프로페탐포스

프로페탐포스
프로페탐포스 구조식 이미지
카스 번호:
31218-83-4
한글명:
프로페탐포스
동의어(한글):
프로페탐포스;(E)-3-(((에틸아미노)메톡시포스피노티오일)옥시)-2-부테노산-1-메틸에틸에스테르
상품명:
PROPETAMPHOS
동의어(영문):
Magget;blotic;deadmag;oms1502;san322i;SAN 322;VEL-4283;ent27989;SAFROTIN;(e)-este
CBNumber:
CB7478592
분자식:
C10H20NO4PS
포뮬러 무게:
281.31
MOL 파일:
31218-83-4.mol
MSDS 파일:
SDS

프로페탐포스 속성

녹는점
<25℃
끓는 점
bp0.005 87-89°
밀도
1.1294 g/cm3 (20 ºC)
증기압
1.9×10-3Pa (20°C)
굴절률
nD20 1.495
저장 조건
2-8°C
용해도
클로로포름(약간 용해됨), 메탄올(약간 용해됨)
수용성
110mg l-1(24°C)
산도 계수 (pKa)
0.94±0.70(Predicted)
Merck
13,7907
BRN
1979853
안정성
감광성, 수분 민감성
EPA
Propetamphos (31218-83-4)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 T,N
위험 카페고리 넘버 25-50/53
안전지침서 37-45-60-61
유엔번호(UN No.) 3018
WGK 독일 3
RTECS 번호 GQ4750000
위험 등급 6.1(b)
포장분류 II
HS 번호 29299090
유해 물질 데이터 31218-83-4(Hazardous Substances Data)
독성 LD50 orally in male rats: 82 mg/kg (Berg, Gothe)
기존화학 물질 KE-21661
유해화학물질 필터링 97-1-367
함량 및 규제정보 물질구분: 유독물질; 혼합물(제품)함량정보: 프로페탐포스 및 이를 1% 이상 함유한 혼합물
그림문자(GHS): GHS hazard pictogramsGHS hazard pictograms
신호 어: Danger
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H330 흡입하면 치명적임 급성 독성 물질 흡입 구분 1, 2 위험 GHS hazard pictograms P260, P271, P284, P304+P340, P310,P320, P403+P233, P405, P501
H410 장기적 영향에 의해 수생생물에 매우 유독함 수생 환경유해성 물질 - 만성 구분 1 경고 GHS hazard pictograms P273, P391, P501
예방조치문구:
P273 환경으로 배출하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.

프로페탐포스 C화학적 특성, 용도, 생산

개요

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.

화학적 성질

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.

용도

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).

일반 설명

Yellow oily liquid. Non corrosive. Used as an insecticide.

공기와 물의 반응

Water soluble.

반응 프로필

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.

건강위험

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.

농업용

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

상품명

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.

신진 대사 경로

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.

신진 대사

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.

프로페탐포스 준비 용품 및 원자재

원자재

준비 용품


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