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(1,2,3,4-Tetrahydroisoquinolin-7-Yl)Methanol Hydrochloride CAS NO 2152636-99-0


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CAS No.:2152636-99-0

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

(1,2,3,4-Tetrahydroisoquinolin-7-Yl)Methanol Hydrochloride is a high-purity pharmaceutical intermediate and building block of significant importance in modern organic synthesis. Its value lies in its role as a key precursor for the development of novel bioactive compounds, particularly in central nervous system (CNS) and oncology research. This compound is essential for research institutions, pharmaceutical R&D departments, and fine chemical manufacturers engaged in the synthesis of complex heterocyclic molecules for drug discovery and process development.

Application

  • Pharmaceutical Intermediate: A critical building block for the synthesis of potential drug candidates targeting neurological disorders.
  • Medicinal Chemistry Research: Used in structure-activity relationship (SAR) studies and the development of novel tetrahydroisoquinoline-based therapeutics.
  • Organic Synthesis: Serves as a versatile chiral precursor for constructing complex alkaloid-like frameworks and other nitrogen-containing heterocycles.
  • Chemical Reference Standard: Employed as a high-purity standard for analytical method development and quality control in API manufacturing.
  • Biochemical Tool Compound: Utilized in biochemical assays to study enzyme inhibition and receptor-ligand interactions.

Basic Information

Product Name (1,2,3,4-Tetrahydroisoquinolin-7-Yl)Methanol Hydrochloride
CAS No. 2152636-99-0
Molecular Formula C10H14ClNO
Molecular Weight 199.68 g/mol
Synonyms 7-(Hydroxymethyl)-1,2,3,4-tetrahydroisoquinoline hydrochloride; 1,2,3,4-Tetrahydro-7-isoquinolinemethanol hydrochloride; 7-(Hydroxymethyl)-THIQ HCl; THIQ-7-CH2OH HCl; (7-THIQ-yl)methanol hydrochloride; 1,2,3,4-Tetrahydroisoquinoline-7-methanol hydrochloride
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Quality Control

Our (1,2,3,4-Tetrahydroisoquinolin-7-Yl)Methanol Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, NMR and IR for structural confirmation, and tests for residual solvents and heavy metals to ensure it meets the stringent requirements for pharmaceutical R&D. Certificates of Analysis (COA) with full traceability are provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed after opening to prevent moisture absorption. Keep away from incompatible materials.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to structure
Identification (NMR) Conforms to structure
Purity (HPLC) ≥ 98.0%
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.

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