Sodium deoxycholate monohydrate - BioReagent, ≥99%(T) , CAS No.145224-92-6

CAS: 145224-92-6 Cat. No.: S755665 Peso molecular: 432.57 Beilstein Registry Number: 3643164 Número EC: 680-423-0 PubChem CID: 23679071
Disponible para pedir
GRADE & PURITY BioReagent ? BioReagent grade — tested suitable for life-science and molecular-biology use. Use for cell culture, assays, and biochemical work needing biological compatibility. ≥99%(T)
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
S755665-5g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
509,90US$
25g
S755665-25g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
1.926,90US$
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Why this grade

BioReagent, ≥99%(T) BioReagent for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Sodium deoxycholate (SDC) monohydrate is a bile acid salt.
Application:
Sodium deoxycholate monohydrate has been used in a study to assess a method for the immobilization of lipoxygenase in an alginate-silicate gel matrix. It has also been used in a study to investigate the in vitro dissolution of gall stones.
Powerful solubilization agent; used in the solubilization of estrogen synthetase from human placental microsomes.

Specifications

Especificaciones y pureza
BioReagent, ≥99%(T)
Mecanismos bioquímicos y fisiológicos
Bile Salt
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Grado
BioReagent
Pureza
≥99%(T)
Nombres e identificadores
PH7.5-9.5 (20 °C, 0.1 M in H 2 O)
Sonrisas canónicasCC(CCC(=O)[O-])C1CCC2C1(C(CC3C2CCC4C3(CCC(C4)O)C)O)C.O.[Na+]
IUPAC Namesodium;(4R)-4-[(3R,5R,8R,9S,10S,12S,13R,14S,17R)-3,12-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoate;hydrate
InChIKeyNDVHNZISGVSFMP-WTCAICSISA-M
INCHI1S/C24H40O4.Na.H2O/c1-14(4-9-22(27)28)18-7-8-19-17-6-5-15-12-16(25)10-11-23(15,2)20(17)13-21(26)24(18,19)3;;/h14-21,25-26H,4-13H2,1-3H3,(H,27,28);;1H2/q;+1;/p-1/t14-,15-,16-,17+,18-,19+,20+,21+,23+,24-;;/m1../s1
Isómeros SMILES C[C@H](CCC(=O)[O-])[C@H]1CC[C@@H]2[C@@]1([C@H](C[C@H]3[C@H]2CC[C@H]4[C@@]3(CC[C@H](C4)O)C)O)C.O.[Na+]
WGK Alemania 3
PubChem CID 23679071
Peso molecular 432.57
Beilstein 3643164

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
ClaseSteroids and steroid derivatives
SubclassBile acids, alcohols and derivatives
Intermediate Tree Nodes Hydroxy bile acids, alcohols and derivatives
Direct ParentDihydroxy bile acids, alcohols and derivatives
Alternative Parents 3-alpha-hydroxysteroids  12-hydroxysteroids  Secondary alcohols  Cyclic alcohols and derivatives  Carboxylic acid salts  Monocarboxylic acids and derivatives  Carboxylic acids  Organic zwitterions  Organic sodium salts  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic homopolycyclic compounds
Substituents Dihydroxy bile acid, alcohol, or derivatives - 3-hydroxysteroid - 12-hydroxysteroid - Hydroxysteroid - 3-alpha-hydroxysteroid - Cyclic alcohol - Carboxylic acid salt - Secondary alcohol - Carboxylic acid derivative - Carboxylic acid - Organic alkali metal salt - Monocarboxylic acid or derivatives - Organic sodium salt - Hydrocarbon derivative - Alcohol - Organic oxide - Organic oxygen compound - Organic salt - Carbonyl group - Organooxygen compound - Organic zwitterion - Aliphatic homopolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as dihydroxy bile acids, alcohols and derivatives. These are compounds containing or derived from a bile acid or alcohol, and which bears exactly two carboxylic acid groups.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
SolubilidadH 2 O: 0.1 M, clear, colorless
Punto de fusión (°C)>300℃
Peso molecular432.600 g/mol
XLogP3
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count5
Rotatable Bond Count4
Exact Mass432.285 Da
Monoisotopic Mass432.285 Da
Topological Polar Surface Area81.600 Ų
Heavy Atom Count30
Formal Charge0
Complexity612.000
Isotope Atom Count0
Defined Atom Stereocenter Count10
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count3
Citations of This Product
Referencias
1. Xiaoting Wang, Shiyao Fu, Ying Han, Xuening Yang, Jing Wang, Xin Yang.  (2025)  Ursolic acid- betulinic acid-CCM NPs: A delivery system for improving the stability and bioavailability of CCM.  FOOD RESEARCH INTERNATIONAL,      [PMID:40032459] [10.1016/j.foodres.2025.115947]
2. Chuyue Xiang, Jian Gao, Haoxin Ye, Gerui Ren, Xiangjuan Ma, Hujun Xie, Sheng Fang, Qunfang Lei, Wenjun Fang.  (2020)  Development of ovalbumin-pectin nanocomplexes for vitamin D3 encapsulation: Enhanced storage stability and sustained release in simulated gastrointestinal digestion.  FOOD HYDROCOLLOIDS,      [PMID:] [10.1016/j.foodhyd.2020.105926]
3. Gerui Ren, Ruiqi Hu, Jiajun Mao, Xinpei Cai, Tianrong Wang, Xin Song, Wentao Wu, Caixin Zhuge, Min Huang, Hujun Xie, Kejun Cheng.  (2026)  From poor solubility to precision delivery: Zein–κ-carrageenan nanovehicles unlock dihydromyricetin's bioactive potential.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:41708022] [10.1016/j.ijbiomac.2026.150961]
Calculadoras de soluciones
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