Product Details
Place of Origin: China
Brand Name: Sunshine
Certification: COA,ISO
Model Number: 474-25-9
Payment & Shipping Terms
Minimum Order Quantity: Negotiation
Price: Negotiation
Packaging Details: Aluminum Foil Bag, Drum
Delivery Time: 7-15 working days
Payment Terms: T/T, L/C, D/A
Supply Ability: 15 Ton/Month
CAS NO:: |
474-25-9 |
Appearance: |
A White Or Almost White Powder |
Molecular Formula:: |
C24H40O4 |
Molecular Weight:: |
392.572g/mol |
EINECS NO:: |
207-481-8 |
MDL NO:: |
MFCD00064142 |
CAS NO:: |
474-25-9 |
Appearance: |
A White Or Almost White Powder |
Molecular Formula:: |
C24H40O4 |
Molecular Weight:: |
392.572g/mol |
EINECS NO:: |
207-481-8 |
MDL NO:: |
MFCD00064142 |
Product Description:
Product Name: Chenodeoxycholic acid CAS NO: 474-25-9
Synonyms:
Cholan-24-oic acid, 3,7-dihydroxy-, (3α,5β,7α)-;
3α,7α-Dihydroxy-5β-cholanic Acid;
anthropododesoxycholicacid;
Chemical & Physical Properties:
Appearance: White to off-white powder
Assay :≥96.00%
Density: 1.128g/cm3
Boiling Point: 547.1℃ at 760 mmHg
Melting Point: 167-171℃
Flash Point: 298.8℃
Water Solubility: PRACTICALLY INSOLUBLE
Safety Information:
RTECS: FZ1980000
Safety Statements: S36/37-S45
HS Code: 2918990090
WGK Germany: 2
Risk Statement: R63
Hazard Code: Xn
Application:
Chenodeoxycholic acid (also known as chenodesoxycholic acid, chenocholic acid and 3α,7α-dihydroxy-5β-cholan-24-oic acid) is a bile acid. It occurs as a white crystalline substance insoluble in water but soluble in alcohol and acetic acid,Salts of this carboxylic acid are called chenodeoxycholates. Chenodeoxycholic acid is one of the main bile acids produced by the liver.
It was first isolated from the bile of the domestic goose, which gives it the "cheno" portion of its name (Greek: χήν = goose).
Chenodeoxycholic acid and cholic acid are the two primary bile acids in humans. Some other mammals have muricholic acid or deoxycholic acid rather than chenodeoxycholic acid.
Chenodeoxycholic acid is synthesized in the liver from cholesterol by a process which involves several enzymatic steps. Like other bile acids, it can be conjugated in the liver with taurine or glycine, forming taurochenodeoxycholate or glycochenodeoxycholate. Conjugation results in a lower pKa. This means the conjugated bile acids are ionized at the usual pH in the intestine and will stay in the gastrointestinal tract until reaching the ileum where most will be reabsorbed. Bile acids form micelles which facilitate lipid digestion. After absorption, they are taken up by the liver and resecreted, so undergoing an enterohepatic circulation. Unabsorbed chenodeoxycholic acid can be metabolised by bacteria in the colon to form the secondary bile acid known as lithocholic acid.
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