CAS 623-05-2|4-Hydroxybenzyl alcohol

Introduction:Basic information about CAS 623-05-2|4-Hydroxybenzyl alcohol, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common Name4-Hydroxybenzyl alcohol
CAS Number623-05-2Molecular Weight124.137
Density1.2±0.1 g/cm3Boiling Point252.0±0.0 °C at 760 mmHg
Molecular FormulaC7H8O2Melting Point114-122 °C(lit.)
MSDSChineseUSAFlash Point145.8±15.0 °C
Symbol
GHS07
Signal WordWarning

Names

Namep-hydroxybenzyl alcohol
SynonymMore Synonyms

4-Hydroxybenzyl alcohol BiologicalActivity

Description4-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].
Related CatalogSignaling Pathways >>Apoptosis >>ApoptosisResearch Areas >>CancerResearch Areas >>Inflammation/ImmunologyResearch Areas >>Neurological DiseaseNatural Products >>Phenols
In Vitro4-Hydroxybenzyl alcohol inhibits proliferation of eEND2 cells and suppresses the migration of eEND2 cells, accompanied by inhibition of actin filament reorganization[2]. 4-Hydroxybenzyl alcohol induces apoptotic death of tumor cells[3].
In Vivo4-Hydroxybenzyl alcohol possesses antiangiogenic, anti-inflammatory and anti-nociceptive activity possibly via its down-regulating activity on NO production[1]. 4-Hydroxybenzyl alcohol (200 mg/kg) efficiently inhibits growth and angiogenesis of developing tumors[3]. 4-Hydroxybenzyl alcohol ameliorates ischemic injury induced by transient focal cerebral ischemia in rats, and this neuroprotective effect may be partly related to attenuate apoptosis pathway[4].
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.

[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.

[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.

[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.

Chemical & Physical Properties

Density1.2±0.1 g/cm3
Boiling Point252.0±0.0 °C at 760 mmHg
Melting Point114-122 °C(lit.)
Molecular FormulaC7H8O2
Molecular Weight124.137
Flash Point145.8±15.0 °C
Exact Mass124.052429
PSA40.46000
LogP0.30
Vapour Pressure0.0±0.5 mmHg at 25°C
Index of Refraction1.596
InChIKeyBVJSUAQZOZWCKN-UHFFFAOYSA-N
SMILESOCc1ccc(O)cc1
Storage condition2-8°C

Safety Information

Symbol
GHS07
Signal WordWarning
Hazard StatementsH319
Precautionary StatementsP305 + P351 + P338
Personal Protective Equipmentdust mask type N95 (US);Eyeshields;Gloves
Hazard CodesXi: Irritant;
Risk PhrasesR36/37/38
Safety PhrasesS26-S24/25
RIDADRNONH for all modes of transport
WGK Germany3
RTECSDA4796800
HS Code29072900

Customs

HS Code2907299090
Summary2907299090 polyphenols; phenol-alcohols。supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward)。VAT:17.0%。tax rebate rate:9.0%。MFN tariff:5.5%。general tariff:30.0%

Articles31

More Articles
Convenient QSAR model for predicting the complexation of structurally diverse compounds with β-cyclodextrins

Bioorg. Med. Chem. 17 , 896-904, (2009)

This paper reports a QSAR study for predicting the complexation of a large and heterogeneous variety of substances (233 organic compounds) with beta-cyclodextrins (beta-CDs). Several different theoret...

High tolerance and physiological mechanism of Zymomonas mobilis to phenolic inhibitors in ethanol fermentation of corncob residue.

Biotechnol. Bioeng. 112 , 1770-82, (2015)

Corncob residue as the lignocellulosic biomass accumulated phenolic compounds generated from xylitol production industry. For utilization of this biomass, Zymomonas mobilis ZM4 was tested as the ethan...

Predicting the substrate specificity of a glycosyltransferase implicated in the production of phenolic volatiles in tomato fruit.

FEBS J. 278(2) , 390-400, (2011)

The volatile compounds that constitute the fruit aroma of ripe tomato (Solanum lycopersicum) are often sequestered in glycosylated form. A homology-based screen was used to identify the gene SlUGT5, w...

Synonyms

4-(Hydroxymethyl)benzolol
(4-Hydroxyphenyl)methanol
Gastrodigenin
p-Methylolphenol
4-hydroxymethyl-phenol
PARA-ALCOHOLPHENOL
4-Hydroxybenzyl alcohol
4-hydroxybenzyl-alcohol
Benzyl alcohol, p-hydroxy- (8CI)
p-(Hydroxymethyl)phenol
p-Hydroxybenzyl
4-(Hydroxymethyl)phenol
RARECHEM AL BD 0098
EINECS 210-768-0
Benzenemethanol, 4-hydroxy-
Benzyl alcohol, p-hydroxy-
4-METHYLOLPHENOL
benzyl alcohol, 4-hydroxy-
P-HYDROXYBENZYL ALCOHOL
MFCD00004658
4-HYDROXY-BENZYL-ALCOHOL
α-Hydroxy-p-cresol
FEMA 3987
Bisoprolol Impurity 19
CAS 946219-29-0|N-(3-chloro-2-methylphenyl)-2-((2-oxo-1-(pyridin-4-ylmethyl)-2,5,6,7-tetrahydro-1H-c
CAS 3588-17-8|trans,trans-Muconic Acid
Recommended......
TOP