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Synonyms: Hydrocortisone 21-phosphate sodium, Cortisol 21-phosphate sodium

| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 2 mg | $30 | - | In Stock | |
| 5 mg | $44 | - | In Stock | |
| 10 mg | $63 | - | In Stock | |
| 25 mg | $98 | - | In Stock | |
| 50 mg | $156 | - | In Stock | |
| 100 mg | $233 | - | In Stock |
| Description | Hydrocortisone phosphate sodium belongs to the category of soft glucocorticoids. It exhibits relatively weak anti-inflammatory effects and has a short retention time in vivo, making it suitable for research on various ocular diseases and gastric ulcers. |
| In vivo | Method: Chronic gastric ulcers were induced in male Wistar rats by applying 100% acetic acid to the gastric serosa. Postoperatively, the rats received daily intraperitoneal injections of Hydrocortisone sodium phosphate (2.5 mg/kg) for 2 consecutive weeks. The animals were sacrificed on day 14, and the ulcer area was measured. Result: Chronic administration of Hydrocortisone sodium phosphate significantly delayed the healing of acetic acid‑induced gastric ulcers, as evidenced by a marked increase in ulcer area compared with the control group that did not receive the drug [1]. Method: Rats with acetic acid‑induced chronic gastric ulcers were given daily intraperitoneal injections of Hydrocortisone sodium phosphate (2.5 mg/kg). On day 7, gastric tissues were collected and subjected to hematoxylin‑eosin (HE) and Azan‑Mallory staining for histological evaluation. Result: In the Hydrocortisone sodium phosphate‑treated group, persistent necrotic debris was still observed at the ulcer site on day 7, along with poor granulation tissue formation, reduced regeneration at the mucosal margins, and a thinner ulcer base compared with controls [1]. |
| Synonyms | Hydrocortisone 21-phosphate sodium, Cortisol 21-phosphate sodium |
| Molecular Weight | 486.40 |
| Formula | C21H29Na2O8P |
| Cas No. | 6000-74-4 |
| Smiles | C[C@@]12[C@](CC[C@]2(O)C(COP([O-])([O-])=O)=O)([H])[C@@]3([H])[C@]([C@@]4(C(CC3)=CC(CC4)=O)C)([H])[C@H](C1)O.[Na+].[Na+] |
| Storage | Keep away from moisture, Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | H2O: 56 mg/mL (115.13 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
H2O
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density. | ||||||||||||||||||||||||||||||||||||
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 µL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 µL Tween 80 and mix well until fully clarified.
3) Add 450 µL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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