Indophenol

Base Information

• Chemical Name: Indophenol
• CAS No.: 500-85-6
• Molecular Formula: C12H9 N O2
• Molecular Weight: 199.209
• Hs Code.: 2925290090
• European Community (EC) Number: 207-913-5
• UNII: BW444H326B
• DSSTox Substance ID: DTXSID2075425
• Nikkaji Number: J9.397A
• Wikipedia: Indophenol
• Wikidata: Q412974
• Metabolomics Workbench ID: 57419
• ChEMBL ID: CHEMBL3306923
• Mol file: 500-85-6.mol

Synonyms:Indophenol

Chemical Property of Indophenol

Chemical Property:

• Vapor Pressure: 1.11E-05mmHg at 25°C
• Melting Point: >300 °C(lit.)
• Boiling Point: 360°Cat760mmHg
• PKA: 8.1, 9.4, 10.6(at 25℃)
• Flash Point: 171.5°C
• PSA: 49.66000
• Density: 1.18g/cm³
• LogP: 2.15980
• Solubility.: Solubility Insoluble in water; soluble in ethanol
• XLogP3: 1.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 199.063328530
• Heavy Atom Count: 15
• Complexity: 316

Purity/Quality:

98%,99%, ^*data from raw suppliers

Indophenol ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C1=CC(=O)C=CC1=NC2=CC=C(C=C2)O
• Uses: Indophenol is an artificial blue metachromatic dye. The formation of Indophenol can be used to determine ammonia and paracetamol by spectrophotometry.

Technology Process of Indophenol

There total 23 articles about Indophenol 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:

4-amino-phenol (123-30-8) + 2,6-dimethyl-3-acetylamino-phenol (28739-71-1) → indophenol (500-85-6)

Guidance literature:

With ammonium persulfate; ammonia; In water; acetone;

Reference yield:

dibromopyrazolone + 4-amino-2,6-dichlorophenol hydrochloride (42486-53-3) → indophenol (500-85-6)

Guidance literature:

With triethylamine; In ethanol;

Reference yield:

phenol (108-95-2,27073-41-2) → indophenol (500-85-6)

Guidance literature:

With ammonia; water; dihydrogen peroxide; sodium carbonate; man den Krystall eines Hydroxylaminsalzes als Katalysator zusetzt;

upstream raw materials:

bis-(4-hydroxyphenyl)methane

benzoquinone N-chloroimine

4,4'-dihydroxydiphenylamine

phenol blue

Downstream raw materials:

4,4'-dihydroxydiphenylamine

2,5-bis(4-hydroxyanilino)-1,4-benzoquinone

4-amino-phenol

hydroquinone

Refernces

• 1、 Guilbault et al.. "". . p. 1897. Retrieved 1966.
• 2、 Krutikova,Krutikov,Erkin. "Polyfluoroalloxy phosphonic and phosphinic acid derivatives: I. 1-Hydroxy-2,2,2-trichloroethylphosphinates". body text. p. 428 - 433. Retrieved 2010/08/04.
• 3、 Tao,Barra. "Inhibition of quinone-imine dye deamination by complexation with para-sulfonated calixarenes". . p. 2158 - 2160. Retrieved 2007/10/03.