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PROPETAMPHOS

Product Name
PROPETAMPHOS
CAS No.
31218-83-4
Chemical Name
PROPETAMPHOS
Synonyms
blotic;Magget;deadmag;oms1502;san322i;SAN 322;(e)-este;ent27989;VEL-4283;SAFROTIN
CBNumber
CB7478592
Molecular Formula
C10H20NO4PS
Formula Weight
281.31
MOL File
31218-83-4.mol
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PROPETAMPHOS Property

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. 
2-8°C
solubility 
Chloroform (Slightly), Methanol (Slightly)
Water Solubility 
110 mg l-1(24°C)
pka
0.94±0.70(Predicted)
Merck 
13,7907
BRN 
1979853
Stability:
Light Sensitive, Moisture Sensitive
EPA Substance Registry System
Propetamphos (31218-83-4)
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Safety

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
Hazardous Substances Data
31218-83-4(Hazardous Substances Data)
Toxicity
LD50 orally in male rats: 82 mg/kg (Berg, Gothe)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H330Fatal if inhaled

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
34371
Product name
Propetamphos
Purity
PESTANAL
Packaging
100mg
Price
$157
Updated
2024/03/01
TRC
Product number
P769600
Product name
Propetamphos(>85%)
Packaging
1g
Price
$605
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
48409
Product name
Propetamphos
Packaging
500mg
Price
$610
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
PST0000258
Product name
PROPETAMPHOS
Purity
95.00%
Packaging
5MG
Price
$501.38
Updated
2021/12/16
AHH
Product number
MT-58191
Product name
Propetamphos
Purity
98%
Packaging
1g
Price
$410
Updated
2021/12/16
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PROPETAMPHOS Chemical Properties,Usage,Production

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.

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.

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.

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.

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®

Safety Profile

Poison by ingestion. Moderately toxic by skin contact. When heated to decomposition it emits very toxic fumes of POx, SOx, and NOx.

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.

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).

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).

PROPETAMPHOS Preparation Products And Raw materials

Raw materials

Isopropyl acetoacetate (2-METHYL-1H-INDOL-3-YL)-OXO-ACETIC ACID ETHYL ESTER Tributylamine THIOPHOSPHORYL CHLORIDE Crotonic acid

Preparation Products

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View Lastest Price from PROPETAMPHOS manufacturers

Hebei Saisier Technology Co., LTD
Product
PROPETAMPHOS 31218-83-4
Price
US $6.00/KG
Min. Order
1KG
Purity
More than 99%
Supply Ability
2000KG/Month
Release date
2024-04-29
Hebei Jingbo New Material Technology Co., Ltd
Product
PROPETAMPHOS 31218-83-4
Price
US $8.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
200000
Release date
2023-11-28

31218-83-4, PROPETAMPHOSRelated Search:

FLUMIOXAZIN Tangeretin IODOFENPHOS Zirconyl chloride octahydrate PHOSPHAMIDON SAFROTIN (TM) SOLUTION 100UG/ML IN ACETONITRILE 1ML PROPETAMPHOS PESTANAL, 100 MG SAFROTIN (TM) SOLUTION 100UG/ML IN TOLUENE 1ML O,O-Dimethyl phosphoramidothioate PROPETAMPHOS safrotin

  • Propetamphos Solution, 100ppm
  • (e)-1-methylethyl3-(((ethylamino)methoxyphosphinothioyl)oxy)-2-butenoate
  • (e)-1-metiletil-3-(((etilamino)metoxifosfinotiol)oxi)-2-butenoato
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  • trans-isopropyl-3-[[(ethylamino)methoxyphosphinothioyl]oxy]crotonate
  • SAFROTIN, 100MG, NEAT
  • 2-Butenoic acid, 3-(ethylamino)methoxyphosphinothioyloxy-, 1-methylethyl ester, (2E)-
  • propetamphos (bsi,iso,ansi,esa)
  • trans-isopropyl-3-[[(ethylamino)methoxyfosfinothioyl]oxy]crotonate isopropyl 3-[[(ethylamino)methoxyphosphinothioyl]oxy]isocrotonate propetamphos (ISO)
  • 1-methylethyl(e)-3-(((ethylamino)methoxyphosphinothioyl)oxy)-2-butenoate
  • 3-(((ethylamino)methoxyphosphinothioyl)oxy)-2-butenoicaci1-methylethyl
  • blotic
  • crotonicacid,3-hydroxy-,isopropylester,o-esterwitho-methylethylphosphor
  • deadmag
  • ent27989
  • o-(1-isopropoxycarbonyl-1-propen-2-yl)-o-methyln-ethyl-phosphoramidothionate
  • 1-METHYL(E)-3-(((ETHYLAMINO)METHOXYPHOSPHINOTHIOYL)OXY.
  • 1-METHETHYL(E)-3-(((ETHYLAMINO)METHOXYPHOSPHINOTHIOYL)OXY.
  • (E)-3-[[(Ethylamino)(methoxy)phosphinothioyl]oxy]-2-butenoic acid isopropyl
  • (E)-3-[[(Ethylamino)(methoxy)phosphinothioyl]oxy]-2-butenoic acid isopropyl ester
  • VEL-4283
  • 3-(((Ethylamino)me
  • Propetamphos Standard
  • (E)-isopropyl 3-(((ethylaMino)(Methoxy)phosphorothioyl)oxy)but-2-enoate
  • Ectomort Centenary
  • Ectomort Jetting Fluid
  • Ectomort Jetting Fluid and Sheep Dip
  • E-Propetamphos
  • Magget
  • Mules-n-Mark II
  • Safrotin (TM) 100mg [31218-83-4]
  • oms1502
  • safrotins200
  • san322i
  • SAFROTIN
  • SAFROTIN (TM)
  • PROPETAMPHOS
  • Safrotin Brush-on Bait
  • Safrotin MC
  • SAN 322
  • Young's Summer Dip
  • PropetaMphos in acetone
  • 'LGC' (1209)
  • (E)-O,2-ISOPROPOXY-CARBONYL-1-METHYLVINYL-O-METHYL-ETHYL PHOSPHORAMIDOTHIOATE
  • Propetamphos 0
  • Propetamphos@1000 μg/mL in Methanol
  • PropetamphosSolution,100mg/L,1ml
  • Propetamphos Solution
  • PropetamphosSolution,1,000mg/L,1ml
  • PropetamphosSolution,1,000mg/L,2x.6ml
  • Propetamphos Solution in Acetonitrile, 1000μg/mL
  • Propetamphos (>85%)
  • Rimantadine Impurity 23
  • Propetamphos Solution in Methanol
  • 31218-83-4
  • C10H20NO4PS
  • INSECTICIDE