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Cresyl violet

Base Information
  • Chemical Name:Cresyl violet
  • CAS No.:18472-89-4
  • Molecular Formula:C19H18 N3 O . Cl
  • Molecular Weight:339.824
  • Hs Code.:2934999090
  • European Community (EC) Number:242-356-1
  • UNII:2AB49C465R
  • DSSTox Substance ID:DTXSID10939892
  • Wikipedia:Cresyl_violet
  • Wikidata:Q5184693
  • Mol file:18472-89-4.mol
Cresyl violet

Synonyms:cresyl violet;cresyl violet acetate;cresyl violet nitrate;cresyl violet, mononitrate;cresyl violet, monoperchlorate

Suppliers and Price of Cresyl violet
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • Cresyl Violet
  • 100mg
  • $ 1175.00
  • Sigma-Aldrich
  • Cresyl Violet HARLECO? Used to stain nuclei and Nissl bodies
  • 25 g
  • $ 406.07
  • American Custom Chemicals Corporation
  • CRESYL VIOLET 95.00%
  • 5MG
  • $ 504.14
  • AHH
  • Cresyl Violet 98%
  • 10g
  • $ 355.00
Total 6 raw suppliers
Chemical Property of Cresyl violet
Chemical Property:
  • Boiling Point:482.3°Cat760mmHg 
  • Flash Point:245.5°C 
  • PSA:55.06000 
  • Density:g/cm3 
  • LogP:0.59340 
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:0
  • Exact Mass:339.1138399
  • Heavy Atom Count:24
  • Complexity:639
Purity/Quality:

98%Min *data from raw suppliers

Cresyl Violet *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Chemical Classes:Dyes -> Azine Dyes
  • Canonical SMILES:CC1=CC2=NC3=C(C=C(C4=CC=CC=C43)N)OC2=CC1=[N+](C)C.[Cl-]
  • Recent NIPH Clinical Trials:Visualization of enteric nervous system by confocal laser endomicroscopy
  • Uses Cresyl Violet is used as a fiducial marker in combined 3-dimensional mass spectrometry and optical tissue imaging.
Technology Process of Cresyl violet

There total 3 articles about Cresyl violet which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With pantetheinase; In aq. phosphate buffer; water; pH=7.4; Enzymatic reaction;
DOI:10.1021/acs.analchem.7b03303
Guidance literature:
With pyroglutamate aminopeptidase 1; at 37 ℃; for 0.5h; pH=7.4; Kinetics; Enzymatic reaction;
DOI:10.1039/c6sc00951d
Guidance literature:
With acetic acid;
upstream raw materials:

2-naphthylamine hydrochloride

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