$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.
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.
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:
Pharmaceutical Research
Chemical Studies
Biological Research
Synthetic Chemistry
Natural Product Research
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.
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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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