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Methyl cholate, 97%
CAS: 1448-36-8 | C25H42O5 | 422.606 g/mol
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Catalog number L05129.06
also known as L05129-06
Price (EUR)
42,70
Each
Quantity:
5 g
Price (EUR)
42,70
Each
Chemical Identifiers
CAS1448-36-8
IUPAC Namemethyl 4-{4,7,11-trihydroxy-9a,11a-dimethyl-hexadecahydro-1H-cyclopenta[a]phenanthren-1-yl}pentanoate
Molecular FormulaC25H42O5
InChI KeyDLYVTEULDNMQAR-UHFFFAOYNA-N
SMILESCOC(=O)CCC(C)C1CCC2C3C(O)CC4CC(O)CCC4(C)C3CC(O)C12C
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White to cream
FormCrystals or powder or crystalline powder
Assay (special)≥96.0 to ≤104.0% (based on elemental C and H)
Elemental AnalysisC: 63.95-78.17% (Theory: 71.06%)
Elemental AnalysisH: 9.01-11.01% (Theory: 10.01%)
Methyl cholate, is used as a bile acid derivative as anti-inflammatory and antitumor agent.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Methyl cholate, is used as a bile acid derivative as anti-inflammatory and antitumor agent.
Solubility
Insoluble in water. Soluble in medium polarity organic solvents.
Notes
Keep container tightly closed in a dry and well-ventilated place. Keep away from oxidizing agents.
Methyl cholate, is used as a bile acid derivative as anti-inflammatory and antitumor agent.
Solubility
Insoluble in water. Soluble in medium polarity organic solvents.
Notes
Keep container tightly closed in a dry and well-ventilated place. Keep away from oxidizing agents.
RUO – Research Use Only
General References:
- S Broderick.; AP Davis.; RP Williams. The triamino-analogue of methyl cholate; a facial amphiphile and scaffold with potential for combinatorial and molecular recognition chemistry. Tetrahedron letters. 1998, 39,(33), 6083-6086.
- JL Scott. Solid-vapor reactions of cholic acid and methyl cholate with acetonitrile: structures and reaction kinetics. J. Chem. Soc., Perkin Trans. 2. 1995, 2,(1), 495-502.