Synonym: 11β,17α,21-Trihydroxypregn-4-ene-3,20-dione; 17-Hydroxycorticosterone; 4-Pregnene-11β,17α,21-triol-3,20-dione; Cortisol; Kendall’s compound F; Reichstein’s substance M
CAS Number: 50-23-7
Empirical Formula (Hill Notation): C21H30O5
Molecular Weight: 362.46
EC Number: 200-020-1
MDL Number: MFCD00011654
Linear Formula: C21H30O5
Product Type: Chemical
FT-IR Spectra for 11β,17α,21-Trihydroxypregn-4-ene-3,20-dione.
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: H4001-25G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: H4001-100G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: H4001-1G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: H4001-10G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: H4001-5G
| application(s) |
cell analysis |
| assay |
≥98% (HPLC) |
| biological source |
synthetic (organic) |
| form |
powder |
| InChI |
1S/C21H30O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h9,14-16,18,22,24,26H,3-8,10-11H2,1-2H3/t14-,15-,16-,18+,19-,20-,21-/m0/s1 |
| InChI key |
JYGXADMDTFJGBT-VWUMJDOOSA-N |
| mp |
211-214 °C (lit.) |
| Quality Level |
300  |
| shipped in |
ambient |
| SMILES string |
[H][C@@]12CCC3=CC(=O)CC[C@]3(C)[C@@]1([H])[C@@H](O)C[C@@]4(C)[C@@]2([H])CC[C@]4(O)C(=O)CO |
| solubility |
water: 0.28 g/L at 25 °C |
| sterility |
non-sterile |
| storage temp. |
room temp |
| Biochem/physiol Actions: |
Primary glucocorticoid secreted by the adrenal cortex. |
| Biochem/physiol Actions: |
Primary glucocorticoid secreted by the adrenal cortex. It has three times the anti-inflammatory potency of corticosterone but much lower Na2+ retention potency. |
| Features and Benefits: |
This compound is featured on the Nuclear Receptors (Steroids) page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here . |
| Packaging: |
1, 5, 10, 25, 100 g in poly bottle |
| Purity |
≥98% (HPLC) |
| mp |
211-214 °C (lit.) |
| Storage Temp. |
room temp |
| UNSPSC |
51111800 |