Description

Oxitriptyline is a high-purity pharmaceutical intermediate and fine chemical compound. It serves as a critical building block in the synthesis of active pharmaceutical ingredients (APIs) and advanced organic molecules. This product is essential for manufacturers and research institutions in the pharmaceutical, biotechnology, and life sciences sectors requiring reliable, high-quality raw materials for their development and production processes.

Application

• Pharmaceutical Intermediate: Key precursor in the synthesis of various therapeutic agents and active pharmaceutical ingredients (APIs).
• Biochemical Research: Used as a standard or reagent in life science research, including metabolic studies and biochemical pathway analysis.
• Organic Synthesis: Serves as a versatile building block for constructing complex organic molecules in medicinal chemistry and process development.
• Reference Standard: Employed as a high-purity analytical standard for quality control and method validation in pharmaceutical laboratories.

Basic Information

Product Name	Oxitriptyline
CAS No.	29541-85-3
Molecular Formula	C10H12N2O3
Molecular Weight	208.21 g/mol
Synonyms	5-Hydroxytryptophan; L-5-HTP; 5-HTP; Oxitriptan; 5-Hydroxy-L-tryptophan; (S)-2-Amino-3-(5-hydroxy-1H-indol-3-yl)propanoic acid; Levothym; Tript-OH
EINECS	249-761-3

Quality Control

Our Oxitriptyline is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets stringent specifications for identity, purity, and potency. Certificates of Analysis (COA) documenting results for assay, related substances, residual solvents, and other critical parameters are available upon request. We adhere to cGMP principles where applicable to support our clients' regulatory requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (15-25°C). Keep the container tightly sealed to protect from moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference standard
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.5% Any single impurity ≤ 0.5%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Specific Rotation	-30° to -34° (c=1 in 1N HCl)

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