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[2-[(4-Methylpiperazin-1-Yl)Methyl]Phenyl]Methanol CAS NO 91904-36-8


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CAS No.:91904-36-8

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

[2-[(4-Methylpiperazin-1-Yl)Methyl]Phenyl]Methanol CAS NO 91904-36-8 is a versatile and important pharmaceutical intermediate characterized by its piperazine and benzyl alcohol functional groups. This compound is critical for the synthesis of active pharmaceutical ingredients (APIs) and other fine chemicals, where its structure serves as a key building block. It is primarily utilized by research institutions and manufacturers in the pharmaceutical, agrochemical, and specialty chemical industries for developing new therapeutic agents and advanced materials.

Application

  • Pharmaceutical Intermediate: A key precursor in the synthesis of complex drug molecules, particularly those targeting neurological and psychiatric conditions.
  • API Synthesis: Used as a building block for constructing active pharmaceutical ingredients (APIs) with specific receptor-binding properties.
  • Agrochemical Research: Serves as an intermediate in the development of novel pesticides and herbicides.
  • Chemical Research & Development: Employed in organic synthesis for creating novel compounds with potential biological activity.
  • Ligand and Catalyst Preparation: Utilized in the preparation of specialized ligands for metal catalysis and asymmetric synthesis.
  • Fine Chemical Production: Integral to the manufacture of high-value, low-volume specialty chemicals.

Basic Information

Item Detail
Product Name [2-[(4-Methylpiperazin-1-Yl)Methyl]Phenyl]Methanol
CAS No. 91904-36-8
Molecular Formula C13H20N2O
Molecular Weight 220.31 g/mol
Synonyms 1-(2-(Hydroxymethyl)benzyl)-4-methylpiperazine; 2-[(4-Methyl-1-piperazinyl)methyl]benzyl alcohol; (2-((4-Methylpiperazin-1-yl)methyl)phenyl)methanol; 91904-36-8; 4-Methyl-1-[(2-(hydroxymethyl)phenyl)methyl]piperazine
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Quality Control

Our [2-[(4-Methylpiperazin-1-Yl)Methyl]Phenyl]Methanol is produced under strict quality management systems to ensure batch-to-batch consistency and high purity suitable for pharmaceutical applications. We provide comprehensive Certificates of Analysis (COA) for each batch, detailing purity, identity, and impurity profiles. Our quality commitment aligns with cGMP standards where applicable, ensuring reliability for critical synthesis workflows.

Storage

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

Specification

Item Specification
Appearance White to off-white powder or crystalline solid
Identification (IR) Conforms to structure
Assay (HPLC) ≥ 98.0%
Water Content (KF) ≤ 1.0%
Residue on Ignition ≤ 0.1%
Related Substances (HPLC) Total impurities ≤ 2.0%

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

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