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Basic Information
CAS No.: 588-59-0
Name: STILBENE
Article Data: 851
Molecular Structure:
Molecular Structure of 588-59-0 (STILBENE)
Formula: C14H12
Molecular Weight: 180.249
Synonyms: Stilbene(8CI); 1,1'-(1,2-Ethenediyl)bis[benzene]; 1,2-Diphenylethene;1,2-Diphenylethylene; Bibenzal; Bibenzylidene; b-Phenylstyrene
Density: 1.044g/cm3
Melting Point: 123.85°C
Boiling Point: 307°Cat760mmHg
Flash Point: 128.5°C
Safety: Poison by intravenous route. Moderately toxic by intraperitoneal route. Violent reaction with O2. When heated to decomposition it emits acrid smoke and irritating fumes.
PSA: 0.00000
LogP: 3.85700
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Chemistry

IUPAC Name: Stilbene
Synonyms of  Stilbene (CAS NO.588-59-0) : 1,1'-(1,2-Ethenediyl)bis[benzene] ; 1,1'-(E)-Ethene-1,2-diyldibenzene ; 1,1'-(Ethene-1,2-diyl)dibenzene ; 1,1'-[(E)-1,2-Ethendiyl]dibenzol
CAS NO: 588-59-0
Molecular Formula  : C14H12
Molecular Weight  :180.25
Molecular Structure of Stilbene :
Index of Refraction: 1.658
Surface Tension: 42.9 dyne/cm
Density: 1.044 g/cm3
Flash Point: 128.5 °C
Enthalpy of Vaporization: 52.57 kJ/mol
Boiling Point: 307 °C at 760 mmHg
Vapour Pressure: 0.00135 mmHg at 25°C

Uses

1. Stilbene (CAS NO.588-59-0) is used in manufacture of dyes and optical brighteners, and also as a phosphor and a scintillator.
2 Stilbene (CAS NO.588-59-0) is one of the gain mediums used in dye lasers.
3.Many stilbene derivates (stilbenoids) are present naturally in plants. An example is resveratrol and its cousin, pterostilbene.
4.Stilbene derivatives especially E(trans) isomer have estrogenic activity so used in making non-steroidal synthetic estrogens as Diethyl stilbestrol, Fosfosterol, Dienesterol

Toxicity Data With Reference

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intraperitoneal 1150mg/kg (1150mg/kg)   Arzneimittel-Forschung. Drug Research. Vol. 19, Pg. 617, 1969.
mouse LD50 intravenous 34mg/kg (34mg/kg)   Arzneimittel-Forschung. Drug Research. Vol. 19, Pg. 617, 1969.

 

Consensus Reports

Reported in EPA TSCA Inventory.

Safety Profile

Poison by intravenous route. Moderately toxic by intraperitoneal route. Violent reaction with O2. When heated to decomposition it emits acrid smoke and irritating fumes.