Description
IUPAC Name: 4-[(E)-3-hydroxyprop-1-enyl]-2-methoxyphenol
InChI: InChI=1S/C10H12O3/c1-13-10-7-8(3-2-6-11)4-5-9(10)12/h2-5,7,11-12H,6H2,1H3/b3-2+
InChIKey: JMFRWRFFLBVWSI-NSCUHMNNSA-N
Canonical SMILES: COC1=C(C=CC(=C1)C=CCO)O
Isomeric SMILES: COC1=C(C=CC(=C1)/C=C/CO)O
Synonyms: CONIFERYL ALCOHOL; 458-35-5; Coniferol; 4-(3-hydroxyprop-1-en-1-yl)-2-methoxyphenol; 32811-40-8; (E)-Coniferyl alcohol; trans-Coniferyl alcohol; gamma-Hydroxyisoeugenol; …
Botanical Source:
Product Overview
High-purity Coniferyl Alcohol, a natural monolignol precursor essential for lignin biosynthesis, is manufactured to exceptional standards for biochemical and pharmaceutical research.
Technical Specifications
- Molecular Formula: C₁₀H₁₂O₃
- Molecular Weight: 180.20 g/mol
- Purity: ≥98% (HPLC)
- Appearance: White to off-white crystalline powder
- Solubility: Soluble in organic solvents
Key Features & Benefits
- Natural phenylpropanoid compound
- Lignin biosynthesis precursor
- Key intermediate in plant metabolism
- Comprehensive Certificate of Analysis
- Full structural verification
Research Applications
-
Biochemical Studies
- Lignin biosynthesis research
- Peroxidase enzyme studies
- Radical pairing investigations
- Phenylpropanoid pathway research
-
Materials Science
- Biobased material development
- Nanocellulose surface modification
- Fenton reaction studies
- Polymer synthesis
-
Enzymatic Research
- Peroxidase activity studies
- FRET monitoring
- Enzyme kinetics
- Active site investigations
Storage & Handling
- Store at the recommended temperature
- Protect from light and moisture
- Avoid repeated freeze-thaw cycles
- Complete degradation within 72h under specific conditions 7
Quality Assurance
- Rigorous quality control
- Complete analytical documentation
- Traceable lot numbers
- Stability monitoring program
Research Support
BIORLAB provides:
- Technical consultation
- Analytical method support
- Stability data
- Application Guidance
Key Research Areas
-
Plant Biochemistry
- Lignin formation studies
- Biochemical pathway analysis
- Intermediate compound research
-
Materials Development
- Biobased materials
- Surface modification
- Polymer synthesis
-
Enzyme Studies
- Peroxidase mechanisms
- Radical formation
- Quinonemethide intermediates
Reaction Characteristics
- Forms phenoxy radicals via peroxidase oxidation
- Undergoes radical pairing reactions
- Produces quinonemethide intermediates
- Susceptible to nucleophilic attack
This premium-grade Coniferyl Alcohol is specifically designed for research institutions advancing plant biochemistry, materials science, and enzyme studies.
For research and development purposes only. Not for human consumption or clinical use.
[Contact BIORLAB’s technical support team for detailed specifications and custom requirements]