CID 629284

Base Information

• Chemical Name: CID 629284
• CAS No.: 146-68-9
• Molecular Formula: C19H13ClIN5O2
• Molecular Weight: 505.702
• Hs Code.: 29339900
• Mol file: 146-68-9.mol

Synonyms:

Chemical Property of CID 629284

Chemical Property:

• Appearance/Colour: slightly yellow powder
• Vapor Pressure: 6.76E-13mmHg at 25°C
• Melting Point: 240 °C (dec.)(lit.)
• Boiling Point: 567.5 °C at 760 mmHg
• Flash Point: 297 °C
• PSA: 80.41000
• LogP: 1.25100
• Storage Temp.: Store at 2-8
• Sensitive.: Light Sensitive
• Solubility.: methanol: water (1:1): 50 mg/mL hot, very faintly turbid, v
• Water Solubility.: soluble
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 3
• Exact Mass: 504.98025
• Heavy Atom Count: 28
• Complexity: 503

Purity/Quality:

99.0% ^*data from raw suppliers

Iodonitrotetrazolium chloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s): F, Xn, Xi
• Hazard Codes: Xn,F,Xi
• Statements: 20/21/22-68/20/21/22-36/37/38-11
• Safety Statements: 36/37-36/37/39-26-22-16

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C2=NN([N+](=N2)C3=CC=C(C=C3)I)C4=CC=C(C=C4)[N+](=O)[O-].[Cl-]
• Description: Iodonitrotetrazolium (INT) (chloride) is a monotetrazolium salt used as an indicator dye. It is reduced to an insoluble formazan that is used as a vital dye or indicator of cellular redox activity. Reduction commonly results from the activity of dehydrogenases, although non-enzymatic electron transfer reactions can occur in the presence of an intermediate electron acceptor. INT is commonly used to measure the respiratory activity of microorganisms in a variety of contexts.
• Uses: Electron acceptor for the colorimetric assay of various dehydrogenases. Iodonitrotetrazolium chloride (INT) on reduction gets converted to iodonitrotetrazolium formazan, a water insoluble violet colored dye or indicator. Hence INT can be used for the colorimetric assay of various dehydrogenases. Iodonitrotetrazolium chloride has been used for the staining of cells. It has been used as a coupling agent in the enzymatic assay of D-arabinitol.

Technology Process of CID 629284

There total 2 articles about CID 629284 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:

n-Butyl nitrite (544-16-1) + INT-formazan (136196-46-8) → 2-(4-iodophenyl)-3-(4-nitrophenyl)-5-phenyl-3H-tetrazol-2-ium chloride (146-68-9)

Guidance literature:

With hydrogenchloride; ethanol;

DOI:10.1021/ja01164a086

Reference yield:

→ 2-(4-iodophenyl)-3-(4-nitrophenyl)-5-phenyl-3H-tetrazol-2-ium chloride (146-68-9)

Guidance literature:

1-(4-Jodphenyl)-5-(4-nitrophenyl)-3-phenylformazan (I), iso-Amylnitrit/HCl, EtOH;

Reference yield:

2-(4-iodophenyl)-3-(4-nitrophenyl)-5-phenyl-3H-tetrazol-2-ium chloride (146-68-9) → INT-formazan (7781-49-9)

Guidance literature:

With Gerovital H₃; xanthine oxidase; xanthin; at 25 ℃; for 0.166667h; pH=7.4; aq. phosphate buffer; Enzymatic reaction;

upstream raw materials:

n-Butyl nitrite

INT-formazan

Downstream raw materials:

INT-formazan

INT-formazan

Refernces

• 1、 -. "Method of measuring substance in sample using a redox reaction". . . Retrieved 2008/06/13.