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Tauro-α-muricholic Acid

Base Information
  • Chemical Name:Tauro-α-muricholic Acid
  • CAS No.:25613-05-2
  • Molecular Formula:C26H45NO7S
  • Molecular Weight:515.712
  • Hs Code.:
  • Mol file:25613-05-2.mol
Tauro-α-muricholic Acid

Synonyms:

Suppliers and Price of Tauro-α-muricholic Acid
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • Tauro-α-muricholicAcidSodiumSalt
  • 2.5mg
  • $ 910.00
  • TRC
  • Tauro-α-muricholicAcidSodiumSalt
  • 1mg
  • $ 520.00
  • TRC
  • Tauro-α-muricholicAcidSodiumSalt
  • 25mg
  • $ 6960.00
  • Medical Isotopes, Inc.
  • Tauro-α-muricholicAcidSodiumSalt
  • 25 mg
  • $ 6750.00
  • Medical Isotopes, Inc.
  • Tauro-α-muricholicAcidSodiumSalt
  • 2.5 mg
  • $ 1250.00
Total 6 raw suppliers
Chemical Property of Tauro-α-muricholic Acid
Chemical Property:
  • Melting Point:>190°C (dec.) 
  • PKA:1.42±0.50(Predicted) 
  • Density:1.264±0.06 g/cm3(Predicted) 
  • Storage Temp.:-20°C Freezer, Under Inert Atmosphere 
  • Solubility.:DMSO (Slightly), Methanol (Slightly) 
Purity/Quality:

98%+ *data from raw suppliers

Tauro-α-muricholicAcidSodiumSalt *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses Tauro-α-muricholic Acid is a bile acid released by the liver and is typically used in cholestasis studies. Tauro-α-muricholic Acid Sodium Salt is a bile acid released by the liver and is typically used in cholestasis studies.
Technology Process of Tauro-α-muricholic Acid

There total 20 articles about Tauro-α-muricholic Acid 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:
Guidance literature:
With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at 20 ℃; for 20h;
DOI:10.5012/bkcs.2013.34.8.2436
Guidance literature:
With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at 20 ℃; for 20h;
DOI:10.5012/bkcs.2013.34.8.2436
Guidance literature:
Multi-step reaction with 3 steps
1: potassium hydroxide / methanol / 2 h / Reflux
2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane; N,N-dimethyl-formamide / 20 h / 20 °C
3: 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 20 h / 20 °C
With 1,8-diazabicyclo[5.4.0]undec-7-ene; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; potassium hydroxide; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.5012/bkcs.2013.34.8.2436
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