Uroxanthin

Base Information

• Chemical Name: Uroxanthin
• CAS No.: 487-60-5
• Molecular Formula: C₁₄H₁₇NO₆
• Molecular Weight: 295.292
• Hs Code.: 29389090
• NSC Number: 87517
• DSSTox Substance ID: DTXSID10862015
• Wikipedia: Indican
• Wikidata: Q105342753
• NCI Thesaurus Code: C152073
• Metabolomics Workbench ID: 123637
• ChEMBL ID: CHEMBL1561942
• Mol file: 487-60-5.mol

Synonyms:1H-Indol-3-ol Hydrogen Sulfate Ester;Indican;Indican Monopotassium Salt;Indican Monosodium Salt;Indoxyl Sulfate;Monopotassium Salt, Indican;Monosodium Salt, Indican;Sulfate, Indoxyl

Chemical Property of Uroxanthin

Chemical Property:

• Appearance/Colour: white to off-white crystalline powder
• Vapor Pressure: 1.43E-15mmHg at 25°C
• Melting Point: 57-58 °C
• Boiling Point: 606.7 °C at 760 mmHg
• PKA: 12.92±0.70(Predicted)
• Flash Point: 320.7 °C
• PSA: 115.17000
• Density: 1.562 g/cm³
• LogP: -0.65340
• Storage Temp.: −20°C
• Solubility.: H2O: 0.1 M at 20 °C, clear to slightly haz
• XLogP3: -0.1
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 3
• Exact Mass: 295.10558726
• Heavy Atom Count: 21
• Complexity: 356

Purity/Quality:

98%, ^*data from raw suppliers

3-Indoxyl-b-D-glucopyranoside trihydrate ^*data from reagent suppliers

Safty Information:

• Pictogram(s): UN NO.
• Hazard Codes: UN NO.
• Safety Statements: 22-24/25

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C2C(=C1)C(=CN2)OC3C(C(C(C(O3)CO)O)O)O
• Uses: colorimetric substrate for laminarinase Indoxyl-β-D-glucoside is a constitute of Isatis indigotica Chinese medicinal herb widely used for the treatment of influenza, viral pneumonia, mumps, pharyngitis, and hepatitis. It is also used in many Chinese medicinal feeds with the effect of reducing stress reaction of livestock and fowls and enhancing immunity.

Technology Process of Uroxanthin

There total 1 articles about Uroxanthin 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-indoxyl-β-D-glucopyranoside (487-60-5,25466-37-9,126787-65-3,134931-83-2)

Guidance literature:

With methanol; ammonia;

DOI:10.1039/jr9270001937

Reference yield:

3-indoxyl-β-D-glucopyranoside (487-60-5,25466-37-9,126787-65-3,134931-83-2) → indoxyl (480-93-3)

Guidance literature:

With Sulfolobus acidocaldarius β-glucosidase; Enzymatic reaction;

DOI:10.1021/acscatal.9b02613

Reference yield:

3-indoxyl-β-D-glucopyranoside (487-60-5,25466-37-9,126787-65-3,134931-83-2) + acetic anhydride (108-24-7) → (1-acetyl-indol-3-yl)-(tetra-O-acetyl-β-D-glucopyranoside) (7497-97-4)

Guidance literature:

With sodium acetate;

Downstream raw materials:

(1-acetyl-indol-3-yl)-(tetra-O-acetyl-β-D-glucopyranoside)

indoxyl

indigo