Leucocrystal Violet - ≥98% , CAS No.603-48-5

CAS: 603-48-5 Cat. No.: L109872 Peso molecular: 373.53 Beilstein Registry Number: 13315 Número EC: 210-043-9

GRADE & PURITY ≥98%

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

Storage

Protected from light,Room temperature

Shipped In

Normal

Specifications

Sinónimos

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

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Protected from light, Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488184204
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488184204
• Sonrisas canónicas: CN(C)C1=CC=C(C=C1)C(C2=CC=C(C=C2)N(C)C)C3=CC=C(C=C3)N(C)C
• IUPAC Name: 4-[bis[4-(dimethylamino)phenyl]methyl]-N,N-dimethylaniline
• InChIKey: OAZWDJGLIYNYMU-UHFFFAOYSA-N
• 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
• Isómeros 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 Alemania: 3
• Peso molecular: 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=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Triphenyl compounds

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: 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
• Descripción: 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.

DOI: 10.1186/s13321-016-0174-y

Mecanismos de acción

Propiedades químicas y físicas

• Sensibilidad: Light sensitive/Air Sensitive
• Punto de fusión (°C): 175-177°C
• Peso molecular: 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

Referencias

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,      [PMID:] [10.1016/j.jwpe.2022.102831]

2. Xiaohai Wu, Siyu Si, Wei Tan, Xin Lu, Fanggui Ye, Shulin Zhao.  (2020)  Preparation of magnetic mesoporous metal-phenolic coordination spheres for extraction of crystal violet and leuco-metabolites in fish.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:33340749] [10.1016/j.chroma.2020.461776]

3. Yaoping Hu, Zhijin Gao.  (2020)  Yellow emissive Se,N-codoped carbon dots toward sensitive fluorescence assay of crystal violet.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:31968303] [10.1016/j.jhazmat.2020.122073]

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).  [PMID:] [10.1039/C7NJ04517D]

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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,      [PMID:] [10.1016/j.snb.2017.06.042]

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,      [PMID:38460698] [10.1016/j.scitotenv.2024.171519]

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,      [PMID:39086255] [10.1039/D4MH00613E]

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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).  [PMID:39930302] [10.1007/s00604-025-07022-2]

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