Description

Deanxit is a pharmaceutical-grade active ingredient, specifically a combination of the compounds melitracen and flupentixol. This product is a critical component in the formulation of antidepressant and anxiolytic medications, offering a balanced pharmacological profile. It is primarily utilized by pharmaceutical manufacturers and research institutions in the development and production of neuropsychiatric treatments. Our supply ensures high purity and batch-to-batch consistency for reliable formulation outcomes.

Application

• Primary use in the formulation of antidepressant pharmaceutical preparations.
• Key active ingredient in anxiolytic (anti-anxiety) medication manufacturing.
• Utilized in clinical research for neuropsychiatric disorder studies.
• Component in combination therapies for mood and behavioral disorders.
• Reference standard in analytical laboratories for quality control testing.
• Used in the development of novel dosage forms, such as sustained-release tablets.

Basic Information

Product Name	Deanxit
CAS No.	76391-77-0
Molecular Formula	C₁₈H₂₃N₅S₂ (Flupentixol) + C₂₁H₂₅N (Melitracen) *
Molecular Weight	Flupentixol: 373.54 g/mol; Melitracen: 291.43 g/mol *
Synonyms	Flupentixol/Melitracen Combination; Deanxit; Flupentixol and Melitracen; Flupentixol Dihydrochloride with Melitracen Hydrochloride; Flupentixol-Melitracen; Neuroleptic-Antidepressant Combination; 2-Trifluoromethyl-9-[3-[4-(2-hydroxyethyl)piperazin-1-yl]propylidene]thiaxanthene with 10-(10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N,N-dimethyl-10H-anthracen-10-amine
EINECS	Contact for details

*Note: Deanxit is a combination product. The formula and weight are provided for the individual active components.

Quality Control

Our Deanxit is manufactured under strict quality management systems. Each batch is tested to ensure it meets stringent pharmaceutical standards, including identity, purity, and content uniformity of both active components. A comprehensive Certificate of Analysis (COA) is provided with every shipment, detailing results from tests such as HPLC assay, related substances, residual solvents, and microbiological limits, ensuring compliance with cGMP guidelines.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). The product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to prevent degradation. Keep the container tightly sealed when not in use.

Specification

Item	Specification
Appearance	White or almost white powder
Identification (HPLC/IR)	Conforms to reference standard
Assay (HPLC)	98.0% - 102.0% (of labeled amount for each component)
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 2.0%
Water Content (KF)	≤ 5.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Heavy Metals	≤ 20 ppm
Microbial Limits	Complies with Ph. Eur. 2.6.12/2.6.13

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