Description

Indoramin Hydrochloride is a selective α-1 adrenergic receptor antagonist. This compound is a critical active pharmaceutical ingredient (API) and a key intermediate in pharmaceutical research and development. It is primarily utilized by pharmaceutical manufacturers and research institutions focused on cardiovascular therapeutics and pharmacological studies.

Application

• Active Pharmaceutical Ingredient (API): Primary use in the formulation of antihypertensive medications.
• Pharmacological Research: Used as a reference standard in studies investigating α-adrenergic receptor mechanisms.
• Chemical Intermediate: Serves as a key building block in the synthesis of more complex pharmaceutical compounds.
• Reference Standard: Essential for quality control laboratories for method development and validation in drug analysis.
• Academic & Institutional Research: Employed in university and institutional labs for cardiovascular and autonomic nervous system research.

Basic Information

Product Name	Indoramin Hydrochloride
CAS No.	33124-53-7
Molecular Formula	C22H25N3O•HCl
Molecular Weight	383.92 g/mol
Synonyms	Indoramin HCl; 1-(4-Amidinophenethyl)-4-(2,3-dihydro-1H-indol-1-yl)piperidine Hydrochloride; 1-[2-(4-Amidinophenyl)ethyl]-4-(indolin-1-yl)piperidine Hydrochloride; Wy-21901; Baratol; Vidora; Indoram; Indoraminium Chloride
EINECS	Contact for details

Quality Control

Our Indoramin Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. A Certificate of Analysis (COA) detailing specifications such as assay, related substances, and residual solvents is provided with every shipment to support your quality assurance protocols.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Due to its hygroscopic nature, protect from moisture and store under inert conditions for long-term stability.

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)	98.0% - 102.0% (on anhydrous basis)
Related Substances (HPLC)	Total impurities ≤ 2.0%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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