RESAZURIN

Base Information

• Chemical Name: RESAZURIN
• CAS No.: 550-82-3
• Deprecated CAS: 153796-08-8
• Molecular Formula: C12H7 N O4
• Molecular Weight: 229.192
• European Community (EC) Number: 208-987-1
• NSC Number: 56323,10438
• UNII: 1FN9YD6968
• DSSTox Substance ID: DTXSID4060280
• Nikkaji Number: J13.744H
• Wikipedia: Resazurin
• Wikidata: Q409628
• Metabolomics Workbench ID: 67611
• ChEMBL ID: CHEMBL1616414
• Mol file: 550-82-3.mol

Synonyms:Resazurin(6CI); 7-Hydroxy-3H-phenoxazin-3-one 10-oxide; 7-Hydroxy-3H-phenoxazine-3-one10-oxide; Alamar Blue; Azoresorcin; Diazoresorcinol; NSC 10438; NSC 56323;Resazoin; Resazurine; Rhodalux

Chemical Property of RESAZURIN

Chemical Property:

• Vapor Pressure: 9.94E-10mmHg at 25°C
• Melting Point: >250°C
• Boiling Point: 477.2°Cat760mmHg
• PKA: 6.71(at 25℃)
• Flash Point: 242.4°C
• Density: 1.57g/cm³
• Solubility.: Solubility Insoluble in water, ether; sparingly soluble in ethan
• XLogP3: -0.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 229.03750770
• Heavy Atom Count: 17
• Complexity: 463

Purity/Quality:

99%, ^*data from raw suppliers

7-HYDROXY-10-OXY-PHENOXAZIN-3-ONE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Dyes -> Azine Dyes
• Canonical SMILES: C1=CC2=C(C=C1O)OC3=CC(=O)C=CC3=[N+]2[O-]
• Uses: As indicator, using a solution of 0.1 g in 20 ml 0.1N NaOH, and water to make 500 ml. pH: 3.8 orange, 6.5 dark violet. In the detection of hyposulfite (sulfoxylate). In food research (reductase test).

Technology Process of RESAZURIN

There total 10 articles about RESAZURIN 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:

recorcinol (108-46-3) → resazurin (550-82-3,153796-08-8)

Guidance literature:

With diethyl ether; nitric acid;

Reference yield:

resazurinyl-β-D-glucopyranoside (132928-74-6) → resazurin (550-82-3,153796-08-8)

Guidance literature:

With H₂O; In water; at 37 ℃; β-D-glucosidase, phosphate buffer, pH, 6.8; K_M value, maximum velocity;

DOI:10.1248/cpb.38.3466

Reference yield:

7-hydroxy-3H-phenoxazin-3-one sodium salt (34994-50-8) → resazurin (550-82-3,153796-08-8)

Guidance literature:

With sulfuric acid; dihydrogen peroxide;

upstream raw materials:

hydroxyquinone

7-hydroxy-3H-phenoxazin-3-one sodium salt

4-nitroso-1,3-benzenediol

recorcinol

Downstream raw materials:

resorufin

carbon dioxide

dihydroxyacetone

7-hydroxy-3H-phenoxazin-3-one sodium salt

Refernces