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EPN

EPN

CAS:
2104-64-5
MF:
C14H14NO4PS
MW:
323.3

Properties

Melting point:
36℃
Boiling point:
371.1°C (estimate)
Density 
1.3 g/cm3
vapor pressure 
3,000 at 100 °C (quoted, Verschueren, 1983)
refractive index 
1.6021 (589.3 nm 25℃)
Flash point:
2 °C
storage temp. 
APPROX 4°C
solubility 
Miscible with acetone, benzene, methanol, isopropanol, toluene, and xylene (Windholz et al., 1983)
Water Solubility 
6.6 mg l-1 (20 °C, est.)
form 
solid
Merck 
13,3656
BRN 
2542580
Exposure limits
NIOSH REL: TWA 0.5 mg/m3, IDLH 5 mg/m3; OSHA PEL: TWA 0.5 mg/m3; ACGIH TLV: TWA 0.5 mg/m3.

Safety Information

Symbol(GHS) 

GHS06,GHS09
Signal word 
Danger
Hazard statements 
H300+H310-H410
Precautionary statements 
P262-P273-P280-P301+P310+P330-P302+P352+P310
Hazard Codes 
T+,N,Xn,F
Risk Statements 
27/28-50/53-36-20/21/22-11
Safety Statements 
22-36/37-45-60-61-16
RIDADR 
3018
OEB
C
OEL
TWA: 0.5 mg/m3 [skin]
WGK Germany 
3
RTECS 
TB1925000
HazardClass 
6.1(a)
PackingGroup 
II
Toxicity
LD50 in female, male rats (mg/kg): 7.7, 36 orally; 25, 230 dermal (Gaines)
IDLA
5 mg/m3

Use

Biological. From the first-order biotic and abiotic rate constants of EPN in estuarine water and sediment/water systems, the estimated biodegradation half-lives were 6.2 and 9.2 days, respectively (Walker et al., 1988). Soil. Though no products were reported, the half-life in soil is 15–30 days (Hartley and Kidd, 1987). Photolytic. EPN may undergo direct photolysis since the insecticide showed some absorption when a 1,4-dioxane was irradiated with UV light (l >290 nm) (Gore et al., 1971). Chemical/Physical. On heating, EPN is converted to the S-ethyl isomer (Worthing and Hance, 1991). Releases toxic fumes of phosphorus, nitrogen and sulfur oxides when heated to decomposition (Sax and Lewis, 1987; Lewis, 1990). Rapidly hydrolyzed in alkaline solutions to p-nitrophenol, alcohol and benzene thiophosphoric acid (Sittig, 1985).

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NitrendipineParathion-methylNimodipineParathionEPNDIMETHYL PHENYLPHOSPHONITE
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