Vat Black 25

Base Information

• Chemical Name: Vat Black 25
• CAS No.: 4395-53-3
• Deprecated CAS: 182893-26-1,51609-92-8,51609-92-8
• Molecular Formula: C45H22N2O5
• Molecular Weight: 670.68
• European Community (EC) Number: 224-519-9
• DSSTox Substance ID: DTXSID0063440
• Nikkaji Number: J88.092B
• Wikidata: Q72516121
• Mol file: 4395-53-3.mol

Synonyms:Anthra[2,1,9-mna]naphth[2,3-h]acridine-5,10,15(16H)-trione,3-(1-anthraquinonylamino)- (7CI,8CI);Indanthrene Olive T (6CI);Ahcovat OliveT;Amanthrene Olive T;Atic Vat Olive D;BelanthreneOlive T;Benzadone Olive T;C.I. 69525;Calcoloid Olive T;Calcoloid Olive TCC;Calcoloid Olive TL;Caledon Olive D;Carbanthrene Olive T;Cibanone Olive FS;Cibanone Olive S;Cibanone Olive SRR;Fenanthren Olive T 3R;HelanthreneOlive BT;Helanthrene Olive T;Indanthren Olive T;Indanthrene Olive T 3R;Mayvat Olive T;Novatic Olive D;Nyanthrene Olive T;Palanthrene Olive T;Palanthrene Olive TR;Pernithrene Olive T;Ponsol Olive TR;Romantrene Olive FT;Romantrene Olive T;Sandothrene Olive NT;Solanthrene Olive T;Tinon Olive S;Tyrian Olive I-T;Vat Black 25;Vat Grey 2Z;

Chemical Property of Vat Black 25

Chemical Property:

• Refractive Index: 1.826
• PKA: -2.72±0.20(Predicted)
• PSA: 130.24000
• Density: 1.527 g/cm³
• LogP: 8.09390
• XLogP3: 9
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 2
• Exact Mass: 670.15287181
• Heavy Atom Count: 52
• Complexity: 1540

Purity/Quality:

99.9% ^*data from raw suppliers

CI VAT BLACK 25 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=CC=C3)NC4=CC5=C(C=C4)C6=CC=C7C8=C(C=CC(=C68)C5=O)C9=C(N7)C1=C(C=C9)C(=O)C2=CC=CC=C2C1=O

Technology Process of Vat Black 25

There total 1 articles about Vat Black 25 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:

Reference yield:

→ 3-(anthraquinon-1-ylamino)anthra(2,1,9-mna)naphth[2,3-h]acridine-5,10,15(16H)-trione (4395-53-3)

Guidance literature:

3-Amino-anthra<2.1.9-mna>naphtha<2.3-h>acridin-5,10,15(16H)-trion (VIe), α-Chloranthrachinon, Naphthalin, Na2CO3, CO;