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Desvenlafaxine (o-Desmethyl Venlafaxine) Fumarate CAS NO 93414-04-1


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CAS No.:93414-04-1

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Desvenlafaxine (o-Desmethyl Venlafaxine) Fumarate is a high-purity active pharmaceutical ingredient (API) and a major active metabolite of the antidepressant venlafaxine. This compound is critical for the development and production of next-generation serotonin-norepinephrine reuptake inhibitor (SNRI) medications. It is primarily required by pharmaceutical manufacturers and advanced research institutions focused on central nervous system (CNS) therapeutics and generic drug formulation.

Application

  • Pharmaceutical API: Core active ingredient in the manufacture of antidepressant medications.
  • Reference Standard: Used in analytical laboratories for quality control, method development, and pharmacokinetic studies.
  • Research & Development: Critical for preclinical and clinical research into mood disorders, neuropathic pain, and other CNS conditions.
  • Generic Drug Formulation: Serves as the key component for developing bioequivalent generic versions of SNRI drugs.
  • Metabolite Studies: Employed in drug metabolism and pharmacodynamics (DMPK) research to understand venlafaxine's activity profile.

Basic Information

Product Name Desvenlafaxine (o-Desmethyl Venlafaxine) Fumarate
CAS No. 93414-04-1
Molecular Formula C18H27NO2 • C4H4O4
Molecular Weight 463.50 g/mol
Synonyms O-Desmethylvenlafaxine Fumarate; Desvenlafaxine Succinate (common misnomer); Pristiq (Trade Name API); WY-45233; (1R,2R)-2-(Dimethylamino)-1-(4-hydroxy-3-methoxyphenyl)propyl cyclohexanol fumarate; 4-[2-(Dimethylamino)-1-(1-hydroxycyclohexyl)ethyl]-2-methoxyphenol fumarate; Venlafaxine Metabolite ODV Fumarate
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Quality Control

Our Desvenlafaxine Fumarate is manufactured under strict quality management systems. Each batch is tested to ensure compliance with high-purity pharmacopeial standards, including identification, assay, and control of specific impurities. A comprehensive Certificate of Analysis (COA) documenting purity, residual solvents, and heavy metals is provided with every shipment to guarantee traceability and regulatory readiness.

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) and must be kept in a dry environment to maintain stability and potency.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference standard
Identification (HPLC) Retention time matches reference
Assay (HPLC) ≥ 98.5%
Related Substances (HPLC) Total impurities ≤ 1.0%
Single Unknown Impurity ≤ 0.5%
Residual Solvents (GC) Complies with ICH Q3C
Heavy Metals ≤ 20 ppm
Loss on Drying ≤ 1.0%
Specific Rotation Contact for details

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

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