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Viaminate CAS NO 53839-71-7


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CAS No.:53839-71-7

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Viaminate is a synthetic retinoid compound with the CAS registry number 53839-71-7, recognized for its potent biological activity in modulating cell growth and differentiation. This high-purity active pharmaceutical ingredient (API) is crucial for developing advanced dermatological and oncological treatments. It is primarily utilized by pharmaceutical manufacturers and R&D institutions focused on creating innovative therapeutic solutions for skin disorders and certain cancers.

Application

  • Pharmaceutical API: Core active ingredient in prescription medications for severe acne, psoriasis, and other keratinization disorders.
  • Dermatological R&D: Key compound in research for next-generation topical and systemic treatments targeting retinoid receptors.
  • Oncology Research: Investigated for its potential role in chemoprevention and differentiation therapy in certain cancer models.
  • Cosmeceutical Actives: Used in the development of high-potency, prescription-strength anti-aging and skin-renewal formulations.
  • Chemical Intermediate: Serves as a sophisticated building block for synthesizing novel retinoid analogs and derivatives.
  • Reference Standard: Provides a certified standard for quality control and analytical testing in pharmaceutical laboratories.

Basic Information

Product Name Viaminate
CAS No. 53839-71-7
Molecular Formula C₂₄H₃₁NO₄
Molecular Weight 397.51 g/mol
Synonyms Retinamidoester; N-(4-Ethoxyphenyl)retinamide; Ethyl p-[(E)-2-(5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)propenyl]benzoate; Viaminati; Tretinoin amide ethoxy derivative; Ro 11-4768; Arotinoid Ethyl Ester; 4-[(E)-2-(5,5,8,8-Tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)prop-1-en-1-yl]phenyl ethylcarbamate
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Quality Control

Our Viaminate CAS NO 53839-71-7 is manufactured under strict quality management systems. Each batch is subjected to comprehensive analytical testing, including HPLC for purity, residual solvent analysis, and identification by IR and NMR, to ensure it meets stringent pharmaceutical-grade specifications. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming compliance with relevant standards.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept under dry, inert conditions to maintain stability and potency.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time matches reference standard
Assay (HPLC) ≥ 98.5%
Related Substances (HPLC) Total impurities ≤ 1.0% Any single impurity ≤ 0.5%
Residual Solvents (GC) Meets ICH Q3C guidelines
Loss on Drying ≤ 0.5%
Heavy Metals ≤ 20 ppm

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

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