Description

Hidrosmin CAS NO 120250-44-4 is a high-purity pharmaceutical intermediate and active ingredient known for its venotonic and vasoprotective properties. This compound is critical for the development and manufacturing of advanced therapeutic formulations targeting chronic venous insufficiency and related vascular disorders. It is primarily utilized by pharmaceutical manufacturers, R&D laboratories, and fine chemical suppliers serving the global healthcare sector.

Application

• Pharmaceutical Active Ingredient: Primary use in the formulation of prescription medications for treating symptoms of chronic venous insufficiency, such as heaviness, pain, and swelling in the legs.
• Vasoprotective Drug Development: Key intermediate in the R&D and production of drugs aimed at improving capillary resistance and reducing vascular permeability.
• Nutraceutical & Dietary Supplements: Incorporated into advanced supplement formulations designed to support vascular health and microcirculation.
• Reference Standard: Serves as a high-purity analytical standard in quality control laboratories for method development, validation, and pharmacopeial testing.
• Cosmeceutical Applications: Used in the development of topical creams and gels aimed at reducing the appearance of dark circles and puffiness related to microvascular issues.
• Clinical Research Material: Supplied as a raw material for preclinical and clinical studies investigating new therapeutic applications for vascular and lymphatic diseases.

Basic Information

Product Name	Hidrosmin
CAS No.	120250-44-4
Molecular Formula	C18H16O8
Molecular Weight	360.32 g/mol
Synonyms	3',5-Di-O-(β-hydroxyethyl) diosmin; Hidrosmina; Hidrosmine; 7-[[6-O-(2-Hydroxyethyl)-β-D-glucopyranosyl]oxy]-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one; Diosmetin 7-O-(6''-O-(2-hydroxyethyl))-β-D-glucopyranoside; Venosmine
EINECS	Contact for details

Quality Control

Our Hidrosmin is manufactured under strict quality management systems to ensure batch-to-batch consistency and compliance with pharmaceutical-grade standards. Each lot is subjected to comprehensive analytical testing, including identity confirmation, purity assay, and impurity profiling. Certificates of Analysis (COA) detailing all test results are provided and can be tailored to meet specific customer or regulatory requirements (e.g., ICH guidelines).

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 2.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%

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