623-05-2
Chemical Structure
4-Hydroxybenzyl alcohol
- CAS No.: 623-05-2
- Formula:C7H8O2
- Molecular Weight:124.14
IUPAC Name: 4-(hydroxymethyl)phenol
InChIKey: BVJSUAQZOZWCKN-UHFFFAOYSA-N
SMILES: OCC1=CC=C(O)C=C1
Biological Activity: 4-Hydroxybenzyl alcohol is a phenolic compound widely distributed in various kinds of plants. Anti-inflammatory, anti-oxidant, anti-nociceptive activity. Neuroprotective effect. Inhibitor of tumor angiogenesis and growth[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
4-Hydroxybenzyl alcohol | 99.83% | 4-Hydroxybenzyl alcohol is a phenolic compound widely distributed in various kinds of plants. Anti-inflammatory, anti-oxidant, anti-nociceptive activity. Neuroprotective effect. Inhibitor of tumor angiogenesis and growth. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
4-Hydroxybenzyl alcohol (Standard) | 98.49% | 4-Hydroxybenzyl alcohol (Standard) is the analytical standard of 4-Hydroxybenzyl alcohol. This product is intended for research and analytical applications. 4-Hydroxybenzyl alcohol is a phenolic compound widely distributed in various kinds of plants. Anti-inflammatory, anti-oxidant, anti-nociceptive activity. Neuroprotective effect. Inhibitor of tumor angiogenesis and growth. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
KSD 2405 | 99.4% | KSD 2405 is an endogenous metabolite. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Salicyl alcohol | 99.26% | Salicyl alcohol (2-Hydroxybenzyl alcohol; Saligenin) is a phenolic alcohol-type topical anesthetic and strong sensitizer with antiseptic, antibacterial and antipyretic activities. Salicyl alcohol serves as a precursor for salicin synthesis. Salicyl alcohol induces contact dermatitis and eczematous skin reactions, and is a well-known allergen identified in phenolic resins. Salicyl alcohol is isolated from the barks of European aspen (Populus tremula), rowan (Sorbus aucuparia) and willow (Salix spp.). Salicyl alcohol is used in studies related to allergic contact dermatitis. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Tyrosol (Standard) | 99.93% | Tyrosol (Standard) is the analytical standard of Tyrosol. This product is intended for research and analytical applications. Tyrosol is a derivative of phenethyl alcohol. Tyrosol attenuates pro-inflammatory cytokines from cultured astrocytes and NF-κB activation. Anti-oxidative and anti-inflammatory effects. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
3-(4-Hydroxyphenyl)-1-propanol | 98.81% | 3-(4-Hydroxyphenyl)-1-propanol (Dihydro-p-coumaryl alcohol) is a metabolite. 3-(4-Hydroxyphenyl)-1-propanol can be isolated from P. radiate callus cultures. 3-(4-Hydroxyphenyl)-1-propanol is associated with CAD activity. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
4-Hydroxybenzylamine (Standard) | ≥98% | 4-Hydroxybenzylamine (Standard) is the analytical standard of 4-Hydroxybenzylamine (HY-W004078). This product is intended for research and analytical applications. 4-Hydroxybenzylamine is a dimerizer and precursor. 4-Hydroxybenzylamine forms cyclic dimers stabilized by O-H/N hydrogen bonds and π-stacking interactions in solution. 4-Hydroxybenzylamine undergoes condensation with formaldehyde to form a 12-atom azacyclophane, facilitated by pre-organization into cyclic dimeric templates. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
4-Aminobenzyl alcohol | 99.95% | 4-Aminobenzyl alcohol is a self-eliminating linker. 4-Aminobenzyl alcohol can be used to synthesize the fluorescent probe MB-Van1 targeting Vanin-1. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
4-Ethylphenol (Standard) | 99.98% | 4-Ethylphenol (Standard) is the analytical standard of 4-Ethylphenol (HY-W012836). This product is intended for research and analytical applications. 4-Ethylphenol is a volatile phenolic compound associated with off-odour in wine. 4-Ethylphenol is a phenolic compound that can be synthesized by intestinal flora. 4-Ethylphenol will be converted to 4-ethylphenyl sulfate (HY-W674241) by Lactobacillus plantarum. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
1,4-Benzenedimethanol (Standard) | ≥98% | 1,4-Benzenedimethanol (Standard) is the analytical standard of 1,4-Benzenedimethanol. This product is intended for research and analytical applications. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Bengamin hydrochloride | Bengamin (4-(Aminomethyl)phenol) hydrochloride is a drug intermediate that can be used for the synthesis of benzylguanidine derivatives, and it possesses antibacterial activity. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. Lim EJ, et al. Anti-angiogenic, anti-inflammatory and anti-nociceptive activity of 4-hydroxybenzyl alcohol. J Pharm Pharmacol. 2007 Sep;59(9):1235-40. [Content Brief]
- [2]. Laschke MW, et al. In vitro and in vivo evaluation of the anti-angiogenic actions of 4-hydroxybenzyl alcohol. Br J Pharmacol. 2011 Jun;163(4):835-44. [Content Brief]
- [3]. Laschke MW, et al. 4-hydroxybenzyl alcohol: a novel inhibitor of tumor angiogenesis and growth. Life Sci. 2013 Jul 19;93(1):44-50. [Content Brief]
- [4]. Yu SS, et al. Neuroprotective effect of 4-hydroxybenzyl alcohol against transient focal cerebral ischemia via anti-apoptosis in rats. Brain Res. 2010 Jan 13;1308:167-75. [Content Brief]