Dexamethasone - BioReagent, Moligand™, for cell culture, ≥97%, powder , CAS No.50-02-2

CAS: 50-02-2 Cat. No.: D754934 分子式: C22H29FO5 分子量: 392.46 Beilstein Registry Number: 2066651 EC番号: 200-003-9
注文可能
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. Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. for Cell culture ? Cell-culture grade — low endotoxin and contaminants to support viable cell growth. Use in mammalian/other cell culture media and supplements. ≥97% powder
Synonyms
Prednisolone F | 9α-Fluoro-16α-methyl-11β,17α,21-trihydroxy-1,4-pregnadiene-3,20-dione | (11β,16α)-9-Fluoro-11,17,21-trihydroxy-16-methylpregna-1,4-diene-3,20-dione | 9α-Fluoro-16α-methylprednisolone | NSC 34521 | MK 125
Storage
Store at 2-8°C,Protected from light
Shipped In
Wet ice
★
Size
USA
ドイツ (EU)*
Price
Qty
25mg
D754934-25mg
在庫あり ≥10
—
$152.90
100mg
D754934-100mg
3 在庫あり
—
$387.90
500mg
D754934-500mg
3 在庫あり
—
$839.90
1g
D754934-1g
3 在庫あり
—
$1,245.90
Enter a quantity for the sizes you want to add.
🧪
Why this grade

BioReagent, Moligand™, for cell culture, ≥97%, powder BioReagent,Moligand™,細胞培養用 for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Protected from light Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

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

📚

Literature proof

Cited in 241 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

概要

Dexamethasone is used to study apoptosis, cell signaling pathways, cell differentiation and gene expression.

Specifications

同義語
Prednisolone F | 9α-Fluoro-16α-methyl-11β,17α,21-trihydroxy-1,4-pregnadiene-3,20-dione | (11β,16α)-9-Fluoro-11,17,21-trihydroxy-16-methylpregna-1,4-diene-3,20-dione | 9α-Fluoro-16α-methylprednisolone | NSC 34521 | MK 125
仕様と純度
BioReagent, Moligand™, for cell culture, ≥97%, powder
生化学的・生理学的メカニズム
Dexamethasone (Hexadecadrol) is a glucocorticoid receptor agonist, apoptosis inducer, and common disease inducer in experimental animals, constructing models of muscle atrophy, hypertension, and depression. Dexamethasone can inhibit the production of infl
保管条件
Store at 2-8°C,Protected from light
入荷
Wet ice
この製品は冷冷この冷このこの製品の運送が必要です。地上およびその他の経済サービスは利用できません。
等級
BioReagent, Moligand™, 細胞培養用
純度
≥97%
製品の性質
ALogP
1.9
名前と識別子
パブケム・シド
カノニカル・スマイル
CC1CC2C3CCC4=CC(=O)C=CC4(C3(C(CC2(C1(C(=O)CO)O)C)O)F)C
IUPAC Name
(8S,9R,10S,11S,13S,14S,16R,17R)-9-fluoro-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-3-one
InChIKey
UREBDLICKHMUKA-CXSFZGCWSA-N
INCHI
1S/C22H29FO5/c1-12-8-16-15-5-4-13-9-14(25)6-7-19(13,2)21(15,23)17(26)10-20(16,3)22(12,28)18(27)11-24/h6-7,9,12,15-17,24,26,28H,4-5,8,10-11H2,1-3H3/t12-,15+,16+,17+,19+,20+,21+,22+/m1/s1
異性体SMILES
C[C@@H]1C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@@]4([C@]3([C@H](C[C@@]2([C@]1(C(=O)CO)O)C)O)F)C
WGKドイツ
2
RTECS
TU3980000
代替CAS番号
23495-06-9,50-02-2
NSC番号
34521
MeSH用語
Decaject;Decaject L.A.;Decaject-L.A.;Decameth;Decaspray;Dexamethasone;Dexasone;Dexpak;Hexadecadrol;Hexadrol;Maxidex;Methylfluorprednisolone;Millicorten;Oradexon
分子量
392.46
Beilstein
2066651
Reaxy-Rn
2341697
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2341697&ln=

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
分類Steroids and steroid derivatives
SubclassHydroxysteroids
Intermediate Tree Nodes Not available
Direct Parent21-hydroxysteroids
Alternative Parents Gluco/mineralocorticoids, progestogins and derivatives  20-oxosteroids  11-beta-hydroxysteroids  17-hydroxysteroids  3-oxo delta-1,4-steroids  Halogenated steroids  Delta-1,4-steroids  Tertiary alcohols  Alpha-hydroxy ketones  Secondary alcohols  Fluorohydrins  Cyclic ketones  Cyclic alcohols and derivatives  Alkyl fluorides  Hydrocarbon derivatives  Organic oxides  Organofluorides  Primary alcohols  
Molecular FrameworkAliphatic homopolycyclic compounds
Substituents Progestogin-skeleton - 21-hydroxysteroid - Pregnane-skeleton - 20-oxosteroid - 3-oxo-delta-1,4-steroid - 3-oxosteroid - 17-hydroxysteroid - 11-hydroxysteroid - 11-beta-hydroxysteroid - 9-halo-steroid - Halo-steroid - Oxosteroid - Delta-1,4-steroid - Alpha-hydroxy ketone - Cyclic alcohol - Tertiary alcohol - Ketone - Fluorohydrin - Halohydrin - Secondary alcohol - Cyclic ketone - Organooxygen compound - Alcohol - Primary alcohol - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Alkyl halide - Alkyl fluoride - Organohalogen compound - Organofluoride - Aliphatic homopolycyclic compound
説明This compound belongs to the class of organic compounds known as 21-hydroxysteroids. These are steroids carrying a hydroxyl group at the 21-position of the steroid backbone.
External Descriptors Pregnane and derivatives [Fig]
3 D構造
インタラクティブ化学構造モデル





証明書(CoA、COO、BSE/TSEと分析図)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

9 results found

Lot NumberCertificate Type日付商品
A2514338Certificate of AnalysisDec 27, 2024 D754934
A2514339Certificate of AnalysisDec 27, 2024 D754934
A2514340Certificate of AnalysisDec 27, 2024 D754934
A2514356Certificate of AnalysisDec 27, 2024 D754934
B2626140Certificate of AnalysisDec 27, 2024 D754934
E2529216Certificate of AnalysisDec 27, 2024 D754934
H2605073Certificate of AnalysisDec 27, 2024 D754934
H2620022Certificate of AnalysisDec 27, 2024 D754934
J2511044Certificate of AnalysisDec 27, 2024 D754934
化学的性質と物理的性質
溶解度methanol: 25 mg/mL
感度Light sensitive
融点(°C)262-264°C
分子量392.500 g/mol
XLogP31.900
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count6
Rotatable Bond Count2
Exact Mass392.2 Da
Monoisotopic Mass392.2 Da
Topological Polar Surface Area94.800 Ų
Heavy Atom Count28
Formal Charge0
Complexity805.000
Isotope Atom Count0
Defined Atom Stereocenter Count8
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
よくある質問と記事
3T3-L1 Adipocyte Differentiation Protocol
For Cell Culture
Glucocorticoids (GCs) and the Glucocorticoid Receptor (GR): Mechanisms, Classification Frameworks, and the Latest Advances (with a Product Selection Table)
Glucocorticoids: Scientific Overview and Key Application Considerations
How to Map the NF-κB Pathway and Choose Inhibitors: Bringing Inflammatory Transcriptional Output into a “Controllable Range” (Tables A–F)
Mechanisms and Experimental Applications of β-GP, Ascorbic Acid, and Dexamethasone in Osteogenic Induction Systems
Neuropathological Mechanisms of Cerebral Infarction
Establishment and Evaluation Methods of Diabetic Animal Models
Inflammatory Signaling Pathway Research Guide: Danger Signal Recognition, Core Signaling Modules, Detection Readouts, and Representative Research Reagents
Applications of Endocrinology/Hormones in Metabolic Regulation, Reproductive Function, and Disease Research
Culture Systems, Molecular Markers, and Research Applications of Major Human Organ Organoids
Standard Operating Procedure for Osteogenic Differentiation of Mesenchymal Stem Cells and Evaluation by ALP and Alizarin Red S Staining
Standard Operating Procedure for Chondrogenic Differentiation of Mesenchymal Stem Cells and Evaluation by Alcian Blue Staining
Standard Operating Procedure for Adipogenic Differentiation of Mesenchymal Stem Cells and Evaluation by Oil Red O Staining
Gentiana Root Extract and Gentiopicroside: Chemical Composition, Antioxidant and Inflammation-Modulating Mechanisms, and Their Potential Effects on Skin Barrier Homeostasis
Antidiabetic Mechanisms, Representative Bioactive Compounds, and Research Applications of Natural Products
Bone Metabolic Disease Animal Models: Modeling Methods and Experimental Evaluation
Skin-Soothing Mechanisms of Avenanthramides: From Natural Oat Defense Molecules to Inflammatory Signaling and Mast Cell Regulation
Citations of This Product
ソリューション計算機
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