ChemicalBook >> CAS DataBase List >>PROPETAMPHOS

PROPETAMPHOS

CAS No.
31218-83-4
Chemical Name:
PROPETAMPHOS
Synonyms
Magget;blotic;deadmag;oms1502;san322i;SAN 322;VEL-4283;ent27989;SAFROTIN;(e)-este
CBNumber:
CB7478592
Molecular Formula:
C10H20NO4PS
Molecular Weight:
281.31
MDL Number:
MFCD00137384
MOL File:
31218-83-4.mol
Last updated:2023-11-28 19:11:11

PROPETAMPHOS Properties

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
FDA UNII G4A07F635U
Pesticides Freedom of Information Act (FOIA) Propetamphos
EPA Substance Registry System Propetamphos (31218-83-4)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS06,GHS09
Signal word  Danger
Hazard statements  H301+H311-H330-H410
Precautionary statements  P273-P280-P301+P310+P330-P302+P352+P312-P304+P340+P310
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
Toxicity LD50 orally in male rats: 82 mg/kg (Berg, Gothe)

PROPETAMPHOS price More Price(6)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 34371 Propetamphos PESTANAL 31218-83-4 100mg $157 2024-03-01 Buy
TRC P769600 Propetamphos(>85%) 31218-83-4 1g $605 2021-12-16 Buy
Medical Isotopes, Inc. 48409 Propetamphos 31218-83-4 500mg $610 2021-12-16 Buy
American Custom Chemicals Corporation PST0000258 PROPETAMPHOS 95.00% 31218-83-4 5MG $501.38 2021-12-16 Buy
AHH MT-58191 Propetamphos 98% 31218-83-4 1g $410 2021-12-16 Buy
Product number Packaging Price Buy
34371 100mg $157 Buy
P769600 1g $605 Buy
48409 500mg $610 Buy
PST0000258 5MG $501.38 Buy
MT-58191 1g $410 Buy

PROPETAMPHOS Chemical Properties,Uses,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

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

Insecticide.

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.

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).

PROPETAMPHOS Preparation Products And Raw materials

Global( 92)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Jingbo New Material Technology Co., Ltd
+8619931165850 hbjbtech@163.com China 1000 58
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
Hubei xin bonus chemical co. LTD
86-13657291602 linda@hubeijusheng.com CHINA 22968 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873 sales@chemdad.com China 39916 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418671 sales@tnjchem.com China 34572 58
AFINE CHEMICALS LIMITED
0571-85134551 info@afinechem.com CHINA 15377 58
Dayang Chem (Hangzhou) Co.,Ltd.
571-88938639 +8617705817739 info@dycnchem.com CHINA 52867 58
GIHI CHEMICALS CO.,LIMITED
+8618058761490 info@gihichemicals.com China 49999 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 57511 58

View Lastest Price from PROPETAMPHOS manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
PROPETAMPHOS pictures 2023-12-25 PROPETAMPHOS
31218-83-4
US $8.00 / kg 1kg 99% 200000 Hebei Jingbo New Material Technology Co., Ltd
  • PROPETAMPHOS pictures
  • PROPETAMPHOS
    31218-83-4
  • US $8.00 / kg
  • 99%
  • Hebei Jingbo New Material Technology Co., Ltd
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 Solution, 100ppm (e)-1-methylethyl3-(((ethylamino)methoxyphosphinothioyl)oxy)-2-butenoate (e)-1-metiletil-3-(((etilamino)metoxifosfinotiol)oxi)-2-butenoato (e)-amidothioat (e)-este 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 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