| Identification | Back Directory | [Name]
PROPETAMPHOS | [CAS]
31218-83-4 | [Synonyms]
blotic
Magget
SAN 322
deadmag
oms1502
san322i
SAFROTIN
ent27989
(e)-este
VEL-4283
Safrotin MC
PROPETAMPHOS
safrotins200
'LGC' (1209)
SAFROTIN (TM)
E-Propetamphos
Propetamphos 0
Mules-n-Mark II
(e)-amidothioat
3-(((Ethylamino)me
Ectomort Centenary
Young's Summer Dip
SAFROTIN, 100MG, NEAT
Ectomort Jetting Fluid
Propetamphos Standard
Safrotin Brush-on Bait
PropetaMphos in acetone
Propetamphos Solution, 100ppm
propetamphos (bsi,iso,ansi,esa)
Safrotin (TM) 100mg [31218-83-4]
Ectomort Jetting Fluid and Sheep Dip
1-METHYL(E)-3-(((ETHYLAMINO)METHOXYPHOSPHINOTHIOYL)OXY.
1-METHETHYL(E)-3-(((ETHYLAMINO)METHOXYPHOSPHINOTHIOYL)OXY.
(e)-1-metiletil-3-(((etilamino)metoxifosfinotiol)oxi)-2-butenoato
trans-isopropyl-3-[[(ethylamino)methoxyphosphinothioyl]oxy]crotonate
3-(((ethylamino)methoxyphosphinothioyl)oxy)-2-butenoicaci1-methylethyl
crotonicacid,3-hydroxy-,isopropylester,o-esterwitho-methylethylphosphor
(E)-isopropyl 3-(((ethylaMino)(Methoxy)phosphorothioyl)oxy)but-2-enoate
(e)-1-methylethyl3-(((ethylamino)methoxyphosphinothioyl)oxy)-2-butenoate
1-methylethyl(e)-3-(((ethylamino)methoxyphosphinothioyl)oxy)-2-butenoate
(E)-3-[[(Ethylamino)(methoxy)phosphinothioyl]oxy]-2-butenoic acid isopropyl
o-(1-isopropoxycarbonyl-1-propen-2-yl)-o-methyln-ethyl-phosphoramidothionate
(E)-O,2-ISOPROPOXY-CARBONYL-1-METHYLVINYL-O-METHYL-ETHYL PHOSPHORAMIDOTHIOATE
(E)-3-[[(Ethylamino)(methoxy)phosphinothioyl]oxy]-2-butenoic acid isopropyl ester
2-Butenoic acid, 3-(ethylamino)methoxyphosphinothioyloxy-, 1-methylethyl ester, (2E)-
trans-isopropyl-3-[[(ethylamino)methoxyfosfinothioyl]oxy]crotonate isopropyl 3-[[(ethylamino)methoxyphosphinothioyl]oxy]isocrotonate propetamphos (ISO) | [EINECS(EC#)]
250-517-2 | [Molecular Formula]
C10H20NO4PS | [MDL Number]
MFCD00137384 | [MOL File]
31218-83-4.mol | [Molecular Weight]
281.31 |
| Chemical Properties | Back Directory | [Description]
Propetamphos technical is a yellowish, oily liquid at room temperature and a moderately
toxic acaricide and insecticide. It is sparingly soluble in water, but very soluble in acetone,
chloroform, ethanol, and hexane. U.S. EPA has classified propetamphos both as a GUP and
RUP, indicating that its handling should be done by certified, qualified, and applicators.
Propetamphos is used to control cockroaches, flies, ants, ticks, moths, fleas, and mosquitoes
in households and where vector eradication is necessary to protect public health. It
is also used in veterinary applications to combat parasites such as ticks, lice, and mites in
livestock. The formulations of propetamphos include aerosols, emulsified concentrates,
liquids, and powders. In veterinary applications, the insecticide is used for the control of
ticks, lice, and mites in livestock. Commercial products include aerosols, emulsified concentrates,
liquids, and powders. | [Melting point ]
<25℃ | [Boiling point ]
bp0.005 87-89° | [density ]
1.1294 g/cm3 (20 ºC) | [vapor pressure ]
1.9×10-3Pa (20°C) | [refractive index ]
nD20 1.495 | [storage temp. ]
APPROX 4°C
| [form ]
neat | [pka]
0.94±0.70(Predicted) | [Water Solubility ]
110 mg l-1(24°C) | [Merck ]
13,7907 | [BRN ]
1979853 | [EPA Substance Registry System]
Propetamphos (31218-83-4) |
| Hazard Information | Back Directory | [Chemical Properties]
Propetamphos technical is a yellowish, oily liquid at room temperature and a moderately
toxic acaricide and insecticide. It is sparingly soluble in water, but very soluble in acetone,
chloroform, ethanol, and hexane. The US EPA has classifi ed propetamphos as a GUP
and RUP, indicating that its handling should be done by certifi ed, qualifi ed applicators.
Propetamphos is used for the control of cockroaches, fl ies, ants, ticks, moths, fl eas, and
mosquitoes in households and where vector eradication is necessary to protect public
health. It is also used in veterinary applications to combat parasites, such as ticks, lice,
and mites in livestock. The formulations of propetamphos include aerosols, emulsifi ed
concentrates, liquids, and powders. Commercial products include aerosols, emulsifi ed
concentrates, liquids, and powders. | [General Description]
Yellow oily liquid. Non corrosive. Used as an insecticide. | [Air & Water Reactions]
Water soluble. | [Reactivity Profile]
An organophosphate derivative. Organophosphates are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides. Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides. | [Health Hazard]
Propetamphos is a moderately toxic organophosphate insecticide. It inhibits the cholinesterase
enzyme in animals and humans leading to overstimulation of the CNS. Prolonged
period of exposures to high concentrations of propetamphos cause poisoning with symptoms
that include, but are not limited to, nausea, headache, dizziness, confusion, numbness,
tingling sensations, incoordination, tremor, abdominal cramps, sweating, blurred
vision, breathing diffi culty, unconsciousness, and convulsions, slow heart beat, respiratory
paralysis, and death. There is no evidence to suggest that propetamphos causes mutagenic,
teratogenic, or carcinogenic effects in animals or humans. | [Uses]
Insecticide. | [Uses]
Propetamphos is used to control household and public health
pests, especially cockroaches, clothes moths and ants. It is also used for
the control of ectoparasites (mites, lice and ticks). | [Uses]
Propetamphos may be used as an analytical reference standard for the determination of the analyte in human tissues, fruits and crops by various chromatography techniques. | [Definition]
ChEBI: Propetamphos is a phosphoramidate ester, an organophosphate insecticide and an isopropyl ester. It has a role as an EC 3.1.1.7 (acetylcholinesterase) inhibitor and an agrochemical. It is functionally related to an isopropyl 3-hydroxybut-2-enoate. | [Agricultural Uses]
Fungicide, Insecticide: Propetamphos is used indoors for the control of structural insects, e. g., ants, cockroaches, fleas, and termites. It is applied in indoor residential, medical, commercial, and industrial buildings, and in food service | [Trade name]
BLOTIC®; OVIDIP®; SAFROTIN®[C]; SAN-52139®; SANDOZ®52139; SERAPHOS®; TSAR®; VEL-4283®; ZOECON® | [Carcinogenicity]
There was no significant treatment-
related increase in the incidence of any tumor type of
cancer among male rats given diets with 0, 6, 12, and 120 ppm
(0, 0.376, 0.632, and 5.891 mg/kg/day (males) and, 0, 0.412,
0.689, and 7.602 mg/kg/day (females), respectively) for
24 months . In females, there was an increase in
pancreatic islet cell adenomas at all dose levels compared
to controls. A significant decrease in body weight was
observed in both sexes at the high dose.
When propetamphos was administered to mice via the
diet at dose levels of 0, 0.5, 1.0, 6.0, and 21 mg/kg/day for
91 weeks, there was no apparent increase in the incidence of
tumors in either sex at dose levels that caused significant
cholinesterase inhibition . There was no adverse effect
on survival of males, but high-dose females had a higher
mortality rate than control females and a shorter survival
time. There were no adverse effects on body weight or bodyweight
gain in either sex. | [Metabolic pathway]
The major pathways of propetamphos detoxification in insect tissue and
in the mouse differ, with the principal route in insects being glutathione
conjugation but O-demethylation in the mouse. Oxidative or hydrolytic
cleavage of the P-O-crotonyl linkage to yield isopropyl acetoacetate,
which is hydrolysed and further metabolised to CO2, is also an important
route. As with mevinphos, which also contains a crotonyl ester group,
de-esterification is not an important detoxification route in animals
and no propetamphos carboxylic acid has been detected in the animal
experiments which have been reported. | [Metabolism]
Propetamphos administered in animals is rapidly
metabolized and excreted mainly via urine and exhaled
air. The major pathways of detoxication in mammals are
O-demethylation and cleavage of the P?O-vinyl linkage to
give isopropyl acetoacetate, which is finally metabolized
to carbon dioxide. Hydrolysis of the carboxylic ester bond
is also involved. Activation by oxidative desulfuration also
occurs. | [Degradation]
The hydrolytic DT50, values at pH 3, 6 and 9 were 11 days, 1 year and
41 days respectively. Propetamphos is stable to light and no degradation
was detected after 70 hours of exposure to sunlight (PM). | [Toxicity evaluation]
The acute oral LD50
for rats is 59.5–119 mg/kg. Inhalation LC50 (4 h) for rats
is 0.69 (female) and >1.5 (male) mg/L air. NOEL (2 yr) for
rats is 6 mg/kg diet (0.3 mg/kg/d). |
| Safety Data | Back Directory | [Hazard Codes ]
T,N | [Risk Statements ]
25-50/53 | [Safety Statements ]
37-45-60-61 | [RIDADR ]
3018 | [WGK Germany ]
3 | [RTECS ]
GQ4750000 | [HazardClass ]
6.1(b) | [PackingGroup ]
II | [HS Code ]
29299090 | [Safety Profile]
Poison by ingestion.
Moderately toxic by skin contact. When
heated to decomposition it emits very toxic
fumes of POx, SOx, and NOx. | [Hazardous Substances Data]
31218-83-4(Hazardous Substances Data) | [Toxicity]
LD50 orally in male rats: 82 mg/kg (Berg, Gothe) |
|
| Company Name: |
BEST-REAGENT
|
| Tel: |
400-1166-196 18981987031 |
| Website: |
http://www.hx-r.com/ |
|