Description

Prednisolamate is a synthetic corticosteroid derivative with significant anti-inflammatory and immunosuppressive properties. This compound is valued for its potent biological activity and serves as a key intermediate in the synthesis of advanced pharmaceutical agents. It is primarily utilized by research institutions and pharmaceutical manufacturers developing treatments for inflammatory conditions, autoimmune disorders, and dermatological applications.

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of potent topical and systemic corticosteroid medications.
• Anti-inflammatory Research: Used in preclinical and clinical research to study mechanisms of inflammation and immune response modulation.
• Dermatology Formulations: Incorporated into creams, ointments, and lotions for treating skin conditions like eczema, psoriasis, and contact dermatitis.
• Veterinary Medicine: Employed in formulations for managing inflammatory and allergic conditions in animals.
• Reference Standard: Serves as a high-purity analytical standard for quality control and regulatory testing in pharmaceutical laboratories.
• Biochemical Studies: Utilized to investigate steroid receptor interactions and metabolic pathways.

Basic Information

Product Name	Prednisolamate
CAS No.	5626-34-6
Molecular Formula	C27H41NO7
Molecular Weight	491.62 g/mol
Synonyms	Prednisolone 21-Diethylaminoacetate; Diethylaminoacetate Prednisolone Ester; NSC-106977; Prednisolone Diethylaminoacetate; 11β,17α,21-Trihydroxypregna-1,4-diene-3,20-dione 21-(diethylamino)acetate; (11β)-11,17,21-Trihydroxypregna-1,4-diene-3,20-dione 21-(2-(diethylamino)acetate); Prednisolone 21-N,N-Diethylglycolate Ester
EINECS	Contact for details

Quality Control

Our Prednisolamate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling via HPLC and other pharmacopeial methods, to ensure it meets stringent specifications for pharmaceutical use. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption, which can affect stability and potency.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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