4-Hydroxybenzyl alcohol

SKU 623-05-2 Category

$35.00

CAS No.: 623-05-2
Molecular Formula C₇H₈O₂
Molecular Weight 124.14g/mol
Purity HPLC>98%
Chemical Family Phenols

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* Warning: BIORLAB’s Natural Compounds are for laboratory research purposes only.

Description


High-purity 4-Hydroxybenzyl alcohol, a naturally occurring aromatic alcohol found in Bacopa monnieri and other organisms, demonstrating significant potential in pharmaceutical and synthetic applications 1.

Technical Specifications

  • Molecular Formula:  C₇H₈O₂
  • Molecular Weight: 124.14 g/mol
  • Purity: ≥98% (HPLC)
  • Appearance: White to off-white crystalline powder
  • Solubility: Slightly soluble in water; soluble in organic solvents

 

IUPAC Name: 4-(hydroxymethyl)phenol

InChI: InChI=1S/C7H8O2/c8-5-6-1-3-7(9)4-2-6/h1-4,8-9H,5H2

InChIKey: BVJSUAQZOZWCKN-UHFFFAOYSA-N

Canonical SMILES: C1=CC(=CC=C1CO)O

Isomeric SMILES: C1=CC(=CC=C1CO)O

Synonyms: 4-hydroxybenzyl alcohol; 623-05-2; 4-(Hydroxymethyl)phenol; p-Hydroxybenzyl alcohol; p-Methylolphenol; 4-Hydroxybenzenemethanol; 4-Methylolphenol; Benzenemethanol, 4-hydroxy-; …

Botanical Source:


 

Key Features & Benefits

  • Natural metabolite compound
  • Synthetic intermediate
  • High chemical purity
  • Comprehensive Certificate of Analysis
  • Full spectroscopic characterization

Physical Properties

  • Melting Point: 114-122°C
  • Boiling Point: 251-253°C
  • Density: 1.1006 (estimated)
  • Refractive Index: 1.5035 (estimated)
  • Form: Crystalline Powder

Research Applications

  1. Pharmaceutical Research

    • Synthetic intermediate
    • Drug development
    • Process optimization
    • Structure-activity studies
  2. Chemical Studies

    • Organic synthesis
    • Method development
    • Reaction mechanisms
    • Process optimization
  3. Biological Research

    • Metabolic studies
    • Pathway analysis
    • Biotransformation research
    • Natural product chemistry

Storage & Handling

  • Store below +30°C
  • Light Sensitive/Air Sensitive
  • Protect from moisture
  • Stock solution guidelines provided
  • Use immediately after opening

Chemical Properties

  • Water Solubility: 6.7g/l at 20°C
  • pKa: 9.82 (25°C)
  • LogP: 0.21
  • Odor: Fruity bitter almond sweet coconut
  • Color: Pink to beige

Quality Assurance

  • GMP-compliant manufacturing
  • Rigorous quality control
  • Complete analytical documentation
  • Traceable lot numbers
  • Stability monitoring program

Key Research Areas

  1. Synthetic Chemistry

    • Intermediate synthesis
    • Process development
    • Method optimization
    • Scale-up studies
  2. Natural Product Research

    • Metabolite studies
    • Pathway analysis
    • Biotransformation
    • Structure elucidation

This premium-grade 4-Hydroxybenzyl alcohol is specifically designed for research institutions and pharmaceutical companies advancing synthetic and analytical research.

For research and development purposes only. Not for human consumption or clinical use.

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Delivery times vary based on order size, We deliver small quantities of compounds within 2 working days, ranging from one week for up to 500 compounds to about 6 weeks for orders exceeding 5,000 compounds.

While our focus is on natural compounds, we can provide information on natural product-like synthetic compounds if requested.

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Yes, we can re-supply active compounds in larger quantities and offer analogs for further testing if hits are discovered.

We offer a wide range of natural compounds including alkaloids, terpenoids, flavonoids, coumarins, peptides, glycosides, and nucleosides isolated from plants.

Our compounds undergo rigorous purification processes and are tested using advanced analytical methods such as NMR, mass spectroscopy, and in some cases, X-ray analysis to ensure >98% purity.

Yes, we offer custom isolation services for specific natural compounds based on client requirements.

We typically offer quantities ranging from 2 mg to 100 mg for screening purposes, with larger amounts available upon request.

We use various physicochemical analytical methods, including NMR (300-500 MHz) and mass spectroscopy, to confirm structures and stereochemistry.

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