/mol
XLogP3
5.700
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
3
Rotatable Bond Count
6
Exact Mass
373.252 Da
Monoisotopic Mass
373.252 Da
Topological Polar Surface Area
9.700 Ų
Heavy Atom Count
28
Formal Charge
0
Complexity
370.000
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
1.
Jun Xiang, Huan Li, Yunhao Hei, Guiying Tian, Lei Zhang, Penggao Cheng, Jianping Zhang, Na Tang.
(2022)
Preparation of highly permeable electropositive nanofiltration membranes using quaternized polyethyleneimine for dye wastewater treatment. Journal of Water Process Engineering,
48
(102831).
2.
Xiaohai Wu, Siyu Si, Wei Tan, Xin Lu, Fanggui Ye, Shulin Zhao.
(2021)
Preparation of magnetic mesoporous metal-phenolic coordination spheres for extraction of crystal violet and leuco-metabolites in fish. JOURNAL OF CHROMATOGRAPHY A,
1636
(461776).
3.
Yaoping Hu, Zhijin Gao.
(2020)
Yellow emissive Se,N-codoped carbon dots toward sensitive fluorescence assay of crystal violet. JOURNAL OF HAZARDOUS MATERIALS,
388
(122073).
4.
Ji Yang, Ming-Hui Wu, Zheng-Zhong Lin, Zhi-Yong Huang.
(2018)
Detection of trace leucomalachite green with a nanoprobe of CdTe quantum dots coated with molecularly imprinted silica via synchronous fluorescence quenching. NEW JOURNAL OF CHEMISTRY,
42
(4):
(2640-2648).
5.
Mi Zhang, Xiaobing He, Jie Wei.
(2018)
A paper-based visible light-responsive imaging material. JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY,
353
(122).
6.
Ji Yang, Zheng-Zhong Lin, Hui-Ping Zhong, Xiao-Mei Chen, Zhi-Yong Huang.
(2017)
Determination of leucomalachite green in fish using a novel MIP-coated QDs probe based on synchronous fluorescence quenching effect. SENSORS AND ACTUATORS B-CHEMICAL,
252
(561).
7.
Jie Tan, Lingdong Kong, Yuwen Wang, Beibei Liu, Yixuan An, Lianghai Xia, Yu Lu, Qing Li, Lin Wang.
(2024)
Direct aqueous photochemistry of methylglyoxal and its effect on sulfate formation. SCIENCE OF THE TOTAL ENVIRONMENT,
924
(171519).
8.
Hao Liu, Zhiming Liu, Hao Zhang, Ke Huang, Xiaohui Liu, Hui Jiang, Xuemei Wang.
(2024)
Mineralized aggregates based on native protein phase transition for non-destructive diagnosis of seborrheic skin by surface-enhanced Raman spectroscopy. Materials Horizons,
9.
Yuwen Wang, Lingdong Kong, Jie Tan, Beibei Liu, Yixuan An, Lianghai Xia, Yu Lu, Qing Li, Lin Wang.
(2024)
Photochemistry of Imidazole-2-carbaldehyde in Droplets as a Potential Source of H2O2 and Its Oxidation of SO2. ENVIRONMENTAL SCIENCE & TECHNOLOGY,
58
(25):
(11096-11104).
10.
Guo Dongying, Yang Hailiang, Zhang Longyue, Dai Ruoyu, Huang Yuankui, Hu Yaoping.
(2025)
Smartphone-assisted detection of methylene blue using leaf-derived, dual-emissive carbon dots as ratiometric fluorescence probes. MICROCHIMICA ACTA,
192
(3):
(1-9).
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10 Citations
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