OlivetolCAS：500-66-3

Potent Antimicrobial Activity

This compound exerts robust fungicidal and bactericidal effects against a broad spectrum of pathogenic microorganisms.

DNA Cleavage Mechanism at High Concentrations

At elevated dosage levels, it promotes DNA cleavage via Cu(II) chloride-mediated oxidative pathways, which occurs under conditions involving molecular oxygen.

Efficacy Against Retroviruses and Malignancies

Clinically validated data confirms its therapeutic effectiveness against retroviral infections such as HIV. Additionally, it has demonstrated significant inhibitory activity against various malignant tumors and carcinoma cell lines.

Physical Stability and Storage Requirements

The compound presents as a stable solid, ranging in color from colorless to beige. Standard storage conditions necessitate an inert atmospheric environment and protection from light exposure to preserve its integrity.

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Product Details

Potent Antimicrobial Properties of Olivetol

Olivetol possesses remarkable antimicrobial activity, exerting both fungicidal and bactericidal effects against a wide array of pathogenic microorganisms.

DNA Strand Scission Mechanism at Elevated Concentrations

Modern research has confirmed that at increased dosage levels, this 3,5-dihydroxypentylbenzene-derived compound is capable of inducing DNA strand scission. The underlying mechanism involves Cu(II) chloride-mediated oxidative cleavage pathways, which take place under conditions containing molecular oxygen

OlivetolCAS：500-66-3

Parameters

Melting point	46-48 °C(lit.)
Boiling point	164 °C
density	1.068±0.06 g/cm3(Predicted)
Fp	>230 °F
storage temp.	Keep in dark place,Inert atmosphere,Room temperature
solubility	Chloroform (Slightly), Methanol (Slightly)
form	Solid
pka	9.59±0.10(Predicted)
color	Colourless to Beige
Stability:	Light Sensitive
InChI	InChI=1S/C11H16O2/c1-2-3-4-5-9-6-10(12)8-11(13)7-9/h6-8,12-13H,2-5H2,1H3
InChIKey	IRMPFYJSHJGOPE-UHFFFAOYSA-N
SMILES	C1(O)=CC(CCCCC)=CC(O)=C1
CAS DataBase Reference	500-66-3(CAS DataBase Reference)
NIST Chemistry Reference	1,3-Benzenediol, 5-pentyl-(500-66-3)
EPA Substance Registry System	Olivetol (500-66-3)

Safety Information

Hazard Codes	Xi
Risk Statements	36/37/38
Safety Statements	26-36/39
WGK Germany	3
RTECS	VH2880000
HS Code	2907290090

Therapeutic Efficacy in Retroviral Infections and Malignancies

These distinct biochemical properties have paved the way for the clinical application of olivetol in treating retroviral infections—particularly human immunodeficiency virus (HIV)—as well as a broad range of malignant neoplasms and carcinomas. Its therapeutic effectiveness in these indications has been validated by clinical documentation.

OlivetolCAS：500-66-3