Corticosterone
SIGMA/C2505 - ≥92%
Synonym: 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
CAS Number: 50-22-6
Empirical Formula (Hill Notation): C21H30O4
Molecular Weight: 346.46
EC Number: 200-019-6
MDL Number: MFCD00037715
Linear Formula: C21H30O4
Product Type: Chemical
| assay | ≥92% |
| biological source | synthetic (organic) |
| form | powder |
| InChI | 1S/C21H30O4/c1-20-8-7-13( |
| InChI key | OMFXVFTZEKFJBZ-HJTSIMOOSA |
| mp | 179-183 °C (lit.) |
| Quality Level | 200 ![]() |
| shipped in | ambient |
| SMILES string | C[C@]12C[C@H](O)[C@H]3[C@ |
| solubility | chloroform: 50 mg/mL, clear, colorless to faintly yellow |
| storage temp. | room temp |
| Application: | Corticosterone has been used: • in chronic treatment to investigate its effect on somatostatin (SST) neurons in mice • as a stress inducing hormone in pregnant mice • to test its effect on depression-related behaviors in mice |
| Biochem/physiol Actions: | Corticosterone is a glucocorticoid secreted by the adrenal cortex that activates both mineralocorticoid and glucocorticoid receptors. |
| Biochem/physiol Actions: | Corticosterone is synthesized from 11-deoxycortisone by the action of enzyme 11β-hydroxylase majorly in adrenal glands. However, it may also be synthesized in non-adrenal tissues including leydig cells of testes and in murine thymus. Corticosterone is released post activation of hypothalamus-pituitary-ad |
| Packaging: | 500 mg in glass bottle |
| Hazard Codes | Xi |
| Risk Statements | 43 |
| Safety Statements | 36 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 3 |
| Purity | ≥92% |
| mp | 179-183 °C (lit.) |
| Storage Temp. | room temp |
| UNSPSC | 51111800 |

