share

Hydrocortisone Sodium Succinate CAS NO 125-04-2


Unit Price:

CAS No.:125-04-2

Grade:Pharmacy Grade

Content:99.0%

Brand:Customizable

Packaging:Customizable

Description

Hydrocortisone Sodium Succinate CAS NO 125-04-2 is the water-soluble sodium salt of hydrocortisone 21-hemisuccinate, a vital corticosteroid prodrug. This formulation is critical for enabling rapid intravenous or intramuscular administration, providing immediate anti-inflammatory and immunosuppressive effects. It is an essential active pharmaceutical ingredient (API) for manufacturers of injectable emergency medications, hospital solutions, and critical care formulations targeting severe allergic reactions, adrenal insufficiency, and inflammatory conditions.

Application

  • Injectable Pharmaceutical Formulations: Primary use in sterile injectable solutions for rapid systemic corticosteroid delivery.
  • Emergency & Critical Care Medicine: Key component in drugs for treating anaphylaxis, septic shock, and acute adrenal crisis (Addisonian crisis).
  • Hospital Compounding: Used in hospital pharmacies for preparing IV infusions and IM injections.
  • Anti-inflammatory & Immunosuppressive Therapy: Management of severe inflammatory conditions like rheumatoid arthritis flares, ulcerative colitis, and systemic lupus erythematosus.
  • Oncology Supportive Care: Used to manage inflammation and side effects associated with certain chemotherapy regimens.
  • Veterinary Pharmaceuticals: Employed in veterinary medicine for anti-inflammatory and shock therapy in animals.

Basic Information

Product Name Hydrocortisone Sodium Succinate
CAS No. 125-04-2
Molecular Formula C25H33NaO8
Molecular Weight 484.52 g/mol
Synonyms Hydrocortisone 21-Hemisuccinate Sodium Salt; Cortisol Sodium Succinate; 11β,17,21-Trihydroxypregn-4-ene-3,20-dione 21-(Sodium Succinate); Solu-Cortef (Pfizer brand name); EINECS 204-731-1; A-Hydrocort; Sodium Hydrocortisone Succinate
EINECS 204-731-1

Quality Control

Our Hydrocortisone Sodium Succinate is manufactured under strict quality systems suitable for pharmaceutical applications. We ensure compliance with relevant pharmacopoeial standards such as USP and EP monographs. Every batch is supported by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles, confirming it meets stringent specifications for use in injectable drug products.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive); the container must be kept tightly sealed in a dry environment to prevent degradation. For long-term storage, consider conditions of 2-8°C.

Specification

Item Specification
Appearance White or almost white, hygroscopic powder
Identification (IR) Conforms
Identification (HPLC) Retention time corresponds to reference standard
Assay (HPLC) 98.0% - 102.0% (on anhydrous basis)
Water (Karl Fischer) ≤ 5.0%
pH (5% Solution) 7.0 - 8.0
Related Substances (HPLC) Individual impurity ≤ 0.5%; Total impurities ≤ 2.0%
Specific Rotation +150° to +158° (c=1 in water)
Bacterial Endotoxins < 0.17 EU/mg (for injectable grade)
Sterility Conforms (for sterile grade)

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.

Complete Your RFQ

0/ 2000

Why choose US

Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.