ChemicalBook > CAS DataBase List > LITHOCHOLIC ACID

LITHOCHOLIC ACID

Product Name
LITHOCHOLIC ACID
CAS No.
434-13-9
Chemical Name
LITHOCHOLIC ACID
Synonyms
Lithocolic acid;NCI-C03861;Lithocholate;(R)-4-((3R,5R,8R,9S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid;NCI-CO-3861;lithocholicaci;LITHOCHOLIC ACID;Lithocholic aCld;Stone cholic acid;Lithocholic Acide
CBNumber
CB2342229
Molecular Formula
C24H40O3
Formula Weight
376.57
MOL File
434-13-9.mol
More
Less

LITHOCHOLIC ACID Property

Melting point:
183-188 °C (lit.)
alpha 
D20 +33.7° (c = 1.5 in abs ethanol); D19 +23.3° (Wieland); D20 +32.1° (Fischer)
Boiling point:
445.09°C (rough estimate)
Density 
1.0454 (rough estimate)
refractive index 
35.5 ° (C=1, EtOH)
Flash point:
9℃
storage temp. 
room temp
solubility 
Chloroform (Slightly), Dichloromethane (Slightly, Heated), DMSO (Slightly, Heated)
pka
4.76±0.10(Predicted)
form 
Powder
color 
White to off-white
optical activity
+3220 (c 1.5, ethanol)
biological source
bovine bile
synthetic
Water Solubility 
18.83ug/L(25 ºC)
Merck 
5545
BRN 
3217757
InChIKey
SMEROWZSTRWXGI-HVATVPOCSA-N
LogP
6.700 (est)
CAS DataBase Reference
434-13-9(CAS DataBase Reference)
EPA Substance Registry System
Lithocholic acid (434-13-9)
More
Less

Safety

Safety Statements 
22-24/25
RIDADR 
UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany 
2
RTECS 
FZ2275000
HS Code 
29181998
Hazardous Substances Data
434-13-9(Hazardous Substances Data)
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H225Highly Flammable liquid and vapour

H370Causes damage to organs

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P403+P233Store in a well-ventilated place. Keep container tightly closed.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
L6250
Product name
Lithocholic acid
Purity
≥95%
Packaging
10g
Price
$77
Updated
2024/03/01
Cayman Chemical
Product number
20253
Product name
Lithocholic Acid
Purity
≥95%
Packaging
5g
Price
$33
Updated
2024/03/01
Cayman Chemical
Product number
20253
Product name
Lithocholic Acid
Purity
≥95%
Packaging
10g
Price
$60
Updated
2024/03/01
Sigma-Aldrich
Product number
L6250
Product name
Lithocholic acid
Purity
≥95%
Packaging
25g
Price
$264
Updated
2024/03/01
Sigma-Aldrich
Product number
L0720800
Product name
Lithocholic acid
Purity
European Pharmacopoeia (EP) Reference Standard
Packaging
l0720800
Price
$220
Updated
2024/03/01
More
Less

LITHOCHOLIC ACID Chemical Properties,Usage,Production

Chemical Properties

white to off-white powder

Uses

LD50(mouse) 3900 mg/kg po

Uses

Cholagogue;Anticholelithogenic

Uses

Lithocholic acid has been used in a study to assess cholestasis and its action on several organs and tissues in rats. It has also been used in a study to investigate the regulation of hepatic phospholipid and bile acid homeostasis through SMAD3 activation by TGFβ.

Uses

A cholic acid derivative as TGR5 modulator. Found in ox bile, human bile, rabbit bile, and in ox and pig gallstones.

Definition

ChEBI: A monohydroxy-5beta-cholanic acid with a alpha-hydroxy substituent at position 3. It is a bile acid obtained from chenodeoxycholic acid by bacterial action.

General Description

Hexagonal leaflets (from alcohols) or prisms (from acetic acid) or white powder.

Air & Water Reactions

Insoluble in water.

Health Hazard

ACUTE/CHRONIC HAZARDS: When heated to decomposition LITHOCHOLIC ACID emits acrid smoke and fumes.

Fire Hazard

Flash point data for LITHOCHOLIC ACID are not available. LITHOCHOLIC ACID is probably combustible.

Biological Activity

lithocholic acid (lca) is a toxic secondary bile acid, causing intrahepatic cholestasis, which has tumor-promoting activity.

in vitro

among 17 kinds of bile acids with respect to inhibition of mammalian dna polymerases, only lca and its derivatives inhibited dna polymerases, while other bile acids did not show inhibitory effect [1].

in vivo

administration of lca and its conjugates to rodents causes intrahepatic cholestasis, which is a pathogenic state characterized by decreased bile flow and the accumulation of bile constituents in the liver and blood [2].

Purification Methods

Lithocholic acid can be purified by conversion to the rather insoluble Na or K salt by addition of the equivalent amount of aqueous NaOH or KOH, filtering off the alkali salt, washing it with ice cold H2O, dissolving it in the least volume of boiling H2O, acidifying with the dilute HCl (slight excess), filtering off the acid, washing with cold H2O and drying it thoroughly in a vacuum. Recrystallise it from Me2CO, EtOH or acetic acid. The methyl ester crystallises from MeOH, with 0.5 mol of MeOH, and has m 92-93o, [] D 25 +34o (MeOH). It has also been purified by recrystallisation from pet ether (b 40-60o) and, after chromatography on Al2O3 in pet ether, gave a labile form m 92-93o which is transformed to the stable form m 125-126o after standing for 2days in a vacuum desiccator. [Hoelm & Mason J Am Chem Soc 62 569 1940, Sarel & Yanuka J Org Chem 24 2018 1959, Beilstein 10 IV 785.]

References

[1] ogawa a, murate t, suzuki m, nimura y, yoshida s. lithocholic acid, a putative tumor promoter, inhibits mammalian dna polymerase beta. jpn j cancer res. 1998 nov;89(11):1154-9.
[2] staudinger jl, goodwin b, jones sa, hawkins-brown d, mackenzie ki, latour a, liu y, klaassen cd, brown kk, reinhard j, willson tm, koller bh, kliewer sa. the nuclear receptor pxr is a lithocholic acid sensor that protects against liver toxicity. proc natl acad sci u s a. 2001 mar 13;98(6):3369-74.

LITHOCHOLIC ACID Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

LITHOCHOLIC ACID Suppliers

MedChemexpress LLC
Tel
021-58955995
Fax
609-228-5909
Email
sales@medchemexpress.cn
Country
United States
ProdList
4861
Advantage
58
AdooQ BioScience, LLC
Tel
+1 (866) 930-6790
Fax
+1 (866) 333-9607
Email
info@adooq.com
Country
United States
ProdList
2782
Advantage
58
Target molecule Corp.
Tel
857-239-0968
Fax
857-239-8801
Email
service1@targetmol.com
Country
United States
ProdList
2559
Advantage
60
Musechem
Tel
+1-800-259-7612
Fax
+1-800-259-7612
Email
info@musechem.com
Country
United States
ProdList
4660
Advantage
60
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32161
Advantage
58
InvivoChem
Tel
+1-708-310-1919 +1-13798911105
Fax
708-557-7486
Email
sales@invivochem.cn
Country
United States
ProdList
6391
Advantage
58
Accela ChemBio Inc.
Tel
+1-858-6993322
Fax
(+1)-858-876-1948
Email
info@accelachem.com
Country
United States
ProdList
18478
Advantage
58
Standardpharm Co. Ltd.
Tel
86-714-3992388
Email
overseasales1@yongstandards.com
Country
United States
ProdList
14332
Advantage
58
BOC Sciences
Tel
+1-631-485-4226
Fax
1-631-614-7828
Email
inquiry@bocsci.com
Country
United States
ProdList
19553
Advantage
58
Cato Research Chemicals Inc.
Tel
020-81215950 4000-868-328
Email
customer@uwalab.com
Country
United States
ProdList
10404
Advantage
58
Aladdin Scientific
Tel
+1-+1(833)-552-7181
Email
sales@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
ApexBio Technology
Tel
--
Fax
--
Email
sales@apexbt.com
Country
United States
ProdList
6251
Advantage
58
BOC Sciences
Tel
16314854226
Email
info@bocsci.com
Country
United States
ProdList
9923
Advantage
65
Abcam
Tel
--
Fax
--
Email
us.orders@abcam.com
Country
United States
ProdList
6001
Advantage
50
Cayman Chemical Company
Tel
--
Fax
--
Email
cayman@caymanchem.com
Country
United States
ProdList
6213
Advantage
81
IsoSciences
Tel
--
Fax
--
Email
info@isosciences.com
Country
United States
ProdList
379
Advantage
58
Fluorochem Ltd.
Tel
--
Fax
--
Email
enquiries@fluorochem.co.uk
Country
United States
ProdList
4583
Advantage
58
MP Biomedicals, LLC. (Division of Valiant FC Co., Ltd.)
Tel
--
Fax
--
Email
serv@mpbio.com
Country
United States
ProdList
1854
Advantage
58
Selleck Chemicals LLC
Tel
--
Fax
--
Email
sales@selleckchem.com
Country
United States
ProdList
1848
Advantage
58
VWR International, LLC.
Tel
--
Fax
--
Email
@sargentwelch.com
Country
United States
ProdList
6262
Advantage
58
Oakwood Products, Inc.
Tel
--
Fax
--
Email
sales@oakwoodchemical.com
Country
United States
ProdList
6193
Advantage
74
TCI America, Inc. (part of Tokyo Chemical Industry)
Tel
--
Fax
--
Email
Angelina.Crew@tcichemicals.com
Country
United States
ProdList
2053
Advantage
58
United States Biological
Tel
--
Fax
--
Email
chemicals@usbio.net
Country
United States
ProdList
6214
Advantage
80
MedChemExpress
Tel
--
Fax
--
Email
sales@medchemexpress.com
Country
United States
ProdList
6398
Advantage
58
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
Cambridge Isotope Laboratories, Inc.
Tel
--
Fax
--
Email
cilsales@isotope.com
Country
United States
ProdList
6598
Advantage
79
CacheSyn Inc.
Tel
--
Fax
--
Email
info@cachesyn.com
Country
United States
ProdList
695
Advantage
50
Selleck Chemicals LLC
Tel
--
Fax
--
Email
info@selleckchem.com
Country
United States
ProdList
824
Advantage
60
ChemService Inc.
Tel
--
Fax
--
Country
United States
ProdList
6379
Advantage
68
INDOFINE Chemical Company, Inc.
Tel
--
Fax
--
Email
chemical@indofinechemical.com
Country
United States
ProdList
6176
Advantage
69
Spectrum Chemicals & Laboratory Products
Tel
--
Fax
--
Email
sales@spectrumchemical.com
Country
United States
ProdList
6699
Advantage
77
HONEST JOY HOLDINGS LIMITED
Tel
--
Fax
--
Email
sales@honestjoy.cn
Country
United States
ProdList
6675
Advantage
54
City Chemical LLC
Tel
--
Fax
--
Email
sales@citychemical.com
Country
United States
ProdList
6708
Advantage
72
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
AK Scientific, Inc.
Tel
--
Fax
--
Email
sales@aksci.com
Country
United States
ProdList
6347
Advantage
65
Sciencelab.com, Inc.
Tel
--
Fax
--
Email
accounting@sciencelab.com
Country
United States
ProdList
4159
Advantage
82
Advance Scientific & Chemical
Tel
--
Fax
--
Email
sales@advance-scientific.com
Country
United States
ProdList
6419
Advantage
71
MP Biomedicals, Inc.
Tel
--
Fax
--
Country
United States
ProdList
6561
Advantage
81
ChromaDex
Tel
--
Fax
--
Email
sales@chromadex.com
Country
United States
ProdList
2501
Advantage
76
Steraloids Inc.
Tel
--
Fax
--
Email
sales@steraloids.com
Country
United States
ProdList
2357
Advantage
68
City Chemicals Corporation
Tel
--
Fax
--
Country
United States
ProdList
6460
Advantage
72
Pfaltz & Bauer, Inc.
Tel
--
Fax
--
Email
sales@pfaltzandbauer.com
Country
United States
ProdList
6828
Advantage
72
Research Plus, Inc.
Tel
--
Fax
--
Email
respls@aol.com
Country
United States
ProdList
3674
Advantage
51
More
Less

View Lastest Price from LITHOCHOLIC ACID manufacturers

Hebei Saisier Technology Co., LTD
Product
LITHOCHOLIC ACID 434-13-9
Price
US $6.00-3.00/KG
Min. Order
1KG
Purity
More than 99%
Supply Ability
2000KG/Month
Release date
2024-04-03
HebeiShuoshengImportandExportco.,Ltd
Product
LITHOCHOLIC ACID 434-13-9
Price
US $6.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
2000KG/Month
Release date
2024-08-09
Hebei Longbang Technology Co., Ltd
Product
LITHOCHOLIC ACID 434-13-9
Price
US $5.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
20TONS
Release date
2024-05-13

434-13-9, LITHOCHOLIC ACIDRelated Search:


  • 17-beta-(1-Methyl-3-carboxypropyl)ethiocholan-3-alpha-ol
  • 17beta-(1-methyl-3-carboxypropyl)etiocholan-3alpha-ol
  • BETA-CHOLANIC ACID-3-ALPHA-OL
  • HYDROYCHOLANIC ACID
  • 3-HYDROXYCHOLANIC ACID
  • 3ALPHA-HYDROXYCHOLANIC ACID
  • 3ALPHA-HYDROXY-5BETA-CHOLANIC ACID
  • 3ALPHA-HYDROXY-5BETA-CHOLAN-24-OIC ACID
  • 5BETA-CHOLAN-24-OIC ACID-3A-OL
  • 5BETA-CHOLAN-24-OIC ACID-3ALPHA-OL
  • 5BETA-CHOLANIC ACID-3ALPHA-OL
  • LITHOCHOLIC ACID
  • Ursodeoxycholic Acid Impurity 3(Ursodeoxycholic Acid EP Impurity C)
  • Lithocolic acid
  • NCI-C03861
  • 3α-Hydroxy-5β-cholan-24-oic acid
  • 3α-Hydroxy-5β-cholanic acid
  • 5β-Cholan-24-oic acid-3α-ol
  • Lithocholic Acide
  • Lithocholic acid,3α-Hydroxy-5β-cholan-24-oic acid, 3α-Hydroxy-5β-cholanic acid, 5β-Cholan-24-oic acid-3α-ol
  • 17β-(1-Methyl-3-car-boxypropyl) etiocholan-3α-ol
  • (4R)-4-[(3R,5R,8R,9S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,]
  • LITHOCHOLIC ACID(RG)
  • 3α-Hydroxy-5β-cholan-24-oic acid, 3α-Hydroxy-5β-cholanic acid, 5β-Cholan-24-oic acid-3α-ol
  • 3β-Hydroxyallocholanic acid
  • NCI-CO-3861
  • Lithocholic acid,98%
  • Lithocholic acid3alpha-Hydroxycholanic acid
  • Lithocholic acid, 98% 5GR
  • 3α-Hydroxy-5β-cholan-24-oate
  • 3α-Hydroxy-5β-cholanoic Acid
  • 5beta-Cholanic Acid-3alpha-ol 3alpha-Hydroxy-5beta-cholanic Acid
  • 3-alpha-hydroxy-5-beta-cholan-24-oicaci
  • 3alpha-hydroxy-5beta-cholan-24-oicaci
  • 3-alpha-hydroxy-5-beta-cholanicaci
  • 3alpha-Hydroxy-5beta-cholanoic acid
  • 3alpha-hydroxy-5beta-cholanoicacid
  • 3-hydroxy-,(3-alpha,5-beta)-cholan-24-oicaci
  • 3-hydroxy-,(3alpha,5beta)-cholan-24-oicaci
  • 3-Hydroxycholan-24-oic acid
  • 3-hydroxycholan-24-oicacid
  • 5beta-Cholan-24-oic acid, 3alpha-hydroxy-
  • 5-beta-Cholanic acid, 3-alpha-hydroxy-
  • Cholan-24-oic acid, 3-hydroxy-, (3alpha,5beta)-
  • Lithocholate
  • Cholan-24-oic acid, 3-hydroxy-, (3α,5β)-
  • Lithocholic aCld
  • LITHOCHOLIC ACID >=95%
  • Ursodeoxycholic Acid EP Impurity C
  • Stone cholic acid
  • (R)-4-((3R,5R,8R,9S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid
  • Chenodeoxycholic Acid Impurity 3
  • Lithocholic acid CRS
  • LithocholicAcid&gt
  • LITHOCHOLIC ACID USP/EP/BP
  • Chenodeoxycholic acid EP Impurity C
  • ALPHA-HYDROXY-5BETA-CHOLANIC ACID
  • Ursodeoxycholic Acid EP Impurity C 434-13-9