Corticosterone
≥98.5% (HPLC)
Manufacturer: Sigma Aldrich
CAS Number: 50-22-6
Synonym(S): 11β,21-Dihydroxy-4-pregnene-3,20-dione, 11β,21-Dihydroxyprogesterone, 4-Pregnene-11β,21-diol-3,20-dione, Kendall’s Compound B, Reichstein’s Substance H
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| 100 MG | 27840-100-MG | In Stock | ₹ 2,446.45 |
| 500 MG | 27840-500-MG | In Stock | ₹ 10,521.90 |
27840 - 100 MG
In Stock
Quantity
1
Base Price: ₹ 2,446.45
GST (18%): ₹ 440.361
Total Price: ₹ 2,886.811
biological source
synthetic
Quality Level
200
Assay
≥98.5% (HPLC)
form
powder or crystals
optical activity
[α]20/D +223±3°, c = 1% in ethanol
mp
179-183 °C (lit.)179-183 °C
functional group
ketone
SMILES string
C[C@]12C[C@H](O)[C@H]3[C@@H](CCC4=CC(=O)CC[C@]34C)[C@@H]1CC[C@@H]2C(=O)CO
InChI
1S/C21H30O4/c1-20-8-7-13(23)9-12(20)3-4-14-15-5-6-16(18(25)11-22)21(15,2)10-17(24)19(14)20/h9,14-17,19,22,24H,3-8,10-11H2,1-2H3/t14-,15-,16+,17-,19+,20-,21-/m0/s1
InChI key
OMFXVFTZEKFJBZ-HJTSIMOOSA-N
Other Options
| Image | Product Name | Manufacturer | Price Range | |
|---|---|---|---|---|
 | Enzo Life Sciences Corticosterone (50mg). CAS: 50-22-6 | Enzo Life Sciences | ₹ 4,620.24 | |
| | VETRANAL™ Corticosterone, ≥98% (HPLC), MilliporeSigma™ Supelco™ | MilliporeSigma Supelco | ₹ 8,470.44 | |
 | Sigma Aldrich Fine Chemicals Biosciences Corticosterone, 50-22-6, MFCD00037715, 100 mg | Sigma Aldrich Fine Chemicals Biosciences | ₹ 4,449.12 | |
 | Corticosterone | Supelco | ₹ 7,090.38 | |
 | Corticosterone | ChemScene | ₹ 7,015.92 - ₹ 29,004.84 | |
 | 50-22-6 | (11β)-11,21-Dihydroxypregn-4-ene-3,20-dione | A2B Chem | ₹ 2,481.24 - ₹ 14,202.96 |
Related Products
Description
- General description: Corticosterone (Cort) is a glucocorticoid hormone.[1] It is also the principal hormone that mediates stress responses in birds.[2] It is the primary adrenal cortical steroid in rat plasma.[3] The influence of maternal Cort exposure on the developing placenta has been studied in a mouse model.[4]
- Application: Corticosterone was used to study the adrenoceptor signaling in rats,[5][6] lizards[7] or in vitro.[8] It was also used in immune suppression experiment.[9]
- Biochem/physiol Actions: Corticosterone is synthesized from cholesterol in the adrenal cortex that activates both mineralocorticoid and glucocorticoid receptors. The role of corticosterones is vital for reproductive processes including ovulation, lutenization, development of oocytes, parturition and lactation. The metabolism of corticosterone is modulated by the enzyme 11β-hydroxysteroid dehydrogenase.[10][11]
- Packaging: Bottomless glass bottle. Contents are inside inserted fused cone.
- Preparation Note: Corticosterone is soluble in chloroform and ethanol.
SAFETY INFORMATION
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Compare Similar Items
Show Difference
biological source: synthetic
Quality Level: 200
Assay: ≥98.5% (HPLC)
form: powder or crystals
optical activity: [α]20/D +223±3°, c = 1% in ethanol
mp: 179-183 °C (lit.)179-183 °C
functional group: ketone
SMILES string: C[C@]12C[C@H](O)[C@H]3[C@@H](CCC4=CC(=O)CC[C@]34C)[C@@H]1CC[C@@H]2C(=O)CO
InChI: 1S/C21H30O4/c1-20-8-7-13(23)9-12(20)3-4-14-15-5-6-16(18(25)11-22)21(15,2)10-17(24)19(14)20/h9,14-17,19,22,24H,3-8,10-11H2,1-2H3/t14-,15-,16+,17-,19+,20-,21-/m0/s1
InChI key: OMFXVFTZEKFJBZ-HJTSIMOOSA-N
biological source: __
Quality Level: 200
Assay: __
form: liquid
optical activity: __
mp: __
functional group: __
SMILES string: [Na]OS(=O)(=O)C=C
InChI: 1S/C2H4O3S.Na/c1-2-6(3,4)5;/h2H,1H2,(H,3,4,5);/q;+1/p-1
InChI key: BWYYYTVSBPRQCN-UHFFFAOYSA-M
biological source: __
Quality Level: 100
Assay: 98%
form: liquid
optical activity: __
mp: __
functional group: __
SMILES string: CN(C)CCN(C)CCO
InChI: 1S/C7H18N2O/c1-8(2)4-5-9(3)6-7-10/h10H,4-7H2,1-3H3
InChI key: LSYBWANTZYUTGJ-UHFFFAOYSA-N
